UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 10-K
(Mark One)
☒
ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the fiscal year ended December 31, 2024
OR
☐
TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the transition period from
to
Commission File Number 001-37894
FULGENT GENETICS, INC.
(Exact name of registrant as specified in its charter)
Delaware
81-2621304
(State or other jurisdiction of
incorporation or organization)
(I.R.S. Employer
Identification No.)
4399 Santa Anita Avenue
El Monte, CA
91731
(Address of principal executive offices)
(Zip Code)
Registrant’s telephone number, including area code: (626) 350-0537
Securities registered pursuant to Section 12(b) of the Act:
Title of each class
Trading Symbol(s)
Name of each exchange on which registered
Common Stock, par value $0.0001 per share
FLGT
The Nasdaq Stock Market
(Nasdaq Global Market)
Securities registered pursuant to Section 12(g) of the Act: None
Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act. YES ☐ NO ☒
Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Act. YES ☐ NO ☒
Indicate by check mark whether the registrant: (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of
1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such
filing requirements for the past 90 days. YES ☒ NO ☐
Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405
of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit
such files). YES ☒ NO ☐
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or
an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging
growth company” in Rule 12b-2 of the Exchange Act.
Large accelerated filer
☐
Accelerated filer
☒
Non-accelerated filer
☐
Smaller reporting company
Emerging growth company
☐
☐
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any
new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Indicate by check mark whether the registrant has filed a report on and attestation to its management’s assessment of the effectiveness of its internal
control over financial reporting under Section 404(b) of the Sarbanes-Oxley Act (15 U.S.C. 7262(b)) by the registered public accounting firm that
prepared or issued its audit report. ☒
If securities are registered pursuant to Section 12(b) of the Act, indicate by check mark whether the financial statements of the registrant included in
the filing reflect the correction of an error to previously issued financial statements. ☐
Indicate by check mark whether any of those error corrections are restatements that required a recovery analysis of incentive-based compensation
received by any of the registrant’s executive officers during the relevant recovery period pursuant to § 240.10D-1(b). ☐
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Act). YES ☐ NO ☒
The aggregate market value of the registrant’s voting and non-voting common equity held by non-affiliates as of June 30, 2024 (computed by
reference to the price at which the registrant’s common stock was last sold on June 28, 2024, the last business day of the registrant’s most recently
completed second fiscal quarter, as reported by the Nasdaq Global Market) was approximately $325.6 million. For purposes of this calculation, it has
been assumed that all shares of the registrant’s common stock held by directors, executive officers and persons beneficially owning 5% or more of
the registrant’s common stock are held by affiliates; however, the treatment of these persons as affiliates for purposes of this calculation is not, and
shall not be considered, a determination as to whether such persons are affiliates of the registrant for any other purpose.
As of February 24, 2025, there were 30,829,454 outstanding shares of the registrant’s common stock.
DOCUMENTS INCORPORATED BY REFERENCE
Certain portions of the registrant’s definitive proxy statement for its 2025 annual meeting of stockholders are incorporated by reference in Part III of
this report.
TABLE OF CONTENTS
Page
Cautionary Note Regarding Forward-Looking Statements..........................................................................................................
i
PART I
1
Item 1.
Business ..................................................................................................................................................................
1
Item 1A.
Risk Factors.............................................................................................................................................................
28
Item 1B.
Unresolved Staff Comments...................................................................................................................................
68
Item 1C.
Cybersecurity ..........................................................................................................................................................
68
Item 2.
Properties ................................................................................................................................................................
71
Item 3.
Legal Proceedings...................................................................................................................................................
71
Item 4.
Mine Safety Disclosures .........................................................................................................................................
71
PART II
72
Item 5.
Market for Registrant’s Common Equity, Related Stockholder Matters and Issuer Purchases of Equity
Securities.................................................................................................................................................................
72
Item 6.
[Reserved] ..............................................................................................................................................................
73
Item 7.
Management’s Discussion and Analysis of Financial Condition and Results of Operations.................................
74
Item 7A.
Quantitative and Qualitative Disclosures About Market Risk................................................................................
85
Item 8.
Financial Statements and Supplementary Data ......................................................................................................
87
Item 9.
Changes in and Disagreements with Accountants on Accounting and Financial Disclosure.................................
87
Item 9A.
Controls and Procedures .........................................................................................................................................
87
Item 9B.
Other Information ...................................................................................................................................................
89
Item 9C.
Disclosure Regarding Foreign Jurisdictions that Prevent Inspections....................................................................
89
PART III
90
Item 10.
Directors, Executive Officers and Corporate Governance......................................................................................
90
Item 11.
Executive Compensation.........................................................................................................................................
90
Item 12.
Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters...............
90
Item 13.
Certain Relationships and Related Transactions, and Director Independence .......................................................
90
Item 14.
Principal Accountant Fees and Services.................................................................................................................
90
PART IV
91
Item 15.
Exhibits and Financial Statement Schedules ..........................................................................................................
91
Item 16.
Form 10-K Summary ..............................................................................................................................................
91
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CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS
This report contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended,
or the Securities Act, and Section 21E of the Securities Exchange Act of 1934, as amended, or the Exchange Act. Forward-looking
statements are statements other than historical facts and relate to future events or circumstances or our future performance, and they
are based on our current assumptions, expectations and beliefs concerning future developments and their potential effect on our
business. The words “believe,” “may,” “will,” “potentially,” “estimate,” “continue,” “anticipate,” “intend,” “could,” “would,”
“project,” “plan,” “expect,” “possible,” “likely,” “probable,” and similar expressions that convey uncertainty of future events or
outcomes identify forward-looking statements.
The forward-looking statements in this report include statements about, among other things:
•
developments, projections, and trends relating to us, our competitors, and our industry;
•
our plans for our business;
•
our ability to integrate any acquired businesses and technologies and to realize the value of any acquired entities, joint
ventures, or investments;
•
our operating performance, including our ability to stabilize the historical fluctuations in our performance and to achieve,
maintain, or grow profitability;
•
the rate and degree of market acceptance and adoption of our tests and testing services and other anticipated trends in our
industry;
•
our competitive advantages and our ability to remain competitive, particularly if the testing markets continue to expand,
and competition becomes more acute;
•
our ability to continue to expand our test menu and introduce other improvements to our tests;
•
our continued ability to offer affordable pricing for our tests, to maintain the low internal costs of our business model, and
to record acceptable margins on our sales;
•
the timing and our ability to develop our drug candidates, to satisfy the U.S. Food and Drug Administration’s, or FDA’s,
regulatory requirements, and to commercialize our drug candidates;
•
the anticipated progress of our drug candidate development programs, including whether our ongoing and potential future
clinical trials will achieve clinically relevant results;
•
our ability to generate data and conduct analyses to support the regulatory approval of our drug candidates and our plans
to pursue discussions with regulatory authorities, and the anticipated timing, scope and outcome of related regulatory
actions or guidance;
•
the success of our competitors’ research and development efforts for drug candidates seeking to treat similar or the same
indication as our drug candidates;
•
our ability to strengthen our existing base of customers by maintaining or increasing demand from these customers;
•
our ability to grow and diversify our customer base;
•
our reliance on a limited number of suppliers and their ability to adapt to possible disruptions in their operations;
•
our use of our laboratory facilities and our ability to adapt in the event we need to relocate or in the event any of our
facilities are damaged or rendered inoperable;
•
our plans for future sales and marketing efforts;
•
advancements in technology by us and our competitors;
•
our use of technology and ability to prevent security breaches; unauthorized use or disclosure of health information,
personal information, or sensitive personal information; loss of data; and other disruptions;
•
our ability to effectively manage any growth we may experience, including expanding our infrastructure, developing
increased efficiencies in our operations, and hiring additional skilled personnel in order to support any such growth;
•
developments with respect to U.S. and foreign laws and regulations applicable to our business, and our ability to comply
with these regulations, and the results or potential liability associated with disclosure pursuant to any voluntary disclosure
process by and between us and applicable regulatory agencies and bodies;
•
our ability to effectively respond to the results of payor audits and government audits and investigations, such as our
currently ongoing U.S. Department of Health Resources and Services Administration, or HRSA, audit and Civil
Investigative Demands, or CIDs;
•
our ability to prevent errors in interpreting the results of our tests so as to avoid product liability and professional liability
claims;
•
our ability to obtain and maintain coverage and adequate reimbursement for our tests and to manage the complexity of
billing and collecting such reimbursement;
•
the state of the U.S. and foreign healthcare markets, including the role of governments in the healthcare industry,
generally, pressures or incentives to reduce healthcare costs while expanding individual benefits, and the impact of
general uncertainty in the U.S. healthcare regulatory environment;
•
our ability to attract, retain, and motivate key scientific and management personnel;
ii
•
our ability to obtain and maintain protection of our trade secrets, licensed intellectual property, patent rights, and other
intellectual property rights and to not infringe upon the rights of others;
•
our expectations regarding inflation and our future expense levels and our ability to appropriately forecast and plan our
expenses;
•
our expectations regarding our future capital requirements and our ability to obtain additional capital if and when needed;
and
•
the impact of the above factors and other future events on the market price of our common stock.
These forward-looking statements are subject to a number of risks and uncertainties, including, among others, those described
under Item 1A, “Risk Factors” and elsewhere in this report. Moreover, we operate in a competitive and rapidly evolving industry, and
new risks emerge from time to time. It is not possible for us to predict all of the risks we may face, nor can we assess the impact of all
factors on our business or the extent to which any factor or combination of factors could cause actual results to differ from our
expectations. In light of these risks and uncertainties, the forward-looking events and circumstances described in this report may not
occur, and actual results could differ materially and adversely from those described in or implied by any forward-looking statements
we make. Although we have based our forward-looking statements on assumptions and expectations that we believe are reasonable,
we cannot guarantee future results, levels of activity, performance or achievements, or other future events. As a result, forward-
looking statements should not be relied on or viewed as predictions of future events, and this report should be read with the
understanding that our actual future results, levels of activity, performance and achievements, or other future events may be materially
different than what we currently expect.
The forward-looking statements in this report speak only as of the date of this document, and except as required by law, we
undertake no obligation to update publicly any forward-looking statements for any reason after the date of this report to conform these
statements to actual results or to changes in our expectations.
We qualify all of our forward-looking statements by this cautionary note.
* * * * * * *
We own registered or unregistered trademark rights to FULGENT®, PICTURE GENETICS®, BEACON®, INFORMDX®,
LUMERA®, and our company name and logo. Any other service marks, trademarks and trade names appearing in this report are the
property of their respective owners. We do not use the ® or ™ symbol in each instance in which one of our trademarks appears in this
report, but this should not be construed as any indication that we will not assert our rights thereto to the fullest extent under
applicable law.
Fulgent Genetics, Inc., together with its subsidiaries and affiliated professional corporations with which the Company has a
management services arrangement, are collectively referred to in this Annual Report on Form 10-K as the “Company,” “Fulgent,”
“we,” “us,” and “our.”
1
PART I
Item 1. Business.
Overview
We are a technology-based company with a well-established laboratory services business and a therapeutic development
business. Our laboratory services business includes technical laboratory and testing services and professional interpretation of
laboratory results by licensed physicians. Our therapeutic development business is focused on developing drug candidates for treating
a broad range of cancers using a novel nanoencapsulation and targeted therapy platform designed to improve the therapeutic window
and pharmacokinetic profile, or PK profile, of new and existing cancer drugs.
Mission and Vision
Founded in 2011, Fulgent began with two simple ideas: flexibility and affordability. We offer and develop flexible and
affordable diagnostic and genetic tests and laboratory services designed to improve patient care and quality of life. We strive to
provide the most effective and wide-ranging genetic and diagnostic testing menu on the market. Our long-term vision is to transform
from a diagnostic business into a fully integrated precision medicine company.
Our Laboratory Services Business
We have broad testing capabilities with a testing and testing services menu that is scalable and affordable to our customers. Our
testing services include:
Comprehensive anatomic pathology testing services, including gastrointestinal pathology, dermatopathology, urologic
pathology, breast pathology, neuropathology, and hematopathology. These services are supported by our expansive geographic
presence with Clinical Laboratory Improvement Amendments of 1988, or CLIA, licensed laboratories in the United States.
Precision diagnostics testing services, including next-generation sequencing, or NGS, tests for biopharma research and
clinical tests for rare disease, hereditary cancer, reproductive health, and many other disease subtypes. Our precision diagnostic testing
also includes specialized oncology services that utilize a wide array of technologies. These services include flow cytometry;
cytogenetic analysis; fluorescence in-situ, or FISH; immunohistochemistry; molecular genetics; NGS; and consultations in
hematopathology and surgical pathology.
We also offer testing services to pharmaceutical or biotech companies, contract research organizations, or CROs, or
sponsored testing programs, which we call BioPharma services.
Picture is a patient-centric telemedicine platform that prioritizes patient convenience and education, giving
consumers the power to initiate testing and access to clinical support. Picture tests help individuals identify important health markers
to empower their personal health journey.
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Our Laboratory Services Technology Platform
Our proprietary technology platform for our laboratory services business includes proprietary gene probes, data suppression and
comparison algorithms, adaptive learning software, and proprietary laboratory information management systems. This platform
provides a broad test menu, the ability to rapidly develop and launch new tests, customizable test offerings, lower cost per test, and
high efficiency. As an example, this technology platform allowed us to rapidly respond to the 2019 novel coronavirus disease, or
COVID-19, pandemic and scale our business to provide COVID-19 tests with reliable results and rapid turnaround time in a way that
surpassed even our largest competitors. We are proud that through this effort we supplied approximately 19.4 million COVID-19 tests
from 2020 through 2023.
Our Therapeutic Development Business - Fulgent Pharma
In 2022, we completed our acquisition of Fulgent Pharma Holdings, Inc., or Fulgent Pharma. Our efforts at Fulgent Pharma are
based on a novel nano-drug delivery platform technology capable of delivering various water insoluble or poorly soluble drugs. Nano-
drug delivery, or nanoencapsulation, refers to a technology where active pharmaceuticals are encapsulated within miniature capsules
to protect and control the release of these pharmaceuticals in a targeted manner. Unlike other nano drug delivery materials such as
Human Serum Albumin, which is only soluble in water, our nano-drug delivery materials used for our drug candidates in development
are soluble not only in water, but also in various organic solvents, as well as capable of hot melt mixing with active pharmaceutical
ingredients, or APIs. We believe these advantages will allow us to generate a much broader range of drug candidate formulations,
particularly amorphous drug candidate formulations, which can be used for both intravenous, or IV, and oral formulations with a goal
to improve the PK profile, as well as safety and efficacy, for encapsulated drugs and therapeutics.
The goal of our nano-drug delivery platform is to develop drug candidates to treat various diseases for which we believe the
current standard of care is inadequate or may be improved. The target markets for these drug candidates are large and well-established,
as shown in the figures below:
Note: U.S. opportunity shown
Sources: Evaluate Pharma, Wall Street research, and management pricing expectations
1.
Head & Neck, or H&N, market opportunity for both 2nd line and 3rd line therapy
2.
Ampullary market opportunity for 2nd line therapy
3
Our current research and development progress for certain of our candidates and assets is shown in the pipeline chart below.
Our Laboratory Services Customers
We currently classify our customers in our laboratory services business by their payor types: (i) Insurance; (ii) Institutional,
including hospitals, medical institutions, other laboratories, governmental bodies, payors, municipalities, and large corporations; and
(iii) Patients who pay directly. Typically, we bill our Institutional customers for our tests, and testing services, and they are responsible
for paying us directly. A small percentage of our customers are patients, who elect to pay for tests or testing services themselves with
out-of-pocket payments after their physicians have ordered our tests or testing services.
We consider each single billing and paying unit to be an individual customer, even though a unit may represent multiple
physicians and healthcare providers ordering tests and testing services. Aggregating customers that are under common control, one of
our customers contributed $62.6 million or 22% of our total revenue in 2024, and $35.7 million or 12% of our total revenue in 2023.
Laboratory Services Sales and Marketing
Our sales and marketing force for our laboratory services business currently consists of internal teams of sales and marketing
professionals, respectively, with deep experience in our industry, as well as a network of primarily U.S. field-based sales
representatives who are knowledgeable about our tests and testing services. Historically, we have significantly relied on organic
growth and word-of-mouth among our customers to generate interest in our tests, which we believe demonstrates the value of our
offerings. In recent years, we have invested significant time and capital to strengthen our sales and marketing efforts, including
increasing the size and restructuring the organization of our internal team, re-focusing our initiatives and strategies, and increasing the
overall scope of our marketing activities. On a regular basis, we continue to evaluate the need to grow the size of our sales team and
marketing resources.
Laboratory Services Research and Development
We have assembled a highly qualified team with expertise in a number of fields important to our business, such as
bioinformatics, genetics, software engineering, laboratory management, drug development, and sales and marketing. This team
conducts all of our research and development activities related to our laboratory services business, including efforts to develop and
curate our expansive library of genetic information and further expand our testing and testing services technology platform.
Fulgent Pharma-Pre-Clinical Studies and Clinical Trials
FID-007 Phase 1/1b Clinical Trial
FID-007, nanoencapsulated paclitaxel, is currently being investigated in the United States to treat patients diagnosed with
various cancers including H&N, ampullary, and pancreatic cancer. We have released preliminary data and completed enrollment for a
Phase1/1b dose escalation/expansion clinical trial for evaluation of FID-007 in treating patients diagnosed with advanced solid tumors.
This Phase 1/1b is being conducted at clinical trial sites in the United States and has enrolled 50 patients. In this trial and to date, we
observed FID-007 to have a manageable safety profile and observed preliminary evidence of anti-tumor activity in heavily pre-treated
patients across various tumor types. The PK observed was linear, dose proportional, and comparable to that of nab paclitaxel. No
neuropathy above grade two was observed.
FID-007 Phase 2 Clinical Trial
We began enrollment of a Phase 2, randomized, multi-center, open-label trial of FID-007 in patients with recurrent or metastatic
H&N squamous cell carcinoma at various sites in the United States in the second quarter of 2024. Up to 46 patients will be randomly
assigned (1:1) to one of two treatment arms: Arm A: FID-007 (75 mg/m2) plus cetuximab or Arm B: FID-007 (125 mg/m2) plus
4
cetuximab. We expect to complete the trial by early 2026. We currently anticipate releasing preliminary data for this trial in or around
June 2025 and final results in or around June 2026. Assuming favorable results, we plan to investigate FID-007 in a Phase 3
registrational clinical trial in patients diagnosed with H&N squamous cell carcinoma, and potentially seek regulatory approval in the
United States through the 505(b)(2) pathway, which may shorten the clinical trial process and accelerate potential commercialization.
FID-022 and ADC Pre-Clinical Development
We are also continuing to engage in other clinical and preclinical development utilizing our nano-drug delivery platform. In our
preclinical studies, we observed our second drug candidate, FID-022, nanoencapsulated SN38, to have superior efficacy over
irinotecan in various xenograft cancer models, including colon, bile duct, ovarian, and pancreatic cancers, with no significant
unexpected toxicity observed in both rat and monkey Good Laboratory Practice, or GLP, toxicity studies. We plan to next evaluate
FID-022 in a Phase 1/1b clinical trial in patients diagnosed with these cancers. The IND for this trial was cleared by the FDA in
January 2025. In connection with this trial, we plan to enroll 42 patients at sites located in the United States and to begin dosing
patients for this trial in mid-2025.
In addition, we have also made a significant advancement in development of antibody drug conjugates, or ADCs, using our
novel patented linker and payload platform technology. In preclinical studies, we observed our ADC to have better efficacy over
different tumors with a broad range of target antigens expression level compared with some of the best ADC benchmarks on the
market in preclinical studies. In the meantime, ADCs honing to novel targets using our novel platform technology are also being
prepared with the goal of generating leading candidates for clinical studies.
Our Suppliers
We rely on a limited number of suppliers for certain laboratory substances used in the chemical reactions incorporated into our
tests and testing services, which we refer to as reagents, as well as for the sequencers and various other equipment and materials we
use in our laboratory operations. In particular, we rely on Illumina, Inc., or Illumina, as the sole supplier of the next generation
sequencers and associated reagents we use to perform our genetic tests and as the sole provider of maintenance and repair services for
these sequencers; on Roche Holdings AG for certain laboratory equipment, supplies, and services for our immunohistochemistry
services; on Beckman Coulter Diagnostics for certain laboratory equipment, supplies, and services for our flow cytometry tests and
testing services; on Leica Biosystems for an automated digital scanning solution to scale up digital pathology operations; and on
Abbott Laboratories for certain laboratory equipment, supplies, and services for our FISH tests and testing services. Additionally, our
therapeutic development business relies on ANP Technologies, Inc. for certain laboratory services, equipment, tools, and drug
intermediates in connection with our research and development efforts. While there are several sequencer suppliers that we believe
could replace Illumina, and while we believe that we have sufficient alternative suppliers for our other needs, our laboratory
operations or therapeutic development efforts could be interrupted if we encounter delays or difficulties in connection with securing
these supplies, services, reagents, sequencers, other equipment, materials, or maintenance and repair services, which could occur for a
variety of reasons, including if we need a replacement or temporary substitute for any of our limited or sole suppliers and are not able
to locate and make arrangements with an acceptable replacement or temporary substitute.
Competition
Our competitors for our laboratory services business include dozens of companies focused on pathology, genetic, and diagnostic
testing services, including specialty and reference laboratories that offer traditional single-gene and multi-gene tests and other
diagnostic test providers. Principal competitors include companies such as Ambry Genetics Corporation, a subsidiary of Tempus AI,
Inc.; Baylor Genetics Management, LLC; Caris Life Sciences, LLC; Exact Sciences Corporation; Foundation Medicine, Inc.; GeneDx
Holdings Corp.; Guardant Health, Inc.; Laboratory Corporation of America Holdings; Myriad Genetics, Inc.; Natera, Inc.;
NeoGenomics, Inc.; PerkinElmer, Inc.; Quest Diagnostics Incorporated; Tempus AI, Inc.; and other commercial and academic
laboratories. Other established and emerging healthcare, information technology, and service companies may develop and sell
competitive tests, which may include informatics analysis, integrated genetic tools, and services for health and wellness. We also
expect to compete in the future with certain developers of traditional in vitro diagnostic test products, which are often packaged as
commercial kits and sold for use in clinical laboratories, due to complex ongoing legal and regulatory reforms occurring in both the
United States and the European Union for in vitro testing products, among other marketplace changes.
Additionally, participants in closely related markets, such as prenatal testing and clinical trial or companion diagnostic testing,
could converge on offerings that are competitive with the type of tests we perform. Our principal competitors in this space include
companies such as Laboratory Corporation of America Holdings; Natera, Inc.; Myriad Genetics, Inc.; Quest Diagnostics Incorporated;
and other commercial and academic laboratories. Instances where potential competitors are aligned with key suppliers or are
themselves suppliers could provide these potential competitors with significant advantages. Further, hospitals, research institutions,
and eventually individual physicians and other practitioners may also seek to perform at their own facilities the type of genetic or
diagnostic testing we would otherwise perform for them. In this regard, continued development of, and potential associated relative
5
decreases in the cost of, equipment, reagents, and other materials and databases and genetic data interpretation services may enable
broader direct participation in genetic testing and analysis and drive down the use of third-party testing companies such as ours.
Moreover, cost decreases and increased direct participation, as well as cost-saving initiatives on the part of government entities and
other insurance payors could intensify the downward pressure on the price for genetic analysis and interpretation generally. Moreover,
the clinical diagnostic testing field continues to undergo significant consolidation, permitting larger clinical laboratory service
providers to increase cost efficiencies and service levels and potentially resulting in more intense competition. The development and
commercialization of new drug candidates is highly competitive. Our competitors include drug delivery platform companies and
505(b)(2) drug developers in the cancer therapeutics area. Principal competitors include companies making nano drugs such as
Bristol-Myers Squibb, academic research institutions, government agencies, and various other public and private research institutions.
We believe we compare favorably with our competitors. However, many of our competitors have longer operating histories;
larger customer bases; more expansive brand recognition; established manufacturing capabilities and facilities; deeper market
penetration; substantially greater financial, technological, research and development resources and selling and marketing capabilities;
and considerably more experience dealing with insurance payors. As a result, they may be able to respond more quickly to changes in
customer requirements or preferences, develop faster and better advancements for their technologies, product candidates and tests,
create and implement more successful strategies for the promotion and sale of their tests, obtain more favorable results from insurance
payors regarding coverage and reimbursement for their offerings, adopt more aggressive pricing policies for their tests, secure supplies
from vendors on more favorable terms, or devote substantially more resources to infrastructure and systems development. In addition,
competitors may be acquired by, receive investments from, or enter into other commercial relationships with larger, well-established,
and well-financed companies. Smaller or early-stage companies may also prove to be significant competitors, particularly through
collaborative arrangements with large and established companies. Further, companies or governments that effectively control access to
genetic or diagnostic testing through umbrella contracts or regional preferences could promote our competitors or prevent us from
performing certain tests in certain territories. We may not be able to compete effectively against these organizations.
Intellectual Property
Intellectual property is essential to our strategy and capturing the value of research output. We rely on a combination of
registered and unregistered intellectual property rights, including trade secrets, certain licenses, patents, trademarks, and customary
contractual protections, to protect our core technology and intellectual property.
We principally rely on trade secrets and know-how to protect the proprietary technology platform we use in our laboratory
services business to develop and maintain our competitive position. We seek to protect our proprietary technology and processes, and
obtain and maintain ownership of certain technologies, in part, through non-disclosure and intellectual property assignment
agreements with our employees, consultants, and commercial partners. In general, these agreements provide that confidential
information concerning our business or financial affairs developed or made known to the individual during the course of the
individual’s relationship with us is to be kept confidential and not disclosed to third parties, except in specific circumstances. In the
case of employees, the agreements further provide that inventions and discoveries conceived or reduced to practice by the individual
that are related to our business, or actual, or demonstrably anticipated, research or development, or made during normal working
hours, on our premises or using our equipment, supplies, or proprietary information, are our exclusive property. In many cases, our
agreements with consultants, outside scientific collaborators, sponsored researchers, and other service providers and advisors require
them to assign, or grant us licenses to, inventions resulting from the work or services they render under such agreements or grant us an
option to negotiate a license to use such inventions. We also seek to preserve the integrity and confidentiality of our proprietary
technology and processes by maintaining physical security of our premises and physical and electronic security of our information
technology systems.
Further, we seek to obtain and maintain patent rights intended to cover the technologies incorporated into, or used to produce,
our drug candidates, the compositions of matter of our drug candidates and their methods of use and manufacture, as well as other
inventions that are important to our business. The patent families comprising our patent portfolio are primarily focused on our nano-
drug delivery platform technology, including FID-007 and FID-022 and other candidates we may develop, for delivery of water
insoluble or poorly soluble drugs for treatments of disease conditions, including cancer. Worldwide, we own or exclusively in-license
over 20 issued or allowed patents and over 10 active patent applications as of December 31, 2024. This includes eight issued or
allowed U.S. patents. Patents in these patent families are expected to expire by 2034, and patent applications in these patent families,
if granted, are expected to expire as far out as 2044, subject to any patent term disclaimers, adjustments, or extensions. Patents and/or
patent applications in these families are active in multiple jurisdictions, including the United States, Australia, Canada, China,
European Patent Organization, Germany, New Zealand, Japan, and Switzerland. In addition to these owned and exclusively licensed
patents and active patent applications, we also license patents on a non-exclusive and/or territory-restricted basis. In particular, as of
December 31, 2024, we own or exclusively in-license 18 issued patents and five patent applications relating to FID-007 and related
formulations. United States and foreign patents (Canada, China, Germany, France, United Kingdom, Japan, Australia, and New
Zealand) were granted in these families, and these patents are expected to expire by 2034, absent any patent term extension. Individual
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patent terms extend for varying periods of time, depending upon the date of filing of the patent application, the date of patent issuance,
and the legal term of patents in the countries in which they are obtained.
We also rely on in-licensing opportunities to develop, strengthen, and maintain our proprietary position in the fields targeted by
our drug candidates, including FID-007 and FID-022. In June 2017, we entered into an exclusive license agreement with ANP
Technologies, Inc., or ANP, as amended on December 28, 2017, and May 1, 2024. Under the agreement, ANP granted us ownership
of certain patents and patent applications, and an exclusive, worldwide, perpetual, irrevocable, and sublicensable license to certain
rights in patents and patent applications under which we may develop and commercialize FID-007 and FID-022 and related
formulations for human therapeutic, prophylactic, and diagnostic uses. We do not currently have any obligations to pay royalties
pursuant to the terms of the ANP License Agreement. The ANP License Agreement term expires upon the date of expiration or the
invalidation of the last of the patents licensed to us unless terminated earlier under its terms. The ANP License Agreement provides
ANP the right to terminate for an uncured breach by us, or if we are insolvent, the subject of a bankruptcy proceeding, or potentially
other reasons. We may terminate the ANP License Agreement at any time on 90 days’ notice.
Additionally, the ANP License Agreement provides that ANP will be responsible for preparing, filing, prosecuting and
maintaining all of the licensed patents at ANP’s expense. If ANP decides that it is not interested in prosecuting or maintaining a
particular licensed patent, it will notify us in writing, we will have the right to assume such responsibilities at our own cost and
expense.
We may also grant a sublicense provided that the sublicensee agrees to (i) be bound by the terms of the ANP License
Agreement; (ii) in the event the sublicensee initiates a proceeding to challenge the enforceability of any licensed patent, ANP may
terminate the sublicense agreement; (iii) the ANP License Agreement controls in the event that there is any inconsistency with the
sublicense agreement; and (iv) the sublicensee will submit quarterly reports to ANP consistent with the reporting provisions in the
ANP License Agreement.
We also own registered and unregistered trademark and service mark rights under applicable U.S. and foreign law to distinguish
and/or protect our brand, including our company name and logo.
Governmental Regulation
U.S. Federal Regulations Applicable to Our Laboratory Operations
As we operate clinical laboratories in the United States, we are required to hold certain federal licenses, certifications, and
permits to conduct our business. Clinical Laboratory Improvement Amendments, or CLIA, establishes quality standards for all
laboratory testing to ensure the accuracy, reliability and timeliness of patient test results. Our laboratories located in California, Texas,
Georgia, Massachusetts, and Arizona are CLIA-certified and are accredited by the College of American Pathologists, or CAP, and the
Centers for Medicare & Medicaid Services, or CMS.
CLIA requires that we hold certificates for each of our laboratories applicable to the categories of testing that each laboratory
performs and that we comply with various standards with respect to personnel qualifications, facility administration, proficiency
testing, quality control and assurance, and inspections. Each of our laboratories must obtain a certificate from CMS, the agency that
enforces CLIA, and CLIA compliance and certification are prerequisites to be eligible to bill government payors and many private
payors for our tests.
Each CLIA certificate is valid for two years from the date of issuance. If one or more of our laboratories is found to be out of
compliance with CLIA requirements, we may be subject to sanctions such as suspension, limitation, or revocation of our CLIA
certificate; a directed plan of correction; on-site monitoring; civil monetary penalties; civil injunctive suits; criminal penalties;
exclusion from the Medicare and Medicaid programs; and significant adverse publicity.
In addition, we elect to participate in the accreditation program of CAP. CMS has deemed CAP standards to be equally or more
stringent than CLIA regulations and has approved CAP as a recognized accrediting organization. An inspection by CAP is performed
in lieu of inspection by CMS for CAP-accredited laboratories. Because we are accredited by the CAP Laboratory Accreditation
Program, we are deemed to also comply with CLIA.
State and Foreign Clinical Laboratory Licensure
Our clinical laboratories are required to maintain certain state laboratory licenses. State laws establish standards for day-to-day
operations of our laboratories, including requirements with respect to the training and skills required of personnel, quality control, and
proficiency testing requirements. If our clinical laboratories are out of compliance with the applicable state regulations, state agencies
may suspend, restrict, or revoke our license to operate our clinical laboratories, assess substantial civil money penalties, or impose
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specific corrective action plans. Any such actions could materially affect our business. Currently, we maintain good standing with all
state authorities.
Additionally, certain states may require licensure for out-of-state laboratories that accept specimens originated from those states.
Our Texas laboratory currently holds the out-of-state licenses from New York, California, Maryland, Pennsylvania, and Rhode Island
to perform testing on specimens from these states, and our California laboratory holds the required out-of-state laboratory licenses
from New York, Maryland, Pennsylvania, and Rhode Island in order to perform testing on specimens from these states. Our
Australian laboratory is also subject to Australian regulatory requirements.
Other states may adopt similar licensure requirements in the future, which could require us to modify, delay, or discontinue our
operations in such jurisdictions. If we identify any other state with such requirements, or if we are contacted by any other state
advising us of such requirements, we intend to follow instructions from the state regulators as to how to comply with such
requirements.
We are also subject to regulation in foreign jurisdictions, which we expect will increase as we continue to expand international
utilization of our tests, or if jurisdictions in which we pursue operations adopt new or modified licensure requirements for U.S.-based
clinical laboratories offering and providing diagnostic testing services to professionals located in those jurisdictions. Foreign licensure
requirements could require review and modification of our tests in order to offer them in certain jurisdictions or could impose other
limitations, such as restrictions on international data transfer or on the transport of human blood or other tissue necessary for us to
perform our tests, that may limit our ability to make our tests available outside of the United States on a broader scale.
U.S. FDA Oversight of Our Tests and Testing Services
The tests and testing services that we offer may be considered medical devices. Pursuant to its authority under the Federal Food,
Drug, and Cosmetic Act, or FDC Act, the FDA has jurisdiction over medical devices, which are defined to include, among other
things, in vitro diagnostic products, or IVDs, used for clinical purposes. The laws and regulations governing the marketing of IVDs are
evolving, are extremely complex, and in many instances, there are no significant regulatory or judicial interpretations of these laws
and regulations. The FDA regulates, among other things, the research, testing, manufacturing, safety, labeling, storage, recordkeeping,
premarket clearance or approval, marketing and promotion, and sales and distribution of medical devices in the United States to
ensure that medical products distributed domestically are safe and effective for their intended uses. In addition, the FDA regulates the
import and export of medical devices. Many of the instruments, reagents, kits, or other consumable products used within our
laboratories are regulated as medical devices and therefore must comply with FDA quality system regulations and certain other device
requirements. We have policies and procedures in place to ensure that we source such materials from suppliers that are in compliance
with any applicable medical device regulatory requirements.
We believe our tests fall within the definition of laboratory developed tests, or LDTs. LDTs, which are a subset of IVDs that are
intended for clinical use and are designed, manufactured, and used within a single laboratory. Although the FDA has statutory
authority to assure that medical devices, including IVDs, are safe and effective for their intended uses, the FDA had historically
exercised enforcement discretion and not enforced applicable provisions of the FDC Act and regulations with respect to LDTs.
However, in May 2024, the FDA issued a final rule aimed at regulating LDTs under the current medical device framework and
phasing out its existing enforcement discretion policy for this category of diagnostic tests; the final rule became effective on July 5,
2024. The LDT enforcement policy phase-out process will occur in gradual stages over a total period of four years, with pre-market
approval applications for high-risk tests to be submitted by the 3.5-year mark. Moderate-risk and low-risks tests are expected to be in
compliance at the four-year mark, although FDA has stated that, if premarket submissions are pending review, it will continue to
exercise enforcement discretion with respect to those tests. The FDA’s final rule is complex and, concurrently, the agency announced
several exceptions from the requirement to comply with full medical device regulatory controls, depending upon the specific nature of
the LDT and the clinical laboratory that is offering such LDT for use by health care providers. Importantly, under the agency’s
transition plan, LDTs that were marketed prior to the official publication date of the final rule (May 6, 2024) are considered to be
“currently marketed” tests. “Currently marketed” tests will become subject to many of the device regulatory controls but are exempted
from the premarket review and FDA authorization requirements, unless or until significant modifications are made to such “currently
marketed” tests. Similarly, the FDA has created a partial enforcement discretion policy for tests approved by the New York
Department of Health’s Clinical Laboratory Evaluation Program, whereby such tests also do not need to undergo FDA premarket
review but must come into compliance with all other device general controls in a staggered fashion between 2025 and 2027. We have
begun the process of evaluating the final rule’s potential impact on our tests, our operations, and our business more generally.
Publication of the LDT final rule prompted the American Clinical Laboratory Association, or ACLA, and one of its members,
on May 29, 2024, as well as the Association for Molecular Pathology, or AMP, and one of its members, on August 19, 2024, to file
complaints against the FDA in the Eastern District of Texas and the Southern District of Texas, respectively. Both complaints allege
that the agency does not have authority to promulgate the LDT final rule and seek to vacate the FDA’s action; the two cases were
subsequently consolidated into a single action pending in the Eastern District of Texas. Briefing is ongoing in the consolidated case
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and the outcome is uncertain. The ongoing litigation could potentially affect the FDA’s plans to implement these new LDT
requirements, making the implementation timeline somewhat uncertain although no preliminary injunction has been issued to date.
Accordingly, the agency has continued its implementation efforts by actively providing guidance and training to clinical laboratories
on how to comply with medical device general controls. Following the November 2024 federal elections, it is unclear whether the
incoming Trump Administration will continue to defend the FDA’s rulemaking action in the consolidated litigation in Texas or if it
will take steps to rescind or modify the LDT final rule. Affected stakeholders also continue to press for a comprehensive legislative
solution to create a harmonized paradigm for oversight of LDTs by both the FDA and CMS, instead of implementation of the FDA’s
final rule, which may be disruptive to the industry and to patient access to certain diagnostic tests. However, this FDA rulemaking was
initiated after years of failed congressional attempts to harmonize the regulatory paradigms applicable to LDTs and other IVDs,
making it unclear whether any legislative efforts would be successful going forward. The outcome of the November 2024 elections on
the composition of the 2025-2026 Congress, with transition of both the Senate and House to Republican control, also creates
uncertainties for the diagnostic industry.
Even though we presently commercialize our tests as LDTs, the FDA may disagree that our currently marketed tests are within
the scope of its LDT criteria, or tests we develop may in the future become subject to more onerous regulation by the FDA. Depending
upon the characteristics and regulatory status of each individual test, we could in the future be required to obtain premarket clearance
for our tests under Section 510(k) of the FDC Act or approval of a pre-market approval application, or PMA. The process for
submitting a 510(k) premarket notification and receiving FDA clearance usually takes from three to twelve months, but it can take
significantly longer, and clearance is never guaranteed. The process for submitting and obtaining FDA approval of a PMA generally
takes from one to three years or even longer, and approval is not guaranteed. PMA approval typically requires extensive clinical data
and can be significantly longer, more expensive and more uncertain than the 510(k) clearance process. If premarket review is required
for some or all of our tests, whether currently marketed or developed in the future, the FDA could require that we stop selling our tests
and testing services pending clearance or approval and conduct clinical testing prior to making submissions to FDA to obtain
premarket clearance or approval. The FDA could also require that we label our tests as investigational or limit the labeling claims we
are permitted to make.
The FDA enforces its medical device requirements by various means, including inspection and market surveillance. If the FDA
finds a violation, it can institute a wide variety of enforcement actions, ranging from an Untitled Letter or Warning Letter to more
severe sanctions, such as: fines, injunctions, and civil penalties; recall or seizure of products; operating restrictions, partial suspension
or total shutdown of production; and criminal prosecution. Failure to comply with any applicable FDA requirements could trigger a
range of enforcement actions by the FDA, including warning letters, civil monetary penalties, fines, injunctions, criminal prosecution,
consent decrees, repairs, replacements, refunds, recalls or seizures of products, operating restrictions, partial suspension or total
shutdown of operations and denial of or challenges to applications for clearance or approval, as well as significant adverse publicity.
Foreign Regulation of Diagnostic Medical Devices
Medical devices, including IVD products, are subject to extensive regulation, such as premarket review, marketing
authorization, or certification, by regulatory agencies or notified bodies in other countries. Regulatory requirements and approval or
certification processes are not harmonized and vary from one country to another, and international regulators and notified bodies are
not bound by the findings of the FDA. The IVDR (as defined and described below) has introduced an enhanced level of EU regulatory
oversight for diagnostic tests developed as LDTs, and Fulgent’s commercial laboratory in California may be considered a health
institution in the context of the IVDR because it provides testing for EU citizens.
In the European Union in particular, IVD products had historically been regulated under EU-Directive 98/79/EC (IVD
Directive) and corresponding national provisions. The IVD Directive required that medical devices meet the essential requirements,
including those relating to device safety and efficacy, set out in an annex of the Directive. According to the IVD Directive, EU
Member States have presumed compliance with these essential requirements for devices that are in conformity with the relevant
national standards transposing the harmonized standards, such as ISO 13485:2016, the quality system standard for medical device
manufacturers.
IVD medical devices, other than devices for performance evaluation, must bear the CE mark of conformity when they are
placed on the European market. The CE mark is a declaration by the manufacturer that the product meets all the appropriate provisions
of the applicable legislation implementing the relevant European Directive. As a general rule, the manufacturer must follow the EU
declaration of conformity procedure to obtain or apply a CE mark. The advertising and promotion of medical devices is also subject to
general principles set forth by EU directives, which establish that devices that are CE marked may only be marketed and advertised in
the EU in accordance with their intended purpose. Specific requirements defined at the EU Member State level may vary between
jurisdictions and may limit or restrict a manufacturer’s promotional communications with healthcare professionals.
In May 2022, the Directive was replaced by the In Vitro Diagnostic Device Regulation, or IVDR, (EU) 2017/746. Unlike the
IVD Directive, the IVDR has binding legal force throughout every Member State. The major goal of the IVDR was to standardize
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diagnostic procedures within the EU, increase reliability of diagnostic analysis and enhance patient safety. Under the IVDR as enacted
by the European Commission, or EC, IVDs are subject to additional legal requirements. Among other things, the IVDR introduced a
new risk-based classification system and requirements for conformity assessments. It also imposes additional requirements relating to
post-market surveillance and submission of post-market performance follow-up reports. Under the IVDR and subsequent
amendments, IVDs already certified under the IVD Directive by a Notified Body may remain on the market until December 31, 2027,
and IVDs certified under the IVD Directive without the involvement of a Notified Body may be placed on, or remain in, the market
for up to two additional years (until December 31, 2029) depending on the classification of the IVD. Nonetheless, the manufacturers
of such devices must comply with specific requirements in the IVDR according to the timelines established, but ultimately, such
products, as with all new IVDs, will have to undergo the IVDR’s conformity assessment procedures. Notified Bodies are entities
accredited by an EU Member State to independently assess whether a product to be placed on the market meets certain preordained
standards and that manufacturing facilities and records comply with applicable requirements such as International Organization for
Standardization, or ISO, standards such as ISO 13485 and ISO 27001. Such international standards establish extensive requirements
for quality assurance and control as well as manufacturing and change control procedures.
The EC has designated 13 Notified Bodies to perform conformity assessments under the IVDR. MedTech Europe has issued
guidance relating to the IVDR in several areas, e.g., clinical benefit, technical documentation, state of art, accessories, and
EUDAMED. On December 5, 2023, the European Commission adopted Implementing Regulation (EU) 2023/2713 designating five
EU Reference Laboratories covering the following types of high-risk, class D IVDs: hepatitis and retroviruses; herpesviruses; bacterial
agents; and respiratory viruses that cause life-threatening diseases. The designated EU Reference Laboratories are responsible for
verifying performance of IVDs in accordance with common specifications, batch testing of class D IVDs, collaborating with Notified
Bodies to develop best practices for IVD conformity assessments, and providing scientific and technical assistance on the
implementation of the IVDR.
We believe that LDTs produced outside of the EU and involving samples obtained from EU citizens must fully comply with the
IVDR and accordingly, we are working towards ISO 13485 compliance and preparing certain of our tests for conformity assessments
by a designated Notified Body. We have made initial submissions to our Notified Body and expect to receive CE marking under the
IVDR for certain of our tests in the future, subject to ongoing review and auditing by the regulatory agency. If we are not able to
obtain and maintain regulatory compliance, we may not be permitted to market our laboratory services in the EU and/or may become
subject to enforcement by EU Competent Authorities, bodies with authority to act on behalf of the government of the applicable EU
Member State to ensure that the requirements of the regulation are met.
Our tests also may become subject to other foreign premarket review, compliance, and regulatory approval regimes applicable
to IVDs as we continue to expand and offer our services internationally.
Regulations Regarding Advertising of Laboratory Services, LDTs, or IVDs
In the United States, our advertising for laboratory services and tests is subject to federal truth-in-advertising laws enforced by
the Federal Trade Commission, or FTC, as well as comparable state consumer protection agencies under similarly broad state laws.
Under the Federal Trade Commission Act, or the FTC Act, the FTC is empowered, among other things, to (a) prevent unfair methods
of competition and unfair or deceptive acts or practices in or affecting commerce; (b) seek monetary redress and other relief for
conduct injurious to consumers; and (c) gather and compile information and conduct investigations relating to the organization,
business, practices, and management of entities engaged in commerce. The FTC has very broad enforcement authority, and failure to
abide by the substantive requirements of the FTC Act and other consumer protection laws can result in administrative or judicial
penalties, including civil penalties, injunctions affecting the manner in which we would be able to market services or products in the
future, or criminal prosecution. Further, as medical devices under the FDA’s LDT Final Rule, certain of our tests will become subject
to the device labeling requirements that presently apply to other FDA-regulated IVD products, which prohibit the distribution of false
or misleading labels or promotional labeling for such products. Enforcement actions by the FDA may include, among other things, the
issuance of untitled or warning letters, injunctions, and civil or criminal penalties.
In addition, when marketing our diagnostic tests to clinical laboratories and medical institutions outside of the United States
(including our operations in Australia), we are subject to foreign regulatory requirements governing promotional statements and IVD
labeling. The legal landscape governing promotional and other marketing activities for diagnostic tests can vary widely from
jurisdiction to jurisdiction, and is often more complex, less clear, or less developed than in the United States.
Rules and Regulations Relating to U.S. Payor Reimbursement for our Tests and Testing Services
CPT Codes
We bill insurance payors, both commercial and government, for our tests and testing services using Current Procedural
Terminology, or CPT, codes, which are published by the American Medical Association, or AMA. CPT codes in their current form
are not readily applied to many of the genetic tests we conduct. For example, for many of our multi-gene panels, there may not be an
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appropriate CPT code for one or more of the genes in a panel, in which case our test may be billed under a miscellaneous code for an
unlisted molecular pathology procedure. Many insurance payors do not have a set reimbursement rate for this miscellaneous code.
Prior to performing a test, we may negotiate the reimbursement rate with the payor if the benefits investigation has determined the test
to be medically necessary, and the payor has issued prior authorization. After we file the claim, we may also need to resubmit
documentation or appeal a denial. All of these issues can cause delay in the reimbursement of the claim or our inability to get
reimbursed.
PAMA
In April 2014, Congress passed the Protecting Access to Medicare Act of 2014, or PAMA, which included substantial changes
to the way in which clinical laboratory services are priced and paid under Medicare’s Clinical Laboratory Fee Schedule, or CLFS. On
June 23, 2016, CMS published the final rule implementing the reporting and rate-setting requirements. Under PAMA, laboratories that
receive the majority of their Medicare revenue from payments made under the CLFS or the Physician Fee Schedule are required to
report private payor payment rates and volumes for clinical diagnostic laboratory tests, or CDLTs, to CMS every three years (or
annually for advanced diagnostic laboratory tests, or ADLT). We do not believe that any of our tests meet the current definition of
ADLT. We, therefore, must report private payor rates for our tests every three years. Laboratories that fail to report the required
payment information may be subject to substantial civil monetary penalties.
As required under PAMA, CMS uses the data reported by laboratories to develop Medicare payment rates for laboratory tests
equal to the volume-weighted median of the private payor payment rates. For tests furnished on or after January 1, 2018, Medicare
payments for CDLTs are based upon reported private payor rates. For a CDLT that is assigned a new or substantially revised CPT
code, the initial payment rate is assigned using the gap-fill methodology, as under prior law.
Since December 2019, Congress has passed a series of laws to modify PAMA’s statutory requirements related to the data
reporting period and phase-in of payment reductions under the CLFS for CDLTs that are not ADLTs. Most recently, on September 26,
2024, Section 221 of the Continuing Appropriations and Extensions Act, 2025, was passed, and it delayed data reporting requirements
for CDLTs that are not ADLTs as well as the phase-in of payment reductions. The next data reporting period for CDLTs that are not
ADLTs will be January 1, 2026 through March 31, 2026, and will be based on the original data collection period of January 1, 2019
through June 30, 2019. After this data reporting period, the three-year data reporting cycle for these tests will resume (e.g., 2028,
2031, etc.).
The same series of laws modified the phase-in of payment reductions resulting from private payor rate implementation so that a
zero percent reduction limit was applied for calendar years, or CYs, 2021 through 2024, as compared to the payment amounts for a
test the preceding year. The Further Continuing Appropriations and Other Extensions Act of 2025 further applied a zero percent
reduction limit for CY 2025. Consequently, payment may not be reduced by more than 15 percent per year for CYs 2026 through
2028 as compared to the payment amount established for a test the prior year.
HRSA Audits and Investigations
In March 2020, the Coronavirus Aid, Relief, and Economic Security Act, or CARES Act, was enacted, providing for
reimbursement to healthcare providers for COVID-19 tests provided to uninsured individuals through a program administered by
HRSA. This program administered by HRSA was the HRSA COVID-19 Claims Reimbursement to Health Care Providers and
Facilities for Testing, Treatment, and Vaccine Administration for the Uninsured Program, or the Uninsured Program. The Uninsured
Program was valid for the period between May 2020 and April 2022, and HRSA announced that the Uninsured Program ceased
accepting COVID-19 testing claims as of March 22, 2022, due to a lack of sufficient funds. The Company recorded approximately
$548.9 million of reimbursements from HRSA under the Uninsured Program during the years ended December 31, 2022, 2021, and
2020.
Similar to other laboratories in the industry, the Company is currently being audited by HRSA with respect to its reimbursement
for COVID-19 tests furnished to patients believed to be uninsured. The Company is fully cooperating and working with HRSA’s
auditors to resolve any issues, including any reimbursed amounts that may need to be returned to HRSA. There is uncertainty with
respect to the methodology HRSA will use and whether and how they will extrapolate audit results. The Company has also received a
Civil Investigative Demand, or CID, issued by the U.S. Department of Justice, or DOJ, related to the DOJ’s investigation as to
whether we submitted or caused to be submitted false claims to the Uninsured Program. We are fully cooperating with the DOJ in
connection with this CID.
See “Contingencies” in Note 8, Debt, Commitments and Contingencies to the Consolidated Financial Statements, and the
paragraphs under the heading entitled “Failure to comply with government laws and regulations related to submission of claims for
our services could result in significant monetary damages and penalties and exclusion from the Medicare and Medicaid programs and
corresponding foreign reimbursement programs. We are also subject to governmental audits and investigations that could result in
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material refunds or settlement. Our business, prospects and financial condition may be adversely affected as the result of the current
HRSA Audit and CIDs.” included in Item 1A “Risk Factors” of this Annual Report.
Rules and Regulations Applicable to Our Pharmaceutical Research and Development Activities
We engage in research and development activities, including pharmaceutical research and development activities through our
wholly owned subsidiary, Fulgent Pharma. Development of therapeutic products is subject to extensive regulation by the FDA and
other regulatory agencies. In particular, government authorities in the United States at the federal, state, and local levels and in other
countries regulate, among other things, the research, development, testing, manufacture, quality control, approval, labeling, packaging,
storage, record-keeping, promotion, advertising, distribution, post-approval monitoring and reporting, marketing and export and
import of therapeutic products. Generally, therapeutic products require government authorization before they may be clinically tested
and commercially marketed for human therapeutic use in the United States and other countries. The precise regulatory requirements
with which we will have to comply are undergoing periodic revisions and refinement.
In the United States, the FDA regulates drugs under the FDC Act and its implementing regulations. The process of obtaining
regulatory approvals and the subsequent compliance with applicable federal, state, local, and foreign statutes and regulations requires
the expenditure of substantial time and financial resources. Failure to comply with the applicable U.S. requirements at any time during
the product development process, approval process or post-market may subject an applicant to administrative or judicial sanctions.
These sanctions could include, among other actions, the FDA’s refusal to approve pending applications, withdrawal of an approval, a
clinical hold, untitled or warning letters, product recalls or market withdrawals, product seizures, total or partial suspension of
production or distribution, injunctions, fines, refusals of government contracts, restitution, disgorgement and civil or criminal
penalties.
The steps required before a therapeutic product may be marketed in the United States are numerous and include, but are not
limited to, the following:
•
completion of non-clinical laboratory tests, animal studies, chemical process development, and formulation studies
according to GLP and other applicable regulations and guidance;
•
the submission to the FDA of an investigational new drug application, or IND, which must become effective before
clinical trials may commence;
•
performance of adequate and well-controlled clinical trials according to good clinical practices, or GCPs, to establish the
safety and efficacy of the drug candidate for its intended use(s);
•
the submission of a New Drug Application, or NDA, to the FDA;
•
satisfactory completion of an FDA inspection of the manufacturing facility or facilities at which the drug candidate is
produced to assess readiness for commercial manufacturing and conformance to the manufacturing-related elements of the
application, to conduct a data integrity audit, and to assess compliance with current Good Manufacturing Practices, or
cGMPs, to assure that the facilities, methods, and controls are adequate; and
•
the FDA's review and approval of the NDA.
The testing and formulation processes required to market a therapeutic product involves substantial time, effort, and financial
resources. The data required to support an NDA are generated in two distinct developmental stages: non-clinical and clinical. The non-
clinical developmental stage generally involves laboratory evaluations of drug chemistry, formulation, and stability, as well as
potential studies to evaluate the molecule’s toxicity in animals, which support subsequent clinical testing. The sponsor must submit the
results of the non-clinical studies, together with manufacturing information, analytical data, any available clinical data or literature and
a proposed clinical protocol, to the FDA as part of the IND. An IND is a request for authorization from the FDA to administer an
investigational new drug to humans and must become effective before human clinical trials may begin.
Clinical Trials
The clinical stage of development involves the administration of the investigational product to volunteers or patients under the
supervision of qualified investigators, generally physicians not employed by or under the trial sponsor’s control, in accordance with
GCP requirements, which include the requirement that all research subjects provide their informed consent for their participation in
any clinical trial. Clinical trials are conducted under protocols detailing, among other things, the objectives of the clinical trial, dosing
procedures, subject selection and exclusion criteria and the parameters to be used to monitor subject safety and assess efficacy. Each
protocol, and any subsequent amendments to the protocol, must be submitted to the FDA as part of the IND. Furthermore, an
institutional review board, or IRB, for each institution participating in the clinical trial must review and approve a new clinical
protocol before a clinical trial commences at that institution and must also approve the information regarding the trial and the consent
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form that must be provided to each research subject or the subject’s legal representative, monitor the trial until completed, and
otherwise comply with IRB regulations.
Clinical trials are typically conducted in three sequential phases that may overlap or be combined:
•
Phase 1: Initial safety study in appropriate human subjects or patients where the candidate therapy is tested for safety,
dosage tolerance, absorption, distribution, metabolism, and excretion.
•
Phase 2: Studies in a limited patient population designed to identify possible adverse effects and safety risks, to determine
the efficacy of the product for specific targeted diseases, and to determine tolerance and optimal dosage.
•
Phase 3: Studies in an expanded patient population to further evaluate clinical efficacy and to further test for safety.
Post-approval trials, sometimes referred to as “Phase 4” clinical trials, may be conducted after initial marketing approval. These
trials are used to gain additional experience from the treatment of patients in the intended therapeutic indication. In certain instances,
FDA may mandate the performance of “Phase 4” clinical trials as a condition of approval of an NDA.
Progress reports detailing the results of the clinical trials, among other information, must be submitted at least annually to the
FDA, and written IND safety reports must be submitted to the FDA and the investigators for serious and unexpected suspected
adverse events, findings from other studies suggesting a significant risk to humans exposed to the investigational drug, findings from
animal or in vitro testing that suggest a significant risk for human subjects, and any clinically important increase in the rate of a
serious suspected adverse reaction over that listed in the protocol or investigator brochure. Congress also recently amended the FDC
Act, in order to require sponsors of a Phase 3 clinical trial, or other “pivotal study” of a new drug to support marketing authorization
(or pivotal trials of medical devices), to design and submit a diversity action plan for such clinical trial. The action plan must include
the sponsor’s diversity goals for enrollment, as well as a rationale for the goals and a description of how the sponsor will meet them.
Sponsors must submit a diversity action plan to the FDA by the time the sponsor submits the relevant clinical trial protocol to the
agency for review. The FDA may grant a waiver for some or all of the requirements for a diversity action plan. It is unknown at this
time how the diversity action plan may affect Phase 3 trial planning and timing or what specific information FDA will expect in such
plans, but if the FDA objects to a sponsor’s diversity action plan or otherwise requires significant changes to be made, it could delay
initiation of the relevant clinical trial. In addition, an IRB on behalf of each institution that is participating in the clinical trial must
conduct a continuing review and reapprove the trial at least annually. Information about certain clinical trials, including details of the
protocol and eventually study results, also must be submitted within specific timeframes to the National Institutes of Health, or NIH,
for public dissemination on the ClinicalTrials.gov data registry. Information related to the investigational product, patient population,
phase of investigation, study sites and investigators, and other aspects of the clinical trial is made public as part of the registration of
the clinical trial. Sponsors are also obligated to disclose the results of their clinical trials after completion. Disclosure of the results of
these trials can be delayed in some cases for up to two years after the date of completion of the trial. Competitors may use this publicly
available information to gain knowledge regarding the progress of development programs. The NIH’s Final Rule on ClinicalTrials.gov
registration and reporting requirements became effective in 2017, and the government has begun enforcing those requirements against
non-compliant clinical trial sponsors.
Clinical trials may not be completed successfully within any specified period, if at all. The FDA or the sponsor may suspend
clinical trials at any time on various grounds, including a finding that the research subjects or patients are being exposed to an
unacceptable health risk. Similarly, an IRB can suspend or terminate approval of a clinical trial at its institution if the clinical trial is
not being conducted in accordance with the IRB’s requirements, or if the drug candidate has been associated with unexpected serious
harm to patients. Additionally, some clinical trials are overseen by an independent group of qualified experts organized by the clinical
trial sponsor, known as a data safety monitoring board or committee. This group provides authorization for whether a trial may move
forward at designated check points based on access to certain data from the trial.
NDA Submission and FDA Review Process
Following completion of the required clinical testing, all of the data are analyzed to assess whether the investigational
therapeutic product is safe and effective for its proposed indicated use or uses. The results of the non-clinical studies and clinical trials,
along with detailed descriptions of the product’s chemistry, manufacturing and controls, or CMC, proposed labeling and other relevant
information are submitted to the FDA as part of an NDA requesting approval to market the product. To support marketing approval,
the data submitted must be sufficient in quality and quantity to establish the safety and efficacy of the investigational product to the
satisfaction of FDA. FDA approval of the NDA must be obtained before a drug may be marketed in the United States.
Under the Prescription Drug User Fee Act, or PDUFA, as amended, each NDA must be accompanied by a significant user fee,
and the sponsor of an approved NDA is also subject to an annual program fee. The FDA typically adjusts these PDUFA user fees on
an annual basis. Fee waivers or reductions are available in certain circumstances, including a waiver of the application fee for the first
application filed by a small business (fewer than 500 employees). Additionally, no user fees are assessed on NDAs for products
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designated as orphan drugs, unless the product also includes a non-orphan indication. Congress is required to re-authorize the agency’s
user fee programs every five years, and current legislative provisions supporting the PDUFA program are set to expire on September
30, 2027.
The FDA reviews all submitted NDAs to ensure that they are sufficiently complete for substantive review before it accepts them
for filing. It may refuse to file the application and request additional information rather than accept an NDA for filing. In this event,
the application must be resubmitted with the additional information. The resubmitted application is also subject to review before the
FDA accepts it for filing. The FDA must make a decision on accepting an NDA for filing within 60 days of receipt and inform the
sponsor by the 74th day after the FDA’s receipt of the submission whether an application is sufficiently complete to permit substantive
review. Once the submission is accepted for filing, the FDA begins an in-depth review of the NDA. Under the goals and policies
agreed to by the FDA under PDUFA, the FDA has 10 months from the filing date, to complete its review of a new molecular-entity, or
NME, NDA and respond to the applicant, and six months from the filing date of an NME NDA designated for priority review. For
non-NME NDAs, such as our current and, potentially, future product candidates, the review goals are 10 months from the date of
receipt for a standard application and six months from the date of receipt for a priority submission. The FDA does not always meet its
PDUFA goal dates for standard and priority NDAs, and the review process is often extended by FDA requests for additional
information or clarification.
Most innovative drug products obtain FDA marketing approval pursuant to an NDA submitted under Section 505(b)(1) of the
FDC Act, commonly referred to as a traditional or “full NDA.” In 1984, with passage of the Drug Price Competition and Patent Term
Restoration Act, informally known as the Hatch-Waxman Act, that established an abbreviated regulatory scheme authorizing the FDA
to approve generic drugs based on an innovator or “reference” product, Congress also enacted Section 505(b)(2) of the FDC Act,
which provides a hybrid pathway combining features of a traditional NDA and a generic drug application. Section 505(b)(2) NDAs
may provide an alternate path to FDA approval for new or improved formulations or new uses of previously approved products; for
example, an applicant may be seeking approval to market a previously approved drug for new indications or for a new patient
population that would require new clinical data to demonstrate safety or effectiveness. Section 505(b)(2) permits the filing of an NDA
in which the applicant relies, at least in part, on information from studies made to show whether a drug is safe or effective that were
not conducted by or for the applicant and for which the applicant has not obtained a right of reference or use (e.g., FDA’s prior
findings of safety and efficacy for an existing product or published literature). A Section 505(b)(2) applicant may eliminate or reduce
the need to conduct certain non-clinical or clinical studies, if it can establish that reliance on studies conducted for a previously
approved product is scientifically appropriate.
Before approving an NDA, the FDA will typically conduct a pre-approval inspection of the manufacturing facilities for the new
product to determine whether the manufacturing processes and facilities comply with cGMP requirements. The FDA will not approve
the product unless it determines that the manufacturing processes and facilities are in compliance with cGMP requirements and
adequate to assure consistent production of the product within required specifications. The FDA also may audit data from clinical
trials to ensure compliance with GCP requirements by each of the entities involved in the clinical trials, including clinical investigators
and any third-party clinical research organizations, or CROs.
Additionally, the FDA may refer applications for novel drug products or drug products that present difficult questions of safety
or efficacy to an advisory committee, typically a panel that includes clinicians and other independent scientific experts, for review,
evaluation and a recommendation as to whether the application should be approved and under what conditions, if any. The FDA is not
bound by recommendations of an advisory committee, but it considers such recommendations when making final agency decisions on
marketing approval. The FDA likely will reanalyze the clinical trial data, which could result in extensive discussions between the
FDA and the applicant during the review process. The FDA also may require development of a risk evaluation and mitigation strategy,
or REMS, plan if it determines that a REMS is necessary to ensure that the benefits of the drug outweigh its risks and to assure the
safe use of the drug. The REMS plan could include medication guides, physician communication plans, assessment plans and/or
elements to assure safe use, such as restricted distribution methods, patient registries or other risk minimization tools. The FDA
determines the requirement for a REMS, as well as the specific REMS provisions, on a case-by-case basis. If the FDA concludes a
REMS plan is needed, the sponsor of the NDA must submit a proposed REMS. The FDA will not approve an NDA without a REMS,
if one is required.
The approval process is lengthy and often difficult, and the FDA may refuse to approve an NDA if the applicable regulatory
criteria are not satisfied or may require additional clinical or other data and information. The FDA reviews an NDA to determine,
among other things, whether a product is safe and effective for its intended use and whether its manufacturing is cGMP-compliant and
capable of assuring and preserving the product’s identity, strength, quality and purity. Based on the FDA’s evaluation of the NDA and
accompanying information, including the results of the inspection of the manufacturing facilities, the FDA may issue either an
approval letter or a Complete Response Letter. An approval letter authorizes commercial marketing of the drug with specific
prescribing information for specific indications. A Complete Response Letter indicates that the review cycle of the application is
complete, and that it will not be approved in its present form. A Complete Response Letter usually describes all of the specific
deficiencies in the NDA and may require substantial additional testing or information for the FDA to reconsider the application. The
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Complete Response Letter may require additional pivotal Phase 3 clinical trial(s) and/or other significant and time-consuming
requirements related to clinical data, non-clinical data or manufacturing processes, among others. If a Complete Response Letter is
issued, the applicant may choose either to resubmit the NDA, addressing all of the deficiencies identified in the letter, or to withdraw
the application. If and when all deficiencies have been addressed to the FDA’s satisfaction in a resubmitted NDA, the FDA will issue
an approval letter. The FDA has committed to reviewing such resubmissions in response to an issued Complete Response Letter in
either two or six months, depending on the type of information included. Even if such data and information are submitted, however,
the FDA may ultimately decide that the NDA does not satisfy the regulatory criteria for approval. Data obtained from clinical trials are
not always conclusive and the FDA may interpret data differently than the applicant interprets the same data.
Even if a product receives marketing approval, the approval may be limited to specific indications and dosages or the indications
for use may otherwise be limited, which could restrict the commercial value of the product. Further, the FDA may require that certain
contraindications, warnings, or precautions be included in the product labeling. The FDA may impose restrictions and conditions on
product distribution, prescribing, or dispensing in the form of a REMS plan, or otherwise limit the scope of any approval. In addition,
the FDA may require post-marketing or Phase 4 clinical trials, designed to further assess a product’s safety and effectiveness, and/or
testing and surveillance programs to monitor the safety of approved products that have been commercialized.
Post-Approval Requirements for Pharmaceutical Products
Following approval of a new therapeutic product, the manufacturer and the approved product are subject to pervasive and
continuing regulation by the FDA, including, among other things, monitoring and record-keeping activities; reporting of adverse
experiences with the product; product samplings and distribution restrictions; complying with promotion and advertising
requirements, which include restrictions on promoting drugs for unapproved uses or patient populations (i.e., “off-label use”) and
limitations on industry-sponsored scientific and educational activities. Although physicians may prescribe legally available products
for off-label uses, manufacturers may not market or promote such uses. The FDA and other agencies actively enforce the laws and
regulations prohibiting the promotion of off-label uses, and a company that is found to have improperly promoted off-label uses may
be subject to significant liability.
Moreover, if there are any modifications to the product, including changes in indications, labeling, or manufacturing processes
or facilities, the applicant may be required to submit and obtain FDA approval of a new NDA or an NDA supplement, which may
require the applicant to develop additional data or conduct additional non-clinical studies and clinical trials. In particular, securing
FDA approval for new indications is similar to the process for approval of the original indication and requires, among other things,
submitting data from adequate and well-controlled clinical trials to demonstrate the product’s safety and efficacy in the new
indication. Even if such trials are conducted, the FDA may not approve any expansion of the labeled indications for use in a timely
fashion, or at all.
In addition, FDA regulations require that products be manufactured in specific approved facilities and in accordance with
cGMP. The cGMP regulations include requirements relating to organization of personnel, buildings and facilities, equipment, control
of components and drug product containers and closures, production and process controls, packaging and labeling controls, holding
and distribution, laboratory controls, records and reports, and returned or salvaged products. Drug manufacturers and other entities
involved in the manufacture and distribution of approved therapeutics are required to register their establishments with the FDA and
certain state agencies and are subject to periodic unannounced inspections by the FDA to assess compliance with cGMP and other
requirements. Changes to the manufacturing process, specifications or container closure system for an approved drug product are
strictly regulated and often require prior FDA approval before being implemented. FDA regulations also require, among other things,
the investigation and correction of any deviations from cGMP and the imposition of reporting and documentation requirements upon
the NDA sponsor and any third-party manufacturers involved in producing the approved therapeutic product. Accordingly, both
sponsors and manufacturers must continue to expend time, money, and effort in the area of production and quality control to maintain
cGMP compliance and other aspects of quality control and quality assurance, and to ensure ongoing compliance with other statutory
requirements of the FDC Act.
Accordingly, even after a new drug approval is granted, the FDA may withdraw the approval if compliance with regulatory
requirements and standards is not maintained, or if problems occur after the product reaches the market. Later discovery of previously
unknown problems with a product, including adverse events of unanticipated severity or frequency, or with manufacturing processes,
or failure to comply with regulatory requirements, may result in revisions to the approved labeling to add new safety information;
imposition of post-market studies or clinical trials to assess new safety risks; or the imposition of distribution or other restrictions
under a REMS plan. Other potential consequences of regulatory non-compliance include, among other things:
•
Restrictions on the marketing or manufacturing of the product, complete withdrawal of the product from the market or
product recalls;
•
fines, warning letters or other enforcement-related letters or clinical holds on post-approval clinical trials;
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•
refusal of the FDA to approve pending NDAs or supplements to approved NDAs;
•
product seizure or detention, or refusal to permit the import or export of products; injunctions or the imposition of civil or
criminal penalties;
•
consent decrees, corporate integrity agreements, debarment, or exclusion from federal health care programs; and/or
•
mandated modification of promotional materials and labeling and the issuance of corrective information.
Expedited Development and Review Programs
The FDA is authorized to designate certain drug products for expedited development or review if they are intended to address an
unmet medical need in the treatment of a serious or life-threatening disease or condition. These programs include fast-track
designation, breakthrough therapy designation, and priority review designation.
To be eligible for a fast-track designation, the FDA must determine, based on the request of a sponsor, that a product is intended
to treat a serious or life-threatening disease or condition and demonstrates the potential to address an unmet medical need by providing
a therapy where none exists or a therapy that may be potentially superior to an existing therapy based on efficacy or safety factors.
Fast-track designation provides opportunities for more frequent interactions with the FDA review team to expedite development and
review of the product. The FDA may also review sections of the NDA for a fast-track product on a rolling basis before the complete
application is submitted, if the sponsor and the FDA agree on a schedule for the submission of the application sections, and the
sponsor pays any required user fees upon submission of the first section of the NDA. In addition, fast-track designation may be
withdrawn by the sponsor or rescinded by the FDA if the designation is no longer supported by data emerging in the clinical trial
process. The sponsor can request the FDA to designate the product for fast-track status any time before receiving NDA approval, but
ideally no later than the pre-NDA meeting.
The FDA also may designate a product for priority review if it is a drug that treats a serious condition and, if approved, would
provide a significant improvement in safety or effectiveness. When a marketing application is submitted with a request for priority
review, the FDA determines on a case-by-case basis whether the proposed drug represents a significant improvement in treatment,
prevention or diagnosis of disease when compared with other available therapies. Significant improvement may be illustrated by
evidence of increased effectiveness in the treatment of a condition, elimination or substantial reduction of a treatment-limiting drug
reaction, documented enhancement of patient compliance that may lead to improvement in serious outcomes, or evidence of safety
and effectiveness in a new subpopulation. A priority review designation is intended to direct overall attention and resources to the
evaluation of such applications, and to shorten the FDA’s goal for taking action on a marketing application from 10 months to six
months from the date of filing for an NME NDA, or from 10 months to six months from the date of receipt for a non-NME NDA.
Additionally, a drug may be eligible for designation as a breakthrough therapy if the product is intended, alone or in
combination with one or more other drugs or biologics, to treat a serious or life-threatening condition and preliminary clinical
evidence indicates that the product may demonstrate substantial improvement over currently approved therapies on one or more
clinically significant endpoints. The FDA must take certain actions with respect to breakthrough therapies, such as holding timely
meetings with and providing advice to the product sponsor, intended to expedite the development and review of an application for
approval of a breakthrough therapy.
Even if a product qualifies for one or more of these programs, the FDA may later decide that the product no longer meets the
conditions for qualification or decide that the time period for FDA review or approval will not be shortened. Fast-track designation,
priority review, and breakthrough therapy designation do not change the standards for approval but may expedite the development or
approval process.
Accelerated Approval Pathway
Products studied for their safety and effectiveness in treating serious or life-threatening illnesses and that provide meaningful
therapeutic benefit over existing treatments may receive accelerated approval from the FDA and may be approved on the basis of
adequate and well-controlled clinical trials establishing that the drug product has an effect on a surrogate endpoint that is reasonably
likely to predict clinical benefit. The FDA may also grant accelerated approval for such a drug when the product has an effect on an
intermediate clinical endpoint that can be measured earlier than an effect on irreversible morbidity or mortality, or IMM, which is
reasonably likely to predict an effect on IMM or other clinical benefit, taking into account the severity, rarity, or prevalence of the
condition and the availability or lack of alternative treatments or on the basis of an effect on a clinical endpoint other than survival or
irreversible morbidity. As a condition of approval, the FDA may require that a sponsor of a drug receiving accelerated approval
perform adequate and well-controlled post-marketing clinical trials to verify and describe the predicted effect on IMM or other clinical
endpoint, and the product may be subject to expedited withdrawal procedures. If the FDA concludes that a drug shown to be effective
can be safely used only if distribution or use is restricted, it will require such post-marketing restrictions, as it deems necessary to
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assure safe use of the product. Drugs granted accelerated approval must meet the same statutory standards for safety and effectiveness
as those granted traditional approval.
For the purposes of accelerated approval, a surrogate endpoint is a marker, such as a laboratory measurement, radiographic
image, physical sign, or other measure that is thought to predict clinical benefit but is not itself a measure of clinical benefit. Surrogate
endpoints can often be measured more easily or more rapidly than clinical endpoints. An intermediate clinical endpoint is a
measurement of a therapeutic effect that is considered reasonably likely to predict the clinical benefit of a drug, such as an effect on
IMM. The FDA has limited experience with accelerated approvals based on intermediate clinical endpoints but has indicated that such
endpoints generally may support accelerated approval when the therapeutic effect measured by the endpoint is not itself a clinical
benefit and basis for traditional approval, if there is a basis for concluding that the therapeutic effect is reasonably likely to predict the
ultimate long-term clinical benefit of a drug.
The accelerated approval pathway is most often used in settings in which the course of a disease is long, and an extended period
of time is required to measure the intended clinical benefit of a drug, even if the effect on the surrogate or intermediate clinical
endpoint occurs rapidly. For example, accelerated approval has been used extensively in the development and approval of drugs for
treatment of a variety of cancers in which the goal of therapy is generally to improve survival or decrease morbidity and the duration
of the typical disease course requires lengthy and sometimes large clinical trials to demonstrate a clinical or survival benefit.
The accelerated approval pathway is usually contingent on a sponsor’s agreement to conduct, diligently, additional post-
approval confirmatory studies to verify and describe the drug’s clinical benefit. As a result, a drug candidate approved on this basis is
subject to rigorous post-marketing compliance requirements, including the completion of Phase 4 or post-approval clinical trials to
confirm the effect on the clinical endpoint. In addition, as part of the Consolidated Appropriations Act for 2023, Congress provided
the FDA additional statutory authority to mitigate potential risks to patients from continued marketing of ineffective drugs previously
granted accelerated approval. Under these recent amendments to the FDC Act, the agency may require a sponsor of a product granted
accelerated approval to have a confirmatory trial underway prior to approval. The sponsor must also submit progress reports on a
confirmatory trial every six months until the trial is completed, and such reports will be published on the FDA’s website. Failure to
conduct required post-approval studies, or to confirm the predicted clinical benefit of the product during post-marketing studies,
allows the FDA to withdraw approval of the drug. Congress also recently amended the law to give the FDA the option of using
expedited procedures to withdraw product approval if the sponsor’s confirmatory trial fails to verify the claimed clinical benefits of
the product. All promotional materials for products approved for marketing under the accelerated approval program are subject to
prior review by the FDA.
Patent Listing and Regulatory Exclusivity under the Hatch-Waxman Act
As noted above, Congress created the 505(b)(2) NDA pathway in 1984 as part of the Hatch-Waxman Act amendments to the
FDC Act. At the same time, it also established an abbreviated regulatory scheme authorizing the FDA to approve generic drugs that
are shown to contain the same active ingredients as, and to be bioequivalent to, drugs previously approved by the FDA pursuant to
NDAs. To obtain approval of a generic drug, an applicant must submit an abbreviated new drug application, or ANDA, to the agency.
An ANDA is a comprehensive submission that contains, among other things, data and information pertaining to the active
pharmaceutical ingredient, bioequivalence, drug product formulation, specifications and stability of the generic drug, as well as
analytical methods, manufacturing process validation data and quality control procedures. ANDAs are “abbreviated” because they
cannot include non-clinical and clinical data to demonstrate safety and effectiveness. Instead, in support of such applications, a generic
manufacturer must rely on the non-clinical and clinical testing conducted for a drug product previously approved under an NDA,
known as the reference listed drug, or RLD. Unlike the ANDA pathway, which does not allow applicants to submit new clinical data
other than bioavailability or bioequivalence data, the 505(b)(2) regulatory pathway does not preclude the possibility that a follow-on
applicant would need to conduct additional clinical trials or nonclinical studies to demonstrate safety or effectiveness of the proposed
change(s) being made to a previously approved drug.
In order for an ANDA to be approved, the FDA must find that the generic version is identical to the RLD with respect to the
active ingredients, the route of administration, the dosage form, the strength of the drug and the conditions of use of the drug. At the
same time, the FDA must also determine that the generic drug is “bioequivalent” to the innovator drug. Under the statute, a generic
drug is bioequivalent to a RLD if “the rate and extent of absorption of the drug do not show a significant difference from the rate and
extent of absorption of the listed drug.” Upon approval of an ANDA, the FDA indicates whether the generic product is
“therapeutically equivalent” to the RLD in the publication, Approved Drug Products with Therapeutic Equivalence Evaluations, or the
Orange Book. Physicians and pharmacists consider a therapeutic equivalent generic drug to be fully substitutable for the RLD. In
addition, by operation of certain state laws and numerous health insurance programs, the FDA’s designation of therapeutic
equivalence often results in substitution of the generic drug without the knowledge or consent of either the prescribing physician or
patient.
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As part of the NDA review and approval process, applicants are required to list with the FDA each patent that has claims that
cover the applicant’s product or method of therapeutic use. Upon approval of a new drug, each of the patents listed in the application
for the drug is then published in the Orange Book. Drugs listed in the Orange Book can, in turn, be cited by potential follow-on
competitors in support of approval of an ANDA or a 505(b)(2) NDA that relies in full or in part on the reference product.
When an ANDA applicant submits its application to the FDA, it is required to certify to the FDA concerning any patents listed
for the reference product in the FDA’s Orange Book. Specifically, the ANDA applicant must certify that: (i) the required patent
information has not been filed; (ii) the listed patent has expired; (iii) the listed patent has not expired, but will expire on a particular
date and approval is sought after patent expiration; or (iv) the listed patent is invalid or will not be infringed by the new product.
Moreover, to the extent that the Section 505(b)(2) NDA applicant is relying on studies conducted for an already approved product, the
applicant also is required to certify to the FDA concerning any patents listed for the NDA-approved product in the Orange Book to the
same extent that an ANDA applicant would.
If the follow-on applicant does not challenge the innovator’s listed patents, FDA will not approve the ANDA or 505(b)(2)
application until all the listed patents claiming the referenced product have expired. A certification that the new product will not
infringe the already approved product’s listed patents, or that such patents are invalid, is called a Paragraph IV certification. If the
follow-on applicant has provided a Paragraph IV certification to the FDA, the applicant must also send notice of the Paragraph IV
certification to the NDA and patent holders once the ANDA or 505(b)(2) NDA has been accepted for filing by the FDA. The NDA
and patent holders may then initiate a patent infringement lawsuit in response to the notice of the Paragraph IV certification. The filing
of a patent infringement lawsuit within 45 days of the receipt of a Paragraph IV certification automatically prevents the FDA from
approving the ANDA or 505(b)(2) NDA until the earlier of 30 months, expiration of the patent, settlement of the lawsuit, or a decision
in the infringement case that is favorable to the ANDA/505(b)(2) applicant.
An ANDA or 505(b)(2) NDA also will not be approved until any applicable non-patent exclusivities listed in the Orange Book
for the referenced product have expired. The Hatch-Waxman Act amendments to the FDC Act provide a five-year period of non-
patent data exclusivity within the United States to the first applicant to gain approval of an NDA for a new chemical entity, or NCE.
For the purposes of this provision, an NCE is a drug that contains no active moiety that has previously been approved by the FDA in
any other NDA. An active moiety is the molecule or ion responsible for the physiological or pharmacological action of the drug
substance. In cases where such NCE exclusivity has been granted, an ANDA or 505(b)(2) NDA may not be filed with the FDA until
the expiration of five years unless the submission is accompanied by a Paragraph IV certification, in which case the applicant may
submit its application four years following the original product approval.
The FDC Act also provides for a period of three years of data exclusivity if an NDA or NDA supplement includes reports of one
or more new clinical investigations, other than bioavailability or bioequivalence studies that were conducted or sponsored by the
applicant, are deemed by the FDA to be essential to the approval of the application or supplement. This three-year exclusivity period
often protects changes to a previously approved drug product, such as new indications, dosage forms, route of administration or
combination of ingredients. Three-year exclusivity would be available for a drug product that contains a previously approved active
moiety, provided the statutory requirement for a new clinical investigation is satisfied. Unlike five-year NCE exclusivity, an award of
three-year exclusivity does not block the FDA from accepting ANDAs or 505(b)(2) NDAs seeking approval for generic versions of
the drug as of the date of approval of the original drug product; rather, this three-year exclusivity covers only the conditions of use
associated with the new clinical investigations and, as a general matter, does not prohibit the FDA from approving follow-on
applications for drugs containing the original active ingredient.
Five-year and three-year exclusivity also will not delay the submission or approval of a traditional NDA filed under Section
505(b)(1) of the FDC Act; however, an applicant submitting a traditional NDA would be required to conduct or obtain a right of
reference to all of the non-clinical studies and adequate and well-controlled clinical trials necessary to demonstrate safety and
effectiveness.
Patent Term Extension
A patent claiming a prescription drug or medical device for which FDA approval is granted may be eligible for a limited patent
term extension under the FDC Act, which permits patent restoration of up to five years for patent term lost during product
development and the FDA regulatory review provided that certain statutory and regulatory requirements are met. The length of the
patent term extension is related to the length of time the drug or medical device is under regulatory review while the patent is in force.
The restoration period granted on a patent covering a new FDA-regulated medical product is typically one-half the time between the
date a clinical investigation on human beings is begun and the submission date of an application for premarket approval of the
product, plus the time between the submission date of an application for approval of the product and the ultimate approval date. Patent
term restoration cannot be used to extend the remaining term of a patent past a total of 14 years from the product’s approval date. Only
one patent applicable to an eligible FDA-approved product is eligible for the extension, and the application for the extension must be
submitted prior to the expiration of the patent in question. A patent that covers multiple products for which approval is sought can
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only be extended in connection with one of the marketing approvals. The U.S. Patent and Trademark Office, or USPTO, reviews and
approves the application for any patent term extension or restoration in consultation with the FDA.
Rules and Regulations Relating to Companion or Complementary Diagnostics
The success of one or more of our drug candidates may depend, in part, on the development and commercialization of either a
companion diagnostic or a complementary diagnostic. Companion diagnostics and complementary diagnostics can identify patients
who are most likely to benefit from a particular drug; identify patients likely to be at increased risk for serious side effects as a result
of treatment with a particular drug; or monitor response to treatment with a particular drug for the purpose of adjusting treatment to
achieve improved safety or effectiveness. Companion diagnostics and complementary diagnostics are regulated as medical devices by
the FDA. The level of risk associated with a new diagnostic test combined with available controls to mitigate risk determines whether
a companion diagnostic device requires PMA approval from the FDA or if it can be cleared by the agency through the 510(k)
premarket notification process based on a showing of substantial equivalence to a commercially available device. For a novel drug for
which a companion diagnostic device is essential for the safe and effective use of the product, the companion diagnostic device should
be developed and PMA-approved or 510(k)-cleared contemporaneously with the FDA’s approval of the drug. The use of the
companion diagnostic device will be stipulated in the labeling of the drug, and vice versa.
Rules and Regulations Relating to Coverage, Pricing, and Reimbursement for Prescription Pharmaceutical Products
Sales of pharmaceutical products approved for marketing by the FDA and foreign regulatory authorities will depend, in part, on
the extent to which such products will be covered by insurance payors, such as government health programs, commercial insurance
and managed care organizations. In the United States no uniform policy of coverage and reimbursement for human drug products
exists. Accordingly, decisions regarding the extent of coverage and the amount of reimbursement to be provided for any of our future
drugs will be made on a payor-by-payor basis. As a result, the coverage determination process is often a time-consuming and costly
process that will require us to provide scientific and clinical support for the use of our drugs to each payor separately, with no
assurance that coverage and adequate reimbursement will be obtained.
The United States government, state legislatures and foreign governments have shown significant interest in implementing cost
containment programs to limit the growth of government-paid health care costs, including price-controls, restrictions on
reimbursement and requirements for substitution of generic products for branded prescription drugs. For example, the federal law
contains provisions that may reduce the profitability of drug products through increased rebates for drugs reimbursed by Medicaid
programs, extension of Medicaid rebates to Medicaid managed care plans, mandatory discounts for certain Medicare Part D
beneficiaries and annual fees based on pharmaceutical companies’ share of sales to federal health care programs. Adoption of general
controls and measures, coupled with the tightening of restrictive policies in jurisdictions with existing controls and measures, could
limit payments for pharmaceutical drugs. The Medicaid Drug Rebate Program requires pharmaceutical manufacturers to enter into and
have in effect a national rebate agreement with the Secretary of the Department of Health and Human Services, or HHS, as a condition
for states to receive federal matching funds for the manufacturer’s outpatient drugs furnished to Medicaid patients. The Patient
Protection and Affordable Care Act, or ACA, enacted in 2010, made several changes to the Medicaid Drug Rebate Program and
expanded the universe of Medicaid utilization subject to drug rebates by requiring pharmaceutical manufacturers to pay rebates on
Medicaid managed care utilization and by enlarging the population potentially eligible for Medicaid drug benefits. In addition, the
Medicare Prescription Drug, Improvement, and Modernization Act of 2003, or MMA, established the Medicare Part D program to
provide a voluntary prescription drug benefit to Medicare beneficiaries. Under Part D, Medicare beneficiaries may enroll in
prescription drug plans offered by private entities that provide coverage of outpatient prescription drugs. Unlike Medicare Part A and
B, Part D coverage is not standardized. While all Medicare drug plans must give at least a standard level of coverage set by Medicare,
Part D prescription drug plan sponsors are not required to pay for all covered Part D drugs, and each drug plan can develop its own
drug formulary that identifies which drugs it will cover and at what tier or level. However, Part D prescription drug formularies must
include drugs within each therapeutic category and class of covered Part D drugs, though not necessarily all the drugs in each category
or class. Any formulary used by a Part D prescription drug plan must be developed and reviewed by a pharmacy and therapeutic
committee. Government payment for some of the costs of prescription drugs may increase demand for products that receive marketing
approval in the future. However, any negotiated prices for future products covered by a Part D prescription drug plan likely will be
lower than the prices we might otherwise obtain. Moreover, while the MMA applies only to drug benefits for Medicare beneficiaries,
private payors often follow Medicare coverage policy and payment limitations in setting their own payment rates. Any reduction in
payment that results from the MMA may result in a similar reduction in payments from non-governmental payors.
For a drug product to receive federal reimbursement under the Medicaid or Medicare Part B programs or to be sold directly to
U.S. government agencies, the manufacturer must extend discounts to entities eligible to participate in the 340B drug pricing program.
The maximum amount that a manufacturer may charge a 340B covered entity for a given product is the average manufacturer price, or
AMP reduced by the rebate amount paid by the manufacturer to Medicaid for each unit of that product. As of 2010, the ACA
expanded the types of entities eligible to receive discounted 340B pricing, although, under the current state of the law, with the
exception of children’s hospitals, these newly eligible entities will not be eligible to receive discounted 340B pricing on orphan drugs.
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In addition, as 340B drug pricing is determined based on AMP and Medicaid rebate data, the revisions to the Medicaid rebate formula
and AMP definition described above could cause the required 340B discount to increase. Pharmaceutical manufacturers, their vendors,
and the federal agency responsible for administering the 340B program, HRSA, have been actively challenging various aspects of the
program and litigation is pending in multiple jurisdictions. The outcome of such lawsuits, as well as potential legislative changes
enacted by Congress or programmatic changes implemented at HRSA by the incoming Trump Administration, may impact the 340B
program in the future.
Moreover, there has been heightened governmental scrutiny over the manner in which manufacturers set prices for their
marketed products, which has resulted in several Congressional inquiries and proposed and enacted federal and state legislation
designed to, among other things, bring more transparency to product pricing, review the relationship between pricing and
manufacturer patient programs, and reform government program reimbursement methodologies for drug products. HHS has solicited
feedback on various measures intended to lower drug prices and reduce the out-of-pocket costs of drugs and has implemented others
under its existing authority. For example, in August 2022 President Biden signed into law the Inflation Reduction Act, or the IRA.
Among other things, the IRA has multiple provisions that may impact the prices of drug products that are both sold into the Medicare
program and throughout the United States starting in 2023, a manufacturer of drugs products covered by Medicare Parts B or D must
pay a rebate to the federal government if their drug product’s price increases faster than the rate of inflation. This calculation is made
on a drug product by drug product basis and the amount of the rebate owed to the federal government is directly dependent on the
volume of a drug product that is paid for by Medicare Parts B or D. Additionally, starting for payment year 2026, CMS is negotiating
drug prices annually for a select number of single source Part D drugs without generic competition. CMS will also negotiate drug
prices for a select number of Part B drugs starting for payment year 2028. If a drug product is selected by CMS for negotiation, it is
expected that the revenue generated from such drug will decrease. CMS has begun to implement these new authorities, entering into
the first set of agreements with pharmaceutical manufacturers to conduct price negotiations in October 2023 and ultimately
announcing the first round of negotiated prices for the first 10 drugs in August 2024; those negotiated “maximum fair prices” will be
effective as of January 1, 2026 (payment year 2026). CMS is currently engaged in its second selection process and is expected to
publish the next 15 drugs selected for negotiation in February 2025. However, the IRA’s impact on the pharmaceutical industry in the
United States remains uncertain, in part because multiple large pharmaceutical companies and other stakeholders (e.g., the U.S.
Chamber of Commerce) have initiated federal lawsuits against CMS arguing the program is unconstitutional for a variety of reasons,
among other complaints. Those lawsuits are currently ongoing.
At the state level, legislatures have increasingly passed legislation and implemented regulations designed to control
pharmaceutical product pricing, including price or patient reimbursement constraints, discounts, restrictions on certain product access
and marketing cost disclosure and transparency measures. In December 2020, the U.S. Supreme Court held unanimously that federal
law does not preempt the states’ ability to regulate pharmacy benefit managers, or PBMs, and other members of the health care and
pharmaceutical supply chain, an important decision that has led to further and more aggressive efforts by states in this area. In mid-
2022, the FTC also launched sweeping investigations into the practices of the PBM industry and published an interim report with its
findings in mid-2024 that could lead to additional federal and state legislative or regulatory proposals targeting such entities’
operations, pharmacy networks, or financial arrangements, including in the 2025-2026 congressional session. Significant efforts to
change the PBM industry as it currently exists in the United States may affect the entire pharmaceutical supply chain and the business
of other stakeholders, including pharmaceutical product developers like us.
As noted above, the marketability of any products for which we receive regulatory approval for commercial sale may suffer if
the government and insurance payors fail to provide adequate coverage and reimbursement. We expect that the increasing emphasis
on cost containment measures in the United States will continue to increase the pressure on pharmaceutical pricing. Coverage policies
and insurance reimbursement rates may change at any time. Even if favorable coverage and reimbursement status is attained for one or
more products for which we receive regulatory approval, less favorable coverage policies and reimbursement rates may be
implemented in the future.
In addition, in most foreign countries, the proposed pricing for a medicinal product must be approved before it may be lawfully
marketed. The requirements governing drug pricing and reimbursement vary widely from country to country. Some countries provide
that drug products may be marketed only after a reimbursement price has been agreed.
Privacy and Security Laws and Regulations and Patient Information Access Laws and Regulations Applicable to our Business
HIPAA and HITECH
Under the Administrative Simplification provisions of the federal Health Insurance Portability and Accountability Act of 1996,
or HIPAA, as amended by the federal Health Information Technology for Economic and Clinical Health Act, or HITECH, the U.S.
Department of HHS has issued regulations, or HIPAA Regulations, that establish uniform standards governing the conduct of certain
electronic healthcare transactions and requirements for protecting the privacy and security of protected health information, or PHI,
used or disclosed by healthcare providers, health plans, and healthcare clearinghouses that conduct certain healthcare transactions
electronically, known as “covered entities.” As a clinical laboratory, we are acting as a covered entity and are subject to HIPAA and
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HITECH. The following four principal regulations with which we are required to comply have been issued in final form under HIPAA
and HITECH: privacy regulations, security regulations, the breach notification rule, and standards for electronic transactions, which
establish standards for common healthcare transactions.
The privacy regulations of HIPAA and HITECH protect medical records and other PHI by limiting their use and release, giving
patients a variety of rights, including the right to access their medical records, and limiting most disclosures of health information to
the minimum amount necessary to accomplish an intended purpose. HIPAA also requires covered entities to enter into business
associate agreements to obtain a written assurance of compliance with HIPAA from individuals or organizations who provide services
to covered entities involving the use or disclosure of PHI, also known as “business associates.” As a general rule, a covered entity or
business associate may not use or disclose PHI, except as permitted under the privacy regulations of HIPAA and HITECH.
Covered entities must also comply with the security regulations of HIPAA and HITECH, which establish requirements for
safeguarding the confidentiality, integrity, and availability of electronic PHI. The HIPAA security regulations, or HIPAA Security
Rule, require the implementation of administrative, physical, and technical safeguards and the adoption of written security policies and
procedures. The HIPAA Security Rule is currently undergoing a proposed update, which, if implemented, will impose more stringent
security measures on covered entities.
In addition, HITECH established, among other things, certain breach notification requirements with which covered entities must
comply. In particular, a covered entity must report breaches of PHI that have not been encrypted or otherwise secured in accordance
with guidance from the Secretary of HHS, or the Secretary. Required breach notices must be made as soon as reasonably practicable,
but no later than sixty days following discovery of the breach. Reports must be made to affected individuals, the Secretary, and,
depending on the size of the breach, the local and national media. Covered entities are also subject to audit under HHS’s HITECH-
mandated audit program and may be investigated in connection with privacy or data security.
There are significant civil and criminal fines and other penalties that may be imposed for violating HIPAA. A covered entity or
business associate is liable for civil monetary penalties for a violation that is based on an act or omission of any of its agents, including
a downstream business associate, as determined according to the federal common law of agency. Penalties for failure to comply with a
requirement of HIPAA and HITECH vary significantly depending on the failure and include civil monetary penalties of up to
approximately $2.1 million per violation of the same requirement per calendar year (as of August 8, 2024, subject to annual inflation
adjustments). A single breach incident may violate multiple requirements, resulting in potential penalties in excess of $2.1 million.
Additionally, a person who knowingly obtains or discloses individually identifiable health information in violation of HIPAA may
face a criminal penalty of up to $50,000 and up to one year of imprisonment. These criminal penalties increase if the wrongful conduct
involves false pretenses or the intent to sell, transfer or use identifiable health information for commercial advantage, personal gain, or
malicious harm. Covered entities are also subject to enforcement by state attorneys general who were given authority to enforce
HIPAA under HITECH. Further, to the extent that we submit electronic healthcare claims and payment transactions that do not
comply with the electronic data transmission standards established under HIPAA and HITECH, payments to us may be delayed or
denied.
In addition to our clinical laboratory services, we provide management and technology services to certain companies,
institutions, and agencies that are covered entities and have entered into business associate agreements with these entities as business
associates. In addition to being directly responsible for compliance with applicable HITECH Act requirements and HIPAA regulations
as a business associate, we have contractually agreed to comply with HITECH and HIPAA Regulations; and in some instances, we
have agreed to indemnify our covered entity clients if we breach our obligations with respect to these laws and regulations and/or in
the event of a reportable breach of PHI.
CMIA
The HIPAA privacy, security, and breach notification regulations establish a uniform federal “floor” but do not supersede state
laws that are more stringent or that provide individuals with greater rights with respect to the privacy or security of, and access to,
their records containing PHI, or insofar as such state laws apply to personal information that is broader in scope than PHI, as defined
under HIPAA. The compliance requirements of these laws, including additional breach reporting requirements, and the penalties for
violation vary widely, and new privacy and security laws in this area are evolving. For example, several states, such as California,
have implemented comprehensive privacy laws and regulations. The California Confidentiality of Medical Information Act, or CMIA,
imposes restrictive requirements regulating the use and disclosure of health information and other personally identifiable information.
In addition to fines and penalties imposed upon violators, some of these state laws also afford private rights of action to individuals
who believe their personal information has been misused. California’s patient privacy laws, for example, provide for penalties of up to
$250,000 and permit injured parties to sue for damages.
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CCPA/CPRA
The California Consumer Privacy Act, or CCPA, and the California Privacy Rights Act, or CPRA, set forth a privacy
framework for covered businesses by creating an expanded definition of personal information, establishing data privacy rights for
California consumers and employees, imposing special rules on the collection of consumer data from minors, and creating a new and
potentially severe statutory damages framework for businesses that violate the CCPA and/or fail to implement reasonable security
procedures and practices to prevent data breaches. Although the CCPA does not directly apply to medical information covered by
HIPAA or CMIA, certain other personal information that our business may collect and use, including through our direct-to-consumer
Picture Genetics platform, is within the scope of the CCPA and does not fall under the CCPA exception. Additionally, the CPRA
protects the rights of our employees who are California residents and provides the California Privacy Protection Agency, or CPPA,
with the power to administer and enforce the CRPA and privacy rights in California. The CPPA has the power to levy fines and bring
other enforcement actions and is in the process of implementing further regulations that could have operational impacts. In addition to
California, 18 other states have passed similar privacy laws, including Colorado, Connecticut, Delaware, Florida, Indiana, Iowa,
Kentucky, Maryland, Montana, Nebraska, New Hampshire, New Jersey, Oregon, Rhode Island, Tennessee, Texas, Utah, and Virginia.
There are also several federal privacy proposals under consideration in Congress, and other states may introduce privacy legislation
for consideration in 2025. These various privacy laws could impact our operations or that of our collaborators and business partners
and impose new regulatory requirements and increase costs of compliance.
Information Blocking Rules
The National Coordinator for Health Information Technology, or ONC, coordinates the ongoing development of standards to
enable interoperable health information technology infrastructure nationwide in the healthcare sector. In May 2020, ONC released the
final Information Blocking Rule to implement the interoperability and patient access provisions of the 21st Century Cures Act, which
took effect in 2021. We need to continually engage in ongoing reviews of all potential practices that could be considered likely to
interfere with access, exchange, or use of electronic health information, as those practices are prohibited by the Information Blocking
Rule unless one of the exceptions outlined in the Information Blocking Rule applies. Among other things, the Information Blocking
Rule requires us to provide patients with on-demand access to laboratory test results. These requirements can be inconsistent with our
obligations under state law and/or medical or ethical standards. It is currently unclear how the ONC will approach delays in providing
patient access in these situations. Health care providers, including laboratories, are subject to “disincentives” for violations of the
Information Blocking Rule. HHS and ONC released a final rule establishing disincentives for health care providers that have
committed information blocking on June 24, 2024, potentially affecting certain providers’ eligibility in the Medicare Promoting
Interoperability Program and Medicare Shared Savings Program. HHS indicated it may establish additional health care provider
disincentives in future rulemaking.
Foreign Laws and Other Laws
We are also subject to foreign privacy laws in the jurisdictions in which we sell our tests, and collect patient samples. The
interpretation, application, and interplay of consumer and health-related data protection laws in the United States, Australia, Europe,
and elsewhere are often uncertain, contradictory, and in flux. For example, the Privacy Act 1988 applies to personal data in Australia.
Additionally, the General Data Protection Regulation, or GDPR, and Cybersecurity Directive applies to personal data in the European
Union. These regulations introduced many changes to privacy and security in the European Union, including stricter rules on consent
and security duties for critical industries, including for the health sector generally and for genetic data specifically. The interpretation
of some rules continues to evolve in guidance from the main regulatory authority, the European Data Protection Board, and some
requirements may be completed by national legislation. This makes it difficult to assess the impact of these foreign data protection
laws on our business at this time.
More generally, foreign laws and interpretations governing data privacy and security are constantly evolving, and it is possible
that laws may be interpreted and applied in a manner that is inconsistent with our current practices, in which case we could be subject
to government-imposed fines or orders requiring that we change our practices. These fines can be very high. For instance, the GDPR
provides for fines of up to approximately $22 million or 4% of a group’s worldwide annual turnover for certain infringements. In
addition, privacy regulations differ widely from country to country and are enforced by individual country data protection authorities,
which have power to enforce privacy regulations. Various data protection authorities have issued fines in the millions of euros for
violations of privacy laws.
Many states have also implemented genetic testing and privacy laws imposing specific patient consent requirements and
requirements for protecting test results. The interplay of federal and state laws may be subject to varying interpretations by courts and
government agencies, creating complex compliance issues for us and our clients and potentially exposing us to additional expense,
adverse publicity, and legal and regulatory liability. Further, as regulatory focus on privacy issues continues to increase, and laws and
regulations concerning the protection of personal information expand and become more complex, these potential risks to our business
could intensify. In addition, the interpretation and application of consumer, health-related, and data protection laws are often
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uncertain, contradictory, and in flux. For example, increasing concerns about health information privacy have recently prompted the
federal government to issue guidance, taking a newly expansive view of the scope of the laws and regulations that they enforce. The
applicability and requirements of these laws and penalties for violations vary widely. Failure to maintain compliance, or changes in
state or federal laws regarding privacy or security, could result in civil and/or criminal penalties and damages and could have a
material adverse effect on our business.
In many activities, including operational use of Artificial Intelligence, or AI, tools, we are subject to emerging regulations and
guidelines. In December 2023, the European Commission, the Council, and the Parliament agreed on the provisional rules that will
comprise the European Union’s Artificial Intelligence Act, the AI Act. This comprehensive EU AI Regulation is broad in scope,
defines high-risk AI activities, and seeks to prohibit certain AI uses. The AI Act will potentially regulate entities that intend to utilize
AI applications in the EU. Anticipated range of fines for entities that are found to violate the AI Act may reach up to EUR 35 million
or up to 7% of the Company’s total worldwide annual turnover for the preceding financial year, whichever is higher. In the United
States, more than thirty states regulate AI, or are considering proposed legislation that would regulate AI, including California,
Georgia, Massachusetts, and Texas, where we conduct operations. Generally, such regulations aim to protect individuals such as
consumers, employees, and/or job applicants from bias, discrimination, and invasion of privacy and to promote transparency with
respect to use of AI by companies.
Additionally, the FTC recently published guidance for companies selling genetic testing products on securing DNA data and
outlined enforcement priorities, anticipating close monitoring of genetic testing companies’ use of AI, including DNA algorithms. The
FTC guidance instructs companies to safeguard consumers from potential detrimental effects of AI usage such as bias, invasion of
privacy, and accuracy; notes that protection of genetic data is FTC’s top priority; and reminds companies to prepare notices regarding
their collection, use, and disclosure of genetic information and to consider affirmative express consent requirements.
Numerous other federal, state, and foreign laws, including consumer protection laws and regulations, govern the collection,
dissemination, use, access to, confidentiality and security of patient health information. In addition, Congress and some states are
considering new laws and regulations that further and more broadly protect the privacy and security of medical records or health
information. With the recent increase in publicity regarding data breaches resulting in improper dissemination of consumer
information, all 50 states have passed laws regulating the actions that a business must take if it experiences a data breach, as defined
by state law, including, in certain instances, prompt disclosure within a specified amount of time to affected individuals. Congress has
also been considering similar federal legislation relating to data privacy and data protection. The FTC and states’ Attorneys General
have also brought enforcement actions and prosecuted some data breach cases as unfair and/or deceptive acts or practices under the
FTC Act and comparable state laws. In addition to data breach notification laws, some states have enacted statutes and rules requiring
businesses to reasonably protect certain types of personal information they hold or to otherwise comply with certain specified data
security requirements for personal information. We intend to continue to comprehensively protect all personal information and to
comply with applicable laws regarding the protection of such information.
In many activities, including the conduct of clinical trials, we are subject to laws and regulations governing data privacy and the
protection of health-related and other personal information. These laws and regulations govern our processing of personal data,
including the collection, access, use, analysis, modification, storage, transfer, security breach notification, destruction, and disposal of
personal data. We must comply with laws and regulations associated with the international transfer of personal data based on the
location in which the personal data originates and the location in which it is processed.
If we or our vendors fail to comply with applicable data privacy or AI laws and directives, or if the legal mechanisms we or our
vendors rely upon to allow for the transfer of personal data from the European Union to the United States (or other countries not
considered by the European Commission to provide an adequate level of data protection) are not considered adequate, we could be
subject to government enforcement actions and significant penalties against us, and our business could be adversely impacted if our
ability to transfer personal data outside of the European Union is restricted, which could adversely impact our operating results. The
GDPR has increased our responsibility and potential liability in relation to European Union personal data that we process, and we may
be required to put in place additional mechanisms to ensure compliance with the GDPR. However, our ongoing efforts related to
compliance with the GDPR may not be successful and could increase our cost of doing business. In addition, data protection
authorities of the different European Union member states may interpret the GDPR differently, and guidance on implementation and
compliance practices is often updated or otherwise revised, which adds to the complexity of processing personal data in the European
Union. In addition to the GDPR, other countries have enacted data protection legislation, which increase the complexity of doing
international business and transferring sensitive personal information from those countries to the United States.
The privacy and security of PHI and personally identifiable information stored, maintained, received, or transmitted, including
electronically, including genetic data, is subject to significant regulation in the United States and abroad. While we strive to comply
with all applicable privacy and security laws and regulations, legal standards for privacy continue to evolve, and any failure or
perceived failure to comply may result in proceedings or actions against us by government entities or others, or could cause
reputational harm, which could have a material adverse effect on our financial condition, prospects, reputation, and operations.
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Healthcare Fraud and Abuse Laws Applicable to our Business
In the United States, we must comply with various fraud and abuse laws, and we are subject to regulation by various federal,
state, and local authorities, including CMS, other divisions of HHS (such as the Office of Inspector General of the Department of
Health and Human Services, or OIG), the DOJ, individual U.S. Attorney’s Offices within the DOJ, and state and local governments.
We also may be subject to foreign fraud and abuse laws in the European Union, Australia, Canada, Japan, Taiwan, and other foreign
countries as a result of the sale of our diagnostic testing services to health care providers, medical institutions, and clinical laboratories
located in such jurisdictions.
Anti-Kickback and Fraud Statutes
In the United States, the federal Anti-Kickback Statute prohibits, among other things, knowingly and willfully offering, paying,
soliciting or receiving remuneration, directly or indirectly, overtly or covertly, in cash or in kind, in order to induce or in return for the
referral of an individual for the furnishing of, or the recommending or arranging for the furnishing of, purchasing, leasing, ordering or
arranging for or recommending purchasing, leasing or ordering of any good, facility, service or item for which payment may be made
in whole or in part by a federal healthcare program. Courts have stated that a financial arrangement may violate the Anti-Kickback
Statute if any one purpose of the arrangement is to encourage patient referrals or other federal healthcare program business, regardless
of whether there are other legitimate purposes for the arrangement. The definition of “remuneration” has been broadly interpreted to
include anything of value, including gifts, discounts, credit arrangements, payments of cash, consulting fees, waivers of co-payments,
ownership interests, and providing anything at less than its fair market value. The Anti-Kickback Statute is broad and may technically
prohibit many innocuous or beneficial arrangements within the healthcare industry, although it does contain several exceptions. HHS
has issued a series of regulatory “safe harbors” setting forth certain provisions that, if met, will immunize the parties to the
arrangement from prosecution under the Anti-Kickback Statute. Although full compliance with the statutory exceptions or regulatory
safe harbors ensures against prosecution under the federal Anti-Kickback Statute, the failure of a transaction or arrangement to fit
within a specific statutory exception or regulatory safe harbor does not necessarily mean that the transaction or arrangement is illegal
or that prosecution under the Anti-Kickback Statute will be pursued. Furthermore, a person or entity does not need to have actual
knowledge of the statute or specific intent to violate it in order to have committed a violation. Penalties for violations of the Anti-
Kickback Statute are severe and include imprisonment, criminal fines, civil monetary penalties, and exclusion from participation in
federal healthcare programs. In addition, a violation of the federal Anti-Kickback Statute can serve as a basis of liability under the
federal False Claims Act (described below). Many states also have anti-kickback statutes, some of which may apply regardless of
payor type.
In addition, in October 2018, the Eliminating Kickbacks in Recovery Act of 2018, or EKRA, was enacted as part of the
Substance Use-Disorder Prevention that Promotes Opioid Recovery and Treatment for Patients and Communities Act. EKRA is an all-
payor anti-kickback law that makes it a criminal offense to pay any remuneration to induce referrals to, or in exchange for, patients
using the services of a recovery home, a substance use clinical treatment facility, or laboratory. However, unlike the federal Anti-
Kickback Statute, EKRA is not limited to services covered by federal or state healthcare programs but applies more broadly to
services covered by “healthcare benefit programs,” including commercial insurers. Although it appears that EKRA was intended to
reach patient brokering and similar arrangements to induce patronage of substance use recovery and treatment, the language in EKRA
is broadly written. Further, certain of EKRA’s exceptions are inconsistent with the federal Anti-Kickback Statute and regulations.
Significantly, EKRA permits the DOJ to issue regulations clarifying EKRA’s exceptions or adding additional exceptions, but such
regulations have not yet been issued.
There are also U.S. federal laws related to healthcare fraud and false statements relating to healthcare matters. The healthcare
fraud statute prohibits, among other things, knowingly and willfully executing a scheme to defraud any healthcare benefit program,
including private payors. A violation of this statute is a felony and may result in fines, imprisonment or exclusion from government
payor programs such as Medicare and Medicaid programs. The false statements statute prohibits knowingly and willfully falsifying,
concealing, or covering up a material fact or making any materially false, fictitious, or fraudulent statement in connection with the
delivery of or payment for healthcare benefits, items or services. Similar to the federal Anti-Kickback Statute, a person or entity does
not need to have actual knowledge of the statute or specific intent to violate it in order to have committed a violation. A violation of
this statute is also a felony and may result in fines, imprisonment or exclusion from government payor programs.
We have adopted policies and procedures designed to comply with these laws, and in the ordinary course of our business, we
conduct internal reviews of our compliance with these laws. However, the rapid growth and international expansion of our diagnostic
testing business may increase the potential of violating these and applicable foreign fraud and abuse laws and regulations. Efforts to
ensure that our internal operations and business arrangements with foreign clinical laboratories and other third parties comply with
applicable laws and regulations will involve substantial costs. Any action brought against us or against our international employees,
customers, or commercial partners for alleged violations of foreign laws or regulations, even if we successfully defend against such an
action, could cause us to incur significant legal expenses and divert our management’s attention from the operation of our business.
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False Claims Act
Another development affecting the U.S. healthcare industry is the increased enforcement of the federal False Claims Act and, in
particular, actions brought pursuant to the False Claims Act’s “whistleblower” or “qui tam” provisions. The False Claims Act imposes
liability on any person or entity that, among other things, knowingly presents, or causes to be presented, a false or fraudulent claim for
payment to the federal government. The qui tam provisions of the False Claims Act allow a private individual to bring an action under
the False Claims Act on behalf of the federal government and permit such an individual to share in any amounts paid by the entity to
the government in fines or settlement. In addition, providers and suppliers must report and return any overpayments received from the
Medicare and Medicaid programs within 60 days of identification. Failure to identify and return such overpayments exposes the
provider or supplier to False Claims Act liability. When an entity is determined to have violated the False Claims Act, it may be
required to pay up to three times the actual damages sustained by the government, plus substantial per-claim civil penalties.
In addition, various states have enacted false claim laws analogous to the federal False Claims Act, although many of these state
laws apply where a claim is submitted to any insurance payor and not merely a government payor program. We have also received a
CID issued by the DOJ pursuant to the False Claims Act related to its investigation of allegations of medically unnecessary laboratory
testing, improper billing for laboratory testing, and remuneration received or provided in violation of the Anti-Kickback Statute and
the Stark Law. Among other things, this CID requests information and records relating to certain of the Company’s customers named
in this CID. We are cooperating with the DOJ in connection with this CID. See Note 8, Debt, Commitments and Contingencies to the
Consolidated Financial Statements,
Civil Monetary Penalties Law
The federal Civil Monetary Penalties Law, or the CMP Law, prohibits, among other things, (1) the offering or transfer of
remuneration to a Medicare or Medicaid beneficiary if the person knows or should know it is likely to influence the beneficiary’s
selection of a particular provider, practitioner, or supplier of services reimbursable by Medicare or Medicaid, unless an exception
applies; (2) employing or contracting with an individual or entity that the provider knows or should know is excluded from
participation in a federal health care program; (3) billing for services requested by an unlicensed physician or an excluded provider;
and (4) billing for medically unnecessary services. The penalties for violating the CMP Law include exclusion, substantial fines, and
payment of up to three times the amount billed, depending on the nature of the offense.
Physician Referral Prohibitions Laws and Regulations
We are also subject to the U.S. federal law directed at “self-referrals,” commonly known as the “Stark Law,” which prohibits a
physician from making referrals for certain designated health services, including laboratory services, that are covered by the Medicare
program, to an entity with which the physician or an immediate family member has a direct or indirect financial relationship, unless an
exception applies. Violation of the Stark Law results in a denial of payment for any services provided pursuant to a prohibited referral.
A physician or entity that engages in a scheme to circumvent the Stark Law’s referral prohibition may be subject to substantial fines
for each such arrangement or scheme. In addition, any person who presents or causes to be presented a claim to the Medicare program
in violation of the Stark Law is subject to substantial civil monetary penalties of an assessment of up to three times the amount
claimed and possible exclusion from participation in federal health care programs. The Stark Law is a strict liability statute, meaning
that a physician’s financial relationship with a laboratory must meet an exception under the Stark Law, or the referrals are prohibited.
Thus, unlike the Anti-Kickback Statute’s safe harbors, if a laboratory’s financial relationship with a referring physician does not meet
the requirements of a Stark Law exception, then the physician is prohibited from making Medicare and Medicaid referrals to the
laboratory and any such referrals will result in overpayments to the laboratory and subject the laboratory to the Stark Law’s penalties.
A violation of the Stark Law can serve as a basis of liability under the federal False Claims Act. Many states, including California,
have comparable laws that are not limited to Medicare referrals. The Stark Law also prohibits state receipt of federal Medicaid
matching funds for services furnished pursuant to a prohibited referral, but this provision of the Stark Law has not been implemented
by regulations.
Physician Sunshine Laws Applicable to our Business
The U.S. Physician Payments Sunshine Act imposes reporting requirements on manufacturers of certain devices, drugs, and
biologics for certain payments and transfers of value by them (and in some cases their distributors) to physicians, teaching hospitals,
and certain advanced non-physician health care practitioners, as well as ownership and investment interests held by physicians and
their immediate family members. The reporting program, known as the Open Payments program, is administered by CMS. A number
of states also have laws similar to the Sunshine Act.
Because we manufacture our own LDTs solely for use by or within our own laboratory, we believe we are exempt from these
reporting requirements. We may become subject to such reporting requirements under the terms of current CMS regulations, however,
if the FDA requires us to obtain premarket authorization for our tests as medical devices (whether because the agency determines that
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one or more of the tests do not fall within the scope of the agency’s existing LDT definition or because of its recently issued final rule
to exercise authority over LDTs as medical devices) or Congress enacts legislative reforms to the federal oversight of LDTs to subject
them to FDA regulation and/or the reporting requirements of the Sunshine Act. It is presently unknown how CMS will respond to the
recently finalized FDA policy change to effectively render all LDTs medical device products under federal law, and whether or when
it will assert that the Sunshine Act’s reporting requirements will begin to apply to the manufacturers of such LDTs. Given that
litigation is ongoing between members of the clinical laboratory industry and FDA/HHS in relation to the May 2024 LDT final rule, it
may be many months or even years before we have clarity on the applicability of state and federal Sunshine Act laws to our business.
Certain states also require medical device manufacturers to maintain compliance programs and/or be licensed as manufacturers or
distributors by a state professional board or health department. Because the FDA’s now-in-effect final rule renders a clinical
laboratory like ours a “medical device manufacturer,” we have begun the process of evaluating whether and to what extent those kinds
of medical device-specific state requirements may be applicable to our operations.
Many EU member states have adopted specific anti-gift statutes that further limit commercial practices for medical devices,
including IVD medical devices, in particular vis-à-vis health care professionals and organizations. Additionally, there has been a
recent trend of increased regulation of payments and transfers of value provided to health care professionals or entities and many EU
member states have adopted national “Sunshine Acts,” which impose reporting and transparency requirements (often on an annual
basis), similar to the requirements in the United States, on medical device manufacturers. Certain countries also mandate
implementation of commercial compliance programs.
We also may become subject to these requirements, as well as applicable state Sunshine Acts, if any therapeutic products
currently in development are successfully approved by FDA, commercialized in the United States, and become eligible for
reimbursement under a federal healthcare program such as Medicare or Medicaid.
Anti-Bribery Laws Applicable to our Business
FCPA
We are subject to the U.S. Foreign Corrupt Practices Act, or FCPA, which prohibits companies and their intermediaries from
making payments in violation of law to non-U.S. government officials for the purpose of obtaining or retaining business or securing
any other improper advantage. The sale of our tests internationally demands a high degree of vigilance in maintaining, implementing
and enforcing a policy against participation in corrupt activity. Other U.S. companies in the medical device and pharmaceutical fields
have faced substantial monetary fines and criminal penalties under the FCPA for allowing their agents to deviate from appropriate
practices in doing business with non-U.S. government officials.
Foreign Laws
We are also subject to similar anti-bribery laws in the foreign jurisdictions in which we operate. In Europe, various countries
have adopted anti-bribery laws providing for severe consequences, in the form of criminal penalties and/or significant fines for
individuals and/or companies committing a bribery offence. For instance, in the United Kingdom, under the Bribery Act of 2010,
which became effective in July 2011, bribery occurs when a person offers, gives, or promises to give a financial or other advantage to
induce or reward another individual to improperly perform certain functions or activities, including any function of a public or private
nature. Bribery of foreign public officials also falls within the scope of the Bribery Act of 2010. An individual found in violation of
the Bribery Act of 2010 faces imprisonment of up to 10 years and could be subject to an unlimited fine, as could commercial
organizations for failure to prevent bribery.
U.S. Prohibitions on the Corporate Practice of Medicine
Numerous states have enacted laws prohibiting business corporations, such as ours, from practicing medicine and employing or
engaging physicians to practice medicine, generally referred to as the prohibition against the corporate practice of medicine. These
laws are designed to prevent interference in the medical decision-making process by anyone who is not a licensed physician. For
example, California’s Medical Board has indicated that determining the appropriate diagnostic tests for a particular condition and
taking responsibility for the ultimate overall care of a patient, including providing treatment options available to the patient, would
constitute the unlicensed practice of medicine if performed by an unlicensed person. Although we have structured our management
services arrangements with our affiliated professional corporations to comply with applicable state corporate practice of medicine
laws, violation of these corporate practice of medicine laws may result in civil or criminal fines, as well as sanctions imposed against
the business corporation and/or the professional through licensure proceedings.
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Environmental and Other Regulatory Requirements Applicable to our U.S. Laboratory Operations
Our facilities are subject on an ongoing basis to federal, state, and local laws and regulations governing the use, storage,
handling, and disposal of regulated medical waste, hazardous waste, and biohazardous waste, including chemicals, biological agents
and compounds and blood and other tissue specimens. Typically, we use licensed or otherwise qualified outside vendors to dispose of
this waste. However, many of these laws and regulations provide for strict liability, holding a party potentially liable without regard to
fault or negligence. As a result, we could be held liable for damages and fines if our, or others’, business operations or other actions
result in contamination of the environment or personal injury due to exposure to hazardous materials. Our costs for complying with
these laws and regulations cannot be estimated or predicted and depends on a number of factors, including the amount and nature of
waste we produce, which depends in part on the number of tests we perform, and the terms we negotiate with our waste disposal
vendors.
Our operations are also subject to extensive requirements established by the U.S. Occupational Safety and Health
Administration relating to workplace safety for healthcare employees, including requirements to develop and implement programs to
protect workers from exposure to bloodborne pathogens by preventing or minimizing any exposure through needlestick or similar
penetrating injuries.
Sustainability
We are committed to operating sustainably and have dedicated the last couple of years to establishing the proper foundation and
internal functions that would enable us to monitor and grow our sustainability strategy. We placed our sustainability efforts and
initiatives under the purview and oversight of the Nominating and Governance Committee. We have also implemented various
policies that outline commitments and establish internal processes with respect to our sustainability efforts. Additionally, we
established a sustainability working group, made up of members of our executive team and senior management.
Environmental Impact
At Fulgent, we prioritize a holistic view of protecting and preserving our precious natural resources, as outlined in our Climate
Policy. We strive to incorporate climate-related risk assessments as part of our leadership team’s regular agenda. Our Board provides
general oversight of energy management, climate risk and opportunities, strategy, and performance. The Board, through our
sustainability working group, provides additional oversight on climate-related projects, goals, and related opportunities.
Employees and Human Capital Resources
We believe growing and retaining a strong team is crucial to our success. As of December 31, 2024, we had 1,313 (U.S. and
international) full-time employees for our laboratory services business, engaged in precision diagnostic and anatomic pathology
testing, BioPharma services, software engineering, laboratory management, sales and marketing, and corporate and administrative
activities, and we have 19 (U.S.-based) full-time employees engaged in research and development for our therapeutic development
business. We offer a comprehensive compensation program that is designed to attract and reward talented individuals who possess the
skills necessary to support our business objectives, assist in the achievement of our strategic goals and create long-term value for our
stockholders. We provide competitive salaries, equity-based compensation, and bonus programs. We also provide an expansive
benefit offering including medical, dental, and vision healthcare coverage; life and accidental death and dismemberment coverage;
optional legal, pet insurance, hospitalization, critical illness and accident coverage; insurance and disability coverage; 401(k)
investment plans with Company matching; tax-advantaged savings accounts; paid time off and leaves of absence; and wellness
programs. We provide added work-life balance to our employees through hybrid work arrangements. None of our employees are
represented by a labor union or covered by collective bargaining agreements, and we believe our overall relationship with our
employees is good.
The following persons currently serve as the directors and executive officers of Fulgent:
Directors and Executive Officers
Position
Ming Hsieh
Chairman of the Board of Directors and Chief Executive Officer
Paul Kim
Chief Financial Officer
Hanlin (Harry) Gao, M.D., Ph.D., D.A.B.M.G., F.A.C.M.G.
Chief Scientific Officer
Jian (James) Xie
President and Chief Operating Officer
Regina (Reggie) Groves
Non-Employee Director
Linda Marsh
Non-Employee Director
Michael Nohaile, Ph.D.
Non-Employee Director
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Employee Training and Engagement
Our dedicated and growing team of over 1,000 employees is a source of pride. They continuously work to expand our testing
solutions and consistently provide the highest quality of care and accuracy. In an effort to recruit the best talent pool and to encourage
the professional and personal development of every employee, we offer reimbursement for qualified educational expenses and
successful completion of undergraduate, graduate, post-graduate, professional training, and licensure courses from accredited colleges,
universities and professional organizations. In the past several years, employees have applied for a variety of courses, including
Stanford Center for Professional Development, Google Project Management Courses, Clinical Genetic Molecular Biologist Scientist
(CGMBS) Training Program, and Bachelor’s Degrees. We also provide mandatory training courses that we believe are important to
our culture, corporate goals, our business and the continued development of our employees, on a variety of topics, including
discrimination, harassment, HIPAA, insider trading, privacy, anti-corruption and anti-bribery, internally and/or through third-party
providers. In 2024, we conducted a recurrent employee feedback survey and utilized the survey results to enhance employee
engagement, implement various improvements to extend continuous learning opportunities and refine our benefit plans for 2025. In
2024, the Training & Development team hosted a series of training sessions for team members, covering key topics such as “The Art
of Giving and Receiving Feedback: 3 Part Series” and “Time Management Training: 3 Part Series”.
Workplace Safety and Health
We are committed to promoting a safe and healthy work environment, to establishing policies and procedures that support the
safety program, and to fostering a workplace that is free from hazards, substance abuse, and violence. We currently operate five
CLIA-certified and CAP-accredited labs across the United States. We seek to surpass the highest standards of diagnostic testing and to
follow applicable safety laws and regulations. We encourage reporting of concerns across all of our physical locations. Because the
health and safety of our employees is our priority, we have established policies and procedures aimed at reducing the risk of
workplace injuries, and we provide regular training to all personnel on workplace safety. In 2024 and 2023, we had 16 and 15
recordable injuries, respectively.
Access and Affordability
Our top priority is the health of patients. We believe no one should have to sacrifice their health due to financial considerations
or other reasons. We work hard to provide patients with access to quality diagnostic testing, regardless of their economic status. We
provide numerous flexible and affordable pay options which include: acceptance of commercial insurance plans; availability of cash
pricing at a discounted rate to make our tests more accessible; financial assistance resources based on various criteria for patients who
are insured with commercial insurance but need additional financial help; a self-pay option for patients who do not meet insurance
coverage policies for testing, have high-deductible plans, or have no insurance coverage; and our Compassionate Care Program, which
offers financial assistance and non-interest payment plans for patients in the United States with no medical insurance and limited
financial resources.
Corporate Information
We were incorporated in Delaware on May 13, 2016. We are the holding company of our subsidiaries, including primarily
Fulgent Therapeutics LLC, which was initially formed in June 2011. On September 30, 2016, Fulgent Therapeutics LLC became our
wholly owned subsidiary in a transaction we refer to as the Reorganization, in which the holders of all equity interests in Fulgent
Therapeutics LLC immediately prior to the Reorganization became all of our stockholders immediately following the Reorganization.
Our headquarters are located at 4399 Santa Anita Avenue, El Monte, California 91731. Our website address is
www.fulgentgenetics.com. The information contained on or that can be accessed through our website is not part of and is not
incorporated into this report by this reference.
Available Information
We file reports with the Securities and Exchange Commission, or the SEC, and make available, free of charge, on or through
our website, our annual reports on Form 10-K, quarterly reports on Form 10-Q, current reports on Form 8-K, proxy and information
statements and amendments to those reports filed or furnished pursuant to Section 13(a) or 15(d) of the Exchange Act as soon as
reasonably practicable after we electronically file such material with, or furnish it to, the SEC on their website. The SEC maintains an
internet site that contains reports, proxy and information statements, and other information regarding issuers that file electronically
with the SEC at www.sec.gov.
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Item 1A. Risk Factors.
Summary of Risk Factors
Investing in our common stock involves a high degree of risk. Before making any investment decision with respect to our
common stock, you should carefully consider the risks described below, together with the other risk factors set forth in this Item 1A,
all other information included in this report, and the other reports and documents filed by us with the SEC. The risk factors described
below are a summary of the principal risk factors associated with an investment in us.
Cybersecurity Risks
•
Actual or attempted security incidents or breaches, loss of data, or other disruptions could expose us to material liability
and materially and adversely affect our business, financial condition, and our reputation.
Business and Strategy Risks
•
Our results of operations may fluctuate significantly from period to period and can be difficult to predict.
•
We have a history of losses, and we may not be able to sustain profitability.
•
We may not be successful in our efforts to integrate any acquired businesses and technologies, and this may adversely
affect our business and results of operations. We may incur unexpected liabilities as a result of our acquisitions.
•
If our laboratory facilities become inoperable, if we are forced to vacate a facility, or if we are unable to obtain additional
laboratory space as and when needed, we would be unable to perform our tests and our business would be harmed.
•
We depend on our information technology systems and any material failure of these systems, due to hardware or software
malfunctions, delays in operation, and/or material failures to implement new or enhanced systems or cybersecurity
breaches, could materially harm our business.
•
Any inability to obtain additional capital when needed and on acceptable terms may limit our ability to execute our
business plans, and our liquidity needs could be materially affected by market fluctuations and general economic
conditions. If we raise funds by issuing equity securities, our stockholders may experience substantial dilution.
•
Impairment charges relating to our goodwill and intangible assets could negatively affect our financial performance.
Reimbursement Risks
•
Our ability to achieve or sustain profitability also depends on our collection of payment for the tests we deliver, which we
may not be able to do successfully.
•
Failure to comply with government laws and regulations related to submission of claims for our services could result in
significant monetary damages and penalties and exclusion from the Medicare and Medicaid programs and corresponding
foreign reimbursement programs. We are also subject to governmental audits and investigations, such as the current
HRSA Audit and CIDs, that could result in material refunds or settlements. Our business, prospects and financial
condition may be adversely affected as the result of the current HRSA Audit and CIDs.
Regulatory Risks
•
Any changes in laws, regulations or the enforcement discretion of the FDA with respect to the marketing of diagnostic
products, or violations of laws or regulations by us, could materially and adversely affect our business, prospects, results
of operations or financial condition.
•
If we fail to comply with applicable federal, state, local and foreign laboratory licensing requirements, we could lose the
ability to perform our tests and experience material disruptions to our business.
•
We are subject to broad legal requirements regarding the information we test and analyze, and any failure to comply with
these requirements could result in materially significant, penalties, materially damage our reputation and materially harm
our business.
•
We conduct business in a heavily regulated industry. Complying with the numerous statutes and regulations pertaining to
our business is expensive and time-consuming, and any failure by us, our consultants or commercial partners to comply
could result in substantial and material penalties.
•
We may be required to modify our business practices, pay fines, incur significant expenses, or experience losses due to
litigation or governmental investigations as a result of voluntary disclosure processes.
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Risk Related to the Development of Drug Candidates
•
Our drug candidates are in early stages of development and may fail or suffer delays that materially and adversely affect
their future commercial viability.
•
Any drug candidate that we may attempt to develop, manufacture, or market in the United States will be subject to
extensive regulation by the FDA, including regulations relating to development, preclinical testing, performance of
clinical trials, manufacturing, and post-approval commercialization and will be subject to extensive regulations outside of
the United States. Satisfaction of these and other regulatory requirements is costly, time-consuming, uncertain, and subject
to unanticipated delays. The time required to obtain FDA approval, and any other required approvals for pharmaceutical
products, including any accelerated approval, is unpredictable but typically requires years to several years and may never
be obtained.
Intellectual Property Risks
•
If we are unable to obtain and maintain patent protection for any drug candidate we develop, our competitors could
develop and commercialize products or technology similar to ours, and our ability to successfully commercialize any drug
candidate we may develop, and our technology, may be adversely affected.
•
We rely on trade secret protection, non-disclosure agreements, and invention assignment agreements to protect our
proprietary information, which may not be effective.
•
Litigation or other proceedings or third-party claims of intellectual property infringement or misappropriation could
require us to spend significant time and money and prevent us from selling our tests or developing drug candidates.
•
We may be subject to claims challenging the inventorship of our patents and other intellectual property.
•
Developments in patent law could have a negative impact on our business.
•
Obtaining and maintaining our patent protection depends on compliance with various procedural, document submission,
fee payment, and other requirements imposed by government patent agencies, and our patent protection could be reduced
or eliminated for non-compliance with these requirements.
•
Our future issued patents covering drug candidates we develop could be found invalid or unenforceable if challenged in
court or before administrative bodies in the United States or abroad.
•
Patent terms may be inadequate to protect our competitive position on our products and services for an adequate amount
of time.
•
If we do not obtain patent term extension and/or data exclusivity for any drug candidate that we may develop, our
business may be materially harmed.
•
We may not be able to enforce our intellectual property rights outside the United States.
•
Third parties may assert that our employees or consultants have wrongfully used or disclosed confidential information or
misappropriated trade secrets.
•
If we fail to comply with our obligations under license or technology agreements with third parties, we could lose license
rights that are important to our business. If our third-party licensors fail to comply with the terms of our license
arrangements, we may be forced to engage in litigation to protect our rights, which may not be successful.
Common Stock Risks
•
An active, liquid trading market for our common stock may not be sustained, which could make it difficult for
stockholders to sell their shares of our common stock.
•
The price of our common stock may be volatile, and you could lose all or part of your investment.
•
Future issuances of our common stock or rights to purchase our common stock, including pursuant to our equity incentive
plan, could result in additional dilution to the percentage ownership of our stockholders and could cause the price of our
common stock to fall.
•
We do not intend to pay dividends on our common stock, so any returns will be limited to the value of our common stock.
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Cybersecurity Risks
Actual or attempted security incidents or breaches, loss of data, or other disruptions could expose us to material liability and
materially and adversely affect our business, financial condition, and our reputation.
In the ordinary course of our business, we generate, collect and store sensitive data, including personal health information, or
PHI; personally identifiable information; intellectual property; and proprietary and other business-critical information, such as
research and development data, commercial data, and other business and financial information. We manage and maintain the data we
generate and collect and store data utilizing a combination of on-site systems and managed data center systems. We also communicate
sensitive patient data when we deliver reports summarizing test results to our customers, which we deliver via our online encrypted
web portal, encrypted email, or fax, or overnight courier. The secure processing, storage, maintenance, and transmission of this
information is vital to our operations and business strategy, and we devote significant resources to protecting the confidentiality and
integrity of this information. While we perform regular audits of our information systems security, we cannot audit our vendors,
suppliers, and customers’ systems in the same way and cannot monitor containment or the spread of malware on those systems, with a
potential resulting impact on our systems.
On occasion, we do encounter attempted security incidents. To date, these incidents have not materially affected our business.
While we are not currently aware of any cyber breaches, attacks, malicious software, or hardware that would materially and adversely
affect our business, such security incident could be present in any of our or our subsidiaries’ systems or in the systems of our
suppliers, customers, vendors, or contractors. When discovered, these incidents could cause us to suffer a material data breach. A
breach or interruption could result in material legal claims or proceedings and could result in material liability or penalties under
federal, state, or foreign laws that protect the privacy of personal information, discussed below under “We are subject to broad legal
requirements regarding the information we test and analyze, and any failure to comply with these requirements could result in
materially significant penalties, materially damage our reputation and materially harm our business.” Additionally, unauthorized
access, manipulation, loss, or dissemination could significantly damage our reputation and disrupt our operations, including our ability
to perform our tests, analyze and provide test results, bill customers or other payors, process claims for reimbursement, provide
customer service, conduct research and development activities, collect, process, and prepare company financial information, conduct
education and outreach activities and manage the administrative aspects of our operations, as described further below under “We
depend on our information technology systems and any material failure of these systems, due to hardware or software malfunctions,
delays in operation, and/or material failures to implement new or enhanced systems or cybersecurity breaches could materially harm
our business.”
Business and Strategy Risks
Our results of operations may fluctuate significantly from period to period and can be difficult to predict.
Our results of operations have experienced fluctuations from period to period, which we expect may continue in the future.
These fluctuations can occur because of a variety of factors, including, among others, the amount and timing of sales of our tests and
testing services, the prices we charge for our tests and testing services, customer or payor mix, general price degradation for our tests
and testing services or other competitive factors, the rate and timing of our billings and collections, our ability to obtain
reimbursement for our tests from insurance payors, our ability to maintain a broad and flexible testing menu, the timing and amount of
our commitments and other payments, and exchange rate fluctuations, as well as the other risk factors discussed in this report. Our
results have been, and may in the future be, impacted by events that may not recur regularly, in the same amounts or at all in the
future. For instance, in 2020, we developed and began offering a series of COVID-19 tests. We experienced substantial revenue
growth in 2020 and 2021 due primarily to the sales of, and growing demand, for these COVID-19 tests, but we have seen a decrease in
our COVID-19 revenue in recent years due to the decline in prevalence of COVID-19. The fluctuations in our operating results may
render period-to-period comparisons less meaningful, and investors should not rely on the results of any one period as an indicator of
future performance. These fluctuations in our operating results could cause our performance in any particular period to fall below the
expectations of securities analysts or investors or guidance we have provided to the public, which could negatively affect the price of
our common stock.
We have a history of losses, and we may not be able to sustain profitability.
We have a history of losses. Although we achieved profitability for the year ended December 31, 2022, we were not profitable
for the years ended December 31, 2023 and 2024, and we may not again be profitable in any future periods. Further, our revenue
levels may not grow at historical rates or at all. We may incur additional losses in the future. While we experienced significant
profitability in connection with the sale of our COVID-19 tests in previous years, the demand for these tests has declined and,
currently, we do not expect future material revenue from the sale of our COVID-19 tests and testing services. Even if there is a
reoccurrence of demand for our COVID-19 tests or other substantial revenue growth, we may be unable to again manage our
resources to effectively respond to this demand such that our revenues would again materially increase. Any losses would have an
adverse effect on our stockholders’ equity and working capital, which could negatively impact our operations and your investment in
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the Company. A failure to sustain or grow our revenue levels and to maintain profitability may negatively affect our business,
financial condition, results of operations and cash flows, and the market price of our common stock may decline or continue to
decline.
We may not be successful in our efforts to integrate any acquired businesses and technologies, and this may adversely affect
our business and results of operations. We may incur unexpected liabilities as a result of our acquisitions.
Our ability to integrate any organizations or technology that we may acquire is subject to a number of risks, including the
following:
•
failure to integrate successfully the personnel, information systems, technology, and operations of the acquired business;
•
failure to maximize the potential financial and strategic benefits of the acquisition;
•
failure to realize the expected synergies of the acquired business;
•
possible impairment of relationships with employees and clients as a result of any integration of new businesses and
management personnel;
•
impairment of goodwill, such as the impairment charge we incurred in the fourth quarter of 2023;
•
increased demand on human resources and operating systems, procedures and controls; and
•
reductions in future operating results as a result of the amortization of intangible assets.
Acquisitions are also accompanied by the risk that obligations and liabilities of an acquired business may not be adequately
reflected in the historical financial statements of that business and the risk that historical financial statements may be based on
assumptions, which are incorrect or inconsistent with our assumptions or approach to accounting policies. The acquisition and
integration of businesses may not be managed effectively, and any failure to manage the integration process could lead to disruptions
in the overall activities of the Company, a loss of clients and revenue, and increased expenses. Further, integration of an acquired
business or technology could involve significant difficulties and could require management and capital resources that otherwise would
be available for ongoing development of our existing business or pursuit of other opportunities. We may also acquire contingent
liabilities in connection with the acquisitions of a business, which may be material, and any estimates we might make regarding any
acquired contingent liabilities and the likelihood that these liabilities will materialize could differ materially from the liabilities
actually incurred. These circumstances could materially harm our business, results of operations, and prospects.
We have previously and may again in the future acquire businesses or assets, form joint ventures, make investments in other
companies or technologies, or establish other strategic relationships, any of which could harm our operating results or dilute
our stockholders’ ownership. These transactions may be subject to federal and state anti-trust laws and regulations, and any
failure to comply, or alleged failure to comply, with these laws and regulations, may adversely affect our business, operating
results and prospects.
As part of our business strategy, we have previously and may again in the future pursue acquisitions of complementary
businesses or assets (such as our acquisitions of Cytometry Specialist, Inc. or CSI; Fulgent Pharma; and Symphony Buyer, Inc., or
Inform Diagnostics), investments in other companies (such as our investment in Helio Health), technology licensing arrangements,
joint ventures, or other strategic relationships. As an organization, we have relatively limited experience with respect to acquisitions,
investments, or the formation of strategic relationships or joint ventures. If we pursue relationships with strategic partners or other
strategic relationships, our ability to establish and maintain these relationships could be challenging due to several factors. Factors
include competition with other testing companies and internal and external constraints placed on pharmaceutical and other
organizations that limit the number and type of relationships they can establish with companies like ours. Moreover, we may not be
able to identify or complete any future acquisition, investment, technology license, joint venture, or other strategic relationship in a
timely manner, on a cost-effective basis, or at all; and we may not realize the anticipated benefits of any acquisition, investment, or
joint venture as needed to recoup our costs.
To finance any acquisitions, investments, joint ventures, or other strategic relationships, we may seek to raise additional funds
through securities offerings, credit facilities, asset sales or collaborations, or licensing arrangements. To the extent these financing
transactions call for the issuance of shares of our capital stock, our existing stockholder would experience dilution in their relative
ownership of shares of our capital stock. Each of these methods of fundraising is subject to a variety of risks, including those
discussed below under “Any inability to obtain additional capital when needed and on acceptable terms may limit our ability to
execute our business plans, and our liquidity needs could be materially affected by market fluctuations and general economic
conditions.” Further, additional funds from capital-raising transactions may not be available when needed, on acceptable terms or at
all. Any inability to fund any acquisitions, investments, or strategic relationships we pursue could cause us to forfeit opportunities we
believe are promising or valuable, which could harm our prospects. If we raise funds by issuing equity securities, our stockholders
may experience substantial dilution.
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Our consummation of future acquisitions may encounter scrutiny under federal and state antitrust laws. For example, our future
acquisitions may be subject to notification under the Hart-Scott Rodino Antitrust Improvements Act of 1976 and to a waiting period
and possible review by the DOJ and the FTC. Any delays, injunctions, conditions or modifications by any of these federal agencies
could have a negative effect on us and result in the abandonment of all or part of otherwise attractive acquisition opportunities. There
can be no assurance as to the cost, scope or impact on our business, results of operations, financial condition or prospects of the
actions that may be required to obtain regulatory approvals. Further, even following completion of an acquisition, applicable
government agencies may disagree with our interpretation of these complicated statutes and regulations. These disagreements,
violations or alleged violations could result in significant civil or criminal penalties and/or equitable actions not in our favor. Any such
circumstances, violations or alleged violations could have a material adverse effect on our business and substantially diminish the
synergies and other advantages which we expect from such acquisition.
Our mix of customers fluctuates from period to period, and our revenue is often concentrated among only a small number of
customers, and the loss of or a reduction in sales to any of our customers could materially harm our business.
The composition and concentration of our customer base often fluctuates from period to period, and in certain prior periods, a
small number of customers accounted for a significant portion of our revenue. When customers who, to our knowledge, are under
common control or otherwise affiliated with each other are aggregated, one of our customers contributed $62.6 million or 22% of our
total revenue during the year ended December 31, 2024. We continue to see significant concentration in a single large customer. For
this customer and for customers generally, tests are purchased on a test-by-test basis and not pursuant to any long-term purchasing
arrangements. As a result, any or all of our customers, including affiliated customers or customers under common control who
purchase large quantities of tests, could decide at any time to decrease, delay, or discontinue their orders from us, which could
adversely affect our revenue. We believe some of these fluctuations in customer demand may be attributable, in part, to the nature of
our business. Our traditional laboratory and testing services customers can experience significant volatility in their testing demand
from period to period in the ordinary course of their operations and certain of these customers are experiencing significant financial
distress. Demand fluctuations, particularly for any large customers, often have a significant impact on our period-to-period
performance regardless of their cause.
For instance, during 2023 and 2024, several projects for our BioPharma services clients were scaled back or terminated. This
was primarily due to those clients experiencing significant financial distress, undergoing restructuring, shifting their focus, reacting to
changing market dynamics, or concluding large clinical trials. We have also experienced recent growth in demand from fertility clinics
and other laboratory customers as a result of our Beacon Expanded Carrier, or Beacon screen. However, if demand for IVF or other
assisted reproductive technologies declines, demand for our Beacon tests and services may also decline. In light of the overturning of
Roe v. Wade, the recent political climate and state court decisions, there is uncertainty regarding the potential regulatory treatment of
embryos, which may cause demand for IVF, or other assisted reproductive technologies, to decline or to decline in certain
jurisdictions. Further, if our laboratory customers decided to perform certain testing services internally, our business and results of
operations could be materially and adversely harmed. Our ability to maintain or increase sales to our existing customers depends on a
variety of factors, including the other risk factors discussed in this report, many of which are beyond our control. Because of these and
other factors, sales to any of our customers, including any key, affiliated, or commonly controlled customers, may not continue in the
amounts or at the rates as they have in the past, and such sales may never reach or exceed historical levels in any future period. The
loss of any of our customers, or a reduction in orders or difficulties collecting payments for tests ordered by any of them, could
significantly reduce our revenue and adversely affect our operating results.
We face intense competition, which could intensify further in the future, and we may fail to maintain or again increase our
revenue levels or sustain profitability if we cannot compete successfully.
We operate our businesses in very competitive and evolving fields. While we believe that we compare favorably to these
competitors, some of our competitors may have technical, competitive, or other advantages over us for the development of
technologies and processes or greater experience in particular diagnostics or therapeutic development areas, and consolidation among
pharmaceutical, diagnostic, and biotechnology companies can enhance these advantages.
More specifically, many of our competitors have longer operating histories, larger customer bases, larger research and
development staffs, more expansive brand recognition, established manufacturing capabilities and facilities, deeper market
penetration, substantially greater financial, technological and research and development resources and selling and marketing
capabilities with established sales forces; and considerably more experience dealing with insurance payors. As a result, they may be
able to respond more quickly to changes in customer requirements or preferences, develop faster and better advancements for their
technologies, product candidates and tests, create and implement more successful strategies for the promotion and sale of their tests,
obtain more favorable results from insurance payors regarding coverage and reimbursement for their offerings, adopt more aggressive
pricing policies for their tests, secure supplies from vendors on more favorable terms or devote substantially more resources to
infrastructure and systems development. In addition, competitors may be acquired by, receive investments from, or enter into other
commercial relationships with larger, well-established and well-financed companies, which may result in even more resources being
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concentrated among our competitors. Smaller or early-stage companies may also prove to be significant competitors, particularly
through collaborative arrangements with large and established companies.
Our laboratory services competitors include dozens of companies focused on pathology, genetic, and diagnostic testing services,
including specialty and reference laboratories that offer traditional single-gene and multi-gene tests. As such, we face intense
competition from other life science, biotechnology, pharmaceutical, research and development, and diagnostic companies. This
competition is subject to rapid change, could be significantly affected by new product or testing introductions, and may intensify
further in the future. With respect to our research and development business, these competitors also compete with us in recruiting and
retaining top qualified scientific and management personnel and establishing clinical trial sites and patient registration for clinical
trials, as well as in acquiring technologies complementary to, or necessary for, our programs. Our commercial opportunities could be
reduced or eliminated if our competitors develop and commercialize products that are safer, more effective, less expensive, more
convenient or easier to administer, or have fewer or less severe effects than any products that we may develop. Our competitors also
may obtain FDA, European Medicines Agency, or EMA, or other regulatory approval for their products more rapidly than we may
obtain approval for our products, which could result in our competitors establishing a strong market position before we are able to
enter the market. Even if our drug candidates achieve marketing approval, they may be priced at a significant premium over
competitive products if any have been approved by then. The key competitive factors affecting the success of our drug candidates are
likely to be their efficacy, safety, and availability of reimbursement, and drugs or drug candidates may compare more favorably than
our drug candidates. We may not be able to compete effectively against competitive organizations. If we are unable to compete
effectively, this could have a material adverse effect on our business and results of operations.
If our laboratory facilities become inoperable, if we are forced to vacate a facility, or if we are unable to obtain additional
laboratory space as and when needed, we would be unable to perform our tests, and our business would be harmed.
We perform our tests at our CLIA-certified laboratories in El Monte, California; Coppell, Texas; Needham, Massachusetts;
Phoenix, Arizona; and Alpharetta, Georgia. Our laboratories and the equipment we use to perform our tests would be costly to replace
and could require substantial lead time to replace and qualify for use. Additionally, any other laboratory facilities or equipment we
may use could be damaged or rendered inoperable by severe weather events, natural disasters (which may be exacerbated by the
effects of climate change), or man-made disasters which could render it difficult or impossible for us to perform our tests for some
period of time. The inability to perform our tests or the backlog that could develop if a laboratory becomes inoperable for even a short
time could result in adversely affected turnaround times, the loss of customers or harm to our reputation. Although we maintain
insurance for damage to our property and disruption of our business, this insurance may not be sufficient to cover all of our potential
losses and may not continue to be available to us on acceptable terms, if at all.
Further, if we need to relocate from one laboratory facility to another laboratory facility or obtain additional laboratory space,
we may have difficulty locating suitable space in a timely manner, on reasonable terms or at all. Even if acceptable space was
available, it would be challenging, time-consuming, and expensive to obtain or transfer the licensure and accreditation required for a
commercial laboratory like ours and the equipment used to perform our tests. These challenges are amplified as we maintain
laboratory space outside the United States. If we are unable to obtain or are delayed in obtaining new laboratory space as needed, we
may not be able to provide our existing tests, provide test results within acceptable turnaround times, or develop and launch new tests,
which could result in harm to our business, reputation, financial condition and results of operations.
We rely on commercial courier delivery services to transport specimens to our laboratory facilities in a timely and cost-
efficient manner, and if these delivery services are disrupted, our business could be materially harmed.
Our business depends on our ability to quickly and reliably deliver test results to our customers. We typically receive specimens
from customers within days of shipment from the United States and outside the United States, or in some cases overnight, for analysis
at our laboratory facilities. Disruptions in delivery service, whether due to labor disruptions, bad weather or natural disasters
(including severe weather, fires or other natural events which may be exacerbated by climate change), labor strikes, work stoppages,
or boycotts, pandemics or epidemics, terrorist acts or threats, force majeure events, or for other reasons, could adversely affect
specimen integrity and our ability to process specimens in a timely manner, provide test results within acceptable turnaround times
and otherwise service our customers. These circumstances could ultimately materially and adversely affect our reputation and our
business. In addition, if we are unable to continue to obtain expedited delivery services on commercially reasonable terms, our
operating results may be materially and adversely affected.
We depend on our information technology systems and any material failure of these systems, due to hardware or software
malfunctions, delays in operation, and/or material failures to implement new or enhanced systems or cybersecurity breaches,
could materially harm our business.
We depend on information technology and telecommunications systems for significant elements of our operations, such as our
laboratory information management systems, including test validation, specimen tracking and quality control; our bioinformatics
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analytical software systems; our reference library of information relating to genetic variants and their role in disease; personal
information storage, maintenance, and transmission; our customer-facing web-based portal and customer service functions; our report
production systems; our billing and reimbursement procedures; our scientific and medical data analysis and other research and
development activities and programs; and our general and administrative activities, including disclosure controls, internal control over
financial reporting and other public reporting functions. In addition, our third-party service providers depend on technology and
telecommunications systems in order to provide contracted services for us. We expect we will need to continue to expand and
strengthen a number of enterprise software systems that affect a broad range of business processes and functions, particularly if and as
our operations grow, including, for example, systems handling human resources, financial and other disclosure controls and reporting,
customer relationship management, regulatory compliance, security controls, and other infrastructure functions.
Information technology and telecommunications systems are vulnerable to disruption and damage from a variety of sources,
including power outages and other telecommunications or network failures, natural disasters, and the outbreak of war or acts of
terrorism. Breaches resulting in the compromise, disruption, degradation, manipulation, loss, theft, destruction, or unauthorized
disclosure of sensitive information can occur in a variety of ways, including but not limited to, negligent or wrongful conduct by
employees or former employees or others with permitted access to our information technology systems and information, or wrongful
conduct by hackers, competitors, or certain governments. Our third-party vendors and business partners face similar risks. Moreover,
despite network security and back-up measures, our servers and other electronic systems are vulnerable to cybersecurity breaches,
such as physical or electronic break-ins, computer viruses, ransomware attacks, phishing schemes, and similar disruptive events. Such
incidents could cause significant downtime or failures of our systems or those used by our third-party service providers. Cyber-attacks
come in many forms, including the deployment of harmful malware or ransomware, exploitation of vulnerabilities, phishing, social
engineering, and other means to compromise the confidentiality, integrity, and availability of our information technology systems and
confidential information. The techniques used by criminal elements to attack computer systems are sophisticated, change frequently
and may originate from less regulated or remote areas of the world. Although we carry property, business interruption, and cyber
liability insurance, the coverage may not be adequate to compensate for all losses that may occur in the event of system downtime or
failure. Any such disruption or loss of information technology or telecommunications systems on which critical aspects of our
operations depend could have a material adverse effect on our business and our reputation.
Additionally, if and as our business grows, we will need to continually improve and expand the scope of our technology systems
in order to maintain their adequacy for the scale of our operations. Any failure to make such improvements or any significant delay in
the planned implementation of new or enhanced systems could render our systems obsolete or inadequate, in which case our service to
our customers and our other business activities could suffer, and we could be more vulnerable to electronic breaches from outside
sources.
If our computer systems are compromised, we could be subject to significant fines, damages, reputational harm, litigation, and
enforcement actions, and we could lose trade secrets, the occurrence of any of which could materially harm our business, in addition
to possibly requiring substantial and material expenditures of resources to remedy.
We rely on a limited number of suppliers and, in some cases, a sole supplier, for certain laboratory substances, equipment and
other materials, and any delays or difficulties securing these materials could disrupt our laboratory operations and materially
harm our business.
We rely on a limited number of suppliers for certain laboratory substances used in the chemical reactions incorporated into our
tests and testing services, which we refer to as reagents, as well as for the sequencers and various other equipment and materials we
use in our laboratory operations. In particular, we rely on Illumina as the sole supplier of the next generation sequencers and
associated reagents we use to perform our genetic tests and as the sole provider of maintenance and repair services for these
sequencers; on Roche Holdings AG for certain laboratory equipment, supplies and services for our immunohistochemistry services; on
Beckman Coulter Diagnostics for certain laboratory equipment, supplies and services for our flow cytometry tests and testing services;
on Leica Biosystems for an automated digital scanning solution to scale up the digital pathology operations; and on Abbott
Laboratories for certain laboratory equipment, supplies and services for our FISH tests and testing services. Additionally, our
therapeutic development business relies on ANP Technologies, Inc. for certain laboratory services, equipment, tools, and drug
intermediates in connection with our research and development efforts. We do not have long-term agreements with most of our
suppliers and, as a result, they could cease supplying these materials and equipment generally to us at any time due to an inability to
reach agreement with us on supply terms, disruptions in their operations, a determination to pursue other activities or lines of business,
or they could fail to provide us with sufficient quantities of materials that meet our specifications, among other reasons. These
suppliers may also be affected by natural disasters such as extreme weather events, fires or flooding (which may be exacerbated as a
result of climate change), pandemics and health events, and disruptions of the global supply chain. While there are several sequencer
suppliers that we believe could replace Illumina, and while we believe that we have sufficient alternative suppliers for our other needs,
transitioning to a new supplier or locating a temporary substitute, if any are available, would be time-consuming and expensive, could
result in interruptions in or otherwise affect the performance specifications of our laboratory operations or could require that we
revalidate our tests. In addition, the use of equipment or materials provided by a replacement supplier could require us to alter our
35
laboratory operations and procedures. Moreover, we believe there are currently only a few manufacturers that are capable of supplying
and servicing certain equipment and other materials necessary for our laboratory operations, including sequencers and various
associated reagents. As a result, replacement equipment and materials that meet our quality control and performance requirements
may not be available on reasonable terms, in a timely manner or at all. If we encounter delays or difficulties securing, reconfiguring or
revalidating the equipment, reagents and other materials required for our tests our operations could be materially disrupted; our
anticipated turnaround times or ability to deliver our testing services in a timely manner could be adversely impacted; our
development efforts may be delayed or interrupted; and our business, financial condition, results of operations and reputation could be
adversely affected.
The loss of any member of our senior management team could adversely affect our business.
Our success depends in large part on the skill, experience, and performance of our executive management team and others in
key leadership positions, especially Ming Hsieh, our founder, Chief Executive Officer and Chairman of our board of directors; Paul
Kim, our Chief Financial Officer; Dr. Hanlin Gao, our Chief Scientific Officer and Laboratory Director; and Jian Xie, our President
and Chief Operating Officer. Additionally, the success of our Fulgent Pharma business depends in large part on the skill, experience,
and performance of Dr. Ray Yin, its President and Chief Scientific Officer. The continued efforts of these persons will be critical to us
as we continue to develop our technologies and focus on growing our business. If we lose one or more of these key executives, we
could experience difficulties maintaining our operations, including our ability to compete effectively, advance our technologies,
develop new tests, and implement our business strategies. All of our executives and employees, including Messrs. Hsieh, Kim, and
Xie; Dr. Yin; and Dr. Gao, are at-will, meaning either we or the executive may terminate his employment at any time. We do not carry
key person insurance for any of our executives or other employees. In addition, we do not have long-term retention agreements in
place with any of our executives or key employees.
We rely on highly skilled personnel in a broad array of disciplines, and if we are unable to hire, retain, or motivate these
individuals, we may not be able to maintain the quality of our tests or grow our business.
Our business, including our research and development programs, laboratory operations, and administrative functions, largely
depend on our continued ability to identify, hire, train, motivate, and retain highly skilled personnel for all areas of our organization,
including biostatisticians, geneticists, software engineers, laboratory directors, and specialists, sales, and marketing experts and other
scientific, technical, and managerial personnel. Competition in our industry for qualified executives and other employees is intense,
and we may not be able to attract or retain the qualified personnel we need to execute our business plans due to high levels of
competition for these personnel among our competitors, other life science businesses, universities, and public and private research
institutions. In addition, our compensation arrangements may not be successful in attracting new employees and retaining and
motivating our existing employees. If we are not able to attract and retain the necessary personnel to accomplish our business
objectives, we may experience constraints that could adversely affect our ability to expand our business and support our clinical
laboratory operations, and our sales and marketing and research and development efforts, which would negatively affect our prospects
for future growth and success.
Our reputation and business could be damaged by negative publicity.
We have been and may again be subject to negative publicity. Reputational risk, including as a result of negative publicity, is
inherent in our business. Negative publicity can result from actual or alleged conduct in a number of areas, including legal and
regulatory compliance, corporate governance, litigation, inadequate protection of health information, illegal or unauthorized acts taken
by third parties that supply products or services to us, and the conduct of our employees or agents. In particular, COVID-19 and access
to fertility services have been politically controversial topics, and our provision of COVID-19 testing and related services has
subjected us to negative publicity and we may again be subject to negative publicity in connection with our testing services provided
to fertility clinics or provided in support of assisted reproductive technology. Negative publicity can damage our reputation and
business even if these statements about us are untrue. Damage to our reputation could adversely impact our ability to attract new and
to maintain existing customers, employees, and business relationships. This damage and these circumstances may have a material
adverse effect on our financial condition, prospects, and results of operations.
We may not be successful in developing and marketing new tests or testing services, which could negatively impact our
performance and prospects.
We believe our future success will depend in part on our ability to continue to expand our test and testing service offerings and
develop and sell new tests and testing services and on our ability to expand our presence in new and existing markets, including our
presence in the molecular diagnostic and cancer testing markets. We may not be successful in launching or marketing any new tests
we may develop; in expanding into any new or existing markets; and, even if we are successful, the demand for our tests or testing
services could decrease or may not continue to increase at historical rates. Development of new tests and testing services is time-
consuming and costly, as development and marketing of new tests and testing services often requires us to conduct research and
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development activities regarding the new tests and to further scale our laboratory processes and infrastructure to be able to analyze
increasing amounts of more diverse data. Further, we may be unable to discover or develop and launch new tests or testing services for
a variety of reasons, including failure of any proposed test to perform as expected, lack of validation or reference data for the test, or
failure to demonstrate the utility of the test. Any new test we are able to discover and develop may not be launched in a timely
manner, meet applicable regulatory standards, successfully compete with other technologies and available tests, avoid infringing the
proprietary rights of others, achieve coverage and adequate reimbursement from insurance payors, be capable of performance at
commercial levels and at reasonable costs, be successfully marketed, or achieve sufficient market acceptance for us to recoup our time
and capital investment in the development of the test. Any failure to successfully develop, market, and sell new tests or testing
services could negatively impact our ability to attract and retain customers, our revenue, and prospects.
The development and use of AI presents risks and challenges that can impact our business, including by posing security risks
to our confidential information, proprietary information, and personal data and could give rise to legal and/or regulatory
actions, damage our reputation, or otherwise materially harm our business.
AI is increasingly being used in the biopharmaceutical, pharmaceutical, technology, and consumer health industries. We
evaluate different AI technologies and identify areas where we can apply AI to improve our operations. We have developed and
incorporated AI technology in certain of our products and services, including for digital pathology. Issues relating to the use of new
and evolving technologies such as AI, machine learning, generative AI, and large language models, may cause us to experience
perceived or actual brand or reputational harm, technical harm, competitive harm, legal liability, cybersecurity risks, privacy risks,
compliance risks, security risks, ethical issues, and new or enhanced governmental or regulatory scrutiny, and we may incur additional
costs to resolve such issues. Litigation or government regulation related to the use of AI may also adversely impact our ability to
develop and offer products that use AI, as well as increase the cost and complexity of doing so. In addition, uncertainties regarding
developing legal and regulatory requirements and standards may require significant resources to modify and maintain business
practices to comply with U.S. and non-U.S. laws concerning the use of AI, the nature of which cannot be determined at this time. In
addition, the European Union recently passed the Artificial Intelligence Act, whose regulations will be developed over the coming
year and, in the United States, the recent Executive Order concerning AI may result in extensive new federal rule-making. Further,
market demand and acceptance of AI technologies are uncertain, and we may be unsuccessful in our product development efforts.
As necessary, we plan to develop policies governing the use of AI to encourage appropriate use of AI by our employees,
contractors, and authorized agents and that our assets, including intellectual property, competitive information, personal information
we may collect or process, and customer information, are protected. Any failure by our personnel, contractors, or other agents to
adhere to any policies that we may establish could violate confidentiality obligations or applicable laws and regulations, jeopardize
our intellectual property rights, cause or contribute to unlawful discrimination, or result in the misuse of personally identifiable
information or the injection of malware into our systems, any of which could have a material adverse effect on our business, results of
operations, and financial condition.
We are exposed to additional business, regulatory, political, operational, financial, and economic risks related to our
international operations.
Our existing customer base includes international customers from a variety of geographic markets. As we expand our direct test
sales in other countries, we are increasingly subject to varied and complex foreign and international laws and regulations, and as part
of our expansion strategy, we aim to conduct targeted marketing outreach activities and, if opportunities arise, engage distributors or
establish other types of arrangements, such as additional joint ventures or other relationships. However, we may never be successful in
achieving these objectives, and even if we are successful, these strategies may not result in meaningful or any increases in our
customer base, test volumes, or revenue.
Doing business internationally involves a number of risks, including, among others:
•
compliance with the laws and regulations of multiple jurisdictions, which may be conflicting or subject to increasing
stringency or other changes, including privacy and data protection regulations, tax laws, tariffs, employment laws,
healthcare regulatory requirements, and other related approvals, including permitting and licensing requirements;
•
logistics associated with the shipment of blood or other tissue specimens, including infrastructure conditions,
transportation delays, and the impact of United States and local laws and regulations, such as export and import permit
requirements or restrictions, tariffs, or other charges and other trade barriers, all of which involve increased risk related to
the trade policies of the current administration, which may threaten existing and proposed trade agreements and impose
more restrictive U.S. export-import regulations that impact our business;
•
limits on our ability to penetrate international markets, including legal and regulatory requirements that would force us to
conduct our tests locally by building additional laboratories or engaging in joint ventures or other relationships in order to
offer our tests in certain countries, which relationships could involve significant time and resources to establish, deny us
control over certain aspects of the foreign operations, or reduce the economic value to us of these operations;
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•
failure by us, any joint venturers, or other arrangements we have or may establish, or by any distributors or other
commercial partners we have engaged or may engage to obtain any regulatory approvals required to market, sell, and use
our tests in various countries;
•
challenges predicting the market for our tests and services generally and tailoring our test menu to meet varying customer
expectations in different countries and territories;
•
difficulties gaining market share in territories in which we do not have a strong physical presence or brand awareness;
•
complexities and difficulties obtaining protection for and enforcing our intellectual property rights;
•
difficulties in staffing and managing foreign operations;
•
complexities associated with managing multiple payor coverage and reimbursement regimes, government payors, or
patient self-pay systems;
•
financial risks, such as longer payment cycles, difficulty collecting trade accounts receivable and the impact of local and
regional financial conditions on demand and payment for our tests;
•
inflationary pressures, such as those the global market is currently experiencing, which have and may increase costs for
materials, supplies, and services;
•
exposure to foreign currency exchange rate fluctuations, conversions of currencies, and the risk of repatriation of certain
foreign currencies;
•
natural disasters; political and economic instability, including wars, terrorism and political unrest, such as conflicts in the
Ukraine and the Middle East and tensions between China and Taiwan; outbreak of disease; boycotts; and other business
restrictions; and
•
regulatory and compliance risks related to applicable anti-bribery laws, including requirements to maintain accurate
information and control over activities that may fall within the purview of these laws.
Any of these factors could significantly harm our existing relationships with international customers or derail our international
expansion plans, which would cause our revenue and results of operations to suffer. Our international business activities are subject to
U.S. economic and trade sanctions, which restrict or otherwise limit our ability to do business in certain designated countries.
In addition, we are exposed to a number of additional risks and challenges related to our joint venture in China. These risks
include, among others, difficulties predicting the market for genetic testing in Asia; competitive factors in this market, including
challenges securing market share; trade wars and tariffs; local differences in customer demands and preferences and the regulatory
environment and regulatory requirements; the interpretation or enforcement of laws, regulations, and rules in China and many of the
other risks of doing business internationally that are discussed above. Although we believe this joint venture could result in expanded
long-term opportunities to address the genetic testing market in Asia, this belief could turn out to be wrong, and we may never realize
these or any other benefits we anticipate from our joint venture. Moreover, any joint venture we may seek to establish may never
produce sufficient revenue for us to recover our capital and other investments in the joint venture, and we could become subject to
liabilities based on our involvement in the joint venture’s operations. The materialization of any of these risks could materially harm
our performance and prospects.
If we are sued for product or professional liability, we could face substantial liabilities that exceed our resources.
Our business depends on our ability to provide reliable and accurate test results, including tests that incorporate rapidly evolving
information about the role of genes and gene variants in disease and clinically relevant outcomes associated with these variants or
pathology services and testing that often rely on human interpretation. Substantial judgment is often required in order to interpret the
results of each test we perform and to produce a report summarizing these results. This is particularly true for our pathology testing
services. Errors, such as failures to detect genomic variants with high accuracy, or mistakes, such as failures to completely and
correctly identify the significance of gene variants, abnormal cells or to detect disease, could subject us to product liability or
professional liability claims. Any such claim against us could result in substantial damages and be costly and time-consuming to
defend. Although we maintain liability insurance, including for errors and omissions, our insurance may not fully protect us from the
financial impact of defending against these types of claims or any judgments, fines, or settlement costs arising out of any such claims.
Additionally, any liability claim brought against us, with or without merit, could increase our insurance rates or prevent us from
securing adequate insurance coverage in the future. Moreover, any liability lawsuit could damage our reputation or force us to suspend
sales of our tests. The occurrence of any of these events could have a material adverse effect on our business, reputation and results of
operations.
Fulgent Pharma’s business involves the testing of new drugs on patients in clinical trials and will continue to involve the
additional testing of drugs on patients in the future. Our involvement in the clinical trials and development process creates a risk of
liability for personal injury to or death of patients, particularly those with life-threatening illnesses, resulting from adverse reactions to
the drugs administered during testing or after product launch, respectively. Although we maintain the types and amounts of insurance
we view as customary and appropriate in the industries and countries in which we operate, if we are required to pay significant
damages or incur significant defense costs in connection with any personal injury claim that is outside the scope of indemnification
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agreements we have with our clients, if any indemnification agreement is not performed in accordance with its terms or if our liability
exceeds the amount of any applicable indemnification limits or available insurance coverage, our financial condition, results of
operations and reputation could be materially and adversely affected.
In addition, insurance coverage is increasingly expensive and difficult to obtain. Inability to obtain or maintain sufficient
insurance coverage at an acceptable cost or to otherwise protect against potential product or other legal or administrative liability
claims could prevent or inhibit customer relationships, the clinical development, commercial production, and sale of any of our
products and drug candidates, which could adversely affect our business.
Any inability to obtain additional capital when needed and on acceptable terms may limit our ability to execute our business
plans, and our liquidity needs could be materially affected by market fluctuations and general economic conditions. If we raise
funds by issuing equity securities, our stockholders may experience substantial dilution.
We expect our capital expenditures and operating expenses to increase over the next several years as we seek to expand our
infrastructure, other commercial operations, and research and development activities. As of December 31, 2024, we had cash, cash
equivalents, and marketable securities of approximately $828.6 million. We may seek to fund future cash needs through securities
offerings, credit facilities, or other debt financings, asset sales, collaborations or licensing arrangements. Additional funding may not
be available to us when needed, on acceptable terms or at all. For example, the COVID-19 pandemic initially caused extreme
disruption and volatility in the global capital markets followed by a period of high market demand for life science and diagnostic
company equities and then a period of less demand for these equities in 2022, 2023, and 2024. These circumstances and high volatility
in capital markets generally may reduce our ability to access capital and/or adversely affect the stability of the depository institutions
maintaining our assets.
If we raise additional funds by issuing equity securities, our existing stockholders could experience substantial dilution.
Additionally, any preferred stock we issue could provide for rights, preferences, or privileges senior to those of our common stock,
and our issuance of any additional equity securities, or the possibility of such an issuance, could cause the market price of our
common stock to decline. The terms of any debt securities we issue or borrowings we incur, if available, could impose significant
restrictions on our operations, such as limitations on our ability to incur additional debt or issue additional equity or other restrictions
that could adversely affect our ability to conduct our business, and would result in increased fixed payment obligations. If we seek to
sell assets or enter into collaborations or licensing arrangements to raise capital, we may be required to accept unfavorable terms or
relinquish or license to a third-party our rights to important or valuable technologies or tests we may otherwise seek to develop
ourselves. Moreover, we may incur substantial costs in pursuing future capital, including investment banking, legal, and accounting
fees, printing and distribution expenses and other similar costs. If we are unable to secure funding if and when needed and on
reasonable terms, we may be forced to delay, reduce the scope of or eliminate one or more sales and marketing initiatives, research
and development programs or other growth plans or strategies. In addition, we may be forced to work with a partner on one or more
aspects of our tests or market development programs or initiatives, which could lower the economic value to us of these tests,
programs or initiatives. Any such outcome could significantly harm our business, performance, and prospects.
Inflation has and may again materially and adversely affect us by materially increasing our costs.
In recent years, inflation has increased throughout the United States economy. Inflation has adversely affected us and may again
adversely affect us by materially increasing the costs of clinical trials and research, the development of our tests and drug candidates,
administration, and other costs of doing business. We have and may again experience material increases in the prices of labor and
other costs of doing business. In an inflationary environment, cost increases may materially outpace our expectations, causing us to
use our cash and other liquid assets faster than forecasted.
If we are unable to maintain effective internal control over financial reporting, investors could lose confidence in the accuracy
and completeness of our reported financial information, and the market price of our common stock could decline.
We are required to maintain internal control over financial reporting and report any material weaknesses in these internal
controls. Section 404 of the Sarbanes-Oxley Act requires that we evaluate and determine the effectiveness of our internal control over
financial reporting and annually provide a management report on these internal controls. We have incurred and expect to continue to
incur significant expenses and devote substantial management effort toward compliance with the auditor attestation requirements of
Section 404 of the Sarbanes-Oxley Act. Although we have implemented systems, processes and controls and performed this
evaluation as of the end of 2024, we will need to maintain and enhance these controls if and as we grow. Moreover, we may need to
hire additional personnel and devote more resources to our financial reporting function in order to do so, which will increase our
operating expenses.
If one or more material weaknesses is identified during the process of evaluating our internal controls or if we do not detect
errors on a timely basis, our financial statements may be materially misstated. In addition, in that event, our management would be
39
unable to conclude that our internal control over financial reporting is effective. In addition, we are required to include an attestation
report on internal control over financial reporting issued by our independent registered public accounting firm. Any failure to develop
or maintain effective controls, or any difficulties encountered in their implementation or improvement, could materially harm our
results of operations, cause us to fail to meet our reporting obligations, result in a restatement of our financial statements for prior
periods, or adversely affect the results of management evaluations and independent registered public accounting firm audits of our
internal control over financial reporting that we are required to include in our periodic reports that will be filed with the SEC. If we or
our auditors were to conclude that our internal control over financial reporting was not effective because one or more material
weaknesses had been identified or if internal control deficiencies result in the restatement of our financial results, investors could lose
confidence in the accuracy and completeness of our financial disclosures and the price of our common stock could decline.
Our disclosure controls and procedures may not prevent or detect all errors or acts of fraud.
We are subject to the periodic reporting and other requirements of the Exchange Act. We have implemented disclosure controls
and procedures designed to provide reasonable assurance that information we must disclose in reports we file or submit under the
Exchange Act is accumulated and communicated to management and recorded, processed, summarized and reported within the time
periods specified in the rules and forms of the SEC. However, any disclosure controls and procedures, no matter how well-conceived
and operated, can provide only reasonable, not absolute, assurance that the objectives of the control system are met. These inherent
limitations include the realities that judgments in decision-making can be faulty and that breakdowns can occur because of simple
errors or mistakes. Additionally, controls can be circumvented by the individual acts of some persons, by collusion of two or more
people or by an unauthorized override of the controls. As a result, because of these inherent limitations in our control system,
misstatements or omissions due to error or fraud may occur and may not be detected, which could result in failures to file required
reports in a timely manner and filing reports containing incorrect information. Any of these outcomes could result in SEC enforcement
actions, monetary fines or other penalties, damage to our reputation and harm to our financial condition and stock price.
Our investments in marketable securities are subject to certain risks which could affect our overall financial condition, results
of operations, or cash flows.
We invest a portion of our available cash and cash equivalents by purchasing marketable securities in a managed portfolio and
direct investments in a variety of debt securities, including corporate debt securities, municipal bonds, U.S. government and agency
debt securities, and debt instruments issued by foreign governments. The primary objective of our investment activity is to maintain
the safety of principal, preserve capital and provide for future liquidity requirements while maximizing yields without significantly
increasing risk. Should any of our investments or marketable securities lose value or have their liquidity impaired, it could materially
affect our overall financial condition. Additionally, should we choose or are required to sell these securities in the future at a loss, our
consolidated operating results or cash flows may be materially and adversely affected.
We maintain cash deposits in excess of federally insured limits. Adverse developments affecting financial institutions,
including bank failures, could adversely affect our liquidity and financial performance.
We maintain our cash, cash equivalents, and marketable securities with high quality, accredited financial institutions. However,
some of these accounts exceed the Federal Deposit Insurance Corporation, or FDIC, insurance limit of $250,000 and, while we believe
the Company is not exposed to significant credit risk due to the financial strength of these depository institutions or investments, if any
such depositary institution fails to return our deposits, or if a depository institution is subject to other adverse conditions in the
financial or credit markets, this could further impact access to our invested cash or cash equivalents and could adversely impact our
operating liquidity and financial performance. Further, the failure or collapse of one or more of these depository institutions or default
on these investments could materially adversely affect our ability to recover these assets and/or materially harm our financial
condition.
We have been the subject of a shareholder class action, which was dismissed without prejudice; and we may be subject to further
shareholder litigation in the future; our costs of defending such litigation, arbitration, and other proceedings and any adverse
outcome of such litigation, arbitration, or other proceeding may have a material adverse effect on our business and the results
of our operations.
We have been, and may from time to time in the future be, involved in and subject to material litigation and other legal
proceedings, including shareholder litigation. These proceedings may not always resolve in our favor and may materially and
adversely affect our business. While the recent shareholder class action was dismissed, it was dismissed without prejudice, so there is
no assurance that another complaint may not be filed in the future. Regardless of outcome, litigation can have an adverse impact on us
due to defense and settlement costs, diversion of management resources, negative publicity, and reputational harm, among other
factors.
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Political uncertainty may have an adverse impact on our operating performance and results of operations.
General political uncertainty may have an adverse impact on our operating performance and results of operations. In particular,
the United States continues to experience significant political events that cast uncertainty on global financial and economic markets,
especially in light of the new administration. It is presently unclear exactly what actions the new administration in the United States
will implement, and if implemented, how these actions may impact the pharmaceutical and diagnostics industries in the United States.
Any actions taken by the new administration may have a negative impact on the United States economies and on our business,
financial conditions, and results of operations.
Impairment charges relating to our goodwill and intangible assets could negatively affect our financial performance.
We have previously and may again in the future pursue acquisitions of complementary businesses or assets, and we may not
realize all the economic benefit from those acquisitions, which could cause an impairment of goodwill or intangibles. We assess
goodwill and indefinite-lived intangibles for impairment at least annually or whenever events or changes in circumstances indicate the
carrying value may not be recoverable. Events and conditions that could result in an impairment of our goodwill and intangible assets
include a decline in our stock price and market capitalization, reduced future cash flow estimates, slower growth rates in industry
segments in which we participate, or other factors leading to reduction in expected long-term growth or profitability. We may be
required to record a significant charge in our consolidated financial statements during the period in which any impairment of our
goodwill or amortizable intangible assets is determined, which may negatively affect our financial condition and results of operations.
For example, during our fiscal 2023 annual goodwill impairment analysis, we fully impaired goodwill of $71.8 million associated with
the acquisition of Inform Diagnostics, $27.5 million associated with the acquisition of CSI, and $21.0 million associated with the
restructuring of Fujian Fujun Gene Biotech Co., Ltd., or FF Gene Biotech, which was principally driven by a sustained decline in our
market price and capitalization.
Changes in financial accounting standards or practices may cause adverse, unexpected financial reporting fluctuations and
affect our reported operating results.
Accounting principles generally accepted in the United States, or U.S. GAAP, is subject to interpretation by the Financial
Accounting Standards Board, or FASB, the SEC, and various bodies formed to promulgate and interpret appropriate accounting
principles. A change in accounting standards or practices can have a significant effect on our reported results and may even affect our
reporting of transactions completed before the change is effective. New accounting pronouncements and varying interpretations of
accounting pronouncements have occurred and may occur in the future. Changes to existing rules or the questioning of current
practices may adversely affect our reported financial results or the way we conduct our business.
We incur costs and demands upon management as a result of complying with the laws and regulations affecting public companies
in the United States, which may adversely affect our operating results.
As a public company listed in the United States, we incur significant additional legal, accounting and other expenses. In
addition, changing laws, regulations and standards relating to corporate governance and public disclosure, including regulations
implemented by the SEC and The Nasdaq Stock Market LLC, may increase legal and financial compliance costs and make some
activities more time-consuming. These laws, regulations and standards are subject to varying interpretations, and as a result, their
application in practice may evolve over time as new guidance is provided by regulatory and governing bodies. We invest resources to
comply with evolving laws, regulations and standards, and this investment may result in increased general and administrative
expenses and a diversion of management’s time and attention from revenue-generating activities to compliance activities. If,
notwithstanding our efforts to comply with these laws, regulations and standards, we fail to comply, regulatory authorities may initiate
legal proceedings against us, and our business may be harmed. As previously disclosed and as set forth in Note 8 “Debt, Commitments
and Contingencies to the Consolidated Financial Statements,” we are under investigation by the SEC for certain alleged violations of
securities laws. While we do not believe that any enforcement recommendation is warranted and deny all liability, we have recorded a
$1.0 million potential liability with respect to this matter. The actual amount of liability, if any, may be materially higher than this
estimate, as discussions are ongoing and there is no formal settlement or final resolution of this matter at this time.
Further, if we fail to comply with these laws, regulations and standards, it might also be more difficult for us to obtain certain
types of insurance, including director and officer liability insurance, and we might be forced to accept reduced policy limits and
coverage or incur substantially higher costs to obtain the same or similar coverage. The impact of these events could also make it more
difficult for us to attract and retain qualified persons to serve on our board of directors, on committees of our board of directors or as
members of senior management.
U.S. federal government contracts are generally subject to terms more favorable to the customer than commercial contracts. If
the U.S. federal government significantly decreased or ceased doing business with us, our business, financial condition and
results of operations would be materially and adversely affected.
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In 2024, we were awarded a contract by the U.S. Department of Veterans Affairs, or VA, to provide hereditary cancer,
pharmacogenetic and other genetic testing to veterans and to their family members. We are also party to a number of other
government contracts.
U.S. federal government contracts, including our contract with the VA, generally contain provisions and are subject to laws and
regulations that give the federal government rights and remedies not typically found in commercial contracts, including provisions
permitting the federal government to:
•
terminate our existing contracts;
•
reduce potential future income from our existing contracts;
•
modify some of the terms and conditions in our existing contracts;
•
suspend or permanently prohibit us from doing business with the federal government or with any specific government
agency;
•
impose fines and penalties;
•
subject the award of some contracts to protest or challenge by competitors, which may require the contracting federal
agency or department to suspend our performance pending the outcome of the protest or challenge and which may also
require the government to solicit new proposals for the contract or result in the termination, reduction or modification of
the awarded contract; and
•
decline to exercise an option to extend an existing multiple year contract.
The U.S. federal government may also terminate a contract either “for convenience” (for instance, due to a change in its
perceived needs or its desire to consolidate work under another contract) or if a default occurs by failing to perform under the contract.
If the federal government terminates a contract for convenience, we generally would be entitled to recover only our incurred or
committed costs, settlement expenses and profit on the work completed prior to termination. If the federal government terminates a
contract based upon a default, we generally would be denied any recovery for undelivered work, and instead may be liable for excess
costs incurred by the federal government in procuring undelivered items from an alternative source and other damages as authorized
by law. In addition, many government contracts are awarded through a rigorous competitive process, which may emphasize price over
other qualitative factors. The U.S. federal government has increasingly relied upon multiple-year contracts with multiple contractors
that generally require those contractors to engage in an additional competitive procurement process for each task order issued under a
contract. This process may result in us facing significant additional pricing pressure and uncertainty and incurring additional
costs. Further, to the extent our performance under a contract does not meet a government agency’s expectations, the customer might
seek to terminate the contract prior to its scheduled expiration date, provide a negative assessment of our performance to government-
maintained contractor past-performance data repositories, fail to award us additional business under existing contracts or otherwise,
and direct future business to our competitors, suspend or debar from contracting with the federal government or any significant
agency, including the VA. These various uncertainties, restrictions, and regulations by government authorities as well as profit and
cost controls, could have a material adverse impact on our business, financial condition and results of operations.
Reimbursement Risks
Our ability to achieve or sustain profitability also depends on our collection of payment for the tests we deliver, which we may
not be able to do successfully.
If insurance payors do not provide coverage and adequate reimbursement for our tests and testing services, our potential for
growth and our ability to collect revenue for these tests and testing services could be limited and our results of operations may be
materially and adversely affected.
Coverage and reimbursement by insurance payors, including managed care organizations, other private health insurers and
government healthcare programs, such as Medicare and Medicaid, for the types of tests we perform can be limited and uncertain. Our
customers may not order our tests or testing services unless insurance payors cover and provide adequate reimbursement for a
substantial portion of the price of the tests. If we are not able to obtain coverage and an acceptable level of reimbursement for our tests
from insurance payors, the patient for whom the test is ordered typically will owe a greater co-insurance, deductible or co-payment
amount or may be expected to pay the entire cost of the test out-of-pocket, which could dissuade practitioners from ordering our tests
and, if ordered, could result in a delay in or decreased likelihood of collecting payment, whether from patients or from insurance
payors. We believe our ability to increase the amount of tests and testing services we sell to our healthcare provider customers and any
corresponding revenue depends in part on our ability to achieve and maintain broad coverage and reimbursement for our tests from
insurance payors.
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Coverage and reimbursement by an insurance payor depend on a number of factors, including a payor’s determination that a test
or testing service is appropriate, medically necessary, and cost-effective. Each payor makes its own decision as to whether to establish
a policy or enter into a contract to cover our tests and the amount it will reimburse for each test, and any determination by a payor
regarding coverage and amount of reimbursement for our tests would likely be made on an indication-by-indication basis. Even if a
test has been approved for reimbursement for any particular indication or in any particular jurisdiction, there is no guarantee this test
will remain approved for reimbursement or that any similar or additional tests will be approved for reimbursement in the future.
Moreover, there can be no assurance that any new tests we launch will be reimbursed at all or at rates comparable to the rates of any
previously reimbursed tests. In addition, the coding procedure used by all insurance payors with respect to establishing payment rates
for various procedures, including our tests, is complex, does not currently adapt well to the tests we perform and may not enable
coverage and adequate reimbursement rates for our tests. If physicians fail to provide appropriate diagnosis codes for tests that they
order, we may not be reimbursed for our tests. Additionally, if we are not able to obtain sufficient clinical information in support of
our tests, insurance payors could designate our tests as experimental or investigational and decline to cover and reimburse our tests
because of this designation. As a result of these factors, obtaining approvals from insurance payors to cover our tests and testing
services and establishing adequate reimbursement levels is an unpredictable, challenging, time-consuming and costly process, and we
may never be successful.
To date, we have contracted directly with national health insurance companies to become an in-network provider and enrolled as
a supplier in the Medicare program and a provider in some state Medicaid programs, and we have also received payment for our tests
from other insurance payors as an out-of-network provider. Although becoming an in-network provider or enrolling as a supplier or
provider means that we have agreed with these payors to provide certain of our tests at negotiated or set fee schedule rates, it does not
obligate any physicians or other practitioners to order our tests or guarantee that we will receive reimbursement for our tests from
these or any other payors at adequate levels. As a result, these payor relationships, any other similar relationships we may establish in
the future, or any additional payments we may receive from other payors as an out-of-network provider, may not amount to acceptable
levels of reimbursement for our tests or meaningful increases in our customer base or the number of tests we sell. We expect to focus
on increasing coverage and reimbursement for our current tests and any future tests we may develop, but we cannot predict whether,
under what circumstances, or at what payment levels payors will cover and reimburse us for our tests. Further, even if we are
successful, we believe it could take several years to achieve coverage and adequate contracted reimbursement with insurance payors.
If we fail to establish and maintain broad coverage and reimbursement for our tests, our ability to maintain or grow our test volume,
customer base, collectability rates and revenue levels could be limited and our future prospects and our business could suffer.
Our collection risks also include the potential for default or bankruptcy by the party responsible for payment and other risks
associated with payment collection generally. Any inability to maintain our past payment collection levels could cause our revenue
and ability to achieve profitability to decline and adversely affect our business, prospects and financial condition.
Failure to comply with government laws and regulations related to submission of claims for our services could result in
significant monetary damages and penalties and exclusion from the Medicare and Medicaid programs and corresponding
foreign reimbursement programs. We are also subject to governmental audits and investigations that could result in material
refunds or settlement. Our business, prospects and financial condition may be adversely affected as the result of the current
HRSA Audit and CIDs.
We are subject to laws and regulations governing the submission of claims for payment for our services, such as those relating
to: coverage of our tests and testing services under Medicare, Medicaid, HRSA, and other state, federal and foreign healthcare
programs; the amounts that we may bill for our services; and the party to which we must submit claims. Our failure to comply with
applicable laws and regulations could result in our inability to receive payment for our services or in attempts by state and federal
healthcare programs, such as HRSA, Medicare and Medicaid, to recover payments already made. Submission of claims in violation of
these laws and regulations, identified through an audit or through the Company’s control processes, can result, as noted above, in
recoupment of payments already received, substantial civil monetary penalties, and exclusion from state and federal healthcare
programs, and can subject us to liability under the federal False Claims Act and similar laws. The failure to report and return an
overpayment to the Medicare or Medicaid programs within 60 days of identifying its existence can give rise to liability under the False
Claims Act. Further, a government agency could attempt to hold us liable for causing the improper submission of claims by another
entity for services that we performed. Similar to other laboratories in the industry, the Company is currently being audited by HRSA
with respect to its reimbursement for COVID-19 tests furnished to patients believed to be uninsured. The Company is fully
cooperating and working with HRSA’s auditors to resolve any issues, including any reimbursed amounts that may need to be returned
to HRSA. There is uncertainty with respect to the methodology HRSA will use and whether and how they will extrapolate audit
results. We have also received a CID issued by the DOJ pursuant to the False Claims Act related to its investigation of allegations of
medically unnecessary laboratory testing, improper billing for laboratory testing, and remuneration received or provided in violation
of the Anti-Kickback Statute and the Stark Law. Among other things, this CID requests information and records relating to certain of
the Company’s customers named in this CID. In addition, we have also received a CID issued by the DOJ related to the DOJ’s
investigation as to whether we submitted or caused to be submitted false claims to the Uninsured Program. We are fully cooperating
with the DOJ in connection with the CIDs that we have received and in connection with the HRSA audit. We cannot currently predict
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when these CIDs and HRSA audit matters will be resolved, the reasonable or likely outcome of these matters, or their potential
impact, which may materially and adversely affect our business, prospects, and financial condition. These matters are not formal
claims and discussions and investigations remain ongoing. As such, we cannot reasonably estimate the loss or range of loss, if any,
that may result from any material government investigations, audits, and reviews in which we are currently involved, given the
inherent difficulty in predicting regulatory action, fines and penalties, if any, and the various remedies and levels of judicial review
available to us in the event of an adverse finding.
See “Contingencies” in Note 8, Debt, Commitments and Contingencies for additional information.
Billing and collection processing for our tests is complex and time-consuming, and any delay in transmitting and collecting
claims could have an adverse effect on our revenue.
Billing for our tests is complex, time-consuming, and expensive. Depending on the billing arrangement and applicable law, we
may bill various different parties for our tests. This includes billing customers directly, as in the case of our hospital and other medical
institution customers, as well as billing through Medicare, Medicaid, insurance companies and patients, all of which may have
different billing requirements. We face increasing risks in our collection efforts due to the complexities of these billing requirements,
including long collection cycles and lower collection rates, which could adversely affect our business, results of operations and
financial condition.
Several factors make this billing process complex, including:
•
contractual restrictions in our customer contracts that may limit our ability to utilize certain third-party billing service
providers;
•
differences between the list price for our tests and the reimbursement rates of payors;
•
compliance with complex federal and state regulations related to billing government healthcare programs, including
Medicare and Medicaid;
•
disputes among payors as to which party is responsible for payment;
•
differences in coverage among payors and the effect of patient co-payments or co-insurance;
•
differences in information and billing requirements among payors;
•
incorrect or missing billing information; and
•
the resources required to manage the billing and claims appeals process.
We have developed internal systems and procedures to handle these billing and collection functions, and have contracted with
third-party providers as needed to assist in our collection efforts, but these systems and internal and external collection functions may
fail or may fail to operate as we intend, particularly as billing for many of our tests from insurance payors is a very complex process.
As a result, these billing complexities, along with the related uncertainty in obtaining payment for our tests, could negatively affect
our revenue and cash flows, our ability to achieve or sustain profitability and the consistency and comparability of our results of
operations. In addition, if claims for our tests are not submitted to payors on a timely basis, or if we are required to switch to a
different provider to handle our processing and collections functions, our revenue and our business could be adversely affected.
Regulatory Risks
Any changes in laws, regulations, or the enforcement discretion of the FDA with respect to the marketing of diagnostic
products, or violations of laws or regulations by us, could materially and adversely affect our business, prospects, results of
operations, or financial condition.
The laws and regulations governing the marketing of diagnostic products are evolving, extremely complex and in many
instances, have no significant regulatory or judicial interpretations of these laws and regulations. Pursuant to its authority under the
federal FDC Act, the FDA has jurisdiction over medical devices, including IVDs, and, therefore, potentially our clinical laboratory
tests. Among other things, pursuant to the FDC Act and its implementing regulations, the FDA regulates the research, testing,
manufacturing, safety, labeling, storage, recordkeeping, premarket clearance or approval, marketing and promotion, and sales and
distribution of medical devices in the United States to ensure that medical products distributed domestically are safe and effective for
their intended uses. In addition, the FDA regulates the import and export of medical devices.
Although the FDA has statutory authority to assure that medical devices and IVDs, including potentially our tests, are safe and
effective for their intended uses, the FDA had historically exercised enforcement discretion and not enforced applicable provisions of
the FDC Act and regulations with respect to LDTs, which are a particular type of medical device. We market our tests as LDTs and
may, in the future, market other tests as LDTs. However, in May 2024, the FDA issued a final rule aimed at regulating LDTs under
the current medical device framework and phasing out its existing enforcement discretion policy for this category of diagnostic tests
over several years. The effective date of the agency’s final rule was July 5, 2024.
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The agency’s final rule provides that the LDT enforcement policy phase-out process would occur in gradual stages over a total
period of four years, with pre-market approval applications for high-risk tests to be submitted by the three-and-a-half-year mark.
Moderate-risk and low-risk tests are expected to be in compliance at the four-year mark, although FDA has stated that if premarket
submissions are pending review it will continue to exercise enforcement discretion with respect to those tests. The FDA’s final rule is
complex and, concurrently, the agency announced several exceptions from the requirement to comply with full medical device
regulatory controls, depending upon the specific nature of the LDT and the clinical laboratory that is offering such LDT for use by
health care providers. Of potential relevance is the agency’s position on LDTs that were marketed prior to the official publication date
of the final rule. Such “currently marketed” tests are subject to many of the device regulatory controls but are exempt from the
premarket review and FDA authorization requirements (unless or until significant modifications are made to such “currently
marketed” tests). Similarly, FDA has created a partial enforcement discretion policy for tests approved by the New York’s Department
of Health, Clinical Laboratory Evaluation Program, or CLEP, whereby such tests also do not need to undergo FDA premarket review
but must come into compliance with all other device general controls in a stagged fashion between 2025 and 2027. We have begun the
process of evaluating the final rule’s potential impact on our tests, our operations, and our business more generally.
On May 29, 2024, ACLA and one of its members filed a complaint against the FDA in the Eastern District of Texas, alleging
that the agency does not have authority to promulgate the LDT final rule and seeking to vacate the FDA’s action. A second lawsuit
was also filed against FDA by AMP on August 19, 2024 in the Southern District of Texas, and subsequently the two cases were
consolidated into a single action pending in the Eastern District of Texas. Briefing is ongoing in the consolidated case, and the
outcome of such litigation is uncertain. The litigation could potentially affect FDA’s plans to implement these new LDT requirements,
making the potential implementation timeline somewhat uncertain, although no preliminary injunction has been issued to date.
Accordingly, the agency has continued its implementation efforts by actively providing guidance and training to clinical laboratories
on how to comply with medical device general controls.
Affected stakeholders also continue to press for a comprehensive legislative solution to create a harmonized paradigm for
oversight of LDTs by both the FDA and CMS, instead of implementation of the proposed FDA administrative action, which may be
disruptive to the industry and to patient access to certain diagnostic tests. However, this FDA rulemaking was initiated after years of
failed congressional attempts to harmonize the regulatory paradigms applicable to LDTs and other IVDs, making it unclear whether
any legislative efforts would be successful going forward.
If FDA prevails in the Texas litigation and is able to fully implement the multi-year phase-in plan for the LDT final rule or
Congress enacts comprehensive legislation to regulate in vitro diagnostics that moots the need for the LDT final rule, or if the FDA
disagrees with our assessment that our tests meet the criteria to be marketed LDTs, we could, for the first time, be subject to
enforcement of a variety of regulatory requirements, including registration and listing, medical device reporting and quality control,
and we could be required to obtain premarket clearance or approval for our existing tests and any new tests we may develop, which
may force us to cease marketing our tests until we obtain the required clearance or approval. The premarket review process can be
lengthy, expensive, time-consuming and unpredictable. Further, obtaining premarket authorization may involve, among other things,
successfully completing clinical trials. Clinical trials require significant time and cash resources and are subject to a high degree of
risk, including risks of experiencing delays, failing to complete the trial or obtaining unexpected or negative results. If we are required
to obtain premarket clearance or approval and/or conduct premarket clinical trials, our development costs could significantly increase,
our introduction of any new tests we may develop may be delayed and sales of our existing tests could be interrupted or stopped. Any
of these outcomes could reduce our revenue or increase our costs and materially adversely affect our business, prospects, results of
operations or financial condition. Moreover, any cleared or approved labeling claims may not be consistent with our current claims or
the test’s indications for use, and they may not be adequate to support continued adoption of and reimbursement for our tests. For
instance, if we are required by the FDA to label our tests as investigational, or if labeling claims the FDA allows us to make are
limited, order levels may decline and reimbursement may be adversely affected. As a result, we could experience significantly
increased development costs and a delay in generating additional revenue from our existing tests or from tests we may develop.
In addition, while we qualify the materials used in our tests and testing services in accordance with the regulations and
guidelines of CLIA, the FDA could promulgate regulations or make policy decisions impacting our ability to purchase materials
necessary for the performance of our tests. If any of the reagents we obtain from suppliers and use in our tests are affected by future
regulatory actions, our business could be adversely affected, including by increasing the cost of testing or delaying, limiting or
prohibiting the purchase of reagents necessary to perform testing with our products.
Failure to comply with any applicable FDA requirements could trigger a range of enforcement actions by the FDA, including
warning letters, civil monetary penalties, injunctions, criminal prosecution, recall or seizure, operating restrictions, partial suspension
or total shutdown of operations and denial of or challenges to applications for clearance or approval, as well as significant adverse
publicity.
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If we fail to comply with applicable federal, state, local and foreign laboratory licensing requirements, we could lose the ability
to perform our tests and experience material disruptions to our business.
We are subject to CLIA, a federal law that establishes quality standards for all laboratory testing and is intended to ensure the
accuracy, reliability, and timeliness of patient results. CLIA requires that we hold a certificate specific to the categories of laboratory
testing that we perform and that we comply with various standards with respect to personnel qualifications, facility administration,
proficiency testing, quality control, quality assurance, and inspections. CLIA certification is required in order for us to be eligible to
bill federal and state healthcare programs, as well as many private insurance payors, for our tests. We have obtained CLIA
certification to conduct our tests at our laboratories in El Monte, California; Coppell, Texas; Needham, Massachusetts; Phoenix,
Arizona; and Alpharetta, Georgia.
In addition, we elect to have our laboratories accredited by CAP. CMS has deemed CAP standards to be equally or more
stringent than CLIA regulations and has approved CAP as a recognized accrediting organization. Inspection by CAP is performed in
lieu of inspection by CMS for CAP-accredited laboratories. Because we are accredited by CAP, we are deemed to also comply with
CLIA. In addition, some countries outside the United States require CAP accreditation as a condition to permitting clinical
laboratories to test samples taken from their citizens. Failure to maintain CAP accreditation could have a material adverse effect on the
sales of our tests and the results of our operations.
We are also required to maintain a license to conduct testing in California. California laws establish standards for day-to-day
operation of our clinical reference laboratory in El Monte, including with respect to the training and skills required of personnel,
quality control and proficiency testing requirements. In addition, because we receive test specimens originating from New York, we
have obtained a state laboratory permit for our California laboratory from the New York State Department of Health, or DOH. The
New York state laboratory laws and regulations are equal to or more stringent than CLIA. In addition, the laboratory director must
maintain a Certificate of Qualification issued by New York’s DOH in permitted categories.
We are subject to on-site routine and complaint-driven inspections under both California and New York state laboratory laws
and regulations. If we are found to be out of compliance with either California or New York requirements, the CA Department of
Public Health or New York’s DOH may suspend, restrict or revoke our license or laboratory permit, respectively (and, with respect to
California, may exclude persons or entities from owning, operating or directing a laboratory for two years following such license
revocation), assess civil monetary penalties, or impose specific corrective action plans, among other sanctions. Any such actions could
materially and adversely affect our business by prohibiting or limiting our ability to offer testing.
We are subject to on-site routine and complaint-driven inspections under California state laboratory laws and regulations. If we
are found to be out of compliance with California requirements, the CA Department of Public Health may suspend, restrict or revoke
our license or laboratory permit, and may exclude persons or entities from owning, operating or directing a laboratory for two years
following such license revocation, assess civil monetary penalties, or impose specific corrective action plans, among other sanctions.
Any such actions could materially and adversely affect our business by prohibiting or limiting our ability to offer testing.
Moreover, certain other states require us to maintain out-of-state laboratory licenses or obtain approval on a test-specific basis to
perform testing on specimens from these states. Additional states could adopt similar licensure requirements in the future, which could
require us to modify, delay or discontinue our operations in such jurisdictions. We are also subject to regulation in foreign
jurisdictions, which we expect will increase as we continue to expand international utilization of our tests or if jurisdictions in which
we pursue operations adopt new or modified licensure requirements for U.S.-based clinical laboratories offering and providing
diagnostic testing services to professionals located in those jurisdictions. Foreign licensure requirements could require review and
modification of our tests in order to offer them in certain jurisdictions or could impose other limitations, such as restrictions on the
domestic transport or importation of human blood or other tissue necessary for us to perform our tests that may limit our ability to
make our tests more widely available outside the United States. Additionally, complying with licensure requirements in new
jurisdictions may be expensive, time-consuming and subject us to significant and unanticipated delays.
Failure to comply with applicable clinical laboratory licensure requirements could result in a range of enforcement actions,
including license suspension, limitation or revocation, directed plan of correction, onsite monitoring, civil monetary penalties, civil
injunctive suits, criminal sanctions and exclusion from the Medicare and Medicaid programs, as well as significant adverse publicity.
Any sanction imposed under CLIA, its implementing regulations or state or foreign laws or regulations governing clinical laboratory
licensure, or our failure to renew our CLIA certificate or any other required local, state or foreign license or accreditation, could have
a material adverse effect on our business, financial condition and results of operations. In such case, even if we were able to bring our
laboratory back into compliance, we could incur significant expenses and lose revenue while doing so.
Failure to obtain necessary foreign regulatory approvals or certifications may adversely affect our ability to expand our
operations internationally.
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An important part of our business strategy is to expand and offer our tests internationally, with patient specimens collected by
laboratory and health care professional customers in foreign countries for processing by our California laboratory. As we continue to
expand our diagnostic offerings into new markets, including in Australia, we will become increasingly subject to or impacted by the
regulatory requirements of foreign jurisdictions, which are varied and complex. Our tests, and certain components of our tests, may be
subject to the regulatory approval requirements in each foreign country in which they are sold by us or a laboratory partner, and our
future performance may depend in part on obtaining any necessary regulatory approvals in a timely manner. For example, we are in
the process of obtaining a CE Mark from the European Commission for certain IVDs being offered to customers in Europe. We are
also in the process of obtaining NATA accreditation in Australia.
We are occasionally required to address inquiries from regulatory authorities in various countries, such as those in the European
Union, regarding the regulatory status of our diagnostic test offerings. If we do not continue to satisfactorily address any such
questions in the future, we may be required to cease offering our products in the relevant country. This may in turn result in similar
concerns, and subsequent cessation of our sources of revenue, in other countries.
Regulatory approval can be a lengthy, expensive and uncertain process. In addition, regulatory processes are subject to change,
and new or changed regulations can result in unanticipated delays and cost increases. For example, the European Commission’s
modernized regulations for in vitro diagnostic products, the IVDR, became effective in May 2022. Among others, the new regulations
introduce risk-based classification for IVDs and will require Notified Body involvement for various classes of devices, including
certain of our tests, which will require us to submit clinical evidence and post-market performance data to regulators. We must also
achieve and maintain International Standards Organization, or ISO, certification of our quality management system to come into
compliance with the IVDR.
We may not be able to obtain foreign regulatory approvals or authorizations for our tests on a timely basis, if at all, which may
cause us to incur additional costs or prevent us from marketing our tests in certain foreign countries.
We are subject to broad legal requirements regarding the information we test and analyze, and any failure to comply with
these requirements could result in materially significant, penalties, materially damage our reputation and materially harm our
business.
Our business is subject to federal and state laws that protect the privacy and security of personal information, including the
HIPAA, HITECH, and similar state laws, as well as numerous other federal, state and foreign laws, including consumer protection
laws and regulations, that govern the collection, dissemination, use, access to, confidentiality and security of patient health
information. In addition, new laws and regulations that further protect the privacy and security of medical records or medical
information are regularly considered by federal and state governments. Further, with the recent increase in publicity regarding data
breaches resulting in improper dissemination of consumer information, federal and state governments have passed or are considering
laws regulating the actions that a business must take if it experiences a data breach, such as prompt disclosure to affected customers.
The FTC and states’ attorneys general have also brought enforcement actions and prosecuted some data breach cases as unfair and/or
deceptive acts or practices under the FTC Act and comparable state laws. In addition to data breach notification laws, some states have
enacted statutes and rules requiring businesses to reasonably protect certain types of personal information they hold or to otherwise
comply with certain specified data security requirements for personal information. We intend to continue to comprehensively protect
all personal information and to comply with all applicable laws regarding the protection of such information.
Any failure to implement appropriate security measures to protect the confidentiality and integrity of personal information or
any breach or other failure of these systems resulting in the unauthorized access, manipulation, disclosure, or loss of this information
could result in our noncompliance with these laws. Penalties for failure to comply with a requirement of HIPAA and HITECH vary
significantly depending on the failure and could include civil monetary or criminal penalties. Additionally, the HIPAA Security Rule
is currently undergoing a proposed update, which, if implemented, will impose more stringent security measures on covered entities.
The European Union formally adopted the GDPR, which applies to all European Union member states. The GDPR introduced
stringent new data protection and operational requirements in the European Union for companies that receive or process personal data
of European residents, as well as substantial fines for breaches of the data protection rules. It has increased our responsibility and
liability in relation to personal data that we process, and we are required to maintain additional mechanisms ensuring compliance with
the GDPR. The GDPR is a complex law, and the regulatory guidance is still evolving, including with respect to how the GDPR should
be applied in the context of clinical studies and the collection, processing, and storage of sensitive personal data, including genetic
information and testing. Furthermore, many of the countries within the European Union are still in the process of drafting
supplementary data protection legislation in key fields where the GDPR allows for national variation, including the fields of clinical
study and other health-related information. Additionally, in 2021, the United Kingdom’s GDPR rules became effective. These
variations in the law may raise our costs of compliance and result in greater legal risks. On July 16, 2020, the highest Court of Justice
of the European Union, or the CJEU, issued a landmark opinion in the case Maximilian Schrems vs. Facebook (Case C-311/18), or
Schrems II. This decision calls into question certain data transfer mechanisms as between the European Union member states and the
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United States. The CJEU is the highest court in Europe, and the Schrems II decision heightens the burden on data importers to assess
U.S. national security laws on their business and future actions of European Union data protection authorities are difficult to predict at
this early date. Consequently, there is some risk of any such data transfers from the European Union being halted by one or more
European Union member states. Any contractual arrangements requiring the transfer of personal data from the European Union to us
in the United States will require greater scrutiny and assessments as required under Schrems II and may have an adverse impact on
cross-border transfers of personal data or increase costs of compliance.
In addition, many states, such as California, have implemented similar privacy laws and regulations, such as the CMIA, that
impose restrictive requirements regulating the use and disclosure of patient health information and other personal information. In
addition to fines and penalties imposed upon violators, some of these state laws also afford private rights of action to individuals who
believe their personal information has been misused. California’s patient privacy laws, for example, provide for penalties of up to
$250,000 and permit injured parties to sue for damages. In addition to the CMIA, California also enacted the CCPA, which became
effective on January 1, 2020. The CCPA has been characterized as the first “GDPR-like” privacy statute to be enacted in the United
States because it mirrors a number of the key provisions of the GDPR. The CCPA establishes a new privacy framework for covered
businesses in the State of California by creating an expanded definition of personal information, establishing new data privacy rights
for California residents, imposing special rules on the collection of personal data from minors, and creating a new and potentially
severe statutory damages framework for violations of the CCPA and for businesses that fail to implement reasonable security
procedures and practices to prevent data breaches. Additionally, the CPRA took full effect on January 1, 2023. The CPRA amends and
expands the CCPA significantly, potentially resulting in further uncertainty, additional costs and expenses in an effort to comply, and
additional harm and liability for failure to comply. Among other things, the CPRA established the CPPA, a new regulatory authority
charged with administering and enforcing the CRPA and privacy rights in California. The CPPA has the power to levy fines and bring
other enforcement actions. The CPRA could impact our operations or that of our collaborators and business partners and impose new
regulatory requirements and increase costs of compliance. In addition to California, 18 other states have passed similar privacy laws,
including Colorado, Connecticut, Delaware, Florida, Indiana, Iowa, Kentucky, Maryland, Montana, Nebraska, New Hampshire, New
Jersey, Oregon, Rhode Island, Tennessee, Texas, Utah, and Virginia. Other states are considering similar legislation, adding to the
complexity, costs, and risk of compliance. Like the GDPR and CCPA, many of these state laws categorize medical or health data,
genetic data, and biometric data that can be used to identify a natural person as “sensitive data” and the processing or collection of
such will require additional compliance obligations.
The interplay of federal and state laws may be subject to varying interpretations by courts and government agencies, creating
complex compliance issues for us and potentially exposing us to additional expense, adverse publicity and liability. Further, as
regulatory focus on privacy issues continues to increase and laws and regulations concerning the protection of personal information
expand and become more complex, these potential risks to our business could intensify. Additionally, the interpretation, application
and interplay of consumer and health-related data protection laws in the United States, Europe and elsewhere are often uncertain,
contradictory and in flux. As a result, it is possible that laws may be interpreted and applied in a manner that is inconsistent with our
current practices. Moreover, these laws and their interpretations are constantly evolving and may become more stringent or inclusive
over time. For example, increasing concerns about health information privacy have recently prompted the federal government to issue
guidance taking a newly expansive view of the scope of the laws and regulations that they enforce. Complying with these laws or any
new laws or interpretations of their application could involve significant time and substantial costs or require us to change our
business practices and compliance procedures in a manner potentially adverse to our business. We may not be able to obtain or
maintain compliance with the diverse privacy and security requirements in all of the jurisdictions in which we currently or plan to do
business, and failure to comply with any of these requirements could result in material civil or criminal penalties, materially harm our
reputation and materially adversely affect our business.
Many states, including California, New York, and Massachusetts, have also implemented genetic testing, informed consent, or
other privacy laws imposing specific patient consent requirements and requirements for protecting certain test results. As regulatory
focus on genetic privacy issues continues to increase and laws and regulations concerning the protection of personal information
expand and become more complex, these potential risks to our business could intensify.
Ethical, legal, and social concerns related to the use of genetic information could reduce demand for our tests.
Genetic testing has raised ethical, legal, and social issues regarding privacy and the appropriate uses of the resulting
information. Government authorities could, for social or other purposes, limit or regulate the use of genetic information or genetic
testing or prohibit testing for genetic predisposition to certain conditions, particularly for those that have no known cure. Similarly,
these concerns may cause patients to refuse to use, or physicians to be reluctant to order, genetic tests such as ours, even if
permissible. These and other ethical, legal, and social concerns may limit market acceptance and adoption of our tests or reduce the
potential markets for our tests, any of which could have an adverse effect on our business, financial condition and results of
operations. In addition, California has enacted the Genetic Information Privacy Act that imposes privacy requirements on direct-to-
consumer genetic testing companies that could change the discussion among patients and physicians related to genetic testing as a
whole and potentially reduce consumer interest in such testing more broadly.
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We conduct business in a heavily regulated industry. Complying with the numerous statutes and regulations pertaining to our
business is expensive and time-consuming, and any failure by us, our consultants, or commercial partners to comply could
result in substantial and material penalties.
Our industry and our operations are heavily regulated by various federal, state, local and foreign laws and regulations, and the
regulatory environment in which we operate could change significantly and adversely in the future. These laws and regulations
currently include, among others:
•
CLIA’s and CAP’s regulation of our laboratory activities;
•
FDA laws and regulations, including but not limited to requirements for offering LDTs following the July 2024 effective
date of the agency’s LDT final rule;
•
federal and state laws and standards affecting reimbursement by government healthcare programs, including certain
coding requirements to obtain reimbursement and certain changes to the payment mechanism for clinical laboratory
services resulting from PAMA;
•
HIPAA and HITECH, which establish comprehensive federal standards with respect to the privacy and security of PHI,
and requirements for the use of certain standardized electronic transactions with respect to transmission of such
information, as well as similar laws protecting other types of personal information;
•
state laws governing the maintenance of personally identifiable information of state residents, including medical
information, and which impose varying breach notification requirements, some of which allow private rights of action by
individuals for violations and also impose penalties for such violations;
•
the federal Anti-Kickback Statute, which generally prohibits knowingly and willfully offering, paying, soliciting or
receiving remuneration, directly or indirectly, in return for or to induce a person to refer to an individual any good,
facility, item or service that is reimbursable under a federal healthcare program;
•
the federal Stark Law, which generally prohibits a physician from making a referral for certain designated health services
covered by the Medicare and Medicaid program, including laboratory and pathology services, if the physician or an
immediate family member has a financial relationship with the entity providing the designated health services;
•
the federal False Claims Act, which imposes civil penalties, and provides for civil whistleblower or qui tam actions,
against individuals or entities for knowingly presenting, or causing to be presented, to the federal government, claims for
payment that are false or fraudulent or making a false statement to avoid, decrease or conceal an obligation to pay money
to the federal government;
•
the federal Civil Monetary Penalties Law, which generally prohibits, among other things, the offering or transfer of
remuneration to a Medicare or Medicaid beneficiary if it is likely to influence the beneficiary’s selection of a particular
provider, practitioner or supplier of services reimbursable by Medicare or Medicaid;
•
EKRA, which imposes criminal penalties for knowing or willful payment or offer, or solicitation or receipt, of any
remuneration, whether directly or indirectly, overtly or covertly, in cash or in kind, in exchange for the referral or
inducement of laboratory testing (among other health care services) covered by healthcare benefit programs (including
commercial insurers) unless a specific exception applies;
•
the ACA, which, among other things, establishes a requirement for providers and suppliers to report and return any
overpayments received from the Medicare and Medicaid programs;
•
other federal and state fraud and abuse laws, such as anti-kickback laws, prohibitions on self-referral, fee-splitting
restrictions, insurance fraud laws, anti-markup laws, prohibitions on the provision of tests at no or discounted cost to
induce physician or patient adoption and false claims acts, some of which may extend to services reimbursable by any
insurance payor, including private payors;
•
the federal Physician Payments Sunshine Act and various state laws on reporting relationships with health care providers
and customers, which could be determined to apply to our LDTs now that they are treated by FDA as medical devices
pursuant to the 2024 final rule;
•
the prohibition on reassignment of Medicare claims and other Medicare and Medicaid billing and coverage requirements;
•
state laws that prohibit other specified healthcare practices, such as billing physicians for tests that they order, waiving
coinsurance, copayments, deductibles and other amounts owed by patients, business corporations practicing medicine or
employing or engaging physicians to practice medicine and billing a state Medicaid program at a price that is higher than
what is charged to one or more other payors;
•
FCPA and applicable foreign anti-bribery laws;
•
federal, state and local regulations relating to the handling and disposal of regulated medical waste, hazardous waste and
biohazardous waste and workplace safety for healthcare employees;
•
laws and regulations relating to health and safety, labor and employment, public reporting, taxation and other areas
applicable to businesses generally, all of which are subject to change, including, for example, the significant changes to
the taxation of business entities were enacted in December 2017; and
•
similar foreign laws and regulations that apply to us in the countries in which we operate or may operate in the future.
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Certain states also require medical device manufacturers to maintain compliance programs and/or be licensed as manufacturers
or distributors by a state professional board or health department. Because the FDA’s now-in-effect final rule renders a clinical
laboratory like ours a “medical device manufacturer,” we have begun the process of evaluating whether and to what extent those kinds
of medical device-specific state requirements may be applicable to our operations.
The genetic testing industry is currently under a high degree of government scrutiny. The OIG and a variety of states’ Attorneys
General have issued fraud alerts regarding a variety of cancer genetic testing fraud schemes, and the DOJ has announced indictments
and guilty pleas in such fraud schemes involving a variety of individuals and entities, including genetic testing and other laboratories,
physicians who ordered genetic testing for a large volume of patients without treating them, and third parties who arranged for the
genetic testing by approaching patients through telemarketing calls, booths at public events, health fairs, and door-to-door visits.
These individuals then shared the proceeds received from Medicare, TRICARE, and other insurance payors, and these activities
allegedly violated the federal Anti-Kickback Statute and other criminal laws. This increased regulatory scrutiny could decrease
demand for our testing services or increase our costs of regulatory compliance, either of which could have a material adverse effect on
our business.
Any future growth of our business, including, in particular, growth of our international business and continued reliance on
consultants, commercial partners and other third parties, may increase the potential for violating these laws. In some cases, our risk of
violating these or other laws and regulations is further increased because of the lack of their complete interpretation by applicable
regulatory authorities or courts, and their provisions are thus open to a variety of interpretations. Our Picture Genetics line of at-home
genetic test offerings are patient-initiated screening tests, which may receive greater scrutiny from regulatory authorities than our
traditional testing services that are offered directly to health care providers.
We have adopted policies and procedures designed to comply with these laws and regulations and, in the ordinary course of our
business, we conduct internal reviews of our compliance with these laws. Our compliance is also subject to review by applicable
government agencies. It is not always possible to identify and deter misconduct by employees, distributors, consultants and
commercial partners, and the precautions we take to detect and prevent this activity may not be effective in controlling unknown or
unmanaged risks or losses or in protecting us from government investigations or other actions or lawsuits stemming from a failure to
comply with applicable laws or regulations. Any action brought against us for violation of these or other laws or regulations, even if
we successfully defend against it, could cause us to incur significant legal expenses, divert our management’s attention from the
operation of our business and materially harm our reputation. In relation to a recent advisory opinion issued by the OIG, the
Company’s subsidiary, Inform Diagnostics, initiated a voluntary disclosure process with the appropriate government contact. The
Company has settled and paid $3.0 million in connection with this voluntary disclosure. If our operations, including the conduct of our
employees, consultants and commercial partners, are found to be in violation of any of these laws and regulations, (including in
connection with the voluntary disclosure process described above), we may be subject to applicable penalties associated with the
violation, including administrative, civil and criminal penalties, damages, fines, individual imprisonment, exclusion from participation
in federal healthcare programs, refunding of payments received by us and curtailment or cessation of our operations, which could
materially harm our reputation, business, prospects or results of operations.
We may be required to modify our business practices, pay fines, incur significant expenses, or experience losses due to
litigation or governmental investigations.
From time to time and in the ordinary course of our business, we have been and again may be subject to litigation or
governmental investigation on a variety of matters in the United States or foreign jurisdictions, including, without limitation,
regulatory, intellectual property, product liability, antitrust, consumer, false claims, whistleblower, qui tam, privacy, anti-kickback,
anti-bribery, environmental, commercial, securities and employment litigation and claims and other legal proceedings that may arise
from the conduct of our business. Healthcare providers and other participants in the healthcare industry have become subject to an
increasing number of lawsuits alleging medical malpractice and related legal theories such as negligent hiring, supervision and
credentialing. As previously disclosed in our periodic reports, we have received a CID, issued by the DOJ, pursuant to the False
Claims Act related to its investigation of allegations of medically unnecessary laboratory testing, improper billing for laboratory
testing, and remuneration received or provided in violation of the Anti-Kickback Statute and the Stark Law. Among other things, this
CID requests information and records relating to certain of our customers named in this CID.
Similar to other laboratories in the industry, we are currently being audited by HRSA with respect to our reimbursement for
COVID-19 tests furnished to patients believed to be uninsured. We recorded approximately $548.9 million of reimbursements from
HRSA under the Uninsured Program during the years ended December 31, 2022, 2021, and 2020. There is uncertainty with respect to
the methodology HRSA will use in its audit and whether and how HRSA will extrapolate audit results. We are working with HRSA’s
auditors to resolve any issues related to its audit, including any reimbursed amounts that may need to be returned to HRSA. We have
also received a CID issued by the DOJ pursuant to the False Claims Act related to the DOJ’s investigation as to whether we submitted
or caused to be submitted false claims to the Uninsured Program.
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We are fully cooperating with the DOJ in connection with the CIDs that we have received and in connection with the HRSA
audit. We cannot currently predict when these CID and HRSA audit matters will be resolved, the reasonable or likely outcome of
these matters, or their potential impact, which may materially and adversely affect our business, prospects, and financial condition.
These matters are not formal claims, and discussions and investigations remain ongoing. As such, we cannot reasonably estimate the
loss or range of loss, if any, that may result from any material government investigations, audits, and reviews in which we are
currently involved, given the inherent difficulty in predicting regulatory action, fines and penalties, if any, and the various remedies
and levels of judicial review available to us in the event of an adverse finding. As a result, we have not recorded any liability related to
these CID or audit matters.
In addition, and as previously disclosed, the SEC is conducting a non-public formal investigation, which relates to (i) the matters
raised in the requests for the CID regarding allegations of medically unnecessary laboratory testing, improper billing for laboratory
testing, and remuneration received or provided in violation of the Anti-Kickback Statute and the Stark Law and (ii) our Exchange Act
reports filed for 2018 through 2020. On May 6, 2024, the SEC staff advised us that the SEC staff made a preliminary determination to
recommend that the SEC file an enforcement action against us based on a corporate negligence theory, which, if authorized, would
allege violations of Sections 17(a)(2) and 17(a)(3) of the Securities Act of 1933, as amended, Sections 13(a), 13(b)(2)(A) and
13(b)(2)(B) of the Exchange Act, and Rules 13a-1, 13a-13, and 12b-20 thereunder. The Company has fully cooperated with the SEC
and its requests, and the Company and the SEC staff are continuing to communicate regarding this matter. While we do not believe
that any enforcement recommendation is warranted and deny all liability, we have recorded a $1.0 million potential liability with
respect to this matter. While we believe this amount is a reasonable and probable estimate, the actual amount of liability, if any, may
be materially higher than this estimate, as discussions are ongoing and there is no formal settlement or final resolution of this matter at
this time.
We cannot predict when these investigations and matters will be resolved, the outcome of the investigations and matters, or the
potential impact on our business, which may ultimately be greater than we expect. Adverse developments in existing litigation claims
or legal proceedings involving us or new claims could require us to establish or increase litigation reserves or enter into unfavorable
settlements or satisfy judgments for monetary damages for amounts in excess of current reserves, which could adversely affect our
financial results. In addition, government investigations and litigation generally may divert the attention of our management team and
resources from our core business. As such, the time and attention of our management team in responding to these matters may limit
their time available to devote to our business, and we may also incur significant expenses or experience losses in relation to these
matters. As a result of these matters, we may also be required to alter the conduct of our operations or be subject to other penalties.
Any of these circumstances may adversely affect our business, prospects, reputation and results of operations.
Healthcare policy changes, including recently enacted and proposed new legislation targeting the U.S. healthcare system, could
cause significant harm to our business, operations and financial condition.
The ACA made a number of substantial changes to the way healthcare is financed both by governmental and private payors. The
ACA also introduced mechanisms to reduce the per capita rate of growth in Medicare spending if expenditures exceed certain targets.
Any such reductions could affect reimbursement payments for our tests. The ACA also contains a number of other provisions,
including provisions governing enrollment in federal and state healthcare programs, reimbursement matters and fraud and abuse,
which we expect will impact our industry and our operations in ways that we cannot currently predict.
In April 2014, Congress passed PAMA, which included substantial changes to the way in which clinical laboratory services are
paid under Medicare CLFS. Under PAMA, certain clinical laboratories are required to periodically report to CMS private payor
payment rates and volumes for their tests, and laboratories that fail to report the required payment information may be subject to
substantial civil monetary penalties. Medicare reimbursement for CDLTs is based on the weighted-median of the payments made by
private payors for these tests, rendering private payor payment levels even more significant than in the past. As a result, future
Medicare payments may fluctuate more often and become subject to the willingness of private payors to recognize the value of
diagnostic tests generally and any given test individually. The impact of this payment system on rates for our tests, including any
current or future tests we may develop, is uncertain.
Additionally, state legislatures have increasingly passed legislation and implemented regulations designed to control the cost of
health care services, including clinical laboratory and pathology services, as well as prescription drug prices. States may pursue a
variety of strategies to control spending growth in health care and pharmaceutical markets, including but not limited to promoting
competition, reducing prices through regulation, imposing spending targets and promoting payment reform. These cost containment
strategies may result in less favorable reimbursement rates and in some cases could negatively impact our ability to change or expand
our clinical testing operations in certain states.
Further, the impact on our business of the expansion of the federal and state governments’ role in the U.S. healthcare industry
generally, including the social, governmental, and other pressures to reduce healthcare costs while expanding individual benefits, is
51
uncertain. Any future changes or initiatives could have a materially adverse effect on our business, financial condition, results of
operations and cash flows.
Changes in laws and regulations, or in their application, may adversely affect our business, financial condition and results of
operations.
The clinical laboratory testing industry is highly regulated, and failure to comply with applicable regulatory, supervisory,
accreditation, registration or licensing requirements may adversely affect our business, financial condition and results of operations. In
particular, the laws and regulations governing the marketing and research of clinical diagnostic testing are extremely complex and in
many instances there are no clear regulatory or judicial interpretations of these laws and regulations, increasing the risk that we may
be found to be in violation of these laws.
Furthermore, the genetic testing industry as a whole is a growing industry and regulatory agencies such as HHS or the FDA may
apply heightened scrutiny to new developments in the field, or the U.S. Congress may do so. For example, since 2017, Congress has
been working on legislation to create an LDT and IVD regulatory framework that would be separate and distinct from the existing
medical device regulatory framework, it remains possible that congressional action in this area could moot the need for the FDA’s
recently issued LDT final rule (discussed further above).
In addition, there has been a recent trend of increased U.S. federal and state regulation, scrutiny and enforcement relating to
payments made to referral sources, which are governed by laws and regulations including the Stark law, the federal Anti-Kickback
Statute, the federal False Claims Act, as well as state equivalents of such laws. For example, EKRA was passed in October 2018 as
part of the Substance Use-Disorder Prevention that Promotes Opioid Recovery and Treatment for Patients and Communities Act.
EKRA imposes criminal penalties for knowing or willful payment or offer, or solicitation or receipt, of any remuneration, whether
directly or indirectly, overtly or covertly, in cash or in kind, in exchange for the referral or inducement of laboratory testing (among
other health care services) payable by a “healthcare benefit program” (which includes private insurance companies), unless a specific
exception applies. We cannot assure you that our relationships with physicians, sales representatives, hospitals, customers, or any
other party will not be subject to scrutiny or will survive regulatory challenge under such laws. If imposed for any reason, sanctions
under the EKRA could have a negative effect on our business.
If the hazardous materials we use in our operations cause contamination or injury, we could be liable for resulting damages.
Our operations require the use of regulated medical waste, hazardous waste and biohazardous waste, including chemicals,
biological agents and compounds and blood and other tissue specimens. We are subject on an ongoing basis to federal, state and local
laws and regulations governing the use, storage, handling and disposal of these hazardous materials and other specified waste
products. Although we typically use licensed or otherwise qualified outside vendors to dispose of this waste, applicable laws and
regulations could hold us liable for damages and fines if our or others’ business operations or other actions result in contamination to
the environment or personal injury due to exposure to hazardous materials. We cannot eliminate the risk of contamination or injury,
and any liability imposed on us for any resulting damages or injury could exceed our resources or any applicable insurance coverage.
The cost to secure such insurance coverage and to comply with these laws and regulations could become more significant in the future
and any failure to comply could result in substantial costs and other business and reputational consequences, any of which could
negatively affect our operating results.
If we were deemed to be an investment company under the Investment Company Act of 1940, as amended, applicable
restrictions could make it impractical for us to continue our business as currently conducted and could have a material
adverse effect on our business, financial condition and results of operations.
Under the Investment Company Act of 1940, or 1940 Act, a company generally will be deemed to be an “investment company”
for purposes of the 1940 Act if (1) it is, or holds itself out as being, engaged primarily, or proposes to engage primarily, in the business
of investing, reinvesting or trading in securities or (2) it engages, or proposes to engage, in the business of investing, reinvesting,
owning, holding or trading in securities and it owns or proposes to acquire investment securities having a value exceeding 40% of the
value of its total assets (exclusive of U.S. government securities and cash items) on an unconsolidated basis. We do not believe that
we are an “investment company,” as such term is defined in either of those sections of the 1940 Act and we intend to conduct our
operations so that we will not be deemed an investment company. However, if we were to be deemed an investment company,
restrictions imposed by the 1940 Act, including limitations on our capital structure and our ability to transact with affiliates, could
make it impractical for us to continue our business as it is currently being conducted and could have a material adverse effect on our
business, financial condition, and results of operations.
Our joint venture in China is subject to risks and uncertainties relating to the laws and regulations of China and the changes
in relations between the United States and China. If the Chinese government determines that our joint venture does not
52
comply with applicable regulations, our business could be adversely affected. If the regulatory agencies of the People’s
Republic of China, or the PRC, determine that the agreements that establish the structure and relationship for our operations
in China do not comply with PRC regulatory restrictions on foreign investment, we could be subject to severe penalties.
Under its current leadership, the government of China has been pursuing economic reform policies, including by encouraging
foreign trade and investment. However, there is no assurance that the Chinese government will continue to pursue such policies, that
such policies will be successfully implemented, that such policies will not be significantly altered, or that such policies will be
beneficial to our partnerships or activities in China. China’s system of laws can be unpredictable, especially with respect to foreign
investment and foreign trade. The United States government has called for substantial changes to foreign trade policy with China and
has raised tariffs on several Chinese goods. China has retaliated with increased tariffs on certain U.S. goods. Moreover, China’s
legislature has adopted a national security law to substantially change the way Hong Kong has been governed since the territory was
handed over by the United Kingdom to China in 1997. This law increases the power of the central government in Beijing over Hong
Kong, limits the civil liberties of residents of Hong Kong and could restrict the ability of businesses in Hong Kong to continue to
conduct business or to continue to with business as previously conducted. The U.S. State Department has indicated that the United
States no longer considers Hong Kong to have significant autonomy from China. The U.S. State Department has recently enacted
sanctions related to China’s governing of Hong Kong. Any further changes in U.S. trade policy could trigger retaliatory actions by
affected countries, including China, resulting in trade wars. Any regulatory changes and changes in United States and China relations
may have a material adverse effect on our partnerships or activities in China, which could materially harm our business and financial
condition.
In addition, there are uncertainties regarding the interpretation and application of PRC laws, rules, and regulations, including,
but not limited to, the laws, rules and regulations governing the validity and enforcement of our joint venture in China. Because many
laws and regulations are relatively new, the interpretations of many laws, regulations and rules are not always uniform. Moreover, the
interpretation of statutes and regulations may be subject to government policies reflecting domestic political agendas. Enforcement of
existing laws or contracts based on existing law may be uncertain and sporadic. We cannot assure you that the PRC regulatory
authorities will not determine that our joint venture in China does not violate PRC laws, rules or regulations. If the PRC regulatory
authorities determine that our current joint venture or any joint ventures, we may enter into in the future are in violation of applicable
PRC laws, rules or regulations, our joint venture in China may become invalid or unenforceable, which will substantially affect our
operations adversely. The PRC has broad discretion in dealing with violations of laws and regulations, including levying fines,
revoking business and other licenses and requiring actions necessary for compliance. In particular, licenses and permits issued or
granted by relevant governmental agencies may be revoked at a later time by other regulatory agencies. We cannot predict the effect
of the interpretation of existing or new PRC laws or regulations on our business. Any of these or similar actions could significantly
disrupt our operations or restrict us from conducting a substantial portion of our operations, which could materially and adversely
affect our business, financial condition and results of operations. There can be no assurance that the United States government will
refrain from imposing additional restrictions or constraints on dealings or investments in China, including our joint venture.
We could be adversely affected by violations of the FCPA and other anti-bribery laws.
Our international operations are subject to various anti-bribery laws, including the FCPA and similar anti-bribery laws in the
non-U.S. jurisdictions in which we operate. The FCPA prohibits companies and their intermediaries from offering, making, or
authorizing improper payments to non-U.S. or foreign officials for the purpose of obtaining or retaining business or securing any other
improper advantage. These laws are complex and far-reaching in nature, and we may be required in the future to alter one or more of
our practices to be in compliance with these laws or any changes to these laws or their interpretation.
We currently engage in significant business outside the United States, and we plan to increase our international operations in the
future. These operations could involve dealings with governments, foreign officials, and state-owned entities, such as government
hospitals, outside the United States. In addition, we may engage distributors, other commercial partners or third-party intermediaries,
such as representatives or contractors, or establish joint ventures or other arrangements to manage or assist with promotion and sale of
our tests abroad and obtaining necessary permits, licenses and other regulatory approvals. Any such third parties could be deemed to
be our agents and we could be held responsible for any corrupt or other illegal activities of our employees or these third parties, even
if we do not explicitly authorize or have actual knowledge of such activities. We have instituted policies, procedures, and internal
controls reasonably designed to promote compliance with the FCPA and other anti-corruption laws and we exercise a high degree of
vigilance in maintaining, implementing and enforcing these policies and controls. However, these policies and controls could be
circumvented or ignored, and we cannot guarantee compliance with these laws and regulations. Any violations of these laws or
allegations of such violations could disrupt our operations, involve significant management distraction, involve significant costs and
expenses, including legal fees, and harm our reputation. Additionally, other U.S. companies in the medical device and pharmaceutical
fields have faced substantial fines and criminal penalties in the recent past for violating the FCPA and we could also incur these types
of penalties, including criminal and civil penalties, disgorgement, and other remedial measures, if we violate the FCPA or other
applicable anti-bribery laws. Any of these outcomes could result in a material adverse effect on our business, prospects, financial
condition, or results of operations.
53
Our services present the potential for embezzlement, identity theft, or other similar illegal behavior by our employees,
consultants, service providers or commercial partners.
Our operations involve the use and disclosure of personal and business information that could be used to impersonate third
parties or otherwise gain access to their data or funds. If any of our employees, consultants, service providers, or commercial partners
takes, converts or misuses these funds or data, we could be liable for any resulting damages, which could harm our financial condition
and damage our business reputation.
We could be adversely affected by alleged violations of the FTC Act or other truth-in-advertising and consumer protection
laws.
In the United States, our advertising for laboratory services is subject to federal truth-in-advertising laws enforced by the FTC,
as well as comparable state consumer protection agencies under similarly broad state laws. Under the FTC Act, the FTC is
empowered, among other things, to (a) prevent unfair methods of competition and unfair or deceptive acts or practices in or affecting
commerce; (b) seek monetary redress and other relief for conduct injurious to consumers; and (c) gather and compile information and
conduct investigations relating to the organization, business, practices, and management of entities engaged in commerce. The FTC
has very broad enforcement authority, and failure to abide by the substantive requirements of the FTC Act and other consumer
protection laws can result in administrative or judicial penalties, including civil penalties, injunctions affecting the manner in which
we would be able to market services or products in the future, or criminal prosecution. In recent years, some companies and
individuals have become more aggressive in attempting to assert consumer protection-type causes of action against competitors based
on their advertising claims or promotional activities. In conjunction with the launch of our Picture Genetics line of at-home genetic
test offerings that are initiated by consumers, we increased our advertising activities that would be subject to federal and state truth-in-
advertising laws. Any actual or perceived non-compliance with those laws could lead to an investigation by the FTC or a comparable
state agency or could lead to allegations of misleading advertising by private plaintiffs. Any such action against us would disrupt our
business operations, cause damage to our reputation, and result in a material adverse effect on our business.
Outside of the United States, the legal landscape governing promotional and other marketing activities for professional
laboratory services and diagnostic tests can vary widely from jurisdiction to jurisdiction, and is often more complex, less clear, or less
developed than in the United States. If our marketing activities are found to be in violation of local laws, regulations or practices, we
may be subject to fines and other penalties and may be required to cease marketing or commercialization activities in such
jurisdiction.
Even if we receive regulatory approval or certification of our IVD medical device products, we will continue to be subject to
extensive regulatory oversight.
Medical devices, including IVDs, are subject to extensive regulation by the FDA in the United States, the European authorities
under the CE Mark process, and comparable regulatory agencies in other territories where we do business such as Japan and Taiwan.
If any of our IVD products are approved by the FDA or other comparable foreign regulatory agencies or certified by Notified Bodies,
we will be required to timely file various reports. If these reports are not filed timely, regulators may impose sanctions and sales of our
products may suffer, and we may be subject to product liability or regulatory enforcement actions, all of which could harm our
business. In addition, the FDA and the FTC regulate the advertising and promotion of medical devices to ensure that their promotional
claims made are consistent with the applicable marketing authorizations, that there are adequate and reasonable data to substantiate the
claims, and that the promotional labeling and advertising is neither false nor misleading in any respect. If the FDA or FTC determines
that any of our promotional claims for IVD products are false, misleading, not substantiated or not permissible, we may be subject to
enforcement actions and we may be required to revise our promotional claims and make other corrections or restitutions. Similar
requirements apply in foreign jurisdictions.
FDA, state and comparable foreign authorities have broad enforcement powers. Our failure to comply with applicable regulatory
requirements could result in enforcement action by the FDA, state or comparable foreign regulatory agencies, which may include any
of the following sanctions:
•
adverse publicity, warning letters, untitled letters, fines, injunctions, consent decrees and civil penalties;
•
repair, replacement, refunds, recalls, termination of distribution, administrative detention or seizures of our products;
•
operating restrictions, partial suspension or total shutdown of production;
•
customer notifications or repair, replacement or refunds;
•
refusing our requests for clearances or approvals of new products, new intended uses or modifications to existing
products;
•
withdrawals of current clearances, approvals or certifications, resulting in prohibitions on sales of our products;
54
•
refusal to issue certificates needed to export products for sale in other countries; and
•
criminal prosecution.
Any of these sanctions could also result in higher than anticipated costs or lower than anticipated sales of our IVD products and
have a material adverse effect on our reputation, business, results of operations and financial condition.
In addition, FDA regulations and guidance are often revised or reinterpreted by the FDA in ways that may significantly affect
our business and our products. Any new statutes, regulations or revisions or reinterpretations of existing regulations may impose
additional costs or lengthen review times of any product candidates or make it more difficult to obtain marketing authorizations for,
manufacture, market or distribute any IVD product candidate we are developing. We cannot determine what effect changes in
regulations, statutes, legal interpretation or policies, when and if promulgated, enacted or adopted may have on our business in the
future. Such changes could, among other things, require: additional testing prior to seeking marketing authorization, changes to
manufacturing methods recalls, replacement or discontinuance of our products or additional record keeping.
The EU’s regulatory landscape for IVD medical devices has also evolved in recent years with adoption of the IVDR to establish
a modernized and more robust EU legislative framework, with the aim of ensuring better protection of public health and patient safety.
We are working towards compliance with the IVDR for certain of our tests and have made initial submissions to our Notified Body for
purposes of the conformity assessment process. We expect to receive CE marking under the IVDR for certain of our tests in the future,
subject to ongoing review and auditing by the regulatory agency. If we are not able to obtain and maintain regulatory compliance, we
may not be permitted to market our laboratory services in the EU or may become subject to enforcement by EU Competent
Authorities.
Risks Related to the Development of Drug Candidates
Our drug candidates are in early stages of development and may fail or suffer delays that materially and adversely affect their
future commercial viability.
We are early in our development efforts. Generally, before obtaining marketing approval for the commercial distribution of drug
candidates, we must conduct preclinical tests and clinical trials to demonstrate sufficient safety and efficacy of our drug candidates in
patients. Failure can occur at any time during the development or clinical trial process and our future clinical trial results may not be
successful. As a result, we may not have, or we may deem it imprudent to use, additional financial resources to continue development
of a drug candidate if there are issues that could delay or prevent marketing approval of, or ability to commercialize, our drug
candidates, including:
•
negative or inconclusive results from clinical trials, or the clinical trials of others for similar drug candidates, leading to a
decision or requirement to conduct additional preclinical testing or clinical trials or abandon a program;
•
therapeutic-related side effects experienced by participants in its clinical trials or by individuals using drugs or other drugs
similar to its drug candidates;
•
delays in submitting INDs or comparable foreign clinical trial applications or delays or failure in obtaining the necessary
approvals from regulators to commence a clinical trial, or a suspension or termination of a clinical trial once commenced;
•
conditions imposed by the FDA or comparable foreign authorities regarding the scope or design of clinical trials;
•
delays in enrolling research subjects or high drop-out rates of research subjects enrolled in clinical trials;
•
delays or difficulties in its clinical trials due to quarantines or other restrictions resulting from pandemics or other public
health emergencies;
•
unfavorable FDA or other regulatory agency inspection and review of a clinical trial site or the manufacturing location(s)
for a drug candidate;
•
inadequate supply or quality of drug candidate clinical material or other raw materials or supplies necessary for the
conduct of our clinical trials;
•
failure of third-party contractors or investigators to comply with regulatory requirements or otherwise meet their
contractual obligations in a timely manner, or at all;
•
delays and changes in regulatory requirements, policy and guidelines, including with respect to our technology in
particular; or
•
varying interpretations of data by the FDA and similar foreign regulatory agencies.
The drug candidates we pursue may not demonstrate the necessary safety or efficacy requirements for marketing approval.
Clinical trials are costly, time consuming, and inherently risky; and we may fail to demonstrate safety and efficacy to the
satisfaction of applicable regulatory authorities, and may never obtain regulatory approval for, or successfully commercialize
certain or any of our drug candidates.
55
Clinical development is expensive, time consuming and involves significant risk. We cannot guarantee that any clinical trials
will be conducted as planned or completed on schedule, if at all. A failure of one or more clinical trials can occur at any stage of
development. Events that may prevent successful or timely completion of clinical development include but are not limited to:
•
potential delays in patient enrollment for our clinical trials due to public health emergencies or pandemics, natural
disasters, staffing shortages, or other events, which may affect our ability to initiate and/or complete preclinical studies,
conduct ongoing clinical trials, and delay initiation of planned and future clinical trials;
•
inability to generate satisfactory preclinical, toxicology or other in vivo or in vitro data or to develop diagnostics capable
of supporting the initiation or continuation of clinical trials;
•
delays in reaching agreement on acceptable terms with CROs, and clinical trial sites, the terms of which can be subject to
extensive negotiation and may vary significantly among different CROs and clinical trial sites;
•
delays or failure in obtaining required an IRB approval for clinical trial site;
•
failure to obtain or delays in obtaining a permit from regulatory authorities to conduct a clinical trial;
•
delays in recruiting or failure to recruit sufficient eligible volunteers or subjects in our clinical trials;
•
failure by clinical trial sites or CROs or other third parties to adhere to clinical trial requirements;
•
failure by our clinical trial sites, CROs or other third parties to perform in accordance with the good clinical practices
requirements of the FDA or applicable foreign regulatory guidelines;
•
subjects withdrawing from our clinical trials;
•
adverse events or other issues of concern significant enough for the FDA, or comparable foreign regulatory authority, to
put a clinical trial or an IND on clinical hold;
•
occurrence of adverse events associated with our drug candidates;
•
changes in regulatory requirements and guidance that require amending or submitting new clinical protocols;
•
the cost of clinical trials of our drug candidates;
•
negative or inconclusive results from our clinical trials which may result in us deciding, or regulators requiring us, to
conduct additional clinical trials or abandon development programs in other ongoing or planned indications for a drug
candidate; and
•
delays in reaching agreement on acceptable terms with third-party manufacturers or an inability to manufacture sufficient
quantities of our drug candidates for use in clinical trials.
Any inability to successfully complete clinical development and obtain regulatory approval for one or more of our drug
candidates could result in additional costs to us or impair our ability to generate revenue. In addition, if we make manufacturing or
formulation changes to our drug candidates, we may need to conduct additional nonclinical studies and/or clinical trials to show that
the results obtained from such new formulation are consistent with previous results. Clinical trial delays could also shorten any periods
during which our drug candidates have patent protection and may allow competitors to develop and bring products to market before
we do, which could impair our ability to successfully commercialize our drug candidates and may harm our business and results of
operation.
Further, a clinical trial may be suspended or terminated by the company, the IRBs of the institutions in which such trials are
being conducted, the Data Safety Monitoring Board, or DSMB, for such trial or by the FDA or other regulatory authorities due to a
number of factors, including failure to conduct the clinical trial in accordance with regulatory requirements or our clinical protocols,
inspection of the clinical trial operations or trial site by the FDA or other regulatory authorities resulting in the imposition of a clinical
hold, unforeseen safety issues or adverse side effects, failure to demonstrate a benefit from using an investigational drug, changes in
governmental regulations, administrative actions or lack of adequate funding to continue the clinical trial. Clinical holds may be
placed prior to a clinical trial even beginning, in order to address potential safety and risk concerns of regulatory authorities, and
partial or complete clinical holds can be imposed at any time during a trial. Furthermore, while we perform certain similar functions
internally, we expect to rely on CROs and clinical trial sites to ensure proper and timely conduct of our clinical trials and while we
expect to enter into agreements governing those CROs’ committed activities we have limited influence over their actual performance.
If there are delays in the completion of, or termination of, any clinical trial of drug candidates, the commercial prospects of
those drug candidates may be harmed. In addition, any delays in completing clinical trials will increase costs, slow down product
development and approval processes, and jeopardize the ability to commence product sales and generate revenue. Any of these
occurrences may materially and adversely affect our business, financial condition, results of operations, and prospects. In addition,
many of the factors that cause, or lead to, a delay in the commencement or completion of clinical trials may also ultimately lead to the
denial of marketing approval of drug candidates.
Our nano-drug delivery platform is being researched and developed and, if approved, will be used as a delivery mechanism for
other pharmaceuticals or therapeutics. To the extent these delivered substances cause undesirable side effects, encounter competition
or experience regulatory limitations either prior or following market approval or are otherwise unavailable to us due to our lack of
rights or ability to utilize supplies of these candidates, the prospects for our drug candidates or, as applicable, approved therapeutics
56
could be materially and negatively affected. In such circumstances, our business, results of operations and the value of our common
stock may decline.
Product development involves a lengthy and expensive process with an uncertain outcome, and results of earlier preclinical
studies and clinical trials may not be predictive of future clinical trial results.
Clinical testing is expensive and generally takes many years to complete, and the outcome is inherently uncertain. Failure can
occur at any time during the clinical development process. Clinical trials may produce negative or inconclusive results, and we or any
current or future collaboration partners may decide, or regulators may require us, to conduct additional clinical trials or non-clinical
studies. We will be required to demonstrate with substantial evidence through well-controlled clinical trials that our drug candidates
are safe and effective for use in a diverse population before we can seek marketing approvals for their commercial sale. The results of
preclinical studies and early clinical trials of our drug candidates may not be predictive of the results of larger, later-stage controlled
clinical trials. Drug candidates that have shown promising results in early-stage clinical trials may still suffer significant setbacks or
failure in subsequent clinical trials. Our clinical trials to date have been conducted on a small number of subjects in limited numbers of
clinical trial sites for a limited number of indications. We will have to conduct larger, well-controlled trials in our proposed indications
to verify the results obtained to date and to support any regulatory submissions for further clinical development. A number of
companies in the biopharmaceutical industry have suffered significant setbacks or failure in advanced clinical trials due to lack of
efficacy or adverse safety profiles despite promising results in earlier, smaller clinical trials.
Moreover, from time to time, we may publish or report interim or preliminary data from our clinical trials. For example, we
have previously announced and included interim data for our drug candidate, FID-007, in this Annual Report. Interim or preliminary
data from clinical trials that we may conduct, including any interim data we have reported for FID-007, may not be indicative of the
final results of the trial and are subject to the risk that one or more of the clinical outcomes may materially change as patient
enrollment continues and more patient data become available. Interim or preliminary data also remain subject to audit and verification
procedures that may result in the final data being materially different from the interim or preliminary data. As a result, interim or
preliminary data should be viewed with caution until the final data is available.
In some instances, there can be significant variability in safety and efficacy results between different clinical trials of the same
drug candidate due to numerous factors, including changes in trial protocols, differences in size and type of the patient populations,
differences in and adherence to the dosing regimen and other trial protocols and the rate of dropout among clinical trial participants.
We therefore do not know whether any clinical trials we may conduct will demonstrate consistent or adequate efficacy and safety
sufficient to obtain marketing approval to market our drug candidates.
Any drug candidate that we may attempt to develop, manufacture, or market in the United States will be subject to extensive
regulation by the FDA, including regulations relating to development, non-clinical testing, performance of clinical trials,
manufacturing and post-approval commercialization and will also be subject to extensive regulations outside of the United
States in relevant jurisdictions. Satisfaction of these and other regulatory requirements is costly, time consuming, uncertain
and subject to unanticipated delays. The time required to obtain FDA approval, and any other required approvals for
pharmaceutical products, is unpredictable but typically requires years to several years and may never be obtained.
Any product that we may wish to develop, manufacture or market in countries other than the United States will also be subject
to numerous foreign regulatory requirements governing the conduct of clinical trials, manufacturing and marketing, pricing and
insurance reimbursement among other things in such countries. The foreign marketing approval process includes all of the risks and
uncertainties associated with FDA approval described above as well as risks attributable to the satisfaction of local regulations in such
foreign jurisdictions.
Obtaining marketing approval for pharmaceutical products requires the submission of extensive non-clinical and clinical data
and supporting information to FDA and comparable regulatory authorities for each therapeutic indication to establish the drug
candidate’s safety and efficacy. Securing marketing approval also typically requires the submission of information about the product
manufacturing process, and in many cases the inspection of manufacturing, processing, and packaging facilities by the applicable
regulatory authorities. Our drug candidates may not be effective, may be only moderately effective or may prove to have undesirable
or unintended side effects, toxicities or other characteristics that may preclude our obtaining marketing approval or prevent or limit
commercial use, or there may be deficiencies in manufacturing compliance by us or by our contract manufacturing organizations and
partners that could result in the candidate not being approved. Moreover, we have not obtained marketing approval for any drug
candidate in any jurisdiction and it is possible that none of our existing drug candidates or any drug candidates we may seek to
develop in the future will ever obtain marketing approval.
Drug candidates could fail to receive, or could be delayed in receiving, marketing approval for many reasons, including any one
or more of the following:
57
•
the FDA, EMA, or comparable foreign regulatory authorities may disagree with the design or implementation of clinical
trials;
•
we may be unable to demonstrate to the satisfaction of the FDA, EMA or comparable foreign regulatory authorities that a
drug candidate is safe and effective for its proposed indication(s) for use;
•
the results of clinical trials may not meet the level of statistical significance required by the FDA, EMA or comparable
foreign regulatory authorities for marketing approval;
•
we may be unable to demonstrate that a drug candidate’s clinical and other benefits outweigh its safety risks;
•
the FDA, EMA or comparable foreign regulatory authorities may disagree with our interpretation of data from non-
clinical studies or clinical trials;
•
the data collected from clinical trials of drug candidates may not be sufficient to support the submission of an application
to obtain marketing approval in the United States or elsewhere;
•
upon review of clinical trial sites and data, the FDA or comparable foreign regulatory authorities may find record keeping
or the record keeping of clinical trial sites to be inadequate or may identify other deficiencies related to the trials;
•
the manufacturing processes or facilities of third-party manufacturers with which we or Fulgent Pharma contract for
clinical and commercial supplies may fail to meet the requirements of the FDA, EMA or comparable foreign regulatory
authorities; or
•
the medical standard of care or the approval policies or regulations of the FDA, EMA or comparable foreign regulatory
authorities may significantly change in a manner that renders our clinical data insufficient for approval.
It is possible that none of the drug candidates we may develop will obtain the marketing approvals necessary for us or our
collaborators to sell the products either in the United States or any other country. Furthermore, approval by the FDA of a therapeutic
product does not assure approval by regulatory authorities outside the United States and vice versa. Even if approval for a therapeutic
product is obtained, such approval may be subject to limitations on the indicated uses or appropriate patient population that could
result in a significantly reduced potential market size for the product.
We intend to develop and seek approval for our drug candidates developed using our nano-drug delivery platform technology,
including FID-007, FID-022, and other candidates it may develop, pursuant to the FDA’s 505(b)(2) pathway. If the FDA determines
that we may not use this regulatory pathway, then we would need to seek regulatory approval via a “full” or “stand-alone” NDA under
Section 505(b)(1) of the FDC Act. This would require us to conduct additional clinical trials, provide additional safety and efficacy
data and other information, and meet additional standards for regulatory approval, including possibly nonclinical data. If this were to
occur, the time and financial resources required to obtain FDA approval, as well as the development complexity and risk associated
with these programs, would likely substantially increase, which could have a material adverse effect on our business and financial
condition.
The Drug Price Competition and Patent Term Restoration Act of 1984, informally known as the Hatch-Waxman Act, added
Section 505(b)(2) to the FDC Act. Section 505(b)(2) permits the filing of an NDA where at least some of the information required for
approval comes from studies and information that were not conducted by or for the applicant and for which the applicant has not
obtained a right of reference. Utilization of the Section 505(b)(2) NDA pathway could expedite the development program for our lead
drug candidates, FID-007 and of FID-022.
Notwithstanding the approval of an increasing number of products by the FDA under Section 505(b)(2) over the last few years,
certain brand-name pharmaceutical companies and others have objected to the FDA’s interpretation of Section 505(b)(2). If the FDA’s
interpretation of Section 505(b)(2) is successfully challenged, or Congress were to amend the statute to alter the currently available
regulatory pathway, the FDA may change its 505(b)(2) policies and practices, which could delay or even prevent the FDA from
approving any NDA we submit under Section 505(b)(2). In addition, the pharmaceutical industry is highly competitive, and Section
505(b)(2) NDAs are subject to special requirements designed to protect the patent rights of sponsors of previously approved drugs
referenced in a Section 505(b)(2) NDA. Even if we are able to utilize the Section 505(b)(2) regulatory pathway for one or more of our
candidates, there is no guarantee this would ultimately lead to faster product development or earlier approval.
Moreover, any delay resulting from our inability to utilize the FDA’s 505(b)(2) pathway could result in new competitive
products reaching the market more quickly than our drug candidates, which may have a material adverse impact on our competitive
position and prospects. Even if we are allowed to use the FDA’s 505(b)(2) pathway for one or more of our drug candidates, we cannot
assure you that such candidates will receive the requisite approvals for commercialization.
58
Our commercial success will depend upon attaining significant market acceptance of our drug candidates, if approved, among
physicians, patients, insurance payors and other members of the medical community.
Even if we obtain regulatory approval for our drug candidates, the approved products may nonetheless fail to gain sufficient
market acceptance among patients, physicians, insurance payors, and other members of the medical community, which is critical to
commercial success. If an approved product does not achieve an adequate level of acceptance, we may not generate significant
product revenues or any profits from operations. The degree of market acceptance of any drug candidate for which we receive
approval depends on a number of factors, including:
•
the efficacy and potential advantages compared to alternative treatments or competitive products;
•
perceptions by the medical community, physicians, and patients, regarding the safety and effectiveness of our products
and the willingness of the target patient population to try new therapies and of physicians to prescribe these therapies;
•
the size of the market for such drug candidate, based on the size of the patient subsets that we are targeting, in the
territories for which we gain regulatory approval and have commercial rights;
•
the safety of the drug candidate as demonstrated through broad commercial distribution;
•
the ability to offer our drug candidates for sale at competitive prices;
•
the availability of adequate coverage and reimbursement for our products from governmental health programs and other
insurance payors;
•
relative convenience and ease of administration compared to alternative treatments;
•
cost-effectiveness of our product relative to competing products;
•
the prevalence and severity of any side effects;
•
the adequacy of supply of our drug candidates;
•
the timing of any such marketing approval in relation to other product approvals;
•
any restrictions on concomitant use of other medications;
•
support from patient advocacy groups; and
•
the effectiveness of sales, marketing and distribution efforts by us and our licensees and distributors, if any.
Our drug candidates may cause undesirable side effects that could delay or prevent their marketing approval, limit the
commercial profile of an approved label, or result in significant negative consequences following marketing approval, if any.
Undesirable side effects caused by our drug candidates could cause us, our collaborators or regulatory authorities, to interrupt,
delay or halt clinical trials. These circumstances could result in a more restrictive label or the delay or denial of marketing approval by
the FDA or other regulatory authorities. Results of our clinical trials or the clinical trials of our collaborators could reveal a high and
unacceptable severity of adverse side effects and it is possible that patients enrolled in these clinical trials could respond in unexpected
ways. Such side effects could also affect patient recruitment or the ability of enrolled patients to complete the trial or result in potential
product liability claims. Further, clinical trials by their nature utilize a sample of the potential patient population. Rare and severe side
effects of our drug candidates may only be uncovered with a significantly larger number of patients exposed to our drug candidates.
In the event that any of our drug candidates receives marketing approval and we, our collaborators or others identify undesirable
side effects caused by a product or any other similar drugs, any of the following adverse events could occur:
•
regulatory authorities may withdraw their approval of the product;
•
additional restrictions may be imposed on the marketing of the particular product or the manufacturing processes for the
product or any component of the product;
•
we may be subject to fines, injunctions or the imposition of civil or criminal penalties;
•
regulatory authorities may require the addition of safety-related labeling statements, such as a “black box” warning or a
contraindication;
•
we may be required to create a Medication Guide outlining the risks of such side effects for distribution to patients or to
implement other aspects of a REMS such as a restricted distribution program or educational programs for prescribers;
•
we could be sued and held liable for harm caused to patients;
59
•
the product may become less competitive; and
•
our reputation may suffer.
In addition, adverse side effects caused by any drugs that may be similar in nature to our drug candidates or in connection with
the nanoencapsulated drugs or therapeutics used in connection with our drug candidates (similar to paclitaxel with FID-007) could
delay or prevent marketing approval of our drug candidates, limit the commercial profile of an approved label for our drug candidates,
or result in significant negative consequences for our drug candidates following marketing approval.
Any of the above-described events could prevent us from achieving or maintaining market acceptance of our drug candidates, if
approved, and could delay, impede and/or substantially increase the costs of commercializing our drug candidates thus significantly
impacting our ability to successfully commercialize our drug candidates and generate revenue. Any of the above described
occurrences may materially and adversely affect our business, financial condition, results of operations and prospects.
If our drug candidates are approved for marketing and commercialization and we are unable to develop sales, marketing and
distribution capabilities on our own or enter into agreements with third parties to perform these functions on acceptable
terms, we will be unable to commercialize successfully any such drug candidates.
We currently have no sales, marketing, or distribution capabilities for prescription pharmaceutical products. If any of our drug
candidates is approved for marketing in the United States or elsewhere, we will need to expand our internal sales, marketing and
distribution capabilities to commercialize such approved drug candidates in the United States and other territories, or we will need to
enter into collaborations with third parties to perform these services. Any internal effort would be expensive and time-consuming, and
we would need to commit significant financial and managerial resources to develop an internal marketing and sales force with
technical expertise and the related supporting distribution, administration and compliance capabilities. If we were to rely on additional
third parties with these capabilities to market our future therapeutics or were to decide to co-promote products with any of our current
or future collaborators, we would need to establish and maintain or revise existing marketing and distribution arrangements with these
partners, and there can be no assurance that we will be able to enter into such arrangements on acceptable terms or at all. Further, there
can be no assurance that these third parties will establish adequate sales and distribution capabilities or be successful in gaining market
acceptance of any approved product. If we are not successful in commercializing any product approved in the future, either on our
own or through third parties, our business, financial condition, results of operations and prospects could be materially and adversely
affected.
We rely on third parties to conduct portions of our clinical trials and certain of our non-clinical studies and intend to continue
to do so. If these third parties do not perform as contractually required, fail to satisfy regulatory or legal requirements, or miss
expected deadlines, our development programs could be delayed with material and adverse effects on our business, financial
condition, results of operations and prospects.
While we expect to continue our current clinical trials and expect to initiate clinical trials in the near term for other drug
candidates, we do not independently conduct clinical trials. In particular, while we perform certain functions internally, we currently
rely and intend to continue to rely on third-party CROs, clinical data management organizations and consultants to help us design,
conduct, supervise and monitor clinical trials of our drug candidates. As a result, we will have less control over the timing, quality and
other aspects of our clinical trials than we would have had we conducted them on our own. There is a limited number of third-party
service providers that specialize or have the expertise required to achieve our business objectives. If any of our relationships with
these third-party CROs or clinical investigators terminate, we may not be able to enter into arrangements with alternative CROs or
investigators or to do so on commercially reasonable terms.
Further, these investigators, CROs and consultants are not our employees, and we have limited control over the amount of time
and resources that they dedicate to our programs. These third parties may have contractual relationships with other entities, some of
which may be our competitors, which may draw time and resources from our programs. The third parties with which we contract
might not be diligent, careful or timely in conducting our non-clinical studies or clinical trials. These third parties may also be
susceptible to disruption as a result of health crises, public health emergencies or periods of societal unrest or conflict. If we cannot
contract with acceptable third parties on commercially reasonable terms, or at all, or if these third parties do not carry out their
contractual duties, satisfy the legal and regulatory requirements for the conduct of non-clinical studies or clinical trials or meet
expected deadlines for any reason, our clinical development programs could be delayed and otherwise adversely affected.
In all events, we will be responsible for ensuring that each of our non-clinical studies and clinical trials is conducted in
accordance with the general investigational plan and protocols for the relevant study or trial. The FDA requires non-clinical studies to
be conducted in accordance with GLP and clinical trials to be conducted in accordance with GCPs including practices and
requirements for designing, conducting, recording and reporting the results of non-clinical studies and clinical trials to assure that data
and reported results are credible and accurate and that the rights, integrity and confidentiality of clinical trial participants are protected.
Our reliance on third parties we do not control will not relieve us of these responsibilities and requirements. Any adverse development
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or delay in our clinical trials could have a material and adverse effect on our business, financial condition, results of operations and
prospects.
We rely on third parties to supply and manufacture our drug candidates, and we expect to continue to rely on third parties to
manufacture and supply our therapeutics, if approved. The development of drug candidates and the commercialization of any
drug candidates, if approved, could be stopped, delayed, or made less profitable if any of these third parties fail to provide us
with sufficient quantities of drug candidates or therapeutics, fail to do so at acceptable quality levels or prices, or fail to
maintain or achieve satisfactory regulatory compliance.
We do not currently have, nor do we plan to acquire, the infrastructure or capability internally to develop and manufacture our
drug candidates for use in the conduct of our trials or for commercial supply, if our therapeutics are approved. Instead, we rely on, and
expect to continue to rely on third-party providers to manufacture the supplies for our non-clinical studies and clinical trials.
We currently rely on a limited number of third-party contract manufacturers for our required raw materials and other
components for our non-clinical research and clinical trials, as well as for the manufacture of supplies for our drug candidates. To the
extent any of our manufacturing partners are unable to fulfill these obligations in a timely manner, our clinical trials may be delayed,
and our business may be adversely affected. In general, reliance on third-party providers may expose us to more risk than if we were
to manufacture our drug candidates ourselves. We do not control the operational processes of the contract manufacturing organizations
with whom we contract, and are dependent on these third parties for the production of our drug candidates in accordance with relevant
regulations (such as cGMP), which include, among other things, quality control and the maintenance of records and documentation.
Intellectual Property Risks
If we are unable to obtain and maintain patent protection for any drug candidate we develop, our competitors could develop
and commercialize products or technology similar to ours, and our ability to successfully commercialize any drug candidate
we may develop, and our technology, may be adversely affected.
Our success depends in large part on our ability to obtain and maintain patent protection in the United States and other countries
with respect to any drug candidate and other technologies we may develop. Given that the development of our drug and therapeutic
technology is at an early stage, our intellectual property portfolio comprises applications and patents with respect to coverage of
certain aspects of our technology and any drug and any drug candidates; however, there can be no assurance that any such patent
applications will issue as granted patents.
Composition of matter patents for biological and pharmaceutical products are generally considered to be the strongest form of
intellectual property protection for those types of products, as such patents provide protection without regard to any method of use.
We cannot be certain, however, that the claims in our future patent applications covering the composition of matter of any drug
candidates will be considered patentable by the United States Patent and Trademark Office (“USPTO”), or by patent offices in foreign
countries, or that the claims in any of its issued patents will be considered valid and enforceable by courts in the United States or
foreign countries.
Furthermore, in some cases, we may not be able to obtain issued claims covering compositions of matter relating to any drug
candidates we develop and instead may need to rely on filing patent applications with claims covering a method of use and/or method
of manufacture. Method of use patents protect the use of a product for the specified method. This type of patent does not prevent a
competitor from making and marketing a product that is identical to any product we develop for an indication that is outside the scope
of the patented method. Moreover, even if competitors do not actively promote their products for its targeted indications, physicians
may prescribe these products “off-label” for those uses that are covered by its method of use patents. Although off-label prescriptions
may infringe or contribute to the infringement of method of use patents, the practice is common, and such infringement is difficult to
prevent or prosecute. There can be no assurance that any such patent applications will issue as granted patents, and even if they do
issue, such patent claims may be insufficient to prevent third parties, such as our competitors, from utilizing our technology. Any
failure to obtain or maintain patent protection with respect to any drug candidate we develop could have a material adverse effect on
our business, financial condition, results of operations, and prospects.
We rely on trade secret protection, non-disclosure agreements. and invention assignment agreements to protect our
proprietary information, which may not be effective.
We rely on trade secret protection, non-disclosure agreements and invention assignment agreements with our employees,
consultants and third parties to protect our confidential and proprietary information. Although our competitors have utilized and are
expected to continue to utilize technologies and methods similar to ours and have aggregated and are expected to continue to
aggregate libraries of genetic information similar to ours, we believe our success will depend in part on our ability to develop
proprietary methods and libraries and to defend any advantages afforded to us by these methods and libraries relative to our
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competitors. If we do not protect our intellectual property and other confidential information adequately, competitors may be able to
use our proprietary technologies and information and thereby erode any competitive advantages our intellectual property and other
confidential information provide us.
We will be able to protect our proprietary trade secret rights from unauthorized use by third parties only to the extent these
rights are effectively maintained as confidential. We expect to rely primarily on trade secret and contractual protections for our
confidential and proprietary information, and we have taken security measures we believe are appropriate to protect this information.
These measures, however, may not provide adequate protection for our trade secrets, know-how, or other confidential information. We
seek to protect our proprietary information by, among other things, entering into confidentiality agreements with employees,
consultants and other third parties. These confidentiality agreements may not sufficiently safeguard our trade secrets and other
confidential information and may not provide adequate remedies in the event of unauthorized use or disclosure of this information.
Enforcing a claim that a party illegally disclosed or misappropriated a trade secret or other proprietary information could be difficult,
expensive, and time-consuming; and the outcome could be unpredictable. In addition, trade secrets or other confidential information
could otherwise become known or be independently developed by others in a manner that could prevent legal recourse by us. If any of
our trade secrets or other confidential or proprietary information were disclosed or misappropriated or if any such information was
independently developed by a competitor, our competitive position could be harmed, and our business could suffer.
Litigation or other proceedings or third-party claims of intellectual property infringement or misappropriation could require
us to spend significant time and money and prevent us from selling our tests or developing drug candidates.
We believe our ability to succeed will depend in part on our avoidance of infringement of patents and other proprietary rights
owned by third parties, including the intellectual property rights of competitors. There are numerous third-party-owned U.S. and
foreign patents, pending patent applications and other intellectual property rights that cover technologies relevant to our testing,
testing services and drug candidates. We may be unaware of patents or other intellectual property rights that a third-party might assert
are infringed by our business, and there may be pending patent applications that, if issued, could be asserted against us. As a result,
our existing or future operations may be alleged or found to infringe existing or future patents or other intellectual property rights of
others. Moreover, as we continue to sell our existing tests and if we launch new tests, commercialize drug candidates and enter new
markets, competitors may claim that our tests or products infringe or misappropriate their intellectual property rights as part of
strategies designed to impede our existing operations or our entry into new markets.
If a patent infringement or misappropriation of intellectual property lawsuit was brought against us, we could be forced to
discontinue or delay our development or sales of any tests or other activities that are the subject of the lawsuit while it is pending, even
if it is not ultimately successful. In the event of a successful claim of infringement against us, we could be forced to pay substantial
damages, including treble damages and attorneys’ fees if we were found to have willfully infringed patents; obtain one or more
licenses, which may not be available on commercially reasonable terms when needed or at all; pay royalties, which may be
substantial; or redesign any infringing tests or other activities, which may be impossible or require substantial time and expense. In
addition, third parties making claims against us for infringement or misappropriation of their patents or other intellectual property
rights could seek and obtain injunctive or other equitable relief, which, if granted, could prohibit us from performing some or all of
our tests. Further, defense against these claims, regardless of their merit or success, could cause us to incur substantial expenses, be a
substantial diversion to our management and other employee resources and significantly harm our reputation. Any of these outcomes
could delay our introduction of new tests, delay commercialization of any approved drug candidates, significantly increase our costs,
or prevent us from conducting certain of our essential activities, which could materially adversely affect our ability to operate and
grow our business.
We may be subject to claims challenging the inventorship of our patents and other intellectual property.
We may be subject to claims that former employees, collaborators or other third parties have an interest in our owned patents,
trade secrets, or other intellectual property as an inventor or co-inventor. For example, we may have inventorship disputes arise from
conflicting obligations of consultants or others who are involved in developing our drugs or drug candidates and other proprietary
technologies we may develop. Litigation may be necessary to defend against these and other claims challenging inventorship or our
ownership of our owned patents, trade secrets, or other intellectual property. If we fail in defending any such claims, in addition to
paying monetary damages, we may lose valuable intellectual property rights, such as exclusive ownership of, or right to use,
intellectual property that is important to our products, drug candidates and other proprietary technologies we may develop. Even if we
are successful in defending against such claims, litigation could result in substantial costs and be a distraction to management and
other employees. Any of the foregoing could have a material adverse effect on our business, financial condition, results of operations
and prospects.
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Developments in patent law could have a negative impact on our business.
From time to time, the Supreme Court, other federal courts, the United States Congress or the USPTO may change the standards
of patentability, and any such changes could have a negative impact on our business.
Three cases involving diagnostic method claims and “gene patents” have been decided by the Supreme Court in recent years. In
March 2012, the Supreme Court issued a decision in Mayo Collaborative v. Prometheus Laboratories, or Prometheus, a case
involving patent claims directed to optimizing the amount of drug administered to a specific patient, holding that the applicable
patents’ claims failed to incorporate sufficient inventive content above and beyond mere underlying natural correlations to allow the
claimed processes to qualify as patent-eligible processes that apply natural laws. In June 2013, the Supreme Court decided Association
for Molecular Pathology v. Myriad Genetics, or Myriad, a case challenging the validity of patent claims relating to the breast cancer
susceptibility genes BRCA1 and BRCA2, holding that isolated genomic DNA that exists in nature, such as the DNA constituting the
BRCA1 and BRCA2 genes, is not patentable subject matter, but that cDNA, which is an artificial construct created from ribonucleic
acid transcripts of genes, may be patent eligible. In June 2014, the Supreme Court decided Alice Corporation Pty. Ltd. v. CLS Bank
International, or Alice, which affirmed the Prometheus and Myriad decisions and provided additional interpretation.
If we make efforts to seek patent protection for our drug candidates, products, technologies, and tests, these efforts may be
negatively impacted by the Prometheus, Myriad and Alice decisions, rulings in other cases or guidance or procedures issued by the
USPTO. However, we cannot fully predict the impact of the Prometheus, Myriad and Alice decisions on the ability of genetic testing,
biopharmaceutical, or other companies to obtain or enforce patents relating to DNA, genes or genomic-related discoveries in the
future, as the contours of when claims reciting laws of nature, natural phenomena or abstract ideas may meet patent eligibility
requirements are not clear and may take years to develop via interpretation at the USPTO and in the courts. There are many previously
issued patents claiming nucleic acids and diagnostic methods based on natural correlations that issued before these recent Supreme
Court decisions and, although many of these patents may be invalid under the standards set forth in these decisions, they are presumed
valid and enforceable until they are successfully challenged and third parties holding these patents could allege that we infringe or
request that we obtain a license under such patents. Whether based on patents issued before or after these Supreme Court decisions,
we could be forced to defend against claims of patent infringement or obtain license rights, if available, under these patents. In
particular, although the Supreme Court has held in Myriad that isolated genomic DNA is not patent-eligible subject matter, third
parties could allege that our activities infringe other classes of gene-related patent claims. There are numerous risks associated with
any patent infringement claim that may be brought against us, as discussed above under “Litigation or other proceedings or third-party
claims of intellectual property infringement or misappropriation could require us to spend significant time and money and prevent us
from selling our tests or developing drug candidates.”
In addition, the Leahy-Smith America Invents Act, or America Invents Act, which was signed into law in 2011, includes a
number of significant changes to U.S. patent law. These changes include a transition from a “first-to-invent” system to a “first-to-file”
system, changes to the way issued patents are challenged, and changes to the way patent applications are disputed during the
examination process. These changes may favor larger and more established companies that have greater resources to devote to patent
application filing and prosecution. The USPTO has developed new regulations and procedures to govern the full implementation of
the America Invents Act, but the impact of the America Invents Act on the cost of prosecuting any patent applications we may file,
our ability to obtain patents based on our discoveries if we pursue them, and our ability to enforce or defend any patents that may issue
remains uncertain.
These and other substantive changes to U.S. patent law could affect our susceptibility to patent infringement claims and our
ability to obtain any patents we may pursue and, if obtained, to enforce or defend them, any of which could have a material adverse
effect on our business.
Obtaining and maintaining our patent protection depends on compliance with various procedural, document submission, fee
payment, and other requirements imposed by government patent agencies, and our patent protection could be reduced or
eliminated for non-compliance with these requirements.
Periodic maintenance fees, renewal fees, annuity fees, and various other government fees on patents and applications will be due
to be paid to the USPTO and various government patent agencies outside of the United States over the lifetime of its owned patents
and applications. The USPTO and various non-U.S. government agencies require compliance with several procedural, documentary,
fee payment, and other similar provisions during the patent application process. In some cases, an inadvertent lapse can be cured by
payment of a late fee or by other means in accordance with the applicable rules. There are situations, however, in which non-
compliance can result in abandonment or lapse of the patent or patent application, resulting in a partial or complete loss of patent
rights in the relevant jurisdiction. In such an event, potential competitors might be able to enter the market with similar or identical
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products or technology, which could have a material adverse effect on our business, financial condition, results of operations, and
prospects.
Worldwide, we own or exclusively in-license over 20 issued or allowed patents and over 10 active patent applications as of
December 31, 2024. This includes eight issued or allowed U.S. patents. Patents in these patent families are expected to expire by
2034, and patent applications in these patent families, if granted, are expected to expire as far out as 2044 subject to any patent term
disclaimers, adjustments, or extensions. Patents and/or patent applications in these families are active in multiple jurisdictions,
including the United States, Australia, Canada, China, European Patent Organization, German, New Zealand, Japan, and Switzerland.
In addition to these owned and exclusively licensed patents and active patent applications, we also license patents on a non-exclusive
and/or territory-restricted basis. Our intellectual property portfolio includes important patents and patent applications directed to our
technologies. This includes patent filings relating to our nano-drug delivery platform technology for delivery of water insoluble or
poorly soluble drugs for treatments of disease conditions, including cancer. In particular, as of December 31, 2024, we own or
exclusively in-license 18 issued patents and five patent applications relating to FID-007 and FID-022. Individual patent terms extend
for varying periods of time, depending upon the date of filing of the patent application, the date of patent issuance, and the legal term
of patents in the countries in which they are obtained.
In June 2017, Fulgent Pharma LLC entered into an exclusive license agreement with ANP, as amended December 28, 2017, and
May 1, 2024. Under the agreement, ANP granted Fulgent Pharma LLC an exclusive, worldwide, perpetual, irrevocable, and
sublicensable license to certain rights in patents and patent applications under which we may develop and commercialize FID-007 and
related formulations for human therapeutic, prophylactic, and diagnostic uses. As of December 31, 2024, this IP suite includes 28
patents and five patent applications that relate to FID-007 and FID-022. Patents and/or patent applications in these families are active
in multiple jurisdictions, including the United States, Australia, Canada, China, European Patent Organization, Germany, New
Zealand, Japan, and Switzerland. Patents in these patent families, if granted, are expected to expire in 2034 subject to any patent term
disclaimers, adjustments, or extensions.
Our future issued patents covering drug candidates we develop could be found invalid or unenforceable if challenged in court
or before administrative bodies in the United States or abroad.
In patent litigation in the United States, defendant counterclaims alleging invalidity or unenforceability are commonplace.
Grounds for a validity challenge could be an alleged failure to meet any of several statutory requirements, including lack of novelty,
obviousness, or non-enablement. Grounds for an unenforceability assertion could be an allegation that someone connected with
prosecution of the patent withheld relevant information from the USPTO, or made a misleading statement, during prosecution. Third
parties may raise claims challenging the validity or enforceability of our owned patents before administrative bodies in the United
States or abroad, even outside the context of litigation. Such mechanisms include re-examination, post-grant review, inter partes
review, interference proceedings, derivation proceedings, and equivalent proceedings in foreign jurisdictions (e.g., opposition
proceedings). Such proceedings could result in the revocation of, cancellation of, or amendment to our future patents in such a way
that they no longer cover its drug candidate or other technologies. The outcome following legal assertions of invalidity and
unenforceability is unpredictable. With respect to the validity question, for example, we cannot be certain that there is no invalidating
prior art, of which we and the patent examiner were unaware during prosecution. If a third-party were to prevail on a legal assertion of
invalidity or unenforceability, we would lose at least part, and perhaps all, of the patent protection on any drug candidates it develops
or other technologies. Such a loss of patent protection would have a material adverse impact on our business, financial condition,
results of operations, and prospects.
Patent terms may be inadequate to protect our competitive position on our products and services for an adequate amount of
time.
Patents have a limited lifespan. Patent terms may be shortened or lengthened by, for example, terminal disclaimers, patent term
adjustments, supplemental protection certificates, and patent term extensions. Although extensions may be available, the life of a
patent, and the protection it affords, is limited. Patent term extensions and supplemental protection certificates, and the like, may be
impacted by the regulatory process and may not significantly lengthen patent term. Non-payment or delay in payment of patent fees or
annuities, delay in patent filings or delay in extension filing, whether intentional or unintentional, may also result in the loss of patent
rights important to our business. In such an event, competitors might be able to enter the market earlier than would otherwise have
been the case. In addition, certain countries have compulsory licensing laws under which a patent owner may be compelled to grant
licenses to other parties. Furthermore, many countries limit the enforceability of patents against other parties, including government
agencies or government contractors. In these countries, the patent owner may have limited remedies, which could materially diminish
the value of any patents.
In the United States and abroad, if all maintenance fees/annuity fees are timely paid, the natural expiration of a patent is
generally 20 years from its earliest non-provisional filing date. The protection a patent affords is limited. Even if patents covering our
products or drug candidates are obtained, once the patent life has expired, we may be open to competition from competitive products.
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Given the amount of time required for the development, testing, and regulatory review of new products and drug candidates, patents
protecting such products or drug candidates might expire before or shortly after such products or drug candidates are commercialized.
As a result, our future owned and licensed patent portfolio may not provide us with sufficient rights to exclude others from
commercializing products or drug candidates similar or identical to ours.
If we do not obtain patent term extension and/or data exclusivity for any drug candidate that we may develop, our business
may be materially harmed.
Depending upon the timing, duration, and specifics of any FDA marketing approval of any drug candidate we may develop, one
or more of our future owned U.S. patents may be eligible for limited patent term extension under the Hatch-Waxman Act. The Hatch-
Waxman Act permits a patent term extension of up to five years as compensation for patent term lost during the FDA regulatory
review process. A patent term extension cannot extend the remaining term of a patent beyond a total of 14 years from the date of
product approval, only one patent may be extended, and only those claims covering the approved drug, a method for using it, or a
method for manufacturing it may be extended. Similar extensions as compensation for patent term lost during regulatory review
processes are also available in certain foreign countries and territories, such as in Europe under a Supplementary Patent Certificate.
However, we may not be granted an extension in the United States and/or foreign countries and territories because of, for example,
failing to exercise due diligence during the testing phase or regulatory review process, failing to apply within applicable deadlines,
failing to apply prior to expiration of relevant future patents, or otherwise failing to satisfy applicable requirements. Moreover, the
applicable time period or the scope of patent protection afforded could be less than we request. If we are unable to obtain patent term
extension, or the term of any such extension is shorter than what we request, our competitors may obtain approval of competing
products following our patent expiration, and our business, financial condition, results of operations, and prospects could be materially
harmed.
We may not be able to enforce our intellectual property rights outside the United States.
The laws of some foreign countries do not protect proprietary rights to the same extent as the laws of the United States, and
many companies have encountered significant challenges in establishing and enforcing their proprietary rights outside the United
States. These challenges can be caused by the absence of rules and methods for the establishment and enforcement of intellectual
property rights in certain jurisdictions. In addition, the legal systems of some countries, particularly developing countries, do not favor
the enforcement of certain intellectual property protection, especially relating to healthcare. These aspects of many foreign legal
systems could make it difficult for us to prevent or stop the misappropriation of our intellectual property rights in these jurisdictions.
Moreover, changes in the law and legal decisions by courts in foreign countries could affect our ability to obtain adequate protection
for our technologies and enforce our intellectual property rights. Many countries have compulsory licensing laws under which a patent
owner may be compelled to grant licenses to third parties. In addition, many countries limit the enforceability of patents against
government agencies or government contractors. In these countries, the patent owner may have limited remedies, which could
materially diminish the value of such patent. If we or any of our licensors is forced to grant a license to third parties with respect to
any patents relevant to our business, our competitive position may be impaired, and our business, financial condition, results of
operations, and prospects may be adversely affected. As a result, our efforts to protect and enforce our intellectual property rights
outside the United States may prove inadequate, in which case our ability to remain competitive and grow our business and revenue
could be materially harmed.
We do not have intellectual property rights in every country throughout the world. Filing, prosecuting, and defending patents on
drug candidates in all countries throughout the world would be prohibitively expensive, and our intellectual property rights in some
countries outside the United States and Europe can be less extensive than those in the United States. In addition, the laws of foreign
countries do not protect intellectual property rights to the same extent as federal and state laws of the United States. Consequently, we
may not be able to prevent third parties from practicing our inventions in all countries outside the United States, or from selling or
importing products made using our inventions in and into the United States or other jurisdictions. Competitors may use our
technologies in jurisdictions where we have not obtained patent protection to develop their own products and, further, may export
otherwise infringing products to territories where we have patent protection but where enforcement is not as strong as that in the
United States. These products may compete with our drug candidates, and our patents or other intellectual property rights may not be
effective or sufficient to prevent them from competing.
Third parties may assert that our employees or consultants have wrongfully used or disclosed confidential information or
misappropriated trade secrets.
We employ individuals who were previously employed at universities and biometric solution, genetic testing, diagnostic, or
other healthcare companies, including our competitors or potential competitors. Further, we may become subject to ownership
disputes in the future arising from, for example, conflicting obligations of consultants or others who are involved in developing our
and other parties’ technologies and intellectual property rights. Although we try to ensure that our employees and consultants do not
use the proprietary information or know-how of others in their work for us, we may be subject to claims that we or our employees or
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consultants have inadvertently or otherwise used or disclosed intellectual property rights, including trade secrets or other proprietary
information, of a former employer or other third-party. Litigation may be necessary to defend against these claims, should they arise.
If we fail in defending against any such claims, we could be subject to monetary damages and the loss of valuable intellectual property
rights or personnel. Even if we are successful in defending against any such claims, litigation could result in substantial costs, distract
management and other employees, and damage our reputation.
If we fail to comply with our obligations under license or technology agreements with third parties, we could lose license rights
that are important to our business. If our third-party licensors fail to comply with the terms of our license arrangements, we
may be forced to engage in litigation to protect our rights, which may not be successful.
We license certain intellectual property, including technologies and patents, from third parties, that is important to our research
and development efforts; and in the future we may enter into additional agreements that provide us with licenses to valuable
intellectual property or technology. For example, our business is substantially dependent upon certain intellectual property rights that
we license from ANP under the ANP License Agreement. Under the ANP License Agreement, ANP granted Fulgent Pharma LLC an
exclusive, worldwide, perpetual, irrevocable, and sublicensable license to certain rights in patents and patent applications under which
we may develop and commercialize FID-007 and FID-022 and related formulations for human therapeutic, prophylactic, and
diagnostic uses. Therefore, our commercial success will depend to a large extent on our ability to maintain and comply with our
obligations under the ANP License Agreement. The ANP License Agreement provides ANP the right to terminate for an uncured
breach by us, or if we are insolvent, the subject of a bankruptcy proceeding, or potentially other reasons. If ANP were to terminate the
ANP License Agreement, the development and commercialization of FID-007 and FID-022 would be adversely affected, our potential
for generating revenue from this program would be adversely affected and attracting new partners would be made more difficult. As a
result, we would likely be subject to increased competition within our market.
We expect that other technology in-licenses that we may enter into in the future will contain similar provisions and impose
similar obligations on us. If we fail to comply with any of the obligations under our license agreements, we may be required to pay
damages and the licensor may have the right to terminate the license. Termination by the licensor could cause us to lose valuable
rights, prevent us from continuing related research and development activities, or otherwise materially and negatively impact our
business. If our licensors fail to abide by the terms of a license agreement, if they fail to enforce licensed intellectual property against
infringing third parties, if the licensed intellectual property is found to be invalid or unenforceable, or if we are unable to enter into
necessary license agreements on acceptable terms or at all, we may be forced to engage in litigation to enforce our rights. This
litigation may not be successful and may consume substantial amounts of time and resources. These circumstances could have a
material adverse effect on our business, development efforts, financial condition, or results of operations.
Common Stock Risks
An active, liquid trading market for our common stock may not be sustained, which could make it difficult for stockholders to
sell their shares of our common stock.
An active trading market for our common stock may not be sustained. Further, Mr. Hsieh, our founder, Chief Executive Officer
and Chairman of our board of directors, beneficially owns approximately 28.3% of our outstanding voting equity as of December 31,
2024. As a result, fewer shares are actively traded in the public market, which reduces the liquidity of our common stock. The lack of
an active trading market could impair our stockholders’ ability to sell their shares at the desired time or at a price considered
reasonable. Further, an inactive trading market may impair our ability to raise capital by selling shares of our common stock in the
future, and may impair our ability to enter into strategic relationships or acquire companies or technologies using shares of our
common stock as consideration.
Our common stock is listed on the Nasdaq Global Market, or Nasdaq, under the symbol “FLGT.” If we fail to satisfy the
continued listing standards of Nasdaq, however, we could be de-listed, which would negatively impact the price and liquidity of our
common stock.
The price of our common stock may be volatile, and you could lose all or part of your investment.
The trading price of our common stock has experienced, and may continue to experience, wide fluctuations and significant
volatility. This volatility may be exacerbated by the relatively small and illiquid market for our common stock. Other factors that may
contribute to this volatility include, among others:
•
actual or anticipated fluctuations in our operating results;
•
competition from existing tests or new tests that may emerge, particularly if competitive factors in our industry, including
prices for testing and testing services, become more acute or the introduction of new products by our competitors;
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•
failures to meet or exceed financial estimates and projections of the investment community or guidance we have provided
to the public;
•
issuance of new or updated research or reports by securities analysts or changed recommendations for our common stock;
•
announcements by us or our competitors of significant acquisitions, investments, strategic relationships, joint ventures,
collaborations or capital commitments;
•
the timing and amount of our investments in our business and the market’s perception of these investments and their
impact on our prospects;
•
actual or anticipated changes in laws or regulations applicable to our business or our tests;
•
whether and when we are able to obtain marketing approval to market any of our drug candidates and the outcome of
meetings with applicable regulatory agencies, including the FDA;
•
the outcome, success, costs and timing of preclinical studies and clinical trials for our current or future drug candidates;
•
failure of any our drug candidates, if approved, to achieve commercial success;
•
additions or departures of key management or other personnel;
•
changes in coverage and reimbursement by current or potential payors;
•
inability to obtain additional funding as and when needed on reasonable terms;
•
disputes or other developments with respect to our or others’ intellectual property rights;
•
product liability claims or other litigation;
•
sales of our common stock by us or our stockholders;
•
general economic, political, industry and market conditions, including factors not directly related to our operating
performance or the operating performance of our competitors, such as increased uncertainty in the U.S. regulatory
environment for healthcare, trade and tax-related matters;
•
events that affect, or have the potential to affect, general economic conditions, including but not limited to political unrest,
global trade wars, natural disasters, act of war, terrorism, or disease outbreaks; and
•
the other risk factors discussed in this report.
In addition, the stock market in general, and the market for the stock of companies in the life sciences and technology industries
in particular, has experienced extreme price and volume fluctuations in recent years that have, at times, been unrelated or
disproportionate to the operating performance of specific companies. These broad market and industry factors may negatively affect
the market price of our common stock, regardless of our actual operating performance. In addition, in the past, following periods of
volatility in the overall market and the market price of a particular company’s securities, securities class action litigation has often
been instituted against such company. This type of litigation, if instituted against us, could result in substantial costs, a diversion of
our management’s attention and resources and could damage our reputation.
Our principal stockholders and management own a significant percentage of our capital stock and are able to exert significant
control over matters subject to stockholder approval.
Our executive officers, directors, beneficial owners of 5% or more of our outstanding voting equity and their respective
affiliates collectively beneficially own approximately 49.8% of our outstanding voting equity as of December 31, 2024, and of this,
Mr. Hsieh, our founder, Chief Executive Officer and Chairman of our board of directors, by himself beneficially owns approximately
28.3% of our outstanding voting equity as of December 31, 2024. As a result, these stockholders have the ability to control matters
submitted to our stockholders for approval, including elections of directors, amendments to our organizational documents or approval
of any merger, sale of assets or other major corporate transaction. This concentration of ownership may prevent or discourage
unsolicited acquisition proposals or offers to acquire our common stock that some of our stockholders feel are in their best interests, as
the interests of these stockholders may not coincide with the interests of our other stockholders and they may act in a manner that
advances their best interests and not necessarily those of all of our stockholders. Further, this concentration of ownership could
adversely affect the prevailing market price for our common stock.
67
Sales of a substantial number of shares of our common stock in the public market, or the perception that such sales could
occur, could cause the price of our common stock to fall.
Sales of a substantial number of shares of our common stock in the public market could occur at any time. Any such sales, or
the perception in the market that sales are pending or could occur, could reduce the market price of our common stock. The vast
majority of the outstanding shares of our common stock are freely tradable without restriction in the public market, subject to certain
volume and manner of sale limitations applicable to shares held by our affiliates, as that term is defined in the Securities Act. In
addition, subject to similar limitations and any other applicable legal and contractual limitations, all of the shares of our common stock
subject to outstanding equity-based awards or reserved for issuance pursuant to such awards we may grant in the future are registered
under the Securities Act or are otherwise eligible under applicable securities laws for free trading in the public market upon their
issuance.
Future issuances of our common stock or rights to purchase our common stock, including pursuant to our equity incentive
plan, could result in additional dilution to the percentage ownership of our stockholders and could cause the price of our
common stock to fall.
To raise capital or for other strategic purposes, we may sell common stock, convertible securities or other equity securities in
one or more transactions at prices and in a manner we determine from time to time. We also may issue common stock or grant other
equity awards for compensatory purposes under our equity incentive plan. If we issue common stock, convertible securities or other
equity securities, including equity awards under our equity incentive plan, our then-existing stockholders could be materially diluted
by such issuances and, if we otherwise issue preferred stock, new investors could gain rights, preferences and privileges senior to the
holders of our common stock, any of which could cause the price of our common stock to decline.
We do not intend to pay dividends on our common stock, so any returns will be limited to the value of our common stock.
We currently anticipate that we will retain any future earnings to finance the continued development, operation and expansion of
our business. As a result, we do not anticipate declaring or paying any cash dividends or other distributions in the foreseeable future.
Further, if we were to enter into a credit facility or issue debt securities or preferred stock in the future, we may become contractually
restricted from paying dividends. If we do not pay dividends, our common stock may be less valuable because stockholders must rely
on sales of their common stock after price appreciation, which may never occur, to realize any gains on their investment.
If securities or industry analysts do not publish research or reports about our business or if they issue an adverse or
misleading opinion regarding our common stock, our stock price and trading volume could decline.
The trading market for our common stock is influenced by the research and reports that industry or securities analysts publish
about us or our business. If one or more of these analysts ceases coverage of us or fails to publish reports on us regularly, we could
lose visibility in the financial markets, which could cause the price and trading volume of our common stock to decline. Further, if any
of these analysts issues an adverse or misleading opinion regarding us, our business model, our industry or our stock performance or if
our operating results fail to meet analyst expectations, the price of our common stock could also decline.
Provisions in our charter documents and Delaware law could discourage, delay or prevent a change in control of our company
or changes in our management and depress the market price of our common stock.
Our certificate of incorporation and bylaws contain provisions that could depress the market price of our common stock by
acting to discourage, delay or prevent a change in control of our company or changes in our management that our stockholders may
deem advantageous. These provisions, among other things:
•
authorize our board of directors to issue, without further action by our stockholders, up to 1.0 million shares of
undesignated or “blank check” preferred stock;
•
prohibit stockholder action by written consent, thus requiring all stockholder actions to be taken at a duly noticed and held
meeting of our stockholders;
•
specify that special meetings of our stockholders can be called only by our board of directors, the Chairman of our board
of directors or our President, thereby eliminating the ability of our stockholders to call special meetings;
•
permit only our board of directors to establish the number of directors and fill vacancies on the board of directors, except
as may be required by law;
•
permit our board of directors to amend our bylaws, subject to the power of our stockholders to repeal any such
amendment;
•
do not permit cumulative voting by our stockholders on the election of directors; and
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•
establish advance notice requirements for stockholders to propose nominees for election as directors or matters to be acted
upon at annual meetings of stockholders.
In addition, we are subject to Section 203 of the Delaware General Corporation Law, or DGCL, which imposes certain
restrictions on mergers, business combinations and other transactions between us and holders of 15% or more of our common stock.
Section 203 may have the effect of discouraging, delaying or preventing a change in control of our company.
Holders of our common stock could be adversely affected if we issue preferred stock.
Pursuant to our certificate of incorporation, our board of directors is authorized to issue up to 1.0 million shares of preferred
stock without any action by our stockholders. Our board of directors also has the power, without stockholder approval, to set the terms
of any series of preferred stock that may be issued, among others, including voting rights, dividend rights and preferences over our
common stock with respect to dividends or in the event of a dissolution, liquidation or winding up. If we issue preferred stock in the
future that has preferences over our common stock with respect to payment of dividends or upon a liquidation, dissolution or winding
up, or if we issue preferred stock that is convertible into our common stock at greater than a one-to-one ratio, the voting and other
rights of the holders of our common stock and the market price of our common stock could be adversely affected.
Our certificate of incorporation designates the Court of Chancery of the State of Delaware as the sole and exclusive forum for
certain types of actions and proceedings that may be initiated by our stockholders, which could limit our stockholders’ ability
to obtain a judicial forum they consider favorable for disputes with us or our directors, officers or other employees.
Our certificate of incorporation and bylaws provide that, unless we consent in writing to the selection of an alternative forum,
the Court of Chancery of the State of Delaware shall be the sole and exclusive forum for:
•
any derivative action brought on our behalf;
•
any direct action brought by a stockholder against us or any of our directors, officers or other employees, alleging a breach
of a fiduciary duty;
•
any action brought by a stockholder against us or any of our directors, officers or other employees, alleging a violation of
the DGCL, our certificate of incorporation or our bylaws; and
•
any action brought by a stockholder against us or any of our directors, officers or other employees, asserting a claim
against us governed by the internal affairs doctrine.
We refer to the forgoing limitations as the Exclusive Forum Provisions. The Exclusive Forum Provisions do not apply to (i)
actions in which the Court of Chancery in the State of Delaware concludes that an indispensable party is not subject to the jurisdiction
of the Delaware courts, and (ii) actions in which a federal court has assumed exclusive jurisdiction of a proceeding.
Accordingly, the Exclusive Forum Provisions do not apply to actions brought to enforce a duty or liability created by the
Exchange Act or the rules and regulations thereunder, or Exchange Act Claims. Further, the clause in our certificate of incorporation
excepting “actions in which a federal court has assumed exclusive jurisdiction of a proceeding” from the Exclusive Forum Provisions
is not intended to mean that a federal court must take any actual or affirmative action to assume jurisdiction over an Exchange Act
Claim, as Section 27 of the Exchange Act creates exclusive federal jurisdiction over all Exchange Act Claims, regardless of whether a
federal court takes any action. The Exclusive Forum Provisions also do not apply to federal and state suits brought to enforce any duty
or liability created by the Securities Act or the rules and regulations thereunder, or Securities Act Claims. To the extent applicable or
enforceable, the Exclusive Forum Provisions may limit a stockholder’s ability to bring a claim in a judicial forum it finds favorable for
disputes with us or our directors, officers or other employees, which may discourage these lawsuits. Alternatively, for Securities Act
Claims, Exchange Act Claims or claims for which a court were to find these Exclusive Forum Provisions inapplicable or
unenforceable for one or more of the specified types of actions or proceedings, we may incur additional costs associated with
resolving these matters in other jurisdictions, which could adversely affect our business, financial condition or results of operations.
Item 1B. Unresolved Staff Comments.
Not applicable.
Item 1C. Cybersecurity.
We recognize the critical importance of maintaining the trust and confidence of customers, clients, patients, business partners,
and employees toward our business and are committed to protecting the confidentiality, integrity, and availability of our business
operations and systems. Our board of directors is actively involved in oversight of our risk management activities, and cybersecurity
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represents an important element of our overall approach to risk management. Our cybersecurity policies, standards, processes,
procedures, and practices are based on recognized frameworks established by the National Institute of Standards and Technology, or
NIST and other applicable industry standards. In general, we seek to address cybersecurity risks through a comprehensive, cross-
functional approach that is focused on preserving the confidentiality, security, integrity, and availability of the information that we
collect and store by identifying, preventing, and mitigating cybersecurity threats and effectively responding to cybersecurity incidents
when they occur.
Risk Management and Strategy; Effect of Risk
We face risks related to cybersecurity such as unauthorized access, cybersecurity attacks, and other security incidents, including
as perpetrated by hackers and unintentional damage or disruption to hardware and software systems, loss of data, and misappropriation
of confidential information. To identify and assess material risks from cybersecurity threats, we maintain a comprehensive
cybersecurity program and regular oversight of our programs for security monitoring for internal and external threats to ensure the
confidentiality and integrity of our information assets. We consider risks from cybersecurity threats alongside other company risks as
part of our overall risk assessment process. We employ a range of tools and services, including regular network and endpoint
monitoring, vulnerability assessments, penetration testing, threat monitoring and tabletop exercises to inform our risk identification
and assessment.
We also identify our cybersecurity threat risks by comparing our processes to standards set by NIST and Center for Internet
Security, as well as by engaging experts to attempt to infiltrate our information systems. To provide for the availability of critical data
and systems, maintain regulatory compliance, manage our material risks from cybersecurity threats, and protect against and respond to
cybersecurity incidents, we also perform periodic risk assessments, which includes cybersecurity risks, monitor emerging data
protection laws and implement changes to our processes that are designed to comply with such laws; through our policies, practices,
and/or contracts (as applicable), require employees and certain third parties to treat confidential information and data with care;
periodically update our relevant policies and procedures; employ technical safeguards that are designed to protect our information
systems from cybersecurity threats, including firewalls, intrusion prevention and detection systems, anti-malware functionality, and
access controls, which are evaluated and improved through vulnerability assessments and cybersecurity threat intelligence; provide
regular, mandatory training for our employees regarding cybersecurity threats as a means to equip them with effective tools and
knowledge necessary to identify or address cybersecurity threats and to communicate our evolving information security policies,
standards, processes and practices; conduct regular phishing email simulations to enhance awareness and responsiveness to possible
threats; conduct annual cybersecurity training for our board of directors and senior management; run tabletop exercises to simulate a
response to a cybersecurity incident and use the findings to improve our processes and technologies; leverage the NIST incident
handling framework to help us identify, protect, detect, respond, and recover when there is an actual or potential cybersecurity
incident; engage consultants to help us oversee and manage cybersecurity risks, processes, and incident response measures; and carry
information security risk insurance that provides protection against the potential losses arising from a cybersecurity incident.
Our incident response plan outlines and coordinates the activities we take to prepare for, detect, respond to, and recover from
cybersecurity incidents, which include processes to triage, assess severity for, escalate, contain, investigate, and remediate the
incident, as well as to comply with potentially applicable legal obligations and mitigate damage to our business and reputation. Our
incident response plan further outlines the roles and responsibilities of various employees, managers, and senior leadership with
respect to performing a materiality assessment and responding to cybersecurity events that are deemed material, as well as provides
rapid escalation procedures after a cybersecurity incident. In the event of an incident, we intend to follow our incident response plan,
which outlines the steps to be followed from incident detection to mitigation, recovery, and notification, including notifying functional
areas (e.g. legal), as well as senior leadership and our board of directors, as appropriate.
Our cyber risk management program is integrated within the Company’s enterprise risk management system and addresses both
the corporate information technology environment and customer-facing products and services. The risk management program is
focused on safeguarding the organization’s digital assets, ensuring continuous business operations, and minimizing the potential
impact of cyber threats. Regular assessments, including penetration tests, are performed. These inputs form the basis of a risk register
that is integrated into the overall enterprise risk management program to further inform the Company’s strategy assessing the
likelihood, impact, and velocity of these risks on a forward-looking basis.
As part of the above processes, we regularly engage with consultants, and other third parties, review our cybersecurity program
to help identify areas for continued focus, improvement, and compliance. We engage them, specifically, to assist us with cybersecurity
risk assessments, external threat environment reviews, internal cybersecurity policy compliance and near-term incident response. Our
processes also address cybersecurity threat risks associated with our use of third-party service providers, including our key suppliers,
which have access to consumer, patient, and employee data or our systems. In addition, cybersecurity considerations affect the
selection and oversight of our third-party service providers. We periodically perform diligence on certain third parties that have access
70
to our systems, data, or facilities that house such systems or data; and we monitor cybersecurity threat risks identified through such
diligence.
We describe whether and how risks from identified cybersecurity threats, including as a result of any previous cybersecurity
incidents, have materially affected or are reasonably likely to materially affect us, including our business strategy, results of
operations, or financial condition under the heading “Actual or attempted security incidents or breaches, loss of data, or other
disruptions could expose us to material liability and materially and adversely affect our business, financial condition, and our
reputation,” which disclosures are incorporated by reference herein.
We have not experienced any material cybersecurity incidents. As of the date of this report, we do not believe that risks from
any cybersecurity threats, including as a result of any previous cybersecurity incidents, have materially affected or are reasonably
likely to affect us, including our business strategy, results of operations or financial condition. However, we are aware that changes in
our IT systems, including those provided by third parties, could expose us to risk in the future. These threats pose a risk to the security
of our systems and networks and the confidentiality, availability, and integrity of our data. Cybersecurity attacks could also include
attacks targeting patient, employee, or customer data or the security, integrity, and/or reliability of the hardware and software we
utilize in our business operations. It is possible that our information technology systems and networks, or those managed or provided
by third parties, could have vulnerabilities, which could go unnoticed for a period of time. While various procedures and controls have
been and are being utilized to mitigate such risks, there can be no guarantee that the actions and controls we have implemented and are
implementing will be sufficient to protect and mitigate associated risks to our systems, information, or other property. For more
information, see the risk factors included in Item 1A of this Annual Report.
Cybersecurity Governance; Management
Cybersecurity is an important part of our risk management processes and an area of focus for our board of directors and
management. In general, our board of directors oversees risk management activities designed and implemented by our management
and considers specific risks, including, for example, risks associated with our strategic plan, business operations, and capital structure.
Our board of directors executes its oversight responsibility for risk management both directly and through delegating oversight of
certain of these risks to its committees, and our board of directors has authorized our audit committee to oversee risks from
cybersecurity threats.
At least quarterly, our board of directors receives an update from management of our cybersecurity threat risk management and
strategy processes, covering topics such as data security posture, any results from third-party assessments, progress towards pre-
determined risk-mitigation-related goals, our incident response plan, material cybersecurity threat risks or incidents and developments,
as well as the steps management has taken to respond to such risks. In such sessions, our board of directors generally receives
materials that include a cybersecurity dashboard and/or other materials discussing current and emerging material cybersecurity threat
risks and describing our ability to mitigate those risks, as well as recent developments, evolving standards, technological
developments, and information security considerations arising with respect to our peers and third parties, and discusses such matters
with our Chief Information Security Officer and/or General Counsel and Chief Privacy Officer. Our board of directors also receive
prompt and timely information regarding any cybersecurity incident that meets established reporting thresholds, as well as ongoing
updates regarding any such incident until it has been addressed.
Members of board of directors are also encouraged to regularly engage in conversations with management on cybersecurity-
related news and events and discuss any updates to our cybersecurity risk management and strategy programs. Material cybersecurity
threat risks are also considered during separate board meeting discussions of important matters like enterprise risk management,
operational budgeting, business continuity planning, mergers and acquisitions, brand management, and other relevant matters. Our
Chief Information Security Officer advises our Board on the specific vulnerabilities we identified and the controls we put in place to
mitigate our risk.
Our cybersecurity program is managed by a dedicated team, which is led by our Chief Information Security Officer, (CISO who
reports to the Chief Operating Officer and has to the ability to communicate directly to our CEO if necessary). Our CISO has over 20
years of IT experience, including over 18 years of cybersecurity experience, holds an M.S. degree in Information Security, and is a
Certified Information Systems Security Professional (CISSP). Our General Counsel and Chief Privacy Officer is an attorney with 18
years of experience, including experience in privacy matters. They are also a Certified Information Privacy Professional (CIPP/US/E),
a Certified Privacy Manager (CIPM), and a Privacy Law Specialist (PLS) with the International Association of Privacy Professionals
(IAPP). As discussed above, our CISO and/or General Counsel and Chief Privacy Officer report to our board of directors about
cybersecurity threat risks, among other cybersecurity related matters, on a quarterly basis.
In addition, our cybersecurity risk management and data strategy processes are further overseen by certain management team
members. Together with CISO and our General Counsel and Chief Privacy Officer, these management team members are regularly
informed about and routinely monitor the prevention, mitigation, detection, and remediation of cybersecurity incidents through their
71
ongoing management of, and participation in, the cybersecurity risk management and strategy processes described above, including
the operation of our incident response plan. Such individuals have extensive prior work experience in various roles involving
managing information security, developing cybersecurity strategy, implementing effective information and cybersecurity programs, as
well as several relevant degrees and certifications.
Item 2. Properties.
Our corporate headquarters and laboratory operations are located in El Monte, California, where we own and occupy 61,612
square feet of building space situated on 2.6 acres of land. We have built a CLIA-certified laboratory at this location. We use these
facilities for laboratory testing and management activities and certain research and development, administrative and other functions.
We have CLIA-certified laboratories located in Coppell, Texas; Alpharetta, Georgia; Phoenix, Arizona; and Needham,
Massachusetts. In Coppell, Texas, we own and occupy approximately 96,500 square feet of building and space situated on 6.8 acres of
land. In Alpharetta, Georgia, we own and occupy approximately 65,000 square feet of building and space situated on 8.5 acres of land.
In Phoenix, Arizona, we lease and occupy approximately 25,000 square feet under a lease that will expire in November 2025. In
Needham, Massachusetts, we lease and occupy approximately 21,000 square feet under a lease that will expire in September 2027. We
use these facilities for laboratory testing and certain administrative and other functions.
We believe our existing facilities are adequate for our current and expected near-term needs and additional space would be
available on commercially reasonable terms if required.
Item 3. Legal Proceedings.
From time to time, we may be involved in legal proceedings arising in the ordinary course of our business. As disclosed in Note
8, Debt, Commitments and Contingencies to the Consolidated Financial Statements, we are engaged in certain legal investigations,
audits and voluntary disclosure processes, and the disclosure set forth in Note 8 relating to these certain legal matters is incorporated
herein by reference.
The outcome of these matters are inherently uncertain, and there can be no assurances that a favorable outcome will be obtained.
Regardless of outcome, litigation can have an adverse impact on us due to defense and settlement costs, diversion of
management resources, negative publicity and reputational harm, among other factors.
Item 4. Mine Safety Disclosures.
Not applicable.
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PART II
Item 5. Market for Registrant’s Common Equity, Related Stockholder Matters and Issuer Purchases of Equity Securities.
Market Information
On September 29, 2016, our common stock was listed for trading on Nasdaq under the symbol “FLGT.” There was no public
market for our common stock prior to September 29, 2016.
Holders of Common Stock
As of February 1, 2025, there were 11 holders of record of our common stock, plus an indeterminate number of additional
stockholders whose shares of our common stock are held on their behalf by brokerage firms or other agents.
Dividend Policy
We currently anticipate that we will retain any future earnings to finance the continued development, operation and expansion of
our business. As a result, we do not anticipate declaring or paying any cash dividends or other distributions in the foreseeable future.
Any determination to pay dividends would be at the discretion of our board of directors and would depend on our results of operation,
financial condition and other factors that our board of directors, in its discretion, considers relevant.
Use of Proceeds from Registered Securities
To date, we have used $190.8 million of the net proceeds from sales of our common stock, of which, $4.5 million was used for
contributions to FF Gene Biotech prior to the FF Gene Biotech Acquisition, $170.5 million was used to fund the Company’s operation
and a business combination, and $15.8 million was used to pay off the investment margin loan. All other net proceeds from sales of
our common stock are invested in investment-grade and interest-bearing securities, such as corporate bonds, municipal bonds, and
U.S. government and U.S. agency debt securities. There has been no material change in the planned use of proceeds from the sales of
our common stock from that described in the Prospectus.
Common Stock Performance Graph
The following graph compares the cumulative total stockholder return, calculated on a dividend-reinvested basis, in Fulgent's
Common Stock, the Nasdaq Composite Index, and the Nasdaq Biotechnology Index for the five years ended December 31, 2024. The
comparison assumes that $100 was invested in the Company’s common stock, the NASDAQ Composite Index, and the Nasdaq
Biotechnology Index as of the market close on December 31, 2019. Note that historic stock price performance is not necessarily
indicative of future stock price performance.
73
Information on Share Repurchases
The number of shares of common stock repurchased by the Company during the year ended December 31, 2024 and the average
price paid per share are as follows:
Period
(a) Total Number
of Shares
Purchased
(b) Average Price
Paid Per Share (1)
(c) Total Number
of Shares
Purchased as Part
of Publicly
Announced Plans
or Programs
(d) Maximum
Dollar Value of
Shares that May
Yet Be Purchased
Under the Plans or
Programs
March 2024 (3/1/2024-3/31/2024)
10,000
$
22.02
10,000
$
150,461,000
Total
10,000
10,000
(1) Includes commissions for the shares repurchased under the stock repurchase program.
Item 6. [Reserved]
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Item 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations.
Forward-Looking Statements
The following discussion and analysis of our financial condition and results of operations should be read together with our
consolidated financial statements and related notes included in this report and contains forward-looking statements within the
meaning of Section 27A of the Securities Act and Section 21E of the Exchange Act. We have omitted discussion of 2022 results where
it would be redundant to the discussion previously included in Item 7 of our 2023 Annual Report on Form 10-K. Forward-looking
statements are statements other than historical facts and relate to future events or circumstances or our future performance, and they
are based on our current assumptions, expectations and beliefs concerning future developments and their potential effect on our
business. The forward-looking statements in this discussion and analysis include statements about, among other things, our future
financial and operating performance, our future cash flows and liquidity and our growth strategies, as well as anticipated trends in
our business and industry. These forward-looking statements are subject to a number of risks and uncertainties, including, among
others, those described under “Item 1A. Risk Factors” in Part I of this report. Moreover, we operate in a competitive and rapidly
evolving industry and new risks emerge from time to time. It is not possible for us to predict all of the risks we may face, nor can we
assess the impact of all factors on our business or the extent to which any factor or combination of factors could cause actual results
to differ from our expectations. In light of these risks and uncertainties, the forward-looking events and circumstances described in
this discussion and analysis may not occur, and actual results could differ materially and adversely from those described in or implied
by any forward-looking statements we make. Although we have based our forward-looking statements on assumptions and
expectations we believe are reasonable, we cannot guarantee future results, levels of activity, performance or achievements or other
future events. As a result, forward-looking statements should not be relied on or viewed as predictions of future events, and this
discussion and analysis should be read with the understanding that actual future results, levels of activity, performance and
achievements may be materially different than our current expectations. The forward-looking statements in this discussion and
analysis speak only as of the date of this report, and except as required by law, we undertake no obligation to update publicly any
forward-looking statements for any reason after the date of this report to conform these statements to actual results or to changes in
our expectations.
Overview
We are a technology-based company with a well-established laboratory services business and a therapeutic development
business. Our laboratory services business includes technical laboratory and testing services and professional interpretation of
laboratory results by licensed physicians. Our therapeutic development business is focused on developing drug candidates for treating
a broad range of cancers using a novel nanoencapsulation and targeted therapy platform designed to improve the therapeutic window
and PK profile of new and existing cancer drugs.
We recorded revenue and net (loss) from operations of $283.5 million and ($42.7) million, respectively, in 2024, compared to
revenue and net (loss) from operations of $289.2 million and ($167.8) million, respectively, in 2023.
2024 Developments
In 2024, we began enrollment of a Phase 2, randomized, multi-center, open-label trial of FID-007 in patients with recurrent or
metastatic H&N squamous cell carcinoma, established seven testing sites, and as of December 31, 2024, we had enrolled 17 patients.
In December 2024, we filed an IND for the investigation of FID-022 in a Phase 1/1b clinical trial, and in January 2025, the IND for
this trial was cleared by the FDA.
Factors Affecting Our Performance
Mix of Tests Delivered
We offer our tests and testing services at different price points, and we incur different amounts and types of costs, depending on
the nature and level of complexity and customization of the test and the specific terms we have negotiated for the tests and testing
services, which can vary from customer to customer. As a result, the mix of tests delivered in any period, and the customers that order
these tests, impacts our financial results for the period.
Mix of Customers and Purchasing Terms
We consider each single billing and paying unit to be an individual customer, even though a unit may represent multiple
physicians and healthcare providers ordering tests. The composition and concentration of our customer base can fluctuate from period
to period, and in certain prior periods, a small number of customers have accounted for a significant portion of our revenue. Generally,
we do not have long-term purchase agreements with any of our customers, including these key customers, and, as result, any or all of
75
them could decide at any time to increase, accelerate, decrease, delay or discontinue their orders from us. Although we believe some
of these fluctuations in customer demand may be attributable in part to the nature of our business, in which our customers can
experience significant volatility in their testing demand from period to period in the ordinary course of their operations, these demand
fluctuations, particularly for our key customers, can have a significant impact on our period-to-period performance regardless of their
cause.
We currently classify our customers into three payor types: (i) Insurance, (ii) Institutional, including hospitals, medical
institutions, other laboratories, governmental bodies, municipalities, and large corporations or (iii) Patients who pay directly.
Typically, we bill our Institutional customers for our tests, and they are responsible for paying us directly and billing their patients
separately or obtaining reimbursement from insurance payors in connection with a patient’s diagnosis related group. A small
percentage of our customers are patients, who elect to pay for tests themselves with out-of-pocket payments after their physicians have
ordered our tests.
We continue to make efforts to diversify our customer market, including building relationships with hospitals and affiliated
specialties related to our service offerings. We are also pursuing relationships with payors, including Medicare, some state Medicaid
programs, and commercial payors, in an effort to obtain coverage and reimbursement for our tests to make them accessible to more
individual physicians. Generally, when we establish these new customer relationships, we agree with the applicable payor, laboratory,
or other customer to provide certain of our tests at negotiated rates, but, subject to limited exceptions, most of these relationships do
not obligate any party to order our tests at any agreed volume or frequency or at all. Further, any relationships we may or have
developed with any government agencies are subject to unique risks associated with government contracts, including cancellation if
adequate appropriations for subsequent performance periods are not made and modification or termination at the government’s
convenience without prior notice. These efforts may not lead to meaningful or any increases in our customer base and may not
improve our ability to achieve or sustain profitability.
Ability to Maintain Our Broad and Flexible Test Menu
We believe the large number of genes we incorporate into our test menu provides a meaningful competitive advantage. We
believe the breadth of genes in our portfolio allows us to provide more comprehensive genetic information and improves our variant
detection rate, which can increase the clinical actionability of the data we produce. The breadth of genes in our portfolio also allows us
to offer hundreds of pre-established, multi-gene panels that focus on specified genetic conditions, including our Focus and
Comprehensive oncology panels and Beacon carrier screening panels and somatic cancer panels. In addition, all of our genetic panel
tests can be adjusted up or down to include more or fewer genes, or customers can design their own panels to their exact
specifications, resulting in a flexible and customizable test menu. We believe our ability to continue to offer more genes and more
ordering flexibility than our competitors could be a key contributor to the long-term growth of our business.
Ability to Maintain Low Internal Costs and Inflation
We have developed various proprietary technologies that improve our laboratory efficiency and reduce the costs we incur to
perform our tests, including our proprietary gene probes, data algorithms, adaptive learning software and genetic reference library.
This technology platform enables us to perform each test and deliver its results at a lower cost to us than many of our competitors, and
this low cost allows us to maintain affordable and competitive pricing for our customers, which we believe encourages repeat ordering
from existing customers and attracts new customers. We believe this low internal cost is a key factor in our ability to grow our
business and obtain margins on our sales that allow us to drive toward sustained profitability.
Investments in our operational capabilities could increase our cost of revenue, but these investments could also, on a near-term
and/or long-term basis, increase our operating efficiencies and lead to cost of revenue decreases. As a result, the amount, timing,
nature and success of these investments, as well as other influences on our cost of revenue from period to period, can impact our costs.
Moreover, changes in our other operating expenses, due to investments in these aspects of our business or other factors, are not taken
into account but impact our overall results, which can limit the utility of cost as an overall cost measurement tool.
Similar to other companies in our industry, we have and may again experience the effects of inflation in the costs of labor,
materials and services in connection with the marketing of our tests and testing services and in connection with our research and
development efforts.
Ability to Obtain Reimbursement and Government Audits and Investigations
Much of our revenue depends on receiving reimbursement for our tests from insurance payors, including our Insurance and
Institutional customers. These payors have complicated rules and procedures regarding submissions for reimbursement and their
reimbursement practices and procedures may vary from period to period. Reimbursed amounts are often subject to audit, and our
ability to collect and retain reimbursement from these payors may vary from period to period. If we are unable to obtain or retain
76
reimbursement during any period, our rate of reimbursement is lower than expected or if reimbursement is delayed, our results of
operations may be correspondingly affected and fluctuate significantly from period to period. As part of our business plan for future
growth, we intend to pursue coverage and reimbursement from insurance payors at a level adequate for us to again achieve and
maintain profitability. However, we cannot predict whether, under what circumstances, or at what payment levels payors will cover
and reimburse for our tests, and even if we are successful, we believe it could take several years to achieve coverage and adequate
contracted reimbursement with insurance payors. To date, we have contracted directly with national health insurance companies to
become an in-network provider and enrolled as a supplier with the Medicare program and some state Medicaid programs, which
means that we have agreed with these payors to provide certain of our tests at negotiated rates. Although this does not guarantee that
we will receive reimbursement for our tests from these or any other payors at adequate levels, we believe our low cost could enhance
our ability to compete effectively in the insurance payor market and our flexibility in establishing relationships with additional
insurance payors in the future. Our level of success in obtaining and maintaining adequate coverage and reimbursement from
insurance payors for our testing services will, we believe, be a key factor in the rate and level of growth of our business over the long
term.
These reimbursement activities also subject us to payor and government audits and investigations such as the HRSA audit and
the CIDs discussed in Note 8, Debt, Commitments and Contingencies to the Consolidated Financial Statements. The results of these
matters and the expenses and use of resources needed in connection with these and similar matters could materially affect our results
of operations.
Foreign Currency Exchange Rate Fluctuations
Some of our business to date has been from non-U.S. customers, and we may record increasing revenue levels from non-U.S.
sources as we focus on growing our international customer base. These revenue sources expose us to fluctuations in our results
associated with changes in foreign currency exchange rates depending on the value of the U.S. dollar compared to the foreign
currencies in which we record revenue. During all periods covered by this report, we consider the estimated effect on our revenue of
foreign currency exchange rate fluctuations to be immaterial; however, the impact of foreign currency exchange rate fluctuations may
increase in future periods as we pursue continued international expansion.
COVID-19 Testing Services
We experienced significant volume growth in 2020, 2021 and 2022 after the launch of our COVID-19 testing services in 2020.
Most of this growth in our testing volume resulted from COVID-19 tests that we conducted for certain counties, states and
municipalities during the pandemic. However, due to decreased demand of COVID-19 testing following the pandemic and our
decision to scale back our COVID-19 testing services, we do not expect material revenue from COVID-19 testing in future periods.
Business Risks and Uncertainties
Our business and prospects are exposed to numerous risks and uncertainties. For more information, see “Item 1A. Risk Factors”
in this report.
Financial Overview
Revenue
Our laboratory service segment generates revenue from molecular testing, including precision diagnostics and anatomic
pathology, BioPharma services, and COVID-19 testing. We recognize revenue upon delivery of a report to the ordering physician or
other customer based on the established billing rate, less contractual and other adjustments, to arrive at the amount we expect to
collect. Our therapeutic development segment is still pre-revenue.
Cost of Revenue
Cost of revenue reflects the aggregate costs incurred in delivering test results and consists of: costs of laboratory reagents and
supplies; personnel costs, including salaries, employee benefit costs, bonuses and equity-based compensation expenses; depreciation
of laboratory equipment; delivery and courier costs relating to the transportation of specimens to be tested; amortization of leasehold
improvements; and allocated overhead expenses, including rent and utilities. Costs associated with performing tests are recorded as
tests are processed.
77
Operating Expenses
Our operating expenses are classified into five categories: research and development; selling and marketing; general and
administrative; amortization of intangible assets; and goodwill impairment loss, if any. For each category except for amortization of
intangible assets and goodwill impairment loss, the largest component is personnel costs, which include salaries, employee benefit
costs, bonuses and equity-based compensation expenses.
Research and Development Expenses
Research and development expenses represent costs incurred to develop our technology and future tests and treatments and our
drug candidates. These costs consist of:
•
personnel costs, including salaries, benefits, and other employee-related costs, such as bonuses and equity-based
compensation expenses;
•
consulting costs, including consulting fees and related travel expenses;
•
laboratory supplies;
•
costs associated with in-process research and conducting clinical studies to develop and support our products;
•
costs related to production of clinical materials;
•
set up costs, including electronic medical record set up costs, costs associated with setting up and conduct clinical studies
at domestic and international sites;
•
costs related to compliance with regulatory requirements; and
•
allocated overhead expenses, including rent, information technology, equipment depreciation and utilities.
We expense all research and development costs in the periods in which they are incurred. We expect our research and
development expenses will continue to increase in absolute dollars, as we expect to continue to invest in research and development
activities and continue to innovate and expand the application of our platform. Furthermore, we expect our research and development
expenses for our therapeutic development segment to increase as we incur incremental expenses associated with our drug candidates
that are currently under development and in clinical trials. Drug candidates in later stages of clinical development generally have
higher development costs, primarily due to the increased size and duration of later-stage clinical trials. Accordingly, we expect to
incur significant research and development expenses in connection with our Phase 2 trials for FID-007 and the initiation of clinical
trials for FID-022.
Selling and Marketing Expenses
Selling and marketing expenses consist of personnel costs, customer service expenses, direct marketing expenses, educational
and promotional expenses, market research and analysis and allocated overhead expenses, including rent and utilities. We expense all
selling and marketing costs as incurred. We expect our selling and marketing expenses will increase in absolute dollars, primarily
driven by our increased investment in sales and marketing, including developing and expanding our sales team, creating and
implementing new sales and marketing strategies and increasing the overall scope of our marketing efforts.
General and Administrative Expenses
General and administrative expenses include executive, finance, accounting, legal and human resources functions. These
expenses consist of personnel costs, audit and legal expenses, consulting costs and allocated overhead expenses, including rent and
utilities. We expense all general and administrative costs as incurred. We expect our general and administrative expenses will continue
to increase in absolute dollars as we seek to continue to scale our operations. We also expect to continue to incur general and
administrative expenses as a result of operating as a public company, including expenses related to compliance with the rules and
regulations of the SEC, and Nasdaq, additional insurance expenses, investor relations activities and other administrative and
professional services.
Goodwill Impairment Loss
A goodwill impairment loss is measured as the amount by which a reporting unit’s carrying value, including goodwill, exceeds
its fair value, not to exceed the carrying amount of goodwill.
78
Amortization of Intangible Assets
Amortization of intangible assets consist of amortization expense on customer relationships, royalty-free technology, trade
name, laboratory information system platform and in-place intangible assets that arose from the business combinations and a patent
acquired. We amortize finite lived intangible assets over the period of estimated benefit using the straight-line method. Indefinite lived
intangible assets are tested for impairment annually or whenever events or circumstances indicate that the carrying amount of the asset
may not be recoverable. If impairment is indicated, we measure the amount of the impairment loss as the amount by which the
carrying amount exceeds the fair value of the asset.
(Benefit from) Provision for Income Taxes
(Benefit from) provision for income taxes consists of U.S. federal and state income taxes. A deferred tax liability is recognized
for all taxable temporary differences, and a deferred tax asset is recognized for all deductible temporary differences, operating losses
and tax credit carryforwards. A valuation allowance is provided when it is more likely than not that some portion or all of a deferred
tax asset will not be realized.
The factors that most significantly impact our effective tax rate include the levels of net earnings and certain deductions,
including those related to equity-based compensation, tax credits, the reclassification of stranded tax effects from other comprehensive
income, and the effect of state income taxes. We expect that these factors could cause our consolidated effective tax rate to differ
significantly from the U.S. federal income tax rate in future periods.
Results of Operations
The table below summarizes the results of our continuing operations for each of the periods presented. Historical results are not
indicative of the results to be expected in the current period or any future period.
Year Ended December 31,
2024
2023
$ Change
% Change
(in thousands, except percentages)
Statement of Operation Data
Revenue
$
283,470
$
289,213
$
(5,743)
(2)%
Cost of revenue
176,255
184,757
(8,502)
(5)%
Gross profit
107,215
104,456
2,759
3%
Operating expenses:
Research and development
48,816
41,440
7,376
18%
Selling and marketing
36,246
41,467
(5,221)
(13)%
General and administrative
88,106
88,999
(893)
(1)%
Amortization of intangible assets
7,965
7,845
120
2%
Goodwill impairment loss
—
120,234
(120,234)
(100)%
Total operating expenses
181,133
299,985
(118,852)
(40)%
Operating (loss) income
(73,918)
(195,529)
121,611
(62)%
Other income (expenses):
Interest income
31,304
21,612
9,692
45%
Interest expense
170
(488)
658
(135)%
Impairment of available-for-sale debt securities
(10,073)
—
(10,073)
*
Other income, net
561
320
241
75%
Total other income, net
21,962
21,444
518
2%
(Loss) income before income taxes
(51,956)
(174,085)
122,129
(70)%
(Benefit from) provision for income taxes
(8,136)
1,154
(9,290)
(805)%
Net (loss) income from consolidated operations
(43,820)
(175,239)
131,419
(75)%
Net loss attributable to noncontrolling interests
1,112
7,414
(6,302)
(85)%
Net (loss) income attributable to Fulgent
$
(42,708)
$
(167,825)
$
125,117
(75)%
* not meaningful
79
Revenue
Year Ended December 31,
2024
2023
$ Change
% Change
(in thousands, except percentages)
Revenue from laboratory services
Precision diagnostics
$
167,745
$
131,990
$
35,755
27%
Anatomic pathology
97,080
104,655
(7,575)
(7)%
BioPharma services
16,338
25,416
(9,078)
(36)%
COVID-19
2,307
27,152
(24,845)
(92)%
Total laboratory services
$
283,470
$
289,213
$
(5,743)
(2)%
Revenue decreased by $5.7 million, or 2%, from $289.2 million in 2023 to $283.5 million in 2024. The decrease in revenue
between periods was driven by decreases of $24.8 million in COVID-19 testing, $9.1 million in BioPharma services, and $7.6 million
in anatomic pathology. However, these declines were offset by an increase of $35.8 million in precision diagnostics.
The decrease in COVID-19 testing services resulted from the cessation of testing operations at the end of March 2023.
Continued COVID-19 revenues after March 2023 are due to variable consideration recognized for services completed in prior periods.
The decrease in anatomic pathology services was due to lower reimbursement rates from insurance payors and client losses. The
decrease in BioPharma services revenue was primarily due to the scaling back or termination of certain projects, as some clients faced
financial distress, underwent restructuring, shifted strategic priorities, adapted to market changes, or completed large clinical trials.
BioPharma services revenue is expected to remain variable due to the long sales cycle and project timing differences. Conversely, the
increase in precision diagnostics revenue was driven by growth in our reproductive health services and legacy diagnostic offerings.
We believe the factors that will affect our ability to grow these revenue streams are 1) the average price point we offer and the
reimbursement rate from insurance payors; 2) the concentration of our payor base; 3) the competitive advantage we have due to our
broad and flexible test menu, detection rate, and turnaround times; and 4) growth in size of an addressable market. Estimated
collection amounts from insurance payors are subject to the complexities and ambiguities of billing, reimbursement regulations and
claims processing, as well as considerations unique to Medicare and Medicaid programs. Because our proprietary technology platform
allows for repaid scaling of a broad, flexible testing menu, we can offer our customers more scalable and affordable testing. Going
forward, we will strive to maintain this competitive advantage and emphasize this in our marketing efforts to grow our testing revenue.
Our customer base includes insurance, institutional, and individual payors. In some periods, our revenue is concentrated on a
smaller number of customers. For the laboratory services segment, aggregating customers that are under common control, one
customer comprised $62.6 million or 22% of our revenue in 2024 and $35.7 million or 12% of our revenue in 2023. To reduce this
revenue risk, we will focus on increasing the number of customers and thereby reducing the concentration.
Revenue from non-U.S. sources increased by $4.1 million, or 20%, from $20.2 million in 2023 to $24.3 million in 2024. The
increase in revenue from non-U.S. sources between periods were primarily due to increased sales of our traditional genetic testing
services to customers in China through our joint venture, which contributed $11.8 million in total revenue in 2024.
Cost of Revenue
Year Ended December 31,
2024
2023
$ Change
% Change
(in thousands, except percentages)
Cost of revenue
$
176,255
$
184,757
$
(8,502)
(5)%
Cost of revenue as a % of revenue
62.2%
63.9%
80
Our consolidated cost of revenue decreased by $8.5 million, or 5%, from $184.8 million in 2023 to $176.3 million in 2024. The
decrease was primarily due to decreases of $6.7 million in consulting and outside labor costs for production, $1.7 million in software
and software licensing expenses, $1.4 million in personnel costs, including equity-based compensation, $0.8 million in shipping
expenses, and $0.2 million in dues and subscriptions expense, related to efforts of optimizing cost structures including bringing certain
operations in house, consolidating laboratory operations, and the cessation of our COVID-19 testing operations, and partially offset by
an increase of $1.8 million in reagent and supply costs and $0.5 million in depreciation expenses.
Our consolidated cost of revenues as a percentage of revenue decreased from 63.9% to 62.2%. Our gross profit increased by
$2.8 million, or 3%, from $104.5 million in 2023 to $107.2 million in 2024. Our gross profit as a percentage of revenue, or gross
margin, increased from 36.1% to 37.8%. This is driven by the efforts of optimizing cost structures as discussed above.
Research and Development
Year Ended December 31,
2024
2023
$ Change
% Change
(in thousands, except percentages)
Research and development
Laboratory services
$
28,424
$
29,748
$
(1,324)
(4)%
Therapeutic development
20,392
11,692
8,700
74%
Total research and development
$
48,816
$
41,440
$
7,376
For the laboratory services segment, the research and development expenses were mainly for advancing our technology and
future testing and testing services. The expenses decreased by $1.3 million, or 4%, from $29.7 million in 2023 to $28.4 million in
2024. The decrease was primarily attributed to reductions of $0.6 million in facility expenses due to the consolidation of office and
laboratory space, $0.3 million in depreciation expenses, $0.2 million in personnel expenses, and $0.1 million in consulting and
external labor expenses.
In 2024, the research and development expenses primarily consisted of $25.3 million in personnel expenses, including bonuses
and equity-based compensation, $1.4 million in reagent and supply costs, $0.6 million in facility expenses, $0.4 million in
depreciation expense, and $0.4 million in software and licensing fees. The 2023 expenses primarily consisted of $25.5 million in
personnel expenses, including bonuses and equity-based compensation, $1.4 million in reagent and supply costs, $1.1 million in
facility expenses, $0.7 million in depreciation expense, and $0.4 million in software and licensing fees.
For the therapeutic development segment, the research and development expenses in 2024 included $10.9 million in CRO costs,
$8.6 million in personnel costs, including equity-based compensation, and $0.7 million in depreciation expenses. In 2023, these
expenses comprised $6.4 million of personnel expenses, including equity-based compensation, $4.5 million in CRO costs, and $0.7
million in depreciation expenses.
Research and development expenses for the therapeutic development segment increased by $8.7 million, or 74%, from $11.7
million in 2023 to $20.4 million in 2024. The increase was primarily driven by increases of $6.4 million in CRO costs and $2.2
million in personnel costs, including equity-based compensation expense. The overall increase was attributed to the advancement and
continuation of the clinical study of FID-007, along with the completion of preclinical work for FID-022. In 2024, approximately $2.1
million was incurred for the preclinical development of FID-022, whereas related costs in 2023 were minimal.
Looking ahead, we expect research and development expenses to continue increasing as clinical trials progress for FID-007,
FID-022, and other preclinical studies.
Selling and Marketing
Our consolidated selling and marketing expenses decreased by $5.2 million, or 13%, from $41.5 million in 2023 to $36.2
million in 2024. The decrease was primarily due to decreases of $1.9 million in facility expenses due to the consolidation of office
space, $1.3 million in consulting and outside labor expenses, $1.0 million in advertising and marketing expenses, $0.9 million in
commissions, $0.6 million in depreciation expenses, $0.3 million in losses of fixed asset disposals, and $0.2 million in software and
software licensing expenses, and partially offset by an increase of $1.0 million personnel costs, including equity-based compensation
expense.
81
General and Administrative
Our consolidated general and administrative expenses decreased by $0.9 million, or 1%, from $89.0 million in 2023 to $88.1
million in 2024. The decrease was primarily due to decreases of $10.1 million in legal and professional fees related to a voluntary
disclosure, see Note 8, Debt, Commitments and Contingencies, of our consolidated financial statements included in this report, $1.6
million in insurance expenses, $0.8 million in provision for credit losses due to subsequent collections from customers who were
previously reserved, and $0.7 million in depreciation expenses and partially offset by increases of $11.4 million in personnel costs,
including equity-based compensation, and $0.8 million in software and software licensing fees.
Amortization of Intangible Assets
Our consolidated amortization of intangible assets represents amortization expenses on the intangible assets that arose from the
business combinations in 2022 and 2021, and a patent purchased in 2021.
Goodwill Impairment Loss
Year Ended December 31,
$
%
2024
2023
Change
Change
(dollars in thousands)
Goodwill impairment loss
Laboratory services
$
—
$
120,234
$
(120,234)
*
Therapeutic development
—
—
—
*
$
—
$
120,234
$
(120,234)
* not meaningful
Goodwill impairment loss for 2023 was comprised of a full goodwill impairment loss of $120.2 million for the laboratory
services reporting unit. There was no goodwill impairment loss for the year ended December 31, 2024. The full impairment was
driven by a sustained decline in our stock price and market capitalization. There was no impairment loss for the therapeutic
development unit for the years ended December 31, 2024 and 2023. See Note 17, Goodwill and Intangible Assets, for more details.
Other Income (Expenses)
Other income, net, is primarily comprised of interest income, which was $31.3 million and $21.6 million for 2024 and 2023,
respectively, and impairment of available-for-sale debt securities of $10.1 million in 2024. This interest income included interest
earned on marketable securities and realized gain or loss on sale of marketable securities. The increase in interest income was
primarily due to increased interest rates on marketable securities relative to the prior comparative period.
(Benefit from) Provision for Income Taxes
(Benefit from) provision for income taxes were ($8.1) million and $1.2 million in 2024 and 2023, respectively. The effective
income tax rate was 16.11% and (0.69)% of loss before income taxes for 2024 and 2023, respectively. The change in the effective tax
rate compared to prior period is due to the valuation allowance in the current period that precludes us from recognizing the benefit
from our net operating losses. The increase in the valuation allowance for 2024 was primarily due to the increase in capitalized
Section 174 expenditures.
See Note 11, Income Taxes, to our consolidated financial statements included in this report for more information regarding our
income taxes.
Net Loss Attributable to Noncontrolling Interest
Net loss attributable to noncontrolling interest represents net loss attributable to minority shareholders from entities not wholly
owned.
82
Liquidity and Capital Resources
Liquidity and Sources of Cash
We had $828.6 million and $847.7 million in cash, cash equivalents, restricted cash, and marketable securities as of
December 31, 2024 and 2023, respectively. Our marketable securities primarily consist of U.S. government and U.S. agency debt
securities, U.S. treasury bills, corporate bonds, municipal bonds, and Yankee debt securities as of December 31, 2024 and 2023.
Our primary uses of cash are for capital expenditures mainly in buildings, building improvements, and equipment, to repurchase
our stock, fund our operations, and to fund strategic acquisitions as we continue to invest in and seek to grow our business. Cash used
to fund operating expenses is impacted by the timing of our expense payments, as reflected in the changes in our outstanding accounts
payable and accrued expenses.
We expect our existing cash, cash equivalent, and short-term marketable securities to continue to be sufficient to meet our
anticipated cash requirements for at least the next 12 months. Cash provided by operations has significantly contributed to our ability
to meet our liquidity needs, including paying for capital expenditures, however, cash provided by our operations has in the past
experienced fluctuations from period to period, which we expect may continue in the future. These fluctuations can occur because of a
variety of factors, including, among others, factors relating to the demand for our tests, the amount and timing of sales, the prices we
charge for our tests due to changes in product mix, customer mix, general price degradation for tests, or other factors, the rate and
timing of our billing and collections cycles and the timing and amount of our commitments and other payments. We intend to improve
our profitability by improving margins and expanding in new markets for our tests, but these efforts are subject to risks, including
those described in Item 1A of this Annual Report, and may not be successful. Moreover, even if our liquidity expectations are correct,
we may still seek to raise additional capital through securities offerings, credit facilities or other debt financings, asset sales or
collaborations or licensing arrangements.
If we raise additional funds by issuing equity securities, our existing stockholders could experience substantial dilution.
Additionally, any preferred stock we issue could provide for rights, preferences or privileges senior to those of our common stock, and
our issuance of any additional equity securities, or the possibility of such an issuance, could cause the market price of our common
stock to decline. The terms of any debt securities we issue or borrowings we incur, if available, could impose significant restrictions
on our operations, such as limitations on our ability to incur additional debt or issue additional equity or other restrictions that could
adversely affect our ability to conduct our business, and would result in increased fixed payment obligations. If we seek to sell assets
or enter into collaborations or licensing arrangements to raise capital, we may be required to accept unfavorable terms or relinquish or
license to a third-party our rights to important or valuable technologies or tests we may otherwise seek to develop ourselves.
Moreover, we may incur substantial costs in pursuing future capital, including investment banking, legal and accounting fees, printing
and distribution expenses and other similar costs. Additional funding may not be available to us when needed, on acceptable terms or
at all. If we are not able to secure funding if and when needed and on reasonable terms, we may be forced to delay, reduce the scope of
or eliminate one or more sales and marketing initiatives, research and development programs or other growth plans or strategies. In
addition, we may be forced to work with a partner on one or more aspects of our tests or market development programs or initiatives,
which could lower the economic value to us of these tests, programs or initiatives. Any such outcome could significantly harm our
business, performance and prospects.
Cash Flows
The following table summarizes cash flows from continuing operations for each of the periods presented:
Year Ended December 31,
2024
2023
(in thousands)
Net cash provided by operating activities
$
21,060
$
27,003
Net cash (used in) provided by investing activities
$
(58,352)
$
38,898
Net cash used in financing activities
$
(4,847)
$
(47,785)
Operating Activities
During the year ended December 31, 2024, our operations provided $21.1 million of cash as compared to $27.0 million in 2023.
The decrease in cash provided from operating activities in 2024 compared to the corresponding 2023 period was primarily due to
timing of cash receipts from customers and cash payments for operating expenses. We expect to incur more operating expenses and
use more cash in operating activities in the coming year as a result of our planned and ongoing clinical trials for FID-007 and FID-
022, and as we continue to invest resources to grow our laboratory services business.
83
Investing Activities
The cash provided by or used in investing activities are impacted by capital expenditures for operation needs and timing of
payments, timing of maturities of marketable securities, and discretionary business combinations and other investment.
Cash used in investing activities in 2024 was $58.4 million, which primarily related to $472.4 million in purchase of marketable
securities, $40.3 million related to the purchase of fixed assets consisting mainly of building, building improvement, and medical
laboratory equipment, and partially offset by $349.8 million related to maturities of marketable securities, $104.3 million related to
proceeds from sales of marketable securities, and $0.3 million related to the sale of fixed assets.
Cash provided by investing activities in 2023 was $38.9 million, which primarily related to $508.6 million related to maturities
of marketable securities, $44.1 million related to proceeds from sales of marketable securities, and $0.8 million related to the sale of
fixed assets, and partially offset by $491.9 million in purchase of marketable securities, $22.2 million related to the purchase of fixed
assets consisting mainly of medical laboratory equipment and building improvement, and $0.4 million related to a business
acquisition.
Financing Activities
Cash used in financing activities in 2024 was $4.8 million, which primarily related to $1.2 million used in the repayment of
notes payable, and $2.9 million used in common stock withholding for employee tax obligations.
Cash used in financing activities in 2023 was $47.8 million, which primarily related to $25.1 million used in the repurchase of
common stock, $15.0 million used in the repayment for the margin account, $4.3 million used in the repayment of notes payable, and
$2.7 million used in common stock withholding for employee tax obligations.
We did not expect to use any credit facilities due to the strong cash position as of December 31, 2024.
Stock Repurchase Program
In March 2022, our Board authorized a $250.0 million stock repurchase program. The stock repurchase program has no
expiration from the date of authorization. Under the stock repurchase program, the Company may repurchase shares from time to time
in the open market or in privately negotiated transactions.
During the year ended December 31, 2024, we repurchased 10,000 shares of our common stock at an aggregate cost of $0.2
million under the stock repurchase program. During the year ended December 31, 2023, we repurchased 1.0 million shares of our
common stock at an aggregate cost of $25.1 million under the stock repurchase program. During the year ended December 31, 2022,
we repurchased 1.8 million shares of our common stock at an aggregate cost of $74.3 million under the stock repurchase program. As
of December 31, 2024, a total of approximately $150.5 million remained available for future repurchases of our common stock under
our stock repurchase programs.
Material Cash Requirements and Contractual Obligations as of December 31, 2024
As of December 31, 2024, we have an outstanding balance of $2.9 million on an installment loan, of which, the current portion
is $0.4 million. See Note 8, Debt, Commitments and Contingencies, of our consolidated financial statements included in this report.
The following summarizes our contractual obligations as of December 31, 2024:
Payments Due by Period
Total
Less than 1 year
1-3 years
3-5 years
More than
5 years
(in thousands)
Operating lease obligations(1)
$
6,651
$
1,707
$
2,128
$
984
$
1,832
Finance lease obligations(2)
783
417
366
—
—
Purchase obligations(3)
40,604
31,638
6,639
2,327
—
Total contractual obligations
$
48,038
$
33,762
$
9,133
$
3,311
$
1,832
84
(1)
Represents non-cancelable operating leases. For further information, refer to Note 9, Leases, to the Consolidated Financial Statements.
(2)
Represents non-cancelable finance leases. For further information, refer to Note 9, Leases, to the Consolidated Financial Statements.
(3)
Represents purchase obligations for medical lab equipment, reagents and other supplies, see Note 8, Debt, Commitment and Contingencies, to the Consolidated
Financial Statements.
Critical Accounting Policies and Use of Estimates
This discussion and analysis is based on our consolidated financial statements included in this report, which have been prepared
in accordance with U.S. GAAP. The preparation of consolidated financial statements in accordance with U.S. GAAP requires
management to make certain estimates, judgments and assumptions and decisions that affect the reported amounts and related
disclosures, including the selection of appropriate accounting principles and the assumptions on which to base accounting estimates.
In making these estimates and assumptions and reaching these decisions, we apply judgment based on our understanding and analysis
of the relevant circumstances, including historical data and experience available at the date of the consolidated financial statements, as
well as various other factors management believes to be reasonable under the circumstances, including but not limited to valuation of
intangible assets and goodwill in recent business combinations. Actual results could differ from our estimates. We are committed to
incorporating accounting principles, assumptions and estimates that promote the representational faithfulness, verifiability, neutrality
and transparency of the accounting information included in our consolidated financial statements.
While our significant accounting policies are described in more detail in the notes to the consolidated financial statements
included in this report, we believe the accounting policies discussed below used in the preparation of our consolidated financial
statements require the most significant estimates, judgments, assumptions and decisions.
Revenue Recognition
We generate revenue from sales of our testing services. We currently receive payments from: insurance, institutional customers,
including hospitals, medical institutions, other laboratories, governmental bodies, municipalities, and large corporations; and patients
who pay directly.
We recognize revenue in an amount that reflects the consideration to which we expect to be entitled in exchange for the transfer
of promised goods or services to our customers.
For insurance payors, in the absence of Medicare coverage, contractually established reimbursement rates or other coverage, we
have concluded that our contracts include variable consideration because the amounts paid by Medicare or commercial health
insurance carriers may be paid at less than our standard rates or not paid at all, with such differences considered implicit price
concessions. Variable consideration attributable to these price concessions measured at the expected value using the “most likely
amount” method under Accounting Standards Codification, or ASC, 606 Revenue from Contracts with Customers, or ASC 606. The
amounts are determined by the historical average collection rates by test type taking into consideration the range of possible outcomes,
the predictive value of our past experiences, the time period of when uncertainties expect to be resolved and the amount of
consideration that is susceptible to factors outside of our influence, such as the judgment and actions of third parties. Such variable
consideration is included in the transaction price only to the extent it is probable that a significant reversal in the amount of cumulative
revenue recognized will not occur when the uncertainties with respect to the amount are resolved. Variable consideration may be
constrained and excluded from the transaction price in situations where there is the absence of a predictable pattern and history of
collectability with a payor.
We re-assess our estimated transaction price at the end of each reporting period, including our assessment of whether our
estimate of variable consideration is constrained to the extent that it is probable that a significant reversal of cumulative revenue will
not occur once any uncertainty is resolved. We record any necessary adjustments in the current period’s revenue. $1.8 million and
$23.0 million variable consideration was recognized as additional revenue in the year ended December 31, 2024 and 2023,
respectively, that related to collections for COVID-19 tests completed in the prior period.
Valuation of Goodwill and Indefinite-Lived Intangible Assets
The valuation of assets acquired in a business combination and asset impairment reviews require the use of significant estimates
and assumptions. The acquisition method of accounting for business combinations requires us to estimate the fair value of assets
acquired, liabilities assumed, and any noncontrolling interest in an acquired business to properly allocate purchase price consideration
between assets that are depreciated or amortized and goodwill.
85
See Note 2, Summary of Significant Accounting Policies, to our consolidated financial statements included in this report for
information about our valuation and assessment process with regard to potential impairment of goodwill and indefinite-lived
intangibles. Also see Note 17, Goodwill and Intangible Assets, to our consolidated financial statements included in this report for
details on the valuation estimate and results for 2024.
There can be no assurance that the estimates and assumptions management made for the purposes of the goodwill or in-process
research & development, or IPR&D, impairment analysis will prove to be accurate predictions of future performance. It is possible
that the conclusions regarding impairment or recoverability of goodwill or intangible assets could change in future periods. We will
continue to monitor the therapeutic development reporting unit. For all IPR&D projects, there are major risks and uncertainties
associated with the timely and successful completion of development and commercialization of these drug candidates, including the
ability to confirm their efficacy based on data from clinical trials, the ability to obtain necessary regulatory approvals, and the ability
to successfully complete these tasks within budgeted costs. We are not able to market a human therapeutic without obtaining
regulatory approvals, and such approvals require completing clinical trials that demonstrate a drug candidate is safe and effective. In
addition, the availability and extent of coverage and reimbursement from insurance payors, including government healthcare programs
and private insurance plans, impact the revenues a product can generate. Consequently, the eventual realized value, if any, of these
acquired IPR&D projects may vary from their estimated fair values.
Recent Accounting Pronouncements
See Note 2, Summary of Significant Accounting Policies, to our consolidated financial statements included in this report for
information about recent accounting pronouncements.
Off-Balance Sheet Arrangements
We did not have, and do not currently have, any off-balance sheet arrangements during the periods presented, as defined in the
rules and regulations of the SEC, that have or are reasonably likely to have a current or future effect on our financial condition,
changes in financial condition, revenue or expenses, results of operations, liquidity, capital expenditures or capital resources that is
material to investors.
Item 7A. Quantitative and Qualitative Disclosures About Market Risk.
We are exposed to market risks from fluctuations in interest rates and foreign currency translation, which may adversely affect
our results of operations and financial condition.
Interest Rate Risk
We invest in marketable debt securities, including corporate debt securities, municipal bonds, U.S. government and agency debt
securities, and debt instruments issued by foreign governments. Our investment policy and strategy are focused on the preservation of
capital and supporting our liquidity requirements. We typically invest in highly rated securities, with the primary objective of
minimizing the potential risk of principal loss. Our investments in fixed rate interest earning securities carry a degree of interest rate
risk. Fixed rate securities may have their fair market value adversely affected due to a rise in interest rates. Unrealized gains or losses
on our marketable debt securities are primarily due to interest rate fluctuations as compared to interest rates at the time of purchase.
We measure our debt securities at fair value with gains and losses recorded in other comprehensive income (loss) until the securities
are sold, less any expected credit losses.
To provide a meaningful assessment of the interest rate risk associated with our investment portfolio, we performed a sensitivity
analysis to determine the impact a change in interest rates would have on the value of the investment portfolio assuming a 100-basis
point parallel shift in the yield curve. Based on investment positions as of December 31, 2024 and 2023, a hypothetical 100 basis point
increase in interest rates across all maturities would result in an incremental decline of $14.5 million and $10.1 million, respectively,
in the fair market value of the portfolio. Such losses would only be realized if we sold the investments prior to maturity.
Foreign Currency Risk
We transact business in multiple currencies, in addition, we translate the assets and liabilities of our non-U.S. dollar functional
currency subsidiaries into U.S. dollars. Foreign assets, liabilities, revenues, as well as costs and expenses denominated in foreign
currencies, expose us to the risk of fluctuations in foreign currency exchange rates against the U.S. dollar. Our foreign currency
exposures are primarily concentrated in the Chinese yuan. For the purpose of analyzing foreign currency exchange risk, we considered
the historical trends in foreign currency exchange rates and determined that it was reasonably possible that adverse changes in
exchange rates of 10% could be experienced in the near term.
86
If an adverse 10% foreign currency exchange rate change was applied to total monetary assets denominated in currencies other
than the functional currencies at the balance sheet date, it would have resulted in decrease in assets of approximately $1.1 million as of
December 31, 2024, and $1.3 million as of December 31, 2023. The impact to income (loss) before income tax was not significant.
87
Item 8. Financial Statements and Supplementary Data.
The information required by this Item 8 immediately follows the signature page to this report and is incorporated herein by
reference.
Item 9. Changes in and Disagreements with Accountants on Accounting and Financial Disclosure.
None.
Item 9A. Controls and Procedures.
Evaluation of Disclosure Controls and Procedures
Disclosure controls and procedures are controls and other procedures of a company that are designed to ensure that information
required to be disclosed by the company in the reports that it files or submits under the Exchange Act is recorded, processed,
summarized and reported within the time periods specified in the SEC’s rules and forms. Disclosure controls and procedures include,
without limitation, controls and procedures designed to ensure that information required to be disclosed by a company in the reports
that it files or submits under the Exchange Act is accumulated and communicated to the Company’s management, including its
principal executive officer and principal financial officer, or persons performing similar functions, as appropriate to allow timely
decisions regarding required disclosure. As required by Rules 13a-15(b) and 15d-15(b) under the Exchange Act, our management,
with the participation of our principal executive officer and principal financial officer, conducted an evaluation of the effectiveness of
our disclosure controls and procedures as of December 31, 2024. Based on this evaluation, our principal executive officer and
principal financial officer concluded that our disclosure controls and procedures were effective as of December 31, 2024.
Internal Control over Financial Reporting
Changes in Internal Control over Financial Reporting.
There has been no change in our internal control over financial reporting during the year ended December 31, 2024, that has
materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.
Management’s Annual Report on Internal Control over Financial Reporting.
Our management is responsible for establishing and maintaining adequate internal control over financial reporting, as defined in
Rule 13a-15(f) of the Exchange Act. Our management conducted an evaluation of the effectiveness of our internal control over
financial reporting based on the framework in Internal Control—Integrated Framework issued by the Committee of Sponsoring
Organizations of the Treadway Commission (2013 framework). Based on this evaluation, management concluded that our internal
control over financial reporting was effective as of December 31, 2024. Management reviewed the results of its assessment with our
Audit and Compliance Committee. The effectiveness of our internal control over financial reporting as of December 31, 2024 has
been audited by Deloitte & Touche LLP, an independent registered public accounting firm, as stated in its report, which is included in
Item 8 of this Annual Report on Form 10-K.
Inherent Limitations on Disclosure Controls and Procedures and Internal Control over Financial Reporting
Management recognizes that any controls and procedures, no matter how well-designed and operated, can provide only
reasonable assurance of achieving their objectives, and management necessarily applies its judgment in evaluating the benefits of
possible controls and procedures relative to their costs. Because of these inherent limitations, our disclosure and internal controls may
not prevent or detect all instances of fraud, misstatements or other control issues. In addition, projections of any evaluation of the
effectiveness of disclosure or internal controls to future periods are subject to risks, including, among others, that controls may
become inadequate because of changes in conditions or that the degree of compliance with policies or procedures may deteriorate.
88
REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM
To the shareholders and the Board of Directors of Fulgent Genetics, Inc.
Opinion on Internal Control over Financial Reporting
We have audited the internal control over financial reporting of Fulgent Genetics, Inc. and subsidiaries (the “Company”) as of
December 31, 2024, based on criteria established in Internal Control – Integrated Framework (2013) issued by the Committee of
Sponsoring Organizations of the Treadway Commission (COSO). In our opinion, the Company maintained, in all material respects,
effective internal control over financial reporting as of December 31, 2024, based on criteria established in Internal Control –
Integrated Framework (2013) issued by COSO.
We have also audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States)
(PCAOB), the consolidated financial statements as of and for the year ended December 31, 2024, of the Company and our report dated
February 28, 2025, expressed an unqualified opinion on those financial statements.
Basis for Opinion
The Company’s management is responsible for maintaining effective internal control over financial reporting and for its assessment of
the effectiveness of internal control over financial reporting, included in the accompanying “Management’s Annual Report on Internal
Control over Financial Reporting.” Our responsibility is to express an opinion on the Company’s internal control over financial
reporting based on our audit. We are a public accounting firm registered with the PCAOB and are required to be independent with
respect to the Company in accordance with the U.S. federal securities laws and the applicable rules and regulations of the Securities
and Exchange Commission and the PCAOB.
We conducted our audit in accordance with the standards of the PCAOB. Those standards require that we plan and perform the audit
to obtain reasonable assurance about whether effective internal control over financial reporting was maintained in all material respects.
Our audit included obtaining an understanding of internal control over financial reporting, assessing the risk that a material weakness
exists, testing and evaluating the design and operating effectiveness of internal control based on the assessed risk, and performing such
other procedures as we considered necessary in the circumstances. We believe that our audit provides a reasonable basis for our
opinion.
Definition and Limitations of Internal Control over Financial Reporting
A company’s internal control over financial reporting is a process designed to provide reasonable assurance regarding the reliability of
financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting
principles. A company’s internal control over financial reporting includes those policies and procedures that (1) pertain to the
maintenance of records that, in reasonable detail, accurately and fairly reflect the transactions and dispositions of the assets of the
company; (2) provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial statements in
accordance with generally accepted accounting principles, and that receipts and expenditures of the company are being made only in
accordance with authorizations of management and directors of the company; and (3) provide reasonable assurance regarding
prevention or timely detection of unauthorized acquisition, use, or disposition of the company’s assets that could have a material effect
on the financial statements.
Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, projections
of any evaluation of effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in
conditions, or that the degree of compliance with the policies or procedures may deteriorate.
/s/ DELOITTE & TOUCHE LLP
Los Angeles, California
February 28, 2025
89
Item 9B. Other Information.
Rule 10b5-1 trading arrangements
During the year ended December 31, 2024, none of our directors or officers adopted or terminated “Rule 10b5-1 trading
arrangement” or “non-Rule 10b5-1 trading arrangement,” as each term is defined in Item 408 of Regulation S-K.
Item 9C. Disclosure Regarding Foreign Jurisdictions that Prevent Inspections.
None.
90
PART III
Item 10. Directors, Executive Officers and Corporate Governance.
The information required by this item is incorporated by reference to the definitive proxy statement for our 2025 annual meeting
of stockholders or an amendment to this report, in either case to be filed with the SEC within 120 days after the end of our fiscal year
ended December 31, 2024.
Item 11. Executive Compensation.
The information required by this item is incorporated by reference to the definitive proxy statement for our 2025 annual meeting
of stockholders or an amendment to this report, in either case to be filed with the SEC within 120 days after the end of our fiscal year
ended December 31, 2024.
Item 12. Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters.
The information required by this item is incorporated by reference to the definitive proxy statement for our 2025 annual meeting
of stockholders or an amendment to this report, in either case to be filed with the SEC within 120 days after the end of our fiscal year
ended December 31, 2024.
Item 13. Certain Relationships and Related Transactions, and Director Independence.
The information required by this item is incorporated by reference to the definitive proxy statement for our 2025 annual meeting
of stockholders or an amendment to this report, in either case to be filed with the SEC within 120 days after the end of our fiscal year
ended December 31, 2024.
Item 14. Principal Accountant Fees and Services.
The information required by this item is incorporated by reference to the definitive proxy statement for our 2025 annual meeting
of stockholders or an amendment to this report, in either case to be filed with the SEC within 120 days after the end of our fiscal year
ended December 31, 2024.
91
PART IV
Item 15. Exhibits and Financial Statement Schedules.
(a)(1)Consolidated Financial Statements.
The following financial statements are included immediately following the signature page hereof and are filed as part of this
report:
Report of Independent Registered Public Accounting Firm (PCAOB ID: 34)
F-2
Consolidated Balance Sheets as of December 31, 2024 and 2023
F-5
Consolidated Statements of Operations for the Years Ended December 31, 2024, 2023, and 2022
F-6
Consolidated Statements of Comprehensive Income (Loss) for the Years Ended December 31, 2024, 2023, and 2022
F-7
Consolidated Statements of Stockholders’ Equity for the Years Ended December 31, 2024, 2023, and 2022
F-8
Consolidated Statements of Cash Flows for the Years Ended December 31, 2024, 2023, and 2022
F-9
Notes to Consolidated Financial Statements
F-10
(a)(2)Financial Statement Schedules.
All financial statement schedules have been omitted, as they are not required, not applicable, or the required information is
otherwise included.
(a)(3)Exhibits.
The information required by this Item 15(a)(3) is set forth on the Exhibit Index immediately preceding the signature page of this
report and is incorporated herein by reference.
Item 16. Form 10-K Summary.
None.
92
EXHIBIT INDEX
Exhibit
Number
Description
Form
File Number
Incorporated by
Reference Exhibit
Filing Date
Filed
Herewith
2.1
Agreement and Plan of Merger, dated September 16,
2016, by and among the registrant, Fulgent
MergerSub, LLC and Fulgent Therapeutics LLC.
S-1/A
333-213469
2.1
9/19/2016
3.1
Certificate of Incorporation of the registrant, as
amended.
10-Q
001-37894
3.1
8/14/2017
3.1.1
Certificate of Amendment to Certificate of
Incorporation of the registrant, dated August 2, 2016.
10-Q
001-37894
3.1.1
8/14/2017
3.1.2
Certificate of Amendment to Certificate of
Incorporation of the registrant, dated May 17, 2017.
10-Q
001-37894
3.1.2
8/14/2017
3.2
Amended and Restated Bylaws.
10-Q
001-37894
3.2
8/4/2023
4.1
Form of Certificate of Common Stock of the
registrant.
S-1/A
333-213469
4.1
9/19/2016
4.2
Description of the registrant’s securities.
X
10.1#
Form of Indemnification Agreement between the
registrant and each of its officers and directors.
S-1
333-213469
10.1
9/2/2016
10.2#
Amended and Restated 2015 Equity Incentive Plan
of Fulgent Therapeutics LLC.
S-1
333-213469
10.2
9/2/2016
10.3#
Form of Notice of Option Grant and Option
Agreement under the Amended and Restated 2015
Equity Incentive Plan of Fulgent Therapeutics LLC.
S-1
333-213469
10.3
9/2/2016
10.4#
Form of Notice of Profits Interest Grant and Profits
Interest Agreement under the Amended and Restated
2015 Equity Incentive Plan of Fulgent Therapeutics
LLC.
S-1
333-213469
10.4
9/2/2016
10.5#
Form of Notice of Restricted Share Unit Grant and
Restricted Share Unit Agreement under the
Amended and Restated 2015 Equity Incentive Plan
of Fulgent Therapeutics LLC.
S-1
333-213469
10.5
9/2/2016
10.6#
2016 Omnibus Incentive Plan of the registrant.
S-1/A
333-213469
10.6
9/26/2016
10.7#
Form of Notice of Stock Option Award and Stock
Option Award Agreement under the 2016 Omnibus
Incentive Plan of the registrant.
S-1
333-213469
10.7
9/2/2016
10.8#
Form of Notice of Restricted Stock Unit Award and
Restricted Stock Unit Agreement under the 2016
Omnibus Incentive Plan of the registrant.
10-K
001-37894
10.8
3/17/2017
10.9#
Form of Option Substitution Award under the 2016
Omnibus Incentive Plan of the registrant.
S-1
333-213469
10.9
9/2/2016
10.10#
Form of Notice of Restricted Stock Unit Substitution
Award and Restricted Stock Unit Agreement under
the 2016 Omnibus Incentive Plan of the registrant.
S-1
333-213469
10.10
9/2/2016
10.11#
Employment Agreement, dated May 25, 2016, by
and among Fulgent Therapeutics LLC, the registrant
and Ming Hsieh.
S-1
333-213469
10.11
9/2/2016
10.12#
Employment Agreement, dated May 25, 2016, by
and among Fulgent Therapeutics LLC, the registrant
and Paul Kim.
S-1
333-213469
10.12
9/2/2016
10.13#
Amended and Restated Employment Agreement,
dated May 25, 2016, by and among Fulgent
Therapeutics LLC, the registrant and Han Lin Gao.
S-1
333-213469
10.13
9/2/2016
10.14#
Severance Agreement, dated July 7, 2016, by and
among Fulgent Therapeutics LLC, the registrant and
Ming Hsieh.
S-1
333-213469
10.14
9/2/2016
10.15#
Severance Agreement, dated July 7, 2016, by and
among Fulgent Therapeutics LLC, the registrant and
Paul Kim.
S-1
333-213469
10.15
9/2/2016
10.16#
Severance Agreement, dated July 7, 2016, by and
among Fulgent Therapeutics LLC, the registrant and
Han Lin Gao.
S-1
333-213469
10.16
9/2/2016
10.17
Contribution and Allocation Agreement, dated May
19, 2016, by and among Fulgent Therapeutics LLC,
Fulgent Pharma LLC and Ming Hsieh.
S-1
333-213469
10.17
9/2/2016
10.18
Form of Fourth Amended and Restated Operating
Agreement of Fulgent Therapeutics LLC, to be in
effect upon completion of the Reorganization.
S-1/A
333-213469
2.1
9/19/2016
10.19
Director Compensation Program of the registrant,
effective as of September 28, 2016 and amended
November 2, 2017.
10-K
001-37894
10.20
3/20/2018
93
Exhibit
Number
Description
Form
File Number
Incorporated by
Reference Exhibit
Filing Date
Filed
Herewith
10.20§
Cooperation Agreement on the Establishment of
Fujian Fujun Gene Biotech Co., Ltd., dated April 25,
2017, by and among Shenzhen Fujin Gene Science &
Technology Co., Ltd., Xilong Scientific Co., Ltd.
and Fuzhou Jinqiang Investment Partnership (LP).
10-Q
001-37894
10.1
8/14/2017
10.21
Fulgent Genetics, Inc. Amended and Restated 2016
Omnibus Incentive Plan.
8-K
001-37894
10.1
5/21/2018
10.22
Fulgent Genetics, Inc. Amended and Restated 2016
Omnibus Incentive Plan.
8-K
001-37894
10.1
9/18/2020
10.23^
Agreement for Purchase and Sale of Property, dated
July 23, 2020, by and between the registrant and
4401 Santa Anita Corporation.
8-K
001-37894
2.1
10/21/2020
10.24#
Employment Agreement, dated March 8, 2021, by
and among Fulgent Therapeutics, LLC, Fulgent
Genetics, Inc. and Jian Xie.
10-K
001-37894
10.37
3/8/2021
10.25#
Severance Agreement, dated March 8, 2021, by and
among Fulgent Therapeutics LLC, Fulgent Genetics,
Inc. and Jian Xie.
10-K
001-37894
10.38
3/8/2021
10.26#^
Amended and Restated Non-Employee Director
Compensation Policy.
10-Q
001-37894
10.1
5/7/2021
10.27§
Restructuring Agreement of Fujian Fujun Gene
Biotech Co., Ltd.
10-Q
001-37894
10.1
8/10/2021
10.28#
Fulgent Genetics, Inc. Incentive Compensation
Recoupment Policy.
8-K
001-37894
10.1
3/29/2022
10.29
Agreement and Plan of Merger, dated as of April 16,
2022, by and among Fulgent Therapeutics LLC,
solely for purpose of Section 6.20, Fulgent Genetics,
Inc., Ducks Acquisition Sub, Inc., Symphony Buyer,
Inc., solely in its capacity as the representative of
Symphony’s securityholders, Avista Capital Partners
IV GP, L.P. and solely for purposes of Section 6.21,
Article VIII and Section 10.14, those company
stockholders set forth on the signature page thereto.
8-K
001-37894
2.1
4/26/2022
10.30#
Amended and Restated Director Compensation
Program of the registrant, dated as of August 1,
2022.
10-Q
001-37894
10.1
11/7/2022
10.31#
Form of Notice of Restricted Stock Unit Award and
Restricted Stock Unit Agreement under the Fulgent
Pharma Holdings, Inc. 2022 Omnibus Incentive Plan.
10-Q
001-37894
10.2
11/7/2022
10.32^
Agreement and Plan of Merger, dated November 7,
2022 by and among Fulgent Genetics, FG Merger
Sub, Inc., Fulgent Pharma Holdings, Inc. and solely
for purposes of Section 2.4, Section 5.5, Article VI,
Section 7.8 and Section 7.14, those company
stockholders set forth on the signature page thereto.
10-Q
001-37894
10.3
11/7/2022
10.33
Rule 10b5-1 Issuer Repurchase Plan, dated
December 12, 2023, by and between Fulgent
Genetics, Inc. and Piper Sandler & Co.
10-K
001-37894
10.41
2/28/2024
10.34^
Second Amendment to Lease Agreement, July 1,
2020 by and between Inform Diagnostics, Inc., p/k/a/
Miraca Life Sciences, Inc. and WPT Land 2 LP.
10-K
001-37894
10.48
2/28/2023
10.35
Lease Agreement of Premises at 15-19 Crawford
Street Needham, Massachusetts, by and between
Inform Diagnostics and Crawford Street DE, LLC.
10-K
001-37894
10.51
2/28/2023
10.36#
Fulgent Pharma Holdings, Inc. 2022 Omnibus
Incentive Plan.
10-K
001-37894
10.52
2/28/2023
10.37*^#
Amended and Restated Director Compensation
Program of the registrant.
10-Q
001-37894
10.1
5/5/2023
10.38
Executive Officer Incentive Plan of the registrant.
10-Q
001-37894
10.3
5/5/2023
10.39
Amended and Restated 2016 Omnibus Incentive
Plan of the registrant.
8-K
001-37894
10.1
5//18/2023
10.40^#
Amended and Restated Executive Officer Incentive
Plan of the registrant.
10-Q
001-37894
10.2
11/3/2023
19.1
Insider Trading Policy.
X
21.1
Subsidiaries of the registrant.
X
23.1
Consent of Deloitte & Touche LLP, independent
registered public accounting firm, relating to the
financial statements of the registrant.
X
24.1
Power of Attorney (included on the signature page
hereto).
X
94
Exhibit
Number
Description
Form
File Number
Incorporated by
Reference Exhibit
Filing Date
Filed
Herewith
31.1
Certification of Principal Executive Officer pursuant
to Rules 13a-14(a) and 15d-14(a) under the
Securities Exchange Act of 1934, as adopted
pursuant to Section 302 of the Sarbanes-Oxley Act
of 2002.
X
31.2
Certification of Principal Financial Officer pursuant
to Rules 13a-14(a) and 15d-14(a) under the
Securities Exchange Act of 1934, as adopted
pursuant to Section 302 of the Sarbanes-Oxley Act
of 2002.
X
32.1*
Certification of Principal Executive Officer and
Principal Financial Officer pursuant to 18 U.S.C.
Section 1350, as adopted pursuant to Section 906 of
the Sarbanes-Oxley Act of 2002.
X
97.1^#
Amended and Restated Incentive Compensation
Recoupment Policy of the registrant.
10-Q
001-37894
10.1
11/3/2023
101.INS
Inline XBRL Instance Document – the instance
document does not appear in
the Interactive Data File because XBRL tags are
embedded within the Inline
XBRL document.
X
101.SCH
Inline XBRL Taxonomy Extension Schema
Document.
X
101.CAL
Inline XBRL Taxonomy Extension Calculation
Linkbase Document.
X
101.DEF
Inline XBRL Taxonomy Extension Definition
Linkbase Document.
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101.LAB
Inline XBRL Taxonomy Extension Label Linkbase
Document.
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101.PRE
Inline XBRL Taxonomy Extension Presentation
Linkbase Document.
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Cover Page Interactive Data File (embedded within
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* This certification is being furnished solely to accompany this report pursuant to 18 U.S.C. 1350, and are not being filed for purposes of Section 18 of the Securities
Exchange Act of 1934, as amended, and is not to be incorporated by reference into any filing of the registrant, whether made before or after the date hereof, regardless
of any general incorporation by reference language in such filing.
# Management contract or compensatory plan, contract or arrangement.
§ Confidential treatment has been granted with respect to portions of this exhibit pursuant to Rule 24b-2 under the Exchange Act, and these confidential portions have
been redacted from the version of this agreement that is incorporated by reference in this report. A complete copy of this exhibit, including the redacted portions, has
been separately furnished to the SEC.
^ Certain exhibits and schedules have been omitted pursuant to Item 601(a)(5) of Regulation S-K. The Company hereby undertakes to furnish supplementally a copy of
any omitted exhibit or schedule upon request by the SEC.
95
SIGNATURES
Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, as amended, the registrant has duly
caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
FULGENT GENETICS, INC.
Date: February 28, 2025
By:
/s/ Ming Hsieh
Ming Hsieh
Chief Executive Officer
POWER OF ATTORNEY
IN WITNESS WHEREOF, each person whose signature appears below constitutes and appoints Ming Hsieh and Paul Kim as
his or her true and lawful agent, proxy and attorney-in-fact, each acting alone, with full power of substitution and resubstitution, for
him or her and in his or her name, place and stead, in any and all capacities, to (i) act on and sign any amendments to this report, with
exhibits thereto and other documents in connection therewith, (ii) act on and sign such certificates, instruments, agreements and other
documents as may be necessary or appropriate in connection therewith, and in each case file the same with the SEC, hereby
approving, ratifying and confirming all that such agent, proxy and attorney-in-fact or any of his substitutes may lawfully do or cause
to be done by virtue thereof.
Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, this report has been signed below by the
following persons on behalf of the registrant in the capacities and on the dates indicated.
Name and Signature
Title
Date
/s/ Ming Hsieh
Chief Executive Officer and Chairman of the Board
February 28, 2025
Ming Hsieh
(principal executive officer)
/s/ Paul Kim
Chief Financial Officer
February 28, 2025
Paul Kim
(principal financial and accounting officer)
/s/ Michael Nohaile
Director
February 28, 2025
Michael Nohaile
/s/ Regina Groves
Director
February 28, 2025
Regina Groves
/s/ Linda Marsh
Director
February 28, 2025
Linda Marsh
F-1
INDEX TO CONSOLIDATED FINANCIAL STATEMENTS
Report of Independent Registered Public Accounting Firm (PCAOB ID: 34)
F-2
Consolidated Balance Sheets as of December 31, 2024 and 2023
F-5
Consolidated Statements of Operations for the Years Ended December 31, 2024, 2023, and 2022
F-6
Consolidated Statements of Comprehensive Income (Loss) for the Years Ended December 31, 2024, 2023, and 2022
F-7
Consolidated Statements of Stockholders’ Equity for the Years Ended December 31, 2024, 2023, and 2022
F-8
Consolidated Statements of Cash Flows for the Years Ended December 31, 2024, 2023, and 2022
F-9
Notes to Consolidated Financial Statements
F-10
F-2
REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM
To the shareholders and the Board of Directors of Fulgent Genetics, Inc.
Opinion on the Financial Statements
We have audited the accompanying consolidated balance sheets of Fulgent Genetics, Inc., and subsidiaries (the “Company”) as of
December 31, 2024, and 2023, the related consolidated statements of operations, comprehensive income (loss), stockholders' equity,
and cash flows, for each of the three years in the period ended December 31, 2024, and the related notes (collectively referred to as the
“financial statements”). In our opinion, the financial statements present fairly, in all material respects, the financial position of the
Company as of December 31, 2024, and 2023, and the results of its operations and its cash flows for each of the three years in the
period ended December 31, 2024, in conformity with accounting principles generally accepted in the United States of America.
We have also audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States)
(PCAOB), the Company's internal control over financial reporting as of December 31, 2024, based on criteria established in Internal
Control – Integrated Framework (2013) issued by the Committee of Sponsoring Organizations of the Treadway Commission and our
report dated February 28, 2025, expressed an unqualified opinion on the Company's internal control over financial reporting.
Basis for Opinion
These financial statements are the responsibility of the Company’s management. Our responsibility is to express an opinion on the
Company’s financial statements based on our audits. We are a public accounting firm registered with the PCAOB and are required to
be independent with respect to the Company in accordance with the U.S. federal securities laws and the applicable rules and
regulations of the Securities and Exchange Commission and the PCAOB.
We conducted our audits in accordance with the standards of the PCAOB. Those standards require that we plan and perform the audit
to obtain reasonable assurance about whether the financial statements are free of material misstatement, whether due to error or fraud.
Our audits included performing procedures to assess the risks of material misstatement of the financial statements, whether due to
error or fraud, and performing procedures that respond to those risks. Such procedures included examining, on a test basis, evidence
regarding the amounts and disclosures in the financial statements. Our audits also included evaluating the accounting principles used
and significant estimates made by management, as well as evaluating the overall presentation of the financial statements. We believe
that our audits provide a reasonable basis for our opinion.
Critical Audit Matters
The critical audit matters communicated below are matters arising from the current-period audit of the financial statements that were
communicated or required to be communicated to the audit committee and that (1) relate to accounts or disclosures that are material to
the financial statements and (2) involved our especially challenging, subjective, or complex judgments. The communication of critical
audit matters does not alter in any way our opinion on the financial statements, taken as a whole, and we are not, by communicating
the critical audit matters below, providing separate opinions on the critical audit matters or on the accounts or disclosures to which
they relate.
Goodwill – Therapeutic Development Reporting Unit – Refer to Notes 2 and 17 to the financial statements
Critical Audit Matter Description
The Company’s evaluation of goodwill for impairment involves the comparison of the fair value of the reporting unit to its carrying
value. The Company used the discounted cash flow model to estimate fair value, which requires management to make significant
estimates and assumptions related to discount rates, forecasts of future revenues and EBITDA (defined as earnings before interest,
income taxes, depreciation and amortization) margin, as well as probability and timing of commercial success. Changes in these
assumptions could have a significant impact on either the fair value, the amount of any goodwill impairment charge, or both. The
goodwill balance was $22.1 million as of December 31, 2024. The fair value of the Therapeutic Development Reporting Unit
exceeded its carrying value by 268% as of the measurement date and, therefore, no impairment was recognized as of December 31,
2024.
We identified goodwill as a critical audit matter because of the significant judgments made by management to estimate the fair value
of the reporting unit. This required a high degree of auditor judgment and an increased extent of effort, including the need to involve
professionals in our firm having fair value expertise when performing audit procedures to evaluate the reasonableness of
management’s estimates and assumptions related to selection of the discount rate.
How the Critical Audit Matter Was Addressed in the Audit
F-3
Our audit procedures related to the discount rate and forecasts used by management to estimate the fair value of the Therapeutic
Development Reporting Unit included the following, among others:
•
We tested the effectiveness of controls over management’s goodwill impairment evaluation, including those over the
determination of the fair value of the reporting unit, such as controls related to management’s selection of the discount
rate, forecasts of future revenue and EBITDA margin, and the probability and timing of commercial success.
•
We evaluated management’s ability to accurately forecast timing of commercial success by comparing actual milestones
achieved to milestone assumptions in management’s historical forecast.
•
We evaluated the reasonableness of management’s forecasts of future revenue and EBITDA margin, including the
probability and timing of commercial success by comparing the forecasts with:
o
Internal communications to management and the Board of Directors.
o
Forecasted information included in Company press releases as well as in analyst and industry reports for the
Company and certain of its peer companies.
o
Relevant regulatory approvals supporting timing of commercial success.
•
With the assistance of professionals in our firm having fair value expertise, we evaluated the reasonableness of the (1)
valuation methodology and (2) discount rate by:
o
Testing the source information underlying the determination of the discount rate and the mathematical accuracy of
the calculation.
o
Developing a range of independent estimates and comparing those to the discount rate selected by management.
Intangible Assets – IPR&D – Refer to Notes 2 and 17 to the financial statements
Critical Audit Matter Description
The Company has in-process research & development (“IPR&D”) that are indefinite-lived intangible assets. As of December 31,
2024, the carrying value of the IPR&D is $64.6 million. Management estimates the fair value of IPR&D annually on its elected
assessment date of December 31, 2024, using a multi-period excess earnings method, which is a specific discounted cash flow
method. The determination of the fair value requires management to make significant estimates and assumptions related to discount
rates, forecasts of future revenues and EBITDA margin, as well as probability and timing of commercial success. Changes in these
assumptions could have a significant impact on the fair value of IPR&D and a significant change in fair value could cause a significant
impairment. The fair value of the IPR&D exceeded its carrying value by 214% as of the measurement date and therefore, no
impairment was recognized as of December 31, 2024.
We identified the IPR&D as a critical audit matter because of the significant judgments made by management to estimate its fair
value. This required a high degree of auditor judgment and an increased extent of effort, including the need to involve professionals in
our firm having fair value expertise when performing audit procedures to evaluate the reasonableness of management’s estimates and
assumptions related to selection of the discount rate.
How the Critical Audit Matter Was Addressed in the Audit
Our audit procedures related to the discount rate and forecasts used by management to estimate the fair value of IPR&D included the
following, among others:
•
We tested the effectiveness of controls over management’s intangible asset impairment evaluation, including those over
the determination of the IPR&D, such as controls related to management’s selection of the discount rate, forecasts of
future revenue, EBITDA margin, and the probability and timing of commercial success.
•
We evaluated management’s ability to accurately forecast timing of commercial success by comparing actual milestones
achieved to milestone assumptions in management’s historical forecast.
•
We evaluated the reasonableness of management’s forecasts of future revenue and EBITDA margin, including the
probability and timing of commercial success by comparing the forecasts with:
o
Internal communications to management and the Board of Directors.
o
Forecasted information included in Company press releases as well as in industry reports and external studies.
o
Relevant regulatory approvals supporting timing of commercial success.
F-4
•
With the assistance of professionals in our firm having fair value expertise, we evaluated the reasonableness of the (1)
valuation methodology and (2) of the discount rates by:
o
Testing the source information underlying the determination of the discount rate and the mathematical accuracy of
the calculation.
o
Developing a range of independent estimates and comparing those to the discount rate selected by management.
/s/ DELOITTE & TOUCHE LLP
Los Angeles, California
February 28, 2025
We have served as the Company’s auditor since 2016.
F-5
CONSOLIDATED FINANCIAL STATEMENTS
FULGENT GENETICS, INC.
Consolidated Balance Sheets
(in thousands, except par value data)
December 31, 2024
December 31, 2023
Assets
Current assets
Cash and cash equivalents
$
55,144
$
97,473
Marketable securities
202,962
326,681
Trade accounts receivable, net of allowance for credit losses of $20,458 and
$25,226
69,021
51,132
Other current assets
26,444
32,559
Total current assets
353,571
507,845
Marketable securities, long-term
570,351
423,571
Intangible assets, net
134,978
143,053
Fixed assets, net
105,549
83,464
Goodwill
22,055
22,055
Redeemable preferred stock investment
—
20,438
Other long-term assets
33,460
34,902
Total assets
$
1,219,964
$
1,235,328
Liabilities and Stockholders’ Equity
Current liabilities
Accounts payable
$
18,364
$
15,360
Accrued liabilities
24,279
30,737
Customer deposit
27,610
22,700
Contract liabilities
2,234
2,874
Notes payable, current portion
412
1,183
Other current liabilities
—
164
Total current liabilities
72,899
73,018
Deferred tax liabilities
6,370
7,962
Unrecognized tax benefits
4,563
5,978
Other long-term liabilities
6,973
15,084
Total liabilities
90,805
102,042
Commitments and contingencies (Note 8)
Stockholders’ equity
Common stock, $0.0001 par value per share, 50,000 shares authorized, 33,614
shares issued and 30,841 shares outstanding, and 32,416 shares issued and 29,653
shares outstanding
3
3
Preferred stock, $0.0001 par value per share, 1,000 shares authorized, no shares
issued or outstanding
—
—
Additional paid-in capital
543,126
501,718
Accumulated other comprehensive (loss) income
(368)
1,205
Retained earnings
590,467
633,175
Total Fulgent stockholders’ equity
1,133,228
1,136,101
Noncontrolling interest
(4,069)
(2,815)
Total stockholders’ equity
1,129,159
1,133,286
Total liabilities and stockholders’ equity
$
1,219,964
$
1,235,328
The accompanying notes are an integral part of these consolidated financial statements.
F-6
CONSOLIDATED FINANCIAL STATEMENTS
FULGENT GENETICS, INC.
Consolidated Statements of Operations
(in thousands, except per share)
Year Ended December 31,
2024
2023
2022
Revenue
$
283,470
$
289,213
$
618,968
Cost of revenue
176,255
184,757
252,067
Gross profit
107,215
104,456
366,901
Operating expenses:
Research and development
48,816
41,440
28,910
Selling and marketing
36,246
41,467
38,918
General and administrative
88,106
88,999
111,074
Amortization of intangible assets
7,965
7,845
6,497
Goodwill impairment loss
—
120,234
—
Restructuring costs
—
—
2,975
Total operating expenses
181,133
299,985
188,374
Operating (loss) income
(73,918)
(195,529)
178,527
Other income (expenses):
Interest income
31,304
21,612
5,624
Interest expense
170
(488)
(1,013)
Impairment of available-for-sale debt securities
(10,073)
—
—
Other income, net
561
320
887
Total other income, net
21,962
21,444
5,498
(Loss) income before income taxes
(51,956)
(174,085)
184,025
(Benefit from) provision for income taxes
(8,136)
1,154
42,102
Net (loss) income from consolidated operations
(43,820)
(175,239)
141,923
Net loss attributable to noncontrolling interests
1,112
7,414
1,480
Net (loss) income attributable to Fulgent
$
(42,708)
$
(167,825)
$
143,403
Net (loss) income per common share attributable to Fulgent:
Basic
$
(1.41)
$
(5.63)
$
4.76
Diluted
$
(1.41)
$
(5.63)
$
4.63
Weighted-average common shares:
Basic
30,235
29,784
30,097
Diluted
30,235
29,784
30,964
The accompanying notes are an integral part of these consolidated financial statements.
F-7
FULGENT GENETICS, INC.
Consolidated Statements of Comprehensive Income (Loss)
(in thousands)
Year Ended December 31,
2024
2023
2022
Net (loss) income from consolidated operations
$
(43,820)
$
(175,239)
$
141,923
Other comprehensive (loss) income
Foreign currency translation loss
(511)
(1,200)
(2,665)
Net (loss) income on available-for-sale debt securities, net of tax
(1,204)
24,717
(19,940)
Net comprehensive (loss) income from consolidated operations
(45,535)
(151,722)
119,318
Net loss attributable to noncontrolling interest
1,112
7,414
1,480
Foreign currency translation loss (gain) attributable to noncontrolling
interest
142
(1,409)
2,461
Comprehensive loss attributable to noncontrolling interest
1,254
6,005
3,941
Comprehensive (loss) income attributable to Fulgent
$
(44,281)
$
(145,717)
$
123,259
The accompanying notes are an integral part of these consolidated financial statements.
F-8
FULGENT GENETICS, INC.
Consolidated Statements of Stockholders’ Equity
(in thousands)
Fulgent
Stockholders’ Equity
Shares
Amount
Additional
Paid-In
Capital
Accumulated
Other
Comprehensive
(Loss) Income
Retained
Earnings
Fulgent
Stockholders’
Equity
Noncontrolling
Interest
Total
Equity
Balance at January 1, 2022
30,160
$
3 $ 501,908 $
(759) $ 657,597 $ 1,158,749
$
7,131
$ 1,165,880
Equity-based compensation
—
—
32,640
—
—
32,640
—
32,640
Exercise of common stock options
5
—
31
—
—
31
—
31
Restricted stock awards
699
—
—
—
—
—
—
—
Common stock withholding for
employee tax obligations
(32)
—
(1,768)
—
—
(1,768)
—
(1,768)
Repurchase of common stock
(1,810)
—
(74,337)
—
—
(74,337)
—
(74,337)
Common stock issued in a business
combination (1)
416
—
28,111
—
—
28,111
—
28,111
Other comprehensive loss, net
—
—
—
(20,144)
—
(20,144)
(2,461)
(22,605)
Net income (loss)
—
—
—
—
143,403
143,403
(1,480)
141,923
Balance at December 31, 2022
29,438
$
3 $ 486,585 $
(20,903) $ 801,000 $ 1,266,685
$
3,190
$ 1,269,875
Equity-based compensation
—
—
42,922
—
—
42,922
—
42,922
Exercise of common stock options
9
—
3
—
—
3
—
3
Restricted stock awards
1,066
—
—
—
—
—
—
—
Common stock withholding for
employee tax obligations
(93)
—
(2,732)
—
—
(2,732)
—
(2,732)
Repurchase of common stock
(953)
—
(25,060)
—
—
(25,060)
—
(25,060)
Common stock issued in a business
combination (1)
186
—
—
—
—
—
—
—
Other comprehensive income, net
—
—
—
22,108
—
22,108
1,409
23,517
Net loss
—
—
—
—
(167,825)
(167,825)
(7,414)
(175,239)
Balance at December 31, 2023
29,653
$
3 $ 501,718 $
1,205
$ 633,175 $ 1,136,101
$
(2,815) $ 1,133,286
Equity-based compensation
—
—
44,481
—
—
44,481
—
44,481
Exercise of common stock options
133
—
51
—
—
51
—
51
Restricted stock awards
1,004
—
—
—
—
—
—
—
Common stock withholding for
employee tax obligations
(125)
—
(2,899)
—
—
(2,899)
—
(2,899)
Repurchase of common stock
(10)
—
(225)
—
—
(225)
—
(225)
Common stock issued in a business
combination (1)
186
—
—
—
—
—
—
—
Other comprehensive loss, net
—
—
—
(1,573)
—
(1,573)
(142)
(1,715)
Net loss
—
—
—
—
(42,708)
(42,708)
(1,112)
(43,820)
Balance at December 31, 2024
30,841
$
3 $ 543,126 $
(368) $ 590,467 $ 1,133,228
$
(4,069) $ 1,129,159
(1) As of December 31, 2022, 371,000 shares of the Company’s common stock were not issued and heldback by the Company as partial security for the
indemnification obligations in connection with the business combination of Fulgent Pharma Holdings, Inc., or Fulgent Pharma, in 2022. 186,000 shares were issued in
November 2023, and the remainder were issued in May 2024 by the Company upon expiration of hold back provisions.
The accompanying notes are an integral part of these consolidated financial statements.
F-9
FULGENT GENETICS, INC.
Consolidated Statements of Cash Flows
(in thousands)
Year Ended December 31,
2024
2023
2022
Cash flow from operating activities
Net (loss) income from consolidated operations
$
(43,820)
$
(175,239)
$
141,923
Adjustments to reconcile net (loss) income to net cash provided by operating activities:
Goodwill impairment loss
—
120,234
—
Equity-based compensation
44,481
42,922
32,640
Depreciation and amortization
24,928
26,143
32,662
(Adjustment) provision for credit losses
(1,730)
(880)
32,596
Noncash lease expense
3,760
6,412
4,913
Loss on disposal of fixed asset
320
305
502
Amortization of (discount) premium of marketable securities
(5,550)
(3,911)
4,767
Deferred taxes
(3,736)
11,466
(8,280)
Unrecognized tax benefits
(1,414)
(3,858)
9,111
Net realized loss on marketable securities
994
589
692
Impairment of available-for-sale debt securities
10,073
—
—
Other
(7)
(21)
(11)
Changes in operating assets and liabilities:
Trade accounts receivable
(16,303)
2,388
68,638
Income tax
9,253
2,759
(14,544)
Other current and long-term assets
199
(3,331)
9,380
Accounts payable
3,066
(6,896)
(25,339)
Contract liabilities
(639)
(325)
(11,497)
Customer deposits
4,917
11,815
(8,887)
Accrued liabilities and other liabilities
(3,961)
2,718
(10,915)
Operating lease liabilities
(3,771)
(6,287)
(4,831)
Net cash provided by operating activities
21,060
27,003
253,520
Cash flow from investing activities
Purchase of marketable securities
(472,415)
(491,914)
(417,982)
Purchases of fixed assets
(40,315)
(22,207)
(18,775)
Purchase of preferred stock of privately held company
—
—
(15,000)
Contingent consideration payout related to a business acquisition
—
—
(10,000)
Maturities of marketable securities
349,795
508,558
232,534
Proceeds from sale of marketable securities
104,270
44,085
140,176
Proceeds from sale of fixed assets
313
775
412
Acquisition of businesses, net of cash acquired
—
(399)
(172,679)
Net cash (used in) provided by investing activities
(58,352)
38,898
(261,314)
Cash flow from financing activities
Common stock withholding for employee tax obligations
(2,899)
(2,732)
(1,768)
Repayment of notes payable
(1,230)
(4,266)
(367)
Principal paid for finance lease
(544)
(730)
(700)
Repurchase of common stock
(225)
(25,060)
(74,337)
Repayment of investment margin loan
—
(15,000)
—
Proceeds from exercise of stock options
51
3
31
Net cash used in financing activities
(4,847)
(47,785)
(77,141)
Effect of exchange rate changes on cash and cash equivalents
(55)
(149)
(453)
Net (decrease) increase in cash, cash equivalents, and restricted cash
(42,194)
17,967
(85,388)
Cash, cash equivalents, and restricted cash at beginning of period
97,473
79,506
164,894
Cash, cash equivalents, and restricted cash at end of period
$
55,279
$
97,473
$
79,506
Supplemental disclosures of cash flow information
Cash and cash equivalents
$
55,144
$
97,473
$
79,506
Restricted cash
135
—
—
Total cash, cash equivalents, and restricted cash
$
55,279
$
97,473
$
79,506
Income taxes paid
$
27,588
$
3,261
$
56,193
Interest Paid
$
512
$
960
$
—
Supplemental disclosures of non-cash investing and financing activities
Stock consideration in a business combination
$
—
$
—
$
28,111
Maturities of marketable securities in ither current assets
$
—
$
—
$
19,120
Purchases of fixed assets in notes payable
$
—
$
—
$
3,833
Purchases of fixed assets in accounts payable
$
1,806
$
1,799
$
2,989
Finance lease right-of-use assets obtained in exchange for lease liabilities
$
—
$
—
$
573
Operating lease right-of-use assets obtained in exchange for lease liabilities
$
1,158
$
2,661
$
52
Operating lease right-of-use assets reduced due to lease modification and termination
$
57
$
142
$
66
Operating lease liabilities removed due to purchasing underlying assets
$
2,799
$
—
$
—
Finance lease right-of-use assets reduced due to lease modification and termination
$
—
$
696
$
—
The accompanying notes are an integral part of these consolidated financial statements.
F-10
FULGENT GENETICS, INC.
Notes to Consolidated Financial Statements
Note 1. Overview and Basis of Presentation
The accompanying consolidated financial statements have been prepared in accordance with accounting principles generally
accepted in the United States, or U.S. GAAP. These financial statements include the assets, liabilities, revenues and expenses of all
subsidiaries and entities in which the Company has a controlling financial interest or is deemed to be the primary beneficiary. In
determining whether the Company is the primary beneficiary of an entity, the Company applies a qualitative approach that determines
whether it has both (i) the power to direct the economically significant activities of the entity and (ii) the obligation to absorb losses of,
or the right to receive benefits from, the entity that could potentially be significant to that entity. The Company uses the equity method
to account for its investments in entities that it does not control, but in which it has the ability to exercise significant influence over
operating and financial policies. All intercompany accounts and transactions are eliminated from the accompanying consolidated
financial statements.
Nature of the Business
Fulgent Genetics, Inc., together with its subsidiaries and affiliated professional corporations, or PCs (collectively referred to as
the Company, unless otherwise noted or the context otherwise requires), is a technology-based company with a well-established
laboratory services business and a therapeutic development business. Its laboratory services business includes technical laboratory and
testing services and professional interpretation of laboratory results by licensed physicians. Its therapeutic development business is
focused on developing drug candidates for treating a broad range of cancers using a novel nanoencapsulation and targeted therapy
platform designed to improve the therapeutic window and pharmacokinetic profile of new and existing cancer drugs. The Company
aims to transform from a genomic diagnostic business into a fully integrated precision medicine company.
Note 2. Summary of Significant Accounting Policies
Use of Estimates
The preparation of consolidated financial statements in conformity with U.S. GAAP requires management to make certain
estimates, judgments and assumptions that affect the reported amounts of assets and liabilities at the date of the financial statements,
as well as the reported amounts of revenue and expenses during the reporting periods. These estimates, judgments, and assumptions
are based on historical data and experience available at the date of the accompanying consolidated financial statements, as well as
various other factors management believes to be reasonable under the circumstances. The Company’s estimates and assumptions may
evolve as conditions change. Actual results could differ significantly from these estimates.
On an on-going basis, management evaluates its estimates, primarily those related to: (i) revenue recognition criteria, (ii)
accounts receivable and allowances for credit losses, (iii) the useful lives of fixed assets and intangible assets, (iv) estimates of tax
liabilities, (v) valuation of goodwill and indefinite-lived intangible assets at time of acquisition and on a recurring basis, and (vi)
valuation of investments.
Principles of Consolidation
The accompanying consolidated financial statements include the accounts of the Company. All intercompany transactions and
balances have been eliminated in consolidation.
Cash and Cash Equivalents
The Company considers all highly liquid investments with original maturities of three months or less at the date of purchase to
be cash equivalents. Cash and cash equivalents include cash held in banks and money market accounts. Cash equivalents are stated at
fair value.
Restricted Cash
Restricted cash consists of legally restricted deposits held in conjunction with a lease contract the Company entered into with a
third-party landlord. A bank guarantee equivalent to six months of gross rent plus tax with an expiry date three months post the lease
expiry is required under the lease contract, and the lease contract will expire in March 2034. Restricted deposit is recorded in other
long-term assets in the Company’s Consolidated Balance Sheets as the balance is not expected to be released to cash within the next
12 months. As of December 31, 2024, the Company had restricted cash of $0.1 million. The Company did not have restricted cash as
of December 31, 2023.
F-11
Marketable Securities
All marketable debt securities, which consist of U.S. government and agency debt securities, U.S. treasury bills, corporate debt
securities, municipal bonds, and Yankee debt securities issued by foreign governments or entities and denominated in U.S. dollars
have been classified as “available-for-sale,” and are carried at fair value. Net unrealized gains and losses, net of any related tax effects,
are excluded from earnings and are included in other comprehensive income (loss) and reported as a separate component of
stockholders’ equity until realized. Realized gains and losses on marketable debt securities are included in interest income, in the
accompanying Consolidated Statements of Operations. The cost of any marketable debt securities sold is based on the specific-
identification method. The amortized cost of marketable debt securities is adjusted for amortization of premiums and accretion of
discounts to maturity. Interest on marketable debt securities is included in interest income. In accordance with the Company’s
investment policy, management invests to diversify credit risk and only invests in securities with high credit quality, including U.S.
government securities.
The Company’s investments in marketable equity securities are measured at fair value with the related gains and losses, realized
and unrealized, recognized in interest income, in the accompanying Consolidated Statements of Operations. The cost of any
marketable equity securities sold is based on the specific-identification method.
For available-for-sale debt securities, in an unrealized loss, the Company determines whether a credit loss exists. The credit loss
is estimated by considering available information relevant to the collectability of the security and information about past events,
current conditions, and reasonable and supportable forecasts. The Company compares the present value of cash flows expected to be
collected from the security with the amortized cost basis of the security. If the present value of cash flows to be collected is less than
the amortized basis of the security, a credit loss exists, and an allowance for credit losses is recorded for the credit loss, limited by the
amount of unrealized loss. Changes in the allowance are recorded in the period of changes as credit loss expense. If the Company has
an intent to sell, or if it is more likely than not that the Company will be required to sell a debt security in an unrealized loss position
before recovery of its amortized cost basis, the Company will write down the security to its fair value and record the corresponding
charge as a component of other income, net.
Trade Accounts Receivable and Allowance for Credit Losses
Trade accounts receivable are stated at the amount the Company expects to collect. The Company maintains an allowance for
credit losses for expected uncollectible trade accounts receivable, which is recorded as an offset to trade accounts receivable, and
changes in allowance for credit losses are classified as a general and administrative expense in the accompanying Consolidated
Statements of Operations. The Company assesses collectability by reviewing trade accounts receivable on a collective basis where
similar risk characteristics exist and on an individual basis when it identifies specific customers that have deterioration in credit
quality such that they may no longer share similar risk characteristics with the other receivables. In determining the amount of the
allowance for credit losses, the Company uses a loss rate model or probability-of-default and loss given default model. Following the
loss rate method, expected credit losses are determined based on an estimated historical loss rate. The probability of default method
allows the ability to define a point of default and measure credit losses for receivables that have reached the point of default for
purposes of calculating the allowance for credit losses. Loss given default represents the likelihood that a receivable that has reached
the point of default will not be collected in full. The Company updates its loss rate and factors annually to incorporate the most recent
historical data and adjusts the quantitative portion of the reserve through its qualitative reserve overlay. The Company looks at
qualitative factors such as general economic conditions in determining expected credit losses.
A roll-forward of the activity in the Company’s allowance for credit losses is as follows:
2024
2023
2022
(in thousands)
Allowance for credit losses at beginning of year
$
25,226
$
41,205
$
11,217
Current period (gain) provision
(1,730)
(880)
32,596
Write-downs
(11,155)
(15,099)
(2,608)
Recoveries of amounts previously charged off
8,117
—
—
Allowance for credit losses at end of year
$
20,458
$
25,226
$
41,205
Preferred Stock Investment
The redeemable preferred stock investment of $20.4 million as of December 31, 2023, represents the fair value of the 7.3
million shares of preferred stock of a privately-held, Cayman Islands company, Laboratory for Advanced Medicine, Inc., or LAMH,
doing business as “Helio Health” that the Company purchased in July 2021. Helio Health is an AI-biotechnology company developing
blood-based early cancer detection tests, and the Company expected to gain access to an emerging liquid biopsy testing technology,
F-12
through this strategic partnership. As the preferred stock had the option to be redeemed, the investment was initially recorded as
available-for-sale debt securities with changes in fair value recorded in other comprehensive income (loss).
On June 19, 2024, the Board of Directors of LAMH approved to spin out certain U.S.-based laboratory and development
operations into a separate, privately-held Delaware corporation, Helio Genomics, Inc., or Helio Genomics. The Company received 7.3
million shares of preferred stock of Helio Genomics in connection with this spin-out.
Post spin-out, Helio Genomics amended and restated its certificate of incorporation on July 25, 2024, which resulted in a change
in stockholder’s rights where the Company no longer holds the right to redeem its preferred stock of Helio Genomics. As a result, the
Company reclassified $0.4 million unrealized gain out of accumulated other comprehensive income (loss) to net income (loss) in the
consolidated financial statements. The Company elected to record its preferred stock investment in Helio Genomics under the
measurement alternative in accordance with ASC 321, defined as cost less impairment, adjusted for subsequent observable price
changes and are periodically assessed for impairment when events or circumstances indicate that a decline in value may have
occurred. As of July 25, 2024, the preferred stock investment carrying value of $9.9 million was recorded as other long-term assets in
the Consolidated Balance Sheets. No impairment loss was recorded as of December 31, 2024.
Post spin-out, the Company retained the original right to redeem its LAMH preferred stock. As the preferred stock had the
option to be redeemed, the investment was recorded as available-for-sale debt securities with changes in fair value recorded in other
comprehensive income (loss). The Company considered a number of factors including, but not limited to: (i) the extent to which the
fair value of the investment is less than its amortized cost; (ii) the financial condition and near-term prospects of the investee, and (iii)
general market conditions. As a result, the Company recognized a $10.1 million credit loss during the year ended December 31, 2024,
recorded as impairment of available-for-sale debt securities in the Consolidated Statements of Operations.
The roll-forward for the allowance for credit losses related to the available-for-sale debt securities is as follows:
2024
2023
2022
(in thousands)
Allowance for credit losses at beginning of year
$
—
$
—
$
—
Current period provision
10,073
—
—
Write-downs
(10,073)
—
—
Allowance for credit losses at end of year
$
—
$
—
$
—
Business Combinations
The Company uses the acquisition method of accounting and allocates the fair value of purchase consideration to the assets
acquired and liabilities assumed from an acquiree based on their respective fair values as of the acquisition date. The excess of the fair
value of purchase consideration over the fair value of these assets acquired and liabilities assumed is recorded as goodwill. When
determining the fair values of assets acquired and liabilities assumed, management makes significant estimates and assumptions,
especially with respect to intangible assets. Critical estimates in valuing intangible assets include, but are not limited to, expected
future cash flows, which includes consideration of future growth and margins, future changes in technology, expected cost and time to
develop in-process research and development, brand awareness and discount rates. Fair value estimates are based on the assumptions
that management believes a market participant would use in pricing the asset or liability.
Fixed Assets
Fixed assets are recorded at cost, net of accumulated depreciation and amortization. Depreciation is recorded using the straight-
line method over the estimated useful lives of the assets. Leasehold improvements are capitalized and amortized over the shorter of
their expected lives or the applicable lease term, including renewal options, if available. Major replacements and improvements are
capitalized, while general repairs and maintenance are expensed as incurred. See Note 5, Fixed Assets, for useful lives for each major
class of fixed assets.
Finite-Lived Intangible assets
Intangible assets, unless determined to be indefinite-lived, are amortized over their estimated useful lives. The Company
amortizes intangible assets on a straight-line basis with definite lives generally over periods ranging from three to 14 years. See Note
17, Goodwill and Intangible Assets, for details of intangible assets.
F-13
Impairment of Long-Lived Assets
The Company evaluates the carrying amount of its long-lived assets whenever events or changes in circumstances indicate that
the assets may not be recoverable. An impairment loss would be recognized when estimated future cash flows expected to result from
the use of an asset and its eventual disposition is less than the carrying amount of the asset.
Goodwill and Indefinite-lived Intangibles
In-process research & development, or IPR&D, costs are considered to be indefinite-lived until the completion or abandonment
of the associated research and development efforts. If and when development is complete, the associated assets would be deemed
finite-lived and would then be amortized based on their respective estimated useful lives at that point in time.
The Company assesses goodwill and indefinite-lived intangibles for impairment on an annual basis and between annual tests if
an event occurs or circumstances change that would more likely than not reduce the fair value of a reporting unit below its carrying
amount. The Company may choose to bypass a qualitative assessment of impairment for any reporting unit and proceed directly to
performing a quantitative assessment. An impairment loss would be recognized for the amount by which the reporting unit's carrying
amount exceeds its fair value.
The Company’s quantitative assessment includes estimating the fair value of each reporting unit and comparing it to its carrying
value. The Company estimates the fair value of reporting units using both income-based and market-based valuation methods and
typically engages a third-party appraisal firm to assist with the valuation. The estimated fair value for each reporting unit is
determined based upon the range of estimated values developed from the income and market-based methods. If the estimated fair
value of a reporting unit exceeds its carrying value, the goodwill is not impaired, and no further review is required.
The income-based fair value methodology is based on a reporting unit’s forecasted future cash flows that are discounted to the
present value using the reporting unit’s weighted-average cost of capital, or WACC. Under the income-based approach, it requires
management’s assumptions and judgments regarding economic conditions in the markets in which the company operates and
conditions in the capital markets, many of which are outside of management’s control. The market-based fair value methodology
looks at the guideline public company valuation method to determine the prices of comparable public companies and looks at merger
and acquisition methods, similar businesses that were sold recently, to estimate the value of the reporting units. Under the market-
based approach, judgment is required in evaluating market multiples and recent transactions.
The Company performed an annual goodwill and intangible asset impairment test on December 31, 2024, and elected to bypass
the optional qualitative test and perform the quantitative assessments for its therapeutic development reporting units, which includes
an indefinite-lived intangible asset.
Reagents and Supplies
The Company maintains reagents and other consumables primarily used in testing which are valued at the lower of cost or net
realizable value. Cost is determined using actual costs on a first-in, first-out basis. The reagents and other consumables were included
in other current assets in the accompanying Consolidated Balance Sheets.
Fair Value of Financial Instruments
The Company’s financial instruments consist principally of cash and cash equivalents, marketable securities, trade accounts
receivable, restricted cash, a redeemable preferred stock investment, preferred stock investments, accounts payable, and accrued
liabilities. The carrying amounts of certain of these financial instruments, including cash and cash equivalents, accounts receivable,
accounts payable, and accrued liabilities approximate fair value due to their short maturities. Fair value of marketable securities, the
redeemable preferred stock investment, and the preferred stock investments is disclosed in Note 4, Fair Value Measurements, to the
accompanying consolidated financial statements.
Concentrations of Credit Risk, Customers and Suppliers
Financial instruments that potentially subject the Company to significant concentrations of credit risk consist primarily of cash
and cash equivalents, trade accounts receivable, and marketable securities. As of December 31, 2024, substantially all of the
Company’s cash and cash equivalents were deposited in accounts at financial institutions, and amounts may exceed federally insured
limits. Management believes that the Company is not exposed to significant credit risk due to the financial strength of the depository
institutions in which its cash and cash equivalents are held.
F-14
In certain periods, a small number of customers has accounted for a significant portion of the Company’s revenue. For the
laboratory services segment, aggregating customers under common control, one customer comprised of $62.6 million or 22% of total
revenue in the year ended December 31, 2024, and the same customer comprised of $35.7 million or 12% of total revenue in the year
ended December 31, 2023. A different customer comprised of $115.6 million or 19% of total revenue in the year ended December 31,
2022. One customer comprised 15% of total accounts receivable, net, as of December 31, 2024, and the same customer comprised
13% of total accounts receivable, net, as of December 31, 2023. For the therapeutic development segment, the Company doesn't have
customers or revenue as it does not have any commercialized or approved drug candidates.
The Company’s therapeutic development business relies on ANP Technologies, Inc. for certain laboratory services, equipment,
tools, and drug intermediates in connection with research and development efforts. The Company also relies on a limited number of
suppliers for certain laboratory substances used in the chemical reactions incorporated into its processes, referred to as reagents, as
well as for the sequencers and various other equipment and materials it uses in its laboratory operations. In particular, the Company
relies on a sole supplier for the next generation sequencers and associated reagents it uses to perform its genetic tests and as the sole
provider of maintenance and repair services for these sequencers. The Company’s laboratory operations would be interrupted if it
encountered delays or difficulties securing these reagents, sequencers, other equipment or materials or maintenance and repair
services, which could occur for a variety of reasons, including if the Company needs a replacement or temporary substitute for any of
its limited or sole suppliers and is not able to locate and make arrangements with an acceptable replacement or temporary substitute.
The Company’s development efforts could also be delayed or interrupted if it is unable to procure items needed for its therapeutic
development activities. The Company believes there are currently only a few other manufacturers that are capable of supplying and
servicing some of the equipment and other materials necessary for its laboratory operations, including sequencers and various
associated reagents.
Leases
The Company determines if an arrangement is a lease at inception by evaluating whether the arrangement conveys the right to
use an identified asset and whether the Company obtains substantially all of the economic benefits from and has the ability to direct
the use of the asset. Operating and finance lease right-of-use assets, or ROU assets, short-term lease liabilities, and long-term lease
liabilities are included in other long-term assets, accrued liabilities, and other long-term liabilities, respectively, in the accompanying
Consolidated Balance Sheets.
Lease ROU assets represent the Company’s right to use an underlying asset for the lease term. Lease liabilities represent the
Company’s obligation to make lease payments arising from the lease. Lease ROU assets and liabilities are recognized at the
commencement date based on the present value of lease payments over the lease term, including options to extend the lease when it is
reasonably certain that the Company will exercise that option. The Company uses its incremental borrowing rate based on the
information available at the commencement date, including inquiries with its bank, in determining the present value of lease payments
when its leases do not provide an implicit or explicit rate. Lease ROU assets consist of initial measurement of lease liabilities, any
lease payments made to lessor on or before the lease commencement date, minus any lease incentive received, and any initial direct
costs incurred by the Company. Operating lease expense for lease payments is recognized on a straight-line basis over the lease term.
For finance lease, ROU assets are amortized on a straight-line basis from the commencement date to the earlier of the end of useful
life of the ROU assets or the end of the lease term. Amortization of ROU assets and interest on the lease liability for finance leases are
included as charges to the accompanying Consolidated Statements of Operations.
Lease ROU assets and liabilities arising from business combinations are recognized and measured at the acquisition dates as if
an acquired lease were a new lease at the date of acquisition using the Company’s incremental borrowing rate unless the discount rate
is implicit in the lease. The Company elects to not to recognize assets or liabilities as of the acquisition dates for leases that, on the
acquisition dates, have a remaining lease term of 12 months or less. The Company also retains the acquirees’ classification of the
leases if there are no modifications as part of the business combinations.
The Company leased out space in buildings it owns to third-party tenants under noncancelable operating leases. The Company
recognized lease payments as income over the lease terms on a straight-line basis and recognized variable lease payments as income in
the period in which the changes in facts and circumstances on which the variable lease payments were based occurred. The net rental
income was included in the other income, net, in the accompanying Consolidated Statements of Operations.
Software for Internal Use
The Company capitalizes certain costs incurred to purchase computer software for internal use. These costs include purchased
software packages for Company use. Capitalized computer software costs are amortized over the estimated useful life of the computer
software, which is generally one to 10 years. Internally developed software costs are capitalized after management has committed to
funding the project, it is probable that the project will be completed and the software will be used for its intended function. Costs that
do not meet that criteria and costs incurred on projects in the preliminary and post-implementation phases are expensed as incurred.
F-15
Reportable Segment and Geographic Information
Reporting segments are identified as components of an enterprise about which separate discrete financial information is
available for evaluation by the chief operating decision-maker in making decisions regarding resource allocation and assessing
performance. The Company’s chief operating decision maker is its Chief Executive Officer. The Company reports its business in two
segments, a laboratory services business and a therapeutic development business. For further financial information about these
segments, including information for each of the last three fiscal years regarding revenue, operating income (loss), and other important
information, see Note 7, Reportable Segment and Geographic Information.
Revenue Recognition
The Company generates revenue from sales of its testing services. The Company currently receives payments from primarily
three different customer types: insurance payors, institutional customers, including hospitals, medical institutions, other laboratories,
governmental bodies, municipalities, and large corporations, and patients who pay directly.
The Company recognizes revenue in an amount that reflects the consideration to which it expects to be entitled in exchange for
the transfer of promised goods or services to its customers. To determine revenue recognition for contracts with customers, the
Company performs the following steps described in ASC 606: (1) identifies the contract with the customer, or Step 1, (2) identifies the
performance obligations in the contract, or Step 2, (3) determines the transaction price, or Step 3, (4) allocates the transaction price to
the performance obligations in the contract, or Step 4, and (5) recognizes revenue when (or as) the entity satisfies a performance
obligation, or Step 5.
The Company’s test results are primarily delivered electronically. The Company bills certain customers for shipping and
handling fees incurred by the Company, and shipping and handling fees billed to customers are included in revenue, and such shipping
and handling fees incurred are included in cost of revenue in the accompanying Consolidated Statements of Operations.
Performance Obligations
Institutional and Patient Direct Pay
The Company’s institutional contracts for its testing services typically have a single performance obligation to deliver testing
services to the ordering facility or patient. In arrangements with institutions, including hospitals, medical institutions, other
laboratories, governmental bodies, municipalities, and large corporations, and patients who pay directly, the transaction price is stated
within the contract and is therefore fixed consideration. For most of the Company’s testing, the Company identified the institutions,
including hospitals, medical institutions, other laboratories, governmental bodies, municipalities, and large corporations, and patients
as the customer in Step 1 and have determined a contract exists with those customers in Step 1. As these contracts typically have a
single performance obligation, no allocation of the transaction price is required in Step 4. Control over testing services is transferred to
the Company’s ordering facility at a point in time. Specifically, the Company determined the customer obtains control of the promised
service upon delivery of test results.
The Company enters into contracts with research institutions to perform testing and research services. Revenue is recognized as
each individual test is completed, as the Company has a right to payment upon completion of each test. While the contract represents a
single performance obligation to provide testing and research services, the revenue is recognized as the individual tests are completed
and the results are delivered to the customer. Each completed test is considered a measurable event that indicates the transfer of
control to the customer, at which point revenue is recognized. The Company regularly reviews its contracts and recognizes revenue in
accordance with the completion of each test, based on the right to payment and the transfer of control.
Insurance
The Company’s insurance contracts for testing services typically have a single performance obligation to deliver testing services
to the ordering facility or patient. For most of the Company’s insurance revenue, the Company identified the patient as the customer in
Step 1 and determined a contract exists with the patient in Step 1. In arrangements with insurance patients, the transaction price is
typically stated within the contract, however, the Company may accept payments from insurance payors that are less than the
contractually stated price, therefore estimation of the transaction price is considered variable consideration. In developing the estimate
of variable consideration, the Company utilizes the expected value method under a portfolio approach. As these contracts typically
have a single performance obligation, no allocation of the transaction price is required in Step 4. Control over testing services is
transferred to the Company’s ordering parties at a point in time. Specifically, the Company determined the customer obtains control of
the promised service upon delivery of the test results.
F-16
Certain incremental costs pertaining to both insurance and institutional, such as commissions, are incurred in obtaining
contracts. Contract costs are capitalized if the Company expects to recover them, and amortization of contract costs is classified in the
general and administrative expense in the Consolidated Statements of Operations. Historically contract costs have not been significant
to the financial statements.
Significant Judgments and Contract Estimates
Accounting for insurance contracts includes estimation of the transaction price, defined as the amount the Company expects to
be entitled to receive in exchange for providing the services under the contract. Due to the Company’s out-of-network status with
various insurance payors, estimation of the transaction price represents variable consideration.
In the absence of Medicare coverage, contractually established reimbursement rates or other coverage, we have concluded that
our contracts include variable consideration because the amounts paid by Medicare or commercial health insurance carriers may be
paid at less than our standard rates or not paid at all, with such differences considered implicit price concessions. Variable
consideration attributable to these price concessions measured at the expected value using the “most likely amount” method under
ASC 606. The amounts are determined by the historical average collection rates by test type taking into consideration the range of
possible outcomes, the predictive value of our past experiences, the time period of when uncertainties expect to be resolved and the
amount of consideration that is susceptible to factors outside of our influence, such as the judgment and actions of insurance payors.
Such variable consideration is included in the transaction price only to the extent it is probable that a significant reversal in the amount
of cumulative revenue recognized will not occur when the uncertainties with respect to the amount are resolved. Variable
consideration may be constrained and excluded from the transaction price in situations where there is no contractually agreed upon
reimbursement coverage or in the absence of a predictable pattern and history of collectability with a payor.
The Company re-assesses its estimated transaction price at the end of each reporting period, including an assessment of whether
the estimate variable consideration is constrained to the extent that is probable that a significant reversal of cumulative revenue will
not occur once any uncertainty is resolved. The Company records any necessary adjustments in the current period’s revenue. $1.8
million and $23.0 million variable consideration was recognized as additional revenue in the years ended December 31, 2024 and
2023, respectively, that related to collections for COVID-19 tests completed in the prior period.
Contract Liabilities
Contract liabilities are recorded when the Company receives payment or bills prior to completing its obligation to transfer goods
or services to a customer, and the Company subsequently recognizes contract liabilities as revenue in the period in which the
applicable revenue recognition criteria, as described above, are met.
Customer Deposit
Customer deposit in the accompanying Consolidated Balance Sheets consists of payments received from customers in excess of
their outstanding trade accounts receivable balances. These deposits will be offset against future testing receivables or refunded to the
customers.
Overhead Expenses
The Company allocates overhead expenses, such as facility, rent, and utilities, to cost of revenue and operating expense
categories based on square footage. As a result, an overhead expense allocation is reflected in cost of revenue and each operating
expense category.
Cost of Revenue
Cost of revenue reflects the aggregate costs incurred in delivering test results and consists of: personnel costs, including salaries,
employee benefit costs, bonuses, and equity-based compensation expenses; costs of laboratory supplies; depreciation of laboratory
equipment; amortization of leasehold and building improvements and allocated overhead. Costs associated with performing tests are
recorded as tests are processed.
Research and Development Expenses
Research and development expenses represent costs incurred to develop the Company’s technology and future tests. These costs
consist of: personnel costs, including salaries, employee benefit costs, bonuses, and equity-based compensation expenses; laboratory
F-17
supplies; consulting costs and allocated overhead. The Company expenses all research and development costs in the periods in which
they are incurred.
Selling and Marketing Expenses
Selling and marketing expenses consist of: personnel costs, including salaries, employee benefit costs, bonuses, and equity-
based compensation expenses; customer service expenses; direct marketing expenses; educational and promotional expenses; market
research and analysis and allocated overhead. The Company expenses all selling and marketing costs as incurred.
General and Administrative Expenses
General and administrative expenses include executive, finance and accounting, legal, and human resources functions. These
expenses consist of: personnel costs, including salaries, employee benefit costs, bonuses, and equity-based compensation expenses;
audit and legal expenses; consulting costs and allocated overhead. The Company expenses all general and administrative expenses as
incurred.
Restructuring Costs
Restructuring costs represent one-time employee termination benefits provided to employees associated with an acquired entity
that were involuntarily terminated. A plan of termination was approved and authorized by management in the second quarter of 2022.
The plan identified specific employees to be terminated and established terms of benefits those employees would receive upon
termination. No additional costs are expected to be incurred under the plan of termination post 2022, and the full amount was paid off
by August 2023.
Income Taxes
Income taxes are accounted for under the asset and liability method. The Company provides for federal, state and foreign
income taxes currently payable, as well as for taxes deferred due to timing differences between reporting income and expenses for
financial statement purposes versus tax purposes. Deferred tax assets and liabilities are recognized for the future tax consequences
attributable to temporary differences between the financial statement carrying amounts of existing assets and liabilities and their
respective tax bases. Deferred tax assets and liabilities are measured using enacted income tax rates expected to apply to taxable
income in the years in which those temporary differences are expected to be recovered or settled. The effect of a change in income tax
rates is recognized as income or expense in the period that includes the enactment date.
The Company recognizes the effect of income tax positions only if those positions are more likely than not to be sustained.
Recognized income tax positions are measured at the largest amount with a greater than 50% likelihood of being realized. Changes in
recognition or measurement are reflected in the period in which the change in judgment occurs. For income tax positions where it is
not more likely than not that a tax benefit will be sustained, the Company does not recognize a tax benefit in its consolidated financial
statements. The Company records interest and penalties related to uncertain tax positions, if applicable, as a component of income tax
expense.
The Company releases income tax effects from other comprehensive income (loss) under the portfolio method. In 2024, the
Company reclassified certain investments out of the available-for-sale debt security category. This reclassification resulted in the
removal of unrealized gains or losses previously recorded in other comprehensive income (loss). The tax effects of these adjustments
have been recognized, as a benefit of $2.1 million, in net loss to avoid stranded tax effects in other comprehensive income (loss).
Equity-Based Compensation
The Company grants various types of equity-based awards to its employees, consultants, and non-employee directors. Equity-
based compensation costs are reflected in the accompanying Consolidated Statements of Operations based upon each award
recipient’s role with the Company. The Company primarily grants to its employees restricted stock unit awards, or RSU awards, that
generally vest over a specified period of time upon the satisfaction of service-based conditions or performance conditions.
Compensation expense for employee RSU awards with a service-based vesting condition is recognized ratably over the vesting period
of the award. Compensation expense for employee RSU awards with a performance condition is based on the probable outcome of
that performance condition. The Company measures compensation expense for equity-based awards granted to employees based on
the fair value of the award on the grant date of the award.
F-18
Foreign Currency Translation and Foreign Currency Transactions
The Company translates the assets and liabilities of its non-U.S. dollar functional currency subsidiaries into U.S. dollars using
exchange rates in effect at the end of each period. Expenses for these subsidiaries are translated using rates that approximate those in
effect during the period. Gains and losses from these translations are recognized in foreign currency translation gain (loss) included in
the accompanying Consolidated Statements of Comprehensive Income (Loss). The Company and its subsidiaries that use the U.S.
dollar as their functional currency remeasure monetary assets and liabilities at exchange rates in effect at the end of each period, and
inventories, property and nonmonetary assets and liabilities at historical rates. Gains and losses from these measurements are included
in other income, net, in the accompanying Consolidated Statements of Operations. Losses from foreign currency exchange were not
significant in 2024, 2023, and 2022.
Comprehensive (Loss) Income
Comprehensive (loss) income is comprised of net (loss) income and other comprehensive (loss) income. Other comprehensive
(loss) income consists of net unrealized gain or loss on available-for-sale debt securities, net of tax, and foreign currency translation
adjustments from its subsidiaries not using the U.S. dollar as their functional currency. Reclassification from other comprehensive
(loss) income to net loss, which includes reclassification of stranded tax effects, was $3.6 million in 2024. Reclassifications from other
comprehensive income (loss) to net earnings were not significant in 2023 or 2022. The tax effects related to net unrealized gain or loss
on available-for-sale debt securities were zero in 2024 and 2023, due to the valuation allowance in the current period that precludes
the Company from recognizing the deferred tax benefit, and $7.2 million in 2022.
Basic and Diluted Net Income or Loss per Share
Basic net income or loss per common share is computed by dividing the net income or loss attributable to common stockholders
by the weighted-average number of common shares outstanding during the period. Diluted net income or loss per common share is
computed by dividing the net income or loss attributable to common stockholders by the weighted-average number of common shares
and dilutive common share equivalents outstanding during the period.
Disaggregation of Revenue
The Company classifies its customers into three payor types: (i) Institutional, including hospitals, medical institutions, other
laboratories, governmental bodies, municipalities, and large corporations, (ii) Insurance, including claim reimbursement from HRSA
for uninsured individuals, or (iii) Patients who pay directly, as the Company believes this best depicts how the nature, amount, timing,
and uncertainty of its revenue and cash flows are affected by economic factors. The following table summarizes revenue from
contracts with customers by payor type for the years ended December 31, 2024, 2023, and 2022.
Year Ended December 31,
2024
2023
2022
(in thousands)
Revenue by payor
Institutional
$
154,733
$
134,191
$
239,961
Insurance
123,924
151,946
377,873
Patient
4,813
3,076
1,134
Total revenue
$
283,470
$
289,213
$
618,968
The insurance revenue category above includes zero for the years ended December 31, 2024 and 2023, and $83.1 million for the
year ended December 31, 2022 for services related to claims covered by the HRSA COVID-19 Uninsured Program.
During the years ended December 31, 2024 and 2023, the Company experienced a change in estimate related to variable
consideration. $1.8 million and $23.0 million variable consideration were recognized in the years ended December 31, 2024 and 2023,
respectively, related to COVID-19 test services completed in the prior periods due to collection efforts, which was included as revenue
from insurance in the table above. The Company estimates variable consideration using the expected value method. Any changes in
variable consideration estimates that affect transactions are accounted for on a cumulative catch-up basis.
Contract Balances
Receivables from contracts with customers - Receivables from contracts with customers are included within trade accounts
receivable on the Consolidated Balance Sheets. Receivables from Insurance and Institutional customers represented 44% and 56%,
respectively, as of December 31, 2024 and 39% and 61%, respectively, as of December 31, 2023.
F-19
Contracts assets and liabilities - Contract assets from contracts with customers associated with contract execution and certain
costs to fulfill a contract are included in other current assets in the accompanying Consolidated Balance Sheets. Contract liabilities are
recorded when the Company receives payment prior to completing its obligation to transfer goods or services to a customer. Contract
liabilities are included in the Consolidated Balance Sheets. Revenues of $2.5 million, $2.2 million and $14.4 million for the years
ended December 31, 2024, 2023, and 2022, respectively, related to contract liabilities at the beginning of the respective periods were
recognized.
Transaction Price Allocated to Future Performance Obligations
ASC 606 issued by the Financial Accounting Standards Board, or FASB, requires that the Company disclose the aggregate
amount of transaction price that is allocated to performance obligations that have not yet been satisfied as of December 31, 2024. ASC
606 provides certain practical expedients that limit the requirement to disclose the aggregate amount of transaction price allocated to
unsatisfied performance obligations.
The Company applied the practical expedient to not disclose the amount of transaction price allocated to unsatisfied
performance obligations when the performance obligation is part of a contract that has an original expected duration of one year or
less. The Company does not have material future obligations associated with its testing services that extend beyond one year.
Prior Period Reclassifications
Certain amounts reported in the prior periods have been reclassified to conform with the current period presentation. In the
Consolidated Statements of Cash Flow, the Company has separated prepaid income taxes from its previous inclusion in other current
and long-term assets and separated customer deposits, and contract liabilities from its previous inclusion in accrued liabilities and
other liabilities. In the Consolidated Statements of Operations, the Company has also separated interest income, and interest expenses
from its previous inclusion in other income, net.
Recent Accounting Pronouncements
The Company evaluates all Accounting Standards Updates, or ASUs, issued by the Financial Accounting Standards Board, or
FASB, for consideration of their applicability. ASUs not included in the Company’s disclosures were assessed and determined to be
either not applicable or are not expected to have a material impact on the Company’s consolidated financial statements or disclosures.
Adopted
In November 2023, the FASB issued ASU 2023-07, Segment Reporting (Topic 280): Improvements to Reportable Segments.
This update improves reportable segment disclosure requirements and requires enhanced disclosures related to significant segment
expenses regularly provided to the CODM, the amount for other segment items with descriptions of the composition, segment profit or
loss, and clarification on if the CODM uses more than one measurement of a segment’s profit or loss in assessing segment
performance and deciding how to allocate resources. We adopted the guidance effective January 1, 2024 for annual reporting, and
January 1, 2025 for interim reporting. Adoption of the guidance has affected the disclosures related to reportable segments, and have
been applied retrospectively to all prior periods presented in the financial statements. For further information, refer to Note 7.
Reportable Segment and Geographic Information for the presentation of the additional required disclosures.
Issued
In December 2023, the FASB issued ASU 2023-09, Income Taxes (Topic 740): Improvement to Income Tax Disclosures. This
update requires more detailed information on certain income tax disclosures including the income tax rate reconciliation and income
taxes paid. Amendments in this update are effective for annual periods beginning December 15, 2024 for public entities, and early
adoption is permitted. This update will result in enhanced income tax disclosures, and the Company does not expect any impact to
income tax expense.
In November 2024, the FASB issued ASU 2024-03, Income Statement-Reporting Comprehensive Income-Expense
Disaggregation Disclosures (Subtopic 220-40): Disaggregation of Income Statement Expenses. This update requires disclosure in the
notes to financial statements, of specified information about certain costs and expenses. Amendments in this update are effective for
annual periods beginning after December 15, 2026, and interim reporting periods beginning after December 15, 2027. Early adoption
is permitted. The Company is currently evaluating the impacts of this amendment on the consolidated financial statements and related
disclosure.
The Company does not expect that any other recently issued accounting guidance will have a significant effect on its
consolidated financial statements.
F-20
Note 3. Equity and Debt Securities
The Company’s equity and debt securities consisted of the following:
December 31, 2024
Amortized
Cost Basis
Unrealized
Gains
Unrealized
Losses
Aggregate
Fair Value
(in thousands)
Equity securities
Long-term
Preferred stock of privately-held companies
$
24,927
$
—
$
—
$
24,927
Total equity securities
24,927
—
—
24,927
Available-for-sale debt securities
Short-term
U.S. government debt securities
75,054
136
(25)
75,165
U.S. agency debt securities
65,490
72
(23)
65,539
U.S. treasury bills
44,366
19
(2)
44,383
Corporate debt securities
19,177
12
(50)
19,139
Municipal bonds
3,719
1
(7)
3,713
Money market accounts
19,720
—
—
19,720
Less: Cash equivalents
(24,696)
(1)
—
(24,697)
Total debt securities due within 1 year
202,830
239
(107)
202,962
After 1 year through 5 years
U.S. government debt securities
379,060
565
(2,283)
377,342
U.S. agency debt securities
144,398
57
(1,507)
142,948
Corporate debt securities
47,801
114
(150)
47,765
Municipal bonds
1,820
2
(4)
1,818
Yankee debt securities
501
—
(23)
478
Total debt securities due after 1 year through 5
years
573,580
738
(3,967)
570,351
Total available-for-sale debt securities
776,410
977
(4,074)
773,313
Total equity and debt securities
$
801,337
$
977
$
(4,074)
$
798,240
F-21
December 31, 2023
Amortized
Cost Basis
Unrealized
Gains
Unrealized
Losses
Aggregate
Fair Value
(in thousands)
Equity securities
Long-term
Preferred stock of privately-held company
$
15,000
$
—
$
—
$
15,000
Total equity securities
15,000
—
—
15,000
Available-for-sale debt securities
Short-term
U.S. government debt securities
119,739
8
(1,765)
117,982
U.S. agency debt securities
72,310
—
(1,414)
70,896
U.S. treasury bills
69,214
36
—
69,250
Corporate debt securities
63,810
—
(792)
63,018
Money market accounts
38,291
—
—
38,291
Municipal bonds
5,557
1
(23)
5,535
Less: Cash equivalents
(38,291)
—
—
(38,291)
Total debt securities due within 1 year
330,630
45
(3,994)
326,681
After 1 year through 5 years
U.S. government debt securities
247,104
1,262
(578)
247,788
U.S. agency debt securities
156,150
161
(490)
155,821
Corporate debt securities
12,885
—
(765)
12,120
Municipal bonds
6,337
2
(48)
6,291
Yankee debt securities
752
—
(60)
692
Redeemable preferred stock investment
20,000
438
—
20,438
Total debt securities due after 1 year through 5
years
443,228
1,863
(1,941)
443,150
After 5 years through 10 years
Municipal bonds
868
1
(10)
859
Total debt securities due after 5 years through 10
years
868
1
(10)
859
Total available-for-sale debt securities
774,726
1,909
(5,945)
770,690
Total equity and debt securities
$
789,726
$
1,909
$
(5,945)
$
785,690
Gross unrealized losses on the Company’s equity and debt securities were $4.1 million and $5.9 million as of December 31,
2024 and 2023, respectively. Proceeds from sale of available-for-sale securities were $104.3 million, $44.1 million, and
$140.2 million in 2024, 2023, and 2022, respectively. Gross realized losses on the Company’s available-for-sale securities were $1.1
million, $0.6 million, and $1.4 million in 2024, 2023, and 2022, respectively, and the gross realized income was insignificant in 2024,
2023, and 2022. The cost of any marketable securities sold is based on the specific-identification method. The Company did not
recognize any credit losses for its marketable available-for sale debt securities in 2024, 2023, and 2022.
See Note 2, Summary of Significant Accounting Policies, for the reclassification of available-for-sale securities to equity
securities and a credit loss of $10.1 million recorded in 2024 related to Helio Health.
F-22
Note 4. Fair Value Measurements
The authoritative guidance on fair value measurements establishes a framework with respect to measuring assets and liabilities
at fair value on a recurring basis and non-recurring basis. Under the framework, fair value is defined as the exit price, or the amount
that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants, as of the
measurement date. The framework also establishes a three-tier hierarchy for inputs used in measuring fair value that maximizes the
use of observable inputs and minimizes the use of unobservable inputs by requiring that the most observable inputs be used when
available. Observable inputs are inputs market participants would use in valuing the asset or liability and are developed based on
market data obtained from sources independent of the Company. Unobservable inputs are inputs that reflect the Company’s
assumptions about the factors market participants would use in valuing the asset or liability and are developed based on the best
information available in the circumstances. The hierarchy consists of the following three levels:
Level 1:
Inputs are quoted prices (unadjusted) in active markets for identical assets or liabilities that the reporting entity can
access at the measurement date.
Level 2:
Inputs other than quoted prices included within Level 1 that are observable for the asset or liability, either directly
or indirectly.
Level 3:
Inputs are unobservable for the asset or liability.
The following tables present information about the Company’s financial assets measured at fair value on a recurring basis, based
on the three-tier fair value hierarchy:
December 31, 2024
Total
Level 1
Level 2
Level 3
(in thousands)
Equity securities, debt securities and cash equivalents
U.S. government debt securities
$
452,507
$
—
$
452,507
$
—
U.S. agency debt securities
208,487
—
208,487
—
Corporate debt securities
66,904
—
66,904
—
U.S. treasury bills
44,383
44,383
—
—
Preferred stock of privately-held companies
24,927
—
—
24,927
Money market accounts
19,720
19,720
—
—
Municipal bonds
5,531
—
5,531
—
Yankee debt securities
478
—
478
—
Total equity securities, debt securities and cash
equivalents
$
822,937
$
64,103
$
733,907
$
24,927
December 31, 2023
Total
Level 1
Level 2
Level 3
(in thousands)
Equity securities, debt securities and cash equivalents
U.S. government debt securities
$
365,770
$
—
$
365,770
$
—
U.S. agency debt securities
226,717
—
226,717
—
Corporate debt securities
75,138
—
75,138
—
U.S. treasury bills
69,250
69,250
—
—
Money market accounts
38,291
38,291
—
—
Redeemable preferred stock investment
20,438
—
—
20,438
Preferred stock of privately-held company
15,000
—
—
15,000
Municipal bonds
12,685
—
12,685
—
Yankee debt securities
692
—
692
—
Total equity securities, debt securities and cash
equivalents
$
823,981
$
107,541
$
681,002
$
35,438
The Company’s Level 1 assets include U.S. treasury bills and money market instruments and are valued based upon observable
market prices. Level 2 assets consist of U.S. government and U.S. agency debt securities, municipal bonds, corporate debt securities
and Yankee debt securities. Level 2 securities are valued based upon observable inputs that include reported trades, broker/dealer
quotes, bids and offers. As of December 31, 2024 and 2023, the Company had preferred stock of two privately held companies, which
were included in other long-term assets in the accompanying Consolidated Balance Sheets that were measured using unobservable
(Level 3) inputs. For the value of the investments in private equity securities, the Company elected to measure them at cost minus
F-23
impairment, as the preferred stock of the privately-held companies did not have a readily determinable fair value, and no impairment
loss was recorded as of December 31, 2024. As of December 31, 2023, the Company also had redeemable preferred stock, and the fair
value of redeemable preferred stock was based on valuation performed by a third-party valuation company utilizing the guideline
public company method under market approach and the discounted cash flow method under income approach. The redeemable
preferred stock has been fully impaired as of December 31, 2024, see Note 2, Summary of Significant Accounting Policies, for more
details.
There were no transfers between fair value measurement levels in 2024, 2023, and 2022.
Note 5. Fixed Assets
Major classes of fixed assets consisted of the following:
Useful Lives
December 31, 2024
December 31, 2023
(in thousands)
Medical lab equipment
1 to 13 Years
$
57,541
$
56,025
Building improvements
6 months to 39 Years
27,924
7,748
Building
25 to 39 Years
21,689
9,781
Computer hardware
1 to 5 Years
7,328
6,805
Computer software
1 to 10 Years
7,214
7,982
Aircraft
7 Years
6,400
6,400
Furniture and fixtures
1 to 11 Years
4,109
3,860
Leasehold improvements
Shorter of lease term or estimated useful life
3,323
11,222
Land improvements
15 Years
904
904
Automobile
3 to 8 Years
581
445
General equipment
5 Years
108
115
Land
17,347
8,800
Assets not yet placed in service
2,792
15,010
Total
157,260
135,097
Less: Accumulated depreciation
(51,711)
(51,633)
Fixed assets, net
$
105,549
$
83,464
Depreciation expense on fixed assets totaled $16.4 million, $17.5 million and $25.5 million for the years ended December 31,
2024, 2023, and 2022, respectively.
Note 6. Other Significant Balance Sheet Accounts
Other current assets consisted of the following:
December 31, 2024
December 31, 2023
(in thousands)
Reagents and supplies
$
8,384
$
5,827
Prepaid expenses
6,629
7,744
Marketable securities interest receivable
6,241
4,994
Prepaid income taxes
3,422
12,675
Other receivable
1,768
1,319
Total
$
26,444
$
32,559
F-24
Accrued liabilities consisted of the following:
December 31, 2024
December 31, 2023
(in thousands)
Payroll liabilities
$
8,210
$
5,741
Accrued bonus and commission
5,803
6,255
Vacation accrual
4,088
3,543
Operating lease liabilities - short term
1,443
3,957
Accrued legal liabilities
1,101
7,026
Other accrued liabilities
3,634
4,215
Total
$
24,279
$
30,737
Accrued legal liabilities as of December 31, 2024 included $1.0 million in connection with the SEC investigation as further
described in Note 8, Debt, Commitments, and Contingencies. Accrued legal liabilities as of December 31, 2023 included a previously
estimated $6.9 million in connection with the Company’s voluntary disclosure process, which was settled at approximately $3.0
million and paid in 2024. Other accrued liabilities included short-term finance lease liabilities, health insurance liabilities, and third-
party billing services.
Other long-term liabilities consisted of the following:
December 31, 2024
December 31, 2023
(in thousands)
Operating lease liabilities, long term
$
4,120
$
7,147
Notes payable, long term
2,493
2,964
Other long-term liabilities
360
4,973
Total
$
6,973
$
15,084
Note 7. Reportable Segment and Geographic Information
The Company has two distinct reportable segments. The laboratory services operating segment offers technical laboratory and
testing services and professional interpretation of laboratory results by licensed physicians who specialize in pathology and oncology.
The therapeutic development operating segment is a pharmaceutical research and development entity.
The Company’s Chief Executive Officer serves as its Chief Operating Decision Maker, or CODM. The CODM oversees the
Company’s operations and evaluates financial data for its two operating segments separately to make resource allocation decisions.
The financial information regularly provided to the CODM includes various performance metrics by reporting segment, such as gross
profit, operating income or loss, income or loss before income taxes, net income or loss from consolidated operations, and net income
or loss attributable to Fulgent, all presented in accordance with U.S. GAAP. Additionally, the CODM receives these metrics on a non-
GAAP basis, which excludes the impact of equity-based compensation expenses, goodwill impairment losses, amortization of
intangible assets, and restructuring costs, if applicable. Although multiple financial metrics are provided, the CODM primarily relies
on adjusted operating income or loss to evaluate segment performance and allocate resources. The balance sheet is presented on a
consolidated basis, as the CODM does not use asset or liability information, including fixed assets, to assess segment performance. As
a result, segment asset and liability details are not disclosed.
There is no inter-segment allocation of interest expense and income taxes. There is no inter-segment revenue and operating
income or loss. The Company did not allocate income tax by segment. Information regarding the Company’s operations and assets for
its reporting segments as well as geographic information are as follows, all dollars are in thousands:
Laboratory
Services
Therapeutic
Development
Total
Fiscal year ended December 31, 2024
Revenue
$
283,470
$
—
$
283,470
Less:
Adjusted cost of revenue
168,456
—
168,456
Adjusted research and development
18,213
15,632
33,845
Adjusted selling and marketing
32,339
—
32,339
Adjusted general and administrative
69,374
928
70,302
Total adjusted operating loss
$
(4,912)
$
(16,560)
$
(21,472)
F-25
Laboratory
Services
Therapeutic
Development
Total
Fiscal year ended December 31, 2023
Revenue
$
289,213
$
—
$
289,213
Less:
Adjusted cost of revenue
175,008
—
175,008
Adjusted research and development
19,577
6,990
26,567
Adjusted selling and marketing
36,503
—
36,503
Adjusted general and administrative
74,982
681
75,663
Total adjusted operating loss
$
(16,857)
$
(7,671)
$
(24,528)
Laboratory
Services
Therapeutic
Development
Total
Fiscal year ended December 31, 2022
Revenue
$
618,968
$
—
$
618,968
Less:
Adjusted cost of revenue
243,363
—
243,363
Adjusted research and development
17,715
746
18,461
Adjusted selling and marketing
34,545
—
34,545
Adjusted general and administrative
101,890
70
101,960
Total adjusted operating income (loss)
$
221,455
$
(816)
$
220,639
Year Ended December 31,
2024
2023
2022
Reconciliation of “adjusted operating (loss) income” to “(loss)
income before income taxes”
Adjusted operating (loss) income
$
(21,472)
$
(24,528)
$
220,639
Less (add):
Equity-based compensation
44,481
42,922
32,640
Amortization of intangible assets
7,965
7,845
6,497
Goodwill impairment loss
—
120,234
—
Restructuring costs
—
—
2,975
Interest income
(31,304)
(21,612)
(5,624)
Interest expense
(170)
488
1,013
Impairment of available-for-sale debt securities
10,073
—
—
Other income, net
(561)
(320)
(887)
Total (loss) income before income taxes
$
(51,956)
$
(174,085)
$
184,025
Significant items by segment excluded from the adjusted operating (loss) income:
Year Ended December 31,
2024
2023
2022
Equity-based compensation
Laboratory services
$
36,951
$
35,649
$
32,640
Therapeutic development
7,530
7,273
—
Total
$
44,481
$
42,922
$
32,640
F-26
Revenue by segment:
Year Ended December 31,
2024
2023
2022
Revenue
Laboratory services:
Precision diagnostics
$
167,745
$
131,990
$
93,685
Anatomic pathology
97,080
104,655
74,799
BioPharma services
16,338
25,416
12,977
COVID-19
2,307
27,152
437,507
Total laboratory services
283,470
289,213
618,968
Therapeutic development
—
—
—
Total
$
283,470
$
289,213
$
618,968
Depreciation and amortization by segment:
Year Ended December 31,
2024
2023
2022
Depreciation and amortization
Laboratory services
$
24,240
$
25,453
$
32,557
Therapeutic development
688
690
105
Total
$
24,928
$
26,143
$
32,662
Interest income and expense by segment:
Year Ended December 31,
2024
2023
2022
Interest income and expense
Laboratory services
Interest income
$
31,304
$
21,612
$
5,624
Interest expense
170
(488)
(1,013)
Therapeutic development
Interest income
—
—
—
Interest expense
—
—
—
Total
$
31,474
$
21,124
$
4,611
Total assets by segment:
December 31, 2024
December 31, 2023
December 31, 2022
Assets
Laboratory services
$
1,131,117
$
1,146,192
$
1,292,821
Therapeutic development
88,847
89,136
93,232
Total
$
1,219,964
$
1,235,328
$
1,386,053
Geographic distribution of revenue:
Year Ended December 31,
2024
2023
2022
Revenue
United States
$
259,132
$
268,977
$
603,148
Foreign
China
12,638
11,446
8,939
Other countries
11,700
8,790
6,881
Total foreign
24,338
20,236
15,820
Total
$
283,470
$
289,213
$
618,968
F-27
Geographic distribution of property, plant and equipment, net:
December 31, 2024
December 31, 2023
December 31, 2022
Fixed assets
United States
$
98,992
$
77,938
$
72,617
Foreign
China
4,616
5,526
8,736
Other countries
1,941
—
—
Total foreign
6,557
5,526
8,736
Total
$
105,549
$
83,464
$
81,353
Note 8. Debt, Commitments and Contingencies
Debt
Notes payable as of December 31, 2024, consisted of $2.9 million of notes payable related to an installment sale contract the
Company entered in February 2022 for a building. The notes payable related to the installment sale are due in February 2030, and the
interest rate is 1.08%. The current portion and noncurrent portion are $0.4 million and $2.5 million, respectively, and the noncurrent
portion is included in the other long-term liabilities in the accompanying Consolidated Balance Sheets. The Company also had notes
payable to Xilong Scientific Co., which were paid off in 2024, and had an interest rate of 4.97%. The interest expenses in 2024 and
2023 were not significant, and was $0.3 million in 2022.
Operating and Finance Leases
See Note 9, Leases, for further information.
Purchase Obligations
The Company entered certain purchase commitments with its vendors, which primarily consist of services, reagent and supplies,
computer software, and medical lab equipment. As of December 31, 2024, the Company had purchase obligations of $40.6 million, of
which $31.6 million is payable within 12 months, and the remainder, $9.0 million, is payable within the next five years.
Contingencies
From time to time, the Company may be subject to legal proceedings and claims arising in the ordinary course of business.
As previously disclosed in the Company’s periodic reports filed pursuant to the Securities Exchange Act of 1934, as amended,
or the Exchange Act, the Company has received a Civil Investigative Demand, or CID, issued by the U.S. Department of Justice, or
the DOJ, pursuant to the False Claims Act related to its investigation of allegations of medically unnecessary laboratory testing,
improper billing for laboratory testing, and remuneration received or provided in violation of the Anti-Kickback Statute and the Stark
Law. Among other things, this CID requests information and records relating to certain of the Company’s customers named in this
CID.
Similar to other laboratories in the industry, the Company is currently being audited by the U.S. Health Resources and Services
Administration, or HRSA, with respect to its reimbursement for COVID-19 tests furnished to patients believed to be uninsured. The
Company recorded approximately $548.9 million of reimbursements from HRSA under the Uninsured Program during the years
ended December 31, 2022, 2021, and 2020. There is uncertainty with respect to the methodology HRSA will use in its audit and
whether and how HRSA will extrapolate audit results. The Company is working with HRSA’s auditors to resolve any issues related to
its audit, including any reimbursed amounts that may need to be returned to HRSA. The Company has also received a CID issued by
the DOJ pursuant to the False Claims Act related to the DOJ’s investigation as to whether the Company submitted or caused to be
submitted false claims to the Uninsured Program.
The Company is fully cooperating with the DOJ in connection with the CIDs that it has received, and in connection with the
HRSA audit. The Company cannot currently predict when these CIDs and HRSA audit matters will be resolved, the reasonable or
likely outcome of these matters, or their potential impact, which may materially and adversely affect the Company’s business,
prospects, and financial condition. These matters are not formal claims, and discussions and investigations remain ongoing. As such,
the Company cannot reasonably estimate the loss or range of loss, if any, that may result from any material government investigations,
audits, and reviews in which it is currently involved, given the inherent difficulty in predicting regulatory action, fines and penalties, if
F-28
any, and the various remedies and levels of judicial review available to the Company in the event of an adverse finding. As a result,
the Company has not recorded any liability related to these CIDs or audit matters.
In addition, and as previously disclosed, the SEC is conducting a non-public formal investigation, which relates to (i) the matters
raised in the requests for the CID regarding allegations of medically unnecessary laboratory testing, improper billing for laboratory
testing, and remuneration received or provided in violation of the Anti-Kickback Statute and the Stark Law and (ii) the Company’s
Exchange Act reports filed for 2018 through 2020. On May 6, 2024, the SEC staff advised the Company that the SEC staff made a
preliminary determination to recommend that the SEC file an enforcement action against the Company based on a corporate
negligence theory, which, if authorized, would allege violations of Sections 17(a)(2) and 17(a)(3) of the Securities Act of 1933, as
amended, Sections 13(a), 13(b)(2)(A) and 13(b)(2)(B) of the Exchange Act, and Rules 13a-1, 13a-13, and 12b-20 thereunder. The
Company has fully cooperated with the SEC and its requests, and the SEC are continuing to communicate regarding this matter. While
the Company does not believe that any enforcement recommendation is warranted and denies all liability, the Company has recorded a
$1.0 million potential liability with respect to this matter. While the Company believes this amount is a reasonable and probable
estimate, the actual amount of liability, if any, may be materially higher than this estimate, as discussions are ongoing, and there is no
formal settlement or final resolution of this matter at this time.
In relation to a recent advisory opinion issued by the Office of Inspector General of the Department of Health and Human
Services, or the OIG, the Company’s subsidiary, Symphony Buyer, Inc., or Inform Diagnostics, initiated a voluntary disclosure
process with the appropriate government contact. The Company had previously estimated and recorded $6.9 million as a liability in its
financial statements in connection with this voluntary disclosure. In December 2024, the Company entered into a settlement
agreement with the DOJ pursuant to which it agreed to pay and paid $3.0 million in resolution of the matters directly related to this
voluntary disclosure.
Note 9. Leases
Lessee
The Company is party as a lessee to various non-cancelable operating leases with varying terms through March 2034 primarily
for laboratory and office space and equipment. The Company has options to renew some of these leases after their expirations. On a
lease-by-lease basis, the Company considers such options, which may be elected at the Company’s sole discretion, in determining the
lease term. The Company also has various finance leases for lab equipment with varying terms through December 2026, of which,
some were acquired in business combinations. The Company does not have any leases with variable lease payments. The Company’s
operating lease agreements do not contain any residual value guarantees, material restrictive covenants, bargain purchase options or
asset retirement obligations.
The Company’s headquarters are located in El Monte, California, which is comprised of various corporate offices and a
laboratory certified under the Clinical Laboratory Improvement Amendments of 1988, or CLIA, accredited by the College of
American Pathologists, or CAP, and licensed by the State of California Department of Public Health. Other CLIA-certified
laboratories are located in Coppell, Texas; Needham, Massachusetts; Phoenix, Arizona; Alpharetta, Georgia. The Company is also in
the process of obtaining NATA accreditation in Dulwich, Australia.
The operating and finance lease right-of-use asset, short-term lease liabilities, and long-term lease liabilities as of December 31,
2024 and 2023 were as follows:
December 31, 2024
December 31, 2023
(in thousands)
Operating lease ROU asset, net
$
5,395
$
10,838
Operating lease liabilities, short term
$
1,443
$
3,957
Operating lease liabilities, long term
$
4,120
$
7,147
Finance lease ROU asset, net
$
771
$
1,316
Finance lease liabilities, short term
$
398
$
544
Finance lease liabilities, long term
$
360
$
760
F-29
The following was operating and finance lease expense:
Year Ended December 31,
2024
2023
2022
(in thousands)
Operating lease cost
$
4,176
$
6,875
$
5,429
Finance lease cost:
Amortization of ROU assets
539
758
683
Interest on lease liabilities
39
80
95
Short-term lease cost
1,346
1,758
1,528
Total lease cost
$
6,100
$
9,471
$
7,735
Supplemental information related to leases was the following:
December 31, 2024
Weighted-average remaining lease term, operating leases
5.95 years
Weighted-average discount rate, operating leases
5.27%
Weighted-average remaining lease term, finance lease
1.90 years
Weighted-average discount rate, finance lease
3.39%
The following is a maturity analysis of operating and finance lease liabilities using undiscounted cash flows on an annual basis
with renewal periods included:
Operating Leases
Finance Lease
(in thousands)
Year ending December 31,
2025
$
1,707
$
417
2026
1,117
366
2027
1,011
—
2028
484
—
2029
500
—
Thereafter
1,832
—
Total lease payments
6,651
783
Less imputed interest
(1,088)
(25)
Total
$
5,563
$
758
Lessor
The Company previously leased out space in buildings it owns to third-party tenants under noncancelable operating leases. As
of December 31, 2024, there were no noncancelable operating leases remaining. Lease income primarily represents fixed lease
payments from tenants recognized on a straight-line basis over the application lease term. Variable lease income represents tenant
payments for real estate taxes, insurance and maintenance.
The lease income was included in other income, net, in the accompanying Consolidated Statements of Operations. An
insignificant amount was recognized in the year ended December 31, 2024. For years ended December 31, 2023 and 2022, $0.2
million and $0.3 million were recognized, respectively. There are no future fixed lease payments from tenants expected, as there were
no remaining noncancelable operating leases as of December 31, 2024.
F-30
Note 10. Equity-Based Compensation
The Company has included equity-based compensation expense as part of cost of revenue and operating expenses in the
accompanying Consolidated Statements of Operations as follows:
Year Ended December 31,
2024
2023
2022
(in thousands)
Cost of revenue
$
7,799
$
9,749
$
8,704
Research and development
14,971
14,873
10,449
Selling and marketing
3,907
4,964
4,373
General and administrative
17,804
13,336
9,114
Total
$
44,481
$
42,922
$
32,640
The actual tax (expense) benefit realized from tax deductions related to awards vested or exercised were ($3.4) million, ($2.7)
million and $2.1 million for the years ended December 31, 2024, 2023, and 2022, respectively.
Award Activity
Option Awards
The following table summarizes activity for options to acquire shares of the Company’s common stock in the years ended
December 31, 2024, 2023, and 2022:
Number
of Shares
Subject to
Options
(in thousands)
Weighted-
Average
Exercise Price
Weighted-
Average
Grant Date Fair
Value
Weighted-
Average
Remaining
Contractual Life
(in years)
Aggregate
Intrinsic
Value
(in thousands)
(1)
Balance at December 31, 2021
216
$
3.42
4.6
$
20,965
Granted
10
$
59.54
$
44.56
Exercised
(5)
$
7.16
$
7.41
Canceled
(9)
$
43.30
$
33.53
Balance at December 31, 2022
212
$
4.21
3.7
$
5,420
Granted
20
$
33.14
$
24.85
Exercised
(9)
$
0.38
$
10.76
Canceled
—
$
—
$
—
Balance at December 31, 2023
223
$
6.96
3.3
$
4,906
Granted
5
$
22.50
$
16.42
Exercised
(133)
$
0.38
$
2.58
Canceled
—
$
—
$
—
Balance at December 31, 2024
95
$
17.07
4.7
$
134
Exercisable as of December 31, 2024
74
$
11.51
3.7
(1)
Aggregate intrinsic value is calculated as the difference between (i) the exercise price of options and (ii) the market value of the Company’s
common stock as of the applicable date.
The total fair value of options that vested during the years ended December 31, 2024, 2023, and 2022 was $0.3 million, $0.2
million and $0.1 million, respectively. As of December 31, 2024, the remaining unrecognized compensation expense related to all
outstanding option awards was $0.5 million and is expected to be recognized over a weighted-average period of 2.2 years.
RSU Awards
RSUs are awards that entitle the holder to receive shares of the Company’s common stock upon satisfaction of vesting
conditions. Each RSU represents the contingent right to receive one share of the Company’s common stock upon vesting and
settlement.
F-31
The following table summarizes activity for RSUs relating to shares of the Company’s common stock in the years ended
December 31, 2024, 2023, and 2022:
Number of
Shares
(in thousands)
Weighted-Average
Grant Date
Fair Value
Balance at December 31, 2021
1,619
$
40.74
Granted
1,895
$
49.98
Vested and settled
(699)
$
34.01
Forfeited
(184)
$
61.11
Balance at December 31, 2022
2,631
$
47.76
Granted
853
$
34.38
Vested and settled
(1,066)
$
43.84
Forfeited
(208)
$
54.72
Balance at December 31, 2023
2,210
$
43.84
Granted
1,142
$
23.47
Vested and settled
(1,004)
$
43.66
Forfeited
(142)
$
37.39
Balance at December 31, 2024
2,206
$
33.85
The RSU awards granted in the years ended December 31, 2024, 2023, and 2022 will result in aggregate equity-based
compensation expense of $26.9 million, $29.3 million and $94.8 million, respectively, to be recognized over the vesting periods from
the grant date of each award granted in the period. As of December 31, 2024, the remaining unrecognized compensation expense
related to all outstanding RSU awards was $64.4 million and is expected to be recognized over a weighted-average period of 2.2 years.
Fair Value Assumptions for Option Awards
The Company uses the Black-Scholes option-pricing model to measure the fair value of option awards. The Black-Scholes
option-pricing model requires the input of various assumptions, each of which is subjective and requires significant judgment. These
assumptions include the following:
•
Expected Term. The expected term represents the period that the Company’s equity-based awards are expected to be
outstanding. The Company determines the expected term assumption based on the vesting terms, exercise terms and
contractual terms of the options.
•
Risk-Free Interest Rate. The Company determines the risk-free interest rate by using the equivalent to the expected term
based on the U.S. Treasury yield curve in effect as of the date of grant.
•
Dividend Yield. The assumed dividend yield is based on the Company’s expectation that it will not pay dividends in the
foreseeable future, which is consistent with its history of not paying dividends.
•
Expected Volatility. The Company calculates expected volatility based on historical volatility data of its stock that is
publicly traded.
•
Forfeiture Rate. The Company accounts for forfeitures as they occur.
Awards to Employees
The table below sets forth the weighted-average assumptions used in the Black-Scholes option-pricing model to estimate the fair
value of options to acquire shares of the Company’s common stock granted to employees during the years ended December 31, 2024,
2023, and 2022.
Year Ended December 31,
2024
2023
2022
Expected term (in years)
6.1
6.1
6.1
Risk-free interest rates
4.3%
3.8%
2.6%
Dividend yield
—
—
—
Expected volatility
82.2%
87.3%
88.7%
F-32
Determination of Fair Value on Grant Dates
The fair value of the shares of the Company’s common stock underlying option and RSU awards is determined by the
Company’s board of directors or the compensation committee thereof based on the closing sales price of the Company’s common
stock on the date of grant as reported by the Nasdaq Global Market.
Note 11. Income Taxes
(Benefit from) provision for income taxes consists of United States federal and state income taxes. A deferred tax liability is
recognized for all taxable temporary differences, and a deferred tax asset is recognized for all deductible temporary differences,
operating losses and tax credit carryforwards. A valuation allowance is provided when it is more likely than not that some portion or
all of a deferred tax asset will not be realized.
The following table summarizes income (loss) before income taxes:
Year Ended December 31,
2024
2023
2022
(in thousands)
U.S. (loss) income before income taxes
$
(46,813)
$
(147,464)
$
189,406
Foreign loss before income taxes
(5,143)
(26,621)
(5,381)
(Loss) income before income taxes
$
(51,956)
$
(174,085)
$
184,025
(Benefit from) provision for income taxes consisted of the following:
Year Ended December 31,
2024
2023
2022
(in thousands)
Current
Federal
$
(2,441)
$
(5,590)
$
31,140
State
(2,107)
(4,722)
19,242
Foreign
148
—
—
Total Current
(4,400)
(10,312)
50,382
Deferred
Federal
(10,313)
(12,771)
(3,763)
State
(734)
4,100
(4,517)
Foreign
602
(188)
224
Change in valuation allowance
6,709
20,325
(224)
Total Deferred
(3,736)
11,466
(8,280)
Total (benefit from) provision for income taxes
$
(8,136)
$
1,154
$
42,102
F-33
Reconciliation of the difference between the federal statutory income tax rate and the effective income tax rate is as follows:
Year Ended December 31,
2024
2023
2022
Tax provision at federal statutory rate
21.00%
21.00%
21.00%
State taxes
-1.70%
0.22%
9.03%
Equity-based compensation
-6.79%
-1.65%
-1.12%
Nondeductible compensation - 162(m)
-2.10%
-0.55%
0.00%
Goodwill impairment
0.00%
-10.62%
0.00%
Amended state tax refunds
8.29%
0.00%
0.00%
Federal return to provision
-2.07%
-0.21%
-3.92%
State return to provision
-0.78%
3.41%
-2.02%
Other permanent differences
1.83%
-1.15%
1.33%
Uncertain tax positions
-1.14%
0.18%
0.92%
Research & development credit
6.95%
3.19%
-2.98%
IRA tax credit
4.82%
0.00%
0.00%
Foreign tax rate differential
-1.68%
-2.42%
0.00%
Stranded tax effect
4.25%
0.00%
0.00%
Foreign NOL carryforward
-1.19%
0.11%
-0.12%
Other
-0.29%
0.00%
0.46%
Change in valuation allowance
-13.29%
-12.20%
0.12%
Effective tax rate
16.11%
-0.69%
22.70%
The following table summarizes the elements of the deferred tax assets (liabilities). Net deferred tax assets are included in other
long-term assets in the Consolidated Balance Sheets.
As of December 31,
2024
2023
(in thousands)
Deferred tax assets
Accrued vacation and other accrued expenses
$
1,775
$
807
Provision for credit losses
2,990
818
Net operating losses
11,875
17,496
Equity-based compensation
2,022
906
State income taxes
284
211
Excess tax basis in FF Gene Biotech net assets
1,527
2,256
Lease liability
789
2,345
Unrealized gain/loss on available-for-sale debt securities
757
406
Research and development credits
2,762
1,258
Section 174 research & experimental expenditures
25,626
18,606
Equity loss in investment
2,965
503
Other
74
107
Gross deferred tax assets
53,446
45,719
Less: Valuation allowance
(22,702)
(15,900)
Net deferred tax assets
30,744
29,819
Deferred tax liabilities
Intangible assets
29,540
30,558
Depreciation
6,198
3,901
Right of use asset
767
2,299
Other
609
1,023
Total deferred tax liabilities
37,114
37,781
Net deferred tax liabilities
$
(6,370)
$
(7,962)
As of December 31, 2024, the Company has $31.5 million estimated federal net operating loss, or NOL, carryforwards and
estimated state NOL carryforwards of $82.6 million. The Company’s state NOLs are scheduled to begin expiring in 2025. The
Company also has foreign NOL carryforwards of $11.0 million which are scheduled to expire from 2025 through 2029. Utilization of
F-34
our net operating loss carryforwards may be subject to annual limitations due to ownership changes as imposed by the Internal
Revenue Code and similar state provisions.
ASC 740-10-30-5 requires that deferred income tax assets be reduced by a valuation allowance if it is more likely than not that
some or all of the deferred income tax assets will not be realized. The Company has evaluated the realizability of its deferred tax
assets and has concluded that it is more likely than not that the Company may not realize the benefit of certain deferred tax assets and,
accordingly, has established a full valuation allowance of $22.7 million on its deferred tax assets as of December 31, 2024. The
Company maintained a full valuation allowance of $15.9 million on its deferred tax assets as of December 31, 2023. The increase in
the valuation allowance of $6.8 million for the year ended December 31, 2024 was primarily due to the increase in capitalized Section
174 expenditures.
The Organization for Economic Cooperation and Development (OECD) has enacted model rules for a new global minimum tax
framework (“BEPS Pillar II”). Various jurisdictions have enacted, or are in the process of enacting, legislation on these rules. We are
closely monitoring developments and are currently evaluating the potential impact in each jurisdiction in which we operate.
Uncertain Tax Positions
The Company is subject to income taxation by the United States government and certain states in which the Company’s
activities give rise to an income tax filing requirement. The Company does not have any significant income tax filing requirements in
any foreign jurisdiction. The Company’s tax returns are subject to statutes of limitations that vary by jurisdiction. As of December 31,
2024, the Company remains subject to income tax examinations in the United States, and various states for tax years 2020 through
2024. However, due to the Company’s NOL carryforwards in various jurisdictions, tax authorities have the ability to adjust
carryforwards related to closed years until the statute expires on the year(s) in which the NOL carryforwards are utilized.
The Company is under examination by certain tax authorities for the 2020 and 2021 tax years. While the timing of the
conclusion of the examination is uncertain, the Company believes that adequate amounts have been reserved for adjustments that may
result.
A reconciliation of the Company’s gross unrecognized tax benefits is as follows:
Year Ended December 31,
2024
2023
2022
(in thousands)
Balance at beginning of year
$
5,833
$
9,742
$
710
Increases to prior year positions
(2,692)
(3,845)
2,843
Increases for current year positions
1,035
(64)
6,189
Balance at end of year
$
4,176
$
5,833
$
9,742
As of December 31, 2024, the Company has $4.2 million of gross unrecognized tax benefits, of which, $2.5 million of
unrecognized tax benefits would affect the effective tax rate if recognized. The Company has accrued $0.4 million and $0.1 million
for interest at December 31, 2024 and 2023, respectively. Although it is possible that the amount of unrecognized benefits with respect
to our uncertain tax positions will increase or decrease in the next 12 months, the Company does not expect material changes.
While the Company believes it has adequately provided for all tax positions, amounts asserted by taxing authorities could differ
from the Company’s accrued positions. Accordingly, additional provisions on federal, state and foreign tax-related matters could be
recorded in future periods as revised estimates are settled or otherwise resolved.
The Company received $40.0 million, $12.5 million, and $0.3 million in income tax refunds in 2024, 2023, and 2022,
respectively. The income tax refunds received, which were due to overpayment in prior years, were not netted in the income tax paid
amounts included in the supplemental disclosure in the accompanying Consolidated Statements of Cash Flows.
In 2024, the Company purchased $27.1 million worth of Investment Tax Credits, or ITCs, under the transferability provisions of
the Inflation Reduction Act of 2022 for $24.6 million in cash. The $2.5 million difference between the purchase price and the face
value of the credits has been recorded as an increase to the Company’s income tax benefit for the period. The $24.6 million cash
payment was included in the income tax paid amounts included in the supplemental disclosure in the accompanying Consolidated
Statements of Cash Flows. The Company has utilized $0.4 million of the acquired credits on its 2023 tax return and carried back the
remainder of $26.7 million to its 2020 tax year and filed a request for a refund. The Company has received the full amount of $26.7
million of ITCs that were carried back to the 2020 tax year in cash in 2024.
F-35
Note 12. Income (Loss) per Share
The following is a reconciliation of the basic and diluted income (loss) per share computations:
Year Ended December 31,
2024
2023
2022
(in thousands)
Net (loss) income attributable to Fulgent
$
(42,708)
$
(167,825)
$
143,403
Weighted-average common shares - outstanding, basic
30,235
29,784
30,097
Weighted-average effect of dilutive securities:
Stock options
—
—
199
Restricted stock units
—
—
613
Contingently issuable shares
—
—
55
Weighted-average common shares - outstanding, diluted
30,235
29,784
30,964
(Loss) income per share:
Basic
$
(1.41)
$
(5.63)
$
4.76
Diluted
$
(1.41)
$
(5.63)
$
4.63
The following securities have been excluded from the calculation of diluted income (loss) per share because their effect would
have been anti-dilutive:
Year Ended December 31,
2024
2023
2022
(in thousands)
Stock options
95
224
10
Restricted stock units
2,206
2,210
728
Contingently issuable shares
—
186
—
The anti-dilutive shares described above were calculated using the treasury stock method. In the years ended December 31, 2024
and 2023, the Company had outstanding stock options and restricted stock units that were excluded from the weighted-average share
calculation for continuing operations due to the Company’s net loss positions. In the year ended December 31, 2023, the Company
also had contingently issuable shares for shares held back in connection with the business combination of Fulgent Pharma, or Pharma
Hold Back Shares. In May 2024, the Company released the remaining Pharma Hold Back Shares such that no shares remain
contingently issuable in connection with the business combination of Fulgent Pharma.
Note 13. Retirement Plans
The Company offers a 401(k) retirement savings plan, or the 401 (k) Plan, for its employees, including its executive officers,
who satisfy certain eligibility requirements. The Internal Revenue Code of 1986, as amended, allows eligible employees to defer a
portion of their compensation, within prescribed limits, on a pre-tax basis through contributions to the 401(k) Plan. The Company
matches contributions to the 401(k) Plan based on the amount of salary deferral contributions the participant makes to the 401(k) Plan.
The Company will match up to 4% of an employee’s compensation that the employee contributes to their 401(k) Plan account. Total
Company matching contributions to the 401(k) Plan were $3.8 million, $3.2 million and $2.5 million in the years ended December 31,
2024, 2023, and 2022, respectively.
Note 14. Related Party
Linda Marsh, who is a member of the Company’s board of directors, is currently the Senior Executive Vice President of AHMC
Healthcare Inc., or AHMC. The Company performs genetic testing and other testing services, on an arms-length basis, for AHMC,
and the Company recognized an insignificant amount, $0.1 million and $1.5 million in revenue in the years ended December 31, 2024,
2023, and 2022, respectively. As of December 31, 2024 and 2023, insignificant amounts were owed to the Company by AHMC,
which is included in trade accounts receivable, net, in the accompanying Consolidated Balance Sheets, in connection with this
relationship.
F-36
Ming Hsieh, is the owner of PTJ Associates Inc., or PTJ. PTJ provides flight services to the Company on an arms-length basis.
In the years ended December 31, 2024, 2023, and 2022 the Company incurred zero, zero and $0.2 million, respectively, in expenses
for flights between California and Texas to transport employees and supplies. As of December 31, 2024 and 2023, no amount was
owed to PTJ by the Company.
Ming Hsieh is also on the board of directors and an approximately 20% owner of ANP Technologies, Inc., or ANP, from which
the Company entered into certain drug-related licensing and development service agreements. The President and Chief Scientific
Officer of Fulgent Pharma, Ray Yin, is the Founder, President, and Chief Technology Officer of ANP. The Company incurred $2.1
million, $2.4 million and $1.2 million, in expenses in the years ended December 31, 2024, 2023, and 2022, respectively, related to the
licensing and development services and purchase of equipment. As of December 31, 2024 and 2023, $0.2 million and zero,
respectively, were owed to ANP by the Company in connection with these relationships. The Company also entered into an employee
service agreement with ANP in April 2023, $0.1 million was recognized in revenue in each of the years ended December 31, 2024 and
2023, and insignificant amounts were owed by ANP in connection with the employee service agreement as of December 31, 2024 and
2023, respectively.
Note 15. Business Combinations
Inform Diagnostics
On April 26, 2022, the Company completed the acquisition of 100% of the outstanding equity of Inform Diagnostics, a leading
national independent pathology laboratory based in Irving, Texas. Under the terms of the Agreement and Plan of Merger, dated April
16, 2022, or the Inform Merger Agreement, the total purchase price payable to the securityholders of Inform Diagnostics was
approximately $170 million, as adjusted for closing cash, closing indebtedness, closing working capital, closing transaction expenses
and other transaction matters. With the addition of Inform Diagnostics, the Company will further expand the Company’s genomic
testing footprint and extend its test menu into breast pathology, gastrointestinal pathology, dermatopathology, urologic pathology,
neuropathology, and hematopathology.
The financial results of Inform Diagnostics are included in the consolidated financial statements from the date of acquisition.
The Company allocated the purchase price to tangible and identified intangible assets acquired and liabilities assumed based on
estimated fair values. The following tables summarizes the consideration paid and the updated amounts of the assets acquired and
liabilities assumed recognized at the acquisition date:
Amounts
(in thousands)
Consideration
Cash, net of cash received
$
137,755
Recognized amounts of identifiable assets acquired and liabilities assumed
Net working capital
$
(15,024)
Fixed assets
20,242
ROU assets - operating
12,653
ROU assets - finance
1,183
Deferred tax assets
3,410
Other long-term assets
4,711
Identifiable intangible assets
57,060
Operating lease liabilities
(12,653)
Finance lease liabilities
(1,183)
Income tax payable
(40)
Other long-term liabilities
(4,449)
Recognized amounts of identifiable assets acquired and liabilities assumed, net
65,910
Goodwill
71,845
Total
$
137,755
The goodwill of $71.8 million arising from the acquisition is attributed to the expected synergies, assembled workforce, other
benefits that will be potentially generated from the combination and deferred tax. The goodwill recognized is not deductible for tax
purposes. The goodwill was subsequently fully impaired in December 2023. Refer to Note 17. Goodwill and Intangible Assets for
more information.
F-37
The identifiable intangible assets acquired consisted of $54.0 million customer relationships with an estimated amortization life
of 14 years, $2.7 million trade name with an estimated amortization life of seven years, and $0.4 million in-place lease intangible asset
to be amortized over the remaining lease term of five years.
The fair value of the customer relationship was estimated using the Multiperiod Excess Earnings Method, or MPEEM, of the
income approach. Under the MPEEM, an intangible asset’s fair value is equal to the present value of the incremental after-tax cash
flows attributable only to the subject intangible asset after deducting contributory asset charges. The incremental after-tax cash flows
attributable to the customer relationships are then discounted to their present value at a risk-adjusted rate of return. The fair value of
the trade name was estimated using the relief from royalty, or RFR, method. The RFR method estimates the portion of the Company’s
earnings attributable to an intangible asset based on the royalty rate the Company would have paid for the use of the asset if it did not
own it. The fair value of in-place lease intangible asset was estimated using the discounted cash flow under the income approach. The
useful lives of the intangible assets for amortization purposes were determined by considering the period of expected cash flows used
to measure the fair values of the intangible assets adjusted as appropriate for entity-specific factors including legal, regulatory,
contractual, competitive, economic and other factors that may limit the useful life. The customer relationships and trade name are
amortized on a straight-line basis over their estimated useful lives.
Revenue and operating loss from the Inform Diagnostics acquisition since the acquisition date were $83.6 million and $17.0
million, respectively, for year ended December 31, 2022, which are included in the accompanying Consolidated Statements of
Operating.
The transaction costs associated with the acquisition of Inform Diagnostics consisted primarily of legal, regulatory and financial
advisory fees of approximately $6.6 million for the year ended December 31, 2022. These transaction costs were expensed as incurred
as general and administrative expense in the respective period.
Unaudited Pro Forma Financial Information
The following unaudited pro forma financial information summarizes the combined results of operations of Fulgent and Inform
Diagnostics as if the companies had been combined as of the beginning of 2021. The pro forma financial information has been
adjusted for the following:
Acquisition-related costs - Acquisition-related costs incurred by both Fulgent and Inform Diagnostics were excluded from the
net income attributable to Fulgent, and total costs were $9.6 million for the year ended December 31, 2022.
Other adjustments to the net income attributable to Fulgent were $0.8 million for the year ended December 31, 2022. Other
adjustments to revenue were $1.0 million for or the year ended December 31, 2022.
Year Ended December
31, 2022
Revenue
$
659,386
Net income attributable to Fulgent
$
140,288
Basic earnings per common share attributable to Fulgent
$
4.66
Diluted earnings per common share attributable to Fulgent
$
4.53
Fulgent Pharma Holdings, Inc
On November 7, 2022, the Company completed the acquisition of 100% of the outstanding equity of Fulgent Pharma, a clinical-
stage, therapeutic development company focused on perfecting drug candidates for treating a broad range of cancers. Under the terms
of the Agreement and Plan of Merger, dated November 7, 2022, or the Pharma Merger Agreement, the total merger consideration was
paid in a combination of cash, the Company’s common stock, or the Stock Consideration, and assumed RSUs subject to customary
adjustments for closing cash, closing indebtedness, transaction expenses and other transaction matters. A portion of the Stock
Consideration was held back for a duration of time after the closing of the transaction to satisfy certain indemnification obligations of
the Pharma Stockholders as described in the Pharma Merger Agreement. The RSUs are subject to vesting over the four-year period
immediately following the date of their original grant, subject to the holder’s continuing service. The integrated companies plan to
offer a vertically integrated solution to combat cancer with the potential to unlock significant long-term upsides for both the
therapeutic and diagnostic businesses, while effectively managing risk.
The financial results of Fulgent Pharma are included in the consolidated financial statements from the date of acquisition. The
Company allocated the purchase price to tangible and identified intangible assets acquired and liabilities assumed based on estimated
fair values. The following tables summarizes the consideration paid and the updated amounts of the assets acquired and liabilities
assumed recognized at the acquisition date:
F-38
The goodwill of $22.1 million arising from the acquisition is attributed to Fulgent Pharma’s rights to intellectual property,
expected synergies, assembled workforce, and other benefits that will potentially be generated from the combination and deferred tax.
The goodwill recognized is not deductible for tax purposes.
The identified intangible assets acquired consisted of $64.6 million in IPR&D. Fulgent Pharma has developed a novel
nanoencapsulation and targeted therapy platform, which is designed to improve the therapeutic window and pharmacokinetic profile
of new and existing cancer drugs. The lead drug candidate, FID-007, is currently being investigated in the United States to treat
patients diagnosed with various cancers including H&N, ampullary, and pancreatic cancer. The Company has released preliminary
data and completed enrollment for a Phase 1/1b dose escalation/expansion clinical trial for evaluation of FID-007 in treating patients
diagnosed with advanced solid tumors. In this trial and to date, the Company has observed FID-007 to have a manageable safety
profile and observed preliminary evidence of anti-tumor activity in heavily pre-treated patients across various tumor types. The fair
value of the IPR&D was estimated using MPEEM. The method involves forecasting after-tax operating income from existing clients,
subtracting the portions attributable to a contributory asset, and discounting the remaining earnings to present value. The useful life of
IPR&D is indefinite.
Revenue and operating loss from the Fulgent Pharma acquisition since the acquisition date are zero and $0.8 million,
respectively, which are included in the accompanying Consolidated Statements of Operations, for the year ended December 31, 2022.
The transaction costs associated with the acquisition of Fulgent Pharma consisted primarily of legal, regulatory and financial
advisory fees of approximately $1.4 million for the year ended December 31, 2022. These transaction costs were expensed as incurred
as general and administrative expense in the respective period.
The $5.0 million restricted cash received represents cash consideration payable pursuant to the share transfer agreement Fulgent
Pharma entered prior to Fulgent Pharma acquisition date. The cash consideration was not paid as of Fulgent Pharma acquisition date
and was included in noncurrent or non-operating liabilities in above table, and the cash consideration was subsequently paid in 2023.
Note 16. Stock Repurchase Program
In March 2022, the Company’s Board authorized a $250.0 million stock repurchase program. Under the stock repurchase
program, the Company may repurchase shares from time to time in the open market or in privately negotiated transactions. The stock
repurchase program has no expiration from the date of authorization. During the year ended December 31, 2024, the Company
repurchased 10,000 shares of its common stock at an aggregate cost of $0.2 million under the stock repurchase program. During the
year ended December 31, 2023, the Company repurchased 1.0 million shares of its common stock at an aggregate cost of $25.1
million under the stock repurchase program. During the year ended December 31, 2022, the Company repurchased 1.8 million shares
of its common stock at an aggregate cost of $74.3 million under the stock repurchase program. As of December 31, 2024, a total of
approximately $150.5 million remained available for future repurchases of its common stock under the stock repurchase program.
Note 17. Goodwill and Intangible Assets
Changes in the carrying amount of goodwill, net of impairment, by reporting unit for the years ended December 31, 2024 and
2023 are as follows:
Laboratory Services
Therapeutic Development
December 31, 2024
December 31, 2023
December 31, 2024
December 31, 2023
(in thousands)
Balance at beginning of year
$
—
$
120,972
$
22,055
$
22,055
Impairment
—
(120,234)
—
—
Foreign currency impact
—
(738)
—
—
Balance at the end of year
$
—
$
—
$
22,055
$
22,055
The Company has identified its laboratory services business and its therapeutic development business as its two operating
segments, and the Company determined that the operating segments represented the two reporting units. The Company tests for
goodwill impairment at the reporting unit level on December 31st of each year and more frequently if events or circumstances indicate
a potential impairment.
Laboratory Services
In 2023, the Company witnessed a continued decline in its share price and market capitalization which prompted a quantitative
impairment analysis as of December 31, 2023, which led to the full impairment of the laboratory services goodwill.
F-39
Therapeutic Development
As of December 31, 2024, the Company performed an updated valuation for the fair values of its therapeutic development
reporting unit and IPR&D due to significant developments in its clinical pipeline. FID-007 was previously in clinical Phase 1/1b as of
the prior reporting period. The Company has released preliminary results for a Phase 1/1b clinical trial of FID-007 in patients
diagnosed with advanced solid tumors and has begun enrollment of a Phase 2 clinical trial evaluating FID-007 in patients diagnosed
with recurrent or metastatic H&N squamous cell carcinoma. The Company has also received clearance from the FDA to commence a
Phase 1/1b clinical trial evaluating FID-022, a candidate using the same nano-drug delivery platform, in patients diagnosed with
certain cancers. These advancements led to a revised assessment of the probability of success for each molecule, and resulted in an
increase to estimated revenue projections.
The fair value of the Company’s therapeutic development reporting unit was calculated using the income approach weighted at
100% with a WACC of 36%. The fair value of the IPR&D was appraised using the income approach known as multi-period excess
earnings method with a WACC of 36%.
Due to these changes, the fair values of the Company’s therapeutic development reporting unit and IPR&D increased
significantly, and are now substantially higher than the carrying value recorded. The fair value of this reporting unit was $201.4
million and exceeded the carrying value of $54.8 million by approximately 268%, and the fair value of IPR&D was $202.7 million
and exceeded the carrying value of $64.6 million by approximately 214%.
There can be no assurance that the estimates and assumptions management made for the purposes of the goodwill or IPR&D
impairment analysis will prove to be accurate predictions of future performance. It is possible that the conclusions regarding
impairment or recoverability of goodwill or intangible assets could change in future periods. Management will continue to monitor the
therapeutic development reporting unit. For all IPR&D projects, there are major risks and uncertainties associated with the timely and
successful completion of development and commercialization of these drug candidates, including the ability to confirm their efficacy
based on data from clinical trials, the ability to obtain necessary regulatory approvals, and the ability to successfully complete these
tasks within budgeted costs. The Company is not able to market a human therapeutic without obtaining regulatory approvals, and such
approvals require completing clinical trials that demonstrate a drug candidate is safe and effective. In addition, the availability and
extent of coverage and reimbursement from insurance payors, including government healthcare programs and private insurance plans,
impact the revenues a product can generate. Consequently, the eventual realized value, if any, of these acquired IPR&D projects may
vary from their estimated fair values.
F-40
Summaries of intangible assets balances as of December 31, 2024 and 2023 were as follows:
Weighted-Average Amortization Period
December 31, 2024
December 31, 2023
(in thousands)
Laboratory Services
Customer Relationships
13 Years
$
83,088
$
83,119
Less: accumulated amortization
(19,079)
(12,586)
Customer relationships, net
64,009
70,533
Royalty-free technology
10 Years
5,069
5,211
Less: accumulated amortization
(1,859)
(1,390)
Royalty-free technology, net
3,210
3,821
Trade name
8 Years
3,790
3,790
Less: accumulated amortization
(1,401)
(906)
Trade name, net
2,389
2,884
Laboratory information system platform
5 Years
1,860
1,860
Less: accumulated amortization
(1,271)
(899)
Laboratory information system platform, net
589
961
In-place lease intangible assets
5 Years
360
360
Less: accumulated amortization
(186)
(116)
In-place lease intangible assets, net
174
244
Purchased patent
10 Years
27
28
Less: accumulated amortization
(10)
(8)
Purchased patent, net
17
20
Total
70,388
78,463
Therapeutic Development
In-process research & development
n/a
64,590
64,590
Total
64,590
64,590
Total intangible assets, net
$
134,978
$
143,053
Acquisition-related intangibles included in the above tables are generally finite-lived and are carried at cost less accumulated
amortization, except for IPR&D, which is related to the acquisition of Fulgent Pharma in 2022 and has an indefinite life until research
and development efforts are completed or abandoned. All other finite-lived acquisition-related intangibles related to the business
combinations are amortized on a straight-line basis over their estimated lives, which approximates the pattern in which the economic
benefits of the intangible assets are expected to be realized.
Amortization of intangible assets was $8.0 million, $7.8 million and $6.5 million in 2024, 2023, and 2022, respectively.
Based on the carrying value of intangible assets recorded as of December 31, 2024, and assuming no subsequent impairment of
the underlying assets, the annual amortization expense for intangible assets is expected to be as follows:
Amounts
(in thousands)
Year ending December 31,
2025
$
7,955
2026
7,654
2027
7,196
2028
7,161
2029
6,904
Thereafter
33,518
Total
$
70,388
F-41
Note 18. Subsequent Event
Stock Repurchase Program
From January 1, 2025 through February 28, 2025, the Company repurchased 0.2 million shares of its common stock for an
aggregate cost of $3.1 million at an average price of $16.61 per share under the stock repurchase program approved in March 2022.
See Note 16, Stock Repurchase Program. As of February 28, 2025, a total of $147.4 million remained available for future repurchases
of its common stock under the stock repurchase program.