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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, 2016
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: 000-24249
Interpace Diagnostics Group, Inc.
(Exact name of registrant as specified in its charter)
Delaware
(State or other jurisdiction of
incorporation or organization)
22-2919486
(I.R.S. Employer
Identification No.)
Morris Corporate Center 1, Building A
300 Interpace Parkway, Parsippany, NJ 07054
(Address of principal executive offices and zip code)
(844) 405-9655
(Registrant's telephone number, including area code)
Securities registered pursuant to Section 12(b) of the Act:
Title of each class
Common Stock, par value $0.01 per share
Name of each exchange on which registered
The Nasdaq Stock Market LLC
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 ☒
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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 and posted on its corporate Web site, if any, every
Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T during the preceding 12 months (or for
such short period that the registrant was required to submit and post such files). Yes ☒ No ☐
Indicate by check mark if disclosure of delinquent filers pursuant to Item 405 of Regulation S-K is not contained herein, and will not
be contained, to the best of registrant’s knowledge, in definitive proxy or information statements incorporated by reference in Part III of
this Form 10-K or any amendment to this Form 10-K. ☐
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller
reporting company. See definitions of “large accelerated filer,” “accelerated filer,” and “smaller reporting company” in rule 12b-2 of the
Exchange Act. (check one):
Large accelerated filer ☐
Accelerated filer ☐
Non-accelerated filer ☐
(Do not check if a smaller reporting
company)
Smaller reporting company ☒
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 common stock, $0.01 par value per share, held by non-affiliates of the registrant on
June 30, 2016, the last business day of the registrant’s most recently completed second fiscal quarter, was $3,349,502 (based on the
closing sales price of the registrant’s common stock on that date). Shares of the registrant's common stock held by each officer and director
and each person who owns 10% or more of the outstanding common stock of the registrant have been excluded because such persons may
be deemed to be affiliates. This determination of affiliate status is not necessarily a conclusive determination for other purposes.
As of March 30, 2017, 6,723,709 shares of the registrant’s common stock, $0.01 par value per share, were issued and outstanding.
DOCUMENTS INCORPORATED BY REFERENCE
Portions of the registrant’s definitive Proxy Statement for the 2017 Annual Meeting of Stockholders, or the Proxy Statement, to be
filed within 120 days of the end of the fiscal year ended December 31, 2016, are incorporated by reference in Part III hereof. Except with
respect to information specifically incorporated by reference in this Annual Report on Form 10-K, the Proxy Statement is not deemed to be
filed as part hereof.
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PART I
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Risk Factors
Item 1. Business
Item
1A.
Item
1B.
Item 2. Properties
Item 3. Legal Proceedings
Item 4. Mine Safety Disclosures
Unresolved Staff Comments
PART II
Quantitative and Qualitative Disclosures about Market Risk
Item 5. Market for our Common Equity, Related Stockholder Matters and Issuer Purchases of Equity Securities
Item 6. Selected Financial Data
Item 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations
Item
7A.
Item 8. Financial Statements and Supplementary Data
Item 9. Changes in and Disagreements with Accountants on Accounting and Financial Disclosure
Item
9A.
Item
9B.
Controls and Procedures
Other Information
PART III
Item
10.
Item
11.
Item
12.
Item
13.
Item
14.
PART IV
Item
15.
Item
16.
Signatures
*Directors, Executive Officers and Corporate Governance
*Executive Compensation
*Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters
*Certain Relationships and Related Transactions, and Director Independence
*Principal Accounting Fees and Services
Exhibits, Financial Statement Schedules
Form 10-K Summary
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* The information required under this item is to be contained in the Proxy Statement for the registrant’s annual meeting of stockholders,
and is incorporated herein by reference. It is anticipated that the Proxy Statement will be filed with the Securities and Exchange
Commission by April 30, 2017.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
FORWARD LOOKING STATEMENT INFORMATION
This Form 10-K 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. Statements that are not
historical facts, including statements about our plans, objectives, beliefs and expectations, are forward-looking statements. Forward-
looking statements include statements preceded by, followed by or that include the words “believes,” “expects,” “anticipates,” “plans,”
“estimates,” “intends,” “projects,” “should,” “could,” “may,” “will,” “can,” “can have,” “likely,” the negatives thereof or similar words and
expressions. These forward-looking statements are contained throughout this Form 10-K, including, but not limited to, statements found
in Part I – Item 1 – “Business” and Part II – Item 7 – “Management’s Discussion and Analysis of Financial Condition and Results of
Operations.”
Forward-looking statements are only predictions and are not guarantees of future performance. These statements are based on current
expectations and assumptions involving judgments about, among other things, future economic, competitive and market conditions and
future business decisions, all of which are difficult or impossible to predict accurately and many of which are beyond our control. These
predictions are also affected by known and unknown risks, uncertainties and other factors that may cause our actual results to be
materially different from those expressed or implied by any forward-looking statement. Many of these factors are beyond our ability to
control or predict. Such factors include, but are not limited to, the following:
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our ability to profitably grow our business, including our ability to finance our business on acceptable terms and
successfully compete in the market;
our ability to obtain broad adoption of and reimbursement for our molecular diagnostic tests in a changing reimbursement
environment;
whether we are able to successfully utilize our operating experience to sell our molecular diagnostic tests;
our limited operating history as a molecular diagnostics company;
our dependence on a concentrated selection of payors for our molecular diagnostic tests;
the demand for our molecular diagnostic tests from physicians and patients;
our reliance on our internal sales forces for business expansion;
our dependence on third parties for the supply of some of the materials used in our molecular diagnostic tests;
our ability to scale our operations, testing capacity and processing technology;
our ability to meet the remaining legacy obligations of our Commercial Services, or CSO, business previously sold or to
meet the acquisition indebtedness related to acquiring our molecular diagnostics businesses;
our ability to comply with the requirements of those certain Senior Secured Promissory Notes, dated as of March 23, 2017,
or the Exchanged Notes, by us and our subsidiary, Interpace Diagnostics, LLC, or Interpace LLC, in favor of the
institutional investor, or the Investor;
the risk of not making our balloon payment of principal and interest due the Investor on June 22, 2018 and the impact on our
business;
the risk of substantial dilution to our stockholders if the Exchanged Notes are converted or exchanged for shares of our
common stock;
the risk of mark-to-market accounting on a quarterly basis for the life of the Exchanged Notes which may impose additional
variability in our financial results;
our ability to obtain further financing or redeem, convert or exchange the remaining Exchanged Notes into equity;
product liability claims against us;
our involvement in current and future litigation against us;
the effect current and future laws, licensing requirements and regulation have on our business including the changing U.S.
Food and Drug Administration, or the FDA, environment as it relates to molecular diagnostics;
the effect of potential adverse findings resulting from regulatory audits of our billing practices and the impact such results
could have on our business;
our exposure to environmental liabilities as a result of our business;
the susceptibility of our information systems to security breaches, loss of data and other disruptions;
our ability to enter into effective electronic data interchange arrangements with our customers
our billing practices and our ability to collect on claims for the sale of our molecular diagnostic tests;
our ability to attract and retain qualified sales representatives and other key employees and management personnel;
competition in the segment of the molecular diagnostics industry in which we operate or expect to operate;
our ability to obtain additional funds in order to implement our business models and strategies;
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
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the results of any future impairment testing for other intangible assets;
our ability to successfully identify, complete and integrate any future acquisitions and the effects of any such items on our
revenues, profitability and ongoing business;
our compliance with our license agreements and our ability to protect and defend our intellectual property rights;
our ability to maintain our listing with The Nasdaq Capital Market, despite our having received notices of non-compliance,
including for failing to have three independent audit committee members and failing to meet the stockholders’ equity
requirement;
the effect of material weaknesses in our disclosure controls and procedures and internal controls;
failure of third-party service providers to perform their obligations to us; and
the volatility of our stock price and fluctuations in our quarterly and annual revenues and earnings.
Please see Part I - Item 1A – “Risk Factors” of this Form 10-K, as well as other documents we file with the U.S. Securities and
Exchange Commission, or the SEC, from time-to-time, for other important factors that could cause our actual results to differ materially
from our current expectations and from the forward-looking statements discussed herein. Because of these and other risks, uncertainties
and assumptions, you should not place undue reliance on these forward-looking statements. In addition, these statements speak only as of
the date of this Form 10-K and, except as may be required by law, we undertake no obligation to revise or update publicly any forward-
looking statements for any reason.
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ITEM 1.
BUSINESS
Company Overview
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
PART I
We are a fully integrated commercial company that provides clinically useful molecular diagnostic tests and pathology services
for improved patient diagnosis and management. We develop and commercialize molecular diagnostic tests and related first line assays
principally focused on early detection of high potential progressors to cancer and leverage the latest technology and personalized medicine
for improved patient diagnosis and management. We currently have three commercialized molecular diagnostic assays in the marketplace
for which we are reimbursed by Medicare and multiple private payors: PancraGEN®, a pancreatic cyst and pancreaticobiliary solid lesion
molecular test that can aid in pancreatic cyst diagnosis and pancreatic cancer risk assessment utilizing our proprietary PathFinder platform;
ThyGenX®, which assesses thyroid nodules for risk of malignancy; and ThyraMIR®, which assesses thyroid nodules for risk of
malignancy utilizing a proprietary gene expression assay. We are also in the process of “soft launching” while we gather additional market
data, BarreGEN®, an esophageal cancer risk classifier for Barrett’s Esophagus that utilizes our PathFinder platform.
Our mission is to provide personalized medicine through molecular diagnostics and innovation to advance patient care based on
rigorous science. We are leveraging our Clinical Laboratory Improvement Amendments, or CLIA, certified and College of American
Pathologists, or CAP, accredited laboratories to develop and commercialize our assays and products. We aim to provide physicians and
patients with diagnostic options for detecting genetic and other molecular mutations that are associated with gastrointestinal and endocrine
cancer. Our customers consist primarily of physicians, hospitals and clinics.
With the completion of the sale of substantially all of our contract sales organization (CSO) business in December 2015 and
transition of related activities through September 2016, we are now concentrating our efforts on our molecular diagnostics business by
offering solutions for determining the presence of certain cancers to clinicians and their patients as well as providing prognostic pre-
cancerous information, which we believe to be an expanding market opportunity. The global molecular diagnostics market is estimated to
be $6.45 billion and is a segment within the approximately $60 billion in vitro diagnostics market. We believe that the molecular
diagnostics market offers significant growth and strong patient value given the substantial opportunity it affords to lower healthcare costs
by helping to reduce unnecessary surgeries and ensuring the appropriate frequency of monitoring. We are keenly focused on growing our
test volumes, securing additional coverage and reimbursement, maintaining our current reimbursement and supporting revenue growth for
our three commercialized innovative tests, introducing related first line product and service extensions, as well as expanding our business
by developing and promoting synergistic products, like BarreGEN®, in our market.
In March 2016, we announced that we implemented a broad-based program to maximize efficiencies and cut costs as we focus on
improving cash flows and profitability while completing our transition to a standalone molecular diagnostics business. In addition to
reducing headcount, we realigned our compensation structure, consolidated positions, eliminated programs and development plans that did
not have near term benefits, and streamlined and right-sized operating systems while reducing overhead. This was done while supporting
the transition of our CSO business to the buyer of that business and continuing to shut-down less profitable CSO contracts that were not
part of the sale of that business.
In August 2016, we announced that the New York State Department of Health had reviewed and approved ThyraMIR®, the
Company’s micro RNA gene-expression based test, for use in New York State. New York State accounts for approximately 5% of the
600,000 Thyroid Fine Needle Aspirate, or FNA, biopsies performed in the U.S. annually according to Thyroid Disease Manager. With this
final approval ThyraMIR® is now available to patients across the U.S.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
In October 2016, we announced that the New York State Department of Health had reviewed and approved for use ThyGenX®,
our NextGen Sequencing oncogene panel for thyroid nodules. The New York State approval of ThyGenX® enables us to test specimens
from patients in New York and therefore, enables us to market both ThyGenX® and ThyraMIR® together in that state. As ThyGenX®
always precedes the running of ThyraMIR®, approximately 80 of ThyGenX® cases warranting reflex to a more sophisticated RNA
assessment via ThyraMIR®. Of the several states that require special licensure to provide testing to patients who reside in their
jurisdiction, New York was the final state to issue a license.
Also, in October 2016, we announced completion and the validation and launch of two new thyroid services, further expanding
our comprehensive support of physicians and health care institutions servicing thyroid patients. Our new cytopathology service is designed
to assist physicians and clinics that prefer to have the initial FNA biopsy assessed by an independent third party versus having it
performed on site.
We have been successfully expanding the reimbursement of our products in 2016. In summary, three of our molecular
diagnostics are now covered by Medicare. Specifically we have made the following progress with payors in 2016:
● In December 2016, we announced that Aetna, the third largest health plan in the United States, agreed to cover our
ThyraMIR® test, the first micro RNA classifier made available for improving the diagnosis of indeterminate thyroid
nodules, for all of Aetna’s approximately 46 million members nationwide, with coverage effective immediately. Our
ThyGenX® and ThyraMIR® thyroid assays are now covered for approximately 200 million patients nationwide,
including through Medicare, national and regional health plans.
● In April 2016, we announced that we received coverage for all of our products by Galaxy Health Network, a national
managed care provider with over 3.5 million covered lives. Galaxy Health Network’s Preferred Provider Organization
includes a network of over 400,000 contracted physicians, 2,700 hospitals and 47,000 ancillary providers.
● In April 2016, we also announced new coding by Novitas Solutions, Inc., or Novitas Solutions, for PancraGEN®.
Novitas Solutions has assigned a new molecular Current Procedural Terminology, or CPT, code to its PancraGEN® test
for pancreatic cysts. Prior to this coding change, the test was covered under a miscellaneous chemistry code, which is used
for billing a wide range of tests across the laboratory industry and does not effectively differentiate between technologies
that have significantly different features and offer unique benefits to patients with specific diseases.
● In February 2016, we announced that we received Medicare approval for coverage of ThyraMIR®. As a
result, ThyraMIR® is now accessible to more than 50 million Medicare covered patients nationwide effective December
14, 2015. ThyGenX® is already covered by Medicare. Therefore, the addition of coverage for ThyraMIR® provides
Medicare covered patients the benefits of the ThyGenX®/ThyraMIR® combination test.
● In January 2016, we announced that our Medicare administrative carrier, or MAC, Novitas Solutions, issued a new local
coverage determination, or LCD, for PancraGEN®. The LCD provides the specific circumstances under which
PancraGEN® is covered. The new policy is non-conditional and may improve the efficiency of the testing process for
doctors and patients. The LCD covers approximately 55 million patients, bringing the total patients covered for
PancraGEN® to nearly 68 million.
Corporate Information
We were originally incorporated in New Jersey in 1986 and began commercial operations as a CSO in 1987. In connection with
our initial public offering, we reincorporated in Delaware in 1998. We currently operate under one operating segment, which is our
molecular diagnostic business. We conduct our business through our wholly-owned subsidiaries, Interpace LLC, which was formed in
Delaware in 2013, and Interpace Diagnostics Corporation (formerly known as RedPath Integrated Pathology, Inc.), which was formed in
Delaware in 2007. Our executive offices are located at Morris Corporate Center 1, Building A, 300 Interpace Parkway, Parsippany, New
Jersey 07054. Our telephone number is (855) 776-6419.
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Our Business
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
We are developing and commercializing molecular diagnostic tests principally focused on early detection high potential
progressors to cancer and leveraging the latest technology and personalized medicine for patient diagnosis and management. We currently
have three commercialized molecular diagnostic assays in the marketplace for which we are reimbursed by Medicare and multiple private
payors: PancraGEN®, a pancreatic cyst and pancreaticobiliary solid lesion molecular test that can aid in pancreatic cyst diagnosis and
pancreatic cancer risk assessment utilizing our proprietary PathFinder platform; ThyGenX®, which assesses thyroid nodules for risk of
malignancy; and ThyraMIR®, which assesses thyroid nodules for risk of malignancy utilizing a proprietary gene expression assay. We are
also in the process of “soft launching” while we gather additional market data, BarreGEN®, an esophageal cancer risk classifier for
Barrett’s Esophagus that utilizes our PathFinder platform.
Our mission is to provide personalized medicine through molecular diagnostics and innovation to advance patient care based on
rigorous science. We are leveraging our CLIA certified and CAP accredited laboratories to develop and commercialize our assays and
products. We aim to provide physicians and patients with diagnostic options for detecting genetic and other molecular mutations that are
associated with gastrointestinal and endocrine cancer. Our customers consist primarily of physicians, hospitals and clinics.
With the completion of the sale of substantially all of our CSO business in December 2015 and transition of related activities
through September 2016, we are now concentrating our efforts on our molecular diagnostics business by offering solutions for determining
the presence of certain cancers to clinicians and their patients as well as providing prognostic pre-cancerous information, which we believe
to be an expanding market opportunity. The global molecular diagnostics market is estimated to be $6.45 billion and is a segment within
the approximately $60 billion in vitro diagnostics market. We believe that the molecular diagnostics market offers significant growth and
strong patient value given the substantial opportunity it affords to lower healthcare costs by helping to reduce unnecessary surgeries and
ensuring the appropriate frequency of monitoring. We are keenly focused on growing our test volumes, securing additional coverage and
reimbursement, maintaining our current reimbursement and supporting revenue growth for our three commercialized innovative tests as
well as expanding our business by developing and promoting synergistic products, like BarreGEN®, in our market.
Strategy
Our primary goal now is to build a leading oncology diagnostics business focused on gastrointestinal and endocrine cancer
markets. We seek to grow our molecular diagnostics business both organically as well as by selective partnering. The key elements of our
strategy to achieve this goal include:
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Continuing to deleverage our balance sheet and improve liquidity;
Leveraging our predictable gastrointestinal and endocrinology businesses, PancraGEN , ThyGenX and ThyraMIR and
focusing on personalized medicine and early intervention related to cancer risk;
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Expanding our soft launch of BarreGEN , our esophageal cancer risk classifier for Barrett’s Esophagus that utilizes our
PathFinder platform, to continue to gather data and seek key reimbursement support while seeking larger partners to collaborate
with us and speed up full market introduction;
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Targeting synergistic product and service opportunities to distribute through our commercial structure;
• Developing and commercializing other related first-line assays and service offerings to assist in the awareness of our current
products and services;
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Expanding our sales staff appropriately while supporting our products with high quality data and studies and seeking dependable
and appropriate reimbursement rates; and
Improving our awareness and opportunities in the public markets.
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Recent Business Developments
Blue Cross Blue Shield Agreement
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
On January 3, 2017, we announced that we had entered into an agreement with the Blue Cross Blue Shield (BCBS) Association’s
Center for Clinical Effectiveness “Evidence Street”, a program that provides us with the opportunity to provide available evidence for our
molecular Thyroid and Pancreas tests, to support further coverage determinations among Blue Cross Blue Shield and other health plans.
International Expansion – Agreement with Best Med Opinion Ltd
On January 20, 2017, we announced that we had entered into an agreement with Best Med Opinion Ltd, or Best Med, of Tel Aviv,
Israel, a provider of second opinion and clinical services for physicians and patients in Israel and several other countries. As part of this
agreement, effective February 1, 2017, Best Med will provide physicians and patients with information regarding our ThyGenX®,
ThyraMIR®, and PancraGEN® tests, and when these tests are selected to support and inform treatment decisions, Best Med will manage
the logistics associated with collecting and shipping samples to our CLIA certified, CAP accredited laboratories and report results back to
the ordering physician. The agreement designates Best Med as the exclusive provider of our products for the country of Israel, and under
the agreement, providers in Israel will be able to order all of our marketed molecular diagnostic products. The agreement is part of our
international expansion efforts to leverage the opportunities for our products outside the U.S. market.
Reporting Segments
We currently operate under one operating segment, which is our molecular diagnostic business. Until December 22, 2015 prior to the
sale of the CSO business, we operated under two reporting segments: Commercial Services and Interpace Diagnostics. The CSO business
is reported as discontinued operations for the periods ended December 31, 2015 and 2016.
Our Business
In August 2014, we acquired certain assets from Asuragen Inc., or Asuragen, in the endocrine and thyroid cancer sectors, and in
October 2014, we acquired our pancreatic and gastrointestinal assets from RedPath Integrated Technologies Inc., or RedPath. In December
2015, we sold the majority of the assets of our CSO business and became a dedicated molecular diagnostics and related first line assays,
company.
We are now a molecular diagnostics company that is focused on improving patient care by resolving diagnostic uncertainty with
evidence that is trustworthy and actionable. Our products and services uniquely combine genomic technology, clinical science and
pathological review to provide answers that give physicians and patients a clear path forward and help avoid risky, costly surgeries that are
often unnecessary.
Our goal is to drive shareholder value by improving patient outcomes and reducing the cost of healthcare.
The role of molecular diagnostic information in medical practice is evolving rapidly. The diagnosis of complex diseases as well as the
role of molecular diagnostics in treatment decisions continue to expand to complement the evaluation performed by pathologists.
Information at the molecular level enables one to understand more fully the makeup and specific subtype of disease to improve diagnosis.
In many cases, the molecular diagnostic information derived can ultimately help guide treatment decisions as part of the standard of care.
We deploy biomarker analysis combined with microRNA expression to improve diagnostic clarity for cancer. In our thyroid and
pancreatic cancer indications, diagnosis can be ambiguous and can lead to indeterminate first line assessments and uncertainty among
physicians regarding how to effectively treat patients. Accordingly, physicians may often select surgery due to lack of confirmation of
disease progression. Our tests are designed to provide clarity of diagnosis that can in turn guide treatment decisions often, eliminating
costly, risky surgeries and other unnecessary medical procedures, improving the lives of patients and saving the healthcare system money.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Patients typically access our tests through their physician during the diagnostic process. All of our testing services are made available
through our clinical reference laboratories located in Pittsburgh, Pennsylvania and New Haven, Connecticut, which are each CLIA
certified and CAP accredited.
The published evidence supporting our tests demonstrates the robustness of our science and clinical studies. Patients and physicians
can access our full list of publications on our website. We continue to build upon our extensive library of clinical evidence. We also
expect to continue expanding our offerings in gastrointestinal and endocrinology cancers, as well as other cancer indications that we
believe will benefit from our technology and approach.
We believe our focus on developing clinically useful tests that change patient care is enabling the company to continue to expand.in
this marketplace. Our thyroid assays, ThyGenX® and ThyraMIR®, are covered by our MAC, Novitas Solutions, and are now covered for
more than 200 million people in the U.S. for use in thyroid cancer diagnosis. Our thyroid assay, PancraGEN®, for pancreatic cancer is also
covered by Novitas Solutions and is now covered for more than 97 million people in the US.
Background
The global molecular diagnostics market is estimated to be $6.45 billion and is a segment within the approximately $60 billion in vitro
diagnostics market.
The molecular diagnostics segment is highly fragmented with numerous science-based companies that have developed clinical tests
that are on the market or ready or near ready to be marketed. A vast majority of these companies have very limited experience bringing a
test to market and many of them do not have the capital to build an infrastructure to effectively commercialize their tests. Due to their
complexity, most molecular diagnostic tests require a specialized go-to-market strategy that includes messaging to physicians, hospitals
and potentially patients and managed care organizations. Additionally, robust data and clinical studies are often necessary to demonstrate
to physicians and managed care organizations the benefit and utility of the assays offered. We believe that developing and delivering these
kinds of messages is one of our core strengths.
Oncology, which represents the third largest segment after infectious disease and blood screening, is one of the fastest growing
segments of the molecular diagnostics market. The Centers for Medicare and Medicaid Services, or CMS, of the Department of Health and
Human Services estimated in June 2014 that there were more than 5,900 independent clinical reference laboratories and specialty clinics,
and more than 8,900 hospital-based laboratories, in the United States.
Our Molecular Diagnostic Tests
We are developing and commercializing molecular diagnostic tests to detect genetic alterations that are associated with
gastrointestinal and endocrine cancer risk, which are principally focused on early detection of high potential progressors to cancer. Our
tests assist healthcare providers in distinguishing between patients at risk for progression to cancer versus non-progressors. Thus, as part of
a comprehensive diagnostic and treatment plan, our tests allow healthcare providers to determine whether surgery or surveillance is most
appropriate. We, therefore, believe our tests can help identify patients at high risk for cancer. We also believe our tests can avoid
unnecessary surgeries in those at low risk, thereby reducing healthcare costs and potential risks associated with surgery.
We offer PancraGEN®, a molecular diagnostic test designed for determining risk of malignancy in pancreatic cysts and solid
pancreaticobiliary lesions, ThyGenX®, a next-generation sequencing test in combination with ThyraMIR®, a novel microRNA gene
expression classifier, designed to assist physicians in distinguishing between benign and malignant genotypes in indeterminate thyroid
nodules, and BarreGEN®, an assay for evaluating Barrett’s Esophagus, an esophageal cancer risk classifier, which we distribute today to
limited customers while we gather additional data, perform clinical studies, seek initial reimbursement and are looking for collaboration
partners.
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Gastrointestinal Cancer Tests
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Our current gastrointestinal cancer risk diagnostic test, PancraGEN® is based on our PathFinderTG platform, or PathFinder.
PathFinder is designed to use advanced clinical algorithms to accurately stratify patients according to risk of cancer by assessing panels of
DNA abnormalities in patients who have pancreaticobiliary lesions (cysts or solid masses) with potential for cancer. PathFinder is
supported by our state of the art CLIA certified, and CAP accredited laboratory in Pittsburgh, Pennsylvania. Our Pittsburgh laboratory is
our major commercial-scale and development Center of Excellence where we process the majority of our current and future oncology
related tests, and we support our gastrointestinal development activities through this laboratory.
Accurate detection of pancreatic cancer risk is crucial. Pancreatic cancer is now the third leading cause of cancer deaths in the U.S.
with an average survival rate of five years. PancraGEN® is designed to determine the risk of malignancy in pancreatic cysts and
pancreaticobiliary solid lesions. We believe that PancraGEN® is the leading integrated molecular diagnostic test for determining risk of
malignancy in pancreatic cysts currently available on the market. We currently estimate that the immediate addressable market for
PancraGEN® is approximately 150,000 indeterminate cysts annually or approximately $350 million annually based on the current size of
the patient population and current and anticipated reimbursement rates. To date, PancraGEN® has been used in about 30,000 clinical
cases. The National Pancreatic Cyst Registry study published in Endoscopy in 2015 demonstrated the clinical validity of PancraGEN® and
that it more accurately determined the malignant potential of pancreatic cysts than the Sendai 2012 EUS criteria for detection of malignant
pancreatic cystic lesions in the context of routine clinical care. The vast majority of all surgeries for pancreatic cysts are for benign disease.
The American College of Gastroenterology (ACG) 2015 Guidelines support the basic principle that too many pancreatic surgeries are
being performed unnecessarily on benign lesions. In addition, the 2016 guidelines published by the American Society of Gastroenterology
Endoscopy (ASGE) included a specific recommendation for use of PancraGEN® in specific circumstances where other types of testing and
analysis have not provided sufficient data on which to determine the best course of action for patient treatment. Accordingly, we believe
that PancraGEN® provides a highly reliable diagnostic option for distinguishing between patients with pancreatic cysts who are at low or
high risk for developing pancreatic cancer.
We have also developed a cancer risk diagnostic assay, BarreGEN®, which is designed to evaluate patients with Barrett’s esophagus,
an upper gastrointestinal condition that can progress into esophageal cancer. BarreGEN®, which utilizes our PathFinder platform, is
distributed today on a limited basis while we gather additional data, perform clinical studies, seek initial reimbursement and are looking
for collaboration partners. We preliminarily estimate that the total market is approximately $2 billion annually based on the current size of
the patient population and anticipated reimbursement rates comparable to those received currently for PancraGEN® for pancreatic cysts.
We are planning to expand our initial soft launch of BarreGEN® in 2017 and seek to partner this product for development and marketing
with a larger partner in the gastrointestinal diagnostic market.
Endocrine Cancer Tests
We currently market and sell a dual platform endocrine cancer risk diagnostic test. The incidence of thyroid nodules is on the rise.
ThyGenX® is a next generation DNA and RNA sequencing oncogene panel and when applied to indeterminate FNA, provides a highly
specific “rule-in” test with over 80% positive predictive value in predicting whether a patient’s thyroid nodule is cancerous. ThyGenX®
works synergistically with our second endocrine cancer diagnostic test ThyraMir®, which is based on microRNA and is designed to
provide a highly sensitive “rule-out” test to accurately categorize a mutation negative indeterminate FNA as being benign or malignant.
Our testing is performed in our state of the art CLIA certified, CAP accredited laboratories in Pittsburgh, Pennsylvania and New Haven,
Connecticut. We estimate the total market for our endocrine cancer diagnostic tests is approximately $350 million annually based on the
current size of the patient population, estimated numbers of indeterminate FNAs and current and anticipated reimbursement rates.
ThyGenX® is used by some customers as a base line oncogene panel assessment and approximately 80% of such users will reflex to also
using ThyraMIR® as a more specific evaluation.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Endocrinologists evaluate thyroid nodules for possible cancer by collecting cells through FNAs that are then analyzed by
cytopathologists to determine whether or not a thyroid nodule is cancerous. It is estimated that up to 20% or up to approximately 100,000
of FNAs analyzed annually yield indeterminate results, meaning they cannot be diagnosed as definitely being malignant or benign by
cytopathology alone. Traditionally, guidelines recommended that some patients with indeterminate cytopathology results undergo surgery
to remove all or part of their thyroid to obtain an accurate diagnosis by looking directly at the thyroid tissue. Historically, in approximately
70% to 80% of these cases, the thyroid nodule proves to be benign. In addition to exposing a patient to unnecessary surgical risk and
incurring costs, surgery can lead to a lifetime of thyroid hormone replacement therapy. Our ThyGenX and ThyraMir
assays, are aimed
at significantly improving the ability of physicians to determine an accurate diagnosis of an indeterminate FNA result.
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Research and Development
We conduct most of our research and development activities at our CLIA certified and CAP accredited laboratories in Pittsburgh,
Pennsylvania and New Haven, Connecticut. Our research and development efforts currently focus on providing data and clinical trials and
analyses necessary to support our existing products on the market. Additionally our research and development activities provide product
line extension of our existing products as well as new product opportunities utilizing our proprietary platforms.
We will also focus our research and development efforts on enhancing existing molecular diagnostic tests as new research becomes
available. We may enter collaborative relationships with research and academic institutions for the development of additional or enhanced
molecular diagnostic tests to further increase the depth and breadth of our molecular diagnostic test offerings. Where appropriate, we may
also enter into licensing agreements with our collaborative partners to both license intellectual property for use in our molecular diagnostic
test panels as well as licensing such intellectual property out, as appropriate.
Customers
Our customers consist primarily of physicians, hospitals and clinics. Our revenue channels include reimbursement by Medicare,
Medicare Advantage, Medicaid, and client billings (for example, hospitals and clinics), and commercial payors.
Marketing
Our commercialization efforts are currently focused in Endocrinology and Gastroenterology. Communication of our molecular
diagnostic marketing messaging and value proposition are done principally through our two field based sales teams of approximately 10
representatives each in Endocrinology and Gastroenterology. Additionally we communicate through print, digital advertising, a web
presence, peer-reviewed publications, and trade show exhibits. We believe that our molecular diagnostic tests provide value to payors,
physicians and patients by lowering healthcare costs through avoidance of unnecessary surgeries, reducing the morbidity associated with
unnecessary surgeries for patients, and providing better diagnostic and prognostic insights to physicians. We support the value propositions
of our molecular diagnostic tests through rigorous science that demonstrates their clinical and analytical validity as well as their clinical
utility, which demonstrates how they actually impact physicians’ decisions.
We also communicate to payors, integrated delivery systems and hospital systems about our molecular diagnostic tests' value through
highly trained professionals who are experienced in reimbursement and business to business selling and through face to face meetings,
phone calls, digital communications and advisory boards. We develop health economic analyses and budget impact models and
incorporate these along with our clinical validation studies, and clinical utility studies to demonstrate our molecular diagnostic tests' value
to this distinct and important constituency.
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Intellectual Property
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Patents, trademarks and other proprietary rights are important to us. We generate our own intellectual property and hold numerous
patents and patent applications covering our existing and future products and technologies. As of December 31, 2016, we owned one
issued United States Patent and three issued patents, one each in Australia, Europe (validated in Germany, France, United Kingdom, and
Ireland) and Japan and nine pending patent applications in the United States and seven pending patent applications in Europe, Australia,
Brazil, Canada, Israel and Japan. Provided all maintenance fees and annuities are paid, our issued United States patent expires in 2034 and
our foreign patents expire in 2027, and our pending patent applications, if issued, are expected to expire between 2027 and 2032, absent
any disclaimers, adjustments or extensions. On March 29, 2017 we were notified by the European Patent Office that our EP patent
#1410739.2 for diagnosing thyroid cancer from a sample based upon at least MIR-375 was issued and, provided all maintenance fees and
annuities are paid, expires in 2031. Our patents are directed to certain of the technologies relating to detecting, diagnosing, and classifying
thyroid tumors, pancreatic cysts and other forms of gastrointestinal disorders, such as Barrett's esophagus.
We also rely on a combination of trade secrets and proprietary processes to protect our intellectual property. We enter into non-
disclosure agreements with certain vendors and suppliers to attempt to ensure the confidentiality of our intellectual property. We also enter
into non-disclosure agreements with our customers. In addition, we require that all our employees sign confidentiality and intellectual
property assignment agreements.
In addition to our own molecular diagnostic test development efforts, we are currently using, and intend to use in the future, certain
tests and biomarkers that have been developed by third parties or by us in collaboration with third parties. While a significant amount of
intellectual property in the field of molecular diagnostic tests is already in the public domain, ThyraMIR , ThyGenX , PancraGEN and
some of the future tests developed by us, or by third parties on our behalf for use in our tests, may require, that we license the right to use
certain intellectual property from third parties and pay customary royalties or make one time payments.
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On August 13, 2014, the Company, consummated an agreement to acquire certain fully developed thyroid and other tests in
development for thyroid cancer, associated intellectual property and a biobank with more than 5,000 patient tissue samples, or the
Acquired Property Asuragen, pursuant to an asset purchase agreement, or the Agreement. The Company paid $8.0 million at closing and
paid an additional $0.5 million to Asuragen for certain integral transition service obligations set forth in a transition services agreement,
entered into concurrently with the Agreement. The Company also entered into two license agreements with Asuragen relating to the
Company’s ability to sell the fully developed diagnostic tests and other tests in development for thyroid cancer. Under the Asuragen
License Agreement, we owed a $500,000 milestone payment, all of which was paid in installments throughout 2016 and paid in full as of
January 13, 2017. We are further obligated to pay royalties on the future net sales of the miRInform® pancreas platform for a period of ten
years following a qualifying sale, on the future net sales of the miRInform® thyroid platform through August 13, 2024 and on certain
other thyroid diagnostics tests for a period of ten years following a qualifying sale.
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Additionally, we have a broad and growing trademark portfolio. We have secured trademark registrations for the marks PancraGEN ,
BarreGEN and miRInform® in the United States, and miRInform® with the World Intellectual Property Organization. We also have
pending trademark applications for our other molecular diagnostic tests in the United States.
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Competition
We compete on the basis of such factors as reputation, service quality, management experience, performance record, customer
satisfaction, ability to respond to specific customer needs, integration skills, product portfolio, and price. Increased competition and/or a
decrease in demand for our services or molecular diagnostic tests may also lead to other forms of competition. We believe that our
business has a variety of competitive advantages that allow us to compete successfully in the marketplace. While we believe we compete
effectively with respect to each of these factors, certain of our competitors are substantially larger than us and have greater capital,
personnel and other resources than we have. Many of our competitors also offer broader product lines outside of the molecular diagnostic
testing market, and many have greater brand recognition than we do. Moreover, our competitors may make rapid technological
developments that may result in our technologies and products becoming obsolete before we recover the expenses incurred to develop
them or before they generate significant revenue. Increased competition may lead to pricing pressures and competitive practices that
could have a material adverse effect on our market share and our ability to attract new business opportunities as well as our business,
financial condition and results of operations.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
We also compete with physicians and the medical community who use traditional methods to diagnose gastrointestinal and endocrine
cancers. In many cases, practice guidelines in the United States have recommended therapies, surveillance or surgery to determine if a
patient’s condition is malignant or benign. As a result, we believe that we will need to continue to educate physicians and the medical
community on the value and benefits of our molecular diagnostic tests in order to change clinical practices and continue to support the use
of molecular diagnostic tests in clinical guidelines.
Specifically, in regard to our thyroid diagnostic tests, Veracyte, Inc., or Veracyte, has a molecular thyroid nodule cancer diagnostic test
tests. Quest Diagnostics Incorporated, or
(Afirma) that is the current market leader and competes with our ThyGenX and ThyraMir
Quest, currently offers a diagnostic test similar to the earlier version of our ThyGenX test and recently announced an agreement to
distribute the Affirma test in partnership with Veracyte. CBLPath, Inc., or CBL, is offering a diagnostic test that analyzes genetic
alterations using next-generation sequencing and in 2016 Rosetta Genomics introduced a thyroid cancer micro RNA assay. Other
competitors include Rosetta Genomics, Accelerate Diagnostics, Inc., Cancer Genetics, Inc., Genomic Health Inc., NeoGenomics Inc. and
Trovagene, Inc.
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We are currently not aware of any direct competitors to PancraGEN that integrate clinical, imaging, cytology, and molecular
information to stratify patients' risk for malignancy and inform physicians on the best course of action, i.e. surgery or surveillance and
surveillance interval length. Recently, University of Pittsburgh Medical Center began offering PanSeq, a Next Generation Sequencing
"gene only" panel that focuses on the analysis of mutations in four oncogenes and three tumor suppressor genes, most of which may help
establish the type of pancreatic cyst present and some of which may help establish the presence of malignancy. All but one of these related
genomic regions are included in PancraGEN . This laboratory test however does not integrate any additional information to fully
characterize a patient's risk for pancreatic cancer. Importantly, there has been no long-term clinical validation or utility studies completed
on any gene panel for pancreatic cyst fluid other than that associated with PancraGEN . PancraGEN has been validated in multiple
studies and peer reviewed publications and has been used in over 30,000 patients. Notably, the Company has validated and is currently
planning the 2017 launch of a DNA only version of PancraGEN , known as PanDNA™.
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It is also possible that we face future competition from laboratory-developed tests, or LDTs, developed by commercial laboratories
such as Quest and other diagnostic companies developing new tests or technologies. Furthermore, we may be subject to competition as a
result of new, unforeseen technologies that may be developed by our competitors in the gastrointestinal and endocrine cancer molecular
diagnostic tests space.
We are aware of companies that are in the process of developing assays and laboratory development tests for Barrett’s esophagus,
such as Cernostics Inc. In addition, NeoGenomics, Inc. is marketing a Barrett’s assay, so it is likely that this space will be competitive in
the future.
Government Regulations and Industry Guidelines
The healthcare industry, and thus our business, is subject to extensive Federal, State, local and foreign regulation. Both Federal and
State governmental agencies continue to subject the healthcare industry to intense regulatory scrutiny, including heightened civil and
criminal enforcement efforts. We believe that we have structured our business operations and relationships with our customers to comply
with applicable legal requirements. However, it is possible that governmental entities or other third parties could interpret these laws
differently and assert otherwise. We discuss below the statutes and regulations that are most relevant to our business and most frequently
cited in enforcement actions.
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Regulations Over Our Clinical Laboratories
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
The conduct and provision of our molecular diagnostic tests are regulated under CLIA. CLIA requires us to maintain Federal
certification. CLIA imposes requirements relating to test processes, personnel qualifications, facilities and equipment, recordkeeping,
quality assurance and participation in proficiency testing. CLIA compliance and certification are also a condition for participation by
clinical laboratories in the Medicare Program and for eligibility to bill for services provided to governmental healthcare program
beneficiaries. As a condition of CLIA certification, our laboratory is subject to survey and inspection every other year, in addition to being
subject to additional random inspections. The biennial survey is conducted by CMS, a CMS agent (typically a State agency), or, if the
laboratory is accredited, a CMS-approved accreditation organization. Sanctions for failure to meet these certification, accreditation and
licensure requirements include suspension, revocation or limitation of a laboratory’s CLIA certification, accreditation or license, which is
necessary to conduct business, cancellation or suspension of the laboratory’s ability to receive Medicare or Medicaid reimbursement, as
well as imposition of plans to correct deficiencies, injunctive actions and civil monetary and criminal penalties. The loss or suspension of a
CLIA certification, imposition of a fine or other penalties, or future changes in the CLIA law or regulations (or interpretation of the law or
regulations) could harm our business. In addition to CLIA requirements, we participate in the oversight program of the CAP. Under CMS
requirements, accreditation by CAP is sufficient to satisfy the requirements of CLIA. CLIA does not preempt State laws that are more
stringent than Federal law. State laws may require additional personnel quality control, record maintenance and/or proficiency testing.
In addition to CLIA certification, we are required to maintain State licenses to conduct testing in our Pittsburgh and New Haven
laboratories. Pennsylvania, New York and Connecticut laws require that we maintain a license and establish standards for the day-to-day
operation of our clinical reference laboratories in Pittsburgh and New Haven. In addition, our clinical reference laboratory is required to be
licensed on a test-specific basis by California, Florida, Maryland, New York (on a test-specific basis) and Rhode Island. California,
Florida, Maryland, New York and Rhode Island laws also mandate proficiency testing for laboratories licensed under the laws of each
respective State regardless of whether such laboratories are located in California, Florida, Maryland, New York or Rhode Island. On
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September 26, 2016 we received approval for our ThyGenX test in New York. We are currently approved to perform ThyGenX ,
ThyraMIR , PancraGEN and BarreGEN in all states including the state of New York. If we were to lose our CAP Accreditation, CLIA
certificate or State licenses for our laboratories, whether as a result of revocation, suspension or limitation, we would no longer be able to
perform our molecular diagnostic tests, which would eliminate a source of revenue, this could have a material adverse effect on our
business, financial condition and results of operations.
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Our Pittsburgh and New Haven laboratories are also subject to licensing and regulation under Federal, State and local laws relating to
hazard communication and employee right-to-know regulations, and the safety and health of laboratory employees. Additionally, our
Pittsburgh and New Haven laboratories are subject to applicable Federal and State laws and regulations and licensing requirements relating
to the handling, storage and disposal of hazardous waste, and laboratory specimens, including the regulations of the Environmental
Protection Agency, the Department of Transportation, and the National Fire Protection Agency. The regulations of the United States
Department of Transportation, Public Health Service and Postal Service apply to the surface and air transportation of laboratory
specimens.
In addition to its comprehensive regulation of safety in the workplace, the United States Occupational Safety and Health
Administration has established extensive requirements relating to workplace safety for healthcare employers whose workers may be
exposed to blood-borne pathogens such as HIV and the hepatitis B virus, by preventing or minimizing any exposure through needle stick or
similar penetrating injuries. Although we believe that we are currently in compliance in all material respects with such Federal, State and
local laws, failure to comply with such laws could subject us to denial of the right to conduct business, fines, criminal penalties and other
enforcement actions.
Further, laboratories that analyze human blood or other biological samples for the diagnosis and treatment of clinical trial subjects
must comply with CLIA, as well as requirements established by Federal law, various States laws and local regulations. In addition, we are
also subject to such laws relating to the handling and disposal of regulated medical waste, hazardous waste and biohazardous waste,
including chemical and biological agents and compounds. Typically, we use outside vendors who are contractually obligated to comply
with applicable laws and regulations to dispose of such waste. These vendors are licensed or otherwise qualified to handle and dispose of
such waste. The failure to meet these requirements may result in civil penalties and suspension or revocation of our CLIA certifications at
our New Haven and Pittsburgh laboratories.
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Potential U.S. Food and Drug Administration Regulation of Diagnostics Tests
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Both United States Federal and State governmental agencies continue to subject the healthcare industry to intense regulatory scrutiny,
including heightened civil and criminal enforcement efforts. As indicated by work plans and reports issued by these agencies, the Federal
government will continue to scrutinize, among other things, the marketing, labeling, promotion, manufacturing and export of molecular
diagnostic tests. While subject to oversight by CMS through its enforcement of CLIA, the FDA has claimed regulatory authority over all
laboratories that produce LDTs, a type of in vitro diagnostic test that is designed, manufactured and used within a single laboratory. The
FDA has regulatory responsibility over, among other areas, instruments, test kits, reagents and other devices used in clinical laboratories to
perform diagnostic testing in the United States.
The FDA has generally exercised enforcement discretion over all LDTs. However, in October 2014, the FDA issued two draft
guidance documents: “Framework for Regulatory Oversight of Laboratory Developed Tests,” which provided an overview of how the
FDA would regulate LDTs through a risk-based approach, and “FDA Notification and Medical Device Reporting for Laboratory
Developed Tests,” which provided guidance on how the FDA intends to collect information on existing LDTs, including adverse event
reports. Pursuant to the Framework for Regulatory Oversight draft guidance, LDT manufacturers would be subject to medical device
registration, listing, and adverse event reporting requirements. LDT manufacturers would be required to either submit a pre-market
application and receive the FDA’s approval before an LDT may be marketed or submit a pre-market notification in advance of marketing.
The Framework for Regulatory Oversight draft guidance states that within six months after the guidance documents are finalized, all
laboratories will be required to give notice to the FDA and provide basic information concerning the nature of the LDTs offered. If the
FDA were to regulate LDTs as proposed under the 2014 draft guidance documents, then it would classify LDTs into one of three classes
according to the current system used to regulate medical devices. Class I devices are those for which reasonable assurance of the safety
and effectiveness can be provided by adherence to the FDA’s general regulatory controls for medical devices. Class II devices are subject
to the FDA’s general controls, and any other special controls as deemed necessary by the FDA to provide reasonable assurance of the
safety and effectiveness of the devices. Class III devices are those devices which are deemed by the FDA to pose the greatest risk, such as
life-sustaining, life-supporting or implantable devices, have a new intended use, or use advanced technology that is not substantially
equivalent to that of a legally marketed device. Under the guidance documents, LDTs would also be subject to significant post-market
requirements as well.
On November 18, 2016, however, the FDA announced that it would not release the final guidance at this time and instead would
continue to work with stakeholders, the new administration and Congress to determine the right approach. On January 13, 2017, the FDA
released a discussion paper on LDTs outlining a possible risk-based approach for FDA and CMS oversight of LDTs. According to the
2017 discussion paper, previously marketed LDTs would not be expected to comply with most or all FDA oversight requirements
(grandfathering), except for adverse event and malfunction reporting. In addition, certain new and significantly modified LDTs would not
be expected to comply with pre-market review unless the agency determines certain tests could lead to patient harm. Since LDTs currently
on the market would be grandfathered in, pre-market review of new and significantly modified LDTs could be phased-in over a four-year
period, as opposed to the nine years proposed in the Framework for Regulatory Oversight draft guidance. In addition, tests introduced after
the effective date, but before their phase-in date, could continue to be offered during pre-market review.
The discussion paper notes that FDA will focus on analytical and clinical validity as the basis for marketing authorization. The FDA
anticipates laboratories that already conduct proper validation should not be expected to experience new costs for validating their tests to
support marketing authorization and laboratories that conduct appropriate evaluations would not have to collect additional data to
demonstrate analytical validity for FDA clearance or approval. The evidence of the analytical and clinical validity of all LDTs will be
made publically available. LDTs are encouraged to submit prospective change protocols in their pre-market submission that outline
specific types of anticipated changes, the procedures that will be followed to implement them and the criteria that will be met prior to
implementation.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Despite the FDA decision to not release the guidance at this time, it can choose to regulate LDTs at any time. Failure to comply with
applicable regulatory requirements could result in enforcement action by the FDA, such as fines, product suspensions, warning letters,
recalls, injunctions and other civil and criminal sanctions. There are other regulatory and legislative proposals that would increase general
FDA oversight of clinical laboratories and LDTs. The outcome and ultimate impact of such proposals on the business is difficult to predict
at this time. We are monitoring developments and anticipate that our products will be able to comply with requirements if ultimately
imposed by the FDA. In the meantime, we maintain our CLIA certification of accreditation, which permits the use of LDTs for diagnostics
purposes.
Healthcare, Fraud, Abuse and Anti-kickback Laws
The Anti-kickback Law makes it a felony for a person or entity, including a laboratory, to knowingly and willfully offer, pay, solicit or
receive remuneration, directly or indirectly, in order to induce business that is reimbursable under any Federal healthcare program. A
violation of the Anti-kickback Law may result in imprisonment of up to five years and fines of up to $250,000 for each offense in the case
of individuals and $500,000 for each offense in the case of organizations. Convictions under the Anti-kickback Law result in mandatory
exclusion from federal healthcare programs for a minimum of five years. In addition, HHS has the authority to impose civil assessments
and fines and to exclude healthcare providers and others engaged in prohibited activities from Medicare, Medicaid and other federal
healthcare programs. Actions, which violate the Anti-kickback Law, also incur liability under the Federal False Claims Act, discussed in
more detail below, which prohibits knowingly presenting, or causing to be presented, a false or fraudulent claim for payment to the U.S.
Government.
Although the Anti-kickback Law applies only to federal healthcare programs, a number of states have passed statutes substantially
similar to the Anti-kickback Law pursuant to which similar types of prohibitions are made applicable to all other health plans and third-
party payors. Federal and state law enforcement authorities scrutinize arrangements between healthcare providers and potential referral
sources to ensure that the arrangements are not designed as a mechanism to induce patient care referrals or induce the purchase or
prescribing of particular products or services. The law enforcement authorities, the courts and Congress have also demonstrated a
willingness to look behind the formalities of a transaction to determine the underlying purpose of payments between healthcare providers
and actual or potential referral sources. Generally, courts have taken a broad interpretation of the scope of the Anti-kickback Law, holding
that the statute may be violated if merely one purpose of a payment arrangement is to induce referrals or purchases.
In addition to the requirements discussed above, several other healthcare fraud and abuse laws could have an effect on our business.
For example, provisions of the Social Security Act permit Medicare and Medicaid to exclude an entity that charges the federal healthcare
programs substantially in excess of its usual charges for its services. The terms "usual charge" and "substantially in excess" are ambiguous
and subject to varying interpretations. Further, the Federal False Claims Act, discussed in more detail below, prohibits a person from
knowingly submitting a claim, making a false record or statement in order to secure payment or retaining an overpayment by the federal
government. In addition to actions initiated by the government itself, the statute authorizes actions to be brought on behalf of the federal
government by a private party having knowledge of the alleged fraud. Because the complaint is initially filed under seal, the action may be
pending for some time before the defendant is even aware of the action. If the government is ultimately successful in obtaining redress in
the matter or if the plaintiff succeeds in obtaining redress without the government's involvement, then the plaintiff will receive a
percentage of the recovery. Finally, the Social Security Act includes its own provisions that prohibit the filing of false claims or submitting
false statements in order to obtain payment. Violation of these provisions may result in fines, imprisonment or both, and possible exclusion
from Medicare or Medicaid programs.
We are also subject to the federal physician self-referral prohibitions, commonly known as the Stark Law. These restrictions generally
prohibit us from billing a patient or any governmental or private payor for any diagnostic services when the physician ordering the service,
or any member of such physician's immediate family, has an investment interest in or compensation arrangement with us, unless the
arrangement meets an exception to the prohibition.
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Annual Report on Form 10-K
Persons or entities found to violate the Stark Law are required to refund any payments received pursuant to a referral prohibited by
these laws to the patient, the payor or the Medicare program, as applicable. Sanctions for a violation of the Stark Law include the
following:
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denial of payment for the services provided in violation of the prohibition;
refunds of amounts collected by an entity in violation of the Stark Law;
a civil penalty of up to $15,000 for each service arising out of the prohibited referral;
possible exclusion from federal healthcare programs, including Medicare and Medicaid; and
a civil penalty of up to $100,000 against parties that enter into a scheme to circumvent the Stark Law's prohibition.
These prohibitions apply regardless of the reasons for the financial relationship and the referral. No finding of intent to violate the
Stark Law is required for a violation. In addition, knowing violations of the Stark Law may also serve as the basis for liability under the
Federal False Claims Act.
We do retain healthcare practitioners as key opinion leaders providing consultation in various aspects of the business. These
arrangements as any arrangement that includes compensation to a healthcare provider may trigger Federal or State anti-kickback and Stark
Law liability. Our arrangements are designed to meet available safe harbors and exceptions provided in the anti-kickback laws and Stark
laws, respectively. There is no guarantee that the government will find that these arrangements are designed properly or that they do not
trigger liability. Under existing laws, all arrangements must have a legitimate purpose and compensation must be fair market value. These
terms require some subjective analysis and there is limited available case law or guidance for the application of these laws to the CLIA
Laboratory industry. Safe harbors in the anti-kickback laws do not necessarily equate to exceptions in the Stark Law; and there is no
guarantee that the government will not have issue with the relationships between the laboratories and the healthcare providers.
HIPAA, Fraud and Privacy Regulations
The Federal government’s efforts to combat fraud in the healthcare setting were consolidated and strengthened under Public Law 104-
191, the Health Insurance Portability and Accountability Act of 1996, or HIPAA. HIPAA established a comprehensive program to combat
fraud committed against all health plans, both public and private by, among other things creating two new Federal offenses: healthcare
fraud (18 U.S. Code § 1347) and false statements relating to healthcare matters (18 U.S. Code § 1035). These provisions prohibit: (1) the
knowing and willful execution, or attempted execution, of a scheme or artifice (a) to defraud any healthcare benefit program (including
private payors), or (b) to obtain, by means of false or fraudulent pretenses, representations, or promises, any of the money or property
owned by, or under the custody or control of, any healthcare benefit program, in connection with the delivery of or payment for healthcare
benefits, items, or services; and (2) the knowing and willful (a) falsification, concealment or covering up of a material fact by any trick,
scheme or device, or (b) making of any materially false, fictitious or fraudulent statement or representation, or making or using any
materially false writing or document knowing the same to contain any materially false, fictitious, or fraudulent statement or entry, in
connection with the delivery of or payment for healthcare benefits, items or services. A violation of these provisions is a felony and may
result in fines, imprisonment and/or exclusion from government-sponsored programs.
HIPAA, along with the Health Information Technology for Economic and Clinical Health Act and the various regulations
promulgated thereunder, also establish uniform standards governing the conduct of certain electronic healthcare transactions and
protecting the security and privacy of individually identifiable health information maintained or transmitted by healthcare providers, health
plans and healthcare clearinghouses, which are referred to as “covered entities.” The regulations promulgated under HIPAA govern: the
Privacy of Individually Identifiable Health Information, restricting the use and disclosure of certain individually identifiable health
information (45 C.F.R. §§ 164.500, et seq.); Administrative Requirements for electronic transactions, establishing standards for common
healthcare transactions, such as claims information, plan eligibility, payment information and the use of electronic signatures (45 C.F.R.
§§ 162.100, et seq.); Security Standards for the Protection of Electronic Protected Health Information, requiring covered entities to
implement and maintain certain security measures to safeguard certain electronic health information (45 C.F.R. §§ 164.302, et seq.); and
Breach Notification, requiring covered entities and their business associates to provide notification following a breach of unsecured
protected health information (45 C.F.R. §§ 164.400, et seq.). As a covered entity, and also in our capacity as a business associate to certain
of our customers, we are subject to these standards. While the government intended this legislation to reduce administrative expenses and
burdens for the healthcare industry, our compliance with certain provisions of these standards entails significant costs for us, and our
failure to comply could lead to enforcement action that could have an adverse effect on our business. If we or our operations are found to
be in violation of HIPAA or its implementing regulations, we may be subject to potentially significant penalties, including civil and
criminal penalties, damages and fines.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
In addition to Federal regulations issued under HIPAA, many States and foreign jurisdictions have enacted privacy and security
statutes or regulations that, in some cases, are more stringent than those issued under HIPAA. In those cases, it may be necessary to
modify our planned operations and procedures to comply with the more stringent laws. If we fail to comply with applicable State laws and
regulations, we could be subject to additional sanctions.
Third Party Coverage and Reimbursement
Our customers bill many different payor groups. The majority of reimbursement dollars for traditional laboratory services are
provided by traditional commercial insurance products, most notably preferred provider organizations, or PPOs, and other managed care
plans, as well as government healthcare programs, such as Medicare and Medicaid. PPOs, HMOs and other managed care plans typically
contract with a limited number of laboratories and then designate the laboratory or laboratories to be used for tests ordered by participating
physicians. We are currently an out-of-network provider with most payors, which means we do not have a contract with payors to pay a
specific rate for our tests. We are subject to applicable State laws regarding who should be billed, how they should be billed, how business
should be conducted, and how patient obligations regarding cost sharing should be handled. In addition, if we become an “in-network”
provider for certain payors in the future, we will also be subject to the terms of contracts (which could include reduced reimbursement
rates) and may be subject to discipline, breach of contract actions, non-renewal or other contractually provided remedies for non-
compliance with the contract's requirements and/or applicable laws.
We generally bill third-party payors and individual patients for testing services on a test-by-test basis. Third-party payors include
Medicare, private insurance companies, institutional direct clients and Medicaid, each of which has different billing requirements.
Medicare reimbursement programs are complex and ambiguous, and are continuously being evaluated and modified by CMS. Our ability
to receive timely reimbursements from third-party payors is dependent on our ability to submit accurate and complete billing statements,
and/or correct and complete missing and incorrect billing information. Missing and incorrect information on reimbursement submissions
slows down the billing process and increases the aging of accounts receivable. We must bill Medicare directly for tests performed for
Medicare patients and must accept Medicare’s fee schedule for the covered tests as payment in full. State Medicaid programs are generally
prohibited from paying more than the Medicare fee schedule. Our Pittsburgh and New Haven laboratories have contracted with a
healthcare billing services management company to work with our in-house staff and help manage our third-party billing.
Some billing arrangements require us to bill multiple payors, and there are several other factors that complicate billing (e.g., disparity
in coverage and information requirements among various payors; and incomplete or inaccurate billing information provided by ordering
physicians). We incur additional costs as a result of our participation in Medicare and Medicaid programs because diagnostic testing
services are subject to complex, stringent and frequently ambiguous federal and state laws and regulations, including those relating to
coverage, billing and reimbursement. Additionally, auditing for compliance with applicable laws and regulations as well as internal
compliance policies and procedures adds further cost and complexity to the billing process. Further, our billing systems require significant
technology investment and, as a result of marketplace demands, we need to continually invest in our billing systems. Changes in laws and
regulations could further complicate our billing and increase our billing expense. CMS establishes procedures and continuously evaluates
and implements changes to the reimbursement process and requirements for coverage.
As an integral part of our billing compliance program, we investigate reported failures or suspected failures to comply with Federal
and State healthcare reimbursement requirements. Any Medicare or Medicaid overpayments are reimbursed by us. As a result of these
efforts, we have periodically identified and reported overpayments, reimbursed the payors for overpayments and taken appropriate
corrective action.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
The majority of our bad debt expense comes from two categories, Medicare Advantage payors, which unlike Medicare or CMS, have
coverages that vary according to specific patient health plans and direct-bill invoices to hospital-based laboratories, who may dispute or
refuse payment. We are taking, and plan to continue to take, steps to improve our collection rates in these two areas. The remainder of our
bad debt expense is primarily due to missing or incorrect billing information on requisitions received from healthcare providers.
Historically, due to the nature of our business, we have performed requested testing and have reported test results regardless of
collectability or form of reimbursement. We submit claims for reimbursement on a best efforts basis including the use of a third-party
revenue cycle management firm. If at times the billing information is incorrect or incomplete, we subsequently attempt to contact the
healthcare provider or patient to obtain any missing information and to rectify incorrect billing information. Missing or incorrect
information on requisitions complicates and slows down the billing process and may also impact bad debt expense. The increased use of
electronic ordering reduces the incidence of missing or incorrect information, and the company is seeking to electronically integrate with
more and more payors and clients.
There are a number of factors that influence coverage and reimbursement for molecular diagnostic tests. In the United States, the
American Medical Association assigns specific CPT codes, which are necessary for reimbursement of molecular diagnostic tests. Once the
CPT code is established, CMS establishes reimbursement payment levels and coverage rules under Medicaid and Medicare, and private
payors establish rates and coverage rules independently. However, the availability of a CPT code is not a guarantee of coverage or
adequate reimbursement levels, and the revenues generated from our tests will depend, in part, on the extent to which third-party payors
provide coverage and establish adequate reimbursement levels.
United States and other government regulations governing coverage and reimbursement for molecular diagnostic testing may affect,
directly or indirectly, the design of our tests and the potential market for their use. The availability of third-party reimbursement for our
tests and services may be limited or uncertain. Third-party payors may deny coverage if they determine that the tests or service has not
received appropriate FDA or other government regulatory clearances, is not used in accordance with cost-effective treatment methods as
determined by the payor, or is deemed by the third-party payor to be experimental, unnecessary or inappropriate. Furthermore, third-party
payors, including Federal and State healthcare programs, government authorities, private managed care providers, private health insurers
and other organizations, are increasingly challenging the prices, examining the medical necessity for, and reviewing the cost-effectiveness
of healthcare products and services, including laboratory tests. Such payors may limit coverage of our tests to specific, limited
circumstances, may not provide coverage at all, or may not provide adequate reimbursement rates, if covered. Further, one payor’s
determination to provide coverage does not assure that other payors will also provide coverage for the test. Adequate third-party
reimbursement may not be available to enable us to maintain price levels sufficient to maintain our revenue and growth. Coverage policies
and third-party reimbursement rates may change at any time.
Government payors, such as Medicare and Medicaid, have taken steps and are expected to continue to take steps to control the cost,
utilization and delivery of healthcare services, including clinical test services. For example, Medicare has adopted policies under which it
does not pay for many commonly ordered clinical tests unless the ordering physician has provided an appropriate diagnosis code
supporting the medical necessity of the test. Physicians are required by law to provide diagnostic information when they order clinical tests
for Medicare and Medicaid patients.
Currently, Medicare does not require the beneficiary to pay a co-payment for diagnostic information services reimbursed under the
Clinical Laboratory Fee Schedule. Certain Medicaid programs require Medicaid recipients to pay co-payment amounts for diagnostic
information services.
The Medicare Part B program contains fee schedule payment methodologies for clinical testing services performed for covered
patients, including a national ceiling on the amount that carriers could pay under their local Medicare clinical testing fee schedules.
Historically, the Medicare Clinical Laboratory Fee Schedule, or CLFS, has been subject to change. In April 2014, the President signed the
Protecting Access to Medicare Act of 2014, or PAMA, which included a substantial new payment system for clinical laboratory tests under
the CLFS. PAMA removed CMS’s authority to adjust the CLFS based and established a new method for setting CLFS rates.
Implementation of this new method for setting CLFS rates begins in 2017. Under PAMA, laboratories that have more than $12,500 in
Medicare revenues from laboratory services and that receive more than 50 percent of their Medicare revenues from laboratory services
would report private payor data from January 1, 2016 through June 30, 2016, to CMS between January 1, 2017 and March 31, 2017. CMS
will post the new Medicare CLFS rates (based on weighted median private payor rates) in November 2015 and the new rates will be
effective beginning on January 1, 2017. Any reductions to payment rates resulting from the new methodology are limited to 10% per test
per year in each of the years 2017 through 2019 and to 15% per test per year in each of the years 2020 through 2022. CMS has issued draft
regulations regarding these changes. Further rule-making from CMS will define the time period and data elements evaluated on an annual
basis to set reimbursement rates. Other than our chemistry testing services, our products are defined as Advanced Diagnostic Laboratory
Tests (ALDTs) and therefore, we believe the pricing provisions of PAMA do not affect a majority of our marketed molecular diagnostic
tests. The only testing for which we bill that is included in the CLFS is our carcinoembryonic antigen (CEA) and Amylase chemistry
testing services. For these services, we provided CMS with the median pricing received from all payers in compliance with PAMA
regulations.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Penalties for violations of laws relating to billing government healthcare programs and for violations of federal and state fraud and
abuse laws include: (1) exclusion from participation in Medicare/Medicaid programs; (2) asset forfeitures; (3) civil and criminal fines and
penalties; and (4) the loss of various licenses, certificates and authorizations necessary to operate our business. Civil monetary penalties
for a wide range of violations may be assessed on a per violation basis. A parallel civil remedy under the federal False Claims Act provides
for penalties on a per violation basis, plus damages of up to three times the amount claimed.
Historically, most Medicare and Medicaid beneficiaries were covered under the traditional Medicare and Medicaid programs
administered by the federal government. Reimbursement from traditional Medicare and Medicaid programs represented approximately
61% of our consolidated net revenues during 2015. Over the last several years, the federal government has continued to expand its
contracts with private health insurance plans for Medicare beneficiaries and has encouraged such beneficiaries to switch from the
traditional programs to the private programs, called “Medicare Advantage” programs. There has been growth of health insurance providers
offering Medicare Advantage programs and of beneficiary enrollment in these programs. In recent years, in an effort to control costs, states
also have mandated that Medicaid beneficiaries enroll in private managed care arrangements.
The current position of the laboratories is that they do not meet the definition of an “Applicable Manufacturer” under Patient
Protection and Affordable Care Act, or PPACA (also known as the Affordable Care Act) and therefore are not subject to the disclosure or
tax requirements contained in PPACA. However, as new regulations are implemented and diagnostic tests reclassified, this may change
and the laboratory business may be subject to PPACA as are other companies. There is no guarantee that our interpretation of the law is
now or will be in the future consistent with government guidance and interpretation.
Employees
As of March 15, 2017, we had approximately 61 employees. We are not party to a collective bargaining agreement with any labor
union.
Corporate History
We were originally incorporated in New Jersey in 1986 and began commercial operations as a CSO in 1987. In connection with our
initial public offering, we reincorporated in Delaware in 1998. We currently operate under one operating segment, which is our molecular
diagnostic business. We conduct our business through our wholly-owned subsidiaries, Interpace LLC, which was formed in Delaware in
2013, and Interpace Diagnostics Corporation (formerly known as RedPath Integrated Pathology, Inc.), which was formed in Delaware in
2007. Our executive offices are located at Morris Corporate Center 1, Building A, 300 Interpace Parkway, Parsippany, New Jersey 07054.
Our telephone number is (855) 776-6419.
Available Information
We maintain an internet website at www.interpacediagnostics.com. Our annual report on Form 10-K, quarterly reports on Form 10-
Q, current reports on Form 8-K, and amendments to those reports are available free of charge through the “Investor Relations” portion of
our website, as soon as reasonably practicable after they are filed with the SEC. The content contained in, or that can be accessed through,
our website is not incorporated into this Form 10-K.
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ITEM 1A.
RISK FACTORS
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
In addition to the other information provided in this Annual Report on Form 10-K, including our financial statements and the related notes
in Part II - Item 8, you should carefully consider the following factors in evaluating our business, operations and financial condition.
Additional risks and uncertainties not presently known to us, which we currently deem immaterial or that are similar to those faced by
other companies in our industry or businesses in general, such as competitive conditions, may also impair our business operations. The
occurrence of any of the following risks could have a material adverse effect on our business, financial condition, results of operations or
cash flows.
RISKS RELATING TO OUR BUSINESS
There are substantial doubts about our ability to continue as a going concern due to our operating history of net losses, negative
working capital and insufficient cash flows, and lack of liquidity to pay our current obligations and if we are unable to continue
our business, our shares may have little or no value.
Our ability to become a profitable operating company is dependent upon our ability to generate revenues and/or obtain financing adequate
to support our cost structure. We do not currently have enough cash on hand to meet our obligations over the next twelve months, and we
cannot provide our stockholders any assurance that we will be able to raise sufficient funding from the generation of revenue, the sale of
our common stock, or through financing to sustain us over the next twelve months.
For the fiscal year ended December 31, 2016, we had an operating loss of $6.4 million. As of December 31, 2016, we had cash and cash
equivalents of $0.6 million and current liabilities of $16.2 million. From September 30, 2016 through December 31, 2016, we provided
working capital by extending our payables primarily by not making timely payments on current obligations and debt incurred prior to the
sale of our CSO business, entering into payment plans, negotiating termination agreements on commitments that were not useful to our
current business and not paying certain severance obligations to terminated employees. We completed four public offerings and a private
placement of warrants from December 22, 2016 through February 8, 2017, which resulted in aggregate gross proceeds to us of
approximately $14.1 million. Of that amount, we used approximately $1.3 million to make the first principal payment on that certain Non-
Negotiable Subordinated Secured Promissory Note, dated as of October 31, 2014, as amended, or the RedPath Note, on December 31,
2016 (which RedPath Note has since been acquired by the Investor and exchanged with the Company for the Exchanged Notes) and
approximately $1.0 million on February 27, 2017 to satisfy severance obligations due to five former senior executives. The proceeds from
the public offerings and private placement have improved our overall cash position. However, we remain in default of certain of our
current obligations and certain vendors have either initiated or threatened litigation against us. The Company must also fund its operating
deficit until a sustainable level of revenue is achieved. These factors have raised substantial doubts about our ability to continue as a going
concern. We may need to attempt to raise additional equity capital by selling shares of common stock or other dilutive or non-dilutive
means, if necessary. However, the doubts raised, relating to our ability to continue as a going concern, may make investing in our
securities an unattractive investment for potential investors. These factors, among others, may make it difficult to raise any additional
capital.
Our molecular diagnostics business has limited revenue, and we expect to incur net losses for the foreseeable future and may never
achieve or sustain profitability.
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In 2014, we acquired RedPath and certain assets from Asuragen. As a result, we now offer PancraGEN , ThyGenX , and ThyraMIR
and to a limited extent, BarreGEN . The revenue generated from our molecular diagnostics business was $13.1 million for the fiscal year
ended December 31, 2016. For the fiscal year ended December 31, 2016, our molecular diagnostics business had an operating loss of
approximately $6.4 million. Although we expect the revenue generated from our molecular diagnostics business to grow in the future,
there can be no assurance that we will achieve revenue sufficient to offset expenses. Over the next several years, we expect to continue to
devote resources to increase adoption of, and reimbursement for, our molecular diagnostic tests and to develop and acquire additional
diagnostic solutions. However, our business may never achieve or sustain profitability, and our failure to achieve and sustain profitability
in the future could have a material adverse effect on our business, financial condition and results of operations.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Our profitability will be impaired by our obligations to make royalty and milestone payments to Asuragen.
In connection with our acquisition of certain assets of Asuragen in 2014, we are obligated to make certain royalty and milestone payments.
Under the Asuragen License Agreement, we owed $500,000, all of which was paid in installments throughout 2016 and paid in full as of
January 13, 2017. We are further obligated to pay royalties on the future net sales of the miRInform® pancreas platform for a period of ten
years following a qualifying sale, on the future net sales of the miRInform® thyroid platform through August 13, 2024 and on certain
other thyroid diagnostics tests for a period of ten years following a qualifying sale.
Even if we are able to successfully launch the above referenced diagnostic tests, our profitability will be impaired by our obligations to
make royalty and milestone payments to Asuragen. Although we believe, under such circumstances, that the increase in revenue will
exceed the corresponding royalty and milestone payments, our obligations to Asuragen could have a material adverse effect on our
business, financial condition and results of operations if we are unable to manage our operating costs and expenses at profitable levels.
Our inability to finance our business on acceptable terms in the future may limit our ability to develop and commercialize new
molecular diagnostic solutions and technologies and grow our business, and potentially force us to seek bankruptcy protection.
We expect capital expenditures and operating expenses to increase over the next several years as we expand our infrastructure and
commercial operations. As of December 31, 2016, we had cash and cash equivalents of $0.6 million, net accounts receivable of $2.2
million, current assets of $4.2 million and current liabilities of $16.2 million. Additionally, from December 22, 2016 through February 8,
2017, we raised gross equity capital of approximately $14.1 million. While our overall cash position has improved, our business is not
currently cash flow breakeven or positive, and as a result, we may need to finance our business in the future through collaborations, equity
offerings, debt financings, licensing arrangements or other dilutive or non-dilutive means. Additional funding may not be available to us
on acceptable terms, or at all. If we raise funds by issuing additional equity securities, dilution to our stockholders could result. Further,
our ability to raise additional financing through equity offerings in the future may be more difficult and costly once we file this Annual
Report on Form 10-K for the fiscal year ended December 31, 2016. At that time, we may lose our eligibility to use our registration
statement on Form S-3 (File No. 333-207263) declared effective by the SEC on October 9, 2015. In addition, we granted each institutional
investor who participated in the registered direct offering completed on January 6, 2017, the right, for a period of 15 months following
January 6, 2017, or until April 6, 2018, to participate in any public or private offering by us of equity securities, subject to certain
exceptions, up to such investor’s pro rata portion of 50% of the securities being offered, or the Participation Right. If we fail to comply
with the applicable provisions of the Participation Right or do not receive waivers from such investors, we may not be able to raise funds
through another equity offering. The incurrence of additional indebtedness or the issuance of certain equity securities could result in
increased fixed payment obligations and could also result in restrictive covenants, such as limitations on our ability to incur additional debt
or issue additional equity, limitations on our ability to acquire or license intellectual property rights, and other operating restrictions that
could adversely affect our ability to conduct our business.
We face new risks with respect to our ability to redeem, convert or pay at maturity our newly issued Exchanged Notes.
On March 23, 2017, we exchanged the RedPath Note in the aggregate outstanding principal amount of $9.34 million, which was acquired
by the Investor, for two new Exchanged Notes aggregating $8.9 million. See “Debt Exchange for RedPath Note.” The Exchanged Notes
mature on June 22, 2018, unless earlier redeemed or, in the case of the Exchanged Convertible Note, converted into our common stock.
The Exchanged Notes are secured by all of our assets and the assets of our subsidiaries, which security interest will be released upon the
reduction of 55% of the face amount of each Exchanged Note.
In the event the Exchanged Notes are not earlier redeemed, or in the case of the Exchanged Convertible Note, converted into our common
stock, and we are unable to pay 125% of the outstanding face value of the Exchanged Notes on June 22, 2018, we may face foreclosure of
our assets by the Investor or Ch. 7 or 11 proceedings, which would likely result in limited if any distribution of our remaining assets to our
common stockholders.
In the event of any of the following with respect to the Exchanged Notes, our stockholders may face substantial dilution due to the
issuance of additional shares of our common stock: (1) the Exchanged Convertible Note is converted into our common stock at a fixed
conversion price of $2.44, (2) we exchange our Exchanged Non-Convertible Note for shares of our common stock, (3) we seek and obtain
stockholder approval and the Investor elects to convert the Exchanged Convertible Note at 88% of the market price of our common stock
at the time of conversion, or (4) we elect to cause the Exchanged Notes to be converted into common stock in the event the volume
weighted average price of our common stock for five consecutive trading days exceeds $3.29, which is 135% of the fixed conversion
price. Through March 30, 2017, the Investor converted $4,321,663 of the Exchanged Convertible Note into 1,730,534 shares of our
common stock.
Further, in the event we seek to redeem one or both of the Exchanged Notes prior to maturity, we would have to pay premiums ranging
from 115% to 125% of the face amount of the Exchanged Notes depending on the time of redemption. In the event of an event of default
or change in control accompanied by an equity conditions failure, in each case as defined in the Exchanged Notes, the Investor may require
us to redeem the Exchanged Convertible Note at a premium taking into account the then market price of our common stock.
Additionally, the nature of various clauses in the Exchanged Notes may be determined to be imbedded derivatives for accounting purposes
which may require mark-to-market accounting on a quarterly basis for the life of the Exchanged Notes and which may therefore impose
additional variability in our financial results.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Our financial results currently depend solely on sales of our molecular diagnostic tests, and we will need to generate sufficient
revenue from these and other molecular diagnostic solutions that we develop or acquire to grow our business.
The majority of our revenue currently is derived from the sale of our molecular diagnostic tests, which we initially launched commercially
in the second half of 2014. We have several additional molecular diagnostics tests and complimentary service extensions that we have
recently launched or are in late stage development, but there can be no assurance that we will be able to successfully commercialize or
sufficiently grow those tests. If we are unable to increase sales of our molecular diagnostic tests, expand reimbursement for these tests, or
successfully develop and commercialize other molecular diagnostic tests, our revenue and our ability to achieve and sustain profitability
would be impaired, and this could have a material adverse effect on our business, financial condition and results of operations.
We have a limited operating history as a molecular diagnostics company, which may make it difficult for you to evaluate the
success of our business to date and to assess our future viability.
We were originally incorporated in New Jersey in 1986 and began commercial operations in 1987. In connection with our initial public
offering, we re-incorporated in Delaware in 1998. From 1987 until the Asset Sale, our operations focused primarily on our CSO business,
which was the personal promotion of pharmaceutical customers’ products through outsourced sales teams. We now conduct our molecular
diagnostics business through our wholly owned subsidiaries, Interpace LLC, which was formed in Delaware in 2013, and Interpace
Diagnostics Corporation, which was formed in Delaware in 2007. We began our own commercial sales of our molecular diagnostic tests in
late 2014. Consequently, any evaluations about our future success, performance or viability may not be as accurate as they could be if we
had a longer operating history.
Recent changes in our senior management team and the lack of shared experience among the current members of our senior
management team could negatively affect our results of operations and our business may be harmed.
Effective as of December 22, 2015, Nancy Lurker resigned as our President and Chief Executive Officer and as a member of our Board.
Our Board appointed Jack E. Stover, previously Chairman of our Audit Committee, as Interim President and Chief Executive Officer, and
subsequently, effective June 21, 2016, Mr. Stover was appointed President and Chief Executive Officer. Additionally, in light of the
departure of our previous Chief Financial Officer, James Early was appointed as Chief Financial Officer effective as of October 11, 2016.
Mr. Early also serves as our principal accounting officer. From August 29, 2016 until October 11, 2016, Mr. Early was engaged by us as a
consultant to perform the role of interim chief financial officer.
As a result of these changes, we may experience disruption or have difficulty in maintaining or developing our business during this
transition. Further, our senior management team has limited experience working together as a group. This lack of shared experience could
negatively impact our senior management team’s ability to quickly and efficiently respond to problems and effectively manage our
business. If our management team is not able to work together as a group, our results of operations may suffer and our business may be
harmed.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
The loss of members of our senior management team or our inability to attract and retain key personnel could adversely affect our
business.
As a small company with 61 employees, the success of our business depends largely on the skills, experience and performance of members
of our senior management team and others in key management positions. The efforts of these persons will be critical to us as we continue
to grow our molecular diagnostics business and develop and/or acquire additional molecular diagnostic tests. If we were to lose one or
more of these key employees, we may experience difficulties in competing effectively, developing our technologies and implementing our
business strategy. In addition, our commercial laboratory operations depend on our ability to attract and retain highly skilled scientists,
including licensed clinical laboratory scientists. We may not be able to attract or retain qualified scientists and technicians in the future due
to the competition for qualified personnel, and we may have to pay higher salaries to attract and retain qualified personnel. We may also
be at a disadvantage in recruiting and retaining key personnel as our small size, limited resources, limited liquidity, work force reductions
in late 2015 and recent changes in our senior management team may be viewed as providing a less stable environment, with fewer
opportunities than would be the case at one of our larger competitors. 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 support our clinical laboratory
and commercialization.
We depend on a few payors for a significant portion of our revenue, and if one or more significant payors stops providing
reimbursement or decreases the amount of reimbursement for our molecular diagnostic tests, our revenue could decline.
Revenue for tests performed on patients covered by Medicare was approximately 1% of our revenue for the fiscal year ended December
31, 2016. The percentage of our revenue derived from significant payors is expected to fluctuate from period to period as our revenue
increases, as additional payors provide reimbursement for our molecular diagnostic tests or if one or more payors were to stop reimbursing
for our molecular diagnostic tests or change their reimbursed amounts.
Since September 2012, Novitas Solutions has been the regional MAC that handles claims processing for Medicare services with
jurisdiction for the PancraGEN , ThyGenX , ThyraMIR and BarreGEN . On a five-year rotational basis, Medicare requests bids for its
regional MAC services. Any future changes in the MAC processing or coding for Medicare claims for our molecular diagnostic tests could
result in a change in the coverage or reimbursement rates for such molecular diagnostic tests, or the loss of coverage.
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Our PancraGEN and ThyGenX tests are reimbursed by Medicare based on applicable CPT codes. PancraGEN is currently reimbursed
by Medicare at $3,038 per test, ThyGenX is currently reimbursed by Medicare at $1,054 a test and ThyraMIR is currently reimbursed
by Medicare at $2,110. Presently, our BarreGEN assay is not reimbursed at all. Any future reduction from the current rate would have a
material adverse effect on business and results of operations.
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Although we have entered into contracts with certain third-party payors which establish in-network allowable rates of reimbursement for
our molecular diagnostic tests, payors may suspend or discontinue reimbursement at any time, may require or increase co-payments from
patients, or may reduce the reimbursement rates paid to us. Any such actions could have a negative effect on our revenue.
If payors do not provide reimbursement, rescind or modify their reimbursement policies or delay payments for our tests, or if we
are unable to successfully negotiate additional reimbursement contracts, our commercial success could be compromised.
Physicians may generally not order our tests unless payors reimburse a substantial portion of the test price. There is uncertainty concerning
third-party reimbursement of any test incorporating new molecular diagnostic technology. Reimbursement by a payor may depend on a
number of factors, including a payor’s determination that tests such as our molecular diagnostic tests are: (a) not experimental or
investigational; (b) pre-authorized and appropriate for the patient; (c) cost-effective; (d) supported by peer-reviewed publications; and (e)
included in clinical practice guidelines. Since each payor generally makes its own decision as to whether to establish a policy or enter into
a contract to reimburse our tests, seeking these approvals is a time-consuming and costly process. Although we have contracted rates of
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reimbursement with certain payors, which establishes in-network allowable rates of reimbursement for our PancraGEN , ThyGenX ,
ThyraMIR and PathFinder TG- Barrett's esophagus tests, payors may suspend or discontinue reimbursement at any time, may require or
increase co-payments from patients, or may reduce the reimbursement rates paid to us. Any such actions could have a negative effect on
our revenue.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
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We have contracted rates of reimbursement with many payors for our PancraGEN , ThyGenX and ThyraMIR tests. Without a
contracted rate for reimbursement, claims may be denied upon submission, and we may need to appeal the claims. The appeals process is
time consuming and expensive, and may not result in payment. We expect to continue to focus resources on increasing adoption of and
coverage and reimbursement for our molecular diagnostic tests. We cannot, however, predict whether, under what circumstances, or at
what payment levels payors will reimburse us for our molecular diagnostic tests, if at all. In addition, the launch of our molecular
diagnostic tests in our PancraGEN , ThyGenX , ThyraMIR and PathFinderTG Barrett's platforms and any other new products we may
acquire or develop in the future may require that we expend substantial time and resources in order to obtain and retain reimbursement.
Also, payor consolidation is underway and creates uncertainty as to whether coverage and contracts with existing payors will remain in
effect. Finally, commercial payors may tie their allowable rates to Medicare rates, and should Medicare reduce their rates, we may be
negatively impacted. If we fail to establish broad adoption of and reimbursement for our molecular diagnostic tests, or if we are unable to
maintain existing reimbursement from payors, our ability to generate revenue could be harmed and this could have a material adverse
effect on our business, financial condition and results of operations.
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We may experience limits on our revenue if physicians decide not to order our molecular diagnostic tests.
If we are unable to create or maintain demand for our molecular diagnostic tests in sufficient volume, we may not become profitable. To
generate demand, we will need to continue to educate physicians and the medical community on the value and benefits of our molecular
diagnostic tests in order to change clinical practices through published papers, presentations at scientific conferences and one-on-one
education by our internal sales force. In addition, our ability to obtain and maintain adequate reimbursement from third-party payors will
be critical to generating revenue.
In many cases, practice guidelines in the United States have recommended therapies or surgery to determine if a patient’s condition is
malignant or benign. Accordingly, physicians may be reluctant to order a diagnostic test that may suggest surgery is unnecessary. In
addition, our molecular diagnostic tests are performed at our laboratories rather than by a pathologist in a local laboratory, so pathologists
may be reluctant to support our molecular diagnostic tests. In addition, guidelines for the diagnosis and treatment of thyroid nodules may
change to recommend another type of treatment protocol, and these changes may result in medical practitioners deciding not to use our
molecular diagnostic tests. These facts may make physicians reluctant to convert to using our molecular diagnostic tests, which could limit
our ability to generate revenue and achieve profitability, which could have a material adverse effect on our business, financial condition
and results of operations.
We may experience limits on our revenue if patients decide not to use our molecular diagnostic tests.
Some patients may decide not to use our molecular diagnostic tests due to price, all or part of which may be payable directly by the patient
if the patient’s insurer denies reimbursement in full or in part. Many insurers seek to shift more of the cost of healthcare to patients in the
form of higher co-payments or premiums. In addition, the current economic environment in the United States has and may continue to
result in the loss of healthcare coverage. Implementation of provisions of PPACA (also known as the Affordable Care Act) also resulted in
the loss of health insurance, and increases in premiums and reductions in coverage, for some patients. These events may result in patients
delaying or forgoing medical checkups or treatment due to their inability to pay for our test, which could have an adverse effect on our
revenue. In addition, the President of the United States has announced that he favors repealing PPACA in 2017, and leaders of the
Republication-controlled federal legislature also have expressed a desire to repeal PPACA. The scope and timing of any legislation to
repeal, amend, replace, or reform PPACA is uncertain, but if such legislation were to become law, it could have a significant impact on the
U.S. healthcare system. We do have a Patient Assistance Program that allows eligible patients to apply for assistance in covering a portion
of their out of pocket obligation; however, there is no guarantee that this Program will be sufficient to influence patients to use our
molecular diagnostic tests.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
If our internal sales force is less successful than anticipated, our business expansion plans could suffer and our ability to generate
revenues could be diminished. In addition, we have limited history selling our molecular diagnostics tests on a direct basis and our
limited history makes forecasting difficult.
If our internal sales force is not successful, or new additions to our sales team fail to gain traction among our customers, we may not be
able to increase market awareness and sales of our molecular diagnostic tests. If we fail to establish our molecular diagnostic tests in the
marketplace, it could have a negative effect on our ability to sell subsequent molecular diagnostic tests and hinder the desired expansion of
our business. We have growing, however limited, historical experience forecasting the direct sales of our molecular diagnostics products.
Our ability to produce product quantities that meet customer demand is dependent upon our ability to forecast accurately and plan
production accordingly.
Due to how we recognize revenue, our quarterly operating results are likely to fluctuate.
We recognize a significant portion of our revenue when the following four revenue recognition criteria are met: persuasive evidence of an
arrangement exists; services have been rendered; the selling price is fixed or determinable; and collectability is reasonably assured. We
have little visibility as to when we will receive payment for our molecular diagnostic tests, and we must appeal negative payment
decisions, which delays collections. For molecular diagnostic tests performed where we have an agreed upon reimbursement rate or we are
able to make a reasonable estimate of reimbursement at the time delivery is complete, such as in the case of Medicare and certain other
payors, we recognize the related revenue upon delivery of a patient report to the prescribing physician based on the established billing rate
less contractual and other adjustments to arrive at the amount that we expect to collect. We determine the amount we expect to collect
based on a per payor, per contract or agreement basis. In situations where we are not able to make a reasonable estimate of reimbursement,
we recognize revenue upon the earlier of receipt of third-party notification of payment or when cash is received. Upon ultimate collection,
the amount received from Medicare and other payors where reimbursement was estimated is compared to previous estimates and the
contractual allowance is adjusted accordingly. These factors will likely result in fluctuations in our quarterly revenue. Should we
recognize revenue from payors on an accrual basis and later determine the judgments underlying estimated reimbursement change, or were
incorrect at the time we accrued such revenue, our financial results could be negatively impacted in future quarters. As a result, comparing
our operating results on a period-to-period basis may not be meaningful. You should not rely on our past results as an indication of our
future performance. In addition, these fluctuations in revenue may make it difficult for us, research analysts and investors to accurately
forecast our revenue and operating results. If our revenue or operating results fall below consensus expectations, the price of our common
stock would likely decline.
We rely on sole suppliers for some of the materials used in our molecular diagnostic tests, and we may not be able to find
replacements or transition to alternative suppliers in a timely manner.
We often rely on sole suppliers for certain materials that we use to perform our molecular diagnostic tests, including Asuragen for our
endocrine cancer diagnostic tests pursuant to our supply agreement with them. We also purchase reagents used in our molecular diagnostic
tests from sole-source suppliers. While we have developed alternate sourcing strategies for these materials and vendors, we cannot be
certain whether these strategies will be effective or the alternative sources will be available in a timely manner. If these suppliers can no
longer provide us with the materials we need to perform our molecular diagnostic tests, if the materials do not meet our quality
specifications, or if we cannot obtain acceptable substitute materials, an interruption in molecular diagnostic test processing could occur.
Any such interruption may directly impact our revenue and cause us to incur higher costs.
We may experience problems in scaling our operations, or delays or reagent and supply shortages that could limit the growth of
our revenue.
If we encounter difficulties in scaling our operations as a result of, among other things, quality control and quality assurance issues and
availability of reagents and raw material supplies, we will likely experience reduced sales of our molecular diagnostic tests, increased
repair or re-engineering costs, and defects and increased expenses due to switching to alternate suppliers, any of which would reduce our
revenues and gross margins.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Although we attempt to match our capabilities to estimates of marketplace demand, to the extent demand materially varies from our
estimates, we may experience constraints in our operations and delivery capacity, which could adversely impact revenue in a given fiscal
period. Should our need for raw materials and reagents used in our molecular diagnostic tests fluctuate, we could incur additional costs
associated with either expediting or postponing delivery of those materials or reagents.
If we are unable to support demand for our molecular diagnostic tests or any of our future tests or solutions, our business could
suffer.
As demand for our molecular diagnostic tests grows, we will need to continue to scale our testing capacity and processing technology,
expand customer service, billing and systems processes and enhance our internal quality assurance program. We will also need additional
certified laboratory scientists and other scientific and technical personnel to process higher volumes of our molecular diagnostic tests. We
cannot assure you that increases in scale, related improvements and quality assurance will be implemented successfully or that appropriate
personnel will be available. Failure to implement necessary procedures, transition to new processes or hire the necessary personnel could
result in higher costs of processing tests or inability to meet demand. There can be no assurance that we will be able to perform our testing
on a timely basis at a level consistent with demand, or that our efforts to scale our operations will not negatively affect the quality of test
results. If we encounter difficulty meeting market demand or quality standards, our reputation could be harmed and our future prospects
and our business could suffer, causing a material adverse effect on our business, financial condition and results of operations.
If we are unable to compete successfully, we may be unable to increase or sustain our revenue or achieve profitability.
We compete with physicians and the medical community who use traditional methods to diagnose gastrointestinal and endocrine cancers.
In many cases, practice guidelines in the United States have recommended therapies or surgery to determine if a patient’s condition is
malignant or benign. As a result, we believe that we will need to continue to educate physicians and the medical community on the value
and benefits of our molecular diagnostic tests in order to change clinical practices. In addition, we face competition from other companies
that offer diagnostic tests. Specifically, in regard to our thyroid diagnostic tests, Veracyte has thyroid nodule cancer diagnostic tests that
compete with our ThyGenX and ThyraMIR tests, which are currently on the market, and Veracyte may be developing additional tests
aimed at FNAs for thyroid cancer. Quest currently offers a diagnostic test similar to the earlier version of our ThyGenX test, and CBL is
offering a diagnostic test that analyzes genetic alterations using next-generation sequencing. Other competitors for our thyroid assays
include Rosetta Genomics, Accelerate Diagnostics, Inc., Cancer Genetics, Inc., Genomic Health Inc., NeoGenomics Inc. and Trovagene,
Inc. While we do not believe we currently have direct competition for PancraGEN in the gastrointestinal market, there is the potential for
indirect competition as well as direct competition due to the limited penetration we currently have of this market.
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It is also possible that we face future competition from LDTs developed by commercial laboratories such as Quest and/or other diagnostic
companies developing new molecular diagnostic tests or technologies. Furthermore, we may be subject to competition as a result of the
new, unforeseen technologies that can be developed by our competitors in the gastrointestinal and endocrine cancer molecular diagnostic
tests space.
To compete successfully, we must be able to demonstrate, among other things, that our molecular diagnostic test results are accurate and
cost effective, and we must secure a meaningful level of reimbursement for our tests. Since our molecular diagnostics business began in
2014, many of our potential competitors have stronger brand recognition and greater financial capabilities than we do. Others may develop
a test with a lower price than ours that could be viewed by physicians and payors as functionally equivalent to our molecular diagnostic
tests, or offer a test at prices designed to promote market penetration, which could force us to lower the price of our molecular diagnostic
tests and affect our ability to achieve and maintain profitability. If we are unable to compete successfully against current and future
competitors, we may be unable to increase market acceptance of our molecular diagnostic tests and overall sales, which could prevent us
from increasing our revenue or achieving profitability and cause the market price of our common stock to decline. As we add new
molecular diagnostic tests and services, we will face many of these same competitive risks for these new molecular diagnostic tests and
services.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Developing new molecular diagnostic tests involves a lengthy and complex process, and we may not be able to commercialize on a
timely basis, or at all, other molecular diagnostic tests we are developing.
Developing new molecular diagnostic tests and solutions will require us to devote considerable resources to research and development. We
may face challenges obtaining sufficient numbers of samples to validate a newly acquired or developed molecular diagnostic test. In order
to develop and commercialize new molecular diagnostic tests, we need to:
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expend significant funds to conduct substantial research and development;
conduct successful analytical and clinical studies;
scale our laboratory processes to accommodate new molecular diagnostic tests; and
build the commercial infrastructure to market and sell new molecular diagnostic tests.
Typically, few research and development projects result in commercial products, and success in early clinical studies often is not replicated
in later studies. At any point, we may abandon development of a molecular diagnostic test or we may be required to expend considerable
resources repeating clinical studies, which would adversely affect the timing for generating revenue from such test. If a clinical validation
study fails to demonstrate the prospectively defined endpoints of the study or if we fail to sufficiently demonstrate analytical validity, we
might choose to abandon the development of the molecular diagnostic test, which could harm our business. In addition, competitors may
develop and commercialize new competing molecular diagnostic tests faster than us or at a lower cost, which could have a material
adverse effect on our business, financial condition and results of operations.
Unfavorable results of legal proceedings could have a material adverse effect on our business, financial condition and results of
operations.
We are and may become subject to various legal proceedings and claims that arise in or outside the ordinary course of business. The
results of legal proceedings cannot be predicted with certainty. Regardless of merit, litigation may be both time-consuming and disruptive
to our operations and cause significant expense and diversion of management attention. If we do not prevail in the legal proceedings, we
may be faced with significant monetary damages or injunctive relief against us that could have a material adverse effect on our business,
financial condition and results of operations. In addition, there can be no assurance that our assumption of the liability for the Settlement
Agreement with the Department of Justice may not lead to greater exposure than we anticipated.
If we are unable to develop or acquire molecular diagnostic tests to keep pace with rapid technological, medical and scientific
change, our operating results and competitive position could be affected.
Recently, there have been numerous advances in technologies relating to diagnostics, particularly diagnostics that are based on genomic
information. These advances require us to continuously develop our technology and to work to develop new solutions to keep pace with
evolving standards of care. Our solutions could become obsolete unless we continually innovate and expand our product offerings to
include new clinical applications. If we are unable to develop or acquire new molecular diagnostic tests or to demonstrate the applicability
of our molecular diagnostic tests for other diseases, our sales could decline and our competitive position could be harmed.
If the U.S. Food and Drug Administration were to begin to enforce regulation of our molecular diagnostic tests, we could incur
substantial costs and delays associated with trying to obtain pre-market clearance or approval and costs associated with complying
with post-market requirements.
Clinical laboratory tests like our molecular diagnostic tests are regulated under CLIA as well as by applicable State laws. Most LDTs are
currently not subject to the FDA's, regulation (although reagents, instruments, software or components provided by third parties and used
to perform LDTs may be subject to regulation). In October 2014, the FDA issued two draft guidance documents: “Framework for
Regulatory Oversight of Laboratory Developed Tests”, which provides an overview of how the FDA would regulate LDTs through a risk-
based approach, and “FDA Notification and Medical Device Reporting for Laboratory Developed Tests”, which provides guidance on how
the FDA intends to collect information on existing LDTs, including adverse event reports. Pursuant to the Framework for Regulatory
Oversight draft guidance, LDT manufacturers will be subject to medical device registration, listing, and adverse event reporting
requirements. LDT manufacturers will be required to either submit a pre-market application and receive the FDA’s approval before an
LDT may be marketed or submit a pre-market notification in advance of marketing. The Framework for Regulatory Oversight draft
guidance states that within six months after the guidance documents are finalized, all laboratories will be required to give notice to the
FDA and provide basic information concerning the nature of the LDTs offered.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
On November 18, 2016, however, the FDA announced that it would not release the final guidance at this time and instead would continue
to work with stakeholders, the new administration and Congress to determine the right approach. On January 13, 2017, the FDA released a
discussion paper on LDTs outlining a possible risk-based approach for FDA and CMS oversight of LDTs. According to the 2017
discussion paper, previously marketed LDTs would not be expected to comply with most or all FDA oversight requirements
(grandfathering), except for adverse event and malfunction reporting. In addition, certain new and significantly modified LDTs would not
be expected to comply with pre-market review unless the agency determines certain tests could lead to patient harm. Since LDTs currently
on the market would be grandfathered in, pre-market review of new and significantly modified LDTs could be phased-in over a four year
period, as opposed to the nine years proposed in the Framework for Regulatory Oversight draft guidance. In addition, tests introduced after
the effective date, but before their phase-in date, could continue to be offered during pre-market review.
The discussion paper notes that FDA will focus on analytical and clinical validity as the basis for marketing authorization. The FDA
anticipates laboratories that already conduct proper validation should not be expected to experience new costs for validating their tests to
support marketing authorization and laboratories that conduct appropriate evaluations would not have to collect additional data to
demonstrate analytical validity for FDA clearance or approval. The evidence of the analytical and clinical validity of all LDTs will be
made publically available. LDTs are encouraged to submit prospective change protocols in their pre-market submission that outline
specific types of anticipated changes, the procedures that will be followed to implement them and the criteria that will be met prior to
implementation.
Despite the FDA decision not release the guidance at this time, it can choose to release the guidance at any time in the future. If the
guidance is released and pre-market review is required, our business could be negatively impacted as a result of commercial delay that
may be caused by the new requirements. The cost of conducting clinical trials and otherwise developing data and information to support
pre-market applications may be significant. If we are required to submit applications for our currently-marketed tests, we may be required
to conduct additional studies, which may be time-consuming and costly and could result in our currently-marketed tests being withdrawn
from the market. Continued compliance with the FDA's regulations would increase the cost of conducting our business, and subject us to
heightened regulation by the FDA and penalties for failure to comply with these requirements. Failure to comply with applicable
regulatory requirements can result in enforcement action by the FDA, such as fines, product suspensions, warning letters, recalls,
injunctions and other civil and criminal sanctions. There are other regulatory and legislative proposals that would increase general FDA
oversight of clinical laboratories and LDTs. The outcome and ultimate impact of such proposals on the business is difficult to predict at
this time. We are monitoring developments and anticipate that our products will be able to comply with requirements that are ultimately
imposed by the FDA. In the meantime, we maintain our CLIA accreditation, which permits the use of LDTs for diagnostics purposes.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
If we fail to comply with Federal, State and foreign laboratory licensing requirements, we could lose the ability to perform our
tests or experience disruptions to our business.
We are subject to CLIA, a Federal law that regulates clinical laboratories that perform testing on specimens derived from humans for the
purpose of providing information for the diagnosis, prevention or treatment of disease. CLIA regulations mandate specific standards in the
areas of personnel qualifications, administration, and participation in proficiency testing, patient test management and quality assurance.
CLIA certification is also required in order for us to be eligible to bill Federal and State healthcare programs, as well as many private third-
party payors, for our molecular diagnostic tests. To renew these certifications, we are subject to survey and inspection every two years.
Moreover, CLIA inspectors may make random inspections of our clinical reference laboratories. We are also required to maintain State
licenses to conduct testing in our New Haven, Connecticut and Pittsburgh, Pennsylvania laboratories. Connecticut and Pennsylvania laws
require that we maintain a license and establishes standards for the day-to-day operation of our clinical reference laboratory in New Haven,
Connecticut and Pittsburgh, Pennsylvania. In addition, our Pittsburgh and New Haven laboratories are required to be licensed on a test-
specific basis by California, Florida, Maryland, New York and Rhode Island. California, Florida, Maryland, New York and Rhode Island
laws also mandate proficiency testing for laboratories licensed under the laws of each respective State regardless of whether such
laboratories are located in California, Florida, Maryland, New York or Rhode Island. In 2016, we received final approval for our
ThyGenX and ThyraMIR assays in New York State. If we were unable to obtain or lose our CLIA certificate for our laboratories,
whether as a result of revocation, suspension or limitation, we would no longer be able to perform our molecular diagnostic tests, which
could have a material adverse effect on our business, financial condition and results of operations. If we were to lose our licenses issued by
New York or by other States where we are required to hold licenses, we would not be able to test specimens from those States. New
molecular diagnostic tests we may develop may be subject to new approvals by governmental bodies such as New York State, and we may
not be able to offer our new molecular diagnostic tests to patients in such jurisdictions until such approvals are received.
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Recent legislation reforming the U.S. healthcare system may have a material adverse effect on our financial condition and
operations.
PPACA makes changes that are expected to significantly impact the pharmaceutical, medical device and clinical laboratory industries.
Beginning in 2013, each medical device manufacturer must pay a sales tax in an amount equal to 2.3% of the price for which such
manufacturer sells its medical devices that are listed with the FDA. The FDA’s final guidance on LDTs may require our molecular
diagnostic tests to be regulated as medical devices. However, consistent with the FDA’s policy of exercising enforcement discretion for
LDTs, our molecular diagnostic tests are not currently listed as medical devices with the FDA. In December 2015, the Consolidated
Appropriations Act was adopted, which included a two-year moratorium on the medical device excise tax. The moratorium will end on
December 31, 2017, and we cannot assure that the tax will not be extended to services such as ours in the future if our tests were to be
regulated as devices. However, in January 2017, Congress introduced the Medical Device Access and Innovation Protection Act, which
could repeal the medical device tax.
Other significant measures contained in PPACA include, for example, coordination and promotion of research on comparative clinical
effectiveness of different technologies and procedures, initiatives to revise Medicare payment methodologies, such as bundling of
payments across the continuum of care by providers and physicians, and initiatives to promote quality indicators in payment
methodologies. PPACA also includes significant new fraud and abuse measures, including required disclosures of financial arrangements
with physician customers, lower thresholds for violations and increasing potential penalties for such violations. In addition, PPACA
establishes an Independent Payment Advisory Board, or IPAB, to reduce the per capita rate of growth in Medicare spending. The IPAB has
broad discretion to propose policies to reduce expenditures, which may have a negative effect on payment rates for services. The IPAB
proposals may affect payments for clinical laboratory services beginning in 2016 and for hospital services beginning in 2020. We are
monitoring the effect of PPACA to determine the trends and any potential changes that may be necessitated by the legislation, any of
which may potentially affect our business.
Following the 2016 U.S. general election, a single party now leads the executive branch and holds majorities in both the U.S. Senate and
House of Representatives. The President of the United States has announced that he favors repealing PPACA in 2017, and leaders of the
Republication-controlled federal legislature also have expressed a desire to repeal PPACA. The scope and timing of any legislation to
repeal, amend, replace, or reform PPACA is uncertain, but if such legislation were to become law, it could have a significant impact on the
U.S. healthcare system.
On January 20, 2017, the new administration signed an executive order directing federal agencies to exercise existing authorities to reduce
burdens associated with PPACA pending further action by Congress. On the same day, the White House issued a regulatory freeze memo
under which rules and guidance published but not yet effective must be frozen for 60 days pending review; rules and guidance submitted
for publication but not yet published must be withdrawn; and rules and guidance not yet submitted for publication must not be submitted
without further direction from the Administration. Since then, further executive orders and statements from the White House and
Congress have addressed potential regulatory changes that could affect us and our customers. Changes to, or repeal of, PPACA may
continue to affect coverage, reimbursement, and utilization of laboratory services, as well as administrative requirements, in ways that are
currently unpredictable.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
In addition to PPACA, the effect of which cannot presently be fully quantified, various healthcare reform proposals have emerged from
Federal and State governments. For example, in February 2012, Congress passed the Middle Class Tax Relief and Job Creation Act of
2012, which reduced the clinical laboratory payment rates on the Medicare CLFS by 2% in 2013. In addition, a further reduction of 2%
was implemented under the Budget Control Act of 2011, which is to be in effect for dates of service on or after April 1, 2013 until fiscal
year 2024. Reductions resulting from the Congressional sequester are applied to total claim payments made; however, they do not
currently result in a rebasing of the negotiated or established Medicare or Medicaid reimbursement rates.
State legislation on reimbursement applies to Medicaid reimbursement and Managed Medicaid reimbursement rates within that State.
Some States have passed or proposed legislation that would revise reimbursement methodology for clinical laboratory payment rates under
those Medicaid programs. We cannot predict whether future healthcare initiatives will be implemented at the Federal or State level or in
countries outside of the United States in which we may do business, or the effect any future legislation or regulation will have on us. The
taxes imposed by Federal legislation, cost reduction measures and the expansion in the role of the U.S. government in the healthcare
industry may result in decreased revenue, lower reimbursement by payors for our tests or reduced medical procedure volumes, all of which
may adversely affect our business, financial condition and results of operations.
Ongoing calls for deficit reduction at the Federal government level and reforms to programs such as the Medicare program to pay for such
reductions may affect the pharmaceutical, medical device and clinical laboratory industries. In particular, recommendations by the
Simpson-Bowles Commission called for the combination of Medicare Part A (hospital insurance) and Part B (physician and ancillary
service insurance) into a single co-insurance and co-payment structure. Currently, clinical laboratory services are excluded from the
Medicare Part B co-insurance and co-payment as preventative services. Combining Parts A and B may require clinical laboratories to
collect co-payments from patients, which may increase our costs and reduce the amount ultimately collected.
In 2013, CMS announced plans to bundle payments for clinical laboratory tests together with other services performed during hospital
outpatient visits under the Hospital Outpatient Prospective Payment System. CMS exempted molecular diagnostic tests from this
packaging provision at that time. It is possible that this exemption could be removed by CMS in future rule making, which might result in
lower reimbursement for tests performed in this setting.
In April 2014, the President signed PAMA, which included a substantial new payment system for clinical laboratory tests under the CLFS.
PAMA removed CMS’s authority to adjust the CLFS based and established a new method for setting CLFS rates. Implementation of this
new method for setting CLFS rates began in 2016. Under PAMA, laboratories that have more than $12,500 in Medicare revenues from
laboratory services and that receive more than 50 percent of their Medicare revenues from laboratory services would report private payor
data from January 1, 2016 through June 30, 2016, to CMS between January 1, 2017 and March 31, 2017. CMS will post the new Medicare
CLFS rates (based on weighted median private payor rates) in November 2016 and the new rates will be effective beginning on January 1,
2018. Any reductions to payment rates resulting from the new methodology are limited to 10% per test per year in each of the years 2017
through 2019 and to 15% per test per year in each of the years 2020 through 2022. CMS has issued draft regulations regarding these
changes. Further rule-making from CMS will define the time period and data elements evaluated on an annual basis to set reimbursement
rates for tests like ours.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Complying with numerous statutes and regulations pertaining to our molecular diagnostics business is an expensive and time-
consuming process, and any failure to comply could result in substantial penalties.
We are subject to regulation by both the Federal government and the States in which we conduct our molecular diagnostics business,
including:
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The Food, Drug and Cosmetic Act, as supplemented by various other statutes;
The Prescription Drug Marketing Act of 1987, the amendments thereto, and the regulations promulgated thereunder
and contained in 21 C.F.R. Parts 203 and 205;
CLIA and State licensing requirements;
Manufacturing and promotion laws;
Medicare billing and payment regulations applicable to clinical laboratories;
The Federal Anti-Kickback Statute, which prohibits knowingly and willfully offering, paying, soliciting, or
receiving remuneration, directly or indirectly, in exchange for or to induce either the referral of an individual, or the
furnishing, arranging for, or recommending of an item or service that is reimbursable, in whole or in part, by a
Federal healthcare program;
The Federal Stark physician self-referral law (and state equivalents), which prohibits a physician from making a
referral for certain designated health services covered by the Medicare 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, unless the financial relationship falls within an applicable exception to the prohibition;
HIPAA, which established comprehensive federal standards with respect to the privacy and security of protected
health information and requirements for the use of certain standardized electronic transactions, and amendments
made in 2013 to HIPAA under the Health Information Technology for Economic and Clinical Health Act, which
strengthen and expand HIPAA privacy and security compliance requirements, increase penalties for violators,
extend enforcement authority to state attorneys general, and impose requirements for breach notification;
The Federal Civil Monetary Penalties Law, which prohibits, among other things, the offering or transfer of
remuneration to a Medicare or state healthcare program 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 a state healthcare program, unless an exception applies;
The Federal False Claims Act, which 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;
Other Federal and State fraud and abuse laws, prohibitions on self-referral, fee-splitting restrictions, prohibitions on
the provision of products at no or discounted cost to induce physician or patient adoption, and false claims acts,
which may extend to services reimbursable by any third-party payor, including private insurers;
The prohibition on reassignment of Medicare claims, which, subject to certain exceptions, precludes the
reassignment of Medicare claims to any other party;
The rules regarding billing for diagnostic tests reimbursable by the Medicare program, which prohibit a physician or
other supplier from marking up the price of the technical component or professional component of a diagnostic test
ordered by the physician or other supplier and supervised or performed by a physician who does not “share a
practice” with the billing physician or supplier; and
State laws that prohibit other specified practices related to billing such as billing physicians for testing that they
order, waiving coinsurance, co-payments, deductibles, and other amounts owed by patients, and billing a State
Medicaid program at a price that is higher than what is charged to other payors.
We have implemented policies and procedures designed to comply with these laws and regulations. We periodically conduct internal
reviews of our compliance with these laws. Our compliance is also subject to governmental review. The growth of our business may
increase the potential of violating these laws, regulations or our internal policies and procedures. The risk of our being found in violation
of these or other laws and regulations is further increased by the fact that many have not been fully interpreted by the regulatory
authorities or the courts, and their provisions are open to a variety of interpretations. Violations of Federal or State regulations may incur
investigation or enforcement action by the FDA, Department of Justice, State agencies, or other legal authorities, and may result in
substantial civil, criminal, or other sanctions. 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 and divert our management’s attention from the operation
of our business. If our operations are found to be in violation of any of these laws and regulations, we may be subject to civil and criminal
penalties, damages and fines, we could be required to refund payments received by us, we could face possible exclusion from Medicare,
Medicaid and other Federal or State healthcare programs and we could even be required to cease our operations. Any of the foregoing
consequences could have a material adverse effect on our business, financial condition and results of operations.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
A failure to comply with Federal and State laws and regulations pertaining to our payment practices could result in substantial
penalties.
We retain healthcare practitioners as key opinion leaders providing consultation in various aspects of our business. These arrangements,
like any arrangement that includes compensation to a healthcare provider, may trigger Federal or State anti-kickback and Stark Law
liability. Our arrangements are designed to meet available safe harbors and exceptions provided in the anti-kickback laws and Stark Laws,
respectively. However, there are no guarantees that the Federal or State governments will find that these arrangements are designed
properly or that they do not trigger liability under Federal and State laws. Under existing laws, all arrangements must have a legitimate
purpose and compensation must be fair market value. These terms require some subjective analysis and there is limited available case law
or guidance for the application of these laws to the CLIA laboratory industry. Safe harbors in the anti-kickback laws do not necessarily
equate to exceptions in the Stark Law, and there is no guarantee that the government will agree with our payment practices with respect to
the relationships between our laboratories and the healthcare providers. A failure to comply with Federal and State laws and regulations
pertaining to our payment practices could result in substantial penalties and adversely affect our business, financial condition and results of
operations.
If we use hazardous materials in a manner that causes contamination or injury, we could be liable for resulting damages.
We are subject to Federal, State and local laws, rules and regulations governing the use, discharge, storage, handling and disposal of
biological material, chemicals and waste. We cannot eliminate the risk of accidental contamination or injury to employees or third parties
from the use, storage, handling or disposal of these materials. In the event of contamination or injury, we could be held liable for any
resulting damages, remediation costs and any related penalties or fines, and any liability could exceed our resources or any applicable
insurance coverage we may have. The cost of compliance with these laws and regulations may become significant, and our failure to
comply may result in substantial fines or other consequences, and either could have a significant impact on our operating results.
Security breaches, loss of data and other disruptions to us or our third-party service providers could compromise sensitive
information related to our business or prevent us from accessing critical information and expose us to liability, which could
adversely affect our business and our reputation.
Our business requires that we and our third-party service providers collect and store sensitive data, including legally protected health
information, personally identifiable information about patients, credit card information, and our proprietary business and financial
information. We face a number of risks relative to our protection of, and our service providers’ protection of, this critical information,
including loss of access, inappropriate disclosure and inappropriate access, as well as risks associated with our ability to identify and audit
such events. The secure processing, storage, maintenance and transmission of this critical information are vital to our operations and
business strategy, and we devote significant resources to protecting such information. Although we take measures to protect sensitive
information from unauthorized access or disclosure, our information technology and infrastructure may be vulnerable to attacks by
hackers or viruses or otherwise breached due to employee error, malfeasance or other activities. While we have not experienced any such
attack or breach, if such event would occur and cause interruptions in our operations, our networks would be compromised and the
information we store on those networks could be accessed by unauthorized parties, publicly disclosed, lost or stolen. Unauthorized access,
loss or dissemination could disrupt our operations, including our ability to process tests, provide test results, bill payors or patients, process
claims, provide customer assistance services, conduct research and development activities, collect, process and prepare company financial
information, provide information about our solution and other patient and physician education and outreach efforts through our website,
manage the administrative aspects of our business and damage our reputation, any of which could adversely affect our business. In
addition, the interpretation and application of consumer, health-related and data protection laws in the United States are often uncertain,
contradictory and in flux. It is possible that these laws may be interpreted and applied in a manner that is inconsistent with our practices.
Complying with these various laws could cause us to incur substantial costs or require us to change our business practices, systems and
compliance procedures in a manner adverse to our business.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
If we are sued for product liability or errors and omissions liability, we could face substantial liabilities that exceed our resources.
The marketing, sale and use of our molecular diagnostic tests could lead to product liability claims if someone were to allege that the
molecular diagnostic test failed to perform as it was designed. We may also be subject to liability for errors in the results we provide to
physicians or for a misunderstanding of, or inappropriate reliance upon, the information we provide. A product liability or errors and
omissions liability claim could result in substantial damages and be costly and time consuming for us to defend. Although we maintain
product liability and errors and omissions insurance, we cannot be certain that our insurance would fully protect us from the financial
impact of defending against these types of claims or any judgments, fines or settlement costs arising out of such claims. Any product
liability or errors and omissions liability claim brought against us, with or without merit, could increase our insurance rates or prevent us
from securing insurance coverage in the future. Additionally, any product liability lawsuit could cause injury to our reputation or cause us
to suspend sales of our products and solutions. The occurrence of any of these events could have a material adverse effect on our business,
financial condition and results of operations.
We may need to increase the size of our organization, and we may experience difficulties in managing this growth.
We are a small company with approximately 61 employees. Future growth will impose significant added responsibilities on members of
management, including the need to identify, attract, retain, motivate and integrate highly skilled personnel. We may increase the number
of employees in the future depending on the progress and growth of our business Our future financial performance and our ability to sell
our existing molecular diagnostic tests and develop and commercialize new molecular diagnostic tests and to compete effectively will
depend, in part, on our ability to manage any future growth effectively. To that end, we must be able to:
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manage our clinical studies effectively;
integrate additional management, administrative, manufacturing and regulatory personnel;
maintain sufficient administrative, accounting and management information systems and controls; and
hire and train additional qualified personnel.
We may not be able to accomplish these tasks, and our failure to accomplish any of them could harm our financial results. We may need to
reduce the size of our organization in order to become profitable and we may experience difficulties in managing these reductions.
Billing for our diagnostic tests is complex, and we must dedicate substantial time and resources to the billing process to be paid for
our molecular diagnostic tests.
Billing for clinical laboratory testing services is complex, time consuming and expensive. Depending on the billing arrangement and
applicable law, we bill various payors, including Medicare, insurance companies and patients, all of which have different billing
requirements. To the extent laws or contracts require us to bill patient co-payments or co-insurance, we must also comply with these
requirements. We may also face increased risk in our collection efforts, including write-offs of doubtful accounts and long collection
cycles, which could have a material adverse effect on our business, results of operations and financial condition. Among others, the
following factors make the billing process complex:
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differences between the list price for our molecular diagnostic tests and the reimbursement rates of payors;
compliance with complex Federal and State regulations related to billing Medicare;
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.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
As we grow and introduce new molecular diagnostic tests, we will need to add new codes to our billing process as well as our financial
reporting systems. Failure or delays in effecting these changes in external billing and internal systems and processes could negatively
affect our revenue and cash flow. Additionally, our billing activities require us to implement compliance procedures and oversight, train
and monitor our employees or contractors, challenge coverage and payment denials, assist patients in appealing claims, and undertake
internal audits to evaluate compliance with applicable laws and regulations as well as internal compliance policies and procedures. Payors
also conduct external audits to evaluate payments, which add further complexity to the billing process. These billing complexities, and the
related uncertainty in obtaining payment for our diagnostic solution, could negatively affect our revenue and cash flow, our ability to
achieve profitability, and the consistency and comparability of our results of operations.
We rely on a third-party to process and transmit claims to payors, and any delay in either could have an adverse effect on our
revenue.
We rely on Quadex, Inc., a third-party provider to provide overall processing of claims and to transmit the actual claims to payors based on
the specific payor billing format. If claims for our molecular diagnostic tests are not submitted to payors on a timely basis, or if we are
required to switch to a different provider to handle claim submissions, we may experience delays in our ability to process these claims and
receipt of payments from payors, which could have a material adverse effect on our business, financial condition and results of operations.
Enacted healthcare reform legislation may increase our costs, impair our ability to adjust our pricing to match any such increased
costs, and therefore could materially and adversely affect our business, financial condition and results of operations.
PPACA entails sweeping healthcare reforms with staggered effective dates from 2010 through 2018, although certain of these effective
dates have been delayed by action of the current administration. While some guidance has been issued under PPACA over the past several
years, many provisions in PPACA require the issuance of additional guidance from the U.S. Department of Labor, the Internal Revenue
Service, the U.S. Department of Health & Human Services, and State governments. This reform includes, but is not limited to: the
implementation of a small business tax credit; required changes in the design of our healthcare policy including providing insurance
coverage to part-time workers working on average thirty (30) or more hours per week; “grandfathering” provisions for existing policies;
“pay or play” requirements; a “Cadillac plan” excise tax; and specifically required “essential benefits,” that must be included in “qualified
plans,” which benefits include coverage for laboratory tests.
Effective January 1, 2014, each State was required to participate in the PPACA marketplace and make health insurance coverage available
for purchase by eligible individuals through a website. While these websites were subject to significant administrative issues leading up to
their inception dates (and, in some cases, thereafter), it is currently estimated that in excess of 11 million individuals nationwide had
enrolled in health insurance coverage through these exchanges as of the end of 2015. It is unclear, however, how many of these individuals
are becoming insured after previously not having health insurance coverage, versus maintaining their plans purchased on the exchanges in
2014 or switching from other health insurance plans.
PPACA also requires “Applicable Manufacturers” to disclose to the Secretary of the Department of Health & Human Services drug
sample distributions and certain payments or transfers of value to covered recipients (physicians and teaching hospitals) on an annual
basis. “Applicable Manufacturers” and “Applicable Group Purchasing Organizations” must also disclose certain physician ownership or
investment interests. The data submitted will ultimately be made available on a public website. Based upon the structure of our
relationship with our clients, we may be included in the definition of “Applicable Manufacturer” for purposes of the disclosure
requirements or may provide services that include the transfer of drug samples and/or other items of value to covered recipients. As such,
we may be required to disclose or provide information that is subject to disclosure. There may be certain risks and penalties associated
with the failure to properly make such disclosures, including but not limited to the specific civil liabilities set forth in PPACA, which
allows for a maximum civil monetary penalty per “Applicable Manufacturer” of $1,150,000 per year. There may be additional risks and
claims made by third parties derived from an improper disclosure that are difficult to ascertain at this time.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
In June 2012, the United States Supreme Court upheld the constitutionality of key provisions of PPACA. PPACA contains numerous
other initiatives that impact the pharmaceutical industry. These include, among other things:
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increasing existing price rebates in Federally funded healthcare programs;
expanding rebates, or other pharmaceutical company discounts, into new programs;
imposing a new non-deductible excise tax on sales of certain prescription pharmaceutical products by prescription
drug manufacturers and importers;
increasing requirements on employer-sponsored health insurance plans, generally, and imposing taxes on certain
high-cost employer-sponsored plans;
creating an independent commission to propose changes to Medicare with a particular focus on the cost of
biopharmaceuticals in Medicare Part D; and
increasing oversight by the FDA of pharmaceutical research and development processes and commercialization
activities.
While PPACA may increase the number of patients who have insurance coverage, its cost containment measures could also adversely
affect reimbursement for any of our molecular diagnostic tests. Cost control initiatives also could decrease the price that we receive for any
molecular diagnostic tests we may develop in the future. If our molecular diagnostic tests are not considered cost-effective or if we are
unable to generate adequate third-party reimbursement for the users of our molecular diagnostic tests, then we may be unable to maintain
revenue streams sufficient to realize our targeted return on investment for our molecular diagnostic tests.
We are currently unable to determine the long-term, direct or indirect impact of such legislation on our business. Since the effect of many
of the provisions of PPACA may not be determinable for a number of years, we do not expect PPACA to have a material adverse impact
on our near term results of operations. However, healthcare reform as mandated and implemented under PPACA and any future Federal or
State mandated healthcare reform could materially and adversely affect our business, financial condition and operations by increasing our
operating costs, including our costs of providing health insurance to our employees, decreasing our revenue, impeding our ability to attract
and retain customers, requiring changes to our business model, or causing us to lose certain current competitive advantages.
However, following the 2016 U.S. general election, a single party now leads the executive branch and holds majorities in both the U.S.
Senate and House of Representatives. The President of the United States has announced that he favors repealing PPACA in 2017, and
leaders of the Republication-controlled federal legislature also have expressed a desire to repeal PPACA. The scope and timing of any
legislation to repeal, amend, replace, or reform PPACA is uncertain, but if such legislation were to become law, it could have a significant
impact on the U.S. healthcare system.
On January 20, 2017, the new administration signed an executive order directing federal agencies to exercise existing authorities to reduce
burdens associated with PPACA pending further action by Congress. On the same day, the White House issued a regulatory freeze memo
under which rules and guidance published but not yet effective must be frozen for 60 days pending review; rules and guidance submitted
for publication but not yet published must be withdrawn; and rules and guidance not yet submitted for publication must not be submitted
without further direction from the Administration. Since then, further executive orders and statements from the White House and
Congress have addressed potential regulatory changes that could affect us and our customers. Changes to, or repeal of, PPACA may
continue to affect coverage, reimbursement, and utilization of laboratory services, as well as administrative requirements, in ways that are
currently unpredictable.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Changes in governmental regulation could negatively impact our business operations and increase our costs.
The pharmaceutical, biotechnology and healthcare industries are subject to a high degree of governmental regulation. Significant changes
in these regulations affecting our business could result in the imposition of additional restrictions on our business, additional costs to us in
providing our molecular diagnostic tests to our customers or otherwise negatively impact our business operations. Changes in
governmental regulations mandating price controls and limitations on patient access to our products could also reduce, eliminate or
otherwise negatively impact our sales.
If we do not increase our revenues and successfully manage the size of our operations, our business, financial condition and results
of operations could be materially and adversely affected.
The majority of our operating expenses are personnel-related costs such as employee compensation and benefits, reagents and disposable
supplies as well as the cost of infrastructure to support our operations, including facility space and equipment. We continuously review our
personnel to determine whether we are fully utilizing their services. If we believe we are not in a position to fully utilize our personnel, we
may make further reductions to our workforce. If we are unable to achieve revenue growth in the future or fail to adjust our cost
infrastructure to the appropriate level to support our revenues, our business, financial condition and results of operations could be
materially and adversely affected.
As a result of certain terminations of employment and change of control features in employment contracts of certain key
employees due to the sale of the CSO business in 2015 and our transition to a standalone molecular diagnostics business,
substantial payments were scheduled during 2016, the nonpayment of which could materially and adversely affect our business,
results of operations and cash flow as well as threaten the continuity of our business.
In late 2015, in connection with the sale of our CSO business and our transition to a standalone molecular diagnostics business, we
implemented work force reductions and made leadership changes. As a result, as of December 31, 2016, we had outstanding past due
severance obligations in the aggregate amount of $2.9 million due to five former senior executives in connection with their respective
separation agreements. Effective January 17, 2017, all five former senior executives each agreed to accept a payment of 35% of the total
severance obligations due to each of them pursuant to their respective separation agreements with us, or an aggregate of approximately
$1.0 million, in satisfaction in full and settlement of an aggregate of approximately $2.9 million in severance payments. Their agreement
was conditioned upon their receipt from us of such payments by March 1, 2017, and our obligation to make such payment was conditioned
upon us consummating a sufficiently large financing (with gross proceeds of approximately $4.0 million) and the prior agreement of our
investment banker and investors in such financing for the use of a portion of such proceeds for such payments. Our registered direct
offering completed on January 25, 2017 satisfied such conditions, and on February 27, 2017, we made payments totaling approximately
$1.0 million to those five former senior executives in satisfaction in full and settlement of an aggregate of approximately $2.9 million in
severance payments. Each of the former senior executives entered into releases with us at the time of receipt of such payments, and in
consideration therefor, releasing us and our directors, officers and agents from any and all claims, losses and damages they have or ever
had against us and our directors, officers and agents.
Additionally, as a result of the sale of the CSO business, we had approximately $675,000 due to former sales representatives and account
managers of our CSO business. During 2016, we made negotiated, monthly payments amounting to approximately $400,000 to these
former sales representatives and expect to continue making such monthly payments until April 2017. We may implement additional
workforce reductions, which could create additional obligations. If we are unable to make these payments or satisfy other obligations
triggered by further workforce reductions, our business, results of operations and cash flow could be materially and adversely affected.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
We may acquire businesses or assets or make investments in other companies or molecular diagnostic technologies that could
harm our operating results, dilute our stockholders’ ownership, increase our debt or cause us to incur significant expense.
As part of our strategy, we may pursue acquisitions of synergistic businesses or molecular diagnostic assets. If we make any further
acquisitions, we may not be able to integrate these acquisitions successfully into our existing business, and we could assume unknown or
contingent liabilities. Any future acquisition by us also could result in significant write-offs or the incurrence of debt and contingent
liabilities, any of which could harm our operating results and financial condition. Integration of an acquired company or business will also
likely require management resources that otherwise would be available for ongoing development of our existing business. We may not
identify or complete these transactions in a timely manner, on a cost-effective basis, or at all, and we may not realize the anticipated
benefits of any acquisition. To finance any acquisitions or investments, we may choose to issue shares of our common stock as
consideration, which would dilute the ownership of our stockholders. If the price of our common stock is low or volatile, we may not be
able to acquire other companies for stock. Alternatively, it may be necessary for us to raise additional funds for these activities through
public or private financings. Additional funds may not be available on terms that are favorable to us, or at all. If these funds are raised
through the sale of equity or convertible debt securities, dilution to our stockholders could result. Consummating an acquisition poses a
number of risks including:
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we may not be able to accurately estimate the financial impact of an acquisition on our overall business;
an acquisition may require us to incur debt or other obligations, incur large and immediate write-offs, issue capital
stock potentially dilutive to our stockholders or spend significant cash, or may negatively affect our operating
results and financial condition;
if we spend significant funds or incur additional debt or other obligations, our ability to obtain financing for
working capital or other purposes could decline;
worse than expected performance of an acquired business may result in the impairment of intangible assets;
we may be unable to realize the anticipated benefits and synergies from acquisitions as a result of inherent risks and
uncertainties, including difficulties integrating acquired businesses or retaining key personnel, partners, customers
or other key relationships, and risks that acquired entities may not operate profitably or that acquisitions may not
result in improved operating performance;
we may fail to successfully manage relationships with customers, distributors and suppliers;
our customers may not accept new molecular diagnostic tests from our acquired businesses;
we may fail to effectively coordinate sales and marketing efforts of our acquired businesses;
we may fail to combine product offerings and product lines of our acquired businesses timely and efficiently;
an acquisition may involve unexpected costs or liabilities, including as a result of pending and future shareholder
lawsuits relating to acquisitions or exercise by stockholders of their statutory appraisal rights, or the effects of
purchase accounting may be different from our expectations;
an acquisition may involve significant contingent payments that may adversely affect our future liquidity or capital
resources;
accounting for contingent payments requires significant judgment and changes to the assumptions used in
determining the fair value of our contingent payments could lead to significant volatility in earnings;
acquisitions and subsequent integration of these companies may disrupt our business and distract our management
from other responsibilities; and
the costs of an unsuccessful acquisition may adversely affect our financial performance.
Additional risks of integration of an acquired business include:
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differing information technology, internal control, financial reporting and record-keeping systems;
differences in accounting policies and procedures;
unanticipated additional transaction and integration-related costs;
facilities or operations of acquired businesses in remote locations and the inherent risks of operating in unfamiliar
legal and regulatory environments; and
new products, including the risk that any underlying intellectual property associated with such products may not
have been adequately protected or that such products may infringe on the proprietary rights of others.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
If our information technology and communications systems fail or we experience a significant interruption in their operation, our
reputation, business and results of operations could be materially and adversely affected.
The efficient operation of our business is dependent on our information technology and communications systems. Increasingly, we are also
dependent upon our ability to electronically interface with our customers. The failure of these systems to operate as anticipated could
disrupt our business and result in decreased revenue and increased overhead costs. In addition, we do not have complete redundancy for
all of our systems and our disaster recovery planning cannot account for all eventualities. Our information technology and
communications systems, including the information technology systems and services that are maintained by third party vendors, are
vulnerable to damage or interruption from natural disasters, fire, terrorist attacks, malicious attacks by computer viruses or hackers, power
loss or failure of computer systems, Internet, telecommunications or data networks. If these systems or services become unavailable or
suffer a security breach, we may expend significant resources to address these problems, and our reputation, business and results of
operations could be materially and adversely affected.
We have and may continue to experience goodwill and other intangible asset impairment charges.
We are required to evaluate goodwill and the carrying value of intangibles at least annually, and between annual tests if events or
circumstances warrant such a test. For the year ended December 31, 2015, we recorded a goodwill impairment charge of $15.7 million
pertaining to the acquisition of RedPath in October 2014 and during the third quarter of 2016, we recorded an impairment charge of $3.4
million related to changes in our development strategy for products acquired from Asuragen.
We review the recoverability of long-lived assets and finite-lived intangible assets whenever events or changes in circumstances indicate
that the carrying value of such assets may not be recoverable. If the sum of the expected future undiscounted cash flows is less than the
carrying amount of the asset, an impairment loss is recognized by reducing the recorded value of the asset to its fair value measured by
future discounted cash flows. This analysis requires estimates of the amount and timing of projected cash flows and, where applicable,
judgments associated with, among other factors, the appropriate discount rate. Such estimates are critical in determining whether any
impairment charge should be recorded and the amount of such charge if an impairment loss is deemed to be necessary. During the fourth
quarter of 2016, due to the decline in market capitalization and other factors, we reviewed the recoverability of long-lived assets and finite-
lived intangible assets and concluded that no further finite-lived intangible assets were impaired.
RISKS RELATING TO THE ASSET SALE
We may not be able to fund the remaining obligations of our previously sold CSO business, which could have a material adverse
effect on our business and results of operations.
In December 2015, we sold a majority of our CSO business to Publicis Healthcare Solutions, Inc., or Publicis, pursuant to an Asset
Purchase Agreement, dated as of October 30, 2015, by and between us and Publicis, or the Asset Purchase Agreement, for a total cash
payment of $28.5 million, or the Asset Sale, including an initial upfront cash payment of $25.5 million and $3.0 million of a working
capital adjustment. We used a significant portion of the net proceeds received at the closing of the Asset Sale to pay the balance of the
outstanding loan under the Credit Agreement, dated October 31, 2014, by and among us, SWK Funding LLC and the financial institutions
party thereto from time to time as lenders, and related fees. As a result of the Asset Sale, not all of our CSO obligations were assumed by
Publicis. These obligations consist of accounts payable, costs relating to the closeout of the portion of the CSO business that principally
related to the provision of services for multiple non-competing brands for different clients, or the ERT Unit, which Publicis did not acquire
in the Asset Sale, and termination of various vendor contracts that had been associated with the CSO business. As such, we continue to pay
some of these obligations, but may not be able to satisfy all of these remaining obligations. If we are unable to satisfy all our remaining
CSO obligations, our business and results of operations could be materially and adversely affected.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
The Asset Purchase Agreement exposes us to contingent liabilities that could have a material adverse effect on our financial
condition.
We have agreed to indemnify Publicis for damages resulting from or arising out of any inaccuracy or breach of any representation,
warranty or covenant of ours in the Asset Purchase Agreement against any and all liabilities of ours not assumed by Publicis in the Asset
Sale and for certain other matters. Significant indemnification claims by Publicis could have a material adverse effect on our financial
condition. We will not be obligated to indemnify Publicis for any breach of certain of the representations and warranties by us under the
Asset Purchase Agreement until the aggregate amount of claims for indemnification exceed $250,000. In the event that claims for
indemnification exceed this threshold, we will be obligated to indemnify Publicis for any damages or loss resulting from such breach up to
25% of the total purchase price paid or due and payable by Publicis to us. Claims for indemnification for breaches of covenants made by
us under the Asset Purchase Agreement and for breaches of representations and warranties classified as fundamental representations or any
provision of the Asset Purchase Agreement relating to taxes will not be subject to the deductible or aggregate liability cap described
above. The Asset Purchase Agreement also allows Publicis to withhold monies due against an earn-out payment if indemnification claims
are asserted. In addition, under the Asset Purchase Agreement, we will retain all of our debts and liabilities not assumed by Publicis.
RISKS RELATING TO OUR INTELLECTUAL PROPERTY
If we breach the Asuragen License Agreement or the CPRIT License Agreement, it could have a material adverse effect on our
sales and commercialization efforts for miRInform® thyroid and pancreas cancer diagnostic tests and other tests in development
for thyroid cancer, and the sale of diagnostic devices and the performance of certain services relating to thyroid cancer.
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We currently license certain patents and know-how from Asuragen relating to (i) miRInform thyroid and pancreas cancer diagnostic tests
and other tests in development for thyroid cancer, or the Asuragen License Agreement, and (ii) the sale of diagnostic devices and the
performance of certain services relating to thyroid cancer, or the CPRIT License Agreement. Under the Asuragen License Agreement, we
are obligated to pay royalties on the future net sales of the miRInform pancreas platform for a period of ten years following a qualifying
sale, on the future net sales of the miRInform thyroid platform through August 13, 2024 and on certain other thyroid diagnostics tests for
a period of ten years following a qualifying sale. Under the CPRIT License Agreement, we are obligated to pay 5% of net sales on sales of
diagnostic devices and the performance of services relating to thyroid cancer, subject to a maximum deduction of 1.5% for royalties paid
to third parties. Both of the Asuragen License Agreement and the CPRIT License Agreement continue until terminated by (i) mutual
agreement of the parties or (ii) either party in the event of a material breach of the respective agreement by the other party. If we
materially breach or fail to perform any provision under the CPRIT License Agreement, Asuragen will have the right to terminate our
license, and upon the effective date of such termination, our right to practice the licensed patent rights would end. To the extent such
licensed patent rights relate to our molecular diagnostic tests currently on the market, we would expect to exercise all rights and remedies
available to us, including attempting to cure any breach by us, and otherwise seek to preserve our rights under the patent rights and other
technology licensed to us, but we may not be able to do so in a timely manner, at an acceptable cost to us or at all. Any uncured, material
breach under these license agreements could result in our loss of rights to practice the patent rights licensed to us under these license
agreements, and to the extent such patent rights and other technology relate to our molecular diagnostic tests currently on the market, it
could have a material adverse effect on our sales and commercialization efforts for miRInform® thyroid and pancreas cancer molecular
diagnostic tests and other tests in development for thyroid cancer, and the sale of molecular diagnostic tests and the performance of certain
services relating to thyroid cancer.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
If we are unable to protect our intellectual property effectively, our business would be harmed.
We rely on patent protection as well as trademark, trade secret and other intellectual property rights protection and contractual restrictions
to protect our proprietary technology. If we fail to protect our intellectual property, third parties may be able to compete more effectively
against us and we may incur substantial litigation costs in our attempts to recover or restrict use of our intellectual property. While we
apply for patents covering our products and technologies and uses thereof, we may fail to apply for patents on important products and
technologies in a timely fashion or at all, or we may fail to apply for patents in relevant jurisdictions. Others could seek to design around
our current or future patented technologies. We may not be successful in defending any challenges made against our patents or patent
applications. Any successful third-party challenge to our patents could result in the unenforceability or invalidity of such patents and
increased competition to our business. The outcome of patent litigation can be uncertain and any attempt by us to enforce our patent rights
against others may not be successful, or, if successful, may take substantial time and result in substantial cost, and may divert our efforts
and attention from other aspects of our business.
Monitoring unauthorized disclosure is difficult, and we do not know whether the steps we have taken to prevent such disclosure are, or
will be, adequate. If we were to enforce a claim that a third-party had illegally obtained and was using our trade secrets, it would be
expensive and time consuming, and the outcome would be unpredictable. Further, competitors could willfully infringe our intellectual
property rights, design around our protected technology or develop their own competitive technologies that arguably fall outside of our
intellectual property rights. Others may independently develop similar or alternative products and technologies or replicate any of our
products and technologies. If our intellectual property does not adequately protect us against competitors’ products and methods, our
competitive position could be adversely affected, as could our business and the results of our operations. To the extent our intellectual
property offers inadequate protection, or is found to be invalid or unenforceable, we would be exposed to a greater risk of competition. If
our intellectual property does not provide adequate coverage of our competitors’ products, our competitive position could be adversely
affected, as could our overall business. Both the patent application process and the process of managing patent disputes can be time
consuming and expensive.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Changes in U.S. patent law could diminish the value of patents in general, thereby impairing our ability to protect our molecular
diagnostic tests.
As is the case with other molecular diagnostics companies, our success is heavily dependent on intellectual property, particularly on
obtaining and enforcing patents. Obtaining and enforcing patents of molecular diagnostics tests, like our molecular diagnostic tests in our
PancraGEN® and miRInform® platforms, involves both technological and legal complexity, and is therefore costly, time-consuming and
inherently uncertain. From time-to-time the U.S. Supreme Court, other Federal courts, the U.S. Congress or the United States Patent and
Trademark Office, or the USPTO, may change the standards of patentability and any such changes could have a negative impact on our
business. For instance, on October 30, 2008, the Court of Appeals for the Federal Circuit issued a decision that methods or processes
cannot be patented unless they are tied to a machine or involve a physical transformation. The U.S. Supreme Court later reversed that
decision in Bilski v. Kappos, finding that the “machine-or-transformation” test is not the only test for determining patent eligibility. The
Court, however, declined to specify how and when processes are patentable. On March 30, 2012, in the case Mayo Collaborative Services
v. Prometheus Laboratories, Inc., the U.S. Supreme Court reversed the Federal Circuit’s application of Bilski and invalidated a patent
focused on a process for identifying a proper dosage for an existing therapeutic because the patent claim embodied a law of nature. On July
30, 2012, the USPTO released a memorandum entitled “2012 Interim Procedure for Subject Matter Eligibility Analysis of Process Claims
Involving Laws of Nature,” with guidelines for determining patentability of diagnostic or other processes in line with the Mayo decision.
On June 13, 2013, in Association for Molecular Pathology v. Myriad Genetics, the Supreme Court held that a naturally occurring DNA
segment is a product of nature and not patent eligible merely because it has been isolated. The Supreme Court did not address the
patentability of any innovative method claims involving the manipulation of isolated genes. On March 4, 2014, the USPTO released a
memorandum entitled “2014 Procedure For Subject Matter Eligibility Analysis Of Claims Reciting Or Involving Laws Of Nature/Natural
Principles, Natural Phenomena, And/Or Natural Products.” This memorandum provides guidelines for the USPTO’s new examination
procedure for subject matter eligibility under 35 U.S.C. §101 for claims embracing natural products or natural principles. On June 12,
2015, the Federal Circuit issued a decision in Ariosa v. Sequenom holding that a method for detecting a paternally inherited nucleic acid of
fetal origin performed on a maternal serum or plasma sample from a pregnant female were unpatentable as directed to a naturally occurring
phenomenon. On July 30, 2015, the USPTO released a Federal Register Notice entitled, “July 2015 Update on Subject Matter Eligibility,”
This Notice updated the USPTO guidelines for the USPTO’s procedure for subject matter eligibility under 35 U.S.C. §101 for claims
embracing natural products or natural principles phenomenon. On May 4, 2016, the USPTO released life science examples that were
intended to be used in conjunction with the USPTO guidance on subject matter eligibility. Although the guidelines and examples do not
have the force of law, patent examiners have been instructed to follow them. What constitutes a law of nature and a sufficient inventive
concept remains uncertain, and it is possible that certain aspects of molecular diagnostics tests would be considered natural laws and,
therefore, ineligible for patent protection. Some aspects of our technology involve processes that may be subject to this evolving standard
and we cannot guarantee that any of our pending or issued claims will be patentable or upheld as valid as a result of such evolving
standards. In addition, patents we own or license that issued before these recent cases may be subject to challenge in court or before the
USPTO in view of these current legal standards. Accordingly, the evolving interpretation and application of patent laws in the United
States governing the eligibility of diagnostics for patent protection may adversely affect our ability to obtain patents and may facilitate
third-party challenges to any owned and licensed patents. Changes in either the patent laws or in interpretations and application of patent
laws may also diminish the value of our existing intellectual property or intellectual property that we continue to develop. We cannot
predict the breadth of claims that may be allowed or enforceable in our patents or in third-party patents.
We may be involved in litigation related to intellectual property, which could be time-intensive and costly and may adversely affect
our business, operating results or financial condition.
We may receive notices of claims of direct or indirect infringement or misappropriation or misuse of other parties’ proprietary rights from
time to time and some of these claims may lead to litigation. We cannot assume that we will prevail in such actions, or that other actions
alleging misappropriation or misuse by us of third-party trade secrets, infringement by us of third-party patents and trademarks or other
rights, or the validity of our patents, trademarks or other rights, will not be asserted or prosecuted against us. We might not have been the
first to make the inventions covered by each of our pending patent applications and we might not have been the first to file patent
applications for these inventions. No assurance can be given that other patent applications will not have priority over our patent
applications. If third parties bring these proceedings against our patents, we could incur significant costs and experience management
distraction. Litigation may be necessary for us to enforce our patents and proprietary rights or to determine the scope, coverage and
validity of the proprietary rights of others. The outcome of any litigation or other proceeding is inherently uncertain and might not be
favorable to us, and we might not be able to obtain licenses to technology that we require on acceptable terms or at all. In addition, if we
resort to legal proceedings to enforce our intellectual property rights or to determine the validity, scope and coverage of the intellectual
property or other proprietary rights of others, the proceedings could be burdensome and expensive, even if we were to prevail. Any
litigation that may be necessary in the future could result in substantial costs and diversion of resources and could have a material adverse
effect on our business, financial condition and operating results.
In the event of a successful claim of infringement against us, we may be required to pay damages and ongoing royalties, and obtain one or
more licenses from third parties, or be prohibited from selling our products. We may not be able to obtain these licenses on acceptable
terms, if at all. We could incur substantial costs related to royalty payments for licenses obtained from third parties, which could
negatively affect our financial results. In addition, our agreements with some of our customers, suppliers or other entities with whom we
do business require us to defend or indemnify these parties to the extent they become involved in infringement claims, including the types
of claims described above. If we are required or agree to defend or indemnify third parties in connection with any infringement claims, we
could incur significant costs and expenses that could have a material adverse effect on our business, financial condition, and results of
operations.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
RISKS RELATING TO OUR CORPORATE STRUCTURE AND OUR COMMON STOCK
We do not meet certain of The Nasdaq Capital Market continued listing requirements and therefore, we risk delisting, which may
decrease our stock price and make it harder for our stockholders to trade our stock.
Our common stock is currently listed for trading on The Nasdaq Capital Market. We do not currently meet certain NASDAQ continued
listing requirements and therefore, risk delisting of our securities. Delisting would have an adverse effect on the price of our common stock
and likely also on our business. Additionally, our ability to publicly or privately sell equity securities and the liquidity of our common
stock could be adversely affected if our common stock was delisted from The Nasdaq Capital Market or if we are unable to transfer our
listing to another U.S. national securities exchange.
NASDAQ has adopted a number of listing standards that are applicable to our common stock for continued listing on The Nasdaq Capital
Market. On December 28, 2016, we effected a one-for-ten reverse split of our issued and outstanding shares of our common stock in order
to achieve the requisite increase in the market price of our common stock to be in compliance with the NASDAQ minimum bid price
requirement in Listing Rule 5550(a)(2). However, we currently are not in compliance with the minimum stockholders’ equity requirement
in NASDAQ Listing Rule 5550(b)(1) (nor the alternatives of market value of listed securities or net income from continuing operations).
We were given until January 9, 2017 to submit a compliance plan for the NASDAQ staff’s consideration, and we timely submitted our
compliance plan on such date. The NASDAQ staff reviewed and considered our compliance plan, and on February 1, 2017, the NASDAQ
staff notified us that we were granted an extension until May 22, 2017 to evidence compliance with the stockholders’ equity requirement.
Pursuant to the terms of the extension, by May 22, 2017, we must choose one of two alternatives to evidence compliance with the
stockholders’ equity requirement. Regardless of which alternative we choose, if we fail to evidence compliance upon filing our Quarterly
Report on Form 10-Q for the period ended June 30, 2017, we may at that time receive a delisting notice. Upon the receipt of such delisting
notice, we would have the right to request a hearing before an independent NASDAQ Listing Qualifications Panel, or the Panel, which
would result in an automatic stay of any suspension or delisting action pending the issuance of the Panel decision following the hearing
and the expiration of any additional extension granted by the Panel. In the event that we do request a hearing, there can be no assurance
that we would be successful in maintaining our listing on The Nasdaq Capital Market. We completed public equity offerings from
December 2016 through February 2017, in part, as a step in our efforts to increase our stockholders’ equity to regain compliance with
NASDAQ Listing Rule 5550(b)(1).
Further, we are also currently not in compliance with the audit committee requirement in NASDAQ Listing Rule 5605(c)(2)(A), although
we intend to appoint an additional independent director to our Board and to the Audit Committee prior to the end of the cure period.
Our common stock currently remains listed on The Nasdaq Capital Market under the symbol “IDXG.” There can be no assurance that we
will be able to regain or maintain compliance with the NASDAQ continued listing requirements, or that our common stock will not be
delisted from The Nasdaq Capital Market in the future. If our common stock is delisted by NASDAQ, it could lead to a number of
negative implications, including an adverse effect on the price of our common stock, increased volatility in our common stock, reduced
liquidity in our common stock, the loss of federal preemption of state securities laws and greater difficulty in obtaining financing. In
addition, delisting of our common stock could deter broker-dealers from making a market in or otherwise seeking or generating interest in
our common stock, could result in a loss of current or future coverage by certain sell-side analysts and might deter certain institutions and
persons from investing in our securities at all. Delisting could also cause a loss of confidence of our customers, collaborators, vendors,
suppliers and employees, which could harm our business and future prospects.
If our common stock is delisted by NASDAQ in the future, our common stock may be eligible to trade on the OTC Bulletin Board, OTC
QB or another over-the-counter market. Any such alternative would likely result in it being more difficult for us to raise additional capital
through the public or private sale of equity securities and for investors to dispose of, or obtain accurate quotations as to the market value
of, our common stock. In addition, there can be no assurance that our common stock would be eligible for trading on any such alternative
exchange or markets. For these reasons and others, delisting could adversely affect the price of our securities and our business, financial
condition and results of operations.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
We have a substantial number of authorized common and preferred shares available for future issuance that could cause dilution
of our stockholders’ interest, adversely impact the rights of holders of our common stock and cause our stock price to decline.
We have a total of 100,000,000 shares of common stock and 5,000,000 shares of preferred stock authorized for issuance. As of March 30,
2017, we had 91,660,799 shares of common stock and 5,000,000 shares of preferred stock available for issuance. As of March 30, 2017,
we have reserved 660,492 shares of our common stock for issuance upon the exercise of outstanding awards under our stock incentive
plan, 853,763 additional shares available for future grants of awards under our stock incentive plan, and 450,820 shares of our common
stock potentially issuable upon conversion of the Exchanged Convertible Note. Under the terms of the Exchanged Convertible Note, we
are required to reserve at least 300% of the number of shares of common stock as shall be necessary from time to time to effect the
conversion of all of the notes outstanding. We may seek financing that could result in the issuance of additional shares of our capital stock
and/or rights to acquire additional shares of our capital stock. We may also make acquisitions that result in issuances of additional shares
of our capital stock. Those additional issuances of capital stock could result in substantial dilution of our existing stockholders.
Furthermore, the book value per share of our common stock may be reduced. This reduction would occur if the exercise price of any issued
warrants, the conversion price of any convertible notes or the conversion ratio of any issued preferred stock is lower than the book value
per share of our common stock at the time of such exercise or conversion. Additionally, new investors in any subsequent issuances of our
securities could gain rights, preferences and privileges senior to those of holders of common stock.
Any weakness in our disclosure controls and procedures and our internal controls could have a material adverse effect on us.
As discussed in “Item 9A-Controls and Procedures,” our senior management has identified material weaknesses in our disclosure controls
and procedures and our internal controls over financial reporting. We cannot assure you that additional material weaknesses will not be
identified in the future. Any such failure could adversely affect our ability to report financial results on a timely and accurate basis, which
could have other material effects on our business, reputation, results of operations, financial condition or liquidity. Material weaknesses in
internal controls over financial reporting or disclosure controls and procedures could also cause investors to lose confidence in our
reported financial information which could have an adverse effect on the trading price of our securities.
We have anti-takeover defenses that could delay or prevent an acquisition and could adversely affect the price of our common
stock.
Our certificate of incorporation, as amended, and amended and restated bylaws include provisions, such as providing for three classes of
directors, which may make it more difficult to remove our directors and management and may adversely affect the price of our common
stock. In addition, our certificate of incorporation, as amended, authorizes the issuance of “blank check” preferred stock, which allows our
Board to create one or more classes of preferred stock with rights and preferences greater than those afforded to the holders of our common
stock. This provision could have the effect of delaying, deterring or preventing a future takeover or a change in control, unless the
takeover or change in control is approved by our Board. We are also subject to laws that may have a similar effect. For example, Section
203 of the General Corporation Law of the State of Delaware prohibits us from engaging in a business combination with an interested
stockholder for a period of three years from the date the person became an interested stockholder unless certain conditions are met. As a
result of the foregoing, it will be difficult for another company to acquire us and, therefore, could limit the price that possible investors
might be willing to pay in the future for shares of our common stock. In addition, the rights of our common stockholders will be subject to,
and may be adversely affected by, the rights of holders of any class or series of preferred stock that may be issued in the future and in this
offering.
We have not declared any cash dividends on our capital stock and do not intend to declare or pay any cash dividends in the
foreseeable future. Future earnings, if any, will be used to finance the future operation and growth of our business. As a result,
capital appreciation, if any, will be your sole source of gain.
We have never paid cash dividends on our capital stock. We do not currently anticipate paying cash dividends on our common stock in the
foreseeable future and we may not have sufficient funds legally available to pay dividends. Even if the funds are legally available for
distribution, we may nevertheless decide not to pay any dividends. We presently intend to retain all earnings for our operations. As a result,
capital appreciation, if any, of our common stock will be your sole source of gain for the foreseeable future.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Our quarterly and annual revenues and operating results may vary, which may cause the price of our common stock to fluctuate.
Our quarterly and annual operating results may vary as a result of a number of factors, including:
•
•
•
•
•
•
•
the commencement, delay, cancellation or completion of sales and marketing programs;
regulatory developments;
uncertainty about when sales of our molecular diagnostic tests will be recognized;
timing and amount of expenses for implementing new programs and accuracy of estimates of resources required for
ongoing programs;
adoption of and coverage and reimbursement for our molecular diagnostic tests;
timing and integration of any acquisitions; and
changes in regulations related to diagnostics, pharmaceutical, biotechnology and healthcare companies.
We believe that quarterly, and in certain instances annual, comparisons of our financial results are not necessarily meaningful and should
not be relied upon as an indication of future performance. Fluctuations in quarterly and annual results could materially and adversely affect
the market price of our common stock in a manner unrelated to our long-term operating performance.
Our stock price is volatile and could be further affected by events not within our control, and an investment in our common stock
could suffer a decline in value.
During 2016, our common stock traded at a low of $0.70 and a high of $19.80. During 2015, our common stock traded at a low of $4.20
and a high of $27.40.* The trading price of our common stock has been and will continue to be subject to:
•
•
•
•
•
•
•
•
•
•
•
general volatility in the trading markets;
significant fluctuations in our quarterly operating results;
significant changes in our cash and cash equivalent reserves;
announcements regarding our business or the business of our competitors;
announcements regarding our equity offerings;
strategic actions by us or our competitors, such as acquisitions or restructurings;
industry and/or regulatory developments;
changes in revenue mix;
changes in revenue and revenue growth rates for us and for the industries in which we operate;
changes in accounting standards, policies, guidance, interpretations or principles; and
statements or changes in opinions, ratings or earnings estimates made by brokerage firms or industry analysts
relating to the markets in which we operate or expect to operate.
*The prices of our common stock listed above have been adjusted to reflect a one-for-ten reverse split on our issued and outstanding
shares of common stock effected on December 28, 2016.
We may be subject to securities litigation, which is expensive and could divert our management's attention.
The market price of our securities may be volatile, and in the past companies that have experienced volatility in the market price of their
securities have been subject to securities class action litigation. We may be the target of this type of litigation in the future. Securities
litigation against us could result in substantial costs and divert our management's attention from other business concerns, which could
seriously harm our business.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
The indemnification rights provided to our directors, officers and employees may result in substantial expenditures by us and may
discourage lawsuits against its directors, officers, and employees.
Our certificate of incorporation, as amended, contains provisions permitting us to enter into indemnification agreements with our directors,
officers, and employees. The foregoing indemnification obligations could result in us incurring substantial expenditures to cover the cost
of settlement or damage awards against directors and officers, which we may be unable to recoup. These provisions and resultant costs
may also discourage us from bringing a lawsuit against our directors and officers for breaches of their fiduciary duties, and may similarly
discourage the filing of derivative litigation by our stockholders against our directors and officers even though such actions, if successful,
might otherwise benefit us and our stockholders.
RISKS RELATED TO THE REVERSE STOCK SPLIT
We completed a reverse stock split of our issued and outstanding shares of common stock on December 28, 2016. However, we
cannot assure you that we will be able to continue to comply with the minimum bid price requirements of The Nasdaq Capital
Market.
On December 28, 2016, we effected a one-for-ten reverse split of our issued and outstanding shares of our common stock in order to
achieve the requisite increase in the market price of our common stock to be in compliance with the NASDAQ minimum bid price
requirement. We cannot assure you that the market price of our common stock will remain at the level required for continuing compliance
with that requirement. It is not uncommon for the market price of a company’s common stock to decline in the period following a reverse
stock split. If the market price of our common stock declines, the percentage decline may be greater than would have occurred in the
absence of a reverse stock split. In any event, other factors unrelated to the number of shares of our common stock outstanding, such as
negative financial or operational results or future announcements of equity offerings, could adversely affect the market price of our
common stock and jeopardize our ability to maintain the NASDAQ minimum bid price requirement. In addition to specific listing and
maintenance standards, NASDAQ has broad discretionary authority over the initial and continued listing of securities, which it could
exercise with respect to the listing of our common stock.
The reverse stock split may decrease the liquidity of the shares of our common stock.
The liquidity of the shares of our common stock may be affected adversely by the reverse stock split given the reduced number of shares
that are outstanding following the reverse stock split, especially if the market price of our common stock does not increase as a result of
the reverse stock split.
Following the reverse stock split, the resulting market price of our common stock may not attract new investors, including
institutional investors, and may not satisfy the investing requirements of those investors. Consequently, the trading liquidity of our
common stock may not improve.
Although we believe that a higher market price of our common stock may help generate greater or broader investor interest, we cannot
assure you that the reverse stock split will result in a share price that will attract new investors, including institutional investors, as some
investors analysts and other stock market participants have negative perceptions of reverse stock splits. In addition, there can be no
assurance that the market price of our common stock will satisfy the investing requirements of those investors. As a result, the trading
liquidity of our common stock may not necessarily improve.
ITEM 1B.
UNRESOLVED STAFF COMMENTS
None.
ITEM 2.
PROPERTIES
Our corporate headquarters are located in Parsippany, New Jersey where we lease approximately 23,000 square feet. The lease runs
through June 2017. Our lab facilities are located in Pittsburgh, Pennsylvania and New Haven, Connecticut, where we lease a total of
approximately 21,400 square feet. Our Pittsburgh, Pennsylvania lease expires on March 31, 2017, and on March 30, 2017 we signed a new
lease for one year commencing April 1, 2017 and ending on March 31, 2018 for an annual rent commitment of $390,000, plus it’s
proportionate share of utilities, with one option to extend the lease for a period of 3 to 5 years. Our New Haven, Connecticut lease is
month-to-month.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Our current facilities in Parsippany, New Jersey are significantly greater than we need, and we believe that there is ample commercial
space available locally in Northern/Central New Jersey. Additionally, our longer-term plans will likely include transferring operations
from New Haven, Connecticut to Pittsburgh, Pennsylvania. Accordingly, we believe that our current facilities are adequate for our current
and foreseeable operations and that suitable additional space will be available if needed.
ITEM 3.
LEGAL PROCEEDINGS
General
We are currently a party to legal proceedings that are incidental to our business and have received threats of litigation regarding past
due amounts for which we are currently negotiating payment plans. As required, we have accrued our estimate of the probable costs for the
resolution of these claims. While management currently believes that the ultimate outcome of these proceedings, individually and in the
aggregate, will not have a material adverse effect on our business, financial condition, results of operations or cash flow, litigation is
subject to inherent uncertainties. Were we to settle a proceeding for a material amount or were an unfavorable ruling to occur, there exists
the possibility of a material adverse impact on our business, financial condition, results of operations or cash flows. To the extent there is a
reasonable possibility that the losses could exceed the amounts already accrued, we will, as applicable, adjust the accrual in the period the
determination is made, disclose an estimate of the additional loss or range of loss, indicate that the estimate is immaterial with respect to
its financial statements as a whole or, if the amount of such adjustment cannot be reasonably estimated, disclose that an estimate cannot be
made. As of December 31, 2016, our accrual for litigation and threatened litigation was not material to the consolidated financial
statements. Legal fees are expensed as incurred.
Prolias Technologies, Inc. v. PDI, Inc.
On April 9, 2015, Prolias Technologies, Inc., or Prolias, filed a complaint, or the Complaint, against us with the Superior Court of
New Jersey (Morris County) in a matter entitled Prolias Technologies, Inc. v. PDI, Inc. (Docket No. MRS-L-000899-15). In the
Complaint, Prolias alleged that we entered into an August 19, 2013 Collaboration Agreement and a First Amendment thereto, or the
Agreement, whereby Prolias and us agreed to work in good faith to commercialize a diagnostic test known as “Thymira.” Thymira is a
minimally invasive diagnostic test that detects thyroid cancer.
Prolias alleged in the Complaint that we wrongfully terminated the Agreement, breached obligations owed to it under the Agreement
and committed torts by (i) failing to effectively and timely validate Thymira, (ii) purchasing a competitor of Prolias and working to
commercialize the competitive product at the expense of Thymira, and (iii) interfering with a license agreement that Prolias had with
Cornell University related to a license for Thymira. Prolias asserted claims against us for breach of contract, breach of the covenant of
good faith and fair dealing, intentional interference with contract and breach of fiduciary duty and seeks to recover unspecified
compensatory damages, punitive damages, interest and costs of suit.
On June 3, 2015, we filed an Answer and Counterclaim in response to the Complaint. In the Answer, we denied that we had any
liability to Prolias for the claims raised in the Complaint. In the Counterclaim, we sought (a) to recover from Prolias the principal amount
of $500,000 plus interest that was due and owing under a March 18, 2014 promissory note that Prolias delivered to us and (b) to compel
Prolias to execute and deliver a $1 million promissory note to memorialize Prolias’ repayment obligations of money we advanced under
the Agreement.
On May 27, 2016, the Court granted the motion by Prolias’ counsel to withdraw from representing Prolias and ordered Prolias to retain
substitute counsel within 30 days.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
On July 6, 2016, we moved to dismiss Prolias’ complaint and strike Prolias’ answer to our counterclaims for failure to retain substitute
counsel within 30 days as required by the Court’s May 27th Order. On August 15, 2016, the Court granted our motion and dismissed
Prolias’ complaint with prejudice and struck Prolias’ answer to our counterclaims. On September 22, 2016, the Court granted our request
to enter default judgment against Prolias for failure to plead or otherwise respond to the counterclaims. Thereafter, on October 13, 2016,
we filed an application to enter final judgment and taxing of costs against Prolias. We requested that the Court enter final judgment against
Prolias and for us in the amount of $621,236, plus ten percent interest continuing to accrue on the principal balance of $500,000 unless and
until paid, attorneys’ fees and costs of $390,769, and a declaratory judgment that Prolias is deemed to have executed and delivered to us a
promissory note in the amount of $1,000,000 under Article 10.2(a) of the Collaboration Agreement. On November 17, 2016, the Court
denied our application without prejudice and with leave to refile.
On February 16, 2017, we refiled our application for final judgment, and on March 9, 2017, the Superior Court of New Jersey entered
a final judgment in our favor against Prolias for the sum of $636,053 plus ten percent interest continuing to accrue on the principal balance
of $500,000 (per diem $136.99) unless and until paid. Final judgment was also entered in our favor, and against Prolias, declaring Prolias
is deemed to have executed and delivered to us a promissory note in the amount of $1,000,000 and Prolias is obligated to repay us the
principal amount and all interest in accordance with the terms of the promissory note and Article 10.2(a) of the Collaboration Agreement
by and between Prolias and us. On March 17, 2017, we requested that the final judgment against Prolias be recorded as a statewide lien.
No assurance can be given that we will be able to recover on the judgment against Prolias.
Swann v. Akorn, Inc., and Interpace Diagnostics Group, Inc.
On May 27, 2016, Michael J. Swann, one of our former employees, filed a complaint against us in the Court of Common Pleas of the
Fifth Judicial Circuit in South Carolina in a matter entitled Michael J. Swann v. Akorn, Inc., and Interpace Diagnostic Group Inc. (Civil
Action No. 2016-CP-40-03362). In the complaint, Mr. Swann alleges, among other things, that he was discriminated against and
wrongfully terminated as a member of a sales force marketing pharmaceutical products of Akorn, Inc., because of an illness suffered by
Mr. Swann. Mr. Swann alleges that he was discriminated against in violation of the Americans with Disabilities Act/Americans with
Disabilities Act Amendments Act and the Family Medical Leave Act and seeks damages for back pay, reinstatement, front pay,
compensatory and punitive damages in an amount not less than $300,000, attorney’s fees and costs. We deny that we are liable to Mr.
Swann for any of the claims asserted and intend to vigorously defend ourselves against those claims.
Brookwood MC Investors, LLC & MCII v, PDI, Inc.
On March 30, 2017, we received a tenancy summons and verified complaint for nonpayment of our Parsippany, New Jersey office
rent. The complaint alleges amounts owing of $203,734 covering unpaid base rent of $54,075 from January through March 2017, as well
as late charges, attorney’s fees, and the redeposit of a security deposit of $136,975. The plaintiff landlord seeks judgement for possession
of the premises. A hearing in the Superior Court of New Jersey, Morris County-Special Civil part, is scheduled for April 21, 2017.
ITEM 4. MINE SAFETY DISCLOSURES
Not applicable.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
PART II
ITEM 5.
MARKET FOR OUR COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER
PURCHASES OF EQUITY SECURITIES
Market Information
Our common stock is traded on The Nasdaq Capital Market under the ticker symbol “IDXG.” On December 28, 2016, we effected a
one-for-ten reverse split of our issued and outstanding shares of our common stock. At the effective time of the reverse split, every 10
shares of common stock issued and outstanding were automatically combined into one share of issued and outstanding common stock,
without any change in the par value per share. Our common stock began trading on The Nasdaq Capital Market on a reverse stock split-
adjusted basis on December 29, 2016. There was no change in our ticker symbol as a result of the reverse stock split.
The price range per share of common stock presented below represents the high and low trading price for our common stock on The
Nasdaq Capital Market for the last two years by quarter. The market prices below give retroactive effect to the one-for-ten reverse split of
our issued and outstanding shares of common stock effected on December 28, 2016.
First quarter
Second quarter
Third quarter
Fourth quarter
Holders of Record
2016
2015
HIGH
LOW
HIGH
LOW
$
$
$
$
4.00 $
5.38 $
4.09 $
13.50 $
2.00 $
2.30 $
1.60 $
0.79 $
21.50 $
18.10 $
27.40 $
19.80 $
13.00
10.00
14.00
4.20
We had 136 stockholders of record as of March 30, 2017. Not reflected in the number of stockholders of record are persons who
beneficially own shares of common stock held in nominee or street name.
Dividends
We have not declared any cash dividends and do not intend to declare or pay any cash dividends in the foreseeable future. Future
earnings, if any, will be used to finance the future operation and growth of our businesses.
Recent Sales of Unregistered Securities
None.
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ITEM 6.
SELECTED FINANCIAL DATA
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
We are a “smaller reporting company” for purposes of the disclosure requirements of Item 301 of Regulation S-K and, therefore, we
are not required to provide this information.
ITEM 7.
MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF
OPERATIONS
The following Management’s Discussion and Analysis of Financial Condition and Results of Operations should be read in
conjunction with our consolidated financial statements and the related notes appearing elsewhere in this Annual Report on Form 10-K.
This discussion and analysis includes certain forward-looking statements that involve risks, uncertainties and assumptions. You should
review the Risk Factors section of this Form 10-K for a discussion of important factors that could cause actual results to differ materially
from the results described in or implied by such forward-looking statements. See Cautionary Note Regarding Forward-Looking
Information at the beginning of this Form 10-K.
COMPANY OVERVIEW
We are a fully integrated commercial company that provides clinically useful molecular diagnostic tests and pathology services.
We develop and commercialize molecular diagnostic tests and related first line assays principally focused on early detection of high
potential progressors to cancer and leverage the latest technology and personalized medicine for improved patient diagnosis and
management. We currently have three commercialized molecular diagnostic assays in the marketplace for which we are reimbursed by
Medicare and multiple private payors: PancraGEN®, a pancreatic cyst and pancreaticobiliary solid lesion molecular test that can aid in
pancreatic cyst diagnosis and pancreatic cancer risk assessment utilizing our proprietary PathFinder platform; ThyGenX®, which assesses
thyroid nodules for risk of malignancy; and ThyraMIR®, which assesses thyroid nodules for risk of malignancy utilizing a proprietary
gene expression assay. We are also in the process of “soft launching” while we gather additional market data, BarreGEN®, an esophageal
cancer risk classifier for Barrett’s Esophagus that utilizes our PathFinder platform.
Our mission is to provide personalized medicine through molecular diagnostics and innovation to advance patient care based on
rigorous science. We are leveraging our Clinical Laboratory Improvement Amendments, or CLIA, certified and College of American
Pathologists, or CAP, accredited laboratories to develop and commercialize our assays and products. We aim to provide physicians and
patients with diagnostic options for detecting genetic and other molecular mutations that are associated with gastrointestinal and endocrine
cancer. Our customers consist primarily of physicians, hospitals and clinics.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
With the completion of the sale of substantially all of our CSO business in December 2015 and transition of related activities
through September 2016, we are now concentrating our efforts on our molecular diagnostics business by offering solutions for determining
the presence of certain cancers to clinicians and their patients as well as providing prognostic pre-cancerous information, which we believe
to be an expanding market opportunity. The global molecular diagnostics market is estimated to be $6.45 billion and is a segment within
the approximately $60 billion in vitro diagnostics market. We believe that the molecular diagnostics market offers significant growth and
strong patient value given the substantial opportunity it affords to lower healthcare costs by helping to reduce unnecessary surgeries and
ensuring the appropriate frequency of monitoring. We are keenly focused on growing our test volumes, securing additional coverage and
reimbursement, maintaining our current reimbursement and supporting revenue growth for our three commercialized innovative tests,
introducing related first line product and service extensions, as well as expanding our business by developing and promoting synergistic
products, like BarreGEN®, in our market.
Operating Activities in 2016
In 2016, we made progress related to laboratory licenses allowing us to market our products, improved reimbursement coverage
and rates and expanding our product offerings while reducing operating costs and continuing to exit the remainder of our CSO business.
In March 2016, we announced that we implemented a broad-based program to maximize efficiencies and cut costs as we focus on
improving cash flows and profitability while completing our transition to a standalone molecular diagnostics business. In addition to
reducing headcount, we have realigned our compensation structure, consolidated positions, eliminated programs and development plans
that did not have near term benefits, and streamlined and right-sized operating systems while reducing overhead. This was done while
supporting the transition of our CSO business to the buyer of that business and continuing to shut-down less profitable CSO contracts that
were not part of the sale of that business.
In August 2016, we announced that the New York State Department of Health had reviewed and approved ThyraMIR®, the
Company’s micro RNA gene-expression based test, in New York State. New York State accounts for approximately 5% of the 600,000
FNA biopsies performed in the U.S. annually according to Thyroid Disease Manager. With this final approval, ThyraMIR® is now
available to patients across the U.S.
In October 2016, we announced that the New York State Department of Health had reviewed and approved ThyGenX®, our
NextGen Sequencing oncogene panel for thyroid nodules. The New York State approval of ThyGenX® enables us to test specimens from
patients in New York and therefore, enables us to market both ThyGenX® and ThyraMIR® together in that state. As ThyGenX® always
precedes the running of ThyraMIR®, approximately 82% of ThyGenX® cases warranting reflex to a more sophisticated RNA assessment
via ThyraMIR®. Of the several states that require special licensure to provide testing to patients who reside in their jurisdiction, New
York was the final state to issue a license.
Also, in October 2016, we announced completion and the validation and launch of two new thyroid services, further expanding
our comprehensive support of physicians and health care institutions servicing thyroid patients. Our new cytopathology service is designed
to assist physicians and clinics that prefer to have the initial FNA biopsy assessed by an independent third party versus having it
performed on site.
Additional Reimbursement Coverage During 2016
Reimbursement progress is key for any molecular diagnostic company. We made progress in both public and private
reimbursement throughout the year. Perhaps our greatest accomplishment in 2016 was our agreement with Aetna to cover our ThyraMIR®
test, which together with their previous approval to cover ThyGenX®, provides 46 million covered patients the opportunity to use both of
our thyroid assays.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
We have been successfully expanding the reimbursement of our products in 2016. In summary, three of our molecular
diagnostics are now covered by Medicare. Specifically we have made the following progress with payors in 2016:
● In December 2016, we announced that Aetna, the third largest health plan in the United States, agreed to cover our
ThyraMIR® test, the first micro RNA classifier made available for improving the diagnosis of indeterminate thyroid
nodules, for all of Aetna’s approximately 46 million members nationwide, with coverage effective immediately. Our
ThyGenX® and ThyraMIR® thyroid assays are now covered for approximately 200 million patients nationwide,
including through Medicare, national and regional health plans.
● In April 2016, we also announced that we received coverage for all of our products by Galaxy Health Network, a
national managed care provider with over 3.5 million covered lives. Galaxy Health Network’s Preferred Provider
Organization includes a network of over 400,000 contracted physicians, 2,700 hospitals and 47,000 ancillary providers.
● In April 2016, we announced new coding by Novitas Solutions for PancraGEN®. Novitas Solutions has assigned a new
molecular CPT code to its PancraGEN® test for pancreatic cysts. Prior to this coding change, the test was covered under a
miscellaneous chemistry code, which is used for billing a wide range of tests across the laboratory industry and does not
effectively differentiate between technologies that have significantly different features and offer unique benefits to
patients with specific diseases.
● In February 2016, we announced that we received Medicare approval for coverage of ThyraMIR®. As a
result, ThyraMIR® is now accessible to more than 50 million Medicare covered patients nationwide effective December
14, 2015. ThyGenX® is already covered by Medicare. Therefore, the addition of coverage for ThyraMIR® provides
Medicare covered patients the benefits of the ThyGenX®/ThyraMIR® combination test.
● In January 2016, we announced that our MAC, Novitas Solutions, issued a new LCD for PancraGEN®. The LCD
provides the specific circumstances under which PancraGEN® is covered. The new policy is non-conditional and may
improve the efficiency of the testing process for doctors and patients. The LCD covers approximately 55 million patients,
bringing the total patients covered for PancraGEN® to nearly 68 million.
Settlements and Debt Exchange for RedPath Note
Settlement Agreement with Former Senior Executives
Effective January 17, 2017, Frank Arena, Jennifer Leonard, Nancy Lurker, Graham G. Miao and Gerald R. Melillo, Jr., all former
senior executives of ours, each agreed to accept a payment of 35% of the total severance obligations due to each of them pursuant to their
respective separation agreements with us, or an aggregate of approximately $1.0 million, in satisfaction in full and settlement of an
aggregate of approximately $2.9 million in severance payments. Their agreement was conditioned upon their receipt from us of such
payments by March 1, 2017. Our obligation to make such payments was conditioned upon us consummating a sufficiently large financing
(with gross proceeds of approximately $4.0 million) and the prior agreement of our investment banker and investors in such financing for
the use of a portion of such proceeds for such payments. Our registered direct offering completed on January 25, 2017 satisfied such
conditions. Each of the former senior executives agreed to enter into releases with us at the time of receipt of such payments, and in
consideration therefor, releasing us and our directors, officers and agents from any and all claims, losses and damages they have or ever
had against us and our directors, officers and agents. Accordingly on February 27, 2017 we paid approximately $1.0 million of the net
proceeds from such registered direct offering to satisfy the obligations due to the five former senior executives and received releases of the
Company and our directors, officers and agents as executed by all five former senior executives at that time.
Debt Exchange for RedPath Note
Exchange Agreement
On March 22, 2017, we entered into an exchange agreement, or the Exchange Agreement, with the Investor. Prior to our entering
into the Exchange Agreement, the Investor acquired the RedPath Note, which was entered into in connection with our acquisition of
RedPath in October 2014. The RedPath Note had an aggregate principal amount of $9,336,250 outstanding and was acquired by the
Investor for $8,869,437.50. The RedPath Equityholder Representative assigned all of its rights, title and interest in the RedPath Note to the
Investor, including, but not limited to, its security interest in all of our assets and the assets of our subsidiaries.
Pursuant to the Exchange Agreement, we and the Investor agreed to exchange the RedPath Note for (i) a senior secured
convertible note in the aggregate principal amount of $5,321,662.50, or the Exchanged Convertible Note, which is convertible into shares
of our common stock in accordance with its terms, and (ii) a senior secured non-convertible note with an aggregate principal amount of
$3,547,775, or the Exchanged Non-Convertible Note, for a combined aggregate principal amount of $8,869,437.50. The Exchanged Notes
will rank senior to all of our outstanding and future indebtedness, other than the indebtedness in favor of our credit line lender and are
secured by a perfected security interest in all of our existing and future assets and those of our subsidiaries. Upon the reduction of 55% of
the aggregate principal amount of each of the Exchanged Notes, the Investor will release its security interest in its entirety.
The closing of the Exchange Agreement occurred on March 23, 2017.
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The Exchanged Notes
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
The Exchanged Notes mature at 125% of the face value on the fifteenth month anniversary of the closing date, or June 22, 2018,
and bear interest quarterly at one and one hundredth percent (1.01%) per annum (as may be adjusted from time to time). Under the terms of
the Exchanged Notes, we have the right to require a redemption of a portion (not less than $500,000) or all of the applicable Exchanged
Notes prior to their maturity at a price equal to 115% of the principal amount of the Exchanged Notes within the first 180 days of issuance,
120% of the principal amount of the Exchanged Notes between 180 and 270 days of issuance, and 125% of the principal amount of the
Exchanged Notes after 270 days of issuance. A mandatory redemption may be required by the Investor in connection with the occurrence
of an event of default or change of control. In each event, the redemption price is subject to a premium on parity, and the Exchanged
Convertible Note redemption may be subject to a premium on parity if certain unfavorable conditions exist, as described therein.
The Exchanged Convertible Note is convertible into shares of our common stock. The Investor may elect to convert all or a
portion of the Exchanged Convertible Note and all accrued and unpaid interest with respect to such portion, if any, into shares of common
stock at a fixed conversion price of $2.44, or the Fixed Conversion Price. In the event we seek and obtain stockholder approval to issue
shares of common stock in connection with the conversion of the Exchanged Convertible Note (which determination shall be at our sole
discretion) from and after the date of the Exchange Agreement, the Exchanged Convertible Note may alternatively be converted, or an
Alternative Conversion, by the Investor at the greater of (i) $0.40 and (ii) lowest of (x) the applicable conversion price as in effect on the
applicable conversion date of the applicable Alternative Conversion, and (y) 88% of the lowest volume-weighted average price of the
common stock during the 10 consecutive trading day period ending and including the date of delivery of the applicable conversion notice.
If the volume-weighted average price of our common stock exceeds 135% of the Fixed Conversion Price, or $3.29, for five consecutive
trading days and no equity conditions failure, as defined, then exists, we have the option to convert the Exchanged Convertible Note into
shares of common stock at the Fixed Conversion Price. We may not effect the conversion of any portion of the Exchanged Convertible
Note, and the Investor shall not have the right to convert any portion of the Exchanged Convertible Note, to the extent that after giving
effect to such conversion, the Investor together with any other persons whose beneficial ownership of our common stock could be
aggregated with the Investor’s collectively would be in excess of 9.99% of the shares of common stock outstanding immediately after
giving effect to such conversion. Additionally, any such conversion will be null and void and treated as if never made.
Through March 30, 2017, the Investor converted $4,321,663 of the Exchanged Convertible Note into 1,730,534 shares of our
common stock.
Security Agreement
As noted above, simultaneously with the sale of the RedPath Note to the Investor, RedPath Equityholder Representative assigned
all of its security interest in our assets and those of our subsidiaries to the Investor. Pursuant to this assignment, on March 23, 2017, we and
our subsidiaries, Interpace Diagnostics Corporation and Interpace LLC, entered into an Amended and Restated Security and Pledge
Agreement, or the Security Agreement, and an Amended and Restated Intellectual Property Security Agreement, or the IP Security
Agreement, with the Investor, evidencing the transfer of security interest in favor of the RedPath Equityholder Representative to the
Investor. In addition, our material subsidiaries entered into a Guaranty in favor of the Investor, to support our obligations pursuant to the
terms of the Exchange Agreement. The Security Agreement, among other things, authorizes the Investor to file UCC-3 financing
statements to transfer the liens on file with the Secretary of State of the State of Delaware to the Investor. The Investor will also have
control of certain deposit accounts in our name. Under the IP Security Agreement, we also granted the Investor the right to assign the liens
on its intellectual property in favor of the RedPath Equityholder Representative to the Investor. The liens in favor of the Investor are senior
to any other of our indebtedness, except the lien in favor of our credit line lender. As noted above, upon the reduction of 55% of the
aggregate principal amount of each of the Exchanged Notes, the Investor will release its security interest in its entirety.
Termination Agreement
Simultaneously with the consummation of the sale of the RedPath Note to the Investor, on March 22, 2017, we and our
subsidiaries entered into a Termination Agreement with the RedPath Equityholder Representative. Under the terms of the Termination
Agreement, RedPath Equityholder Representative agreed to terminate certain royalty and milestone rights, or the Royalties, provided
under that certain Contingent Consideration Agreement, dated October 31, 2014, entered into in connection with the our acquisition of
RedPath. In addition, the RedPath Equityholder Representative agreed to terminate its rights, granted under that certain Agreement and
Plan of Merger, dated October 31, 2014, among RedPath, us and certain other parties, to designate an observer to be present in an observer
capacity at meetings of our board of directors, or the Board Observer Rights. As consideration for the termination of its Royalties and
Board Observer Rights, we agreed to issue warrants to purchase up to an aggregate of 100,000 shares of our common stock, or the RedPath
Warrants, to certain former equityholders of RedPath, as designated by the RedPath Equityholder Representative. We have 10 days from
the instruction of the RedPath Equityholder Representative to effect the issuance of any of the RedPath Warrants.
The RedPath Warrants will have an exercise price of $4.69 per share, which is subject to adjustment in the event of certain stock
dividends and distributions, stock splits, stock combinations, reclassifications or similar events affecting our common stock. The RedPath
Warrants will be exercisable at any time on or after the six-month anniversary of the issuance date, or September 22, 2016 and will survive
until the fifth anniversary of that date.
If at any time we grant, issue or sell any instruments that are convertible into or exercisable or exchangeable for common stock or
rights to purchase stock, warrants, securities or other property pro rata to all of the stockholders, or the Purchase Rights, then the holder of
a RedPath Warrant will be entitled to acquire, on the terms applicable to such Purchase Rights, the aggregate Purchase Rights which the
holder could have acquired if the holder had held the number of shares of common stock acquirable upon complete exercise of the
RedPath Warrant immediately before the date on which a record is taken or otherwise determined for the grant, issuance or sale of such
Purchase Rights. In addition, during such time as the RedPath Warrants are outstanding, if we declare any dividend or other distribution of
our assets (or rights to acquire its assets) to all of the stockholders, by way of return of capital or otherwise, or a Distribution, then, in each
such case, the holder will be entitled to participate in such Distribution to the same extent that the holder would have participated therein if
the holder had held the number of shares of common stock acquirable upon complete exercise of the RedPath Warrant immediately before
the date of which a record is taken or otherwise determined for participation in such Distribution.
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Recent Equity Financings
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
From December 22, 2016 through February 8, 2017, we completed four public offerings of common stock and a private placement
of warrants, which resulted in aggregate gross proceeds to us of approximately $14.1 million. A description of the financings is as follows:
● On December 22, 2016, we completed a registered direct public offering with a single institutional investor, or the Registered Direct
Offering, to sell 200,000 shares of our common stock at a price of $5.30 per share and prefunded warrants to purchase 160,000 shares
of our common stock at a price of $5.20 per warrant, with each warrant having an exercise price of $0.10 per share. The warrants were
immediately exercised. The Registered Direct Offering resulted in gross proceeds to us of approximately $1.9 million. We used
approximately $1.3 million to make the first quarterly payment of principal under the RedPath Note due to the Redpath Equityholder
Representative.
● On January 6, 2017, we completed a registered direct public offering, or the Second Registered Direct Offering, to sell 630,000 shares
of our common stock at a price of $6.81 per share to certain institutional investors. The Second Registered Direct Offering resulted in
gross proceeds to us of approximately $4.2 million. We are using the net proceeds from the Second Registered Direct Offering for
working capital, repayment of indebtedness and general corporate purposes. In addition, we granted each institutional investor who
participated in the Second Registered Direct Offering the right, for a period of 15 months following January 6, 2017, or until April 6,
2018, to participate in any public or private offering by us of equity securities, subject to certain exceptions, up to such investor’s pro
rata portion of 50% of the securities being offered.
● On January 25, 2017, we completed a registered direct public offering, or the Third Registered Direct Offering, to sell 855,000 shares
of our common stock and a concurrent private placement of warrants to purchase 855,000 shares of our common stock, or the
Warrants, to the same investors participating in the Third Registered Direct Offering, or the Private Placement. The Warrants and the
shares of our common stock issuable upon the exercise of the Warrants were not registered under the Securities Act and were sold
pursuant to the exemption provided in Section 4(a)(2) under the Securities Act and Rule 506(b) of Regulation D promulgated
thereunder. The shares of common stock sold in the Third Registered Direct Offering and the Warrants issued in the concurrent
Private Placement were issued separately but sold together at a combined purchase price of $4.69 per share of common stock and
accompanying Warrant. The Third Registered Direct Offering resulted in gross proceeds to us of approximately $4 million. We are
using the net proceeds from the Third Registered Direct Offering for working capital, repayment of indebtedness and general
corporate purposes and also used approximately $1.0 million to satisfy the obligations due to the five former senior executives.
● On February 8, 2017, we completed an underwritten, confidentially marketed public offering, or the CMPO, to sell 1,200,000 shares
of our common stock at a price of $3.00 per share. In addition, we granted the underwriters an option to purchase up to an additional
9% of the total number of shares of common stock sold by us in the CMPO, solely for the purpose of covering over-allotments, if any.
The underwriters exercised the over-allotment option in full. The CMPO resulted in gross proceeds to us of approximately $3.9
million. We are using the proceeds from the CMPO for working capital, repayment of indebtedness and liabilities and for general
corporate purposes.
Certain Defaults of Current Obligations
From September 30, 2016 through December 31, 2016, we provided working capital by extending our payables primarily by not
making timely payments on current obligations and debt incurred prior to the sale of our CSO business, entering into payment plans,
negotiating termination agreements on commitments that were not useful to our current business and not paying certain severance
obligations to terminated employees. Despite the $14.1 million of capital we have raised from December 2016 through February 2017, we
remain in default of certain of our current obligations, as set forth below:
● We received a Notice of Default dated December 12, 2016 for non-payment of November and December rent for our Parsippany,
New Jersey facility, or the Parsippany Lease, which has been substantially vacant since the sale of the CSO business in December
2015. In the notice, the landlord stated the amount of rent due, $112,519, had been deducted from a security deposit of $136,975.
We paid the past due November 2016 rent and half of the December 2016 rent. The lease term for the property ends on June 30,
2017. On March 30, 2017, we received a tenancy summons and verified complaint for nonpayment of our Parsippany, New Jersey
office rent. The complaint alleges amounts owing of $203,734 covering unpaid base rent of $54,075 from January through March
2017, as well as late charges, attorney’s fees, and the redeposit of a security deposit of $136,975. The plaintiff landlord seeks
judgement for possession of the premises. A hearing in the Superior Court of New Jersey, Morris County-Special Civil part, is
scheduled for April 21, 2017.
● Pursuant to the terms of our Credit and Security Agreement dated September 28, 2016 with SCM Specialty Finance
Opportunities Fund, L.P., or the Credit Agreement, the default under the Parsippany Lease creates a cross-default under the Credit
Agreement. We have not yet drawn down on the credit facility as we are negotiating revisions to certain covenants in the Credit
Agreement, and we will not be permitted to draw down under the credit facility until the default referred to above is cured and until
expiration of the Exchanged Notes.
● Currently, we are seeking to restructure past due vendor claims of approximately $2.6 million, which includes approximately
$1.8 million due to certain vendors with whom we had stopped making payments in September 2016. As of March 1, 2017 we
reinitiated payments with certain of those vendors and are continuing negotiations with others regarding scheduled payments. As of
the date of this Annual Report on Form 10-K, we have outstanding royalty obligations totaling approximately $0.8 million and
$0.3 million of outstanding state tax liabilities due to various taxing authorities.
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DESCRIPTION OF REPORTING SEGMENTS
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
We currently operate under one operating segment, which is our molecular diagnostic business. Until December 22, 2015 prior to the
sale of the CSO business, we operated under two reporting segments: Commercial Services and Interpace Diagnostics. The CSO business
is reported as discontinued operations through December 31, 2016 and has been reclassified to discontinued operations in the periods
ended December 31, 2015 to conform to the current period presentation.
CRITICAL ACCOUNTING POLICIES
We prepare our consolidated financial statements in accordance with U.S. generally accepted accounting principles, or GAAP. The
preparation of financial statements and related disclosures in conformity with GAAP requires management to make judgments, estimates
and assumptions at a specific point in time that affect the amounts reported in our consolidated financial statements and disclosed in the
accompanying notes. These assumptions and estimates are inherently uncertain. Outlined below are accounting policies, which are
important to our financial position and results of operations, and require our management to make significant judgments in their
application. Some of those judgments can be subjective and complex. Management’s estimates are based on historical experience,
information from third-party professionals, facts and circumstances available at the time and various other assumptions that are believed to
be reasonable. Actual results could differ from those estimates. Additionally, changes in estimates could have a material impact on our
consolidated results of operations in any one period. For a summary of all of our significant accounting policies, including the accounting
policies discussed below, see Note 1, Nature of Business and Significant Account Policies, to our consolidated financial statements
included in this Annual Report on Form 10-K.
Revenue and Cost of Services
We recognize revenue from services rendered when the following four revenue recognition criteria are met: persuasive evidence of
an arrangement exists; services have been rendered; the selling price is fixed or determinable; and collectability is reasonably assured.
Our revenue is generated using our proprietary tests. Our performance obligation is fulfilled upon the completion, review and release
of test results. In conjunction with fulfilling these services, we bill the third-party payor or hospital. We recognize our revenue related to
billings for Medicare, Medicare Advantage, and hospitals on an accrual basis, net of contractual adjustment, when a contract is in place, a
reliable pattern of collectability exists and collectability is reasonably assured. Contractual adjustments represent the difference between
the list prices and the reimbursement rate set by Medicare and Medicare Advantage, the contractual rate or the amounts agreed to with
hospitals.
Until a contract has been negotiated with a commercial insurance carrier or governmental program, the services may or may not be
covered by these entities existing reimbursement policies. In the absence of an agreement with the patient or other clearly enforceable
legal right to demand payment, the related revenue is only recognized upon the earlier of payment notification or cash receipt.
Accordingly, we recognize revenue from commercial insurance carriers, government programs, and direct-bill healthcare providers
without contracts, when payment is received.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Persuasive evidence of an arrangement exists and delivery is deemed to have occurred upon completion, review, and release of the test
results at which time we will bill the third-party payor or hospital. The assessment of the fixed or determinable nature of the fees charged
for diagnostic testing performed, and the collectability of those fees, requires significant judgment by our management. Our management
believes that these two criteria have been met when there is contracted reimbursement coverage or a predictable pattern of collectability
with individual third-party payors or hospitals and accordingly, recognizes revenue upon delivery of the test results. In the absence of
contracted reimbursement coverage or a predictable pattern of collectability, we believe that the fee is fixed or determinable and
collectability is reasonably assured only upon request of third-party payor notification of payment or when cash is received, and we
recognize revenue at that time.
Cost of services consists primarily of the costs associated with operating our laboratories and other costs directly related to our tests.
Personnel costs, which constitute the largest portion of cost of services, include all labor related costs, such as salaries, bonuses, fringe
benefits and payroll taxes for laboratory personnel. Other direct costs include, but are not limited to, laboratory supplies, certain consulting
expenses, and facility expenses.
Goodwill
We allocate the cost of acquired companies to the identifiable tangible and intangible assets acquired and liabilities assumed, with the
remaining amount classified as goodwill. Since the entities we have acquired do not have significant tangible assets, a significant portion
of the purchase price has been allocated to intangible assets and goodwill. The identification and valuation of these intangible assets and
the determination of the estimated useful lives at the time of acquisition, as well as the completion of impairment tests require significant
management judgments and estimates. These estimates are made based on, among other factors, reviews of projected future operating
results and business plans, economic projections, anticipated highest and best use of future cash flows and the market participant cost of
capital. The use of alternative estimates and assumptions could increase or decrease the estimated fair value of goodwill and other
intangible assets, and potentially result in a different impact to our results of operations. Further, changes in business strategy and/or
market conditions may significantly impact these judgments and thereby impact the fair value of these assets, which could result in an
impairment of the goodwill or intangible assets.
We test goodwill for impairment at least annually (as of December 31) and whenever events or circumstances change that indicate
impairment may have occurred. A significant amount of judgment is involved in determining if an indicator of impairment has occurred.
Such indicators may include, among others: a significant decline in our expected future cash flows; a sustained, significant decline in our
stock price and market capitalization; a significant adverse change in legal factors or in the business climate of the industries in which we
operate; unanticipated competition; and slower growth rates. Any adverse change in these factors could have a significant impact on the
recoverability of goodwill, the indefinite-lived intangible asset and our consolidated financial results.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
In 2015, we recorded $15.7 million of impairment charges relating to the impairment of our goodwill balance pertaining to the
RedPath acquisition in October 2014. See Note 7, Goodwill and Other Intangible Assets, to the consolidated financial statements for more
details.
Long-Lived Assets, including Finite-Lived Intangible Assets
We review the recoverability of long-lived assets and finite-lived intangible assets whenever events or changes in circumstances
indicate that the carrying value of such assets may not be recoverable. If the sum of the expected future undiscounted cash flows is less
than the carrying amount of the asset, an impairment loss is recognized by reducing the recorded value of the asset to its fair value
measured by future discounted cash flows. This analysis requires estimates of the amount and timing of projected cash flows and, where
applicable, judgments associated with, among other factors, the appropriate discount rate. Such estimates are critical in determining
whether any impairment charge should be recorded and the amount of such charge if an impairment loss is deemed to be necessary. In
2016, we recorded $3.4 million of impairment charges relating to the impairment of our certain intangible assets pertaining to the
Asuragen acquisition in August 2014.
Contingencies
In the normal course of business, we are subject to various contingencies. Contingencies are recorded in the consolidated financial
statements when it is probable that a liability will be incurred and the amount of the loss can be reasonably estimated, or otherwise
disclosed, in accordance with ASC 450, Contingencies. Significant judgment is required in both the determination of probability and the
determination as to whether a loss is reasonably estimable. In the event we determine that a loss is not probable, but is reasonably possible,
and it becomes possible to develop what we believe to be a reasonable range of possible loss, then we will include disclosures related to
such matter as appropriate and in compliance with ASC 450. To the extent there is a reasonable possibility that the losses could exceed the
amounts already accrued, we will, when applicable, adjust the accrual in the period the determination is made, disclose an estimate of the
additional loss or range of loss, indicate that the estimate is immaterial with respect to its financial statements as a whole or, if the amount
of such adjustment cannot be reasonably estimated, disclose that an estimate cannot be made. We are currently involved in certain legal
proceedings and, as required, have accrued our estimate of the probable costs for the resolution of these claims. These estimates are
developed in consultation with outside counsel and are based upon an analysis of potential results, assuming a combination of litigation
and settlement strategies. Predicting the outcome of claims and litigation, and estimating related costs and exposures, involves substantial
uncertainties that could cause actual costs to vary materially from estimates.
Income Taxes
Income taxes are based on income for financial reporting purposes calculated using our expected annual effective rate and reflect a
current tax liability or asset for the estimated taxes payable or recoverable on the current year tax return and expected annual changes in
deferred taxes.
We account for income taxes using the asset and liability method. This method requires recognition of deferred tax assets and
liabilities for expected future tax consequences of temporary differences that currently exist between tax bases and financial reporting
bases of our assets and liabilities based on enacted tax laws and rates. Deferred tax expense (benefit) is the result of changes in the
deferred tax asset and liability. A valuation allowance is established, when necessary, to reduce the deferred income tax assets when it is
more likely than not that all or a portion of a deferred tax asset will not be realized.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
We operate in multiple tax jurisdictions and provide taxes in each jurisdiction where we conduct business and are subject to taxation.
The breadth of our operations and the complexity of the various tax laws require assessments of uncertainties and judgments in estimating
the ultimate taxes we will pay. The final taxes paid are dependent upon many factors, including negotiations with taxing authorities in
various jurisdictions, outcomes of tax litigation and resolution of proposed assessments arising from federal and state audits. We have
established estimated liabilities for uncertain federal and state income tax positions. Uncertain tax positions are recognized in the financial
statements when it is more likely than not (for example, a likelihood of more than fifty percent) that a position taken or expected to be
taken in a tax return would be sustained upon examination by tax authorities that have full knowledge of all relevant information. A
recognized tax position is then measured as the largest amount of benefit that is greater than fifty percent likely to be realized upon
ultimate settlement. We adjust our accruals for unrecognized tax benefits as facts and circumstances change, such as the progress of a tax
audit. We believe that any potential audit adjustments will not have a material adverse effect on our financial condition or liquidity.
However, any adjustments made may be material to our consolidated results of operations or cash flows for a reporting period. Penalties
and interest, if incurred, would be recorded as a component of current income tax expense.
Significant judgment is also required in evaluating the need for and magnitude of appropriate valuation allowances against deferred
tax assets. We currently have significant deferred tax assets resulting from net operating loss carryforwards and deductible temporary
differences. The realization of these assets is dependent on generating future taxable income. We perform an analysis quarterly to
determine whether the expected future income will more likely than not be sufficient to realize the deferred tax assets. Our recent
operating results and projections of future income weighed heavily in our overall assessment. The existing and forecasted levels of pretax
earnings for financial reporting purposes are not sufficient to generate future taxable income and realize our deferred tax assets and, as a
result, we established a full federal and state valuation allowance for the net deferred tax assets at December 31, 2016 and 2015, as we
determined that it was more likely than not that these assets would not be realized.
Stock Compensation Costs
The compensation cost associated with the granting of stock-based awards is based on the grant date fair value of the stock award. We
recognize the compensation cost, net of estimated forfeitures, over the shorter of the vesting period or the period from the grant date to the
date when retirement eligibility is achieved. Forfeitures are initially estimated based on historical information and subsequently updated
over the life of the awards to ultimately reflect actual forfeitures. As a result, changes in forfeiture activity can influence the amount of
stock compensation cost recognized from period-to-period.
We primarily use the Black-Scholes option pricing model to determine the fair value of stock options and stock-based stock
appreciation rights (SARs). The determination of the fair value of stock-based payment awards is made on the date of grant and is affected
by our stock price as well as assumptions made regarding a number of complex and subjective variables. These assumptions include: our
expected stock price volatility over the term of the awards; actual and projected employee stock option exercise behaviors; the risk-free
interest rate; and expected dividend yield.
Changes in the valuation assumptions could result in a significant change to the cost of an individual award. However, the total cost
of an award is also a function of the number of awards granted, and as result, we have the ability to manage the cost and value of our
equity awards by adjusting the number of awards granted.
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CONSOLIDATED RESULTS OF OPERATIONS
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
The following table sets forth the selected statement of comprehensive loss data as a percentage of revenue for the periods
indicated. The trends illustrated in this table may not be indicative of future operating results.
Years Ended December 31,
2016
2016
2015
2015
Revenue, net
Cost of revenue
Gross profit
Operating expenses:
$
Sales and marketing
Research and development
General and administrative
Acquisition related amortization expense
Asset impairment
Loss on extinguishment of debt
Goodwill impairment
Change in fair value of contingent consideration
Total operating expenses
Operating loss
Interest expense
Other income (expense), net
Loss from continuing operations before tax
Benefit from income taxes from continuing operations
Loss from continuing operations
(Loss) income from discontinued operations
Gain on sale of assets
Income from discontinued operations
Provision for income tax on discontinued operations
Income from discontinued operations, net of tax
13,085
6,641
6,444
5,462
1,647
10,504
3,770
3,363
-
-
(11,860)
12,886
(6,442)
(2,144)
14
(8,572)
(162)
(8,410)
(886)
1,326
440
362
78
100.0% $
50.8%
49.2%
41.7%
12.6%
80.3%
28.8%
25.7%
0.0%
0.0%
-90.6%
98.5%
-49.2%
-16.4%
0.1%
-65.5%
-1.2%
-64.3%
-6.8%
10.1%
3.4%
2.8%
0.6%
9,432
6,910
2,522
10,358
2,292
16,922
3,812
-
1,873
15,666
(7,993)
42,930
(40,408)
(3,705)
(93)
(44,206)
(13,136)
(31,070)
10,341
21,634
31,975
12,261
19,714
100.0%
73.3%
26.7%
109.8%
24.3%
179.4%
40.4%
0.0%
19.9%
166.1%
-84.7%
455.2%
-428.4%
-39.3%
-1.0%
-468.7%
-139.3%
-329.4%
109.6%
229.4%
339.0%
130.0%
209.0%
Net loss
$
(8,332)
-63.7% $
(11,356)
-120.4%
Revenue, net
Consolidated revenue for the year ended December 31, 2016 increased by $3.7 million, or 38.7%, to $13.1 million, compared to the
year ended December 31, 2015. This increase was principally attributable to increased test and collection volume of ThyGenX and
ThyraMIR , and an increase in reimbursements, principally for ThyraMIR tests.
®
®
®
Cost of revenue
Consolidated cost of revenue for the year ended December 31, 2016 decreased by $0.3 million, or 3.9%, to $6.6 million, compared to
the year ended December 31, 2015. This decrease was attributable to lower lab supplies expense and improved efficiencies as part of a
broad-based program to maximize efficiencies and cut costs.
Gross profit
Consolidated gross profit for the year ended December 31, 2016 increased $3.9 million, or 155.5%, to $6.4 million, compared to the
year ended December 31, 2015. This increase was related to the favorable impact of the increase in revenue and reimbursement of our
Thyroid tests along with the lower cost of revenue described above.
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Sales and marketing expense
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Sales and marketing expense was $5.5 million for the year ended December 31, 2016 and as a percentage of revenue was 41.7%. For
the year ended December 31, 2015 the expense was $10.4 million and as a percentage of revenue was 109.8%. The decrease in sales and
marketing expense principally reflects a reduction in sales personnel and the consolidation of marketing activities under a broad-based
program to maximize efficiencies and cut costs in 2016.
Research and development
Research and development expense was $1.6 million and as a percentage of revenue was 12.6%. For the year ended December 31,
2015, the expense was $2.3 million and as a percentage of revenue, was 24.3%. This was primarily due to a study that ended in 2015 that
had a total expense of approximately $0.5 million.
General and administrative
General and administrative expense for the year ended December 31, 2016 was $10.5 million as compared to $16.9 million for the
year ended December 31, 2015. This decrease was primarily attributable to a decrease in stock compensation of $3.1 million, a net
reduction in executive severance costs of $1.3 million, and $0.8 million in salary costs due to reduced headcount. In 2015, there was $1.8
million in stock compensation expense relating to the accelerated vesting of equity attributable to the CSO sale in December 2016, which
is a portion of the $3.1 million decrease in stock compensation discussed above. As a percentage of revenue, general and administrative
expense was 80.3% for the year ended December 31, 2016 as compared to 179.4% for the year ended December 31, 2015.
Acquisition related amortization expense
During the years ended December 31, 2016 and December 31, 2015, we recorded amortization expense of approximately $3.8 million
for both periods. Amortization expense pertains to RedPath and Asuragen acquired intangible assets.
Asset impairment
During the year ended December 31, 2016, we incurred an asset impairment charge of approximately $3.4 million related to the
PancraMIR and Biobank assets associated with the acquisition of certain assets from Asuragen.
®
Loss on extinguishment of debt
In connection with paying off our credit agreement in 2015, we incurred approximately $1.9 million in expense consisting of $1.4
million in exit fee expense (net), $0.2 million in accelerated deferred financing costs, and $0.3 million in the acceleration of the loan
origination fee. See Note 17, Long-Term Debt, in the Consolidated Financial Statements for more details.
Goodwill impairment
During the year ended December 31, 2015, we recognized an impairment charge of $15.7 million related to the goodwill associated
with the Redpath acquisition in October 2014. See Note 7, Goodwill and Other Intangible Assets, in the Consolidated Financial Statements
for more details.
Change in fair value of contingent consideration
During the year ended December 31, 2016, we had an $11.9 million reduction to our contingent consideration liability and recognized
the credits to operating expenses in 2016. Lower future revenue projections resulted in reduced projected royalties due to the former
equityholders of Asuragen and RedPath.
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Operating loss
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
There were operating losses from continuing operations of $6.4 million and $40.4 million during the years ended December 31, 2016
and 2015, respectively. The decrease in operating loss from continuing operations in the year ended December 31, 2016 was primarily
attributable to the decrease in operating expenses discussed above.
Interest expense
There was interest expense of $2.1 million and $3.7 million during the years ended December 31, 2016 and December 31, 2015,
respectively. The decrease in interest expense in the year ended December 31, 2016 was primarily attributable to the paying off of our $20
million credit agreement in December 2015.
Provision for income taxes
We had income tax benefits of approximately $0.2 million and $13.1 million for the years ended December 31, 2016 and December
31, 2015, respectively. Income tax benefits for the years ended December 31, 2016 and December 31, 2015 were primarily due to the
reclassification of CSO as discontinued operations and the tax adjustments associated with that reclass.
Income (loss) from discontinued operations, before tax
We had a loss from discontinued operations of $0.9 million for the year ended December 31, 2016 as compared to income from
discontinued operations of $10.3 million for the year ended December 31, 2015. This decrease was primarily related to a full year of CSO
operations within discontinued operations in 2015.
Gain (loss) on sale
In 2016, the gain on sale of $1.3 million related to the final working capital adjustment regarding the sale of the CSO business in
December of 2015. In 2015, we sold substantially all of our CSO business to Publicis for an aggregate cash purchase price at closing of
approximately $28.5 million, which resulted in a net gain on sale of approximately $21.6 million. In the first quarter of 2015, we recorded
a gain on sale of the business of Group DCA, LLC, or Group DCA, of approximately $0.2 million. In the fourth quarter of 2015, we
recorded a loss on the disposal of Group DCA of $1.2 million. See Note 4, Discontinued Operations, in the Consolidated Financial
Statements for more details.
LIQUIDITY AND CAPITAL RESOURCES
For the fiscal year ended December 31, 2016, we had an operating loss of $6.4 million. As of December 31, 2016, we had cash and
cash equivalents of $0.6 million and current liabilities of $16.2 million. From September 30, 2016 through December 31, 2016, we
provided working capital by extending our payables primarily by not making timely payments on current obligations and debt incurred
prior to the sale of our CSO business, entering into payment plans, negotiating termination agreements on commitments that were not
useful to our current business and not paying certain severance obligations to terminated employees.
It is anticipated that we will require additional capital to fund our operations. There is no guarantee that additional capital will be
raised to fund our operations in 2017 and beyond, but we intend to meet our capital needs by driving revenue growth, containing costs as
well as exploring other options.
We completed four public offerings and a private placement of warrants from December 22, 2016 through February 8, 2017, which
resulted in aggregate gross proceeds to us of approximately $14.1 million. See “Recent Equity Financings”. Of that amount, we used
approximately $1.3 million to make the first principal payment on the RedPath Note on December 31, 2016 (which RedPath Note has
since been acquired by the Investor and exchanged with the Company for the Exchanged Notes) and approximately $1.0 million on
February 27, 2017 to satisfy severance obligations due to five former senior executives. The proceeds from the public offerings and private
placement have improved our overall cash position. However, as we continue to fund our operating deficit with proceeds from these
offerings, we remain in default of certain of our current obligations and certain vendors have threatened litigation against us. See “Certain
Defaults of Current Obligations”.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Additionally, on March 23, 2017, we completed the exchange of the RedPath Note, which was acquired by the Investor, for two new
Exchanged Notes aggregating $8.9 million. The Exchanged Notes consist of (i) a senior secured convertible note in the aggregate principal
amount of $5.3 million which is convertible into shares of our common stock, in accordance with its terms, and (ii) a senior secured non-
convertible note with an aggregate principal amount of $3.6 million, for a combined aggregate principal amount of $8.9 million. The
Exchanged Notes rank senior to all of our outstanding and future indebtedness, other than the indebtedness in favor of our credit line
lender and are secured by a perfected security interest in all of our existing and future assets and those of our subsidiaries. Upon the
reduction of 55% of the aggregate principal amount of each of the Exchanged Notes, the Investor will release its security interest in its
entirety. See “Debt Exchange for RedPath Note.” We believe the restructuring of the remaining balance of our $9.34 million of secured
debt due under the RedPath Note also improved our liquidity principally by reducing our currently due debt obligations in 2017 by
approximately $4 million.
On September 28, 2016, the Company and its wholly owned direct and indirect subsidiaries, Interpace LLC and Interpace Diagnostics
Corporation, entered into the Credit Agreement with SCM Specialty Finance Opportunities Fund, L.P., or the Lender. Pursuant to and
subject to the terms of the Credit Agreement, the Lender agreed to provide a revolving loan, or the Loan, to us in the maximum principal
amount of $1.2 million. The maturity date of the Loan is September 28, 2018. The Loan bears interest at an annual rate equal to the Prime
Rate (as defined in the Credit Agreement) plus 2.75%, payable in cash monthly in arrears. The interest rate will be increased by 5.0% in
the event of a default under the Credit Agreement. Events of default under the Credit Agreement, some of which are subject to certain cure
periods, include a failure to pay or perform obligations when due, the making of a material misrepresentation to the Lender, the rendering
of certain judgments or decrees against us and our subsidiaries and the initiation, voluntarily or involuntarily, of a bankruptcy or similar
proceeding against us or our subsidiaries. As mentioned above, pursuant to the terms of the Credit Agreement, the default under the
Parsippany Lease creates a cross-default under the Credit Agreement. We have not yet drawn down on the credit facility as we are
negotiating revisions to certain covenants in the Credit Agreement, and we will not be permitted to draw down under the credit facility
until the default referred to above is cured and until expiration of the Exchanged Notes. See “Certain Defaults of Current Obligations.”
Also on September 28, 2016, we and our subsidiaries acknowledged and agreed to an Intercreditor Agreement by and between the
Lender and the RedPath Equityholder Representative, or the Intercreditor Agreement, pursuant to which the Lender has a first lien security
interest on all of the accounts receivable (and related intangibles) of us and our subsidiaries and the RedPath Equityholder Representative
has a second lien security interest, subordinated to the Lender, on all the accounts receivables (and related intangibles) of us and our
subsidiaries. In addition, pursuant to the Intercreditor Agreement, the RedPath Equityholder Representative has a first lien security interest
on all other assets of us and our subsidiaries and the Lender has no lien with respect to such other assets. As mentioned above, the
RedPath Equityholder Representative assigned all of its rights, title and interest in the RedPath Note, including, but not limited to, its
security interest in all of our assets and the assets of our subsidiaries, to the Investor in connection with the consummation of the sale of
the RedPath Note to the Investor.
During the year ended December 31, 2016, net cash used in operating activities was $8.9 million, of which $6.9 million was used in
continuing operations and $2.0 million was used in discontinued operations. The main component of cash used in operating activities
during the year ended December 31, 2016 was our loss from continuing operations of $8.4 million. During the year ended December 31,
2015, net cash used in operating activities was $19.8 million, of which $28.4 million was used in continuing operations and $8.6 million
was provided by discontinued operations. The main component of cash used in operating activities during the year ended December 31,
2015 was our loss from continuing operations of $31.1 million.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
For the year ended December 31, 2016, there was no cash from investing activities. For the year ended December 31, 2015 net cash
provided by investing activities was approximately $26.4 million of which $0.3 million was used in continuing operations and $26.7
million was provided by discontinued operations primarily related to the net proceeds we received from the sale of CSO of $26.8 million.
For the year ended December 31, 2016, there was net cash provided from financing activities of $1.2 million, of which $1.7 million
resulted from the issuance of common stock in our first registered direct offering completed on December 22, 2016, which was partially
offset by the $0.5 million in payments of contingent consideration. For the year ended December 31, 2015, net cash used in financing
activities was $21.6 million as we paid off our $20.0 million credit agreement that we entered into in 2014.
Off-Balance Sheet Arrangements
We do not have any off-balance sheet arrangements.
Inflation
We do not believe that inflation had a significant impact on our results of operations for the periods presented. On an ongoing basis,
we attempt to minimize any effects of inflation on our operating results by controlling operating costs and whenever possible, seeking to
insure that billing rates reflect increases in costs due to inflation.
ITEM 7A.
QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
We are a “smaller reporting company” for purposes of the disclosure requirements of Item 305 of Regulation S-K and, therefore, we
are not required to provide this information.
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ITEM 8.
FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Financial statements and the financial statement schedule specified by this Item 8, together with the reports thereon of BDO USA,
LLP, are presented following Item 15 of this Annual Report on Form 10-K.
ITEM 9.
CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL
DISCLOSURES
None.
ITEM 9A.
CONTROLS AND PROCEDURES
Disclosure Controls and Procedures
Our management, with the participation of our Chief Executive Officer and Chief Financial Officer, evaluated the effectiveness of our
disclosure controls and procedures pursuant to Rule 13a-15 under the Exchange Act as of December 31, 2016. In designing and evaluating
the disclosure controls and procedures, management recognizes that any controls and procedures, no matter how well designed and
operated, can provide only reasonable assurance of achieving the desired control objectives including that information we are required to
disclose in reports that we file or submit under the Exchange Act is recorded, processed, summarized, and reported within the time periods
specified in the SEC rules and forms, and that such information is accumulated and communicated to our management, including our Chief
Executive Officer and Chief Financial Officer, as appropriate, to allow timely decisions regarding required disclosure. In addition,
management is required to apply its judgment in evaluating the benefits of possible disclosure controls and procedures relative to their
costs to implement and maintain.
Based on their evaluation, our Chief Executive Officer and Chief Financial Officer concluded that our disclosure controls and
procedures were not effective at the reasonable assurance level as of December 31, 2016 as a result of a material weakness. Specifically, as
of December 31, 2016, the following material weaknesses existed:
● We lack a sufficient complement of personnel to appropriately account for, review, and disclose the completeness and
accuracy of transactions entered into by the Company.
● We lack sufficient qualified resources to ensure the appropriate design and operating effectiveness of our internal control
over financial reporting. Specifically, ineffective monitoring controls related to our accounting and reporting functions
around management review were not adequately designed and/or operating effectively and resulted in adjustments to our
financial statements and disclosures.
Management believes that the material weaknesses noted are due in part to the small size of the staff resulting from staff downsizing
and cost containment. As part of our remediation plan, we intend to take steps to improve our financial reporting and implement new
policies, procedures and controls in addition to seeking external assistance with a review of transactions recorded and classified in the
financial statements, as well as the accounting and related disclosures for complex accounting matters when necessary.
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Management's Annual Report on Internal Control over Financial Reporting
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Our management is responsible for establishing and maintaining adequate internal control over financial reporting, as such term is
defined in Exchange Act Rule 13a-15(f).
All internal control systems, no matter how well designed, have inherent limitations including the possibility of human error and the
circumvention or overriding of controls. Further, because of changes in conditions, the effectiveness of internal controls may vary over
time. 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. Accordingly, even those
systems determined to be effective can provide us only with reasonable assurance with respect to financial statement preparation and
presentation.
Our management has assessed the effectiveness of internal control over financial reporting as of December 31, 2016, following the
criteria set forth by the Committee of Sponsoring Organizations of the Treadway Commission in Internal Control - Integrated Framework
(2013), updated and reissued by the Committee and Sponsoring Organizations (the Integrated Framework). Based on their assessment
under the Integrated Framework, our management has concluded that our disclosure controls and procedures were not effective at the
reasonable assurance level as of December 31, 2016 as a result of the continuing existence of the material weakness in our controls related
to our identification and accounting for contingent consideration and related interest costs associated with seller financing and a material
weakness identified related to our accounting for, review of, and disclosure of the completeness and accuracy of transaction that we enter
into.
Changes in Internal Control over Financial Reporting
There has not been any change in our system of internal control over financial reporting during the fiscal year ended December 31,
2016, that has materially affected, or is reasonably likely to materially affect, internal control over financial reporting.
ITEM 9B.
OTHER INFORMATION
None.
PART III
ITEM 10.
DIRECTORS, EXECUTIVE OFFICERS AND CORPORATE GOVERNANCE
Information relating to directors and executive officers of the registrant that is responsive to Item 10 of this Annual Report on Form
10-K will be included in our Proxy Statement for our 2017 annual meeting of stockholders and such information is incorporated by
reference herein.
ITEM 11.
EXECUTIVE COMPENSATION
Information relating to executive compensation that is responsive to Item 11 of this Annual Report on Form 10-K will be included in
our Proxy Statement for our 2017 annual meeting of stockholders and such information is incorporated by reference herein.
ITEM 12.
SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT AND RELATED
STOCKHOLDER MATTERS
Information relating to security ownership of certain beneficial owners and management that is responsive to Item 12 of this Annual
Report on Form 10-K will be included in our Proxy Statement for our 2017 annual meeting of stockholders and such information is
incorporated by reference herein.
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Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
ITEM 13.
CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS, AND DIRECTOR INDEPENDENCE
Information relating to certain relationships and related transactions that is responsive to Item 13 of this Annual Report on Form 10-K
will be included in our Proxy Statement for our 2017 annual meeting of stockholders and such information is incorporated by reference
herein.
ITEM 14.
PRINCIPAL ACCOUNTING FEES AND SERVICES
Information relating to principal accounting fees and services that is responsive to Item 14 of this Annual Report on Form 10-K will
be included in our Proxy Statement for our 2017 annual meeting of stockholders and such information is incorporated by reference herein.
ITEM 15.
EXHIBITS, FINANCIAL STATEMENT SCHEDULES
(a) The following documents are filed as part of this Form 10-K:
PART IV
(1)
(2)
Financial Statements – See Index to Financial Statements on page F-1 of this Form 10-K.
Financial Statement Schedule
Schedule II: Valuation and Qualifying Accounts
All other schedules are omitted because they are not applicable or the required information is shown in the financial statements or
notes thereto.
(3) Exhibits
Exhibit No.
2.1
2.2
2.3
3.1
3.2
3.3
3.4
Description
Asset Purchase Agreement, dated August 13, 2014, by and between Interpace Diagnostics, LLC and Asuragen, Inc.,
incorporated by reference to the designated exhibit of the Company’s Quarterly Report on Form 10-Q for the quarter
ended September 30, 2014, filed with the SEC on November 5, 2014
Agreement and Plan of Merger, dated October 31, 2014, by and among RedPath Integrated Pathology, Inc., the
Company, Interpace Diagnostics, LLC, RedPath Acquisition Sub, Inc. and RedPath Equityholder Representative,
LLC, incorporated by reference to the designated exhibit of the Company’s Annual Report on Form 10-K for the year
ended December 31, 2014, filed with the SEC on March 5, 2015
Asset Purchase Agreement, dated as of October 30, 2015, by and between Publicis Touchpoint Solutions, Inc. and PDI,
Inc. is incorporated by reference to Exhibit 2.1 of the Company’s Current Report on Form 8-K, filed with the SEC on
November 2, 2015
Certificate of Incorporation of PDI, Inc. (n.k.a. Interpace Diagnostics Group, Inc.), incorporated by reference to the
designated exhibit of the Company’s Registration Statement on Form S-1 (File No. 333-46321), filed with the SEC on
May 19, 1998
Certificate of Amendment of Certificate of Incorporation of PDI, Inc. (n.k.a. Interpace Diagnostics Group, Inc.),
incorporated by reference to the designated exhibit of the Company’s Annual Report on Form 10-K for the year ended
December 31, 2001, filed with the SEC on March 13, 2002
Certificate of Amendment to the Certificate of Incorporation of PDI, Inc. (n.k.a. Interpace Diagnostics Group, Inc.),
incorporated by reference to the designated exhibit of the Company’s Quarterly Report on Form 10-Q for the quarter
ended June 30, 2012, filed with the SEC on August 14, 2012
Amended and Restated By-Laws of PDI, Inc. (n.k.a. Interpace Diagnostics Group, Inc.), incorporated by reference to
the designated exhibit of the Company’s Annual Report on Form 10-K for the year ended December 31, 2013, filed
with the SEC on March 6, 2014
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Table of Contents
Exhibit No.
3.5
3.6
3.7
4.1
4.2
10.1*
10.2*
10.3*
10.4*
10.5*
10.6*
10.7*
10.8*
10.9*
10.10*
10.11*
10.12*
10.13
10.14
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Description
Certificate of Amendment to the Certificate of Incorporation of PDI, Inc. (n.k.a. Interpace Diagnostics Group, Inc.),
incorporated by reference to the designated exhibit of the Company’s Form 8-K filed with the SEC on December 23,
2015
Certificate of Amendment to the Certificate of Incorporation of PDI, Inc. (n.k.a. Interpace Diagnostics Group, Inc.),
incorporated by reference to the designated exhibit of the Company’s Form 8-K filed with the SEC on December 23,
2015
Certificate of Amendment to the Certificate of Incorporation of Interpace Diagnostics Group, Inc., incorporated by
reference to the designated exhibit of the Company’s Current Report on Form 8-K filed with the SEC on December 28,
2016
Specimen Certificate Representing the Common Stock, incorporated by reference to the designated exhibit of the
Company’s Registration Statement on Form S-1 (File No. 333-46321), filed with the SEC on May 19, 1998
Form of Prepaid Common Stock Purchase Warrant, incorporated by reference to the designated exhibit of the
Company’s Current Report on Form 8-K filed with the SEC on December 19, 2016
2000 Omnibus Incentive Compensation Plan, incorporated by reference to the designated exhibit of the Company’s
Current Report on Form 8-K filed with the SEC on October 20, 2014
Executive Deferred Compensation Plan, incorporated by reference to the designated exhibit of the Company’s Annual
Report on Form 10-K for the year ended December 31, 2009, filed with the SEC on March 8, 2010
Amended and Restated 2004 Stock Award and Incentive Plan, incorporated by reference to the designated exhibit of
the Company’s definitive proxy statement filed with the SEC on April 28, 2004
Form of Restricted Stock Unit Agreement for Employees, incorporated by reference to the designated exhibit of the
Company’s Annual Report on Form 10-K for the year ended December 31, 2008, filed with the SEC on March 8, 2009
Form of Stock Appreciation Rights Agreement for Employees, incorporated by reference to the designated exhibit of
the Company’s Annual Report on Form 10-K for the year ended December 31, 2008, filed with the SEC on March 8,
2009
Form of Restricted Stock Unit Agreement for Directors, incorporated by reference to the designated exhibit of the
Company’s Annual Report on Form 10-K for the year ended December 31, 2008, filed with the SEC on March 8, 2009
Form of Restricted Share Agreement, incorporated by reference to the designated exhibit of the Company’s Annual
Report on Form 10-K for the year ended December 31, 2009, filed with the SEC on March 8, 2010
Offer Letter between the Company and Graham G. Miao, dated October 14, 2014, incorporated by reference to the
designated exhibit of the Company’s Current Report on Form 8-K filed with the SEC on October 20, 2014
Employment Separation Agreement between the Company and Graham G. Miao, incorporated by reference to the
designated exhibit of the Company’s Current Report on Form 8-K filed with the SEC on October 20, 2014
Confidential Information, Non-Disclosure, Non-Competition, Non-Solicitation and Rights to Intellectual Property
Agreement between the Company and Graham G. Miao, dated October 14, 2014, incorporated by reference to the
designated exhibit of the Company’s Current Report on Form 8-K filed with the SEC on October 20, 2014
Form of Restricted Stock Unit Inducement Agreement, by and between the Company and Graham G. Mio,
incorporated by reference to the designated exhibit of the Company’s Current Report on Form 8-K filed with the SEC
on October 20, 2014
Stock Appreciation Rights Inducement Agreement by and between the Company and Graham G. Miao, incorporated
by reference to the designated exhibit of the Company’s Current Report on Form 8-K filed with the SEC on October
20, 2014
Morris Corporate Center Lease, incorporated by reference to the designated exhibit of the Company’s Quarterly
Report on Form 10-Q for the quarter ended September 30, 2009, filed with the SEC on November 5, 2009
Non-negotiable Subordinated Secured Promissory Note, dated October 31, 2014, by the Company and Interpace
Diagnostics, LLC in favor of RedPath Equityholder Representative, LLC, incorporated by reference to the designated
exhibit of the Company’s Annual Report on Form 10-K for the year ended December 31, 2014, filed with the SEC on
March 5, 2015
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Exhibit No.
10.15
10.16
10.17
10.18
10.19
10.20
10.21
10.22
10.23
10.24
10.25
10.26
10.27
10.28
10.29
10.30
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Description
Amendment No. 1 to Note, dated July 30, 2015, by and between Redpath Equityholder Representative, LLC, a
Delaware limited liability company, and the Company, incorporated by reference to the designated exhibit of the
Company’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2015, filed with the SEC on
November 12, 2015
Limited Waiver, Consent and Amendment No. 2 to Note, dated October 30, 2015, by and among RedPath
Equityholder Representative, LLC, PDI, Inc., and Interpace Diagnostics, LLC, incorporated by reference to the
designated exhibit of the Company’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2015, filed
with the SEC on November 12, 2015
Contingent Consideration Agreement, dated October 31, 2014, by and among the Company, Interpace Diagnostics,
LLC and RedPath Equityholder Representative, LLC, incorporated by reference to the designated exhibit of the
Company’s Annual Report on Form 10-K for the year ended December 31, 2014, filed with the SEC on March 5, 2015
Settlement Agreement, dated January 28, 2013, by and between RedPath Integrated Pathology, Inc. (now known as
Interpace Diagnostics Corporation) and the United States of America, incorporated by reference to the designated
exhibit of the Company’s Annual Report on Form 10-K for the year ended December 31, 2014, filed with the SEC on
March 5, 2015
License Agreement, dated August 13, 2014, by and between Interpace Diagnostics, LLC and Asuragen, Inc.,
incorporated by reference to the designated exhibit of the Company’s Quarterly Report on Form 10-Q for the quarter
ended September 30, 2014, filed with the SEC on November 5, 2014
CPRIT License Agreement, dated August 13, 2014, by and between Interpace Diagnostics, LLC and Asuragen, Inc.,
incorporated by reference to the designated exhibit of the Company’s Quarterly Report on Form 10-Q for the quarter
ended September 30, 2014, filed with the SEC on November 5, 2014
Supply Agreement, dated August 13, 2014, by and between Interpace Diagnostics, LLC and Asuragen, Inc.,
incorporated by reference to the designated exhibit of the Company’s Quarterly Report on Form 10-Q for the quarter
ended September 30, 2014, filed with the SEC on November 5, 2014
Guaranty, dated August 13, 2014 by the Company in favor of Asuragen, Inc., incorporated by reference to the
designated exhibit of the Company’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2014, filed
with the SEC on November 5, 2014
Lease, dated October 10, 2007, by and between Spring Way Center, LLC and RedPath Integrated Pathology, Inc.
(now known as Interpace Diagnostics, LLC), incorporated by reference to the designated exhibit of the Company’s
Annual Report on Form 10-K for the year ended December 31, 2014, filed with the SEC on March 5, 2015
Lease Renewal, dated April 3, 2013, by and between Spring Way Center, LLC and RedPath Integrated Pathology, Inc.
(now known as Interpace Diagnostics, LLC), incorporated by reference to the designated exhibit of the Company’s
Annual Report on Form 10-K for the year ended December 31, 2014, filed with the SEC on March 5, 2015
Lease, dated June 28, 2015, by and between WE 2 Church Street South LLC and JS Genetics, LLC, incorporated by
reference to the designated exhibit of the Company’s Annual Report on Form 10-K for the year ended December 31,
2014, filed with the SEC on March 5, 2015
Amendment No. 1 to Lease, dated September 18, 2007, by and between WE 2 Church Street South LLC and JS
Genetics, LLC, incorporated by reference to the designated exhibit of the Company’s Annual Report on Form 10-K
for the year ended December 31, 2014, filed with the SEC on March 5, 2015
Amendment No. 2 to Lease, dated August 29, 2008, by and between WE 2 Church Street South LLC and JS Genetics,
LLC, incorporated by reference to the designated exhibit of the Company’s Annual Report on Form 10-K for the year
ended December 31, 2014, filed with the SEC on March 5, 2015
Amendment No. 3 to Lease, dated April 8, 2009, by and between WE 2 Church Street South LLC and JS Genetics,
LLC, incorporated by reference to the designated exhibit of the Company’s Annual Report on Form 10-K for the year
ended December 31, 2014, filed with the SEC on March 5, 2015
Amendment No. 4 to Lease, dated September 16, 2010, by and between WE 2 Church Street South LLC and JS
Genetics, LLC, incorporated by reference to the designated exhibit of the Company’s Annual Report on Form 10-K
for the year ended December 31, 2014, filed with the SEC on March 5, 2015
Amendment No. 5 to Lease, dated September 15, 2011, by and between WE 2 Church Street South LLC and JS
Genetics, LLC, incorporated by reference to the designated exhibit of the Company’s Annual Report on Form 10-K
for the year ended December 31, 2014, filed with the SEC on March 5, 2015
69
Table of Contents
Exhibit No.
10.31
10.32
10.33*
10.34*
10.35*
10.36*
10.37*
10.38*
10.39*
10.40
10.41
10.42
10.43
10.44*
10.45*
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
Description
Amendment No. 6 to Lease, dated March 5, 2014, by and between WE 2 Church Street South LLC and JS Genetics,
LLC, incorporated by reference to the designated exhibit of the Company’s Annual Report on Form 10-K for the year
ended December 31, 2014, filed with the SEC on March 5, 2015
Amendment No. 7 to Lease, dated August 29, 2014, by and between WE 2 Church Street South LLC and JS Genetics,
LLC, incorporated by reference to the designated exhibit of the Company’s Annual Report on Form 10-K for the year
ended December 31, 2014, filed with the SEC on March 5, 2015
Amendment Agreement, dated December 7, 2015, by and between PDI, Inc. (n.k.a. Interpace Diagnostics Group, Inc.)
and Nancy S. Lurker, incorporated by reference to the designated exhibit of the Company’s Current Report on Form 8-
K filed with the SEC on December 8, 2015
Agreement and General Release, dated January 6, 2016, by and between Gerald Melillo and PDI, Inc. (n.k.a. Interpace
Diagnostics Group, Inc.), incorporated by reference to the designated exhibit of the Company’s Current Report on
Form 8-K filed with the SEC on January 1, 2016
Agreement and General Release, dated January 15, 2016, by and between Nancy S. Lurker and PDI, Inc. (n.k.a.
Interpace Diagnostics Group, Inc.), incorporated by reference to the designated exhibit of the Company’s Current
Report on Form 8-K, filed with the SEC on January 22, 2016.
Severance Agreement and General Release, dated March 28, 2016, by and between Graham Miao and Interpace
Diagnostics Group, Inc., incorporated by reference the designated exhibit of the Company’s Current Report on Form 8-
K, filed with the SEC on March 29, 2016.
Employment Separation Agreement between Interpace Diagnostics Group, Inc. and Nat Krishnamurti, effective as of
June 22, 2016, incorporated by reference to the designated exhibit of Amendment No. 2 to the Company’s Current
Report on Form 8-K filed with the SEC on June 22, 2016.
Confidential Information, Non-Disclosure, Non-Solicitation, Non-Compete and Rights to Intellectual Property
Agreement between Interpace Diagnostics Group, Inc. and Nat Krishnamurti, dated as of June 22, 2016, incorporated
by reference to the designated exhibit of Amendment No. 2 to the Company’s Current Report on Form 8-K filed with
the SEC on June 22, 2016.
Form of Indemnification Agreement by and between Interpace Diagnostics Group, Inc. and its directors and executive
officers, incorporated by reference to the designated exhibit to the Company’s Current Report on Form 8-K filed with
the SEC on August 8, 2016.
Credit Agreement and Security Agreement, dated as of September 28, 2016, by and among Interpace Diagnostics
Group, Inc., Interpace Diagnostics Corporation, Interpace Diagnostics, LLC and SCM Specialty Finance Opportunities
Fund, L.P., incorporated by reference to the designated exhibit to the Company’s Current Report on Form 8-K filed
with the SEC on October 4, 2016.
Intercreditor Agreement, dated as of September 28, 2016, by and between SCM Specialty Finance Opportunities Fund,
L.P. and RedPath Equityholder Representative, LLC and acknowledged and agreed to by Interpace Diagnostics Group,
Inc., Interpace Diagnostics, LLC and Interpace Diagnostics Corporation, incorporated by reference to the designated
exhibit to the Company’s Current Report on Form 8-K filed with the SEC on October 4, 2016.
Third Amendment to Non-Negotiable Subordinated Secured Promissory Note, dated as of September 30, 2016, by and
among Interpace Diagnostics Group, Inc., Interpace Diagnostics, LLC and RedPath Equityholder Representative, LLC,
incorporated by reference to the designated exhibit to the Company’s Current Report on Form 8-K filed with the SEC
on October 4, 2016.
Management Engagement Letter, effective as of October 11, 2016, by and between Early Financial Consulting, LLC
and Interpace Diagnostics Group, Inc., incorporated by reference to the designated exhibit to the Company’s Current
Report on Form 8-K filed with the SEC on October 14, 2016.
Incentive Stock Option Agreement between Interpace Diagnostics Group, Inc. and Jack E. Stover, incorporated by
reference to the designated exhibit to the Company’s Current Report on Form 8-K filed with the SEC on October 20,
2016.
Incentive Stock Option Agreement between Interpace Diagnostics Group, Inc. and James Early, incorporated by
reference to the designated exhibit to the Company’s Current Report on Form 8-K filed with the SEC on October 20,
2016.
70
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Exhibit No.
10.46*
10.47
10.48*
10.49
10.50
10.51
21.1
23.1
31.1
31.2
32.1
32.2
*
101
Description
Form of Incentive Stock Option Agreement, incorporated by reference to the designated exhibit to the Company’s
Current Report on Form 8-K filed with the SEC on October 20, 2016.
Fourth Amendment to Non-Negotiable Subordinated Secured Promissory Note, dated as of October 31, 2016, by and
among Interpace Diagnostics Group, Inc., Interpace Diagnostics, LLC and RedPath Equityholder Representative, LLC,
incorporated by reference to the designated exhibit to the Company’s Current Report on Form 8-K filed with the SEC
on November 3, 2016.
Employment Agreement, dated as of October 28, 2016, by and between Interpace Diagnostics Group, Inc. and Jack E.
Stover, incorporated by reference to the designated exhibit to the Company’s Current Report on Form 8-K filed with the
SEC on November 3, 2016.
Fifth Amendment to Non-Negotiable Subordinated Secured Promissory Note, dated as of November 16, 2016, by and
among Interpace Diagnostics Group, Inc., Interpace Diagnostics, LLC and RedPath Equityholder Representative, LLC,
incorporated by reference to the designated exhibit to the Company’s Quarterly Report on Form 10-Q filed with the
SEC on November 17, 2016.
Placement Agency Agreement by and between Interpace Diagnostics Group, Inc. and Maxim Group, LLC, incorporated
by reference to the designated exhibit of the Company’s Current Report on Form 8-K filed with the SEC on December
19, 2016
Form of Securities Purchase Agreement by and between Interpace Diagnostics Group, Inc. and certain purchasers named
therein, incorporated by reference to the designated exhibit of the Company’s Current Report on Form 8-K filed with
the SEC on December 19, 2016
Subsidiaries of the Registrant, filed herewith
Consent of BDO USA, LLP, filed herewith
Certification of Chief Executive Officer Pursuant to Section 302 of the Sarbanes-Oxley Act of 2002, filed herewith
Certification of Chief Financial Officer Pursuant to Section 302 of the Sarbanes-Oxley Act of 2002, filed herewith
Certification of Chief Executive Officer Pursuant to 18 U.S.C. Section 1350, as adopted Pursuant to Section 906 of the
Sarbanes-Oxley Act of 2002, filed herewith
Certification of Chief Financial Officer Pursuant to 18 U.S.C. Section 1350, as adopted Pursuant to Section 906 of the
Sarbanes-Oxley Act of 2002, filed herewith
Denotes compensatory plan, compensation arrangement or management contract.
The following financial information from this Annual Report on Form 10-K for the fiscal year ended December 31,
2016 formatted in XBRL (Extensible Business Reporting Language) and furnished electronically herewith: (i) the
Condensed Consolidated Balance Sheets; (ii) the Condensed Consolidated Statements of Operations; (iii) the
Condensed Consolidated Statements of Cash Flows; and (iv) the Notes to Condensed Consolidated Financial
Statements.
ITEM 16.
Form 10-K Summary
The Company has opted to not provide a summary.
71
Table of Contents
Interpace Diagnostics Group, Inc.
Annual Report on Form 10-K
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.
Date: March 31, 2017
INTERPACE DIAGNOSTICS GROUP,
INC.
/s/ Jack E. Stover
Jack E. Stover
President and Chief Executive Officer
Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, this report has been signed by the following
persons on behalf of the registrant and in the capacities indicated and on the dates indicated.
Name
Title
/s/ Jack E. Stover
Jack E. Stover
/s/ James Early
James Early
/s/ Stephen J. Sullivan
Stephen J. Sullivan
/s/ Joseph Keegan
Joseph Keegan
President, Chief Executive Officer and Director
(Principal Executive Officer)
Chief Financial Officer
(Principal Financial Officer & Principal Accounting Officer)
Chairman of the Board of Directors
Director
72
Date
March 31, 2017
March 31, 2017
March 31, 2017
March 31, 2017
Table of Contents
Interpace Diagnostics Group, Inc.
(formerly known as PDI, Inc.)
Index to Consolidated Financial Statements
and Financial Statement Schedules
Report of Independent Registered Public Accounting Firm
Consolidated Financial Statements
Consolidated Balance Sheets at December 31, 2016 and 2015
Consolidated Statements of Comprehensive Loss for the years ended December 31, 2016 and 2015
Consolidated Statements of Stockholders’ Equity for the years ended December 31, 2016 and 2015
Consolidated Statements of Cash Flows for the years ended December 31, 2016 and 2015
Notes to Consolidated Financial Statements
Schedule II. Valuation and Qualifying Accounts
F-1
Page
F-2
F-3
F-4
F-5
F-6
F-7
F-38
Table of Contents
Report of Independent Registered Public Accounting Firm
The Board of Directors and Stockholders of Interpace Diagnostics Group, Inc.:
We have audited the accompanying consolidated balance sheets of Interpace Diagnostics Group, Inc. (formerly known as PDI, Inc.)
as of December 31, 2016 and 2015, and the related consolidated statements of comprehensive loss, stockholders' equity, and cash flows
for the years ended December 31, 2016 and 2015. In connection with our audits of the financial statements, we have also audited the
financial statements schedule listed in the accompanying index. These financial statements and schedule are the responsibility of the
Company's management. Our responsibility is to express an opinion on these financial statements and schedule based on our audits.
We conducted our audits in accordance with the standards of the Public Company Accounting Oversight Board (United States). Those
standards require that we plan and perform the audits to obtain reasonable assurance about whether the financial statements are free of
material misstatement. The Company is not required to have, nor were we engaged to perform, an audit of its internal control over
financial reporting. Our audits included consideration of internal control over financial reporting as a basis for designing audit procedures
that are appropriate in the circumstances, but not for the purpose of expressing an opinion on the effectiveness of the Company's internal
control over financial reporting. Accordingly, we express no such opinion. An audit also includes examining, on a test basis, evidence
supporting the amounts and disclosures in the financial statements, assessing the accounting principles used and significant estimates
made by management, and evaluating the overall presentation of the financial statements and schedule. We believe that our audits provide
a reasonable basis for our opinions.
In our opinion, the consolidated financial statements referred to above present fairly, in all material respects, the financial position of
Interpace Diagnostics Group, Inc. at December 31, 2016 and 2015, and the results of its operations and its cash flows for the years ended
December 31, 2016 and 2015, in conformity with accounting principles generally accepted in the United States of America.
Also, in our opinion, the related financial statement schedule, when considered in the relation to the basic consolidated financial
statements taken as a whole, presents fairly in all material respects the information set forth therein.
The accompanying consolidated financial statements have been prepared assuming that the Company will continue as a going
concern. As described in Note 3 to the consolidated financial statements, the Company has suffered recurring losses from continuing
operations that raise substantial doubt about its ability to continue as a going concern. Management's plans in regard to these matters are
also described in Note 3. The consolidated financial statements do not include any adjustments that might result from the outcome of this
uncertainty.
/s/ BDO USA, LLP
Woodbridge, New Jersey
March 31, 2017
F-2
Table of Contents
INTERPACE DIAGNOSTICS GROUP, INC.
CONSOLIDATED BALANCE SHEETS
(in thousands, except share and per share data)
ASSETS
Current assets:
Cash and cash equivalents
Short-term investments
Accounts receivable, net
Other current assets
Current assets from discontinued operations
Total current assets
Property and equipment, net
Other intangible assets, net
Other long-term assets
Non-current assets from discontinued operations
Total assets
LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities:
Accounts payable
Accrued salary and bonus
Other accrued expenses
Current portion of long-term debt, net of debt discount
Current liabilities from discontinued operations
Total current liabilities
Contingent consideration
Long-term debt, net of debt discount
Other long-term liabilities
Total liabilities
Commitments and contingencies (Note 10)
Stockholders’ equity:
December 31,
December 31,
2016
2015
$
$
$
602 $
-
2,209
1,415
14
4,240
929
36,358
251
-
41,778 $
2,326 $
3,551
6,236
-
4,128
16,241
7,254
7,908
3,844
35,247
8,310
106
2,806
2,569
5,374
19,165
1,460
43,492
3,255
340
67,712
1,560
2,424
5,961
1,164
12,264
23,373
17,890
7,233
6,178
54,674
Preferred stock, $.01 par value; 5,000,000 shares authorized, no shares issued and outstanding
Common stock, $.01 par value; 100,000,000 shares authorized; 2,230,506 and 1,870,506
shares issued, respectively; 2,176,252 and 1,766,252 shares outstanding, respectively
Additional paid-in capital
Accumulated deficit
Accumulated other comprehensive income
Treasury stock, at cost (54,254 and 104,254 shares, respectively)
Total stockholders' equity
Total liabilities and stockholders' equity
$
-
-
22
127,736
(119,584)
-
(1,643)
6,531
41,778 $
19
132,690
(111,252)
13
(8,432)
13,038
67,712
The accompanying notes are an integral part of these consolidated financial statements
F-3
Table of Contents
INTERPACE DIAGNOSTICS GROUP, INC.
CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS
(in thousands, except for per share data)
For The Years Ended December 31,
2016
2015
Revenue, net
Cost of revenue (excluding amortization of $3,770 and $3,812 respectively)
$
Gross profit
Operating expenses:
Sales and marketing
Research and development
General and administrative
Acquisition related amortization expense
Asset impairment
Loss on extinguishment of debt
Goodwill impairment
Change in fair value of contingent consideration
Total operating expenses
Operating loss
Interest expense
Other income (expense), net
Loss from continuing operations before tax
Benefit from income taxes from continuing operations
Loss from continuing operations
Discontinued Operations
(Loss) income from discontinued operations
Gain on sale of assets
Income from discontinued operations
Provision for income tax on discontinued operations
Income from discontinued operations, net of tax
Net loss
Other comprehensive income (loss):
Unrealized holding loss on available-for-sale securities, net
Comprehensive loss
Basic and diluted (loss) income per share of common stock:
From continuing operations
From discontinued operations
Net loss per basic and diluted share of common stock
Weighted average number of common shares and common share equivalents outstanding:
Basic
Diluted
$
$
$
$
$
13,085 $
6,641
6,444
5,462
1,647
10,504
3,770
3,363
-
-
(11,860)
12,886
(6,442)
(2,144)
14
(8,572)
(162)
(8,410)
(886)
1,326
440
362
78 $
9,432
6,910
2,522
10,358
2,292
16,922
3,812
-
1,873
15,666
(7,993)
42,930
(40,408)
(3,705)
(93)
(44,206)
(13,136)
(31,070)
10,341
21,634
31,975
12,261
19,714
(8,332) $
(11,356)
-
(8,332) $
(3)
(11,359)
(4.63) $
0.04
(4.59) $
1,816
1,816
(20.08)
12.74
(7.34)
1,548
1,548
The accompanying notes are an integral part of these consolidated financial statements
F-4
Table of Contents
INTERPACE DIAGNOSTICS GROUP, INC.
CONSOLIDATED STATEMENTS OF STOCKHOLDERS' EQUITY
(in thousands)
For The Years Ended December 31,
2015
2016
Amount
Shares
Amount
Shares
Common stock:
Balance at January 1
Common stock issued
Common stock issued through offering
Exercise of warrants
Restricted stock issued
Restricted stock forfeited
Balance at December 31
Treasury stock:
Balance at January 1
Treasury stock reissued
Treasury stock purchased
Balance at December 31
Additional paid-in capital:
Balance at January 1
Common stock issued
Common stock issued through offering, net of expenses
Issuance of warrants
Exercise of warrants
Common stock issued through ATM
Restricted stock issued
Treasury stock reissued
Stock-based compensation expense
Balance at December 31
Accumulated deficit:
Balance at January 1
Net loss
Balance at December 31
Accumulated other comprehensive (loss) income:
Balance at January 1
Unrealized holding loss on available-for-sale securities, net of tax
Realized loss, net of tax
Balance at December 31
Total stockholders' equity
1,870 $
-
200
160
-
-
2,230
104
(50)
-
54
$
19
-
2
1
-
-
22
(8,432)
6,789
-
(1,643)
132,690
-
857
832
15
-
-
(6,789)
131
127,736
(111,252)
(8,332)
(119,584)
13
-
(13)
-
6,531
1,656 $
132
-
-
87
(5)
1,870
120
(50)
34
104
$
17
1
-
-
1
-
19
(14,334)
6,110
(208)
(8,432)
134,339
2
-
-
-
451
(9)
(6,110)
4,017
132,690
(99,896)
(11,356)
(111,252)
16
(3)
-
13
13,038
The accompanying notes are an integral part of these consolidated financial statements
F-5
Table of Contents
INTERPACE DIAGNOSTICS GROUP, INC.
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(unaudited, in thousands)
Cash Flows From Operating Activities
Net loss
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation and amortization
Realignment accrual accretion
Interest accretion
Provision for bad debt
Other current assets
Gain on sale of discontinued operations
Stock-based compensation
Goodwill impairment
Asset impairment
Non-cash loss on debt extinguishment
Change in fair value of contingent consideration
Deferred taxes
Realized gain on benefit plan
Other changes in assets and liabilities:
Decrease (increase) in accounts receivable
Decrease (increase) in unbilled receivable
Decrease in other current assets
Decrease in other long-term assets
Increase in accounts payable
(Decrease) in unearned contract revenue
Decrease in current portion of long-term debt
(Decrease) increase in accrued salaries and bonus
Decrease in accrued liabilities
(Decrease) increase in long-term liabilities
Net cash used in operating activities
Cash Flows From Investing Activities
Purchase of property and equipment
Net proceeds from sale of assets
Net cash provided by investing activities
Cash Flows From Financing Activities
Repayment of financing arrangement
Payments of contingent consideration
Debt extinguishment costs
Issuance of common stock, net of expenses
Cash paid for repurchase of restricted shares
Net cash provided by (used in) financing activities
Net decrease in cash and cash equivalents
Cash and cash equivalents – beginning
Cash and cash equivalents – ending
Cash paid for taxes
Cash paid for interest
For The Years Ended December 31,
2016
2015
$
(8,332) $
(11,356)
4,483
34
2,144
899
102
-
131
-
3,363
(11,860)
-
(4)
4,766
16
1,478
3,004
143
(11)
(1,333)
(637)
(4,992)
(2,334)
(8,940)
-
-
-
-
(475)
-
1,707
-
1,232
(7,708)
8,310
602 $
71 $
- $
5,030
139
1,095
802
979
(21,634)
4,017
15,666
635
476
(7,993)
(1,167)
-
(5,486)
(181)
2,350
3,286
1,019
(5,201)
-
895
(3,389)
176
(19,842)
(353)
26,751
26,398
(20,000)
-
(1,600)
451
(208)
(21,357)
(14,801)
23,111
8,310
242
3,128
$
$
$
The accompanying notes are an integral part of these consolidated financial statements
F-6
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
1. Nature of Business and Significant Accounting Policies
Nature of Business
Interpace Diagnostics Group, Inc. (the “Company”) is a fully integrated commercial company that provides clinically useful molecular
diagnostic tests and pathology services. The Company develops and commercializes molecular diagnostic tests and related first line
assays principally focused on early detection of high potential progressors to cancer and leverages the latest technology and
personalized medicine for improved patient diagnosis and management. The Company currently has three commercialized molecular
diagnostic assays in the marketplace for which it is reimbursed by Medicare and multiple private payors: PancraGEN®, a pancreatic
cyst and pancreaticobiliary solid lesion molecular test that can aid in pancreatic cyst diagnosis and pancreatic cancer risk assessment
utilizing our proprietary PathFinder platform; ThyGenX®, which assesses thyroid nodules for risk of malignancy; and ThyraMIR®,
which assesses thyroid nodules for risk of malignancy utilizing a proprietary gene expression assay. The Company is also in the process
of “soft launching” while gathering additional market data, BarreGEN®, an esophageal cancer risk classifier for Barrett’s Esophagus
that utilizes the Company’s PathFinder platform.
Principles of Consolidation
The accompanying consolidated financial statements have been prepared in accordance with U.S. generally accepted accounting
principles (“GAAP”). The consolidated financial statements include the accounts of Interpace Diagnostics Group, Inc., Interpace
Diagnostics Corporation and Interpace Diagnostics, LLC.
Discontinued operations include the Company's wholly-owned subsidiaries: Group DCA, LLC (“Group DCA”); InServe Support
Solutions (Pharmakon); and TVG, Inc. (TVG, dissolved December 31, 2014) and its Commercial Services (“CSO”) business unit. All
significant intercompany balances and transactions have been eliminated in consolidation.
Effective December 31, 2015, the Company has one reporting segment: the Company's molecular diagnostics business, after the
divestiture of its CSO business on December 22, 2015, see Note 4, Discontinued Operations for further information. The Company's
current reporting segment structure is reflective of the way the Company's management views the business, makes operating decisions
and assesses performance. This structure allows investors to better understand Company performance, better assess prospects for future
cash flows, and make more informed decisions about the Company.
Accounting Estimates
The preparation of consolidated financial statements in conformity with GAAP requires management to make estimates and
assumptions that affect the amounts of assets and liabilities reported and disclosure of contingent assets and liabilities at the date of the
financial statements and the reported amounts of revenues and expenses during the reporting period. Management's estimates are based
on historical experience, facts and circumstances available at the time, and various other assumptions that are believed to be reasonable
under the circumstances. Significant estimates include accounting for business combinations, valuation allowances related to deferred
income taxes, contingent consideration, allowances for doubtful accounts and notes, revenue recognition, income tax accruals, and asset
impairments. The Company periodically reviews these matters and reflects changes in estimates as appropriate. Actual results could
materially differ from those estimates.
Cash and Cash Equivalents
Cash and cash equivalents include unrestricted cash accounts, money market investments and highly liquid investment instruments with
original maturity of three months or less at the date of purchase.
F-7
Table of Contents
Discontinued Operations
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
The Company accounts for business dispositions and its businesses held for sale in accordance with ASC 205-20, Discontinued
Operations. ASC 205-20 requires the results of operations of business dispositions to be segregated from continuing operations and
reflected as discontinued operations in current and prior periods. See Note 4, Discontinued Operations for further information.
Receivables and Allowance for Doubtful Accounts
The Company’s accounts receivable are generated using its proprietary tests. The Company’s services are fulfilled upon completion of
the test, review and release of the test results. In conjunction with fulfilling these services, the Company bills the third-party payor or
hospital. The Company recognizes accounts receivable related to billings for Medicare, Medicare Advantage, and hospitals (direct-bill
clients) on an accrual basis, net of contractual adjustment, when collectability is reasonably assured. Contractual adjustments represent
the difference between the list prices and the reimbursement rate set by Medicare and Medicare Advantage, or the amounts billed to
hospitals. The Company records an Allowance for Doubtful accounts based on the collection history for PancraGen® hospital roster
billings (direct bill clients) and for Medicare Advantage billings for PancraGen® and ThyGenix®. Since Medicare has fixed
reimbursement rates, there is no Allowance for Doubtful Accounts associated with Medicare.For non-paying roster accounts, balances
may be written off to bad debt after twelve months. Medicare Advantage accounts may be written off to bad debt after several appeals,
which in some cases may take longer than twelve months.
The Company provides services to commercial insurance carriers or governmental programs that do not have a contract in place for its
proprietary tests, which may or may not be covered by these entities existing reimbursement policies. In addition, the Company does
not enter into direct agreements with patients that commit them to pay any portion of the cost of the tests in the event that their
commercial insurance carrier or governmental program does not pay the Company for its services. In the absence of an agreement with
the patient, or other clearly enforceable legal right to demand payment from commercial insurance carriers or governmental agencies,
no accounts receivable is recognized. The Company does not record an Allowance for Doubtful Accounts for the commercial insurance
or governmental programs since the revenue is recorded mainly on a cash basis.
Other current assets
Other current assets consisted of the following as of December 31, 2016 and 2015:
Indemnification assets
Letters of credit
Other receivables
Other
Total other current assets
Property and Equipment
December 31,
2016
875 $
-
325
215
1,415 $
December 31,
2015
875
360
1,048
286
2,569
$
$
Property and equipment are stated at cost less accumulated depreciation. Depreciation and amortization is recognized on a straight-line
basis, using the estimated useful lives of: seven to ten years for furniture and fixtures; two to five years for office and computer
equipment; five to seven years for lab equipment; and leasehold improvements are amortized over the shorter of the estimated service
lives or the terms of the related leases which are currently four to five years. Repairs and maintenance are charged to expense as
incurred. Upon disposition, the asset and related accumulated depreciation are removed from the related accounts and any gains or
losses are reflected in operations.
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Software Costs
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
Internal-Use Software - It is the Company’s policy to capitalize certain costs incurred in connection with developing or obtaining
internal-use software. Capitalized software costs are included in property and equipment on the consolidated balance sheet and
amortized over the software’s useful life, generally three to seven years. Software costs that do not meet capitalization criteria are
expensed immediately.
External-Use Software - It is the Company’s policy to capitalize certain costs incurred in connection with developing or obtaining
external-use software. Capitalized software costs are included in property and equipment on the consolidated balance sheet and
amortized over the software’s useful life, generally three years. Software costs that do not meet capitalization criteria are expensed
immediately.
See Note 6, Property and Equipment and Note 4, Discontinued Operations for further information.
Goodwill
The Company allocates the cost of acquired companies to the identifiable tangible and intangible assets acquired and liabilities
assumed, with the remaining amount classified as goodwill. Since the entities the Company has acquired do not have significant
tangible assets, a significant portion of the purchase price has been allocated to intangible assets and goodwill. The identification and
valuation of these intangible assets and the determination of the estimated useful lives at the time of acquisition, as well as the
completion of impairment tests require significant management judgments and estimates. These estimates are made based on, among
other factors, reviews of projected future operating results and business plans, economic projections, anticipated highest and best use of
future cash flows and the market participant cost of capital. The use of alternative estimates and assumptions could increase or decrease
the estimated fair value of goodwill and other intangible assets, and potentially result in a different impact to the Company’s results of
operations. Further, changes in business strategy and/or market conditions may significantly impact these judgments and thereby
impact the fair value of these assets, which could result in an impairment of the goodwill or intangible assets.
The Company tests its goodwill for impairment at least annually (as of December 31) and whenever events or circumstances change
that indicate impairment may have occurred. A significant amount of judgment is involved in determining if an indicator of impairment
has occurred. Such indicators may include, among others: a significant decline in its expected future cash flows; a sustained, significant
decline in its stock price and market capitalization; a significant adverse change in legal factors or in the business climate; unanticipated
competition; and slower growth rates. Any adverse change in these factors could have a significant impact on the recoverability of
goodwill and its consolidated financial results. If the Company's projected long-term sales growth rate, profit margins, or terminal rate
change, or the assumed weighted-average cost of capital is considerably higher, future testing may indicate impairment in this reporting
unit and, as a result, all or a portion of these assets may become impaired.
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Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
During the Company's 2015 annual impairment test of goodwill, it was determined that the goodwill was impaired and the entire
balance should be written off, mainly due to the decline in market capitalization and reduced forecast expectations. As a result the
Company recognized an impairment loss of $15.7 million.
Long-Lived Assets, including Finite-Lived Intangible Assets
Finite-lived intangible assets are stated at cost less accumulated amortization. Amortization of finite-lived acquired intangible assets is
recognized on a straight-line basis, using the estimated useful lives of the assets of approximately two years to nine years in acquisition
related amortization expense in the consolidated statements of comprehensive loss.
The Company reviews the recoverability of long-lived assets and finite-lived intangible assets whenever events or changes in
circumstances indicate that the carrying value of such assets may not be recoverable. If the sum of the expected future undiscounted
cash flows is less than the carrying amount of the asset, an impairment loss is recognized by reducing the recorded value of the asset to
its fair value measured by future discounted cash flows. This analysis requires estimates of the amount and timing of projected cash
flows and, where applicable, judgments associated with, among other factors, the appropriate discount rate. Such estimates are critical
in determining whether any impairment charge should be recorded and the amount of such charge if an impairment loss is deemed to be
necessary.
During 2015, as a result of the decline in market capitalization and other indicators, such as reduced forecast expectations, the
Company reviewed the recoverability of long-lived assets and finite-lived intangible assets. The Company concluded that the carrying
values of such assets were recoverable as of December 31, 2015, and no impairment of such assets was necessary. During the year
ended December 31, 2016, the Company recorded an asset impairment charge of approximately $3.4 million, resulting from a decline in
market value of PancraMIR and Biobank assets associated with the acquisition of certain assets from Asuragen. See Note 7, Goodwill
and Other Intangible Assets for further information.
®
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Contingencies
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
In the normal course of business, the Company is subject to various contingencies. Contingencies are recorded in the consolidated
financial statements when it is probable that a liability will be incurred and the amount of the loss is reasonably estimable, or otherwise
disclosed, in accordance with ASC 450, Contingencies. Significant judgment is required in both the determination of probability and
the determination as to whether a loss is reasonably estimable. In the event the Company determines that a loss is not probable, but is
reasonably possible, and it becomes possible to develop what the Company believes to be a reasonable range of possible loss, then the
Company will include disclosures related to such matter as appropriate and in compliance with ASC 450. To the extent there is a
reasonable possibility that the losses could exceed the amounts already accrued, the Company will, when applicable, adjust the accrual
in the period the determination is made, disclose an estimate of the additional loss or range of loss, indicate that the estimate is
immaterial with respect to its financial statements as a whole or, if the amount of such adjustment cannot be reasonably estimated,
disclose that an estimate cannot be made. The Company is currently involved in certain legal proceedings and, as required, the
Company has accrued its estimate of the probable costs for the resolution of these claims. These estimates are developed in consultation
with outside counsel and are based upon an analysis of potential results, assuming a combination of litigation and settlement strategies.
Predicting the outcome of claims and litigation, and estimating related costs and exposures, involves substantial uncertainties that could
cause actual costs to vary materially from estimates.
In connection with the October 31, 2014 acquisition of RedPath Integrated Pathology, Inc. (“RedPath”), the Company assumed a
liability for a January 2013 settlement agreement (the “Settlement Agreement”) entered into by the former owners of RedPath with the
United States Department of Justice (“DOJ”). Under the terms of the Settlement Agreement, the Company is obligated to make
payments to the DOJ. These payments are due March 31st following the calendar year that the revenue milestones are achieved. See
Note 10, Commitments and Contingencies for further information.
Revenue and Cost of Services
The Company's revenue is generated using the Company's proprietary tests. The Company's performance obligation is fulfilled upon
completion, review and release of test results and subsequently billing the third-party payor or hospital. The Company recognizes
revenue related to billings for Medicare, Medicare Advantage, and hospitals on an accrual basis, net of contractual adjustment, when
there is a predictable pattern of collectability. Contractual adjustments represent the difference between the list prices and the
reimbursement rate set by Medicare and Medicare Advantage, or the amounts billed to hospitals, which approximates the Medicare rate.
Upon ultimate collection, the amount received from Medicare, Medicare Advantage and hospitals with a predictable pattern of payment
is compared to the previous estimates and the contractual allowance is adjusted, if necessary. Amounts not collected are charged to bad
debt expense.
Until a contract has been negotiated with a commercial insurance carrier or governmental program, the services may or may not be
covered by these entities existing reimbursement policies. In addition, the Company does not enter into direct agreements with patients
that commit them to pay any portion of the cost of the tests in the event that insurance declines to reimburse us. In the absence of an
agreement with the patient or other clearly enforceable legal right to demand payment, the related revenue is only recognized upon the
earlier of payment notification or cash receipt. Accordingly, the Company recognizes revenue from commercial insurance carriers and
governmental programs without a contract, when payment is received.
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Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
Persuasive evidence of an arrangement exists and delivery is deemed to have occurred upon completion, review, and release of the test
results by the Company. The assessment of the fixed or determinable nature of the fees charged for diagnostic testing performed, and
the collectability of those fees, requires significant judgment by management. Management believes that these two criteria have been
met when there is contracted reimbursement coverage or a predictable pattern of collectability with individual third-party payors or
hospitals and accordingly, recognizes revenue upon delivery of the test results. In the absence of contracted reimbursement coverage or
a predictable pattern of collectability, the Company believes that the fee is fixed or determinable and collectability is reasonably
assured only upon request of third-party payor notification of payment or when cash is received, and recognizes revenue at that time.
Cost of services consists primarily of the costs associated with operating the Company's laboratories and other costs directly related to
the Company's tests. Personnel costs, which constitute the largest portion of cost of services, include all labor related costs, such as
salaries, bonuses, fringe benefits and payroll taxes for laboratory personnel. Other direct costs include, but are not limited to, laboratory
supplies, certain consulting expenses, and facility expenses.
Stock-Based Compensation
The compensation cost associated with the granting of stock-based awards is based on the grant date fair value of the stock award. The
Company recognizes the compensation cost, net of estimated forfeitures, over the shorter of the vesting period or the period from the
grant date to the date when retirement eligibility is achieved. Forfeitures are initially estimated based on historical information and
subsequently updated over the life of the awards to ultimately reflect actual forfeitures. As a result, changes in forfeiture activity can
influence the amount of stock compensation cost recognized from period to period.
The Company primarily uses the Black-Scholes option-pricing model to determine the fair value of stock options and SARs. The
determination of the fair value of stock-based payment awards is made on the date of grant and is affected by the Company’s stock
price as well as assumptions made regarding a number of complex and subjective variables. These assumptions include: expected stock
price volatility over the term of the awards; actual and projected employee stock option exercise behaviors; the risk-free interest rate;
and expected dividend yield. The fair value of restricted stock units, or RSUs, and restricted shares is equal to the closing stock price on
the date of grant.
See Note 12, Stock-Based Compensation for further information.
Treasury Stock
Treasury stock purchases are accounted for under the cost method whereby the entire cost of the acquired stock is recorded as treasury
stock. Upon reissuance of shares, the Company records any difference between the weighted-average cost of such shares and any
proceeds received as an adjustment to additional paid-in capital.
Rent Expense
Minimum rental expenses are recognized over the term of the lease. The Company recognizes minimum rent starting when possession
of the property is taken from the landlord, which may include a construction period prior to occupancy. When a lease contains a
predetermined fixed escalation of the minimum rent, the Company recognizes the related rent expense on a straight-line basis and
records the difference between the recognized rental expense and the amounts payable under the lease as a deferred rent liability. The
Company may also receive tenant allowances including cash or rent abatements, which are reflected in other accrued expenses and
long-term liabilities on the consolidated balance sheet. These allowances are amortized as a reduction of rent expense over the term of
the lease. Certain leases provide for contingent rents that are not measurable at inception. These contingent rents are primarily based
upon use of utilities and the landlord’s operating expenses. These amounts are excluded from minimum rent and are included in the
determination of total rent expense when it is probable that the expense has been incurred and the amount is reasonably estimable.
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Income taxes
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
Income taxes are based on income for financial reporting purposes calculated using the Company’s expected annual effective rate and
reflect a current tax liability or asset for the estimated taxes payable or recoverable on the current year tax return and expected annual
changes in deferred taxes. Any interest or penalties on income tax are recognized as a component of income tax expense.
The Company accounts for income taxes using the asset and liability method. This method requires recognition of deferred tax assets
and liabilities for expected future tax consequences of temporary differences that currently exist between tax bases and financial
reporting bases of the Company’s assets and liabilities based on enacted tax laws and rates. Deferred tax expense (benefit) is the result
of changes in the deferred tax asset and liability. A valuation allowance is established, when necessary, to reduce the deferred income
tax assets when it is more likely than not that all or a portion of a deferred tax asset will not be realized.
The Company operates in multiple tax jurisdictions and pays or provides for the payment of taxes in each jurisdiction where it conducts
business and is subject to taxation. The breadth of the Company’s operations and the complexity of the tax law require assessments of
uncertainties and judgments in estimating the ultimate taxes the Company will pay. The final taxes paid are dependent upon many
factors, including negotiations with taxing authorities in various jurisdictions, outcomes of tax litigation and resolution of proposed
assessments arising from federal and state audits. Uncertain tax positions are recognized in the financial statements when it is more
likely than not (i.e., a likelihood of more than fifty percent) that a position taken or expected to be taken in a tax return would be
sustained upon examination by tax authorities that have full knowledge of all relevant information. A recognized tax position is then
measured as the largest amount of benefit that is greater than fifty percent likely to be realized upon ultimate settlement. The Company
adjusts accruals for unrecognized tax benefits as facts and circumstances change, such as the progress of a tax audit. The Company
believes that any potential audit adjustments will not have a material adverse effect on its financial condition or liquidity. However, any
adjustments made may be material to the Company’s consolidated results of operations or cash flows for a reporting period. Penalties
and interest, if incurred, would be recorded as a component of current income tax expense.
Significant judgment is also required in evaluating the need for and magnitude of appropriate valuation allowances against deferred tax
assets. Deferred tax assets are regularly reviewed for recoverability. The Company currently has significant deferred tax assets
resulting from net operating loss carryforwards and deductible temporary differences, which should reduce taxable income in future
periods, if generated. The realization of these assets is dependent on generating future taxable income.
Income (Loss) per Share
Basic earnings per common share are computed by dividing net income by the weighted average number of shares outstanding during
the year including any unvested share-based payment awards that contain nonforfeitable rights to dividends. Diluted earnings per
common share are computed by dividing net income by the sum of the weighted average number of shares outstanding and dilutive
common shares under the treasury method. Unvested share-based payment awards that contain nonforfeitable rights to dividends or
dividend equivalents (whether paid or unpaid), are participating securities and are included in the computation of earnings per share
pursuant to the two-class method. As a result of the losses incurred in both 2016 and 2015, the potentially dilutive common shares have
been excluded from the earnings per share computation for these periods because its inclusion would have been anti-dilutive.
Reverse stock split
On December 28, 2016, the Company effected a one-for-ten reverse split of its issued and outstanding shares of common stock in order
to achieve the requisite increase in the market price of our common stock to be in compliance with the NASDAQ minimum bid price
requirement. All share amounts in prior periods have been adjusted to reflect the reverse split.
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Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
2. Recent Accounting Standards
In August 2014, the Financial Accounting Standards Board (“FASB”) issued guidance on determining when and how to disclose going-
concern uncertainties in the financial statements. The new standard requires management to perform interim and annual assessments of
an entity’s ability to continue as a going concern within one year of the date the financial statements are issued. An entity must provide
certain disclosures if conditions or events raise substantial doubt about the entity’s ability to continue as a going concern. The guidance
applies to all entities and is effective for annual periods ending after December 15, 2016, and interim periods thereafter, with early
adoption permitted. The Company adopted this standard in 2016.
In February 2016, the FASB issued ASU 2016-02, Leases (Topic 842), which when effective will require organizations that lease assets
(e.g., through "leases") to recognize assets and liabilities for the rights and obligations created by the leases on the balance sheet. A
lessee will be required to recognize assets and liabilities for leases with terms that exceed twelve months. The standard will also require
disclosures to help investors and financial statement users better understand the amount, timing and uncertainty of cash flows arising
from leases. The disclosures include qualitative and quantitative requirements, providing additional information about the amounts
recorded in the financial statements. The guidance is effective for annual periods beginning after December 15, 2018, and interim
periods within those annual periods. Early adoption is permitted. The Company is currently evaluating the impact of this standard on its
consolidated financial position and results of operations.
In May 2016, the FASB issued ASU 2016-12, "Revenue from Contract with Customers - Narrow-Scope Improvements and Practical
Expedients". In April 2016, the FASB issued ASU 2016-10, "Revenue from Contracts with Customers - Identifying Performance
Obligations and Licensing". In March 2016, the FASB issued ASU 2016-08, "Revenue from Contract with Customers - Principal versus
Agent Considerations (Reporting Revenue Gross versus Net)". In August 2015, the FASB issued ASU 2015-14 deferring the effective
date to annual and interim periods. In May 2014, the FASB issued ASU 2014-09, "Revenue from Contracts with Customers". The core
principle of these ASUs are that an entity should recognize revenue to depict the transfer of promised goods or services to customers in
an amount that reflects the consideration to which the entity expects to be entitled in exchange for those goods or services. The
amendments in ASU 2016-12 affect only the narrow aspects of the guidance, such as assessing the collectability criterion and
accounting for contracts that do not meet the criterion, presentation of sales and other similar taxes collected from customers, non-cash
consideration, and contract modifications at transition. ASU 2016-10 clarifies two aspects of the guidance: identifying performance
obligations and the licensing implementation. The intention of ASU 2016-08 is to improve the operability and understandability of the
implementation guidance on principal versus agent considerations. ASU 2015-14 defers the effective date to annual and interim periods
beginning on or after December 15, 2017, and early adoption will be permitted, but not earlier than the original effective date of annual
and interim periods beginning on or after December 15, 2016, for public entities. ASU 2014-09 is a comprehensive new revenue
recognition model for revenue from contract with customers. The Company is evaluating the potential impact of the new guidance and
will adopt these ASUs when effective.
3. Liquidity
The accompanying consolidated financial statements have been prepared on a basis that assumes that the Company will continue as a
going concern and that contemplates the continuity of operations, the realization of assets and the satisfaction of liabilities and
commitments in the normal course of business. As of December 31, 2016, the Company had cash and cash equivalents of $0.6 million,
net accounts receivable of $2.2 million, current assets of $4.2 million and current liabilities of $16.2 million. For the year ended
December 31, 2016, the Company incurred a net loss of $8.3 million and cash used in operating activities was $8.9 million.
On December 22, 2016, the Company completed a registered direct public offering, which resulted in gross proceeds to the Company of
approximately $1.9 million, (net proceeds of $1.7 million after expenses). In 2017, the Company closed on three equity offerings
raising gross proceeds of $12.2 million. See Note 19, Subsequent Events, of Notes to the Consolidated Financial Statements.
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Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
The Company also entered into a Credit Agreement with SCM Specialty Finance Opportunities Fund, L.P. on September 28, 2016 as
described further below, on which it has not yet drawn.and may not be able to draw down any funds in the near future. The Company
also anticipates operating losses to continue for the foreseeable future due to, among other things, costs related to its commercial
operations, developing products and product candidates, right sizing and reorganizing its administrative organization and winding down
activities and managing obligations related to its discontinued operations.
On September 28, 2016 (the “Closing Date”), the Company and its wholly-owned direct and indirect subsidiaries, Interpace
Diagnostics, LLC (“Interpace LLC”) and Interpace Diagnostics Corporation (“IDC” and together with Interpace LLC, its
“Subsidiaries”), entered into a Credit Agreement (the “Credit Agreement”) with SCM Specialty Finance Opportunities Fund, L.P. (the
“Lender”). Pursuant to and subject to the terms of the Credit Agreement, the Lender agreed to provide a revolving loan (the “Loan”) to
the Company in the maximum principal amount of $1.2 million (“Facility Cap”). The maturity date of the Loan is September 28, 2018.
The Loan bears interest at an annual rate equal to the Prime Rate (as defined in the Credit Agreement) plus 2.75%, payable in cash
monthly in arrears. The interest rate will be increased by 5.0% in the event of a default under the Credit Agreement. Events of default
under the Credit Agreement, some of which are subject to certain cure periods, include a failure to pay or perform obligations when due,
the making of a material misrepresentation to the Lender, the rendering of certain judgments or decrees against the Company and its
Subsidiaries and the initiation, voluntarily or involuntarily, of a bankruptcy or similar proceeding against the Company or its
Subsidiaries.
Also on the Closing Date, the Company and its Subsidiaries acknowledged and agreed to an Intercreditor Agreement (the “Intercreditor
Agreement”) by and between the Lender and the RedPath Equityholder Representative pursuant to which the Lender has a first lien
security interest on all of the accounts receivable (and related intangibles) of the Company and its Subsidiaries and the RedPath
Equityholder Representative has a second lien security interest, subordinated to the Lender, on all the accounts receivables (and related
intangibles) of the Company and its Subsidiaries. In addition, pursuant to the Intercreditor Agreement, the RedPath Equityholder
Representative has a first lien security interest on all other assets of the Company and its Subsidiaries and the Lender has no lien with
respect to such other assets. As discussed below, the RedPath Equityholder Representative assigned all of its rights, title and interest in
the RedPath Note, including, but not limited to, its security interest in all of our assets and the assets of the Company subsidiaries, to the
Investor in connection with the consummation of the sale of the RedPath Note to the Investor.
The Company agreed to pay certain out-of-pocket costs and expenses incurred by the Lender in connection with the Credit Agreement
and related documents, the administration of the Loan and related documents and the enforcement or protection of the Lender’s rights.
The Lender is also entitled to: (a) a $12,000 origination fee; (b) a monthly unused line fee equal to the amount which is one-twelfth of
one percent (0.083%) of the difference between (i) the outstanding balance of the Loan during the preceding month, and (ii) the Facility
Cap on the date of determination; (c) a monthly collateral management fee equal to one-sixth of one percent (0.1666%) of the average
daily balance under the Credit Agreement outstanding during the preceding month; and (d) a termination fee equal to (i) two percent
(2%) of the Facility Cap if the Credit Agreement is terminated before the first anniversary of the Closing Date (the “First
Anniversary”), or (ii) one percent (1%) of the Facility Cap if the Credit Agreement is terminated after the First Anniversary. The
Company must also pay certain fees in the event that (a) the amount outstanding under the Credit Agreement exceeds the availability
under the Credit Agreement’s borrowing base, and (b) receivables are not properly deposited in the appropriate lockbox account.
The Credit Agreement contains customary representations and warranties in favor of the Lender and certain covenants, including,
among other things, financial covenants relating to loan turnover rates, liquidity and revenue targets.
As of March 27, 2017 the Company had not borrowed any funds under the Credit Agreement and funds may not be available to the
Company for the forseeable future.
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Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
On March 23, 2017, the Company entered into an exchange agreement (the “Exchange Agreement”), with an institutional investor (the
“Investor”). Prior to the Company entering into the Exchange Agreement, the Investor acquired that certain Non-Negotiable
Subordinated Secured Promissory Note, dated as of October 31, 2014, as amended (the “RedPath Note”), issued by the Company and
the Company’s subsidiary, Interpace, LLC, in favor of RedPath Equityholder Representative, LLC (the “RedPath Equityholder
Representative”) on behalf of the former equityholders of RedPath. The RedPath Note, which was entered into in connection with the
Company’s acquisition of RedPath in October 2014, had an aggregate principal amount of $9,336,250 outstanding and was acquired by
the Investor for $8,869,437.50. The RedPath Equityholder Representative assigned all of its rights, title and interest in the RedPath Note
to the Investor, including, but not limited to, its security interest in all of the assets of the Company and the assets of the Company’s
subsidiaries.
Pursuant to the Exchange Agreement, the Company and the Investor agreed to exchange the RedPath Note for (i) a senior secured
convertible note in the aggregate principal amount of $5,321,662.50 (the “Exchanged Convertible Note”), which is convertible into
shares of the Company’s common stock, in accordance with its terms, and (ii) a senior secured non-convertible note with an aggregate
principal amount of $3,547,775 (the “Exchanged Non-Convertible Note” and collectively, the “Exchanged Notes”), for a combined
aggregate principal amount of $8,869,437.50. The Exchanged Notes will rank senior to all of the Company’s outstanding and future
indebtedness, other than the indebtedness in favor of the Company’s credit line lender and are secured by a perfected security interest in
all of the existing and future assets of the Company and those of the Company’s subsidiaries. Upon the reduction of 55% of the
aggregate principal amount of each of the Exchanged Notes, the Investor will release its security interest in its entirety.
The Exchanged Notes mature at 125% of the face value on the fifteenth month anniversary of the closing date, or June 22, 2018, and
bear interest quarterly at one and one hundredth percent (1.01%) per annum (as may be adjusted from time to time). As of March 30,
2017, the Investor had converted approximately 80% of the Exchanged Convertible Note to common stock, converting $4,321,663 of
the Exchanged Convertible Note into 1,730,534 shares of common stock.
Due to the Company’s operating deficit and past due vendor debt the Company will require additional capital to meet its obligations.
There is no guarantee that additional capital will be raised to fund its operations in 2017 and beyond, but the Company intends to meet
its capital needs by driving revenue growth, containing costs as well as exploring other options. These liquidity factors have raised
substantial doubts about our ability to continue as a going concern. We plan to attempt to raise additional equity capital by selling
shares of common stock, if necessary, through one or more additional public offerings or private placements. However, the doubts
raised, relating to our ability to continue as a going concern, may make investing in our securities an unattractive investment for
potential investors. These factors, among others, may make it difficult to raise any additional capital.
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4. Discontinued Operations
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
On December 22, 2015, the Company completed the Company's sale of substantially all of the assets, the goodwill and ongoing
business comprising the Company’s CSO business to Publicis Healthcare Solutions, Inc., formerly known as Publicis Touchpoint
Solutions, Inc. (the “Buyer”), pursuant to the Asset Purchase Agreement, dated as of October 30, 2015, by and between the Buyer and
the Company (the “Asset Purchase Agreement”), for an aggregate cash purchase price at the closing of approximately $28.5 million
(the “Closing Purchase Price”), subject to a post-closing working capital adjustment, and the assumption by the Buyer of certain
specified liabilities. The Closing Purchase Price includes a $25.5 million cash payment (the “Base Cash Payment”), and an estimated
closing date working capital adjustment cash payment of $3 million. Under the Asset Purchase Agreement, the Company was also
entitled to receive an earn-out payment in 2017 equal to one-third of the 2016 revenues generated by the Commercial Services Business
under certain specified contracts and client relationships, less the amount of the Base Cash Payment. The Company will not receive the
earn-out payment discussed above.
The Company used the net proceeds from the transactions contemplated by the Asset Purchase Agreement to pay the balance of the
outstanding loan under the Credit Agreement and related fees, as described further in Note 17, Long-Term Debt.
In connection with the closing of the transactions contemplated by the Asset Purchase Agreement, on December 22, 2015, the
Company entered into a transition services agreement with the Buyer, pursuant to which the Company provided certain services to the
Buyer for up to six months following the closing, and a restrictive covenant agreement with the Buyer, pursuant to which, among other
things, the Company would be prohibited from competing with the Commercial Services Business until December 31, 2020.
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Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
The Asset Purchase Agreement also required the Company change its name, and, as a result the Company changed its name from “PDI,
Inc.” to “Interpace Diagnostics Group, Inc.”
A reconciliation of the gain on sale for the Company's CSO business for the years ended December 31, 2016 and 2015 is as follows:
(in thousands)
Purchase price
Working capital adjustment
Total consideration
Assets and liabilities sold, net
Transaction costs
Gain on sale
Gain on Sale
2016
2015
$
-
1,326
1,326
-
-
1,326 ** $
25,467
3,067
28,534
(5,311)
(1,806)
21,417*
$
$
* Does not include $0.2 million gain on sale of the Group DCA business in 2015
** In 2016, the gain on sale was used to offset liabilities owed to the Buyer which resulted in net cash proceeds of
approximately $0.1 million.
As a result of the sale, the gain on sale and all operations from the CSO business were classified as discontinued operations for all
periods presented. On December 31, 2014, the Company classified Group DCA as held-for-sale and wrote the assets of the business
down to their fair values as the assets have become impaired. In the first quarter of 2015, the Company recorded a gain on sale of its
Group DCA business of $0.2 million. On December 29, 2011, the Company entered into an agreement to sell certain assets of its
Pharmakon business unit to Informed Medical Communications, Inc. Informed in exchange for potential future royalty payments and an
ownership interest in Informed. In the fourth quarter of 2012, the Company wrote-off all of the assets related to the sale of Pharmakon
to Informed as it believes that these assets have become impaired. On July 19, 2010, the Board approved closing the TVG business
unit. The Company notified employees and issued a press release announcing this decision on July 20, 2010. The Consolidated
Statements of Comprehensive Loss reflect the presentation of Commercial Services, Group DCA, Pharmakon, and TVG as
discontinued operations in all periods presented.
The table below presents the significant components of Commercial Services, Group DCA's, Pharmakon's and TVG’s results included
i n Loss from Discontinued Operations, Net of Tax in the consolidated statements of comprehensive loss for the years ended
December 31, 2016 and 2015.
Revenue, net
(Loss) income from discontinued operations
Gain on sale of assets
Income from discontinued operations, before tax
Income tax expense
Income from discontinued operations, net of tax
For the Years Ended December 31,
2016
2015
$
1,644 $
134,850
(886)
1,326
440
362
78 $
10,341
21,634
31,975
12,261
19,714
$
F-18
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
The assets and liabilities classified as discontinued operations relate to Commercial Services, Group DCA, Pharmakon, and TVG. As of
December 31, 2016 and December 31, 2015, these assets and liabilities are in the accompanying balance sheets as follows:
CSO
$
For the Years Ended December 31,
2016
DCA/
TVG
Total
CSO
2015
DCA/
TVG
Total
- $
-
-
-
-
14
14
14 $
- $
-
-
-
-
- $
- $
-
-
-
-
14
14
14 $
890 $
-
1,272
1,966
3,296 $
16
2,062
5,374
190
-
190
5,564 $
3,767 $
11
3,036
5,092
4,128
4,128 $
11,906
11,906 $
- $
-
-
-
-
150
150
150 $
- $
-
-
358
358
358 $
3,296
16
2,062
5,374
190
150
340
5,714
3,767
11
3,036
5,450
12,264
12,264
- $
-
-
-
-
-
-
- $
890 $
-
1,272
1,966
4,128
4,128 $
Accounts receivable, net
Unbilled receivable, net
Other
Current assets from discontinued
operations
Property and equipment, net
Other
Long-term assets from discontinued
operations
Total assets
Accounts payable
Unearned contract revenue
Accrued salary and bonus
Other
Current liabilities from discontinued
operations
Total liabilities
5. Fair Value Measurements
$
$
$
The Company's financial assets and liabilities reflected at fair value in the consolidated financial statements include: cash and cash
equivalents; short-term investments; accounts receivable; other current assets; accounts payable; and contingent consideration. Fair
value is the price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market
participants at the measurement date. In determining fair value, the Company uses various methods including market, income and cost
approaches. Based on these approaches, the Company often utilizes certain assumptions that market participants would use in pricing
the asset or liability, including assumptions about risk and/or the risks inherent in the inputs to the valuation technique. These inputs
can be readily observable, market-corroborated, or generally unobservable inputs. The Company utilizes valuation techniques that
maximize the use of observable inputs and minimize the use of unobservable inputs. Based upon observable inputs used in the valuation
techniques, the Company is required to provide information according to the fair value hierarchy. The fair value hierarchy ranks the
quality and reliability of the information used to determine fair values into three broad levels as follows:
Level 1: Valuations for assets and liabilities traded in active markets from readily available pricing sources for market transactions
involving identical assets or liabilities.
Level 2: Valuations for assets and liabilities traded in less active dealer or broker markets. Valuations are obtained from third-party
pricing services for identical or similar assets or liabilities.
Level 3: Valuations for assets and liabilities include certain unobservable inputs in the assumptions and projections used in
determining the fair value assigned to such assets or liabilities.
F-19
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Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
In instances where the determination of the fair value measurement is based on inputs from different levels of the fair value hierarchy,
the level in the fair value hierarchy within which the entire fair value measurement falls is based on the lowest level input that is
significant to the fair value measurement in its entirety. The Company's assessment of the significance of a particular input to the fair
value measurement in its entirety requires judgment, and considers factors specific to the asset or liability. The valuation methodologies
used for the Company's financial instruments measured on a recurring basis at fair value, including the general classification of such
instruments pursuant to the valuation hierarchy, is set forth in the tables below.
Assets:
Cash and cash equivalents:
Cash
Money market funds
Liabilities:
Contingent consideration:
Asuragen
RedPath
Assets:
Cash and cash equivalents:
Cash
Money market funds
Marketable securities:
Money market funds
Mutual funds
U.S. Treasury securities
Government agency securities
Liabilities:
Contingent consideration:
Asuragen
RedPath
As of December 31, 2016
Carrying
Amount
Fair
Value
Fair Value Measurements
As of December 31, 2016
Level 2
Level 1
Level 3
$
$
$
$
$
$
$
$
$
$
602 $
-
602 $
602 $
-
602 $
1,545 $
5,969
7,514 $
1,545 $
5,969
7,514 $
602 $
-
602 $
- $
-
- $
- $
-
- $
- $
-
- $
-
-
-
1,545
5,969
7,514
As of December 31, 2015
Carrying
Amount
Fair
Value
Fair Value Measurements
As of December 31, 2015
Level 2
Level 1
Level 3
7,534 $
776
8,310 $
48 $
58
1,115
131
1,352 $
7,534 $
776
8,310 $
48 $
58
1,115
131
1,352 $
4,628 $
13,921
18,549 $
4,628 $
13,921
18,549 $
7,534 $
776
8,310 $
48 $
58
1,115
131
1,352 $
— $
—
— $
— $
—
— $
— $
—
—
—
— $
— $
—
— $
—
—
—
—
—
—
—
—
4,628
13,921
18,549
The fair value of marketable securities is valued using market prices in active markets (level 1). As of December 31, 2016 and 2015,
the Company did not have any marketable securities in less active markets (level 2) or without observable market values that would
require a high level of judgment to determine fair value (level 3).
F-20
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
In connection with the acquisition of the Acquired Property from Asuragen and acquisition of RedPath, the Company recorded $4.5
million and $22.1 million of contingent cash consideration related to deferred payments and revenue based payments, respectively. The
Company determined the fair value of the contingent consideration based on a probability-weighted income approach derived from
revenue estimates. The fair value measurement is based on significant inputs not observable in the market and thus represents a Level 3
measurement. There was an $11.9 million net reduction in the fair value of the contingent consideration during the period ended
December 31, 2016. There was an $8.0 million net reduction in the fair value of the contingent consideration during the period ended
December 31, 2015. The contingent consideration currently consists of $0.3 million in current liabilities and $7.2 million in long-term
liabilities. A rollforward of the carrying value of the contingent consideration from continuing operations for the years ended December
31, 2015 and 2016 is as follows:
Balance as of January 1, 2015
Accretion
Payments
Adjustment to fair value
Balance as of December 31, 2015
Accretion
Payments
Adjustment to fair value
Balance as of December 31, 2016
Asuragen
RedPath
Total
4,476 $
-
-
152
4,628
325
(475)
(2,933)
1,545 $
22,066 $
-
-
(8,145)
13,921
975
-
(8,927)
5,969 $
26,542
-
-
(7,993)
18,549
1,300
(475)
(11,860)
7,514
$
$
The Company considers carrying amounts of accounts receivable, accounts payable and accrued expenses to approximate fair value due
to the short-term nature of these financial instruments. There is no fair value ascribed to the letters of credit as management does not
expect any material losses to result from these instruments because performance is not expected to be required.
Long-term debt with an aggregate principal amount of approximately $9.34 million has an approximate fair value of $8.9 million based
upon the March 23, 2017 Exchange Agreement.
Certain of the Company's non-financial assets, such as other intangible assets and goodwill are measured at fair value on a nonrecurring
basis when there is an indicator of impairment and recorded at fair value only when an impairment charge is recognized.
Pancreas
Biobank
Total
Pancreas
Biobank
Total
Carrying Amount as of
December 31, 2016
Fair Value Measurements as of
December 31, 2016
Level 2
Level 3
Level 1
$
$
- $
-
- $
- $
-
- $
- $
-
- $
-
-
-
Carrying Amount as of
December 31, 2015
Fair Value Measurements as of
December 31, 2015
Level 2
Level 1
Level 3
$
$
2,625 $
1,034
3,659 $
- $
-
- $
- $
-
- $
2,625
1,034
3,659
Carrying Amount as of
December 31, 2015
Fair Value Measurements as of
December 31, 2015
Level 2
Level 3
Level 1
Goodwill
$
- $
- $
- $
-
F-21
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Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
6. Property and Equipment
Property and equipment consisted of the following as of December 31, 2016 and 2015:
Furniture and fixtures
Office equipment
Computer equipment
Internal-use software
Leasehold improvements
Less accumulated depreciation
December 31,
2016
2015
667 $
1,503
3,473
113
878
6,634
(5,705)
929 $
2,862
2,475
3,476
7,438
4,762
21,013
(19,553)
1,460
$
$
Depreciation expense from continuing operations was approximately $0.5 million and $0.6 million for the years ended December 31,
2016 and 2015, respectively. There was no internal-use software amortization expense included in depreciation and amortization
expense for either period as that was all recorded in discontinued operations. During the year ended December 31, 2015, the Company
recorded a non-cash charge of approximately $0.6 million for the write-down of fixed assets within Loss from discontinued operations
based on the decision to sell the Commercial Services business. As of December 31, 2016, there was no unamortized balance of
capitalized external-use software.
The decrease in gross property and equipment and accumulated depreciation in 2016 was the result of the expiration of the leases on
the Company’s former office buildings and the removal of the assets associated with those buildings as well as the removal of obsolete
software. These amounts were fully depreciated and had no impact on the statement of comprehensive loss in 2016.
7. Goodwill and Other Intangible Assets
Goodwill
During the Company's annual impairment testing of goodwill as of December 31, 2015, the Company recognized an impairment loss of
$15.7 million within goodwill impairment in the consolidated statement of operations and comprehensive loss. A rollforward of the
carrying value of goodwill from continuing operations from January 1, 2015 to December 31, 2015 is as follows:
RedPath
January 1,
$
15,545
Additions
$
—
Adjustments
$
121
$
Impairments
(15,666)
December 31,
—
$
2015
Other Intangible Assets
The net carrying value of the identifiable intangible assets as of December 31, 2016 and December 31, 2015 is as follows:
Diagnostic assets:
Asuragen acquisition:
Thyroid
Pancreas
Biobank
RedPath acquisition:
Pancreas test
Barrett's test
Total
As of December 31,
2016
Carrying
Amount
As of December 31,
2015
Carrying
Amount
Life
(Years)
9
-
-
7
9
$
$
8,519 $
-
-
16,141
18,351
43,011 $
8,519
2,882
1,575
16,141
18,351
47,468
Diagnostic lab:
CLIA Lab
Accumulated Amortization
Net Carrying Value
2.3
$
$
$
F-22
609 $
(7,262) $
36,358 $
609
(4,585)
43,492
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
Amortization expense was approximately $3.8 million for the years ended December 31, 2016 and 2015, respectively. Estimated
amortization expense for the next five years is as follows:
2017
2018
2019
2020
2021
$
4,272 $
5,292 $
5,292 $
5,292 $
4,908
In 2016, the Company recorded an asset impairment charge of approximately $3.4 million resulting from a decline in the market value
of PancraMIR and Biobank assets associated with the acquisition of certain assets from Asuragen.
®
8. Retirement Plans
The Company offers an employee 401(k) saving plan. Under the Interpace Diagnostics Group, Inc. 401(k) Plan, employees may
contribute up to 50% of their pre- or post-tax base compensation. The Company currently offers a safe harbor matching contribution
equal to 100% of the first 3% of the participant’s contributed base salary plus 50% of the participant’s base salary contributed
exceeding 3% but not more than 5%. Participants are not allowed to invest any of their 401(k) funds in the Company’s common
stock. The Company’s total contribution expense from continuing operations related to the 401(k) plan for the years ended
December 31, 2016 and December 31, 2015 was approximately $0.1 million and $0.1 million, respectively.
9. Accrued Expenses and Other Long-Term Liabilities
Other accrued expenses consisted of the following as of December 31, 2016 and 2015:
Accrued royalties
Insurance and benefit accruals
Indemnification liability
Contingent consideration
Rent payable
DOJ settlement
Accrued professional fees
Taxes payable
Unclaimed property
Directors fees and insurance
All others
Total other accrued expenses
Other long-term liabilities consisted of the following as of December 31, 2016 and 2015:
Rent payable
Uncertain tax positions
DOJ settlement (indemnified by RedPath)
Other
Total other long-term liabilities
F-23
December 31,
2016
December 31,
2015
711 $
40
875
260
110
80
1,746
526
565
40
1,283
6,236 $
111
366
875
659
127
250
775
591
546
107
1,554
5,961
December 31,
2016
December 31,
2015
- $
3,594
250
-
3,844 $
52
3,425
2,500
201
6,178
$
$
$
$
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
10. Commitments and Contingencies
The Company leases facilities and certain equipment under agreements classified as operating leases, which expire at various dates
through 2017. Substantially all of the property leases provide for increases based upon use of utilities and landlord’s operating
expenses as well as pre-defined rent escalations. Total expense from continuing operations under these agreements for the years ended
December 31, 2016 and 2015 was approximately $0.9 million and $0.8 million, respectively.
As of December 31, 2016, contractual obligations with terms exceeding one year and estimated minimum future rental payments
required by non-cancelable operating leases with initial or remaining lease terms exceeding one year are as follows:
Operating lease obligations
Contractual obligation
Total
Litigation
Less than
Total
1 Year
1 to 3
Years
3 to 5
Years
After
5 Years
$
$
285 $
-
285 $
285 $
-
285 $
- $
-
- $
- $
-
- $
-
-
-
Due to the nature of the businesses in which the Company is engaged it is subject to certain risks. Such risks include, among others,
risk of liability for personal injury or death to persons using products the Company promotes or commercializes. There can be no
assurance that substantial claims or liabilities will not arise in the future due to the nature of the Company’s business activities and
recent increases in litigation related to healthcare products. As part of the closeout of its CSO operations, the Company seeks to reduce
its potential liability under its service agreements through measures such as contractual indemnification provisions with customers (the
scope of which may vary from customer to customer, and the performance of which is not secured) and insurance. The Company could,
however, also be held liable for errors and omissions of its employees in connection with the services it performs that are outside the
scope of any indemnity or insurance policy. The Company could be materially adversely affected if it were required to pay damages or
incur defense costs in connection with a claim that is outside the scope of an indemnification agreement; if the indemnity, although
applicable, is not performed in accordance with its terms; or if the Company’s liability exceeds the amount of applicable insurance or
indemnity.
The Company routinely assesses its litigation and threatened litigation as to the probability of ultimately incurring a liability, and
records its best estimate of the ultimate loss in situations where the Company assesses the likelihood of loss as probable. The Company
accrues for a liability when it is both probable that a liability has been incurred and the amount of the loss can be reasonably estimated.
Significant judgment is required in both the determination of probability and the determination as to whether a loss is reasonably
estimable. In addition, in the event the Company determines that a loss is not probable, but is reasonably possible, and it becomes
possible to develop what the Company believes to be a reasonable range of possible loss, then the Company will include disclosures
related to such matter as appropriate and in compliance with ASC 450. To the extent there is a reasonable possibility that the losses
could exceed the amounts already accrued, the Company will, as applicable, adjust the accrual in the period the determination is made,
disclose an estimate of the additional loss or range of loss, indicate that the estimate is immaterial with respect to its financial
statements as a whole or, if the amount of such adjustment cannot be reasonably estimated, disclose that an estimate cannot be made. As
of September 30, 2016, the Company's accrual for litigation and threatened litigation was not material to the consolidated financial
statements.
In connection with the October 31, 2014 acquisition of RedPath, the Company assumed a liability for the Settlement Agreement entered
into by the former owners of RedPath with the DOJ. Under the terms of the Settlement Agreement, the Company is obligated to make
payments to the DOJ for the calendar years ended December 31, 2014 through 2017, up to a maximum of $3.0 million.
F-24
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
Payments are due March 31st following the calendar year that the revenue milestones are achieved. In May 2016, the Company
renegotiated payment terms with the DOJ related to a $250,000 payment associated with performance in fiscal 2014 that resulted in an
agreement that the Company pay $85,000 on July 31, 2016, $85,000 on October 31, 2016 and $80,000 on February 28, 2017.
Accordingly, $170,000 was paid to the DOJ in 2016. For the year ended December 31, 2016, the Company has $0.3 million recorded
as its best estimate of the amount that remains to be paid under the Settlement Agreement based on its estimate of future revenues,
which is included in other long-term liabilities.
Prolias Technologies, Inc. v. PDI, Inc.
On April 8, 2015, Prolias Technologies, Inc.(“Prolias”) filed a complaint (the “Complaint”) against the Company with the Superior
Court of New Jersey (Morris County) in a matter entitled Prolias Technologies, Inc. v. PDI, Inc. (Docket No. MRS-L-899-15). In the
Complaint, Prolias alleges that it and the Company entered into an August 19, 2013 Collaboration Agreement and a First Amendment
thereto (collectively, the “Agreement”) whereby Prolias and the Company agreed to work in good faith to commercialize a diagnostic
test known as "Thymira." Thymira is a minimally invasive diagnostic test that is being developed to detect thyroid cancer. Prolias
alleges in the Complaint that the Company wrongfully terminated the Agreement, breached obligations owed to it and committed torts.
After various motions on October 13, 2016, the Company filed an application to enter final judgment and taxing of costs against Prolias.
The Company requested that the Court enter final judgment against Prolias and for the Company in the amount of $621,236, plus ten
percent interest continuing to accrue on the principal balance of $500,000 unless and until paid, attorneys’ fees and costs of $390,769,
and a declaratory judgment that Prolias is deemed to have executed and delivered to the Company a promissory note in the amount of
$1,000,000 under Article 10.2(a) of the Collaboration Agreement. On November 17, 2016, the Court denied the Company’s application
without prejudice and with leave to refile.
On February 16, 2017, the Company refiled its application for final judgment, and on March 9, 2017, the Superior Court of New Jersey
entered a final judgment in the Company’s favor against Prolias for the sum of $636,053 plus ten percent interest continuing to accrue
on the principal balance of $500,000 (per diem $136.99) unless and until paid. Final judgment was also entered in the Company’s favor,
and against Prolias, declaring Prolias is deemed to have executed and delivered to the Company a promissory note in the amount of
$1,000,000 and Prolias is obligated to repay the Company the principal amount and all interest in accordance with the terms of the
promissory note and Article 10.2(a) of the Collaboration Agreement by and between Prolias and the Company. On March 17, 2017, the
Company requested that the final judgment against Prolias be recorded as a statewide lien. No assurance can be given that the Company
will be able to recover on the judgment against Prolias.
Swann v. Akorn, Inc., and Interpace Diagnostics Group, Inc.
On May 27, 2016, Michael J. Swann, one of the Company’s former employees, filed a complaint against the Company in the Court of
Common Pleas of the Fifth Judicial Circuit in South Carolina in a matter entitled Michael J. Swann v. Akorn, Inc., and Interpace
Diagnostic Group Inc. (Civil Action No. 2016-CP-40-03362). In the complaint, Mr. Swann alleges, among other things, that he was
discriminated against and wrongfully terminated as a member of a sales force marketing pharmaceutical products of Akorn, Inc.,
because of an illness suffered by Mr. Swann. Mr. Swann alleges that he was discriminated against in violation of the Americans with
Disabilities Act/Americans with Disabilities Act Amendments Act and the Family Medical Leave Act and seeks damages for back pay,
reinstatement, front pay, compensatory and punitive damages in an amount not less than $300,000, attorney’s fees and costs. The
Company denies that it is liable to Mr. Swann for any of the claims asserted and intends to vigorously defend itself against those
claims.
Severance
In 2015, in connection with the sale of the majority of the CSO business and the implementation of a broad-based program to maximize
efficiencies and cut costs, the Company reduced headcount and incurred severance obligations to terminated employees that amounted
to approximately $3.7 million.
During the first quarter ended March 31, 2016 the Company recorded additional severance obligations as it continued to right-size the
organization and wind down its CSO business. The Company recorded obligations of $1.1 million, $0.5 million of which was recorded
in continuing operations.
The current severance liability as of December 31, 2016 is approximately $3.1 million, of which $2.2 million resides in continuing
operations and $0.9 million is in discontinued operations. The severance liability as of December 31, 2015 was approximately $3.7
million, of which $2.7 million resided in continuing operations and $1.0 million was in discontinued operations. In January 2017, five
former executives agreed to a settlement of their severance obligations agreeing to 35% of the total amount due them. These remaining
obligations were paid out in February 2017 in payments totaling approximately $1.0 million. See Note 19, Subsequent Events, for
further detail.
F-25
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
11. Preferred Stock and Equity Offerings
The board of directors (the “Board”) of the Company is authorized to issue, from time-to-time, up to 5,000,000 shares of preferred stock
in one or more series. The Board is authorized to fix the rights and designation of each series, including dividend rights and rates,
conversion rights, voting rights, redemption terms and prices, liquidation preferences and the number of shares of each series. As of
December 31, 2016 and 2015, there were no issued and outstanding shares of preferred stock.
Equity offering – 2016
On December 22, 2016, the Company completed the Registered Direct Offering to sell 200,000 shares of its common stock at a price of
$5.30 per share and prefunded warrants to purchase 160,000 shares of its common stock at a price of $5.20 per warrant, with each
warrant having an exercise price of $0.10 per share. The warrants were immediately exercised. The Registered Direct Offering resulted
in gross proceeds of approximately $1.9 million (net proceeds of approximately $1.7 million after approximately $0.2 million of related
expenses). In 2017, the Company has had three additional direct offerings. See Note 19, Subsequent Events, for more details.
Equity offering - 2015
On November 2, 2015, the Company entered into a Controlled Equity Offering Sales Agreement (the “Sales Agreement”), with Cantor
Fitzgerald & Co. (“Cantor”) pursuant to which the Company could offer and sell shares of its common stock, par value $0.01 per share,
having an aggregate offering price of up to $5,000,000 from time to time through Cantor as the Company's sales agent, subject to the
limitations set forth in the Sales Agreement.
Under the Sales Agreement, Cantor could sell the shares of common stock by any method permitted by law deemed to be an “at-the-
market” offering as defined in Rule 415 of the Securities Act of 1933, as amended, including, but not limited to, sales made directly on
The NASDAQ Global Market, on any other existing trading market for the shares of common stock or to or through a market maker.
Cantor agreed in the Sales Agreement to use its commercially reasonable efforts to sell the shares of common stock in accordance with
the Company’s instructions (including any price, time or size limit or other customary parameters or conditions the Company may
impose). The Company was not obligated to make any sales of common stock under the Sales Agreement.
The Company paid Cantor a commission of 3.0% of the aggregate gross proceeds from each sale of shares of common stock and agreed
to provide Cantor with customary indemnification and contribution rights. In the fourth quarter of 2015, there were 59,070 shares of
common stock sold under this program with net proceeds to the Company of approximately $0.5 million. There were no shares of
common stock sold under this program in 2016.
F-26
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
12. Stock-Based Compensation
The Company’s stock-incentive program is a long-term retention program that is intended to attract, retain and provide incentives for
talented employees, officers and directors, and to align stockholder and employee interests. Currently, the Company is able to grant
options, SARs and restricted shares from the Interpace Diagnostics Group, Inc. Amended and Restated 2004 Stock Award and
Incentive Plan, (the “Amended 2004 Plan”). In 2015, the Board and stockholders approved the Amended 2004 Plan, which amended
the Company’s pre-existing Amended and Restated 2004 Stock Award and Incentive Plan which had replace the 1998 Stock Option
Plan, or the 1998 Plan, and the 2000 Omnibus Incentive Compensation Plan, or the 2000 Plan. The Amended 2004 Plan authorized an
additional 2,450,000 shares for new awards and combined the remaining shares available under the original Amended and Restated
Plan. Eligible participants under the Amended 2004 Plan include officers and other employees of the Company, members of the Board
and outside consultants, as specified and designated by the Compensation of the Board of Directors.. Unless earlier terminated by
action of the Board, the Amended 2004 and Plan will remain in effect until such time as no stock remains available for delivery and the
Company has no further rights or obligations under the Amended 2004 Plan with respect to outstanding awards thereunder.
Historically, stock options have been granted with an exercise price equal to the market value of the common stock on the date of grant,
expire10 years from the date they are granted, and generally vested over a two-year period for members of the Board of Directors and a
three-year period for employees. Upon exercise, new shares can be issued by the Company. The Company granted stock options in
2016, which vest monthly over a one-year period. SARs are generally granted with a grant price equal to the market value of the
common stock on the date of grant, vest one-third each year on the anniversary of the date of grant and expire five years from the date
of grant. The restricted shares and restricted stock units granted to employees generally have a three year cliff vesting period and are
subject to accelerated vesting and forfeiture under certain circumstances. Restricted shares and restricted stock units granted to board
members generally have a three year graded vesting period and are subject to accelerated vesting and forfeiture under certain
circumstances.
The Company primarily uses the Black-Scholes option-pricing model to determine the fair value of stock options and SARs. The
determination of the fair value of stock-based payment awards on the date of grant using an option-pricing model is affected by the
Company’s stock price as well as assumptions regarding a number of complex and subjective variables. These variables include the
Company’s expected stock price volatility over the term of the awards, actual and projected employee stock option exercise behaviors,
risk-free interest rate and expected dividends. Expected volatility is based on historical volatility. As there is no trading volume for the
Company’s options, implied volatility is not representative of the Company’s current volatility so the historical volatility of the
Company's common stock is determined to be more indicative of the Company’s expected future stock performance. The expected life
is determined using the safe-harbor method. The Company expects to use this simplified method for valuing employee options and
SARs grants until more detailed information about exercise behavior becomes available over time. The Company bases the risk-free
interest rate on U.S. Treasury zero-coupon issues with remaining terms similar to the expected term on the options or SARs. The
Company does not anticipate paying any cash dividends in the foreseeable future and therefore uses an expected dividend yield of zero
in the option valuation model. The Company is required to estimate forfeitures at the time of grant and revise those estimates in
subsequent periods if actual forfeitures differ from those estimates. The Company uses historical data to estimate pre-vesting option
forfeitures and records stock-based compensation expense only for those awards that are expected to vest. The Company recognizes
compensation cost, net of estimated forfeitures, arising from the issuance of stock options and SARs on a straight-line basis over the
vesting period of the grant.
The estimated compensation cost associated with the granting of restricted stock and restricted stock units is based on the fair value of
the Company’s common stock on the date of grant. The Company recognizes the compensation cost, net of estimated forfeitures,
arising from the issuance of restricted stock and restricted stock units on a straight-line basis over the shorter of the vesting period or
the period from the grant date to the date when retirement eligibility is achieved.
In December 2015, the Company sold its CSO business, which triggered a change in control clause for all outstanding equity grants
within the Amended 2004 Plan. As such, all unvested restricted stock, RSUs, and performance and non-performance SARs were
accelerated and the Company recorded that additional expense in the fourth quarter of 2015. The impact of the acceleration on
continuing operations was approximately $2.0 million, which was recorded in general and administrative expenses within the
consolidated statement of comprehensive loss.
F-27
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
The following table provides the weighted average assumptions used in determining the fair value of the stock options granted during
the year ended December 31, 2016 and non-performance based SARs granted during the year ended December 31, 2015.
Risk-free interest rate
Expected life (in years)
Expected volatility
Dividend yield
December 31,
2016
0.66%
4.7
145.71%
-
December 31,
2015
1.02%
3.5
54.47%
-
The weighted-average fair value of stock options granted during the year ended December 31, 2016 was estimated to be $1.40. The
weighted-average fair value of non-performance based SARs granted during the year ended December 31, 2015 was estimated to be
$5.30. There were no options or SARs exercised in 2016 or 2015. Historically, shares issued upon the exercise of options have been
new shares and have not come from treasury shares.
As of December 31, 2015, there was no unamortized compensation cost.
The impact of SARs, performance shares, RSUs and restricted stock on net loss for the years ended December 31, 2016 and 2015 is as
follows:
SARs
Performance awards
RSUs and restricted stock
Options
Total stock-based compensation expense
2016
2015
- $
-
109
22
131 $
823
254
2,940
-
4,017
$
$
A summary of stock option and SARs activity for the year ended December 31, 2016, and changes during such year, is presented
below:
Weighted-
Average
Grant
Shares
Price
Weighted-
Average
Remaining Aggregate
Intrinsic
Contractual
Period (in
years)
Value
Outstanding at January 1, 2016
Granted
Exercised
Forfeited or expired
Outstanding at December 31, 2016
102,680 $
87,871
-
-
190,551
46.71
1.60
2.74 $
9.80
25.80
5.42
Exercisable at December 31, 2016
117,334
41.05
2.69
Vested and expected to vest
183,229
26.88
5.25
-
-
632
106
580
F-28
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
A summary of the status of the Company’s nonvested options for the year ended December 31, 2016, and changes during such year, is
presented below:
Nonvested at January 1, 2016
Granted
Vested
Forfeited
Nonvested at December 31, 2016
Weighted-
Average
Grant Date
Fair Value
-
1.37
1.37
-
1.37
Shares
- $
87,871
(14,654)
-
73,217 $
The aggregate fair value of SARs and options vested during the years ended December 31, 2016 and 2015 was $0.02 million and $1.7
million, respectively. The weighted-average grant date fair value of SARs vested during the year ended December 31, 2015 was $1.66.
A summary of the Company’s nonvested shares of restricted stock and restricted stock units for the year ended December 31, 2016, and
changes during such year, is presented below:
Weighted-
Average
Grant Date
Shares
Fair Value
Average
Remaining Aggregate
Intrinsic
Vesting
Period (in
years)
Nonvested at January 1, 2016
Granted
Vested
Forfeited
Nonvested at December 31, 2016
- $
131,688 $
- $
(29,319) $
102,369 $
-
2.51
-
2.56
2.49
- $
-
-
-
2.14 $
Value
-
-
-
-
502
The aggregate fair value of restricted stock and restricted stock units vested during each of the years ended December 31, 2016 and
2015 was zero and $5.4 million, respectively. The weighted-average grant date fair value of restricted stock and restricted stock units
vested during the year ended December 31, 2015 was $2.73.
13. Revenue Sources
The Company's customers consist primarily of physicians, hospitals and clinics. Its revenue channels include Medicare, Medicare
Advantage, Medicaid, Client Billings (hospitals, etc.), and Commercial Payors. The following sets forth the net revenue generated by
revenue channel accounted for more than 10% of the Company's revenue from continuing operations during the period presented. The
revenue from Medicare Advantage in 2016 was less than 10% of the Company’s total.
Customer
Medicare
Commercial Payors
Client Billings
Medicare Advantage
Years Ended December 31,
2015
2016
$
$
$
$
5,344 $
3,150 $
2,955 $
1,170 $
4,046
1,252
1,944
1,700
F-29
Table of Contents
14. Income Taxes
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
The benefit from income taxes on continuing operations for the years ended December 31, 2016 and 2015 is comprised of the
following:
Current:
Federal
State
Total current
Deferred:
Federal
State
Total deferred
Benefit for income taxes
2016
2015
$
$
(154) $
(8)
(162)
-
-
-
(162) $
(11,244)
(725)
(11,969)
-
(1,167)
(1,167)
(13,136)
The Company performs an analysis each year to determine whether the expected future income will more likely than not be sufficient
to realize the deferred tax assets. The Company's recent operating results and projections of future income weighed heavily in the
Company's overall assessment. As a result of this analysis, the Company continues to maintain a full valuation allowance against its
federal and state net deferred tax assets at December 31, 2016 as the Company believes that it is more likely than not that these assets
will not be realized. A portion of the deferred tax liability that was recorded in purchase accounting in the prior year served a source of
future income to support realization of some of its pre-acquisition deferred tax assets. In prior year, the valuation release associated with
realization of the pre-acquisition deferred tax assets resulted in an income tax benefit of approximately $1.1 million to be recorded in
connection with purchase accounting as ASC 805. In the current year, the company maintains a full Valuation Allowance in
consolidation and no separate company deferred tax liability recorded will be recorded.
The tax effects of significant items comprising the Company’s deferred tax assets and (liabilities) as of December 31, 2016 and 2015
are as follows:
Deferred tax assets included in other current assets
Allowances and reserves
Compensation
Valuation allowance on deferred tax assets
Noncurrent deferred tax assets (liabilities) included in other long-term assets:
State net operating loss carryforwards
Federal net operating loss carryforwards
Credit carryforward
State taxes
Property, plant and equipment
Intangible assets
Other reserves - restructuring
Deferred revenue
Valuation allowance on deferred tax assets
Noncurrent deferred tax liabilities, net
F-30
2016
2015
9,715 $
1,292
(11,007)
-
7,338
51,685
250
1,124
1,464
(8,411)
19
4
(53,473)
-
- $
8,458
2,176
(10,634)
-
7,126
46,166
248
1,124
2,350
(10,992)
208
4
(46,234)
-
-
$
$
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
The Company's current deferred tax asset and noncurrent deferred tax liability are included within Other current assets and Other long-
term liabilities, respectively, within the consolidated balance sheet as of December 31, 2016. Federal tax attribute carryforwards at
December 31, 2016, consist primarily of approximately $147.7 million of federal net operating losses. In addition, the Company has
approximately $105.0 million of state net operating losses carryforwards. The utilization of the federal carryforwards as an available
offset to future taxable income is subject to limitations under federal income tax laws. If the federal net operating losses are not
utilized, they begin to expire in 2027, and current state net operating losses not utilized begin to expire this year.
The NOL carry forwards are subject to review and possible adjustment by the Internal Revenue Service and state tax authorities.
During December 2016 through February 2017, the Company executed four equity offerings issuing approximately 3.1 million shares
of common stock. NOL, and tax credit carry forwards may become subject to an annual limitation in the event of certain cumulative
changes in the ownership interest of significant stockholders over a three year period in excess of 50%, as defined under Sections 382
and 383 of the Internal Revenue Code of 1986, as amended, or the Code, as well as similar state tax provisions. This could limit the
amount of NOLs that we can utilize annually to offset future taxable income or tax liabilities. The amount of the annual limitation, if
any, will be determined based on the value of our company immediately prior to an ownership change. Subsequent ownership changes
may further affect the limitation in future years. Additionally, U.S. tax laws limit the time during which these carry forwards may be
applied against future taxes, therefore, we may not be able to take full advantage of these carry forwards for federal income tax
purposes. We are currently evaluating the ownership history of our company to determine if there were any ownership changes as
defined under Section 382(g) of the Code and the effects any ownership change may have had.
A reconciliation of the difference between the federal statutory tax rates and the Company's effective tax rate from continuing
operations is as follows:
Federal statutory rate
State income tax rate, net of Federal tax benefit
Meals and entertainment
Contingent consideration
Goodwill impairment
Valuation allowance
Other non-deductible
Discontinued operations allocation
Net change in Federal and state reserves
Effective tax rate
2016
2015
34.0%
6.0%
(0.3%)
42.4%
-
(78.8%)
(3.3%)
1.9%
-
1.9%
35.0%
2.1%
(0.1%)
6.2%
(12.4%)
(27.7%)
(0.6%)
27.1%
-
29.6%
The following table summarizes the change in uncertain tax benefit reserves for the two years ended December 31, 2016:
Balance of unrecognized benefits as of January 1, 2015
Additions for tax positions related to the current year
Additions for tax positions of prior years
Reductions for tax positions of prior years
Balance as of December 31, 2015
Additions for tax positions related to the current year
Additions for tax positions of prior years
Reductions for tax positions of prior years
Balance as of December 31, 2016
F-31
Unrecognized
Tax Benefits
$
$
$
1,117
—
—
—
1,117
—
—
—
1,117
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
As of December 31, 2016 and 2015, the total amount of gross unrecognized tax benefits was $1.1 million in each year. The total
amount of unrecognized tax benefits that, if recognized, would affect the effective tax rate as of December 31, 2016 and 2015 was $1.1
million in each year.
The Company recognized interest and penalties of $0.2 million related to uncertain tax positions in income tax expense during each of
the years ended December 31, 2016 and 2015. At December 31, 2016 and 2015, accrued interest and penalties, net were $2.6 million
and $2.4 million, respectively, and included in the Other long-term liabilities in the consolidated balance sheets.
The Company and its subsidiaries file a U.S. Federal consolidated income tax return and consolidated and separate income tax returns
in numerous states and local tax jurisdictions. The following tax years remain subject to examination as of December 31, 2016:
Jurisdiction
Federal
State and Local
Tax Years
2013 - 2016
2012 - 2016
To the extent there was a failure to file a tax return in a previous year; the statute of limitation will not begin until the return is filed.
There were no examinations in process by the Internal Revenue Service as of December 31, 2016. In 2014, the Company was selected
for examination by the Internal Revenue Service for the tax periods ending December 31, 2012 and December 31, 2011 that concluded
in 2015.
15. Historical Basic and Diluted Net Loss per Share
On December 28, 2016, the Company effected a one-for-ten reverse split of the issued and outstanding shares of its common stock in
order to achieve the requisite increase in the market price of its common stock to be in compliance with the NASDAQ minimum bid
price requirement. At the effective time of the reverse split, every 10 shares of common stock issued and outstanding were
automatically combined into one share of issued and outstanding common stock, without any change in the par value per share. All
historical share amount shave been adjusted to reflect the split.
A reconciliation of the number of shares used in the calculation of basic and diluted earnings per share for the years ended
December 31, 2016 and 2015 is as follows:
Basic weighted average number of of common shares
Potential dilutive effect of stock-based awards
Diluted weighted average number of common shares
F-32
Years Ended December 31,
2015
2016
1,816
-
1,816
1,548
-
1,548
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
The following outstanding stock-based awards were excluded from the computation of the effect of dilutive securities on loss per share
for the following periods as they would have been anti-dilutive:
Options
Stock-settled stock appreciation rights (SARs)
Restricted stock units (RSUs)
16. Segment Information
Years Ended December 31,
2015
2016
87,871
102,680
102,369
292,920
-
102,680
-
102,680
The accounting policies followed by the Company's molecular diagnostics business are described in Note 1, Nature of Business and
Significant Accounting Policies.
Effective December 31, 2015, the Company has one reporting segment: the Company's molecular diagnostics business, after the
divestiture of its CSO business on December 22, 2015. The Company realigned its reporting segments due to the integration of
RedPath and acquiring certain assets from Asuragen, to reflect the Company's current and going forward business strategy. The
Company's current reporting segment structure is reflective of the way the Company's management views the business, makes operating
decisions and assesses performance. This structure allows investors to better understand Company performance, better assess prospects
for future cash flows, and make more informed decisions about the Company.
The Company's molecular diagnostics business focuses on developing and commercializing molecular diagnostic tests, leveraging the
latest technology and personalized medicine for better patient diagnosis and management. Through the Company's molecular
diagnostics business, the Company aims to provide physicians and patients with diagnostic options for detecting genetic and other
molecular alterations that are associated with gastrointestinal and endocrine cancers, which are principally focused on early detection of
high potential progressors to cancer. Customers in the Company's molecular diagnostics segment consist primarily of physicians,
hospitals and clinics. The service offerings throughout the segment have similar long-term average gross margins, contract terms, types
of customers and regulatory environments. They are promoted through one centrally managed marketing group and the chief operating
decision maker views their results on a combined basis.
17. Long-Term Debt
On October 31, 2014, the Company and its subsidiary, Interpace LLC, entered into an agreement to acquire RedPath (the
“Transaction”). In connection with the Transaction, the Company entered into a the RedPath Note. This RedPath Note was
subsequently exchanged on March 23, 2017. See note 19, Subsequent Events. Accordingly, the RedPath Note has been classified as
long-term debt on the balance sheet with no current portion due.
Originally, the RedPath Note was $11.0 million, interest-free and payable in eight equal consecutive quarterly installments beginning
October 1, 2016. On September 30, the Company and the RedPath Equityholder Representative amended the RedPath Note to extend
the due date of the first installment to November 1, 2016. Effective October 31, 2016, the Company and the RedPath Equityholder
Representative amended the RedPath Note to further extend the due date of the first installment to November 20, 2016. On November
16, 2016, the Company and the RedPath Equityholder Representative amended the RedPath Note to extend the due date of the first
installment to December 31, 2016, to add as an event of default the failure of the Company to maintain a minimum net cash balance
from operations of no less than $400,000, excluding proceeds from borrowed money, at the end of every week and to add a reporting
requirement for the Company to provide to the RedPath Equityholder Representative, on a weekly basis, a 13-week cash flow forecast
commencing November 22, 2016. On December 29, 2016 the Company made the first installment payment under the amended
agreement of approximately $1.3 million. Subsequent payments on the RedPath Note were to be made on the first day of each fiscal
quarter, beginning on April 1, 2017. See Note 19, Subsequent Events for updates to the RedPath Note.
F-33
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
In the second quarter of 2015, the final working capital adjustment was made, reducing the balance of the RedPath Note to
approximately $10.7 million. In December 2015, pursuant to the sale of substantially all of the CSO business, the RedPath Note was
amended so that the CSO sales proceeds would not have to be applied against the RedPath Note payable balance.
The obligations of the Company under the RedPath Note were guaranteed by the Company and its subsidiaries pursuant to a Guarantee
and Collateral Agreement (the “Subordinated Guarantee”) in favor of the RedPath Equityholder Representative. Pursuant to the
Subordinated Guarantee, the Company and its subsidiaries also granted a security interest in substantially all of their assets, including
intellectual property, to secure their obligations to the RedPath Equityholder Representative. Based on the Company's incremental
borrowing rate under its Credit Agreement, the fair value of the RedPath Note at the date of issuance was $7.5 million. During the
years ended December 31, 2016 and 2015, the Company accreted approximately $0.8 million and $0.8 million into interest expense,
respectively, for each period. As of December 31, 2016, the balance of the Note was approximately $7.9 million and the unamortized
discount was $1.4 million.
In addition, the Company entered into the Credit Agreement with SWK Funding LLC (the “Agent”) and the lenders party thereto in
connection with the Transaction in the aggregate principal amount of $20.0 million (the “SWK Loan”). The maturity date of the SWK
Loan was October 31, 2020. The Company received net proceeds of approximately $19.6 million following payment of certain fees
and expenses in connection with the Credit Agreement.
Upon the sale of substantially all of the CSO business on December 22, 2015, the Company used a portion of the net proceeds from the
transaction to pay the balance of the outstanding SWK Loan in the aggregate principal amount of $20.0 million, and an exit fee and
expenses of approximately $1.6 million. In connection with the termination of the Credit Agreement, the Guarantee and Collateral
Agreement, dated October 31, 2014, by the Company and certain of its subsidiaries in favor of the Agent was also terminated on
December 22, 2015.
F-34
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
18. Supplemental Cash Flow Information
The following table represents cash flows provided by (used in) the Company's discontinued operations for the years ended December
31, 2016 and 2015:
Net cash (used in) provided by operating activities of discontinued operations
Net cash provided by investing activities of discontinued operations
For The Years Ended December 31,
2016
2015
$
$
(2,000) $
9,160
- $
26,721
19. Subsequent Events
Equity Offerings
On January 6, 2017, the Company completed a registered direct public offering (the “Second Registered Direct Offering”) to sell
630,000 shares of its common stock at a price of $6.81 per share to certain institutional investors. The Second Registered Direct
Offering resulted in gross proceeds to the Company of approximately $4.2 million. The Company is using the net proceeds from the
Second Registered Direct Offering for working capital, repayment of indebtedness and general corporate purposes.
In addition, the Company granted each institutional investor who participated in the Second Registered Direct Offering the right, for a
period of 15 months following January 6, 2017, or until April 6, 2018, to participate in any public or private offering by the Company
of equity securities, subject to certain exceptions, up to such investor’s pro rata portion of 50% of the securities being offered.
On January 25, 2017, the Company completed a registered direct public offering (the “Third Registered Direct Offering”) to sell
855,000 shares of its common stock and a concurrent private placement (the “Private Placement”) to sell warrants to purchase 855,000
shares of our common stock ( the “Warrants”) to the same investors participating in the Third Registered Direct Offering. The Warrants
and the shares of its common stock issuable upon the exercise of the Warrants were not registered under the Securities Act of 1933, as
amended ( the “Securities Act”) and were sold pursuant to the exemption provided in Section 4(a)(2) under the Securities Act and Rule
506(b) promulgated thereunder. The shares of common stock sold in the Third Registered Direct Offering and the Warrants issued in
the concurrent Private Placement were issued separately but sold together at a combined purchase price of $4.69 per share of common
stock and accompanying Warrant. The Third Registered Direct Offering resulted in gross proceeds to the Company of approximately $4
million. The Company is using the net proceeds from the Third Registered Direct Offering for working capital, repayment of
indebtedness and general corporate purposes, and used approximately $1.0 million to satisfy severance obligations due to five former
senior executives.
On February 3, 2017 the Company completed a confidentially marketed public offering (the “CMPO”) to sell 1,200,000 shares of its
common stock at $3.00 per share with an overallotment option of 9% to certain institutional and retail investors. The Company intends
to use the proceeds from the CMPO for working capital, repayment of indebtedness and liabilities and for general corporate purposes.
F-35
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
Debt Exchange for RedPath Note
On March 23, 2017, the Company entered into an exchange agreement (the “Exchange Agreement”), with an institutional investor
(the “Investor”). Prior to the Company entering into the Exchange Agreement, the Investor acquired the RedPath Note. The
RedPath Note, which was entered into in connection with the Company’s acquisition of RedPath in October 2014, had an aggregate
principal amount of $9.3 million outstanding and was acquired by the Investor for $8.9 million. The RedPath Equityholder
Representative assigned all of its rights, title and interest in the RedPath Note to the Investor, including, but not limited to, its
security interest in all of the assets of the Company and the assets of the Company’s subsidiaries.
Pursuant to the Exchange Agreement, the Company and the Investor agreed to exchange the RedPath Note for (i) a senior secured
convertible note in the aggregate principal amount of $5.3 million (the “Exchanged Convertible Note”), which is convertible into
shares of the Company’s common stock,in accordance with its terms, and (ii) a senior secured non-convertible note with an
aggregate principal amount of $3.6 million (the “Exchanged Non-Convertible Note” and collectively, the “Exchanged Notes”), for
a combined aggregate principal amount of $8.9 million. The Exchanged Notes rank senior to all of the Company’s outstanding and
future indebtedness, other than the indebtedness in favor of the Company’s credit line lender and are secured by a perfected
security interest in all of the existing and future assets of the Company and those of the Company’s subsidiaries. Upon the
reduction of 55% of the aggregate principal amount of each of the Exchanged Notes, the Investor will release its security interest in
its entirety.
The Exchanged Notes mature at 125% of the face value on the fifteenth month anniversary of the closing date, or June 22, 2018,
and bear interest quarterly at one and one hundredth percent (1.01%) per annum (as may be adjusted from time to time). Under the
terms of the Exchanged Notes, the Company has the right to require a redemption of a portion (not less than $500,000) or all of the
applicable Exchanged Notes prior to their maturity at a price equal to 115% of the principal amount of the Exchanged Notes within
the first 180 days of issuance, 120% of the principal amount of the Exchanged Notes between 180 and 270 days of issuance, and
125% of the principal amount of the Exchanged Notes after 270 days of issuance. A mandatory redemption may be required by the
Investor in connection with the occurrence of an event of default or change of control. In each event, the redemption price is
subject to a premium on parity, and the Exchanged Convertible Note redemption may be subject to a premium on parity if certain
unfavorable conditions exist.
The Exchanged Convertible Note is convertible into shares of the Company’s common stock. The Investor may elect to convert all
or a portion of the Exchanged Convertible Note and all accrued and unpaid interest with respect to such portion, if any, into shares
of common stock at a fixed conversion price of $2.44. In the event the Company seeks and obtains stockholder approval to issue
shares of common stock in connection with the conversion of the Exchanged Convertible Note (which determination shall be at the
Company’s sole discretion) from and after the date of the Exchange Agreement, the Exchanged Convertible Note may alternatively
be converted (“Alternative Conversion”) by the Investor at the greater of (i) $0.40 and (ii) lowest of (x) the applicable conversion
price as in effect on the applicable conversion date of the applicable Alternative Conversion, and (y) 88% of the lowest volume-
weighted average price of the common stock during the 10 consecutive trading day period ending and including the date of delivery
of the applicable conversion notice. If the volume-weighted average price of the common stock exceeds 135% of the Fixed
Conversion Price, or $3.29, for five consecutive trading days and no equity conditions failure then exists, the Company has the
option to convert the Exchanged Convertible Note into shares of common stock at the Fixed Conversion Price. The Company shall
not effect the conversion of any portion of the Exchanged Convertible Note, and the Investor shall not have the right to convert any
portion of the Exchanged Convertible Note, to the extent that after giving effect to such conversion, the Investor together with any
other persons whose beneficial ownership of the Company’s common stock could be aggregated with the Investor’s collectively
would be in excess of 9.99% of the shares of common stock outstanding immediately after giving effect to such conversion.
Additionally, any such conversion will be null and void and treated as if never made. As of March 30, 2017, the Investor had
converted approximately 80% of the Exchanged Convertible Note to common stock, converting $4,321,663 of the Exchanged
Convertible Note into 1,730,534 shares of common stock.
In the event the Company seeks and obtains stockholder approval to issue shares of common stock in connection with the
conversion of the Exchanged Convertible Note (which determination shall be at the Company’s sole discretion) from and after the
date of the Exchange Agreement, the Exchanged Convertible Note may alternatively be converted (“Alternative Conversion”) by
the Investor at the greater of (i) $0.40 and (ii) lowest of (x) the applicable conversion price as in effect on the applicable conversion
date of the applicable Alternative Conversion, and (y) 88% of the lowest volume-weighted average price of the common stock
during the 10 consecutive trading day period ending and including the date of delivery of the applicable conversion notice. If the
volume-weighted average price of the common stock exceeds 135% of the Fixed Conversion Price, or $3.29, for five consecutive
trading days and no equity conditions failure then exists, the Company has the option to convert the Exchanged Convertible Note
into shares of common stock at the Fixed Conversion Price. The Company shall not effect the conversion of any portion of the
Exchanged Convertible Note, and the Investor shall not have the right to convert any portion of the Exchanged Convertible Note, to
the extent that after giving effect to such conversion, the Investor together with any other persons whose beneficial ownership of
the Company’s common stock could be aggregated with the Investor’s collectively would be in excess of 9.99% of the shares of
common stock outstanding immediately after giving effect to such conversion. Additionally, any such conversion will be null and
void and treated as if never made.
F-36
Table of Contents
Interpace Diagnostics Group, Inc.
Notes to the Consolidated Financial Statements
(tabular information in thousands, except share and per share data)
The Company entered into an engagement letter with Maxim Group LLC (“Maxim”). Maxim will be paid $150,000 upon issuance
of the Exchanged Notes as a deposit. In the event that the Exchanged Notes are converted on multiple tranches, Maxim will be paid
a cash fee of 6.5% of the New Notes converted on each occasion. However, Maxim will be paid a cash fee of the principal of the
Exchanged Notes being cash redeemed on each occasion and, regardless of any remaining principal amount ,will be paid at least
3.25% at the end of the Exchanged Note term in 15 months.
Termination Agreement
Simultaneously with the consummation of the sale of the RedPath Note to the Investor, on March 22, 2017, the Company and its
subsidiaries entered into a Termination Agreement with the RedPath Equityholder Representative. Under the terms of the
Termination Agreement, RedPath Equityholder Representative agreed to terminate certain royalty and milestone rights
(collectively, the “Royalties”) provided under that certain Contingent Consideration Agreement, dated October 31, 2014, entered
into in connection with the Company’s acquisition of RedPath. In addition, the RedPath Equityholder Representative agreed to
terminate its rights, granted under that certain Agreement and Plan of Merger, dated October 31, 2014, among RedPath, the
Company and certain other parties, to designate an observer to be present in an observer capacity at meetings of the Company’s
board of directors (the “Board Observer Rights”). As consideration for the termination of its Royalties and Board Observer Rights,
the Company agreed to issue warrants (the “RedPath Warrants”) to purchase up to an aggregate of 100,000 shares of the
Company’s common stock to certain former equityholders of RedPath, as designated by the RedPath Equityholder Representative.
The Company has 10 days from the instruction of the RedPath Equityholder Representative to effect the issuance of any RedPath
Warrants. The RedPath Warrants will have an exercise price of $4.69 per share, which is subject to adjustment in the event of
certain stock dividends and distributions, stock splits, stock combinations, reclassifications or similar events affecting the common
stock. The RedPath Warrants will be exercisable at any time on or after the six-month anniversary of the issuance date, or
September 22, 2016 (the “Initial Exercise Date”), and will survive until the fifth anniversary of the Initial Exercise Date.
If at any time the Company grants, issues or sells any instruments that are convertible into or exercisable or exchangeable for
common stock or rights to purchase stock, warrants, securities or other property pro rata to all of the stockholders (the “Purchase
Rights”), then the holder of a RedPath Warrant will be entitled to acquire, on the terms applicable to such Purchase Rights, the
aggregate Purchase Rights which the holder could have acquired if the holder had held the number of shares of common stock
acquirable upon complete exercise of the RedPath Warrant immediately before the date on which a record is taken or otherwise
determined for the grant, issuance or sale of such Purchase Rights. In addition, during such time as the RedPath Warrants are
outstanding, if the Company declares any dividend or other distribution of its assets (or rights to acquire its assets) to all of the
stockholders, by way of return of capital or otherwise (a “Distribution”), then, in each such case, the holder will be entitled to
participate in such Distribution to the same extent that the holder would have participated therein if the holder had held the number
of shares of common stock acquirable upon complete exercise of the RedPath Warrant immediately before the date of which a
record is taken or otherwise determined for participation in such Distribution.
Agreement with Former Senior Executives
Effective January 17, 2017, five former senior executives of the Company each agreed to accept a payment of 35% of the total
severance obligations due to each of them pursuant to their respective separation agreements with the Company, or an aggregate of
approximately $1.0 million, in satisfaction and settlement of an aggregate of approximately $2.9 million in severance payments.
Their agreement was conditioned upon their receipt from the Company of such payments by March 1, 2017. The Company’s
obligation to make such payments was conditioned upon the Company consummating a sufficiently large financing (with gross
proceeds of approximately $4.0 million) and the prior agreement of the Company’s investment banker and investors in such
financing for the use of a portion of such proceeds for such payments. Each of the former senior executives agreed to enter into
releases with the Company at the time of receipt of such payments, and in consideration therefor, releasing the Company and its
directors, officers and agents from any and all claims, losses and damages they have or ever had against the Company and its
directors, officers and agents. As described previously in this note, the financing was obtained and the severance was paid on
February 27, 2017. As the severance payments were contingent on the Company receiving a minimum of $4 million in financing in
2017, the full amount of the severance accrual was maintained at December 31, 2016. The reduction of the liability will be
reflected in the financial statements in the first quarter of 2017.
Brookwood MC Investors, LLC & MCII v, PDI, Inc.
On March 30, 2017, the Company received a tenancy summons and verified complaint for nonpayment of its Parsippany, New
Jersey office rent. The complaint alleges amounts owing of $203,734 covering unpaid base rent of $54,075 from January through
March 2017, as well as late charges, attorneys fees, and the redeposit of a security deposit of $136,975. The plaintiff landlord seeks
judgement for possession of the premises. A hearing in the Superior Court of New Jersey, Morris County-Special Civil part, is
scheduled for April 21, 2017.
F-37
Table of Contents
INTERPACE DIAGNOSTICS GROUP, INC.
VALUATION AND QUALIFYING ACCOUNTS
YEARS ENDED DECEMBER 31, 2016 AND 2015
($ in thousands)
Additions
Description
2015
Allowance for doubtful accounts
Allowance for doubtful notes
Tax valuation allowance
2016
Allowance for doubtful accounts
Allowance for doubtful notes
Tax valuation allowance
Balance at
Beginning Charged to Deductions
Operations
(Reductions)
of Period
Other
(1)
Balance at
end
of Period
$
$
$
$
$
$
-
1,626
55,126
802
1,646
56,868
802
20
-
899
-
-
- $
- $
1,742 $
(1,338) $
- $
7,612 $
802
1,646
56,868
363
1,646
64,480
(1) Includes payments and actual write offs, as well as changes in estimates in the reserves.
F-38
Interpace Diagnostics Group, Inc.
Subsidiaries
Exhibit 21.1
Interpace Diagnostics, LLC, a Delaware limited liability company, is a wholly-owned subsidiary of Interpace Diagnostics Group, Inc.
Interpace Diagnostics Corporation, a Delaware corporation, is a wholly-owned subsidiary of Interpace Diagnostics, LLC.
JS Genetics, Inc., a Delaware corporation, is a wholly-owned subsidiary of Interpace Diagnostics, LLC.
Consent of Independent Registered Public Accounting Firm
Exhibit 23.1
Interpace Diagnostics Group, Inc.
Parsippany, New Jersey
We hereby consent to the incorporation by reference in the Registration Statements on Form S-3 (No. 333-207263) and Form S-8 (No.
333-61231, 333-60512, 333-177969, 333-201070, and 333-214260) of Interpace Diagnostics Group, Inc. of our report dated March 31,
2017, relating to the consolidated financial statements and financial statement schedule, which is included in this Annual Report on Form
10-K. Our report contains an explanatory paragraph regarding the Company’s ability to continue as a going concern.
/s/ BDO USA, LLP
Woodbridge, New Jersey
March 31, 2017
Exhibit 31.1
CERTIFICATION PURSUANT TO SECTION 302
OF THE SARBANES-OXLEY ACT OF 2002
I, Jack E. Stover, certify that:
1.
2.
3.
4.
a.
b.
c.
d.
5.
a.
b.
I have reviewed this Annual Report on Form 10-K for the year ended December 31, 2016 of Interpace Diagnostics Group, Inc.
(the “registrant”);
Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact
necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading
with respect to the period covered by this report;
Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all
material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods
presented in this report;
The registrant's other certifying officer and I are responsible for establishing and maintaining disclosure controls and
procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined
in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have:
Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed
under our supervision, to ensure that material information relating to the registrant, including its consolidated
subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is
being prepared;
Designed such internal control over financial reporting, or caused such internal control over financial reporting to be
designed under our supervision, 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;
Evaluated the effectiveness of the registrant's disclosure controls and procedures and presented in this report our
conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by
this report based on such evaluation; and
Disclosed in this report any change in the registrant's internal control over financial reporting that occurred during the
registrant's most recent fiscal quarter (the registrant's fourth fiscal quarter in the case of annual report) that has
materially affected, or is reasonably likely to materially affect, the registrant's internal control over financial
reporting; and
The registrant's other certifying officer and I have disclosed, based on our most recent evaluation of internal control over
financial reporting, to the registrant's auditors and the audit committee of the registrant's board of directors (or persons
performing the equivalent functions):
All significant deficiencies and material weaknesses in the design or operation of internal control over financial
reporting which are reasonably likely to adversely affect the registrant's ability to record, process, summarize and
report financial information; and
Any fraud, whether or not material, that involves management or other employees who have a significant role in the
registrant's internal control over financial reporting.
Date: March 31, 2017
/s/ Jack E. Stover
Chief Executive Officer
(Principal Executive Officer)
Exhibit 31.2
CERTIFICATION PURSUANT TO SECTION 302
OF THE SARBANES-OXLEY ACT OF 2002
I, James Early, certify that:
1.
2.
3.
4.
a.
b.
c.
d.
5.
a.
b.
I have reviewed this Annual Report on Form 10-K for the year ended December 31, 2016 of Interpace Diagnostics Group, Inc.
(the “registrant”);
Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact
necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading
with respect to the period covered by this report;
Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all
material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods
presented in this report;
The registrant's other certifying officer and I are responsible for establishing and maintaining disclosure controls and
procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined
in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have:
Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed
under our supervision, to ensure that material information relating to the registrant, including its consolidated
subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is
being prepared;
Designed such internal control over financial reporting, or caused such internal control over financial reporting to be
designed under our supervision, 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;
Evaluated the effectiveness of the registrant's disclosure controls and procedures and presented in this report our
conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by
this report based on such evaluation; and
Disclosed in this report any change in the registrant's internal control over financial reporting that occurred during the
registrant's most recent fiscal quarter (the registrant's fourth fiscal quarter in the case of annual report) that has
materially affected, or is reasonably likely to materially affect, the registrant's internal control over financial
reporting; and
The registrant's other certifying officer and I have disclosed, based on our most recent evaluation of internal control over
financial reporting, to the registrant's auditors and the audit committee of the registrant's board of directors (or persons
performing the equivalent functions):
All significant deficiencies and material weaknesses in the design or operation of internal control over financial
reporting which are reasonably likely to adversely affect the registrant's ability to record, process, summarize and
report financial information; and
Any fraud, whether or not material, that involves management or other employees who have a significant role in the
registrant's internal control over financial reporting.
Date: March 31, 2017
/s/ James Early
Chief Financial Officer
(Principal Financial Officer)
CERTIFICATION PURSUANT TO
18 U.S.C. SECTION 1350,
AS ADOPTED PURSUANT TO
SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002
Exhibit 32.1
In connection with the Annual Report of Interpace Diagnostics Group, Inc. (the “Company”) on form 10-K for the fiscal year ended
December 31, 2016 as filed with the Securities and Exchange Commission on the date hereof (the “Report”), I, Jack E. Stover, as Chief
Executive Officer of the Company, certify, pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley
Act of 2002, to the best of my knowledge, that:
(1)
(2)
The Report fully complies with the requirements of section 13(a) or 15(d) of the Securities Exchange Act of 1934, as amended;
and
The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations
of the Company.
Date: March 31, 2017
/s/ Jack E. Stover
Chief Executive Officer
(Principal Executive Officer)
A signed original of this written statement required by Section 906 has been provided to the Company and will be retained by the
Company and furnished to the Securities and Exchange Commission or its staff upon request.
CERTIFICATION PURSUANT TO
18 U.S.C. SECTION 1350,
AS ADOPTED PURSUANT TO
SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002
Exhibit 32.2
In connection with the Annual Report of Interpace Diagnostics Group, Inc. (the “Company”) on form 10-K for the fiscal year ended
December 31, 2016 as filed with the Securities and Exchange Commission on the date hereof (the “Report”), I, James Early, as Chief
Financial Officer of the Company, certify, pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley
Act of 2002, to the best of my knowledge, that:
(1)
(2)
The Report fully complies with the requirements of section 13(a) or 15(d) of the Securities Exchange Act of 1934, as amended;
and
The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations
of the Company.
Date: March 31, 2017
/s/ James Early
Chief Financial Officer
(Principal Financial Officer)
A signed original of this written statement required by Section 906 has been provided to the Company and will be retained by the
Company and furnished to the Securities and Exchange Commission or its staff upon request.