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SenesTech, Inc

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FY2018 Annual Report · SenesTech, Inc
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2018Annual Report

The SenesTech Mission & Vision

SenesTech, Inc. is very much aware of the problems that have developed as a result of worldwide use of poisons to 
try and reduce the issue of rodents and the effect they have on the environment. With this in mind, SenesTech has 
instituted a sustainability planning and governance committee as an internal watchdog to ensure we work towards 
improving our world and not causing more harm to it.

SenesTech’s underlying goals are:

1.  Reduce the harmful effects and dependency on poisons, which historically have not been effective, 

in the world of rodent control through our proven scienti c methods;

2. 

Improve the health, safety, and well-being of humanity worldwide by reducing the negative impact 
of rodents causing diseases, food contamination, and consumption; 

3.  Provide an economic value to our shareholders through the increased use of our products to 

address current rodent issues while expanding our product base to include other opportunities as 
they are presented.

We have broken these goals down into 3 sections: PLANET, PEOPLE, and PROGRESS.

Planet

People

Progress

 • Reduce  the  poison  currently  being  used  (ineffectively)  to  reduce  the  rodent 

population, which accumulates in the soil and our water sources.

 • Reduce the negative impact of poisons on secondary or predatory species that 
consume the poison directly or feed on the target species, this includes accidental 
consumption by humans, often children.

 • As we continue to increase our product demand, we are working (successfully) 
to reduce waste generated and energy used per liter of manufactured product, 
all  while  decreasing  our  COGS.  We  also  both  use  recycled  goods  (of ce  and 
manufacturing) and recon gure manufacturing equipment when possible.

 • With the decreased amount of food consumed or contaminated by rodents (by 
utilizing ContraPest®) the world food shortage/hunger problem can be reduced 
in many nations where humans do not have enough food to feed their population.

 • Rodents  are  responsible  for  the  transfer  of  many  diseases  that  are  harmful  to 
humans, domestic animals, and other food sources. The reduction in rats alone 
will have a positive impact on our general health.

 • Our  employees  are  committed  to  helping  on  a  local  level  with  the  donation  of 
their  time,  money,  and  services  which  are  provided  to  various  community 
organizations. The most recent indication of this was the honor of receiving the 
Flagstaff Volunteer Business of the year for 2018.

 • Our  home  of ce  is  pet-friendly  with  employees  often  bringing  their  pets  (from 
dogs to lizards) to work with them. Many employees enjoy this bene t (especially 
the dogs) and will “make the rounds” to receive treats during the day.

 • At SenesTech, we embrace diversity in our workforce which is also reflected in our 
Board of Directors. The majority of both the Board and of cers are female, and the 
ages of the employees range from their 20’s to 80’s.

•  We continue to work on teaching PMP’s and the general public on the harm that 
poisons have on our society and the planet while providing a scienti cally proven 
alternative to address the rodent problem.

•  With the increased use of ContraPest we can reduce the dependency on harmful 
poisons  and  have  a  measured  increase  in  the  use  and  locations  of  where  the 
product can be deployed.

•  We  will  continue  to  educate  end-users  on  the  scienti c  basis  for  the  need  of 
an alternative to poison through public forums and research papers which was 
started in 2019.

“Non-responsiveness – also 
known colloquially as ‘resistance’ 
– is directly related to current 
practices in rodent control and is 
immediately relevant in Europe 
and the U.S.” 

-Dr. Stephen Shuster
Professor of Invertebrate Zoology at 
Northern Arizona University

Why ContraPest

Rats Love It.

We Keep PMPs Happy.

Customers Will Love It.

 It’s Liquid: 

 Work that Pays Off:

Rats need to consume 10% of 
their body weight in liquid each 
day

 Appealing Bait: 

Our sweet and fatty bait is 
designed to be attractive to rats 
even when other food sources are 
present.

 Combat Bait Aversion: 

Rats do not show adverse affects 
after consuming ContraPest, 
meaning bait aversion is less of 
an issue.

ContraPest minimizes the chance 
of populations rebounding 
after successful treatment, 
giving PMPs con dence that rat 
infestations are under control.

 Versatile Tool:

Can amplify a current IPM 
program or be used as a stand 
alone non-lethal solution.

 Targeted Approach: 

ContraPest does not require 
standardized placement, treat 
only the areas that need it while 
getting successful results.

 Proactive, not Reactive: 
ContraPest targets a source 
of infestations…reproduction, 
treating the entire population, 
not just the individual rat.

 Peace of Mind: 

Studies have shown no behavioral 
changes or illness in rats, 
reducing risk of predation and 
secondary exposure.
 No Accumulation Effect: 

Reduced risk in non-targets due 
to low concentrations of the 
actives and short half life.

To Our Shareholders

2018  established  SenesTech’s  revenue  growth  potential.    Without 
any recent industry models for growing a novel approach to solve the 
global pest-management problem, we began the journey with a new 
concept: non-lethal population control. Our target goal in 2018 was to 
determine the optimal course for our commercialization success.  The 
logical start was to offer ContraPest®, our fertility control tool, to the 
pest-management industry.   The reality quickly emerged that early 
adopters and end-users had a pressing need and therefore demand 
that was ahead of the industry’s adoption timing. With that, we have 
much to discuss in the 2018 annual report.  Here is some background 
on the need for our solution and our approach.

When it comes to rats and rodents, we usually talk about three main 
challenges:

1.  Rodents destroy food through consumption and contamination,

2.  Rats damage infrastructure, and 

3.  Rats transmit disease, deadly pathogens to animals and humans 

and poisons to wildlife.

application  for  the  base  formulation,  to  an  “issued”  patent.    The 
patent issued May 1, 2018. The total process took 6 years of laborious 
explanation and defense.

“Effective  Solutions”  stems  from  the  history  of  rodent  control  and 
pest  management.    For  years,  traditional  rodenticides  have  worked 
short term by killing rats.  However, you can never kill them all and it 
only takes a breeding pair and their young to rebound the population 
with 15,000 individuals over a year.  This rodent reproductive strategy 
provides room for rat infestations to become evident in a short period 
of time (3-4 months).  Due to the principles of sound science, it also 
has been shown that some of the rats that aren’t killed are resistant 
to the poisons and are selected to give birth to rodenticide-resistant 
pups.  Through the development of a fertility control contraceptive, 
we  have  successfully  produced  an  effective  long-term  sustainable 
solution of a non-lethal approach that targets both male and female 
rats. Our recent scienti c publication demonstrates that our solution 
will not lead to resistance and help attenuate the threat of growing 
poison-resistant populations around the world.  

Centuries of trying have shown that reducing the risks by attempting 
to  control  infestations  and  population  growth  using  lethal  means 
cannot solve the problem.  The heart of the problem is reproduction.  
Rats  are  one  of  the  most  successful  mammalian  species  on  earth 
because they can breed their way out of any threat to their species 
survival.  The evidence is clear!

The  task  of  implementing  our  vision  and  addressing  our  mission  is 
not “easy” but the steps are fairly “simple”.  We strive to deliver the 
following:

1.  Reduce harmful effects of current rodent management practices, 
which have historically not been effective, in the world of rodent 
control by addressing the root cause of the problem, reproduction, 
using proven scienti c methods;

2.  Improve the health, safety, and well-being of humanity worldwide 
by  reducing  the  negative  impact  of  rodent  pest  infestations  on 
food security, disease, and the environment;

3.  Provide value to our stakeholders through the increased use of our 
products to address current rodent pest issues while expanding 
our product base to meet the demands of a changing world as they 
are presented;

We intend to accomplish this following our “tag line”
Sound Science.  Effective Solutions.

“Sound Science” is how SenesTech began in 2004, with two scientists 
destined to make a difference in this world.  At the heart of it, Sound 
Science is the methodology of going from a concept that the world’s 
scienti c  community  has  imagined,  to  developing  a  formulation  for 
practical  application.    Since  science  is  ever  evolving,  the  principles 
developed in our viable product allowed us to continuously utilize new 
scienti c discoveries to make the most optimal product for the market 
and  to  solve  our  customers  rodent  problems.    In  2018,  we  moved 
our  scienti c  discovery  (intellectual  property)  from  a  provisional 

Our Mission
SenesTech is committed to providing sustainable, humane treatment 
of  animals,  improving  the  quality  of  all  human  life,  and  enhancing 
environmental stewardship through global application of our effective 
solution in fertility control technology. This statement is our promise 
and  commitment  to  our  stakeholders:  employees,  customers, 
regulators, the public, and our investors.

Our  flagship  product  ContraPest  is  evidence  of  the  value  in  “Sound 
Science.  Effective  Solutions.”    Fertility  control  in  the  form  of  a 
contraceptive is a solution to the root of the problem not a temporary 
strategy  such  as  lethal  rodenticides.  Therefore,  ContraPest,  is  an 
effective long-term solution that dramatically reduces the exponential 
reproduction rate. And the  rst indication of success you can see is 
smaller  numbers  of  recently  weaned  juvenile  rats  that  are  easy  to 
distinguish from much larger adult rats.

ContraPest  is  a  highly  attractive,  liquid  bait  containing  the  active 
ingredients (AI) 4-vinylcyclohexene diepoxide, or VCD, and triptolide, 
a  plant-derived  chemical,  delivered  in  a  proprietary  trade  secret 
emulsion with a high fat content and sweet taste.

•  Rats  repeatedly  feed  on  ContraPest  because  of  the  nutrition 
and taste, and absence of any adverse effects.  Their fertility is 
reduced as they consume the bait. The active ingredients target 
both male and female rodents resulting in sustained contraception 
with continued consumption

•  Sustained  impact  and  compared  to  anticoagulant  rodenticides 

avoid population “rebound” 

•  When lethal means are used, the death rate is always less than 

birth rate for rats

•  Because rats are territorial the immediate reduction of rats around 
any food source provides an open banquet, less competitive food 
supply to new invading rats  

•  Designed to minimize risk to handlers, non-targets and other animals

While  ContraPest  is  a  product  with  wide-ranging  applicability,  2018 
provided the evidence that our commercialization is best focused on 
very speci c verticals: animal housing markets, commercial markets, 
and food markets.

Animal Housing Markets
SenesTech understands the dif cult balance required to manage pests 
in the human-animal conflict in a responsible and safe way. We must 
create  a  balanced  management  strategy  as  we  provide  for  human 
needs  while  at  the  same  time  being  good  stewards  of  our  animal 
populations.    Secondary  exposure  (animals  consuming  poisoned 
rodents) has become an increasing concern with non-target animals, 
especially  in  environments  where  other  animals  or  wildlife  reside.  
SenesTech’s goal has always been to provide a better environment for 
animals, which is why we developed ContraPest. The animal housing 
markets that have speci cally emerged this year are animal research 
facilities,  animal  sanctuaries,  and  zoos.  As  of  this  writing  we  have 
expanded our deployments in more than a dozen zoos, half a dozen 
sanctuaries, and a few research facilities.  

Commercial/Structural Markets
When  commercial  buildings  provide  the  critical  infrastructure  of 
our  economy,  nothing  is  more  essential  than  effectively  managing 
rodent  control  within  these  physical  structures.    However,  building 
management is not the only factor to consider when selecting optimal 
products for  your  rodent  management  program.  Managing the risk 
of exposure is critical to the health and wellbeing of the people who 
work  in  and  around  these  properties.    Additionally,  construction  of 
new  buildings  frequently  displaces  rats  that  migrate  into  adjacent 
properties.  The urban rodent management challenge captures all of the 
issues of commercial buildings and must integrate that management 
with the human pressures of behavior, health, and sanitation.  No one 
deserves to live with rat infestations.  We have been fortunate to have 
been invited into some of the largest and challenging cities of the US 
to  develop  strategies  and  products,  that  ultimately  deliver  the  right 
solution  for  municipalities  and  commercial  business  success  –  all 
while keeping control of daily operations.  Our largest sale to date has 
been to the city of Washington DC with deployment in the  rst of 8 
wards.  Washington DC will indeed be a lead customer and flagship 
deployment.  Toward the end of the quarter we began a small project 
for the city of St. Louis which is expanding in 2019.  The Gateway Arch 
Park and numerous city buildings are included in the expansion.

Food Markets
Today’s consumers have demanded a new emphasis on food safety 
and humane treatment of protein production animals, and the industry 
must answer with newer and better solutions in their facilities.  One 
key  emphasis  area  is  more  effective  vector  control,  and  inspection 
audits  by  regulatory  agencies  and  third-parties.    Rodents  are  an 
increasing health hazard and present a challenge to these industries 
owing to their potential to cause product and  nancial losses.  These 
concerns  are  compounded  by:  the  increasing  global  demand  for 
food,  concerns  for  humane  conditions  for  production  animals,  the 
increasing demands of biosecurity programs and reducing the risk of 
infectious disease transmission.

In 2018, our expected largest geographical market began to open with 
state approval for sales in California. As California is the  fth largest 
economy in the world, the total addressable market begs “all-in” efforts.  
In addition, California is one of the most environmentally conscientious 
states in the US.  Currently, there are 16 municipalities within the state 
that  have  regulations  demanding  a  poison-free  approach  to  rodent 
control.    In  February  of  this  year,  AB1788  was  introduced,  cleared 
in  committee,  and  is  on  the  way  to  become  law  banning  Second 
Generation  Anti-coagulant  Rodenticides  (SAGARs)  statewide.    Our 
pro le  in  the  state  has  been  raised  by  the  discussion  over  this  bill, 
and we are in the  rst quarter of 2019 answering the call to action for 
the many leading stakeholders in California.  In short, we are further 
re ning our market verticals into the California geography.  

While  many  of  these  deployments  were  limited  in  nature,  they  all 
are expected to reach maturity in 2019.  2018 was also a gratifying 
year with respect to the  nancials, as we completed our  rst year of 
commercial launch. Our revenues were $300,000 for the year, a six-
fold  increase  over  2017.  We  hope  that  a  “six-fold”  increase  will  be 
conservative  when  2019  concludes.  We  successfully  transformed 
from  the  “licensing”  business  model  of  a  research  company  to  a 
fully  operating  commercial  company,  while  holding  the  line  on  our 
operating expense. In our manufacturing operation we have increased 
our  ef ciency  “25-fold”  and  improved  our  margin  by  approximately 
16%.  Our strategy encouraged by many of our investors was to build 
the business, identify the target customers, focus on the right market 
at the right time, and as is the culture of our company, “stay the course” 
to open the market to our novel innovation. We also were prudent in 
our capital market activities, not wanting to dilute our shareholders 
unnecessarily.

Corporate Social Responsibility is vital to the growth of our economy 
that is not at the expense of our global values.  The guiding principles 
of our Sustainability planning and governance committee are captured 
in  initiatives  that  focus  on:  PLANET,  PEOPLE,  and  PROGRESS.    Our 
immediate reach will target the problems that have been created as 
a result of the worldwide use of poisons.  Poisons bio-accumulate in 
our environment threatening both humans, animals, our watersheds, 
and the total environment we live in.  Our internal watch-dog strategy 
will ensure our every step works toward improving our world via our 3 
focus points.  The very nature of our product is a giant  rst step and 
2019 will provide more insight for our journey ahead.  

The heart of our corporate social responsibility effort is rooted in the 
people  that  make  up  SenesTech.    Our  employees  are  committed  to 
helping  on  a  local  level  with  the  donation  of  their  time,  money,  and 
services  which  are  provided  to  various  community  organizations, 
ranging  from  Sharon’s  Attic,  Housing  Solutions,  the  Flagstaff  Food 
Bank,  to  High  Country  Puppy  Rescue.    We  were  honored  to  receive 
the  Flagstaff  Volunteer  Business  of  the  year  for  2018  and  hope  we 
have  inspired  other  businesses  to  consider  their  Corporate  Social 
Responsibility.    Look  for  our  2019  CSR  report  to  be  impacting  and 
reflective of “who we are.” 

2018 has been a good year and 2019 holds the promise and clarity of 
a fantastic year. 

D L
Dr. Loretta Mayer

tt M

l Dyer
D Ch
Dr. Cheryl Dyer

“We were thrilled to  nd ContraPest to 
control our rodent population. We’ve seen 
a dramatic reduction in the numbers of 
rodents in our barn. With ContraPest, we 
can just put out the product and over a 
short amount of time, and the rodents 
stop reproducing. We are thrilled 
to have found Senestech!”

- Kim Meagher
Wildhorse Ranch Rescue, Inc

Our Markets

Animal Markets

Commercial Markets

Food Markets

The SenesTech team understands the 
dif cult balance required to manage 
pests in a responsible and safe way 
without compromising the health and 
welfare of the animals in your care. 
Secondary exposure from poisons 
has become an increasing concern 
with non-target animals, especially in 
environments where other animals or 
wildlife reside.

When commercial buildings are the 
core of your business, nothing is more 
essential than effectively managing 
rodent control within the physical 
structures themselves. However, 
building management is not the only 
factor to consider when selecting 
optimal products for your rodent 
management program.

Today’s emphasis on food safety 
has resulted in increased scrutiny 
on manufacturing and processing 
facilities. One facet of this emphasis 
is the move toward more effective 
vector control due to the pressure of 
inspections by regulatory agencies 
and third-party auditors.

The Challenge
n
Rat Reproduction

mating rats can be responsible 
Under ideal conditions, two mating rats can be responsible 
n one year, making it dif cult to 
for 15,000 descendants within one year, making it dif cult to 
maintain control of rat infestations.
ations.

Population growth like this can lead to continued 
an lead to continued 
infrastructure damage and product loss.
roduct loss.

Sound Science.

How it Works
ContraPest is a proven solution!

 Place bait stations in suspected foraging 
locations to deploy SenesTech control bait

 Replace SenesTech control bait with 

ContraPest in con rmed foraging locations.

 Rats consume ContraPest and it reduces their 

fertility.

 Rat populations decrease and ContraPest 

reduces the rebound effect.

 Rat populations continue to decrease and 

fewer bait stations are needed.

 Rat populations are under control and your 

customers are happy!

The Solution
Fertility Control

While there are many ro
While there are many rodent control tools designed to 
bring rat populations down q
bring rat populations down quickly, without fertility control, 
survivors can reproduce, rebounding the population back to its 
survivors can reproduce, reboun
initial size within 3 to 6 months. 
in

ContraPest® is an innovati
ContraPest® is an innovative technology that targets the 
reproductive capab
reproductive capabilities of Norway and roof rats.

Effective Solutions.

Animal Facility
Case Study

ContraPest successfully suppressed rat 
infestations on a 117-acre research facility in 
the southeastern U.S. that is home to sensitive 
wildlife. 

When ContraPest was added to existing protocol, 
the rat activity was reduced by an average of 23%.

Multi-Family Urban House
Case Study

ContraPest successfully suppressed rat 
infestations in a multi-family housing complex 
located in a dense urban area of New York.

With the implementation of ContraPest into the 
IMP program, it allowed the PMP to focus efforts 
on prevention versus battling the infestation.   

“Each year, rats destroy 
approximately 20% of all 
the agricultural products
 in the world.” 

-U.S. Fish & Wildlife Service

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549

–––––––––––––––

FORM 10-K

–––––––––––––––

(Mark One)
(cid:54)

ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the fi scal year ended December 31, 2018

OR

(cid:133)

TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from                to

Commission fi le number: 001-37941

–––––––––––––––
SENESTECH, INC.
(Exact name of registrant as specifi ed in its charter)
–––––––––––––––

Delaware
(State or other jurisdiction of incorporation or organization)

20-2079805
(I.R.S. Employer Identification Number)

3140 N. Caden Court, Suite 1, Flagstaff , AZ 86004
(Address of principal executive offi  ces, including zip code)
Registrant’s telephone number, including area code: (928) 779-4143

Securities registered pursuant to Section 12(b) of the Act:

Title of each class
Common Stock, $0.001 par value

Name of each exchange on which registered
The NASDAQ Stock Market LLC (NASDAQ Capital Market)

Securities registered pursuant to Section 12(g) of the Act: NONE
–––––––––––––––

Indicate by check mark if the registrant is a well-known seasoned issuer, as defi ned in Rule 405 of the Securities Act. Yes (cid:133) No (cid:54)

Indicate by check mark if the registrant is not required to fi le reports pursuant to Section 13 or 15(d) of the Securities Exchange Act. Yes (cid:133) No (cid:54)

Indicate by check mark whether the registrant (1) has fi led all reports required to be fi led 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 fi le such reports), and (2) has been subject to such fi ling requirements for the past 90 
days. Yes (cid:54) No (cid:133)

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T 

(§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such fi les). Yes (cid:54) No (cid:133)

Indicate by check mark if disclosure of delinquent fi lers 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 defi nitive proxy or information statements incorporated by reference in Part III of this Form 10-K or any amendment to this Form 10-K. (cid:54)

Indicate by check mark whether the registrant is a large accelerated fi ler, an accelerated fi ler, a non-accelerated fi ler, a smaller reporting company or an emerging 
growth company. See the defi nitions of “large accelerated fi ler,” “accelerated fi ler,” “smaller reporting company” and “emerging growth company” in Rule 12b-2 of the 
Exchange Act.:

Large accelerated filer (cid:133)

Accelerated filer (cid:133)

Non-accelerated filer (cid:133)

Smaller reporting company (cid:54)

Emerging growth company (cid:54)

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised 

fi nancial accounting standards provided pursuant to Section 13(a) of the Exchange Act. (cid:54)

Indicate by check mark whether the registrant is a shell company (as defi ned in Rule 12b-2 of the Exchange Act). Yes (cid:133) No (cid:54)

Indicate by check mark whether the registrant is a shell company (as defi ned in Rule 12b-2 of the Exchange Act). Yes (cid:133) No (cid:54)

The aggregate market value of the registrant’s common stock held by non-affi  liates on June 29, 2018 (the last business day of the registrant’s most recently completed 
second fi scal quarter) as reported by The NASDAQ Capital Market on such date was approximately $26,395,959. There were 18,040,497 shares of the registrant’s common 
stock outstanding on June 29, 2018.

The number of shares of common stock outstanding as of [March 29], 2019: 23,560,864

Portions of the defi nitive proxy statement to be fi led with the Commission within 120 days of the end of the fi scal year and delivered to stockholders in connection 

with the 2019 Annual Meeting of Stockholders are incorporated by reference into Part III of this Annual Report on Form 10-K.

DOCUMENTS INCORPORATED BY REFERENCE

SENESTECH, INC.
FORM 10-K
TABLE OF CONTENTS

PART I

Item 1
Business  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Item 1A Risk Factors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Item 1B Unresolved Staff Comments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Properties  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Item 2
Legal Proceedings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Item 3
Mine Safety Disclosures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Item 4

PART II

Item 5

Market for Registrant’s Common Equity, Related Stockholder Matters and 

Issuer Purchases of Equity Securities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Item 6
Selected Financial Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Management’s Discussion and Analysis of Financial Condition and Results of Operations . . . . . . . . . .
Item 7
Item 7A Quantitative and Qualitative Disclosures About Market Risk  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Financial Statements and Supplementary Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Item 8
Item 9
Changes in and Disagreements with Accountants on Accounting and Financial Disclosure . . . . . . . . . .
Item 9A Controls and Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Item 9B Other Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

PART III

Item 10 Directors, Executive Officers and Corporate Governance  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Executive Compensation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Item 11
Security Ownership of Certain Beneficial Owners and Management and 
Item 12

Related Stockholder Matters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Item 13 Certain Relationships and Related Transactions, and Director Independence . . . . . . . . . . . . . . . . . . . . .
Principal Accounting Fees and Services . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Item 14

PART IV

Exhibits, Financial Statement Schedules  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Item 15
Item 16
Form 10-K Summary  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
SIGNATURES  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

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i

CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS

This Annual Report on Form 10-K contains “forward-looking statements” within the meaning of the safe-harbor provisions 
of  the  U.S.  Private  Securities  Litigation  Reform Act  of  1995.  Forward-looking  statements  can  often  be  identifi ed  by  words 
such as: “expect,” “believe,” “estimate,” “plan,” “strategy,” “future,” “potential,” “continue,” “may,” “should,” “will,” and similar 
references to future periods. Examples include, among others, statements about:

•  Our commercialization and promotion strategy and plans, including key elements to our business strategy, how we 
commercialize, our sales approach, our areas and markets of focus, our pricing strategy, our strategic relationships and 
which geographic markets we target;

•  The potential market opportunities for commercializing our product candidates and the role we expect ContraPest® 

to hold within the market;

•  Our seeking further regulatory approvals for our product candidates;

•  The anticipated results and eff ects of our products, including those indicated in studies;

•  Our expectations regarding the potential market size for our products;

•  Estimates of our cash fl ow, expenses, capital requirements and need for additional fi nancing;

•  Our ability to enter into strategic arrangements and to achieve the expected results from such arrangements;

•  The initiation, timing, progress and results of fi eld studies and other studies and trials and our research and development 

programs;

•  Our ability to develop and manufacture our products in a commercially effi  cient manner;

•  The scope of protection we are able to obtain and maintain for our intellectual property rights covering our product 

candidates;

•  Our fi nancial performance;

•  Developments and projections relating to our competitors and our industry;

•  Our expectation regarding our pricing strategy and our ability to sell our products at commercially reasonable values;

•  Our beliefs and expectations related to pending litigation; and

•  Our expectation regarding the commercialization of ContraPest and generation of related revenue.

Forward-looking statements are neither historical facts nor assurances about future performance. Instead, they are only 
predictions, based on current beliefs, expectations and assumptions about the future of our business and other future conditions. 
Forward-looking  statements  are  subject  to  known  and  unknown  risks,  uncertainties  and  changes  in  circumstances  that  are 
diffi  cult to predict and many of which are outside of our control. Actual events and results may diff er materially. Therefore, you 
should not rely on any of these forward-looking statements.

Any forward-looking statement made by us in this report is based only on information available to us on the date of this 
report. Except as may be required by law, we undertake no obligation to publicly update any forward-looking statement, whether 
as a result of new information, future developments or otherwise.

Our forward-looking statements can be aff ected by inaccurate assumptions we might make or by known or unknown risks, 
uncertainties and other factors. We discuss many of these risks, uncertainties and other factors in this Annual Report on Form 
10-K in greater detail under the Item 1A — “Risk Factors.” We caution readers that our business and fi nancial performance are 
subject to substantial risks and uncertainties.

ContraPest is a registered trademark of SenesTech Inc. This Annual Report on Form 10-K may also include trademarks and 
trade names owned by other parties, and all other such trademarks and trade names mentioned in this Annual Report on Form 
10-K are the property of their respective owners.

ii

Item 1.  Business.

Overview

PART I

SenesTech,  Inc.  (referred  to  in  this  report  as  “SenesTech,”  the  “Company,”  “we”  or  “us”)  was  formed  in  July  2004  and 
incorporated in the state of Nevada. The Company subsequently reincorporated in the state of Delaware in November 2015. Our 
corporate headquarters is in Flagstaff , Arizona. We have developed and are commercializing a global, proprietary technology 
for managing animal pest populations, initially rat populations, through fertility control.

Although a myriad of tools are available to fi ght rat infestations, communities continue to face challenges in controlling today’s 
infestations.  Infestations  result  in  incredible  infrastructure  damage,  as  well  as  pose  additional  risks  to  the  health  and  food 
security of communities. In addition to these challenges, the pest management industry and Pest Management Professionals 
(PMPs) are being increasingly asked for new solutions to help solve the problem. With growing concerns about rat resistance 
to rodenticides and a growing interest in non-lethal options, it is becoming increasingly important for PMPs to have new tools 
at their disposal. Our goal is to provide customers with not only a solution to combat their most diffi  cult infestations, but also 
off er a non-lethal option to serve customers that are looking to decrease or remove the amount of poison used in their pest 
management programs.

Our fi rst fertility control product, ContraPest, is a liquid bait containing the active ingredients 4-vinylcyclohexene diepoxide 
(VCD) and triptolide. When consumed, ContraPest targets reproduction, limiting fertility in male and female rats beginning 
with  the  fi rst  breeding  cycle  following  consumption.  ContraPest  is  being  marketed  for  use  in  controlling  rat  populations, 
specifi cally Norway and roof rats. On August 23, 2015, the United States Environmental Protection Agency (EPA) granted 
registration  approval  for  ContraPest  as  a  Restricted  Product  Due  to  Professional  Expertise  (referred  to  in  this  report  as  a 
“Restricted Use designation”), eff ective August 2, 2016. On October 18, 2018, the EPA approved the removal of the Restricted 
Use designation. We believe ContraPest is the fi rst and only non-lethal, fertility control product approved by the EPA for the 
management of rodent populations.

In  addition  to  the  EPA  registration  of  ContraPest  in  the  U.S.,  we  must  obtain  registration  from  the  various  state  regulatory 
agencies prior to selling in each state. As of the date of this report, we have received registration for ContraPest in all 50 states 
and the District of Columbia, 23 of which have approved the removal of the Restricted Use designation.

We  expect  to  continue  to  pursue  regulatory  approvals  and  amendments  to  existing  registration  in  the  United  States  for 
ContraPest, and if ContraPest begins to generate suffi  cient revenue, regulatory approvals for any additional jurisdictions beyond 
the United States. The Company also continues to develop other potential additional fertility control and animal health products 
for additional species.

Current Challenges in Pest Control Methodologies

Despite  current  pest  control  methodologies,  ranging  from  sanitation  and  physical  approaches  to  biological  and  chemical 
approaches, rat infestations continue to be a signifi cant problem. While deploying these methodologies can lead to an initial 
decrease in rat populations, rat infestations persist. As these infestations persist, so does the damage associated with them. 
Rodents  cause  signifi cant  damage  to  public  infrastructure  by  undermining  foundations  with  burrowing  and  by  gnawing  on 
electrical wiring and insulation, fi reproofi ng systems and electronic and computer equipment. Rats also pose additional risks to 
the health and food security of communities.

While lethal poisons have been at the forefront of pest management programs to curb these infestations and the associated 
damage, they have not provided consistent, sustained results. This is because rats reproduce at an extremely rapid rate. This 
rapid rate of reproduction can be seen in the “population rebound” that typically follows the initial decline in rodent populations 
that are exposed to lethal poisons. After the initial decline in the infestation, surviving rodents have plentiful food and harborage 
creating conditions in which rats can quickly reproduce. A single pair of rats in the wild can, under ideal breeding conditions, 
contribute over 15,000 progenies in their expected lifespan of 8-12 months. This means that PMPs typically need to visit a site 
often to combat not only the initial infestation, but also subsequent “rebounds.”

1

Additionally, studies have shown that rodents will generally not consume food that they have seen adversely aff ect other rodents, 
which is referred to as “bait shyness.” When the adverse eff ects of lethal products are displayed by rodents, other rodents in 
the vicinity typically avoid the areas where these poisons were located. Finally, there is the potential that rats may develop a 
resistance to certain lethal rodenticides, further contributing to a potential failure of existing pest management approaches. 
Widespread resistance to rodenticides has been identifi ed as a problem in Europe, and recent research indicates this may be 
an  emerging  issue  in  the  U.S.  as  well. This  requires  property  owners  and  PMPs  to  continuously  apply,  on  a  rotating  basis, 
rodenticides that vary in active ingredients and formulations in an eff ort to control these populations without favoring resistance 
to a particular poison.

Integrated Pest Management and Fertility Control

The most eff ective, long-term way to manage rodents is by using a combination of tools that work together to magnify the 
effi  cacy of the pest management protocol. Integrated pest management is based upon this concept. Regulatory agencies and 
industry  experts  recognize  that  fertility  control  is  or  can  be  an  essential  component  of  safe  and  sustainable  integrated  pest 
management.

ContraPest is an innovative technology with an approach that targets the reproductive capabilities of both sexes in rat populations, 
inducing  egg  loss  in  female  rats  and  impairing  sperm  development  in  males.  Our  proprietary  formulation  addresses  key 
biological traits of rats, making it a more targeted solution. Targeting both males and females allows us to drive populations 
down and to sustain that population reduction. Its effi  cacy has been demonstrated in numerous internal and third-party studies.

Using  a  proprietary  bait  delivery  method,  ContraPest  is  dispensed  in  a  highly  palatable  liquid  formulation  that  promotes 
sustained consumption by rat communities, helping keep populations down. Rats require 10% of their body weight in water 
per day, making Contrapest an attractive bait to add to pest management programs. The high fat content and sweet taste leads 
to repeat consumption even among sought after food sources. In both fi eld and laboratory settings, ContraPest was chosen by 
rats even in the presence of abundant water sources and plentiful food options including animal feed, trash, and other options. 
Consumption of ContraPest does not cause illness in rats and therefore it does not change behavior or result in “bait shyness.”

Adding ContraPest to an integrated pest management program allows PMPs to bring the populations down and keep them at a 
more manageable level by preventing reproduction and therefore limiting population rebounds. Knowing the populations are 
lower should allow PMPs to be more focused on preventing future invasions and maintenance instead of continually needing to 
respond to population spikes. ContraPest’s delivery system is designed to minimize handler exposure and is dispensed inside 
tamper-resistant bait stations, minimizing risks to handlers and non-target species.

We believe ContraPest can establish a new paradigm in rodent control, allowing for a decreased reliance on poisons through the 
off ering of a stand-alone non-lethal option, where requested by the customer or required by circumstances.

ContraPest is a versatile tool that can be used as a standalone non-lethal solution or within integrated pest management program 
to help reduce reproduction and magnify the success of integrated infestation control methodologies.

Chemical

ContraPest®

Biological

Physical/Mechanical

Cultural/Sanitation

Prevention

Approved for use in indoor, non-food areas, and outdoors within one foot of a man-made structure, ContraPest gives PMPs 
an integral tool that can be deployed to fi ght rat infestations in a variety of settings. This is particularly important given that 
infested areas may include a diverse set of variables. ContraPest is currently dispensed from a tank and tray, housed inside a 
tamper resistant bait station.

2

Other Applications

We have also begun exploring diverse applications with a variety of collaborators. We have conducted proof of concept studies 
with feral dogs on the Navajo Reservation in New Mexico with a grant from the USDA, and we have collected rabies and 
geographic data on stray dogs in the Tibetan refugee camps of Mainpat, India. We completed a collaboration with Texas A&M 
University in June 2016 to test the potential of our product candidates to manage feral pigs. Studies have also been conducted 
for proof of concept in Australia with wallaby, rat, and mouse populations and in New Zealand with rats and brushtail possums. 
We have also conducted early trials with cats in collaboration with the University of Florida.

These diverse studies seek to provide evidence of the potential for ContraPest and the continued development of fertility control 
technology in general.

Business Strategy

Our  goal  is  to  become  a  leader  in  fertility  control  technology  designed  to  limit  the  adverse  eff ects  of  rodent  infestations, 
including infrastructure damage and risks to our communities’ health and food security. Key elements of our strategy are:

•  Work to maximize market acceptance for, and generate sales of, our products;

•  Manage the infrastructure for sales, marketing and distribution of ContraPest and any other product candidates for 

which we may receive regulatory approval;

• 

• 

Seek additional regulatory approvals for ContraPest and, to the extent we believe there is commercial viability, our 
other product candidates;

Further  develop  our  manufacturing  processes  to  contain  costs  while  being  able  to  scale  to  meet  future  demand  of 
ContraPest and any other product candidates for which we receive regulatory approval;

•  Continue product development of ContraPest and advance our research and development activities and, as our operating 

budget permits, advance the research and development programs for other product candidates;

•  Maintain, expand and protect our intellectual property portfolio; and

•  Add operational, fi nancial and management information systems and personnel, including personnel to support our 

product development and commercialization eff orts and operations as a public company.

3

Manufacturing, Marketing and Distribution

Commercialization Plans

Structural Accounts

National Retailers

Zoos
Animal Sanctuary
Animal Research

Food Production
Food Storage
Ag (Pig)

Hospitality
Theme Parks

Municipalities
Transit

We began to fully commercialize ContraPest and to generate revenue from the sale of ContraPest in the second quarter of 
2018. Our target market segments for ContraPest include structural accounts (multi-family housing); national retailers; zoos 
and animal sanctuaries; food production and agriculture (e.g., meat packing facilities, dairy production plants, vegetable and 
fruit preparation facilities farms, storage facilities and protein production facilities (including cattle, sheep, pig and poultry 
facilities));  hospitality  and  theme  parks  (e.g.,  major  restaurant  chains  and  hotels)  and  municipalities  (e.g.,  subways,  transit 
systems and public housing agencies).

We market ContraPest both to pest management companies and directly to target segments, using a direct PMP sales channel, 
indirectly through distributor sales, and a direct sales force to targeted customer segments. In addition, we have been pursuing 
strategic relationships with large pest management companies and affi  nity groups for the distribution and sale of ContraPest.

Sales Approach

In the U.S., ContraPest is most commonly deployed and serviced by a licensed PMP, although some customers have in house 
pest management service personnel. In some circumstances, customers of pest management services will direct these PMPs to 
use certain products in the provision of their service.

Many of our potential customers purchase their products through a network of distributors. The advantages to us of selling 
through such distributors include:

• 

• 

Immediate availability of a fi eld sales force experienced in selling rodent control products;

Familiarity with our target customers and the challenges they face;

•  Our  fi eld  personnel,  customer  service,  accounts  receivable,  and  shipping  and  handling  teams  can  be  smaller,  thus 

reducing fi xed operational costs; and

•  Less need to substantially expand the sales force as our product gains traction with new customers.

Because of the unique nature of our technology, pest management companies generally have an interest in learning more about 
ContraPest. Consequently, we plan to continue to foster these discussions, to exchange data, and to negotiate agreements with 
carefully selected partners to maximize the appropriate deployment of our product.

We  plan  to  be  deeply  involved  in  the  initial  deployment  of  ContraPest  and  assist  with  in-depth  product  training,  business 
development, and the creation of sales and marketing tools.

4

Third-Party Arrangements

As a result of our sales approach and target markets, we are party to the following arrangements:

Distribution – In the U.S., ContraPest is primarily deployed and serviced by licensed PMPs. These PMPs typically purchase 
their  supplies  through  distributors. Accordingly,  we  have  agreements  with  seven  distributors,  and  intend  to  add  additional 
distributors from time to time. We also have the ability to sell directly to large pest control companies or other entities that 
provide in-house pest control.

Subject  to  obtaining  necessary  regulatory  approvals,  we  plan  to  market  ContraPest  in  additional  international  jurisdictions, 
including Europe. Our expectation is that we will stage these market launches after gaining further success in the United States 
or we fi nd partners to fi nance the cost of the regulatory approval process and launches. However, we have not yet entered into 
any binding agreements related to these matters.

Pricing and Value

Our pricing strategy takes into account the cost of goods sold, the cost of competitive products and the value of our product to 
the end user. We believe ContraPest will be perceived as a signifi cant value as a complement to existing pest control products 
or  as  a  non-lethal  stand-alone  solution  for  managing  rat  infestations  and,  as  such,  should  command  a  premium  price.  Our 
experience is that potential customers understand the advantages of ContraPest and become enthusiastic about its use. We plan 
to continue to use promotional eff orts to support the value message and to justify our product’s premium price, built around the 
following proposed advantages:

•  ContraPest as a proven technology with:

•  A targeted delivery for maximum effi  cacy;

•  A proprietary gravity feeding system that optimizes consumption.

•  ContraPest  can  be  used  as  an  anchor  for  an  integrated  pest  management  program,  or  as  a  stand-alone  solution  to 

decrease reliance on poisons or other lethal options.

•  ContraPest  is  designed,  formulated  and  dispensed  to  be  low  hazard  for  handlers  and  non-targeted  species  such  as 

wildlife, livestock and pets.

We also focus on specifi c advantages for the individual customer and expect to position our product as having the following 
additional general advantages:

• 

• 

Savings by reducing loss or contamination of food inventories;

Savings by reducing damage to infrastructure;

•  Creation of a more predictable cost model based on prevention vs. treatment of spikes in population seen with rebound 

eff ect;

•  Reduction in disease vectors and clean-up costs with reduction of rat carcasses;

• 

Savings in reduction of the use of other integrated pest management protocols as populations decrease with ContraPest 
deployment; and

• 

Public relations advantages when reducing usage of poisons and other lethal products.

Focus Areas & Key Markets

As part of an integrated pest management program, ContraPest can target rat fertility and off er stable population control, to 
combat the most diffi  cult rat infestations and assist in keeping manageable population levels going forward. This can limit the 
rebound eff ect seen with traditional rodent control measures, and with lower population levels in place, PMPs are able to reduce 

5

the number of ContraPest stations to accommodate a lower population, increasing their work fl ow effi  ciency and saving time to 
focus on integrating other integrated pest management tools to focus on prevention and maintenance rather than responding to 
population spikes.

Target  markets  include  specifi c  customers  looking  to  reduce  the  level  of  lethal  poisons  as  part  of  their  pest  management 
program including settings such as zoos, animal sanctuaries and island ecologies. As a stand-alone option, ContraPest can off er 
a non-lethal approach to helping PMPs bring and keep rat populations down.

Raw Materials and Manufacturing Process

ContraPest  contains  two  active  ingredients, VCD,  an  industrial  chemical,  and  triptolide,  a  plant  derived  chemical  from  the 
Thunder God Vine, Tripterygium wilfordii. ContraPest also contains several other inactive ingredients. Currently, we source 
VCD from standard industrial chemical supply providers. Triptolide is derived from the Thunder God Vine, which is commonly 
cultivated and harvested wild in southeastern China and other Asian countries, and is available from a variety of sources. The 
process to purify triptolide for use in ContraPest is expensive, and we are currently investigating other, less costly sources of 
triptolide.

Our manufacturing process involves the incorporation of our two active ingredients, in low concentrations, into several inert 
ingredients. Once incorporated, the entire product goes through a micro-encapsulation process in order to stabilize the fi nal 
formulation. Stabilizing the product in this manner allows it to be delivered to rodents in a non-lethal and eff ective manner.

Currently, we have production scale capability in our facilities in Arizona to manufacture ContraPest. Our internal production 
capabilities allow us to meet our current and anticipated demand during 2019 for ContraPest.

Scientifi c Background Regarding our Product

ContraPest is a liquid bait containing the active ingredients VCD and triptolide. When consumed, ContraPest targets reproduction, 
limiting fertility in male and female rats beginning with the fi rst breeding cycle following consumption.

The female rat is born with a fi nite number of eggs, also called oocytes, and she remains fertile and will reproduce until the 
day she dies. Within the ovary, eggs are contained in structures called follicles. The non-regenerating and most immature stage 
of follicles is called primordial. The primordial follicles mature through several stages from primary to secondary to antral 
follicles and ultimately ovulate. Once the primordial follicles have become depleted, ovarian failure occurs, which terminates 
reproductive capability.

VCD has been well studied and causes specifi c loss of ovarian small follicles (both primordial and primary). Because oocytes 
do not regenerate, loss of these follicles leads to ovarian failure. Following repeated dosing, VCD causes ovarian failure in 
rats. However, daily dosing of rats with VCD does not produce generalized toxicity nor does it aff ect other tissues. A rat that 
consumes VCD will continue to reproduce until the pool of growing follicles are depleted through ovulation or atresia, which 
is the natural removal of follicles, which can take up to three months.

The  second  active  ingredient,  triptolide,  stops  growing  follicles  and  exerts  a  signifi cant  suppression  of  male  fertility  by 
preventing sperm maturation impairing the movement of sperm. Female rats treated with triptolide ovulate fewer eggs because 
the follicles stop growing. Triptolide does not aff ect primordial follicles, but when used in combination with VCD, the result is 
contraception. The combination of VCD and triptolide profoundly eff ects the male.

6

Both VCD and triptolide are supported by evidence regarding their safety and mechanism of action. Additionally, recent studies, 
both in the lab and in the fi eld, have documented their eff ect in fertility reduction and therefore reduction in rat populations. The 
graph below displays the total numbers of pups after two breeding rounds in one study.

170
160
150
140
130
120
110
100
90
80
70
60
50
40
30
20
10
0

s
p
u
P

t
a
R

f
o
r
e
b
m
u
N

Total Number of Rat Pups

154

Control

Group

2

ContraPest

Figure: Total number of rat pups born after consumption of ContraPest. Sixteen female rats (n=8 control and n=8 treatment) 
were provided ContraPest or inactive bait for 15 days and bred with proven male breeders. After two breeding rounds, the 
number of pups was totaled. The bar on the left shows the number of pups born to control females while the bar on the right 
shows the number of pups born to females that consumed ContraPest.

Other Potential Products

We have developed a pipeline of potential additional fertility control and animal health products, with diverse applications, as 
outlined in the following chart and in more detail below. As we focus on the commercialization of ContraPest, only minimal 
progress is expected on new product development during the coming year.

Product Candidate/Area
Feral animal fertility control Pilot study
Non-surgical spay and 
neutering
Boar taint
Animal cancer treatment

Development Status

Segment

Primary Target

Population management

Feral dogs and hogs

Pilot study
Laboratory and initial pilot study Food production and safety
Concept

Companion animal health

Companion animal health

Companion dogs and cats
Boars
Companion dogs

Boar Taint Product Candidate

Boar taint is the off ensive odor or taste that can be evident during the cooking or eating of pork or pork products caused by 
hormones, called pheromones, present in non-castrated boars once they reach puberty. Castration without anesthesia shortly 
after  birth  is  currently  the  standard  procedure  used  to  eliminate  boar  taint,  but  it  results  in  lower  meat  production  due  to 
decreased weight gain, which is an eff ect of castration. This process also introduces a surgical risk of infection and can raise 
safety issues for workers.

If we are successful at developing a boar taint product candidate, we expect that it will target testosterone production and will be 
easily administered to feedlots and will have none of the safety issues associated with castration. The next step will be continued 
scientifi c and fi eld studies followed by submission to and approval by the appropriate regulatory agencies.

7

 
 
 
Feral Animal Fertility Control Product Candidate

Feral dogs and hogs present problems both in the United States and internationally. The negative impacts of feral dogs include 
threats to human health and safety, agriculture, natural resources and property. Feral pigs can be aggressive and are known for 
damaging crops and transmitting diseases to humans, livestock and other wildlife.

Current strategies for controlling feral animal populations are often ineff ective, diffi  cult to conduct and costly. Studies have 
shown that our fertility control technology is eff ective in both these species. Further development on this product candidate is 
on hold, but we intend to pursue this further as resources become available.

Companion Animal Product Candidates

We  would  like  to  develop  the  following  products  for  use  in  companion  animals  such  as  domestic  dogs  and  cats.  However, 
applications for companion animals require FDA approval, which is a much longer and more expensive regulatory process. Our 
expectation is that we will pursue these technologies through research and development arrangements with other stakeholders.

•  Non-Surgical  Spay  and  Neutering  Product  Candidate.  Based  on  a  low  average  of  $100  for  each  spay  or  neuter 
procedure, the spay and neutering of companion animals constitutes a signifi cant market in the United States alone, 
with  few  eff ective  non-surgical  alternatives.  We  are  developing  a  product  that  can  be  easily  administered  to  the 
companion animal orally or by injection in combination with vaccinations. No surgery is required and the surgical 
risks of infection and pain could be eliminated. This product candidate targets the ovaries and testes and is delivered 
through  a  proprietary  drug  delivery  methodology.  Early  fi eld  studies  with  feral  dogs  showed  encouraging  signs  of 
effi  cacy.

•  Animal Cancer Treatment Product Candidate. Cancer therapy for companion animals is often not a viable option since 
chemotherapy can be a long, painful and expensive process. However, we have developed a manufacturing technology 
that allows the chemotherapeutics to be encapsulated and delivered directly to the aff ected tissues without causing the 
side eff ects to the immune, hypothalamic systems or neuro pathways.

Competition

Currently,  we  are  unaware  of  any  other  non-lethal  fertility  control  products  that  target  rodents. There  are  complementary 
products that are used for managing rodent infestations, which include rodenticides, kill devices and traps, as well as other 
integrated pest management approaches such as exclusion and sanitation improvements.

While ContraPest can be used as a non-lethal, stand-alone solution, we also believe that it has a valuable role within a successful 
integrated pest management protocol. By targeting the reproduction of rats, ContraPest can off er a proven solution that allows 
pest managers to reduce even the most challenging rat infestations, helping keep populations down thus enabling them to focus 
their eff orts on complementary techniques.

Government Regulation and Product Approval

Federal, state and local government authorities in the United States regulate, among other things, the testing, manufacturing, 
quality control, approval, labeling, packaging, storage, record-keeping, distribution and marketing of the products we develop. 
Our wildlife and pest fertility control products must be approved by the EPA Offi  ce of Pesticide Programs, or OPP, before 
they  can  be  legally  marketed  and  sold  in  the  United  States. The  process  for  obtaining  regulatory  approval  and  compliance 
with appropriate federal, state and local regulations is rigorous and requires the expenditure of substantial time and fi nancial 
resources.

Additional product candidates in our pipeline may require approval from other government agencies, namely the USDA and 
FDA. In 2015, the FDA and EPA entered into a “data sharing” agreement to streamline data review and speed the regulatory 
process avoiding redundancy where possible, which may facilitate the approval process of our additional product candidates 
with the FDA.

8

United States Review and Approval Processes

In the United States, the EPA regulates the sale, distribution and use of any pesticide under the Federal Insecticide, Fungicide 
and Rodenticide Act, or FIFRA. The EPA’s defi nition of a pesticide includes “any substance or mixture of substances intended 
for preventing, destroying, repelling, or mitigating any pest.” FIFRA defi nes a pest as “any insect, rodent, nematode, fungus, 
or weed.” To register a new product with the EPA, all active ingredients within the product must be registered with the EPA.

The EPA granted registration approval for ContraPest eff ective August 2, 2016. This EPA approval was granted on a restricted-use 
basis, including indoor and limited outdoor use, and is based on a liquid formation. On October 18, 2018, the EPA removed the 
Restricted Use designation. We intend to diligently pursue additional related regulatory approvals from the EPA to support our 
product evolution, including seeking approval for full outdoor use, alternative formulations and for additional rodent species. In 
addition to the EPA registration of ContraPest in the U.S., we must obtain registration from the various state regulatory agencies 
prior to selling in each state. To date, we have received registration for ContraPest in all 50 states and the District of Columbia, 
23 of which have approved the removal of the Restricted Use designation.

International Review and Approval Processes

We  are  researching  potential  additional  international  markets  and  will  evaluate  regulatory  landscapes  of  each  prospective 
market. Country-specifi c regulatory laws have provisions that include requirements for certain labeling, safety, effi  cacy and 
manufacturers’ quality control procedures to assure the consistency of the products, as well as company records and reports. 
Some  specifi c  in-country  studies  will  be  required  for  particular  countries  but  others  will  generally  accept  an  EPA  or  EU 
compliant dossier.

Personnel

As of December 31, 2018, we had 40 full-time, and four part-time employees including a total of two with Ph.D. degrees. Within 
our workforce, 21 employees are engaged in research and development and 23 in sales, business development, fi nance, legal, 
human resources, facilities, information technology and general management and administration.

With more focus on commercialization of ContraPest, we expect certain fi eld support employees currently classifi ed as research 
and development will be refocused on sales and marketing eff orts and thus, reclassifi ed as such.

None of our employees are represented by labor unions or covered by collective bargaining agreements.

Intellectual Property and Other Proprietary Rights

Maintaining a strong position in the rodenticide market requires constant innovation along with a healthy research program 
to evolve product lines to remain competitive and relevant to the needs of the changing global marketplace. We protect the 
intellectual property resulting from these eff orts with the broadest international patent protections available. Our proprietary 
data and trade secrets are protected with vigilance and attention to data exchanges among employees, consultants, collaborators 
and research and trade partners. We further strengthen our market position employing international regulatory expertise.

Patent Filings

Our intellectual property portfolio supporting ContraPest consists of nine international patent fi lings (in the United States, 
Europe,  Canada,  Brazil,  Russia,  Japan,  Mexico,  South  Korea,  and Australia)  addressing  the  ContraPest  compound.  Claims 
directed toward the compound include composition-of-matter involving a diterpenoid epoxide or salts thereof in combination 
with an organic diepoxide, use claims for inducing follicle depletion and for reducing the reproductive capability of a mammalian 
animal or non-human mammalian population. Issued claims will have a patent term extending to 2033 or longer based on patent 
term determinations in each of the fi ling countries. The novelty of ContraPest extends to its method of fi eld distribution and 
has required innovation to perfect the dosing of our product to rodents. We have fi led United States and international patent 
applications covering our novel bait station device to eff ectively and effi  ciently deliver our rodent bait at individual bait sites that 
would, if issued, off er patent term protection through at least 2036.

9

License Agreements

We have an exclusive patent license with the University of Arizona for background intellectual property that we plan to 
employ for future product development in the domestic animal fertility control market. The patent claims in the United States, 
Australia and New Zealand cover the use of 4-vinylcyclohexene diepoxide to deplete ovarian follicles in individual mammals 
and mammal populations. The license agreement, signed in 2005, will terminate with the last-to-expire patent claims, which 
have a term extending to 2026.

Trade Secrets and Trademarks

Beyond our patent right holdings, we broaden our intellectual property position with trademark, trade secret, know-how 
and continuous scientifi c discovery to accompany our product development eff orts. We protect these proprietary assets with 
a  combination  of  confi dentiality  terms  in  all  commercial  agreements  or  stand-alone  confi dentiality  agreements  along  with 
rights-ownership agreements and structured information transfer understandings prior to beginning any collaborative projects. 
We own and maintain the ContraPest trademark and intend to register new trademarks for products from our evolving rodenticide 
product line and for products for mammalian species beyond rodentia.

Data Sets

We  have  exclusive  use  status  with  the  EPA  for  the  data  sets  we  have  developed  and  submitted  to  the  EPA  as  part  of 
our  application  for  ContraPest. The  exclusive  use  status  applies  to  new  active  ingredients  and  the  fi nal  formulation  of  the 
ContraPest product for a period of 10 years. For fi ve years after the 10-year period of exclusivity, if another applicant or the 
EPA Administrator chooses to rely on one or more data sets that we submitted in support of an application submitted by another 
applicant, the new applicant must make a binding off er to compensate us and certify to the EPA that it has done so. If we and 
the off eror cannot reach agreement on the terms of the compensation for the use of such data sets, FIFRA requires resolution by 
binding arbitration. The EPA rules do not describe how the compensation should be determined, and there is publicly available 
information about some, but not all, binding arbitration decisions. See Item 1A, “Risk Factors,” for more information regarding 
our intellectual property and other proprietary rights.

Available Information

We  electronically  fi le  with  the  Securities  and  Exchange  Commission  (“SEC”)  our  Annual  Reports  on  Form  10-K, 
Quarterly Reports on Form 10-Q, Current Reports on Form 8-K and amendments to those reports fi led or furnished pursuant to 
Section 13(a) or 15(d) of the Securities Exchange Act of 1934. We make available on our website at www.senestech.com, free 
of charge, copies of these reports, as soon as reasonably practicable after electronically fi ling such reports with, or furnishing 
them to, the Securities and Exchange Commission. The information contained in, or that can be accessed through, our website 
is not part of, and is not incorporated into, this Annual Report on Form 10-K.

Item 1A.  Risk Factors

As discussed under Item 1 of Part I, “Business — Cautionary Note Regarding Forward-Looking Statements,” our actual 
results could diff er materially from those expressed in our forward-looking statements. Factors that might cause or contribute to 
such diff erences include, but are not limited to, those discussed below. Additional risks and uncertainties not presently known 
to us, or that we currently deem immaterial, may also impair our business operations. If any of the following risks occur, our 
business,  fi nancial  condition,  operating  results,  cash  fl ows  and  the  trading  price  of  our  common  stock  could  be  materially 
adversely aff ected.

10

Risks Relating to our Business

Our future success is dependent on the commercialization of ContraPest and regulatory approval and commercialization of 
our other product candidates.

The  EPA  granted  registration  approval  for  ContraPest  eff ective August  2,  2016  and  as  of  July  12,  2018,  we  have  received 
registration for ContraPest in all 50 states and the District of Columbia. However, we have not yet had meaningful sales of 
ContraPest, which is our only product to date that is available for commercialization and the generation of revenue.

We cannot commercialize our other product candidates in the U.S. without fi rst obtaining regulatory approval for each product 
and each use pattern from the EPA or, if applicable, the Food and Drug Administration, or FDA, and from any related applicable 
state authorities. Before obtaining regulatory approvals for the commercial sale of any product candidate for a target indication, 
the law requires that applicants demonstrate through laboratory and fi eld studies and related data that the product candidate 
will perform its intended function without causing unreasonable adverse eff ects on the environment. The EPA or a comparable 
foreign regulatory authority may require more information, including additional data to support approval that may delay or 
prevent approval.

ContraPest  and  our  other  product  candidates,  if  approved,  may  not  achieve  adequate  market  acceptance  necessary  for 
commercial success

Even following receipt of regulatory approval for ContraPest or future regulatory approval of our other product candidates, such 
products may not gain market acceptance. Market acceptance of any of our product candidates for which we receive approval 
depends on a number of factors, including:

•  The effi  cacy and safety of such product candidates as demonstrated in trials;

•  The uses, indications or limitations for which the product candidate is approved;

•  The potential and perceived advantages of product candidates over alternative or complementary products;

• 

Product labeling or product insert requirements of the EPA or other regulatory authorities;

•  The timing of market introduction of our products as well as future competitive or alternative products;

•  Relative convenience and ease of use;

•  The eff ectiveness of our sales and marketing eff orts and those of our collaborators; and

•  Unfavorable publicity relating to the product.

Depending on the commercial success of ContraPest, we may require additional capital to fund our operations. Failure to 
obtain this necessary capital if needed may force us to delay, limit, or terminate our product development eff orts or other 
operations.

Commercialization of ContraPest and developing further product candidates, including conducting experiments and fi eld studies, 
obtaining  and  maintaining  regulatory  approval  and  commercializing  any  products  approved  for  sale,  is  a  time-consuming, 
expensive and uncertain process that takes years to complete. We expect our expenses to continue to increase in connection 
with our ongoing activities, particularly as we advance our commercialization activities. We plan to substantially expand our 
operations, and as a result of many factors, some of which may be currently unknown to us, our expenses may be higher than 
expected.  Securing  additional  fi nancing  may  divert  our  management  from  their  day-to-day  activities,  which  may  adversely 
aff ect our ability to develop and commercialize our product candidates, including ContraPest. In addition, we cannot guarantee 
that future fi nancing will be available in suffi  cient amounts or on terms acceptable to us, if at all. If we are unable to raise 
additional capital when required or on acceptable terms, we may be required to:

• 

Signifi cantly  delay,  scale  back  or  discontinue  the  development  or  commercialization  of  our  product  candidates, 
including ContraPest;

11

• 

Seek strategic partners for the manufacturing, sales and distribution of ContraPest or any of our other product candidates 
at  an  earlier  stage  than  otherwise  would  be  desirable  or  on  terms  that  are  less  favorable  than  might  otherwise  be 
available; and

•  Relinquish, or license on unfavorable terms, our rights to technologies or product candidates that we otherwise would 

seek to develop or commercialize ourselves.

The occurrence of any of the events described above would have a material adverse eff ect on our business, operating results 

and prospects and on our ability to develop our product candidates.

If we cannot successfully commercialize our products, especially ContraPest, we will not become profi table.

If any of our approved product candidates fail to achieve market acceptance, we will not be able to generate signifi cant revenues, 
which would compromise our ability to become profi table. Furthermore, the commercial success of ContraPest will depend on 
a number of factors, including the following:

•  The development of a commercial organization or establishment of a commercial arrangement with a commercial 

infrastructure;

•  Establishment of a commercially viable pricing;

•  Our ability to manufacture quantities of ContraPest using commercially acceptable processes and at a scale suffi  cient 

to meet anticipated demand and enable us to reduce our cost of manufacturing;

•  Our success in educating end users about the benefi ts, administration, and use of ContraPest;

•  The  eff ectiveness  of  our  own  or  our  potential  strategic  partners’  marketing,  sales  and  distribution  strategy,  and 

operations; and

•  A continued acceptable safety profi le of ContraPest.

Many of these factors are beyond our control. If we are unable to successfully commercialize ContraPest, we may not be able 
to earn suffi  cient revenues to continue our business.

ContraPest is the fi rst product we have marketed, and if we are unable to establish and maintain an eff ective sales force 
and marketing and distribution infrastructures, or enter into and rely upon acceptable third party relationships, we may be 
unable to generate any revenue.

We established and are continuing to develop a fully functional infrastructure for the sales, marketing, and distribution of our 
products and the cost of establishing and maintaining such an infrastructure may exceed the cost-eff ectiveness of doing so. In order 
to market ContraPest and any other products that may be approved by the EPA and comparable foreign regulatory authorities, we 
must continue to build our sales, marketing, managerial and other non-technical capabilities or make arrangements with third 
parties to perform these services for which we would incur substantial costs. If we are unable to establishand maintain adequate 
sales, marketing, and distribution capabilities, whether independently or with third parties, we may not be able to generate additional 
product revenue and may not become profi table. Without an eff ective internal commercial organization or the support of a third 
party to perform sales and marketing functions, we may be unable to compete successfully against more established companies.

Regulatory approval processes of the EPA and comparable foreign regulatory authorities are lengthy, time-consuming and 
unpredictable, and if we are ultimately unable to obtain regulatory approval for our product candidates, our business may fail.

Although we obtained EPA approval for ContraPest in less than one year, the EPA review process for a product with one or more 
new active ingredients typically takes approximately two years to complete and approval is never guaranteed. Our other product 
candidates could fail to receive marketing approval from the EPA or, with respect to ContraPest or our other product candidates, 
from a comparable foreign regulatory authority for many reasons, including:

•  Disagreement over the design or implementation of our trials;

• 

Failure to demonstrate a product candidate is safe;

12

• 

Failure to demonstrate a product candidate’s benefi ts outweigh its risks;

•  Disagreement over our interpretation of data;

•  Disagreement over whether to accept effi  cacy results from trials;

•  The insuffi  ciency of data collected from trials to obtain regulatory approval;

• 

Irreparable or critical compliance issues relating to our manufacturing process; or

•  Changes in the approval policies or regulations that render our data insuffi  cient for approval.

Any of these factors, some of which are beyond our control, could jeopardize our ability to obtain regulatory approval for and 
successfully market any of our product candidates. Any such setback in our pursuit of regulatory approval could have a material 
adverse eff ect on our business and prospects.

Even following receipt of any regulatory approval for ContraPest and our other product candidates, we will continue to face 
extensive regulatory requirements and our products may face future development and regulatory diffi  culties.

Even  following  receipt  of  any  regulatory  approval  for  ContraPest  or  our  product  candidates,  such  products  will  be  subject 
to  ongoing  requirements  by  the  EPA  and  comparable  state  and  foreign  regulatory  authorities  governing  the  manufacture, 
quality control, further development, labeling, packaging, storage, distribution, safety surveillance, import, export, advertising, 
promotion, recordkeeping, and reporting of safety and other post-market information. The safety profi le of any product will 
continue  to  be  closely  monitored  by  the  EPA  and  comparable  foreign  regulatory  authorities  after  approval.  If  the  EPA  or 
comparable foreign regulatory authorities become aware of new safety information after approval of ContraPest or any other 
product candidate, a number of potentially signifi cant negative consequences could result, including:

•  We may be forced to suspend marketing of such product;

•  Regulatory authorities may withdraw their approvals of such product after certain procedural requirements have been 

met;

•  Regulatory authorities may require additional warnings on the label that could diminish the usage or otherwise limit 

the commercial success of such product;

•  The  EPA  or  other  regulatory  bodies  may  issue  safety  alerts,  press  releases,  or  other  communications  containing 

warnings about such product;

•  The EPA may require the establishment or modifi cation of restricted use or a comparable foreign regulatory authority 
may require the establishment or modifi cation of a similar strategy that may, for instance, restrict distribution of our 
product and impose burdensome implementation requirements on us;

•  We may be required to change the way the product is administered or conduct additional trials;

•  We could be sued and held liable for harm caused;

•  We may be subject to litigation or product liability claims; and

•  Our reputation may suff er.

Any of these events could prevent us from achieving or maintaining market acceptance of the particular product candidate, if 
approved, and could signifi cantly harm our business, results of operations and prospects.

Moreover,  existing  government  regulations  may  change  and  additional  government  regulations  may  be  enacted  that  could 
prevent, limit, or delay regulatory approval of ContraPest or any other product candidates. If we are slow or unable to adapt to 
changes in existing requirements or the adoption of new requirements or policies, or if we are not able to maintain regulatory 
compliance, we may lose any marketing approval that we may have obtained and/or be subject to fi nes or enhanced government 
oversight  and  reporting  obligations,  which  would  adversely  aff ect  our  business,  prospects,  and  ability  to  achieve  or  sustain 
profi tability.

13

Even following receipt of any regulatory approval for ContraPest and our other product candidates, we will continue to be 
subject to regulation of our manufacturing processes and advertising practices.

As  a  manufacturer  of  pest  control  products,  we  are  subject  to  continual  government  oversight  and  periodic  inspections  by 
the EPA and other regulatory authorities. If we or a regulatory agency discover problems with a facility where our products 
are  manufactured,  a  regulatory  agency  may  impose  restrictions  on  the  manufacturing  facility,  including  requiring  recall  or 
withdrawal of the product from the market or suspension of manufacturing until certain procedural requirements have been 
met. The occurrence of any such event or penalty could limit our ability to market ContraPest or any other product candidates 
and generate revenue.

In addition, the EPA strictly regulates the advertising and promotion of pest control products, and these pest control products 
may only be marketed or promoted for their EPA approved uses, consistent with the product’s approved labeling. Advertising 
and promotion of any product candidate that obtains approval in the U.S. will be heavily scrutinized by the EPA, other applicable 
state regulatory agencies and the public. Violations, including promotion of our products for unapproved or off -label uses, are 
subject to enforcement actions, inquiries and investigations, and civil, criminal and/or administrative sanctions imposed by the 
EPA.

Failure to obtain regulatory approval in foreign jurisdictions would prevent ContraPest or any other product candidates 
from being marketed in those jurisdictions.

To market and sell our products globally, we must obtain separate marketing approvals and comply with numerous and varying 
regulatory requirements. The approval procedure varies among countries and can involve additional testing. The time required 
to obtain approval may diff er substantially from that required to obtain EPA approval. Obtaining foreign regulatory approvals 
and maintaining compliance with foreign regulatory requirements could result in signifi cant delays, diffi  culties, and cost for us 
and could delay or prevent the introduction of our products in certain countries. Approval by the EPA does not ensure approval 
by regulatory authorities in other countries or jurisdictions, but EPA approval may infl uence decisions by the foreign regulatory 
authority. If we are unable to obtain approval of ContraPest or for any of our other product candidates by regulatory authorities 
in  the  world  market,  the  commercial  prospects  of  that  product  candidate  may  be  signifi cantly  diminished  and  our  business 
prospects could decline.

We have internal manufacturing capabilities to meet our current demand for ContraPest, however, we must develop additional 
manufacturing capability or rely upon third parties to manufacture our products to meet future demand.

Our existing internal manufacturing platform is adequate for meeting our current demand for ContraPest. We may be required 
to spend signifi cant time and resources to expand these manufacturing facilities to fully meet future demand. If we are unable 
to develop full-scale manufacturing capabilities, we may not be able to meet demand of our products without relying on third 
party manufacturers, which could adversely aff ect our operations or fi nancial condition.

We will need to expand our operations and grow the size of our organization, and we may experience diffi  culties in managing 
this growth.

As of December 31, 2018, we had 40 full-time and four part-time employees. As our development and commercialization plans 
and strategies develop, or as a result of acquisitions, we will need additional managerial, operational, sales, marketing, scientifi c, 
fi nancial headcount, and other resources. Our management, personnel, and systems currently in place may not be adequate 
to  support  this  future  growth.  Future  growth  would  impose  signifi cant  added  responsibilities  on  members  of  management, 
including:

•  Managing our trials eff ectively, which we anticipate being conducted at numerous fi eld study sites;

• 

Identifying, recruiting, maintaining, motivating and integrating additional employees with the expertise and experience 
we will require;

•  Managing our internal development eff orts eff ectively while complying with our contractual obligations to licensors, 

licensees, contractors and other third parties;

•  Managing additional relationships with various strategic partners, suppliers, and other third parties;

14

• 

Improving  our  managerial,  development,  operational,  marketing,  production,  and  fi nance  reporting  systems  and 
procedures; and

•  Expanding our facilities.

Our failure to accomplish any of these tasks could prevent us from successfully growing our business.

We depend on key personnel to operate our business. If we are unable to retain, attract, and integrate qualifi ed personnel, 
our ability to develop and successfully grow our business could be harmed.

We  believe  that  our  future  success  is  highly  dependent  on  the  contributions  of  our  signifi cant  employees,  as  well  as  our 
ability to attract and retain highly skilled and experienced sales, research and development, and other personnel in the U.S. 
and  internationally. All  of  our  employees,  including  our  co-founders  (one  of  which  is  also  our  chief  executive  offi  cer),  are 
free to terminate their employment relationship with us at any time, subject to any applicable notice requirements, and their 
knowledge of our business and industry would be diffi  cult to replace. If one or more of our co-founders, executive offi  cers or 
signifi cant employees terminates his or her employment or becomes disabled or experiences long-term illness, we may not be 
able to replace their expertise, fully integrate new personnel or replicate the prior working relationships, and the loss of their 
services might signifi cantly delay or prevent the achievement of our research, development and business objectives. Qualifi ed 
individuals with the breadth of skills and experience in our industry that we require are in high demand, and we may incur 
signifi cant costs to attract them. Many of the other companies that we compete against for qualifi ed personnel have greater 
fi nancial and other resources, diff erent risk profi les, and a more established history in the industry. They also may provide more 
diverse opportunities and better chances for career advancement. Additionally, our facilities are located in Arizona, which may 
make attracting and retaining qualifi ed scientifi c and technical personnel from outside of Arizona diffi  cult. Our failure to attract 
or retain key personnel could impede the achievement of our research, development, and commercialization objectives.

We have not fully designed, implemented or assessed our internal control over fi nancial reporting. If we experience material 
weaknesses in the future or otherwise fail to maintain an eff ective system of internal controls, we may not be able to accurately 
or timely report our fi nancial condition or results of operations, which may adversely aff ect investor confi dence in us and, as 
a result, the value of our common stock.

A material weakness is a defi ciency, or combination of defi ciencies, in internal control over fi nancial reporting such that there 
is a reasonable possibility that a material misstatement of our fi nancial statements will not be prevented or detected on a timely 
basis. There are currently no material weaknesses in our internal controls over fi nancial reporting and we are in the process of 
implementing measures designed to further improve our internal control over fi nancial reporting, including how to remediate 
any identifi ed material weakness in our internal controls, including:

• 

• 

the establishment of formalized accounting policies and procedures and internal controls; and

the implementation of manual and automated controls to support our overall control environment and the segregation 
of duties and procedures.

This annual report does not include an attestation report of the company’s registered public accounting fi rm due to a transition 
period established by rules of the SEC for smaller reporting companies and emerging growth companies. As a result, we have 
not yet fully assessed our internal control over fi nancial reporting and are unable to assure that the measures we have taken to 
date, together with any measures we may take in the future, will be suffi  cient to remediate the control defi ciencies that led to our 
material weaknesses in our internal control over fi nancial reporting, or to avoid potential future material weaknesses.

If we are unable to design and implement an eff ective system of internal control over fi nancial reporting, successfully remediate 
any existing or future material weaknesses in our internal control over fi nancial reporting, or identify any additional material 
weaknesses,  the  accuracy  and  timing  of  our  fi nancial  reporting  may  be  adversely  aff ected,  we  may  be  unable  to  maintain 
compliance  with  securities  law  requirements  regarding  timely  fi ling  of  periodic  reports  and  Nasdaq  listing  requirements, 
investors may lose confi dence in our fi nancial reporting, and our stock price may decline as a result.

15

We may be subject to legal proceedings in the ordinary course of our business that could result in signifi cant harm to our 
business, fi nancial condition and operating results.

We could be subject to legal proceedings and claims from time to time in the ordinary course of our business, including actions 
arising from tort, contract or other claims. See Item 3, “Legal Proceedings,” for more information. Litigation is expensive, 
time consuming, and could divert management’s attention away from running our business. The outcome of litigation or other 
proceedings is subject to signifi cant uncertainty, and it is possible that an adverse resolution of one or more such proceedings 
could result in reputational harm and/or signifi cant monetary damages, injunctive relief or settlement costs that could adversely 
aff ect  our  results  of  operations  or  fi nancial  condition  as  well  as  our  ability  to  conduct  our  business  as  it  is  presently  being 
conducted. Insurance might not cover such claims, might not provide suffi  cient payments to cover all the costs to resolve one 
or more such claims, and might not be available on terms acceptable to us. In addition, regardless of merit or outcome, claims 
brought  against  us  that  are  uninsured  or  underinsured  could  result  in  unanticipated  costs,  which  could  harm  our  business, 
fi nancial condition and operating results and reduce the trading price of our stock.

Product liability lawsuits against us could cause us to incur substantial liabilities and to limit commercialization of any 
products that we may develop.

We face an inherent risk of product liability exposure related to the use of ContraPest and any of our other products. If we cannot 
successfully defend ourselves against claims from our product users, we could incur substantial liabilities. Regardless of merit 
or eventual outcome, liability claims may result in:

•  Decreased demand for any product that we may develop;

•  Termination of fi eld studies or other research and development eff orts;

• 

• 

• 

Injury to our reputation and signifi cant negative media attention;

Signifi cant costs to defend the related litigation;

Substantial monetary awards to plaintiff s;

•  Loss of revenue;

•  Diversion of management and scientifi c resources from our business operations; and

•  The inability to commercialize our product candidates.

We  may  be  unable  to  obtain  commercially  reasonable  product  liability  insurance  for  any  products  approved  for  marketing. 
Large judgments have been awarded in class action lawsuits based on products that had unanticipated side eff ects, including, 
without limitation, any potential adverse eff ects of our products on humans or other species. A successful product liability claim 
or series of claims brought against us, particularly if judgments exceed our insurance coverage, could decrease our cash and 
adversely aff ect our business.

Business or supply chain disruptions could seriously harm our future revenues and fi nancial condition and increase our 
costs and expenses.

Our operations could be subject to a variety of potential business disruptions, including power shortages, telecommunications 
failures,  water  shortages,  fl oods,  fi res,  earthquakes,  extreme  weather  conditions,  medical  epidemics  and  other  natural  or 
manmade  disasters  or  other  interruptions,  for  which  we  are  predominantly  self-insured. We  do  not  carry  insurance  for  all 
categories of risk that our business may encounter. The occurrence of any of these business disruptions could seriously harm 
our  operations  and  fi nancial  condition  and  increase  our  costs  and  expenses.  Moreover,  we  rely  on  various  third  parties  to 
supply various ingredients and other items which are critical for producing our product candidates. Our ability to produce our 
product candidates would be disrupted if the operations of these suppliers are aff ected by a manmade or natural disaster or 
other business interruption. The ultimate impact on our operations from any business interruption impacting us or any of our 
signifi cant suppliers is unknown, but our operations and fi nancial condition would likely suff er adverse consequences. Further, 
any signifi cant uninsured liability may require us to pay substantial amounts, which would adversely aff ect our business, results 
of operations, fi nancial condition, and cash fl ows from future prospects.

16

We are dependent on triptolide, a key ingredient for ContraPest, which has limited sources and must be in a very refi ned 
condition.

If we are unable to develop additional sources of or alternatives to triptolide, a key ingredient for ContraPest, our long term 
ability to produce ContraPest at a cost eff ective price could be in jeopardy. If market demand for triptolide causes the price 
to increase beyond our ability to market at a competitive price or causes the quality of the refi ned ingredient to be less than 
needed for our production, our ability to commercialize ContraPest could be limited or delayed, which would adversely aff ect 
our business, results of operations and fi nancial condition.

A variety of risks associated with marketing our product candidates internationally could materially adversely aff ect our 
business.

We plan to seek regulatory approval of our product candidates outside of the U.S. and, accordingly, we expect that we will be 
subject to additional risks related to operating in foreign countries if we obtain the necessary approvals, including:

•  Diff ering regulatory requirements in foreign countries;

•  Unexpected changes in tariff s, trade barriers, price and exchange controls and other regulatory requirements;

•  Economic weakness, including infl ation or political instability in particular foreign economies and markets;

•  Compliance with tax, employment, immigration and labor laws for employees living or traveling internationally;

• 

• 

Foreign taxes, including withholding of payroll taxes;

Foreign  currency  fl uctuations,  which  could  result  in  increased  operating  expenses  and  reduced  revenue,  and  other 
obligations incident to doing business in another country;

•  Diffi  culties staffi  ng and managing foreign operations;

•  Workforce uncertainty in countries where labor unrest is more common than in the United States;

• 

Potential liability under the U.S. Foreign Corrupt Practices Act of 1977, as amended, or the FCPA, or comparable 
foreign regulations;

•  Challenges enforcing our contractual and intellectual property rights, especially in those foreign countries that do not 

respect and protect intellectual property rights to the same extent as the United States;

• 

Production  shortages  resulting  from  any  events  aff ecting  raw  material  supply  or  manufacturing  capabilities 
internationally; and

•  Business interruptions resulting from geopolitical actions, including war and terrorism.

These  and  other  risks  associated  with  our  international  operations  may  materially  adversely  aff ect  our  ability  to  attain  or 
maintain profi table operations.

We are subject to anti-corruption and anti-money laundering laws with respect to our operations and noncompliance with 
such laws can subject us to criminal and/or civil liability and harm our business.

We are subject to the FCPA, which is the U.S. domestic bribery statute contained in 18 U.S.C. §201, the U.S. Travel Act, the 
USA PATRIOT Act and other anti-bribery and anti-money laundering laws in countries in which we conduct our business. 
Anti-corruption laws are interpreted broadly and prohibit companies and their employees and third-party intermediaries from 
authorizing, off ering or providing, directly or indirectly, improper payments or benefi ts to recipients in the public or private 
sector. As  we  commercialize  our  product  candidates  and  commence  international  sales  and  business,  we  may  engage  with 
collaborators and third-party intermediaries to sell our products internationally and to obtain necessary permits, licenses and 
other  regulatory  approvals. We  or  our  third-party  intermediaries  may  have  direct  or  indirect  interactions  with  offi  cials  and 
employees of government agencies or state-owned or affi  liated entities. We may be found liable for the corrupt or other illegal 
activities of these third-party intermediaries, our employees, representatives, contractors, partners and agents, even if we do not 
explicitly authorize such activities.

17

Noncompliance with anti-corruption and anti-money laundering laws could subject us to whistleblower complaints, investigations, 
sanctions, settlements, prosecution, other enforcement actions, disgorgement of profi ts, signifi cant fi nes, damages, other civil 
and criminal penalties or injunctions, suspension and/or debarment from contracting with certain persons, the loss of export 
privileges, reputational harm, adverse media coverage and other collateral consequences. Responding to any action will likely 
result  in  a  materially  signifi cant  diversion  of  management’s  attention  and  resources  and  signifi cant  defense  costs  and  other 
professional fees.

If we are unable to obtain or protect intellectual property rights, our competitive position could be harmed.

We depend on our ability to protect our proprietary technology. We rely on trade secret, patent, copyright and trademark laws, 
and confi dentiality, licensing, and other agreements with employees and third parties, all of which off er only limited protection. 
Our commercial success will depend in part on our ability to obtain and maintain intellectual property protection in the United 
States and other countries with respect to our proprietary technology and products. Where we deem appropriate, we seek to 
protect our proprietary position by fi ling patent applications in the U.S. and internationally related to our novel technologies 
and products that are important to our business. Patent positions can be highly uncertain, involve complex legal and factual 
questions and be the subject of litigation. As a result, the issuance, scope, validity, enforceability, and commercial value of our 
patents, including those patent rights licensed to us by third parties, are highly uncertain.

The steps we have taken to protect our proprietary rights may not be adequate to preclude misappropriation of our proprietary 
information or infringement of our intellectual property rights, both inside and outside the U.S. The rights already granted 
under any of our currently issued patents and those that may be granted under future issued patents may not provide us with 
the proprietary protection or competitive advantages we are seeking. If we are unable to obtain and maintain protection for 
our technology and products, or if the scope of the protection obtained is not suffi  cient, our competitors could develop and 
commercialize technology and products similar or superior to ours, and our ability to successfully commercialize our technology 
and products may be adversely aff ected.

With  respect  to  patent  rights,  we  do  not  know  whether  any  of  our  pending  patent  applications  for  any  of  our  technologies 
or  products  will  result  in  the  issuance  of  patents  that  protect  such  technologies  or  products,  or  if  our  licensed  patent  will 
eff ectively prevent others from commercializing competitive technologies and products. Our pending patent applications cannot 
be enforced against third parties practicing the technology claimed in such applications unless and until a patent issues from 
such applications. Further, the examination process may require us to narrow the claims for our pending patent applications, 
which may limit the scope of patent protection that may be obtained if these applications issue. Because the issuance of a patent 
is not conclusive as to its inventorship, scope, validity, or enforceability, issued patents that we own or have licensed from third 
parties may be challenged in the courts or patent offi  ces in the U.S. and internationally. Such challenges may result in the loss 
of patent protection, the narrowing of claims in such patents, or the invalidity or unenforceability of such patents, which could 
limit our ability to stop others from using or commercializing similar or identical technology and products, or limit the duration 
of the patent protection for our technology and products. Protecting against the unauthorized use of our patented technology, 
trademarks, and other intellectual property rights, is expensive, diffi  cult, and in some cases, may not be possible. In some cases, 
it may be diffi  cult or impossible to detect third party infringement or misappropriation of our intellectual property rights, even 
in relation to issued patent claims, and proving any such infringement may be even more diffi  cult.

Intellectual property rights do not necessarily address all potential threats to any competitive advantage we may have.

The degree of future protection aff orded by our intellectual property rights is uncertain because intellectual property rights have 
limitations, and may not adequately protect our business, or permit us to maintain our competitive advantage. The following 
examples are illustrative:

•  Others may be able to make compounds that are the same as or similar to our future products but that are not covered 

by the claims of the patents that we own or have exclusively licensed;

•  We might not have been the fi rst to fi le patent applications covering certain of our inventions;

•  Others may independently develop similar or alternative technologies or duplicate any of our technologies without 

infringing on our intellectual property rights;

• 

Issued patents that we own or have exclusively licensed may not provide us with any competitive advantages, or may 
be held invalid or unenforceable, as a result of legal challenges by our competitors;

18

•  Our competitors might conduct research and development activities in the U.S. and other countries that provide a safe 
harbor from patent infringement claims for certain research and development activities, as well as in countries where 
we do not have patent rights and then use the information learned from such activities to develop competitive products 
for sale in our major commercial markets;

•  We may not develop additional proprietary technologies that are patentable; and

•  The patents of others may have an adverse eff ect on our business.

Our technology may be found to infringe third party intellectual property rights.

Third parties may in the future assert claims or initiate litigation related to their patent, copyright, trademark and other intellectual 
property rights in technology that is important to us. The asserted claims and/or litigation could include claims against us, 
our  licensors,  or  our  suppliers  alleging  infringement  of  intellectual  property  rights  with  respect  to  our  product  candidates 
or  components  of  those  products.  Regardless  of  the  merit  of  the  claims,  they  could  be  time  consuming,  resulting  in  costly 
litigation and diversion of technical and management personnel, or require us to develop noninfringing technology or enter into 
license agreements. We cannot assure you that licenses will be available on acceptable terms, if at all. Furthermore, because 
of the potential for signifi cant damage awards, which are not necessarily predictable, it is not unusual to fi nd even arguably 
unmeritorious claims resulting in large settlements. If any infringement or other intellectual property claim made against us by 
any third party is successful, or if we fail to develop noninfringing technology or license the proprietary rights on commercially 
reasonable terms and conditions, our business, operating results, and fi nancial condition could be materially adversely aff ected.

If our product candidates, methods, processes, and other technologies infringe the proprietary rights of other parties, we could 
incur substantial costs and we may have to:

•  Obtain licenses, which may not be available on commercially reasonable terms, if at all;

•  Redesign our product candidates or processes to avoid infringement;

• 

• 

Stop using the subject matter claimed in the patents held by others;

Pay damages; or

•  Defend litigation or administrative proceedings which may be costly whether we win or lose, and which could result 

in a substantial diversion of our fi nancial and management resources.

We  may  need  to  license  intellectual  property  from  third  parties,  and  such  licenses  may  not  be  available  or  may  not  be 
available on commercially reasonable terms.

A third party may hold intellectual property, including patent rights that are important or necessary to the development of our 
product candidates. It may be necessary for us to use the patented or proprietary technology of a third party to manufacture or 
otherwise commercialize our own technology or products, in which case we would be required to obtain a license from such 
third party. Licensing such intellectual property may not be available or may not be available on commercially reasonable terms, 
which could have a material adverse eff ect on our business and fi nancial condition.

Risks Related to our Capital Stock

We have incurred signifi cant operating losses every quarter since our inception and anticipate that we will continue to incur 
signifi cant operating losses in the future.

Investment  in  product  development  is  highly  speculative  because  it  entails  substantial  upfront  capital  expenditures  and 
signifi cant risk that any potential product candidate will fail to demonstrate adequate effi  cacy or an acceptable safety profi le, 
gain regulatory approval, or become commercially viable. To date, we have fi nanced our operations primarily through research 
grants as well as through the sale of equity securities and debt fi nancings. Until August 2, 2016, we did not have any products 
approved by a regulatory authority for marketing or commercial sale, and we have generated minimal revenue from product 
sales to date. We continue to incur signifi cant research, development, and other expenses related to our ongoing operations, 
including sales, marketing, and distribution functionality. As a result, we are not profi table and have incurred losses in every 

19

reporting period since our inception. For the years ended December 31, 2018 and 2017, we reported net losses of $12.2 million 
and $12.3 million, respectively. As of December 31, 2018, we had an accumulated defi cit since inception of $85.8 million.

Since inception, we have dedicated a majority of our resources to the discovery and development of our proprietary product 
candidates. We expect to continue to incur signifi cant expenses and operating losses for the foreseeable future. The size of our 
losses will depend, in part, on the rate of future expenditures and our ability to generate revenues. In particular, we expect to 
incur substantial and increased expenses as we:

•  Attempt to achieve market acceptance for our products;

•  Continue to establish an infrastructure for the sales, marketing and distribution of ContraPest and any other product 

candidates for which we may receive regulatory approval;

• 

Scale up manufacturing processes and quantities to prepare for the commercialization of ContraPest and any other 
product candidates for which we receive regulatory approval;

•  Continue the research and development of ContraPest and our other product candidates, including engaging in any 

necessary fi eld studies;

• 

Seek regulatory approvals for ContraPest in various jurisdictions and for our other product candidates;

•  Expand  our  research  and  development  activities  and  advance  the  discovery  and  development  programs  for  other 

product candidates;

•  Maintain, expand and protect our intellectual property portfolio; and

•  Add operational, fi nancial and management information systems and personnel, including personnel to support our 

clinical development and commercialization eff orts and operations as a public company.

We may encounter unforeseen expenses, diffi  culties, complications, delays, and other unknown factors that may adversely aff ect 
our fi nancial condition. Our prior losses and expected future losses have had, and will continue to have, an adverse eff ect on our 
fi nancial condition. If ContraPest or any other product candidate does not gain suffi  cient regulatory approval, or if approved, 
fails to achieve market acceptance, we may never become profi table. Even if we achieve profi tability in the future, we may not 
be able to sustain profi tability in subsequent periods. Our failure to become and remain profi table would decrease the value of 
our company and could impair our ability to raise capital, expand our business, diversify our product off erings or continue our 
operations. A decline in the value of our company could cause you to lose all or part of your investment.

If we are unable to continue as a going concern, our securities will have little or no value.

We have incurred operating losses since our inception, and we expect to continue to incur signifi cant expenses and operating 
losses for the foreseeable future. If we encounter signifi cant issues or delays in the commercialization of ContraPest, these 
prior losses and expected future losses could have an adverse eff ect on our fi nancial condition, negatively impact our ability 
to fund continued operations, our ability to obtain additional fi nancing in the future and our ability to continue as a going 
concern. There  are  no  assurances  that  such  fi nancing,  if  necessary,  will  be  available  to  us  at  all  or  will  be  available  in 
suffi  cient amounts or on reasonable terms. Our fi nancial statements do not include any adjustments that may result from 
the outcome of this uncertainty. If we are unable to generate additional funds in the future through fi nancings, sales of our 
products, licensing fees, royalty payments, or from other sources or transactions, we will exhaust our resources and will be 
unable to continue operations. If we cannot continue as a going concern, our stockholders would likely lose most or all of 
their investment in us.

Raising additional capital may cause dilution to our existing stockholders, restrict our operations, or require us to relinquish 
rights to our technologies or product candidates.

Until such time, if ever, as we can generate suffi  cient product revenues, we expect to fi nance our cash needs primarily through 
the sale of equity securities, debt fi nancings, credit facilities and government and foundation grants. We may also seek to raise 
capital through third party collaborations, strategic alliances and similar arrangements. We currently do not have any committed 
external source of funds. Raising funds in the future may present additional challenges and future fi nancing may not be available 

20

in suffi  cient amounts or on terms acceptable to us, if at all. The terms of any fi nancing arrangements we enter into may adversely 
aff ect the holdings or the rights of our stockholders and the issuance of additional securities by us, or the possibility of such 
issuance, may cause the market price of our shares to decline.

Certain of our outstanding warrants contain provisions that impose limitations on our ability to participate in certain variable 
rate  transactions,  including  at-the-market  transactions,  which  may  limit  our  opportunities  to  obtain  fi nancing  in  suffi  cient 
amounts or on acceptable terms. The sale of additional equity or convertible debt securities would dilute all of our stockholders, 
and if such sales occur at a deemed issuance price that is lower than the current exercise price of our outstanding warrants sold 
to investors in November 2017, the exercise price for those warrants would adjust downward to the deemed issuance price 
pursuant to price adjustment protection contained within those warrants.

The incurrence of indebtedness through credit facilities would result in increased fi xed payment obligations and, potentially, 
the imposition of restrictive covenants. Those covenants may include limitations on our ability to incur additional debt, making 
capital expenditures or declaring dividends, and may impose limitations on our ability to acquire, sell, or license intellectual 
property rights and other operating restrictions that could adversely impact our ability to conduct our business.

If  we  raise  additional  funds  through  collaborations,  strategic  alliances,  or  licensing  arrangements  or  other  marketing  or 
distribution  arrangements  with  third  parties,  we  may  have  to  relinquish  valuable  rights  to  our  technologies,  future  revenue 
streams, research programs or product candidates, or grant licenses on terms that may not be favorable to us. If we are unable 
to expand our operations or otherwise capitalize on our business opportunities, our business, fi nancial condition and results of 
operations could be materially adversely aff ected.

If we are unable to raise additional funds through equity or debt fi nancings when needed, we may be required to delay, limit, 
reduce or terminate our product development or commercialization eff orts, or grant others rights to develop and market product 
candidates that we would otherwise prefer to develop and market ourselves.

Our  share  price  may  be  volatile,  which  could  subject  us  to  securities  class  action  litigation  and  your  investment  in  our 
securities could decline in value.

Our stock could be subject to wide fl uctuation in response to many risk factors listed in this section, and others beyond our 
control, including:

•  Market acceptance and commercialization of our products;

•  Our being able to timely demonstrate achievement of milestones, including those related to revenue generation, cost 

control, cost eff ective source supply, and regulatory approvals;

•  Our ability to remain listed on the Nasdaq Capital Market;

•  Results and timing of our submissions with the regulatory authorities;

• 

Failure or discontinuation of any of our development programs;

•  Regulatory developments or enforcements in the United States and non-U.S. countries with respect to our products or 

our competitors’ products;

• 

Failure to achieve pricing acceptable to the market;

•  Regulatory actions with respect to our products or our competitors’ products;

•  Actual or anticipated fl uctuations in our fi nancial condition and operating results, or our continuing to sustain operating 

losses;

•  Competition from existing products or new products that may emerge;

•  Announcements  by  us  or  our  competitors  of  signifi cant  acquisitions,  strategic  arrangements,  joint  ventures, 

collaborations, or capital commitments;

• 

Issuance of new or updated research or reports by securities analysts;

21

•  Announcement  or  expectation  of  additional  fi nancing  eff orts,  particularly  if  our  cash  available  for  operations 

signifi cantly decreases or if the fi nancing eff orts result in a price adjustment to certain outstanding warrants;

• 

• 

Fluctuations in the valuation of companies perceived by investors to be comparable to us;

Share price and volume fl uctuations attributable to inconsistent trading volume levels of our shares;

•  Additions or departures of key management or scientifi c personnel;

•  Disputes or other developments related to proprietary rights, including patents, litigation matters, and our ability to 

obtain patent protection for our technologies;

•  Entry by us into any material litigation or other proceedings;

• 

Sales of our common stock by us, our insiders, or our other stockholders;

•  Exercise of outstanding warrants;

•  Market conditions for equity securities; and

•  General economic and market conditions unrelated to our performance.

Furthermore, the capital markets can experience extreme price and volume fl uctuations that may aff ect the market prices of 
equity securities of many companies. These broad market and industry fl uctuations, as well as general economic, political, 
and market conditions such as recessions, interest rate changes, or international currency fl uctuations, may negatively impact 
the  market  price  of  shares  of  our  common  stock.  In  addition,  such  fl uctuations  could  subject  us  to  securities  class  action 
litigation, which could result in substantial costs and divert our management’s attention from other business concerns, which 
could seriously harm our business. You may not realize any return on your investment in us and may lose some or all of your 
investment.

An active market in the shares may not continue to develop in which investors can resell our common stock.

We cannot predict the extent to which an active market for our common stock will continue to develop or be sustained, or how 
the development of such a market might aff ect the market price for our common stock. Market conditions in eff ect at the time 
you acquire our stock may not be indicative of the price at which our common stock will trade in the future. Investors may not 
be able to sell their common stock at or above the price they acquired it.

If  securities  or  industry  analysts,  or  other  sources  of  information,  do  not  publish  research,  or  publish  inaccurate  or 
unfavorable research or other information about our business, our stock price and trading volume could decline.

The trading market for our common stock may depend on the research, reports and other information that securities or industry 
analysts, or other third party sources of information, publish about us or our business. We do not have any control over these 
analysts or other third party sources of information. From time to time inaccurate or unfavorable research or other information 
about our business, fi nancial condition, results of operations and stock ownership may be published. We cannot assure that 
analysts will cover us or provide favorable coverage. If one or more of the analysts who cover us downgrade our stock or change 
their opinion of our stock, our share price could decline. If one or more of these analysts cease coverage of us or fail to regularly 
publish reports on us, we could lose visibility in the fi nancial markets, which could cause our stock price or trading volume to 
decline. If incorrect or misleading information is disseminated publicly by third parties about us, our stock price could decline.

Future sales, or the possibility of future sales, of a substantial number of our common shares could adversely aff ect the price 
of the shares and dilute stockholders.

Future sales of a substantial number of shares of our common stock, or the perception that such sales will occur, could cause 
a decline in the market price of our common stock. This is particularly true if we sell our stock at a discount. As of March 25, 
2019, we had 3,181,841 shares of our common stock subject to outstanding warrants that contain anti-dilution adjustments 
that provide for an adjustment to the exercise price for certain dilutive issuances of securities. If we off er or issue additional 
securities  at  a  deemed  price  lower  than  the  current  exercise  price  of  these  outstanding  warrants,  these  warrants  will  adjust 

22

pursuant to the price adjustment protection contained within these warrants. For example, our Rights Off ering during 2018 
resulted in an additional downward adjustment of the exercise price of these warrants from $1.50 per share to $0.95 per share. 
Any future issuance of common stock or securities convertible or exercisable into our common stock could cause a further 
downward adjustment of the exercise price of these warrants to the deemed issuance price if the issuance price is less than the 
exercise price of the warrants at the time of the new issuance.

Also, in the future, we may issue additional shares of our common stock or other equity or debt securities convertible into 
common stock in connection with a fi nancing, acquisition, litigation settlement, employee arrangements, or otherwise. Any 
such  issuance  could  result  in  substantial  dilution  to  our  existing  stockholders  and  could  cause  our  common  share  price  to 
decline.

In connection with our Rights Off ering, each of our directors and offi  cers was subject to certain lock-up agreements that expired 
in November 2018. Also in connection with our Rights Off ering, we sold 5,357,052 shares of common stock, which are generally 
not subject to lock-up agreements and may be sold by the holder at any time, and warrants to purchase 5,357,052 shares of 
common stock, which are exercisable immediately by the holder. If these stockholders sell substantial amounts of common 
shares in the public market, or if the market perceives that such sales may occur, the market price of our common shares and our 
ability to raise capital through an issue of equity securities in the future could be adversely aff ected.

We may not be able to comply with all applicable listing requirements or standards of The NASDAQ Capital Market and 
NASDAQ could delist our common stock.

Our common stock is listed on the Nasdaq Capital Market. In order to maintain that listing, we must satisfy minimum fi nancial 
and other continued listing requirements and standards. On January 3, 2018, we received a defi ciency letter from the listing 
qualifi cations staff  of the Nasdaq Stock Market, notifying us that, for the prior 30 consecutive business days, the closing bid 
price of our common stock was not maintained at the minimum required closing bid price of at least $1.00 per share as required 
for continued listing on the Nasdaq Capital Market. In accordance with Nasdaq Listing Rules, we had an initial compliance 
period of 180 calendar days, until July 2, 2018, to regain compliance with this requirement. On June 5, 2018, we received notice 
from the listing qualifi cations staff  of the Nasdaq Stock Market, notifying us that the closing bid price of our common stock 
was greater than $1.00 per share for ten consecutive business days and that we had regained compliance with the minimum bid 
price requirement.

On  September  26,  2018,  we  received  a  defi ciency  letter  from  the  listing  qualifi cations  staff   of  the  Nasdaq  Stock  Market, 
notifying us that, for the prior 30 consecutive business days, the closing bid price of our common stock was not maintained 
at the minimum required closing bid price of at least $1.00 per share as required for continued listing on the Nasdaq Capital 
Market. In accordance with Nasdaq Listing Rules, we had an initial compliance period of 180 calendar days, until March 25, 
2019, to regain compliance with this requirement. On March 20, 2019 we received notice from the listing qualifi cations staff  of 
the Nasdaq Stock Market, notifying us that the closing bid price of our common stock was greater than $1.00 per share for ten 
consecutive business days and that we had regained compliance with the minimum bid price requirement.

We cannot provide any assurance that our stock price will maintain the minimum bid price requirements of Nasdaq or that 
we will be able to satisfy any other continued listing requirement of the Nasdaq Stock Market. In the event that our common 
stock is not eligible for quotation on another market or exchange, trading of our common stock could be conducted in the 
over-the-counter market or on an electronic bulletin board established for unlisted securities such as the Pink Sheets or the OTC 
Bulletin Board. In such event, it could become more diffi  cult to dispose of, or obtain accurate price quotations for, our common 
stock, and there would likely be a reduction in our coverage by security analysts and the news media, which could cause the 
price of our common stock to decline further. In addition, it may be diffi  cult for us to raise additional capital if we are not listed 
on a major exchange.

Our corporate documents and Delaware law and certain warrants contain provisions that could discourage, delay or prevent 
a change in control of our company.

Provisions in our certifi cate of incorporation and our amended and restated bylaws may discourage, delay or prevent a merger 
or acquisition involving us that our stockholders may consider favorable. For example, our certifi cate of incorporation currently 
provides for a staggered board of directors, whereby directors serve for three-year terms, with approximately one-third of the 
directors coming up for reelection each year. Having a staggered board will make it more diffi  cult for a third party to obtain 
control of our board of directors through a proxy contest, which may be a necessary step in an acquisition of us that is not 

23

favored by our board of directors. Additionally, warrants we issued in November 2017 and June 2018 and the warrants included 
in the units issuable in the Rights Off ering provide a Black Scholes value based payment in connection with certain transactions 
that may discourage, delay or prevent a merger or acquisition. We may issue additional warrants with similar terms.

We  are  also  subject  to  the  anti-takeover  provisions  of  Section  203  of  the  Delaware  General  Corporation  Law.  Under  these 
provisions, if anyone becomes an “interested stockholder,” we may not enter into a “business combination” with that person 
for three years without special approval, which could discourage a third party from making a takeover off er and could delay or 
prevent a change of control. For purposes of Section 203, “interested stockholder” means, generally, someone owning 15% or 
more of our outstanding voting stock or an affi  liate of ours that owned 15% or more of our outstanding voting stock during the 
past three years, subject to certain exceptions as described in Section 203.

We are an “emerging growth company” as that term is used in the JOBS Act, and we intend to take advantage of reduced 
disclosure and governance requirements applicable to emerging growth companies, which could result in our common stock 
being less attractive to investors and adversely aff ect the market price of our common stock or make it more diffi  cult to raise 
capital as and when we need it.

We  are  an  “emerging  growth  company”  as  that  term  is  used  in  the  JOBS Act,  and  we  intend  to  take  advantage  of  certain 
exemptions from various reporting requirements that are applicable to other public companies that are not emerging growth 
companies including, but not limited to, not being required to comply with the auditor attestation requirements of Section 404 
of  the  Sarbanes-Oxley  Act,  reduced  disclosure  obligations  regarding  executive  compensation  in  our  periodic  reports  and 
proxy statements, exemptions from the requirements of holding a nonbinding advisory vote on executive compensation and 
stockholder approval of any golden parachute payments not previously approved, and exemptions from any rules that the Public 
Company Accounting Oversight Board may adopt requiring mandatory audit fi rm rotation or a supplement to the auditor’s 
report  on  the  fi nancial  statements. We  currently  intend  to  take  advantage  of  some  of  the  reduced  regulatory  and  reporting 
requirements that will be available to us under the JOBS Act, so long as we qualify as an “emerging growth company.” For 
example, so long as we qualify as an “emerging growth company,” we may elect not to provide you with certain information, 
including certain fi nancial information and certain information regarding compensation of our executive offi  cers, that we would 
have otherwise been required to provide in fi lings we make with the SEC, which may make it more diffi  cult for investors and 
securities analysts to evaluate us.

Because of the exemptions from various reporting requirements provided to us as an “emerging growth company,” we may be 
less attractive to investors and it may be diffi  cult for us to raise additional capital as and when we need it. We may take advantage 
of these reporting exemptions until we are no longer an emerging growth company, which in certain circumstances could be for 
up to fi ve years. If some investors fi nd our common stock less attractive as a result, there may be a less active trading market 
for our common stock and our stock price may be more volatile. Investors may be unable to compare our business with other 
companies in our industry if they believe that our fi nancial accounting is not as transparent as other companies in our industry. 
If we are unable to raise additional capital as and when we need it, our business, results of operations, fi nancial condition and 
cash fl ows, and future prospects may be materially and adversely aff ected.

Item 1B.  Unresolved Staff  Comments.

Not applicable

Item 2.  Properties.

As of December 31, 2018, our corporate headquarters is located in Flagstaff , Arizona, where we lease and occupy 17,797 
square feet of offi  ce and industrial space pursuant to a lease that commenced on December 20, 2011 and expires on December 31, 
2019. Our manufacturing facility is located within our corporate headquarters, occupying 4,865 square feet of the total space. 
We believe that we will be able to extend this lease or relocate to nearby facilities.

On November 16, 2016, we leased an additional 1,954 square feet of research and development space, also in Flagstaff , 
Arizona. This lease expired on November 15, 2018 and was extended for 24 months, through November of 2020. We believe 
that our existing facilities are adequate and meet our current needs for business, manufacturing and research.

24

Item 3.  Legal Proceedings.

On February 20, 2018, New Enterprises, Ltd. (“New Enterprises”), fi led lawsuit against the Company and Roth Capital 
Partners, LLC (“Roth”) in the U.S. District Court for the District of Arizona (the “Court”). The complaint alleges nine counts 
against the Company, including that: the Company engaged in common law fraud and securities fraud to induce the chairman 
of  New  Enterprises  into  investing  in  the  Company;  failed  to  register  New  Enterprises’  requested  transfer;  breached  stock 
certifi cates and the lock-up contract; tortuously interfered with prospective business advantage; and conversion. New Enterprises 
is seeking monetary damages, including compensatory damages, punitive damages, and attorney’s fees. On April 23, 2018, the 
Company moved to dismiss each of the claims alleged against the Company, and on May 18, 2-18, Roth moved to dismiss each 
of the claims alleged against it. The motions to dismiss were fully briefed, the Court issued an order granting the motions to 
dismiss, dismissing each of the claims alleged in the Complaint but allowed New Enterprises to fi le a motion for leave to fi le an 
Amended Complaint seeking to cure the defi ciencies in its claims. On January 25, 2019, New Enterprises moved for leave to fi le 
an amended complaint, alleging similar claims against the Company and Roth. The Company and Roth have fi led oppositions to 
New Enterprises’ motion, New Enterprises fi led its reply, and the motion is currently under advisement with the Court. Roth has 
made a claim for indemnifi cation to the Company based on contractual indemnifi cation agreements, but to date, the Company 
has not accepted Roth’s indemnifi cation demand.

On April 20, 2018, the Company’s former Executive Vice President and Chief Operating Offi  cer Andrew Altman fi led a 
charge of employment discrimination with the Equal Employment Opportunity Commission (EEOC) against the Company. 
Mr. Altman claimed that he was terminated after he expressed opposition to an email Cheryl Dyer, Chief Research Offi  cer, had 
sent out to the management team, in which she criticized a Mormon newspaper. The Company fi led a position statement on 
May 21, 2018. No substantive action has been taken since then, and the Company has not heard anything further either from 
the EEOC or Mr. Altman’s attorneys.

Item 4.  Mine Safety Disclosures.

Not applicable.

25

PART II

Item 5.  Market for Registrant’s 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 symbol “SNES.” Our common stock was initially 

listed for trading on the NASDAQ Capital Market on December 8, 2016

Holders

As of March 28, 2019, there were approximately 626 holders of record of our common stock. Because many shares of our 
common stock are held by brokers and other institutions on behalf of stockholders, we are unable to determine the total number 
of benefi cial owners represented by these holders of record.

Dividends

We have never declared or paid any cash dividends on our common stock. We currently intend to retain all available funds 
and any future earnings to support our operations and fi nance the growth and development of our business. We do not intend 
to pay cash dividends on our common stock for the foreseeable future. Any future determination related to our dividend policy 
will be made at the discretion of our board of directors and will depend upon, among other factors, our results of operations, 
fi nancial condition, capital requirements, contractual restrictions, business prospects and other factors our board of directors 
may deem relevant.

Recent Sales of Unregistered Securities

None.

Purchases of Equity Securities by the Company

We withhold (repurchase) shares of common stock in connection with the vesting of restricted shares to satisfy required 
tax withholding obligations. The following table sets forth information regarding purchases of our equity securities during the 
three months ended December 31, 2018:

(a)
Total number 
of shares 
purchased(1)

(b)
Average price 
paid per 
share(1)

— $ 
— $ 
17,375 $ 
17,375 $ 

—
—
0.70
0.70

(c)
Total number 
of shares 
purchased as 
part of publicly 
announced 
plans or 
programs

(d)
Approximate 
dollar value 
of shares that 
may yet be 
purchased 
under the plans 
or programs

— $ 
— $ 
— $ 
— $ 

—
—
—
—

Period
October 1, 2018 to October 31, 2018 . . . . . . . . . . . . .
November 1, 2018 to November 30, 2018  . . . . . . . . .
December 1, 2018 to December 31, 2018 . . . . . . . . . .
Total  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

(1)  Fully vested shares of common stock withheld (purchased) by us in satisfaction of required withholding tax liability upon 

vesting of restricted stock.

Item 6.  Selected Financial Data.

Not applicable.

26

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 condensed consolidated fi nancial statements and related notes. Some statements and information contained 
in  this  Management’s  Discussion  and Analysis  of  Financial  Condition  and  Results  of  Operations,  notes  to  our  condensed 
consolidated fi nancial statements and elsewhere in this report are not historical facts but are forward-looking statements within 
the meaning of Section 27A of the Securities Act of 1933, as amended (the “Securities Act”), and Section 21E of the Securities 
Exchange Act of 1934, as amended (the “Exchange Act”). In some cases, readers can identify forward- looking statements 
by  terms  such  as  “may,”  “will,”  “should,”  “expect,”  “plan,”  “intend,”  “forecast,”  “anticipate,”  “believe,”  “estimate,”  “predict,” 
“potential,” “continue,” or the negative of these terms or other comparable terminology, which when used are meant to signify 
the statement as forward-looking. These forward-looking statements include, but are not limited to, our expectations regarding 
new accounting standards on our fi nancial results, our expectations regarding our critical accounting policies; our expectations 
regarding our current operating plan, including operating expenses, product sales and revenue expectations, profi tability and 
cash  fl ows,  anticipated  revenue  and  sales  of  our  equity  securities,  our  beliefs  regarding  the  use  of  stock-based  awards  as  a 
compensation tool, our beliefs regarding certain tax positions, our beliefs regarding our revenue targets and the suffi  ciency of our 
liquidity and capital resources, our beliefs regarding ongoing litigation, our expectations regarding our signifi cant employees, 
our  expectations  regarding  commercialization  of  ContraPest  and  product  development  of  our  other  product  candidates,  our 
expectations regarding our sales channel, including distributors, our expectations regarding regulatory approval of our products 
or product candidates, the continued listing of our common stock on The Nasdaq Capital Market, statements about our plans, 
objectives, expectations and intentions and other statements that are not historical facts. These forward-looking statements are 
not guarantees of future performance and involve known and unknown risks, uncertainties and situations that are diffi  cult to 
predict and that may cause our own, or our industry’s actual results, to be materially diff erent from the future results that are 
expressed or implied by these statements. Accordingly, actual results may diff er materially from those anticipated or expressed 
in such statements as a result of a variety of factors, including those discussed in Item 1A of Part II of this Report, entitled “Risk 
Factors,” and those contained from time to time in our other fi lings with the Securities and Exchange Commission. Readers 
are cautioned not to place undue reliance on the forward-looking statements, which speak only as of the date made. Except as 
required by law, we undertake no obligation to update any forward-looking statement, whether as a result of new information, 
future events or otherwise.

Overview

Since  our  inception  in  2004,  we  have  devoted  substantially  all  of  our  resources  to  organizing  and  staffi  ng  our  company, 
conducting research and development activities for our product candidates, business planning, raising capital and acquiring 
and developing product and technology rights. Until August 2016, we did not have any products approved for sale, and we have 
generated minimal revenue from product sales to date. We have primarily funded our operations to date with proceeds from 
the sale of common stock and preferred stock, the issuance of convertible and other promissory notes and, to a lesser extent, 
payments received in connection with research grants and licensing fees. Through December 31, 2017, we had received net 
proceeds of $61.7 million from our sales of common stock, preferred stock and issuance of convertible and other promissory 
notes and an aggregate of $1.7 million from research grants and licensing fees and an aggregate of $0.4 million in product sales. 
At December 31, 2018, we had an accumulated defi cit of $85.8 million and cash and cash equivalents of $4.9 million.

We  have  incurred  signifi cant  operating  losses  every  year  since  our  inception.  Our  net  losses  were  $12.2  million  and 
$12.3 million for the years ended December 31, 2018 and 2017 respectively. We expect to continue to incur signifi cant expenses 
and generate operating losses for at least the next 12 months.

We have historically utilized, and intend to continue to utilize, various forms of stock-based awards in order to hire, retain 
and motivate talented employees, consultants and directors and encourage them to devote their best eff orts to our business and 
fi nancial success. In addition, we believe that our ability to grant stock-based awards is a valuable and necessary compensation 
tool that aligns the long-term fi nancial interests of our employees, consultants and directors with the fi nancial interests of our 
stockholders.

As  a  result,  a  signifi cant  portion  of  our  operating  expenses  includes  stock-based  compensation  expense.  Stock-based 
compensation  expense  has  been,  and  will  continue  to  be  for  the  foreseeable  future,  a  signifi cant  recurring  expense  in  our 
business and an important part of our compensation strategy. Specifi cally, our stock-based compensation expense for the year 
ended December 31, 2018 and December 31, 2017 was $3.4 million and $3.7. million, respectively, which represented 28.6% 
and 30.0%, respectively, of our total operating expenses for those periods.

27

Components of our Results of Operations

Net Sales

Net sales are comprised primarily of sales, net of discounts and promotions, of ContraPest and related components, to our 

distributors and customers.

Prior to 2017, all of our revenue was derived from payments received in connection with research grants and licensing fees 
received under the former license agreement with Neogen. We recognized $0 revenue for the years ended December 31, 2018 
and December 31, 2017, respectively, for services performed under NIH grants and in licensing fees under our former license 
agreement with Neogen. We do not anticipate additional grant revenue under the NIH grants or additional revenue from our 
former license agreement with Neogen.

Operating Expenses

Research and Development Expenses

Research and development expenses consist primarily of costs incurred in connection with the research and development of 
ContraPest and our other product candidates, which include:

•  Employee  related  expenses,  including  salaries,  related  benefi ts,  travel  and  stock-based  compensation  expense  for 

employees engaged in research and development functions;

•  Expenses incurred in connection with the development of our product candidates; and

• 

Facilities, depreciation and other expenses, which include direct and allocated expenses for rent and maintenance of 
facilities, insurance and supplies.

We expense research and development costs as incurred.

We continue to investigate other applications of our core technology to other product candidates, which includes laboratory 
tests and academic collaborations. We also continue to develop our supply chain, particularly identifying and improving our 
sourcing of triptolide, a key active ingredient for our product candidates. At this time, we cannot reasonably estimate the costs 
for further development of ContraPest or the cost associated with the development of any of our other product candidates.

We plan to continue to hire employees to support our research and development eff orts and anticipate that we will continue 
to  utilize  various  forms  of  stock-based  compensation  awards  in  order  to  attract  and  retain  employees  for  our  research  and 
development eff orts. As a result, we anticipate that stock-based compensation expense will continue to represent a signifi cant 
portion of our research and development expenses for the foreseeable future.

Selling, General and Administrative Expenses

Selling, general and administrative expenses consist primarily of salaries and related costs, including stock-based compensation, 
for personnel in executive, fi nance, sales, marketing and administrative functions. Selling, general and administrative expenses 
also include direct and allocated facility-related costs as well as professional fees for legal, consulting, accounting and audit 
services.

We anticipate that our selling, general and administrative expenses may increase in the future as we increase our headcount to 
support commercialization of ContraPest and further development of our product candidates. We also anticipate that we will 
incur increased accounting, audit, legal, regulatory, compliance, director and offi  cer insurance costs as well as investor and 
public relations expenses associated with being a public company.

We plan to continue to hire employees to support our commercialization of ContraPest and further development of our product 
candidates and anticipate that we will continue to utilize various forms of stock-based compensation awards in order to attract 
and retain qualifi ed employees. As a result, we anticipate that stock-based compensation expense will continue to represent a 
signifi cant portion of our selling, general and administrative expenses for the foreseeable future.

28

Interest Income.

Interest income consists primarily of interest income earned on cash and cash equivalents. Prior to 2017, our interest income has 
not been signifi cant due to nominal cash and investment balances and low interest earned on invested balances.

Interest Expense.

Interest expense consists primarily of interest accrued on our capital lease and note commitments.

Other Income (Expense), Net.

Other income (expense), net, consists primarily of recognized change in value of short-term investments and income (expense) 
related  to  the  year-over-year  fair  market  value  adjustment  of  our  derivative  warrant  and  losses  associated  with  the  early 
extinguishment of debt.

Income Taxes

Deferred tax assets and liabilities are determined based on diff erences between the fi nancial statement and tax basis of assets 
and liabilities, as well as a consideration of net operating loss and credit carry forwards, using enacted tax rates in eff ect for the 
period in which the diff erences are expected to impact taxable income. A valuation allowance is established, when necessary, 
to reduce deferred tax assets to the amount that is more likely than not to be realized. The Company’s eff ective tax rate for 
the years ended December 31, 2018 and December 31, 2017 has been aff ected by the valuation allowance on the Company’s 
deferred tax assets.

Since our inception, we have not recorded any U.S. federal or state income tax benefi ts for the net losses we have incurred 
in  each  year  or  for  our  earned  research  and  development  tax  credits,  due  to  our  uncertainty  of  realizing  a  benefi t  from 
those  items. At  December  31,  2018,  the  Company  has  federal  and  state  net  operating  loss  carryforwards  of  approximately 
$51.1  million  and  $37.6  million,  respectively,  not  considering  the  IRC  Section  382  annual  limitation  discussed  below. The 
federal loss carryforwards begin to expire in 2023, unless previously utilized. Additionally, the utilization of the net operating 
loss carryforwards are subject to an annual limitation under Section 382 and 383 of the Internal Revenue Code od 1986, and 
similar state tax provisions due to ownership change limitations that have occurred previously or that could occur in the future. 
These ownership changes limit the amount of net operating loss carryforwards and other deferred tax assets that can be utilized 
to off set future taxable income and tax, respectively. In general, an ownership change, as defi ned by Section 382 and 383. results 
from transactions increasing ownership of certain stockholders or public groups in the stock of the corporation by more than 
50 percent points over a three-year period. The Company has not conducted an analysis of an ownership change under section 
382. To the extent that a study is completed and an ownership change is deemed to occur, the Company’s net operating losses 
could be limited.

29

Comparison of the Years December 31, 2018 to 2017

The following table summarizes our results of operations for the years ended December 31, 2018 and 2017:

SENESTECH, INC.
STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(In thousands, except shares and per share data)

For the Years Ended 
December 31,

2018

2017

Net Sales . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Cost of sales  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Gross profit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

297 $ 
241
56

Operating expenses:

Research and development . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Selling, general and administrative . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total operating expenses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

2,404
9,532
11,936

52
45
7

3,191
9,132
12,323

Net operating loss . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

(11,880)

(12,316)

Other income (expense):

Interest income . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Interest expense . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Interest expense, related parties  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Other income (expense)  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total other income (expense) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

25
(74)
—
21
(28)

29
(85)
(1)
87
30

Net loss and comprehensive loss  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Warrant andtdilution price protection adjustment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Net loss attributable to common shareholders  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Loss per share attributable to common shareholders, basic and diluted . . . . . . . . . . . . . . .  $ 

(11,908) $ 
333
(12,241) $ 
(0.63) $ 

(12,286)
—
(12,286)
(1.12)

Weighted average common shares outstanding - basic and fully diluted . . . . . . . . . . . . . . 

19,402,091

10,920,909

Net Sales

Net sales, shown net of sales discounts and promotions, were $297,000 for the year ended December 31, 2018, compared to 
$52,000 for year ended December 31, 2017. The increase in our net product sales of $245,000 was a result of increased sales 
of ContraPest to our distributors as a result of increased marketing eff orts and sales promotions. We expect net product sales to 
continue to increase year over year for the foreseeable future.

Cost of Goods Sold

Cost of goods sold was $241,000, or 81.1% of net sales, for the year ended December 31, 2018, compared to $45,000, or 
86.5%  of  net  sales  for  year  ended  December  31,  2017. The  increase  in  cost  of  goods  sold  of  $196,000,  was  driven  by  the 
cost of increased sales, increased sales discounts and promotions as well as increased scrap related to product manufactured 
during scale up activities that were ultimately deemed unsellable. The decrease as a percentage of sales was a result of process 
improvement effi  ciencies. We anticipate cost of goods sold as a percentage of sales will improve for the foreseeable future due 
to manufacturing effi  ciencies as a result of the scale up activities.

Gross Profi t

Gross profi t for the year ended December 31, 2018 was $56,000 or 18.9% of net sales, compared to a gross profi t of $7,000 
or 13.5% of net sales, for the year ended December 31, 2017. The increase in gross profi t was a direct result of increased sales 
volume as described above, partially off set by increased sales discounts and promotions as well as increased scrap related to 
scale up activities.

30

Research and Development Expenses

Year Ended 
December 31,

Increase 
(Decrease)

2018

2017
(in thousands)

Direct research and development expenses:

Personnel related (including stock-based compensation) . . . . . . . . . .  $ 
Facility related . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Other . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total research and development expenses  . . . . . . . . . . . . . . . . . . . . . . .  $ 

1,548 $ 
234
622
2,404 $ 

1,840 $ 
293
1,058
3,191 $ 

(292)
(59)
(436)
787

Research and development expenses were $2.4 million for the year ended December 31, 2018, compared to $3.2 million for the 
year ended December 31, 2017. The $800,000 decrease in research and development expenses was primarily due to decreases 
in consulting and legal expenses, primarily related to regulatory aff airs, of $384,000, stock compensation expenses of $271,000, 
rent and facilities of $60,000 and a reduction of manufacturing equipment maintenance of $134,000, off set by increases in travel 
related to customer support expense of $30,000 and depreciation expense of $290,000 due to equipment adds during 2018.

We continue to investigate other applications of our core technology to other product candidates, which includes laboratory 
tests and academic collaborations. We also continue to develop our supply chain, particularly identifying and improving our 
sourcing of triptolide and other ingredients for our product and product candidates.

Selling, General and Administrative Expenses

Selling, general and administrative expenses were $9.5 million for the year ended December 31, 2018, compared to $9.1 million 
for the year ended December 31, 2017. The increase of $0.4 million in selling, general and administrative expenses was primarily 
due to an increase of $307,000 in recruiting and other benefi t expenses and an increase of $125,000 in legal expenses as a result 
of ongoing litigation, off set by a decrease of $32,000 in stock-based compensation expense.

Interest Expense Net

We recorded $49,000 of interest expense, net for the year ended December 31, 2018, compared to $57,000 for the year ended 
December 31, 2017. The decrease in interest expense, net of $8,000 was the result of decreased debt in the form of notes payable 
due primarily to the sale of a vehicle and related debt reduction in April 2018.

Other Income (Expense), Net

We recorded $21,000 of other income, net for the year ended December 31, 2018, compared to $87,000 of other income for the 
year ended December 31, 2017. The $66,000 net decrease in other income was primarily due to lower income recognized for 
year-over-year fair market value adjustment of our convertible promissory notes and a $10,000 loss on the early extinguishment 
of a note payable during 2018.

Liquidity and Capital Resources

Since our inception, we have sustained signifi cant operating losses in the course of our research and development activities 
and commercialization eff orts and expect such losses to continue for the near future. We have generated limited revenue to 
date from product sales, research grants and licensing fees received under our former license agreement with Neogen. In 2017, 
we began full scale marketing of our fi rst product, ContraPest, and we continue to develop other product candidates, which 
are in various phases of development. We have funded our operations to date through the sale of equity securities, including 
convertible preferred stock, common stock and warrants to purchase common stock, debt fi nancing, consisting primarily of 
convertible notes; and, to a lesser extent, payments received in connection with product sales, research grants and licensing fees. 
Through December 31, 2018, we had received net proceeds of $61.7 million from our sales of common stock, preferred stock 
and warrant exercises and issuance of convertible and other promissory notes, and an aggregate of $1.7 million from licensing 
fees and an aggregate of $0.4 million from product sales. At December 31, 2018, we had an accumulated defi cit of $85.8 million 
and cash and cash equivalents of $4.9 million.

31

Our ultimate success depends upon the outcome of a combination of factors, including: (i) successful commercialization of 
ContraPest and ongoing regulatory approval of our other product candidates; (ii) market acceptance, commercial viability and 
profi tability of ContraPest and other products; (iii) the ability to market our products and establish an eff ective sales force and 
marketing infrastructure to generate signifi cant revenue; (iv) the success of our research and development; (v) the ability to 
retain and attract key personnel to develop, operate and grow our business; and (vi) our ability to meet our working capital 
needs.

Based upon our current operating plan, we expect that cash and cash equivalents and highly liquid, short term investments at 
December 31, 2018, in combination with anticipated revenue and additional sales of our equity securities, will be suffi  cient 
to fund our current operations for at least the next 12 months. However, if anticipated revenue targets and margin targets are 
not achieved and we are unable to raise necessary capital through the sale of our securities, we may seek to reduce operating 
expenses, and take other measures that could impair our ability to be successful and operate as a going concern. In any event, 
we are likely to require additional capital in order to fund our operating losses and research and development activities until 
we become profi table. We may never achieve profi tability or generate positive cash fl ows, and unless and until we do, we will 
continue to need to raise capital through equity or debt fi nancing. If such equity or debt fi nancing is not available at adequate 
levels or on acceptable terms, we may need to delay, limit or terminate commercialization and development eff orts.

Additional Funding Requirements

We expect our expenses to increase in connection with our ongoing activities, particularly as we market and focus on sales of 
ContraPest, and as we advance fi eld studies of our product candidates in development. In addition, we will continue to incur 
costs associated with operating as a public company. As a result, we anticipate requiring additional funding during 2019.

In particular, we expect to incur substantial and increased expenses as we:

•  Work to maximize market acceptance for, and generate sales of, our products;

•  Manage the infrastructure for the sales, marketing and distribution of ContraPest and any other product candidates for 

which we may receive regulatory approval;

•  Continue the development of ContraPest and our other product candidates, including engaging in any necessary fi eld 

studies;

• 

• 

Seek additional regulatory approvals for ContraPest and our other product candidates;

Scale up manufacturing processes and quantities to meet future demand of ContraPest and any other product candidates 
for which we receive regulatory approval;

•  Continue product development of ContraPest and advance our research and development activities and advance the 

research and development programs for other product candidates;

•  Maintain, expand and protect our intellectual property portfolio; and

•  Add operational, fi nancial and management information systems and personnel, including personnel to support our 

product development and commercialization eff orts and operations as a public company.

Cash Flows

The following table summarizes our sources and uses of cash for each of the years presented:

Cash used in operating activities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Cash used in investing activities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Cash provided by financing activities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Net increase (decrease) in cash and cash equivalents . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 

(9,129) $ 
5,016
6,932
2,819 $ 

(9,321)
(5,902)
5,498
(9,725)

Year Ended 
December 31,

2018

2017

32

Operating Activities.

During the year ended December 31, 2018, operating activities used $9.1 million of cash, primarily resulting from our net 
loss of $11.9 million and changes in our operating assets and liabilities of $1.0 million, partially off set by non-cash charges 
of  $3.8  million.  Our  net  loss  was  primarily  attributed  to  research  and  development  activities  and  our  selling,  general  and 
administrative expenses, as we generated limited product sales and no research grant and licensing revenue during the period. 
Net cash used by changes in our operating assets and liabilities for the year ended December 31, 2018 consisted primarily of a 
$29,000 decrease in accrued expenses and accounts payable, an increase in inventories of $721,000, a net increase in accounts 
receivable and deposits of $113,000 and an increase in prepaid expenses of $172,000

During the year ended December 31, 2017, operating activities used $9.3 million of cash, primarily resulting from our net 
loss of $12.3 million and changes in our operating assets and liabilities of $1.0 million, partially off set by non-cash charges of 
$4.0 million. Our net loss was primarily attributed to research and development activities and our general and administrative 
expenses,  as  we  generated  limited  product  sales,  research  grant  and  licensing  revenue  during  the  period.  Net  cash  used  by 
changes in our operating assets and liabilities for the year ended December 31, 2017 consisted primarily of a $742,000 decrease 
in accrued expenses and accounts payable, an increase in inventories of $483,000 and an increase in accounts receivable and 
deposits  of  $14,000,  partially  off set  by  a  decrease  in  prepaid  expenses  of  $167,000. The  decrease  in  accrued  expenses  and 
accounts payable was primarily a result of a $1.0 million payment to Neogen in fulfi llment of our settlement agreement in 
January  2017,  off set  by  decreased  payments  of  accrued  expenses  and  accounts  payable  as  a  result  of  negotiation  of  better 
payable terms and management of payment timing.

Investing Activities.

During  the  year  ended  December  31,  2018,  we  generated  $5.0  million  of  cash  in  investing  activities,  which  consisted  of 
$5 million in the sale of short term, highly liquid investments and $185,000 generated from the sale of equipment, off set by 
$239,000 used in the purchases of property and equipment.

During the year ended December 31, 2017, we used $5.9 million of cash in investing activities, which consisted of $5 million in 
the purchase of short term, highly liquid investments and $898,000 used in the purchases of property and equipment.

Financing Activities.

During the year ended December 31, 2018, net cash provided by fi nancing activities was $6.9 million as a result of $5.1 million 
in proceeds from the issuance of common stock, net, $2.2 million in proceeds from warrant exercises and $9,000 in proceeds 
from issuances of notes, off set by $293,000 of repayments of related to notes payable and notes payable, related party, $71,000 
in  repayments  of  capital  lease  obligations  and  $58,000  of  payments  for  employee  withholding  taxes  related  to  share-based 
awards.

During the year ended December 31, 2017, net cash provided by fi nancing activities was $5.5 million as a result of $5.2 million 
of net proceeds from the issuance of shares of common stock in a public off ering in November 2017 as discussed elsewhere in 
this Annual Report on Form 10-K, $6,000 of proceeds received from the exercise of stock options and warrants, and $437,000 
of proceeds received from our issuance of notes payable, all of which were partially off set by payments of $97,000 related to the 
notes payable, and $95,000 in repayments of capital lease obligations.

Recent Developments

Our common stock is listed on the Nasdaq Capital Market. In order to maintain that listing, we must satisfy minimum fi nancial 
and other continued listing requirements and standards. On January 3, 2018, we received a defi ciency letter from the listing 
qualifi cations staff  of the Nasdaq Stock Market, notifying us that, for the prior 30 consecutive business days, the closing bid 
price of our common stock was not maintained at the minimum required closing bid price of at least $1.00 per share as required 
for continued listing on the Nasdaq Capital Market. In accordance with Nasdaq Listing Rules, we had an initial compliance 
period of 180 calendar days, until July 2, 2018, to regain compliance with this requirement. On June 5, 2018, we received notice 
from the listing qualifi cations staff  of the Nasdaq Stock Market, notifying us that the closing bid price of our common stock 
was greater than $1.00 per share for ten consecutive business days and that we had regained compliance with the minimum bid 
price requirement.

33

On  September  26,  2018,  we  received  a  defi ciency  letter  from  the  listing  qualifi cations  staff   of  the  Nasdaq  Stock  Market, 
notifying us that, for the prior 30 consecutive business days, the closing bid price of our common stock was not maintained 
at the minimum required closing bid price of at least $1.00 per share as required for continued listing on the Nasdaq Capital 
Market. In accordance with Nasdaq Listing Rules, we had an initial compliance period of 180 calendar days, until March 25, 
2019, to regain compliance with this requirement. On March 20, 2019 we received notice from the listing qualifi cations staff  of 
the Nasdaq Stock Market, notifying us that the closing bid price of our common stock was greater than $1.00 per share for ten 
consecutive business days and that we had regained compliance with the minimum bid price requirement.

We cannot provide any assurance that our stock price will maintain the minimum bid price requirements of Nasdaq or that 
we will be able to satisfy any other continued listing requirement of the Nasdaq Stock Market. In the event that our common 
stock is not eligible for quotation on another market or exchange, trading of our common stock could be conducted in the 
over-the-counter market or on an electronic bulletin board established for unlisted securities such as the Pink Sheets or the OTC 
Bulletin Board. In such event, it could become more diffi  cult to dispose of, or obtain accurate price quotations for, our common 
stock, and there would likely be a reduction in our coverage by security analysts and the news media, which could cause the 
price of our common stock to decline further. In addition, it may be diffi  cult for us to raise additional capital if we are not listed 
on a major exchange.

Critical Accounting Policies and Signifi cant Judgments and Estimates

Our  fi nancial  statements  are  prepared  in  accordance  with  generally  accepted  accounting  principles  in  the  United  States,  or 
U.S. GAAP. The preparation of our fi nancial statements and related disclosures requires us to make estimates and judgments 
that aff ect the reported amounts of assets, liabilities, revenue, costs and expenses, and the disclosure of contingent assets and 
liabilities in our fi nancial statements. We base our estimates on historical experience, known trends and events and various 
other factors that we believe are reasonable under the circumstances, the results of which form the basis for making judgments 
about the carrying values of assets and liabilities that are not readily apparent from other sources. We evaluate our estimates and 
assumptions on an ongoing basis. Our actual results may diff er from these estimates under diff erent assumptions or conditions.

While our signifi cant accounting policies are described in more detail in Note 2 — Summary of Signifi cant Accounting Policies 
to our fi nancial statements included elsewhere in this Annual Report on Form 10-K, we believe that the following accounting 
policies are those most critical to the judgments and estimates used in the preparation of our fi nancial statements.

Revenue Recognition

Eff ective January 1, 2018, the Company adopted ASC 606 — Revenue from Contracts with Customers. Under ASC 606, the 
Company  recognizes  revenue  from  the  commercial  sales  of  products,  licensing  agreements  and  contracts  to  perform  pilot 
studies by applying the following steps: (1) identify the contract with a customer; (2) identify the performance obligations 
in the contract; (3) determine the transaction price; (4) allocate the transaction price to each performance obligation in the 
contract; and (5) recognize revenue when each performance obligation is satisfi ed. For the comparative periods, revenue has not 
been adjusted and continues to be reported under ASC 605 — Revenue Recognition. Under ASC 605, revenue is recognized 
when the following criteria are met: (1) persuasive evidence of an arrangement exists; (2) the performance of service has been 
rendered to a customer or delivery has occurred; (3) the amount of fee to be paid by a customer is fi xed and determinable; and 
(4) the collectability of the fee is reasonably assured.

There was no impact on the Company’s fi nancial statements as a result of adopting ASC 606 for the years ended December 31, 
2018 and 2017, respectively.

Stock-Based Compensation

We recognize compensation costs related to stock options granted to employees based on the estimated fair value of the awards 
on the date of grant, net of estimated forfeitures, in accordance with ASC Topic 718 — Stock Compensation (“ASC 718”). We 
estimate the grant date fair value of the awards, and the resulting stock-based compensation expense, using the Black-Scholes 
option pricing model. The grant date fair value of stock-based awards is expensed on a straight-line basis over the vesting period 
of the respective award. We account for stock-based compensation arrangements with non-employees using a fair value approach. 
The fair value of these stock options is measured using the Black-Scholes option-pricing model refl ecting the same assumptions 
as applied to employee options in each of the reported periods, other than the expected life, which is assumed to be the remaining 
contractual life of the option. The fair value of the stock options granted to non-employees is re-measured as the stock options 
vest and is recognized in the statements of operations and comprehensive loss during the period the related services are rendered.

34

We recorded stock-based compensation expense of approximately $3.4 million and $3.7 million for the years ended December 31, 
2018 and 2017 respectively. We expect to continue to grant stock options and other equity-based awards in the future, and to the 
extent that we do, our stock-based compensation expense recognized in future periods will likely increase.

The Black-Scholes option pricing model requires the use of highly subjective and complex assumptions, which determine the 
fair value of stock-based awards. If we had made diff erent assumptions, our stock-based compensation expense, net loss and 
loss per share of common stock could have been signifi cantly diff erent. Our assumptions are as follows:

•  Expected term.  The expected term represents the period that the stock-based awards are expected to be outstanding. 
Our historical share option exercise experience does not provide a reasonable basis upon which to estimate an expected 
term because of a lack of suffi  cient data. Therefore, we estimate the expected term by using the simplifi ed method, 
which calculates the expected term as the average of the time-to-vesting and the contractual life of the options.

•  Expected volatility.  Expected volatility is derived from the average historical volatilities of publicly traded companies 
within  our  industry  that  we  consider  to  be  comparable  to  our  business  over  a  period  approximately  equal  to  the 
expected term. We intend to continue to consistently apply this process using the same or similar public companies 
until a suffi  cient amount of historical information regarding the volatility of our own common stock price becomes 
available, or unless circumstances change such that the identifi ed companies are no longer similar to us, in which case, 
more suitable companies whose share prices are publicly available would be utilized in the calculation.

•  Risk-free interest rate.  The risk-free interest rate is based on the U.S. Treasury yield in eff ect at the time of grant for 

zero coupon U.S. Treasury notes with maturities approximately equal to the expected term.

•  Expected dividend.  The expected dividend is assumed to be zero as we have never paid dividends and have no current 

plans to pay any dividends on our common stock.

•  Expected  forfeitures.  We  use  historical  data  to  estimate  pre-vesting  option  forfeitures  and  record  stock-based 
compensation expense only for those awards that are expected to vest. To the extent actual forfeitures diff er from the 
estimates, the diff erence will be recorded as a cumulative adjustment in the period that the estimates are revised.

Signifi cant Factors, Assumptions and Methodologies Used in Determining Fair Value of Our Common Stock

As  noted  above,  we  are  required  to  estimate  the  fair  value  of  the  common  stock  underlying  our  stock-based  awards  when 
performing the fair value calculations using the Black-Scholes option-pricing model. In the absence of an active market for 
our common stock, we utilized methodologies in accordance with the framework of the American Institute of Certifi ed Public 
Accountants’  Technical  Practice  Aid,  Valuation  of  Privately-Held  Company  Equity  Securities  Issued  as  Compensation,  to 
estimate  the  fair  value  of  our  common  stock.  In  addition,  we  have  conducted  periodic  assessments  of  the  valuation  of  our 
common stock.

The  assumptions  underlying  these  valuations  represent  management’s  best  estimates,  which  involve  inherent  uncertainties 
and  the  application  of  management’s  judgment.  If  we  had  made  diff erent  assumptions  than  those  used,  the  amount  of  our 
stock-based compensation expense, net income and net income per share amounts could have been signifi cantly diff erent. The 
fair value per share of our common stock for purposes of determining stock-based compensation expense is the closing price 
of our common stock as reported on the applicable grant date. The compensation cost that has been included in the statements 
of operations and comprehensive loss for all stock-based compensation arrangements is as follows:

Selling, general and administrative expenses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Research and development expense . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total stock-based compensation expense . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 

The intrinsic value of stock options outstanding as of December 31, 2018 is $0.

Years Ended 
December 31,

2018

2017

(in thousands)
3,306 $ 
106
3,412 $ 

3,338
377
3,715

35

Emerging Growth Company Status

The Jumpstart Our Business Startups Act of 2012, or the JOBS Act, permits an “emerging growth company” such as us to take 
advantage of an extended transition period to comply with new or revised accounting standards applicable to public companies 
until those standards would otherwise apply to private companies. We have irrevocably elected to “opt out” of this provision 
and, as a result, we intend to comply with new or revised accounting standards when they are required to be adopted by public 
companies that are not emerging growth companies.

Off -Balance Sheet Arrangements

None.

Item 7A.  Quantitative and Qualitative Disclosures about Market Risk.

Not applicable.

36

Item 8.  Financial Statements and Supplementary Data.

SENESTECH, INC.
INDEX TO CONSOLIDATED FINANCIAL STATEMENTS

Report of Independent Registered Public Accounting Firm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Balance Sheets as of December 31, 2018 and 2017 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Statements of Operations and Comprehensive Loss for the years ended December 31, 2018 and 2017 . . . . . . . . . . . . 

Statements of Stockholders’ Equity for the years ended December 31, 2018 and 2017  . . . . . . . . . . . . . . . . . . . . . . . . 

Statements of Cash Flows for the years ended December 31, 2018 and 2017 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Notes to Financial Statements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

F-2

F-3

F-4

F-5

F-6

F-7

F-1

SENESTECH, INC.
REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM

To the Board of Directors and
Stockholders of SenesTech, Inc.

Opinion on the Financial Statements

We  have  audited  the  accompanying  balance  sheets  of  SenesTech,  Inc.  (the  Company)  as  of  December  31,  2018  and  2017, 
and  the  related  statements  of  income,  comprehensive  income,  stockholders’  equity,  and  cash  fl ows  for  each  of  the  years  in 
the two-year period ended December 31, 2018, and the related notes and schedules (collectively referred to as the fi nancial 
statements). In our opinion, the fi nancial statements present fairly, in all material respects, the fi nancial position of the Company 
as of December 31, 2018 and 2017, and the results of its operations and its cash fl ows for each of the years in the two-year 
period ended December 31, 2018, in conformity with accounting principles generally accepted in the United States of America.

Basis for Opinion

These fi nancial statements are the responsibility of the Company’s management. Our responsibility is to express an opinion on 
the Company’s fi nancial statements based on our audits. We are a public accounting fi rm registered with the Public Company 
Accounting  Oversight  Board  (United  States)  (PCAOB)  and  are  required  to  be  independent  with  respect  to  the  Company 
in accordance with the U.S. federal securities laws and the applicable rules and regulations of the Securities and Exchange 
Commission and the PCAOB.

We conducted our audits in accordance with the standards of the PCAOB. Those standards require that we plan and perform 
the audit to obtain reasonable assurance about whether the fi nancial statements are free of material misstatement, whether due 
to error or fraud. The Company is not required to have, nor were we engaged to perform, an audit of its internal control over 
fi nancial reporting. As part of our audits, we are required to obtain an understanding of internal control over fi nancial reporting, 
but not for the purpose of expressing an opinion on the eff ectiveness of the Company’s internal control over fi nancial reporting. 
Accordingly, we express no such opinion.

Our audits included performing procedures to assess the risks of material misstatement of the fi nancial statements, whether due 
to error or fraud, and performing procedures that respond to those risks. Such procedures included examining, on a test basis, 
evidence regarding the amounts and disclosures in the fi nancial statements. Our audits also included evaluating the accounting 
principles used and signifi cant estimates made by management, as well as evaluating the overall presentation of the fi nancial 
statements. We believe that our audits provide a reasonable basis for our opinion.

The accompanying fi nancial statements have been prepared assuming that the Company will continue as a going concern. As 
discussed in Note 1 to the fi nancial statements, the Company suff ered a net loss from operations and has a net capital defi ciency, 
which raises substantial doubt about its ability to continue as a going concern. Management’s plans regarding those matters are 
also described in Note 1. The fi nancial statements do not include any adjustments that might result from the outcome of this 
uncertainty.

/s/ M&K CPAS, PLLC

We have served as the Company’s auditor since 2014.

Houston, TX

March 29, 2019

F-2

SENESTECH, INC.
BALANCE SHEETS
(In thousands, except shares and per share data)

December 31,
2018

December 31,
2017

ASSETS

Current assets:

Cash . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Investment in securities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Accounts receivable  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Prepaid expenses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Inventory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Deposits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total current assets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Property and equipment, net . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Total assets  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 

LIABILITIES AND STOCKHOLDERS’ EQUITY

Current liabilities:

Short-term debt . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Accounts payable  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Accrued expenses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Notes payable, related parties . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total current liabilities  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Long-term debt, net . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Deferred rent . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total liabilities. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Commitments and contingencies (See note 15) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Stockholders’ equity:

Common stock, $0.001 par value, 100,000,000 shares authorized, 23,471,999 and 

16,404,195 shares issued and outstanding at December 31, 2018 and December 31, 
2017, respectively . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Additional paid-in capital . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Accumulated deficit  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total stockholders’ equity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

4,920 $ 
—
139
342
1,261
9
6,671

1,083
7,754 $ 

219 $ 
173
771
—
1,163

261
16
1,440

—

2,101
5,023
16
170
540
19
7,869

1,454
9,323

177
391
589
12
1,169

591
41
1,801

—

24
92,128
(85,838)
6,314

16
81,103
(73,597)
7,522

Total liabilities and stockholders’ equity  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 

7,754 $ 

9,323

See accompanying notes to fi nancial statements.

F-3

SENESTECH, INC.
STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(In thousands, except shares and per share data)

For the Years 
Ended December 31,

2018

2017

Net Sales . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Cost of sales  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Gross profit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

297 $ 
241
56

Operating expenses:

Research and development . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Selling, general and administrative . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total operating expenses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

2,404
9,532
11,936

52
45
7

3,191
9,132
12,323

Net operating loss . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

(11,880)

(12,316)

Other income (expense):

Interest income . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Interest expense . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Interest expense, related parties  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Other income (expense)  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total other income (expense) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

25
(74)
—
21
(28)

29
(85)
(1)
87
30

Net loss and comprehensive loss  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Deemed dividend-warrant antidilution price protection adjustment. . . . . . . . . . . . . . . . . . 
Net loss attributable to common shareholders  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Loss per share attributable to common shareholders, basic and diluted . . . . . . . . . . . . . . .  $ 

(11,908) $ 
333
(12,241) $ 
(0.63) $ 

(12,286)
—
(12,286)
(1.12)

Weighted average common shares outstanding - basic and fully diluted . . . . . . . . . . . . . . 

19,402,091

10,920,909

See accompanying notes to fi nancial statements.

F-4

SENESTECH, INC.
STATEMENT OF CHANGES IN CONVERTIBLE PREFERRED STOCK AND STOCKHOLDERS’ 
EQUITY (DEFICIT)
(In thousands, except shares and per share data)

Common Stock

Shares

Amount

Additional
Paid-In
Capital

Stock
Subscribed
not Issued

Shares

Amount

Accumulated
Other
Comprehensive
Loss

Accumulated
Deficit

Total
Stockholders’
Equity
 (Deficit)

Balance, December 31, 2016 . . . 

10,157,292

$ 

10

$ 

72,069

8,500

$ 

59

$ 

— $ 

(61,311) $ 

10,827

Issuance of common stock sold 

for cash, net of fees . . . . . . . . . . 

5,860,000

Issuance of common stock 

for services . . . . . . . . . . . . . . . . . 

168,206

Issuance of common stock 

for services, related parties  . . . . 

204,683

Issuance of common stock options 
for services . . . . . . . . . . . . . . . . . 

Cashless exercise of options . . . . . . 

Net loss for the year ended 

—

14,014

December 31, 2017 . . . . . . . . . . 

—

6

—

—

—

—

—

5,247

—

—

552

659

2,576

—

—

(8,500)

(59)

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

5,253

493

659

2,576

—

(12,286)

(12,286)

Balance, December 31, 2017 . . . 

16,404,195

$ 

16

$ 

81,103

— $ 

— $ 

— $ 

(73,597) $ 

7,522

Issuance of common stock sold 

for cash, net of fees . . . . . . . . . . 

5,357,052

Issuance of common stock for 

services  . . . . . . . . . . . . . . . . . . . 

221,193

Stock-based compensation . . . . . . . 

—

Issuance of common stock upon 

exercise of warrants . . . . . . . . . . 

1,475,659

Issuance of common stock upon 
cashles exercise of stock 
options . . . . . . . . . . . . . . . . . . . . 

Issuance of warrants . . . . . . . . . . . . 

Warrant antidilution price protection 
adjustment . . . . . . . . . . . . . . . . . 

Option forfeitures and expirations . . .

Net loss for the year ended 

13,900

December 31, 2018 . . . . . . . . . . 

—

Balance, December 31, 2018 . . . 

23,471,999

$ 

5

—

—

2

—

—

24

5,127

36

1,691

2,212

—

1,693

333

(67)

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

(333)

5,132

36

1,691

2,214

—

1,693

—

(67)

—

—

—

(11,908)

(11,908)

$ 

92,128

— $ 

— $ 

— $ 

(85,838) $ 

6,314

The accompanying notes are an integral part of these fi nancial statements.

F-5

SENESTECH, INC.
STATEMENTS OF CASH FLOWS
(In thousands)

CASH FLOWS FROM OPERATING ACTIVITIES

Net loss . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Adjustments to reconcile net loss to net cash used in operating activities:

(11,908) $ 

(12,286)

For the Years 
Ended December 31,

2018

2017

Gain on investments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Amortization of discounts on investments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Depreciation and amortization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Stock-based compensation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Loss on sale of equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Loss on early extinguishment of debt . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
(Gain) loss on remeasurement of common stock warrant liability . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
(Increase) decrease in current assets:

Accounts receivable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Prepaid expenses  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Inventory  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Deposits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Increase (decrease) in current liabilities:

Accounts payable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Accrued contract cancellation settlement  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Accrued expenses. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Deferred rent  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Net cash used in operating activities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

CASH FLOWS FROM INVESTING ACTIVITIES

Purchase of securities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Proceeds received on sale of securities  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Proceeds received on sale of equipment  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Purchase of property and equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Net cash provided by (used in) investing activities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

CASH FLOWS FROM FINANCING ACTIVITIES

Proceeds from the issuance of common stock, net  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Proceeds from the issuance of notes payable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Repayments of notes payable, net  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Repayments of notes payable, related parties  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Repayments of capital lease obligations  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Proceeds from the exercise of warrants . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Payment of employee withholding taxes relating to share-based awards  . . . . . . . . . . . . . . . . . . . . . . . . 
Net cash provided by financing activities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

NET CHANGE IN CASH  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
CASH AT BEGINNING OF PERIOD  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
CASH AT END OF PERIOD  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 

(47)
—
447
3,413
15
10
1

(123)
(172)
(721)
10

(218)
—
189
(25)
(9,129)

—
5,070
185
(239)
5,016

5,132
9
(281)
(12)
(71)
2,213
(58)
6,932

2,819
2,101
4,920

$ 

SUPPLEMENTAL INFORMATION:

Interest paid . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Income taxes paid . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 

NON-CASH INVESTING AND FINANCING ACTIVITIES:

Deemed dividend . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Purchases of equipment under capital lease obligations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 

$ 
74
— $ 

333
37 $ 

See accompanying notes to fi nancial statements.

(36)
17
391
3,728
—
—
(69)

(6)
167
(483)
(10)

40
(1,000)
218
8
(9,321)

(5,004)
—
—
(898)
(5,902)

5,253
437
(73)
(24)
(95)
—
—
5,498

(9,725)
11,826
2,101

87
—

—
316

F-6

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

1. Organization and Description of Business

SenesTech, Inc. (referred to as “SenesTech,” the “Company,” “we” or “us”) was formed in July 2004 and incorporated in the state 
of Nevada. The Company subsequently reincorporated in the state of Delaware in November 2015. Our corporate headquarters 
is in Flagstaff , Arizona. We have developed and are commercializing a global, proprietary technology for managing animal pest 
populations, primarily rat populations, through fertility control.

SenesTech,  Inc.  (referred  to  in  this  report  as  “SenesTech,”  the  “Company,”  “we”  or  “us”)  was  formed  in  July  2004  and 
incorporated in the state of Nevada. The Company subsequently reincorporated in the state of Delaware in November 2015. Our 
corporate headquarters is in Flagstaff , Arizona. We have developed and are commercializing a global, proprietary technology 
for managing animal pest populations, initially rat populations, through fertility control.

Although a myriad of tools are available to fi ght rat infestations, communities continue to face challenges in controlling today’s 
infestations.  Infestations  result  in  incredible  infrastructure  damage,  as  well  as  pose  additional  risks  to  the  health  and  food 
security of communities. In addition to these challenges, the pest management industry and Pest Management Professionals 
(PMPs) are being increasingly asked for new solutions to help solve the problem. With growing concerns about rat resistance 
to rodenticides and a growing interest in non-lethal options, it is becoming increasingly important for PMPs to have new tools 
at their disposal. Our goal is to provide customers with not only a solution to combat their most diffi  cult infestations, but also 
off er a non-lethal option to serve customers that are looking to decrease or remove the amount of poison used in their pest 
management programs.

Our fi rst fertility control product, ContraPest, is a liquid bait containing the active ingredients 4-vinylcyclohexene diepoxide 
(VCD) and triptolide. When consumed, ContraPest targets reproduction, limiting fertility in male and female rats beginning 
with  the  fi rst  breeding  cycle  following  consumption.  ContraPest  is  being  marketed  for  use  in  controlling  rat  populations, 
specifi cally Norway and roof rats. On August 23, 2015, the United States Environmental Protection Agency (EPA) granted 
registration  approval  for  ContraPest  as  a  Restricted  Product  Due  to  Professional  Expertise  (referred  to  in  this  report  as  a 
“Restricted Use designation”), eff ective August 2, 2016. On October 18, 2018, the EPA approved the removal of the Restricted 
Use designation. We believe ContraPest is the fi rst and only non-lethal, fertility control product approved by the EPA for the 
management of rodent populations.

In  addition  to  the  EPA  registration  of  ContraPest  in  the  U.S.,  we  must  obtain  registration  from  the  various  state  regulatory 
agencies prior to selling in each state. As of the date of this report, we have received registration for ContraPest in all 50 states 
and the District of Columbia, nine of which have approved the removal of the Restricted Use designation.

We expect to continue to pursue regulatory approvals and amendments to existing registration in the United States for ContraPest, 
as well as regulatory approvals for any additional jurisdictions beyond the United States. The Company also continues to pursue 
other potential additional fertility control and animal health products for additional species.

Besides providing just the product, SenesTech provides PMPs with product training, and supports the PMPs by creating tools, 
training  and  awareness  campaigns  to  help  inform  their  customers,  specifi cally  within  the  food  safety  industry  and  larger 
residential customers, such as Home Owners Associations (“HOAs”), on the benefi ts of including ContraPest into their IPM 
protocols.

Going Concern

Although our audited fi nancial statements for the year ended December 31, 2018 were prepared under the assumption that 
we would continue our operations as a going concern, the report of our independent registered public accounting fi rm that 
accompanies our fi nancial statements for the year ended December 31, 2018 contains a going concern qualifi cation in which 
such fi rm expressed substantial doubt about our ability to continue as a going concern, based on the fi nancial statements at that 
time. Specifi cally, as noted above, we have incurred operating losses since our inception, and we expect to continue to incur 
signifi cant expenses and operating losses for the foreseeable future. These prior losses and expected future losses have had, and 
will continue to have, an adverse eff ect on our fi nancial condition. If we cannot continue as a going concern, our stockholders 
would likely lose most or all of their investment in us.

F-7

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

1. Organization and Description of Business (cont.)

Potential Need for Additional Capital

Since our inception, we have sustained signifi cant operating losses in the course of our research and development activities 
and expect such losses to continue for the near future. We have generated limited revenue to date from product sales, research 
grants and licensing fees received under our former license agreement with Neogen. In 2017, we began to prepare and launch 
commercialization of our fi rst product, ContraPest. We have funded our operations to date through the sale of equity securities, 
including convertible preferred stock, common stock and warrants to purchase common stock. Such sales include:

(i)  an initial public off ering of 1,875,000 shares of our common stock on December 8, 2016 with warrants to purchase 
an  additional  187,500  shares  issued  to  Roth  Capital  Partners,  LLC  with  an  exercise  price  of  $9.60  per  share,  as 
underwriter,

(ii)  a public off ering on November 21, 2017 of 5,860,000 shares of our common stock at $1.00 per share with warrants 
issued to investors to purchase an additional 4,657,500 shares of our common stock with an initial exercise price of 
$1.50  per  share  that  subsequently  adjusted  downward  to  $0.95  per  share  pursuant  to  antidilution  price  protection 
contained within those warrants, and warrants issued to Roth Capital Partners, LLC, as underwriter, to purchase an 
additional 945,000 shares with an exercise price of $1.50 per share,

(iii) a private placement of warrants to purchase 1,133,909 shares of common stock in June 2018 with an exercise price 
of  $1.82  per  share  in  connection  with  an  inducement  agreement  with  a  holder  of  outstanding  warrants  issued  in 
November 2017 to exercise its original warrant representing 1,133,909 shares at an exercise price of $1.50 per share; 
and

(iv)  a rights off ering in August 2018 (the “Rights Off ering”), where we accepted subscriptions for 5,357,052 units for a 
purchase price of $1.15 per unit, with each unit consisting of one share of our common stock and one warrant, with 
each warrant exercisable for one share of our common stock at an exercise price of $1.15 per share, and warrants 
issued to an affi  liate of Maxim Group, LLC, as dealer-manager, to purchase an additional 267,853 shares at $1.725 per 
share.

We have also raised capital through debt fi nancing, consisting primarily of convertible notes; and, to a lesser extent, payments 
received in connection with product sales, research grants and licensing fees.

Through December 31, 2018, we had received net proceeds of $61.7 million from our sales of common stock, preferred stock 
and warrant exercises and issuance of convertible and other promissory notes, an aggregate of $1.7 million from licensing fees 
and an aggregate of $0.4 million in net product sales. At December 31, 2018, we had an accumulated defi cit of $85.8 million 
and cash and cash equivalents of $4.9 million.

Our ultimate success depends upon the outcome of a combination of factors, including: (i) successful commercialization of 
ContraPest  and  ongoing  regulatory  approvals  of  our  other  product  candidates,  (ii)  market  acceptance,  commercial  viability 
and profi tability of ContraPest and other products; (iii) the ability to market our products and establish an eff ective sales force 
and marketing infrastructure to generate signifi cant revenue; (iv) the success of our research and development; (v) our ability 
to retain and attract key personnel to develop, operate and grow our business; and (vi) our ability to meet our working capital 
needs.

Based upon our current operating plan, we expect that cash and cash equivalents and highly liquid, short term investments at 
December 31, 2018, in combination with anticipated revenue and additional sales of our equity securities, will be suffi  cient 
to fund our current operations for at least the next 12 months. However, if anticipated revenue targets and margin targets are 
not achieved and we are unable to raise necessary capital through the sale of our securities, we may seek to reduce operating 
expenses and are likely to require additional capital in order to fund our operating losses and research and development activities 
until we become profi table. We may never achieve profi tability or generate positive cash fl ows, and unless and until we do, 

F-8

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

1. Organization and Description of Business (cont.)

we will continue to need to raise capital through equity or debt fi nancing. If such equity or debt fi nancing is not available at 
adequate levels or on acceptable terms, we may need to delay, limit or terminate commercialization and development eff orts.

Major Customer

The Company has two major customers that accounted for approximately 52% and 13% and $157,000 and $38,000 of sales for 
the year ended December 31, 2018 and 91% and $127,000 of total accounts receivable at December 31, 2018. The Company 
expects to maintain this relationship with the customer.

2. Summary of Signifi cant Accounting Policies

Use of Estimates

The preparation of the fi nancial statements in conformity with accounting principles generally accepted in the United States of 
America (“U.S. GAAP”) requires management to make estimates and assumptions that aff ect the reported amounts of assets 
and liabilities and disclosure of contingent assets and liabilities at the date of the fi nancial statements and reported amounts 
of revenues and expenses during the reporting period. The signifi cant estimates in the Company’s fi nancial statements include 
the valuation of preferred stock, common stock and related warrants, and other stock-based awards. Actual results could diff er 
from such estimates.

Reclassifi cations

Certain prior year amounts have been reclassifi ed to conform to the current year presentation. These reclassifi cations had no 
impact on net earnings, fi nancial position or cash fl ows.

Cash and Cash Equivalents

The Company considers money market fund investments to be cash equivalents. The Company had cash equivalents of $0 and 
$3 at December 31, 2018 and December 31, 2017, respectively, included in cash as reported.

Investments in Securities

The Company uses cash holdings to purchase highly liquid, short term, investment grade securities diversifi ed among security 
types, industries and issuers. All of the Company’s investment securities are measured at fair value. The Company’s investment 
securities primarily consist of municipal debt securities, corporate bonds, U.S. agency securities and commercial paper and 
highly-liquid money market funds.

Accounts Receivable

Accounts receivable consist primarily of trade receivables. The Company provides an allowance for doubtful trade receivables 
equal to the estimated uncollectible amounts. That estimate is based on historical collection experience, current economic and 
market conditions and a review of the current status of each customer’s trade accounts receivable. The allowance for doubtful 
trade receivables was less than $1 at December 31, 2018 and $0 at December 31, 2017, respectively.

Inventories

Inventories are stated at the lower of cost or market value, using the fi rst-in, fi rst-out convention. Inventories consist of raw 
materials and fi nished goods.

F-9

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

2. Summary of Signifi cant Accounting Policies (cont.)

Prepaid Expenses

Prepaid expenses consist primarily of payments made for director and offi  cer insurance, director compensation, rent, legal and 
inventory purchase deposits and seminar fees to be expensed in the current year.

Property and Equipment

Property and equipment are stated at cost less accumulated depreciation. Equipment held under capital leases are stated at the 
present value of minimum lease payments less accumulated amortization.

Depreciation  on  property  and  equipment  is  computed  using  the  straight-line  method  over  the  estimated  useful  lives  of  the 
respective assets. The cost of leasehold improvements is amortized over the life of the improvement or the term of the lease, 
whichever is shorter. Equipment held under capital leases are amortized over the shorter of the lease term or estimated useful 
life of the asset. The Company incurs maintenance costs on its major equipment. Repair and maintenance costs are expensed 
as incurred.

Impairment of Long-Lived Assets

Long-lived assets, such as property and equipment, are reviewed for impairment whenever events or changes in circumstances 
indicate that the carrying amount of an asset may not be recoverable. If circumstances require long-lived assets or asset groups 
to be tested for possible impairment, the Company compares the undiscounted cash fl ows expected to be generated from the use 
of the asset or asset group to its carrying amount. If the carrying amount of the long-lived asset or asset group is not recoverable 
on an undiscounted cash fl ow basis, an impairment charge is recognized to the extent that the carrying amount exceeds its fair 
value. Fair value is determined through various valuation techniques, such as discounted cash fl ow models and the use of third- 
party independent appraisals. The Company has not recorded an impairment of long-lived assets since its inception.

Revenue Recognition

Eff ective January 1, 2018, the Company adopted ASC 606 — Revenue from Contracts with Customers. Under ASC 606, the 
Company  recognizes  revenue  from  the  commercial  sales  of  products,  licensing  agreements  and  contracts  to  perform  pilot 
studies by applying the following steps: (1) identify the contract with a customer; (2) identify the performance obligations in the 
contract; (3) determine the transaction price; (4) allocate the transaction price to each performance obligation in the contract; 
and (5) recognize revenue when each performance obligation is satisfi ed. For the comparative periods, revenue has not been 
adjusted and continues to be reported under ASC 605 — Revenue Recognition. Under ASC 605, revenue is recognized when the 
following criteria are met: (1) persuasive evidence of an arrangement exists; (2) the performance of service has been rendered 
to  a  customer  or  delivery  has  occurred;  (3)  the  amount  of  the  fee  to  be  paid  by  a  customer  is  fi xed  and  determinable;  and 
(4) the collectability of the fee is reasonably assured. The performance obligations identifi ed by the Company under Accounting 
Standards Codifi cation (“ASC”) Topic 606, Revenue From Contracts With Customers, are straightforward and similar to the 
unit of account and performance obligation determination under ASC Topic 605, Revenue Recognition. There was no impact 
on the Company’s fi nancial statements as a result of adopting ASC 606 for the twelve months ended ended December 31, 2018 
and 2017, respectively.

The Company recognizes revenue when it leaves their dock at a fi xed selling price and payment terms of 30 to 120 days from 
invoicing. The Company recognizes other revenue earned from pilot studies upon the performance of specifi c services under 
the respective service contract.

F-10

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

2. Summary of Signifi cant Accounting Policies (cont.)

Research and Development

Research and development costs are expensed as incurred. Research and development expenses primarily consist of salaries and 
benefi ts for research and development employees, stock-based compensation, consulting fees, lab supplies, costs incurred related 
to conducting scientifi c trials and fi eld studies, and regulatory compliance costs. Also, included in research and development 
expenses is an allocation of facilities related costs, including depreciation of research and development equipment.

Stock-based Compensation

Employee  stock-based  awards,  consisting  of  restricted  stock  units  and  stock  options  expected  to  be  settled  in  shares  of  the 
Company’s  common  stock,  are  recorded  as  equity  awards. The  grant  date  fair  value  of  these  awards  is  measured  using  the 
Black-Scholes option pricing model. The Company expenses the grant date fair value of its stock options on a straight-line basis 
over their respective vesting periods. Performance-based awards are expensed over the performance period when the related 
performance goals are probable of being achieved.

For equity instruments issued to non-employees, the stock-based consideration is measured using a fair value method. The 
measurement of the stock-based compensation is subject to re-measurement as the underlying equity instruments vest.

Income Taxes

The Company accounts for income taxes under the asset and liability method, which requires the recognition of deferred tax 
assets and liabilities for the expected future tax consequences of events that have been included in the fi nancial statements. 
Under this method, deferred tax assets and liabilities are determined based on the diff erences between the fi nancial statements 
and tax bases of assets and liabilities and net operating loss carryforwards using enacted tax rates in eff ect for the year in which 
the diff erences are expected to reverse. The eff ect of a change in tax rates on deferred tax assets and liabilities is recognized in 
the period that includes the enactment date.

The Company records net deferred tax assets to the extent it believes these assets will more likely than not be realized. These 
deferred tax assets are subject to periodic assessments as to recoverability and if it is determined that it is more likely than not 
that the benefi ts will not be realized, valuation allowances are recorded which would increase the provision for income taxes. In 
making such determination, the Company considers all available positive and negative evidence, including future reversals of 
existing taxable temporary diff erences, projected future taxable income, tax planning strategies and recent fi nancial operations.

The Company applies a more-likely-than-not recognition threshold for all tax uncertainties. Only those benefi ts that have a 
greater than fi fty percent likelihood of being sustained upon examination by the taxing authorities are recognized. Based on 
its evaluation, the Company has concluded there are no signifi cant uncertain tax positions requiring recognition in its fi nancial 
statements.

The  Company  recognizes  interest  and/or  penalties  related  to  uncertain  tax  positions  in  income  tax  expense. There  are  no 
uncertain tax positions as of December 31, 2018 or December 31, 2017 and as such, no interest or penalties were recorded in 
income tax expense.

On December 22, 2017, the SEC staff  issued Staff  Accounting Bulletin No. 118 (“SAB 118”) which provides guidance on 
accounting for the tax eff ects of the Tax Cuts and Job Act of 2017 (the “Tax Act”). SAB 118 provides a measurement period 
that should not extend beyond one year from the date of enactment for companies to complete the accounting under ASC 740, 
Income Taxes. The Company is still analyzing the Tax Act and the impact, if any, it will have.

Comprehensive Loss

Net loss and comprehensive loss were the same for all periods presented; therefore, a separate statement of comprehensive loss 
is not included in the accompanying fi nancial statements.

F-11

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

2. Summary of Signifi cant Accounting Policies (cont.)

Loss Per Share Attributable to Common Stockholders

Basic  loss  per  share  attributable  to  common  stockholders  is  calculated  by  dividing  the  net  loss  attributable  to  common 
stockholders  by  the  weighted  average  number  of  common  shares  outstanding  during  the  period.  Diluted  loss  per  share 
attributable to common stockholders is computed by dividing the loss attributable to common stockholders by the weighted 
average number of common shares and potentially dilutive securities outstanding for the period determined using the treasury 
stock and if-converted methods. For purposes of the computation of diluted loss per share attributable to common stockholders, 
common stock purchase warrants, restricted stock units and common stock options are considered to be potentially dilutive 
securities but have been excluded from the calculation of diluted loss per share attributable to common stockholders because 
their eff ect would be anti-dilutive given the net loss reported for the years ended December 31, 2018 and 2017. Therefore, basic 
and diluted loss per share attributable to common stockholders was the same for all periods presented.

The following table sets forth the outstanding potentially dilutive securities that have been excluded in the calculation of diluted 
loss per share attributable to common stockholders (in common stock equivalent shares):

Common stock purchase warrants  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Restricted stock unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Common stock options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

December 31,

2018

11,226,821
136,245
1,721,771
12,084,837

2017
6,431,785
287,885
1,651,800
8,371,470

In May 2014 the FASB issued ASU 2014-09, Revenue from Contracts with Customers. Since ASU 2014-09 was issued, several 
additional ASUs have been issued to clarify various elements of the guidance. These standards provide guidance on recognizing 
revenue, including a fi ve-step model to determine when revenue recognition is appropriate. The standard requires that an entity 
recognize revenue to depict the transfer of control of promised goods or services to customers in an amount that refl ects the 
consideration to which the entity expects to be entitled in exchange for those goods or services. Eff ective January 1, 2018, the 
Company adopted ASU 2014-09, “Revenue from Contracts with Customers” using the modifi ed retrospective method to all 
contracts that were not completed as of the date of adoption. The results of operations for reported periods after January 1, 2018 
are presented under this amended guidance, while prior period amounts are reported in accordance with ASC 605 — Revenue 
Recognition. There was no material impact on our fi nancial position, results of operations, or cash fl ows. See Note 2 — Summary 
of Signifi cant Accounting Policies — Revenue Recognition.

In August 2016, the FASB issued ASU 2016-15, Statement of Cash Flows (Topic 230): Classifi cation of Certain Cash Receipts 
and Cash Payments. The amendments in this ASU provide guidance on the following eight specifi c cash fl ow classifi cation issues: 
(1) debt prepayment or debt extinguishment costs; (2) settlement of zero-coupon debt instruments or other debt instruments with 
coupon interest rates that are insignifi cant in relation to the eff ective interest rate of the borrowing; (3) contingent consideration 
payments  made  after  a  business  combination;  (4)  proceeds  from  the  settlement  of  insurance  claims;  (5)  proceeds  from  the 
settlement of corporate-owned life insurance policies, including bank-owned life insurance policies; (6) distributions received 
from equity method investees; (7) benefi cial interests in securitization transactions; and (8) separately identifi able cash fl ows 
and application of the predominance principle. The amendments of this ASU are eff ective for reporting periods beginning after 
December 15, 2017, with early adoption permitted. The Company has adopted the provisions of ASU 2016-15 on its fi nancial 
statements. There was no material impact on our fi nancial position, results of operations, or cash fl ows.

In January 2016, the FASB issued ASU 2016-01, Recognition and Measurement of Financial Assets and Financial Liabilities 
(“ASU 2016-01”). This standard aff ects the accounting for equity instruments, fi nancial liabilities under the fair value option 
and the presentation and disclosure requirements of fi nancial instruments. ASU 2016-01 is eff ective the fi rst quarter of 2018. 
The Company has adopted the provisions of ASU 2016-01 on its fi nancial statements. There was no material impact on our 
fi nancial position, results of operations, or cash fl ows.

F-12

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

2. Summary of Signifi cant Accounting Policies (cont.)

Accounting Standards Issued But Not Yet Adopted:

In February 2016, the FASB issued ASU 2016-02, Leases (“ASU 2016-02”). This standard amends various aspects of existing 
accounting guidance for leases, including the recognition of a right-of-use asset and a lease liability on the balance sheet for all 
leases with terms longer than 12 months. Leases will be classifi ed as either fi nance or operating, with classifi cation aff ecting 
the  pattern  of  expense  recognition  in  the  income  statement. This  standard  also  introduces  new  disclosure  requirements  for 
leasing arrangements. ASU 2016-02 is eff ective for fi scal years beginning after December 15, 2018, including interim periods 
within those fi scal years for public business entities. Early adoption is permitted and the new standard must be adopted using a 
modifi ed retrospective approach, and provides for certain practical expedients. At December 31, 2018, the Company had future 
minimum lease payments on its operating leases of $316 that would be recorded as a capital lease liability on its balance sheet. 
The Company plans to adopt ASU 2016-02 on its fi nancial statements and related disclosures at March 31, 2019.

3. Fair Value Measurements

We  invest  in  various  short  term,  highly  liquid  fi nancial  instruments,  which  may  include  municipal  debt  securities,  corporate 
bonds, U.S. agency securities and commercial paper. We value these instruments at fair value. The accounting guidance for fair 
value, among other things, establishes a consistent framework for measuring fair value and expands disclosure for each major 
asset and liability category measured at fair value on either a recurring or nonrecurring basis. Fair value is defi ned as the price that 
would be received to sell an asset or paid to transfer a liability (an exit price) in an orderly transaction between market participants 
at the reporting date. The framework for measuring fair value consists of a three-level valuation hierarchy that prioritizes the 
inputs  to  valuation  techniques  used  to  measure  fair  value  based  upon  whether  such  inputs  are  observable  or  unobservable. 
Observable inputs refl ect market data obtained from independent sources, while unobservable inputs refl ect market assumptions 
made by the reporting entity. The three-level hierarchy for the inputs to valuation techniques is briefl y summarized as follows:

Level 1 — Inputs are unadjusted, quoted prices in active markets for identical assets or liabilities at the measurement 
date;

Level 2 — Inputs are observable, unadjusted quoted prices in active markets for similar assets or liabilities, unadjusted 
quoted prices for identical or similar assets or liabilities in markets that are not active, or other inputs that are observable 
or can be corroborated by observable market data for substantially the full term of the related assets or liabilities; and

Level 3 — Unobservable inputs that are signifi cant to the measurement of the fair value of the assets or liabilities that 
are supported by little or no market data.

An asset’s or liability’s fair value measurement level within the fair value hierarchy is based on the lowest level of any input 
that is signifi cant to the fair value measurement. Valuation techniques used need to maximize the use of observable inputs and 
minimize the use of unobservable inputs.

Assets and liabilities measured at fair value are based on one or more of the following three valuation techniques:

A.  Market  approach:  Prices  and  other  relevant  information  generated  by  market  transactions  involving  identical  or 

comparable assets or liabilities.

B.  Cost approach: Amount that would be required to replace the service capacity of an asset (replacement cost).

C.  Income approach: Techniques to convert future amounts to a single present amount based upon market expectations, 

including present value techniques, option-pricing and excess earnings models.

The Company’s cash equivalents, which include money market funds, are classifi ed as Level 1 because they are valued using 
quoted market prices. The Company’s marketable securities consist of securities and are generally classifi ed as Level 2 because 
their value is based on valuations using signifi cant inputs derived from or corroborated by observable market data.

F-13

 
 
 
SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

3. Fair Value Measurements (cont.)

In certain cases where there is limited activity or less transparency around the inputs to valuation, securities are classifi ed as 
Level 3. Level 3 liabilities consist of common stock warrant liability.

Items Measured at Fair Value on a Recurring Basis

The following table sets forth the Company’s fi nancial instruments that were measured at fair value on a recurring basis by level 
within the fair value hierarchy (in thousands):

Financial Assets:

Money market funds . . . . . . . . . . . . . . . . . . . . . . $ 

Corporate fixed income debt securities . . . . . . . .

Total  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . $ 

Financial Liabilities:

Common stock warrant liability(1) . . . . . . . . . . . . $ 
Total  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . $ 

Level 1

Level 2

Level 3

Total

December 31, 2018

— $ 

—

— $ 

— $ 
— $ 

— $ 

—

— $ 

— $ 
— $ 

— $ 

—

— $ 

— $ 
— $ 

3

—

—

—
—

Level 1

Level 2

Level 3

Total

December 31, 2017

Financial Assets:

Money market funds . . . . . . . . . . . . . . . . . . . . . . $ 

3 $ 

— $ 

Corporate fixed income debt securities . . . . . . . .

—

5,023

Total  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . $ 

3 $ 

5,023 $ 

Financial Liabilities:

Common stock warrant liability(1) . . . . . . . . . . . . $ 
Total  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . $ 

— $ 
— $ 

— $ 
— $ 

— $ 

—

— $ 

— $ 
— $ 

3

5,023

5,026

—
—

(1)  The change in the fair value of the common stock warrant and convertible notes payable for the twelve months ended 
December 31, 2018 and 2017 was recorded as a decrease to other income (expense) and interest expense of $1 and $1, 
respectively, in the statements of operations and comprehensive loss.

Financial Instruments Not Carried at Fair Value

The carrying amounts of the Company’s fi nancial instruments, including accounts payable and accrued liabilities, approximate 
fair value due to their short maturities. The estimated fair value of the convertible notes and other notes, not recorded at fair 
value, are recorded at cost or amortized cost which was deemed to estimate fair value.

Note 4 — Investment in Securities

As  of  December  31,  2017,  investment  in  securities  held  to  maturity  primarily  consisted  of  corporate  fi xed  income  securities. 
investment in securities primarily consisted of corporate fi xed income securities. These investments are in short term, highly liquid 
investments which are recorded at cost plus or minus market fl uctuation and gains and losses are recognized as the sale or redemption 
of the securities is realized. Gains and losses are included in non-operating other income (expense) on the condensed statement of 
operations  and  are  derived  using  the  specifi c  identifi cation  method  for  determining  the  cost  of  the  securities  sold.  Interest  and 
dividends on investment securities are included in interest and other income, net, in the condensed statements of operations.

The Company did not have any held to maturity securities at December 31, 2017.

F-14

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

5. Credit Risk

The  Company  is  potentially  subject  to  concentrations  of  credit  risk  in  its  accounts  receivable.  Credit  risk  with  respect  to 
receivables  is  limited  due  to  the  number  of  companies  comprising  the  Company’s  customer  base. Although  the  Company 
is directly aff ected by the fi nancial condition of its customers, management does not believe signifi cant credit risks exist at 
December 31, 2018. The Company does not require collateral or other securities to support its accounts receivable.

6. Prepaid expenses

Prepaid expenses consist of the following:

December 31,

2018

2017

Director compensation  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Director, officer and other insurance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Marketing programs and conferences . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Legal retainer  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Inventory purchase deposits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Professional service retainer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Rent . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Equipment service deposits  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Engineering, software licenses and other . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total prepaid expenses  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 

100 $ 
121
53
25
—
8
19
3
13

342 $ 

66
33
—
25
20
8
—
7
11
170

7. Property and Equipment

Property and equipment, net consist of the following:

December 31,

Useful Life

2018

2017

Research and development equipment . . . . . . . . . . . . . . . . . . . . . . . . . . 
Office and computer equipment  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Autos . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Furniture and fixtures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Leasehold improvements  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Less accumulated depreciation and amortization . . . . . . . . . . . . . . . . . . 
Total  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

5 years $ 
3 years
5 years
7 years
*

$ 

1,552 $ 
742
54
37
283
2,668
1,585
1,083 $ 

1,349
672
305
34
283
2,643
1,189
1,454

*  Shorter of lease term or estimated useful life

Depreciation and amortization expense was approximately $447 and $391 for the year ended December 31, 2018 and 2017, 

respectively.

F-15

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

8. Accrued Expenses

Accrued expenses consist of the following:

December 31,

2018

2017

Compensation and related benefits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Accrued Litigation  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Personal property and franchise tax  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Board Compensation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Other . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total accrued expenses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 

479 $ 
269
23
—
—

771 $ 

9. Borrowings

A summary of the Company’s borrowings, including capital lease obligations, is as follows:

Short-term debt:

At December 31,

2018

2017

Current portion of long-term debt  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Total short-term debt . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 

Long-term debt:

Capital lease obligations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
Other unsecured promissory notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Less: current portion of long-term debt . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total long-term debt . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 

219
219 $ 

232 $ 
248
480
219
261 $ 

Capital Lease Obligations

304
269
—
16
—
589

177
177

272
496
768
177
591

Capital lease obligations are for computer and lab equipment leased through GreatAmerica Financial Services, Thermo Fisher 
Scientifi c, Navitas Credit Corp., Wells Fargo and ENGS Commercial Finance Co. These capital leases expire at various dates 
through July 2023 and carry interest rates ranging from 6.0% to 11.6%.

Other Promissory Notes

Also included in the table above are three notes payable to Direct Capital, one note to M2 Financing and one note to Fidelity 
Capital, all for the fi nancing of fi xed assets. These notes expire at various dates through June 2022 and carry interest rates 
ranging from 4.3% to 13.8%.

10. Notes Payable, Related Parties

A summary of the Company’s notes payable, related parties is as follows:

Unsecured promissory note, interest rate of 4.25% and 8% per annum . . . . . . . . . . . . . . .  $ 
Total notes payable, related parties . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Less: current portion of notes payable, related parties . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total notes payable, long-term . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 

December 31,
2018

— $ 
—
—
— $ 

2017

12
12
12
—

F-16

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

10. Notes Payable, Related Parties (cont.)

In April 2013, the Company and a previous employee entered into an agreement to settle all outstanding obligations consisting 
of a promissory note of $40, dated March 2009, and deferred salaries amounting to $72. The note and salary obligation provided 
for interest of 8% and 4.25%, respectively. The note required monthly payments of $1 and matured in May 2018. The deferred 
salary obligation required monthly payments of $1 and matured in June 2018.

Amounts outstanding on these obligations were $0 and $12 at December 31, 2018 and 2017, respectively.

Interest  expense  on  the  notes  payable,  related  parties,  was  $1  and  $1  for  the  years  ended  December  31,  2018  and  2017, 
respectively.

11. Common Stock Warrants and Common Stock Warrant Liability

The table summarizes the common stock warrant activity as of December 31, 2018 as follows:

Common Stock Warrants
Outstanding at December 31, 2016 . . . . . . . . . . . . . . . . . . 

Common Stock Offering Warrants Issued . . . . . . . . . . . . . 
Common Stock Offering Underwriter Warrants . . . . . . . . 
Outstanding at December 31, 2017 . . . . . . . . . . . . . . . . . . 

Warrants issued . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Common Stock Offering Warrants Issued . . . . . . . . . . . . . 
Common Stock Offering – Dealer Manager Warrants . . . . 
Warrants exercised  . . . . . . . . . . . . . . . . . . . . . . . . . . 
Expired Warrants. . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Outstanding at December 31, 2018 . . . . . . . . . . . . . . . . . . 

Number of 
Warrants

829,285

4,657,500
945,000
6,431,785

1,133,909
5,357,052
267,853
(1,475,659)
(488,119)
11,226,821

Date 
Issued

Term

Exercise Price

November 2017
November 2017

5 years
5 years

June 2018
August 2018
August 2018

5 Years
5 Years
5 Years

$ 
$ 

$ 
$ 
$ 

1.50(1)
1.50

1.82
1.15(1)
1.725

(1)  The common stock warrants issued in November 2017 with an initial exercise price of $1.50 per share adjusted downward 
to $0.95 per share eff ective July 24, 2018 in connection with our Rights Off ering, and may be subject to further downward 
adjustments, pursuant to antidilution price adjustment protection contained within those warrants.

On November 21, 2017, the Company issued a total of 4,657,500 detachable common stock warrants issued with the second 
public off ering of 5,860,000 shares of its common stock at $1.00 per share. The common stock warrant is exercisable until 
fi ve years from the date of grant. The common shares of the Company’s stock and detachable warrants exist independently as 
separate securities. As such, the Company estimated the fair value of the common stock warrants, exercisable at $1.50 per share, 
to be $661 using a lattice model based on the following signifi cant inputs: Common stock price of $1.00; comparable company 
volatility of 73.8%; remaining term 5 years; dividend yield of 0% and risk-free interest rate of 1.87. The initial exercise price of 
these warrants was $1.50 per share, which adjusted downward to $1.47 on July 24, 2018, the record date of the Right’s Off ering 
and downward to $0.95 per share on August 13, 2018, the date of the Rights Off ering, pursuant to antidilution price adjustment 
protection contained within these warrants. Per guidance of ASC 260, the Company recorded a deemed dividend of $333 on 
the 3,181,841 unexercised warrants that contained this antidilution price adjustment protection provision and was calculated as 
the diff erence between the fair value of the warrants immediately prior to downward exercise price adjustment and immediately 
after the adjustment using a Black Scholes model based on the following signifi cant inputs: On July 24, 2018: Common stock 
price of $1.38; comparable company volatility of 72.4%; remaining term 4.33 years; dividend yield of 0% and risk-free interest 
rate of 2.83. On August 13, 2018: Common stock price of $1.02; comparable company volatility of 74.0%; remaining term 4.25 
years; dividend yield of 0% and risk-free interest rate of 2.75.

On  June  20,  2018,  the  Company  entered  into  an  agreement  with  a  holder  of  1,133,909  of  the  November  2017  warrants  to 
exercise its original warrant representing 1,133,909 shares of Common Stock for cash at the $1.50 exercise price for gross 

F-17

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

11. Common Stock Warrants and Common Stock Warrant Liability (cont.)

proceeds of $1.7 million and the Company issued to holder a new warrant to purchase 1,133,909 shares of Common Stock 
at an exercise price of $1.82 per share. The new warrant did not contain the antidilution price adjustment protection that was 
contained within the exercised warrants. In June 2018, the Company recorded stock compensation expense of $1.7 million 
representing  the  fair  value  of  the  of  1,133,909  inducement  warrants  issued. The  Company  estimated  the  fair  value  of  the 
common stock warrants, exercisable at $1.82 per share, to be $1.7 million using a Black Scholes model based on the following 
signifi cant inputs: Common stock price of $2.11; comparable company volatility of 72.6%; remaining term 5 years; dividend 
yield of 0% and risk-free interest rate of 2.8%. Also in June 2018, an additional 341,750 of the November 8, 2017 warrants that 
were in the money at the time of exercise, were exercised for gross proceeds of $513.

On August  13,  2018,  in  connection  with  a  Rights  Off ering  of  5,357,052  shares  of  its  common  stock,  the  Company  issued 
5,357,052 warrants to purchase shares of its common stock at an exercise price of $1.15 per share. The Company estimated the 
fair value of the common stock warrants, exercisable at $1.15 per share, to be $3.6 million using a Monte Carlo model based 
on the following signifi cant inputs: common stock price of $0.94; comparable company volatility of 159.0%; remaining term 
5 years; dividend yield of 0% and risk-free interest rate of 2.77%.

In connection with the closing of the Rights Off ering, the Company issued a warrant to purchase 267,853 shares of common 
stock to Maxim Partners LLC, an affi  liate of the dealer-manager of the Rights Off ering. The Company estimated the fair value 
of the common stock warrants, exercisable at $1.725 per share, to be $169 using a using a Monte Carlo model based on the 
following signifi cant inputs: common stock price of $0.94; comparable company volatility of 159.0%; remaining term 5 years; 
dividend yield of 0% and risk-free interest rate of 2.77%.

Common Stock Warrant Issued to Underwriter of Common Stock Off ering

In November 2017, the Company issued to Roth Capital Partners, LLC, as underwriter, a warrant to purchase 945,000 shares of 
common stock at an exercise price of $1.50 per share as consideration for providing services in connection with our common 
stock off ering. The warrant was fully vested and exercisable on the date of issuance. The common stock warrant is exercisable 
until fi ve years from the date of grant. The Company estimated the fair value of the common stock warrants, exercisable at $1.50 
per share, to be $134 using a lattice model based on the following signifi cant inputs: Common stock price of $1.00; comparable 
company volatility of 73.8%; remaining term 5 years; dividend yield of 0% and risk-free interest rate of 1.87%.

University of Arizona Common Stock Warrant

In  connection  with  the  June  2015  amended  and  restated  exclusive  license  agreement  with  the  University  of  Arizona 
(“University”), the Company issued to the University a common stock warrant to purchase 15,000 shares of common stock 
at an exercise price of $7.50 per share. The warrant was fully vested and exercisable on the date of grant, and expires, if not 
exercised, fi ve years from the date of grant. In the event of a “terminating change” of the Company, as defi ned in the warrant 
agreement, the warrant holder would be paid in cash the aggregate fair market value of the underlying shares immediately prior 
to the consummation of the terminating change event. Due to the cash settlement provision, the derivative warrant liability was 
recorded at fair value and is revalued at the end of each reporting period. The changes in fair value are reported in other income 
(expense) in the statements of operations and comprehensive loss. The estimated fair value of the derivative warrant liability 
was $53 at the date of grant.

The estimated fair value of the derivative warrant liability was $0 at December 31, 2018. As this derivative warrant liability 
is revalued at the end of each reporting period, the fair values as determined at the date of grant and subsequent periods was 
based on the following signifi cant inputs using a Monte Carlo option pricing model: common stock price of $7.91; comparable 
company volatility of 77.7% of the underlying common stock; risk-free rates of 1.93%; and dividend yield of 0%; including 
the probability assessment of a terminating change event occurring. The change in fair value of the derivative warrant liability 
was $1 for year ended December 31, 2018 and was recorded in other income (expense) in the accompanying statements of 
operations and comprehensive loss.

F-18

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

12. Stockholders’ Defi cit

Capital Stock

The Company was organized under the laws of the state of Nevada on July 27, 2004 and was subsequently reincorporated 
under the laws of the state of Delaware on November 10, 2015. In connection with the reincorporation, as approved by the 
stockholders, the Company changed its authorized capital stock to consist of (i) 100 million shares of common stock, $.001 
par value, and (ii) 2 million shares of preferred stock, $0.001 par value, designated as Series A convertible preferred stock. In 
December 2015, the Company amended its Certifi cate of Incorporation to change its authorized capital stock to provide for 
15 million authorized shares of preferred stock of which 7,515,000 was designated as Series B convertible preferred stock, par 
value $.001 per share.

Prior to November 10, 2015, the Company’s authorized capital stock consisted of 100 million shares of common stock, $.001 
par value, and 10 million shares of preferred stock, $.001 par value.

Common Stock

The Company had 23,471,999 and 16,404,195 shares of common stock issued and outstanding as of December 31, 2018 and 
2017, respectively. During the year ending December 31, 2018, the Company issued 7,021,092 shares of common stock as 
follows:

• 

• 

• 

• 

• 

• 

an aggregate of 5,357,052 shares in connection with a Rights Off ering generating net proceeds to the Company of 
approximately $5.1 million,

an aggregate of 1,475,659 shares for net proceeds of $2.1 million for the exercise of the Company’s November 2017 
warrants (see Note 10 — Common Stock Warrants and Common Stock Warrant Liability for further details),

13,900 shares for the cashless exercise of stock options to employees,

32,625 shares to a former employee for the net settlement of restricted stock units whose vesting accelerated upon the 
termination of their employment contract,

37,162 shares to a Board member in net settlement of Board compensation totaling $28 and

151,406 shares for the net settlement of restricted stock units that vested during the period.

Rights Off ering

On August 13, 2018, the Company closed a Rights Off ering. Pursuant to the Rights Off ering, the Company accepted subscriptions 
for 5,357,052 units for a purchase price of $1.15 per unit, with each unit consisting of one share of the Company’s common 
stock, par value $0.001 per share, and one warrant. Each warrant included in the unit was exercisable for one share of the 
Company’s  common  stock  at  an  exercise  price  of  $1.15  per  share. At  closing  of  the  Rights  Off ering,  the  Company  issued 
5,357,052 shares of its common stock and 5,357,052 warrants to purchase shares of its common stock at an exercise price of 
$1.15 per share. The Rights Off ering generated net proceeds to the Company of approximately $5.1 million after the payment 
of fees and expenses related to the Rights Off ering. In connection with the closing of the Rights Off ering, the Company issued 
a warrant to purchase 267,853 shares of common stock to Maxim Partners LLC, an affi  liate of the dealer-manager of the Rights 
Off ering.

On November 8, 2017, the Company issued 5,860,000 shares of its common stock with a total of 4,657,500 detachable common 
stock warrants for net proceeds of $5.2 million in a second public off ering of the Company’s common stock. In connection 
with this common stock off ering, the Company issued to Roth Capital Partners, LLC, as underwriter, warrants to purchase an 
additional 945,000 shares of common stock.

F-19

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

12. Stockholders’ Defi cit (cont.)

In addition, during the year ended December 31, 2017, the Company issued an aggregate of 386,903 shares of common stock 
as follows: 48,240 shares to consultants for services, valued at $137, to settle previous claims; 14,404 shares for the cashless 
exercise  of  stock  options,  137,354  shares  to  certain  employees  and  Board  members  in  net  settlement  of  bonus  and  Board 
compensation totaling $115 and 187,295 shares for the net settlement of restricted stock units that vested during the period.

13. Stock-based Compensation

On June 12, 2018, the Company’s stockholders approved the 2018 Equity Incentive Plan (the “2018 Plan”) to replace the Company’s 
2015 Equity Incentive Plan (the “2015 Plan”). The 2018 Plan authorized the issuance of 1,000,000 shares of our common stock. 
In addition, up to 2,874,280 shares of our common stock currently reserved for issuance under the 2015 Plan became available 
for issuance under the 2018 Plan to the extent such shares were available for issuance under the 2015 Plan as of June 12, 2018 or 
cease to be subject to awards outstanding under the 2015 Plan, such as by expiration, cancellation, or forfeiture of such awards.

The stock-based awards are generally issued with a price equal to no less than fair value at the date of grant. Options granted 
under the 2018 Plan generally vest immediately, or ratably over a two- to 36-month period coinciding with their respective 
service periods; however, participants may exercise their options prior to vesting as provided by the 2018 Plan. Unvested shares 
issued for options exercised early may be subject to a repurchase by the Company if the participant terminates, at the original 
exercise price. Options under the 2018 Plan generally have a contractual term of fi ve years. Certain stock option awards provide 
for accelerated vesting upon a change in control.

As of December 31, 2018, the Company had 1,849,569 shares of common stock available for issuance under the 2018 Plan.

The Company measures the fair value of stock options with service-based and performance-based vesting criteria to employees, 
directors and consultants on the date of grant using the Black-Scholes option pricing model. The fair value of equity instruments 
issued to non-employees is re-measured as the award vests. The Black-Scholes valuation model requires the Company to make 
certain estimates and assumptions, including assumptions related to the expected price volatility of the Company’s stock, the 
period under which the options will be outstanding, the rate of return on risk-free investments, and the expected dividend yield 
for the Company’s stock.

The weighted-average assumptions used in the Black-Scholes option-pricing model used to calculate the fair value of options 
granted during the year ended December 31, 2017, were as follows:

Expected volatility  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Expected dividend yield . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Expected term (in years) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Risk-free interest rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Employee
71.6% to 83.7%

—
3.0 to 3.5

1.45% to 1.84%

Non-Employee
N/A
N/A
N/A
N/A

The weighted-average assumptions used in the Black-Scholes option-pricing model used to calculate the fair value of options 
granted during the year ended December 31, 2018, were as follows:

Expected volatility  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Expected dividend yield . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Expected term (in years) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Risk-free interest rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Employee
71.0% –79.8%

—
3.0–3.5

1.58%–2.89%

Non-Employee
N/A
N/A
N/A
N/A

Due  to  the  Company’s  limited  operating  history  and  lack  of  company-specifi c  historical  or  implied  volatility,  the  expected 
volatility assumption was determined based on historical volatilities from traded options of biotech companies of comparable 
in size and stability, whose share prices are publicly available. The expected term of options granted to employees is calculated 

F-20

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

13. Stock-based Compensation (cont.)

based on the mid-point between the vesting date and the end of the contractual term according to the simplifi ed method as 
described in SEC Staff  Accounting Bulletin 110 because the Company does not have suffi  cient historical exercise data to provide 
a reasonable basis upon which to estimate the expected term due to the limited period of time its awards have been outstanding. 
For non-employee options, the expected term of options granted is the contractual term of the options. The risk-free rate by 
reference to the implied yields of U.S. Treasury securities with a remaining term equal to the expected term assumed at the 
time of grant. The expected dividend assumption is based on the Company’s history and expectation of dividend payouts. The 
Company has not paid and does not intend to pay dividends on its shares of capital stock.

The table summarizes the stock option activity, for both plans, for the periods indicated as follows:

Weighted 
Average 
Exercise Price 
Share

Number of 
Options

Outstanding at December 31, 2016 . . . . . . . . . . . . . . .
Granted . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Exercised . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Forfeited  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Expired . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Outstanding at December 31, 2017 . . . . . . . . . . . . . . .
Granted . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Exercised . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Forfeited  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Expired . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Outstanding at December 31, 2018 . . . . . . . . . . . . . . .
Exercisable at December 31, 2018 . . . . . . . . . . . . . . .

1,477,300 $ 
258,500 $ 
(18,000) $ 
(1,000) $ 
(65,000) $ 
1,651,800 $ 
179,471 $ 
(49,000) $ 
(50,500) $ 
(10,600) $ 
1,721,171 $ 
1,443,296 $ 

1.61
4.62
0.50
0.50
10.22
1.67
1.53
0.50
—
—
1.57
1.56

Weighted 
Average 
Remaining 
Contractual 
Per Term 
(years)

Aggregate 
Intrinsic 
Value(1)

5.8 $ 
5.0 $ 

9,662
34

3.7 $ 
4.4 $ 

4.0 $ 
3.5 $ 

—
—

—
—

(1)  The aggregate intrinsic value on the table was calculated based on the diff erence between the estimated fair value of the 
Company’s stock and the exercise price of the underlying option. The estimated stock values used in the calculation was 
$0.59 and $0.72 per share for each of the years ended December 31, 2018 and 2017 respectively.

The weighted average grant date fair value of options granted to employees for the year Ended December 31, 2017 was $1.53 
per share.

The stock-based compensation expense was recorded as follows:

Years Ended December 31,

2018

2017

Research and development . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 
General and administrative . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Total stock-based compensation expense . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 

106 $ 

3,306
3,412 $ 

377
3,338
3,715

The allocation between research and development and general and administrative expense was based on the department and 
services performed by the employee or non-employee.

Included in the table above, the Company recorded stock-based compensation expense of $137 and $137 for the years ended 
December 31, 2018 and 2017, respectively, for stock options granted to non-employees.

F-21

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

13. Stock-based Compensation (cont.)

At December 31, 2018, the total compensation cost related to non-vested options not yet recognized was $577, which will be 
recognized over a weighted average period of 27 months, assuming the employees complete their service period required for 
vesting.

Eff ective July 2015, the Company’s stockholders approved the 2015 Equity Incentive Plan (the “2015 Plan”), which permits the 
issuance of up to 2,000,000 shares reserved for the grant of stock options, stock appreciation rights, restricted stock units and 
other stock-based awards for employees, directors or consultants.

Restricted Stock Units

The following table summarizes restricted stock unit activity for the years ended December 31, 2017 and 2016:

Weighted 
Average Grant 
Date Fair Value 
Per Units

Number of 
Units

Outstanding as of December 31, 2016 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Granted . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Vested . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Forfeited  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Outstanding as of December 31, 2017 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Granted . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Vested . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Forfeited  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Outstanding as of December 31, 2018 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

455,430 $ 
117,885(1) $ 
(282,344) $ 
(3,086) $ 
287,885 $ 
75,732(2) $ 
(223,795) $ 
(3,577) $ 
136,345 $ 

0.76
6.95
1.75
—
1.86
1.62
2.56
6.99
0.98

(1)  40,000 restricted stock units were granted on March 27, 2017 with a weighted average grant date fair value of $8.35, 17,885 
restricted stock units were granted on May 19, 2017 with a weighted average grant date fair value of $6.99 and 60,000 
restricted stock units were granted on June 19, 2017 with a weighted average grant date fair value of $6.00.

(2)  12,820 restricted stock units were granted on June 12, 2017 with a weighted average grant date fair value of $0.65 and 

62,912 restricted stock units were granted on June 12, 2018 with a weighted average grant date fair value of $1.82

14. Income Taxes

The  components  of  the  pretax  loss  from  operations  for  the  years  ended  December  31,  2018  and  2017  are  as  follows  (in 
thousands)

U.S. Domestic . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Foreign  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Pretax loss from operations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

2018

2017

(11,908)
—
(11,908)

(12,286)
—
(12,286)

F-22

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

14. Income Taxes (cont.)

The provision for income taxes from continuing operations for the years ended December 31, 2018 and 2017 are as follows (in 
thousands):

Current

Federal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
State . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Foreign  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total current  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Deferred

Federal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
State . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Foreign  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total deferred  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total income tax expense (benefit) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Tax Rate Reconciliation

2018

2017

—
—
—
—

—
—
—
—
—

—
—
—
—

—
—
—
—
—

A reconciliation on income taxes to the amount computed by applying the statutory federal income tax rate to the net loss is 
summarized as follows (in thousands):

12/31/18

12/31/17

Income tax benefit at statutory rates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
State income tax, net of federal benefit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Permanent items . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Stock-based compensation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Tax Rate Adjustment – TCJA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Change in rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Stock Compensation DTA Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Change in Valuation Allowance  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
RTP and Other . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Income tax expense (benefit)  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

(2,501)
(331)
8
697
7,758
941
5,794
(12,673)
307
—

(4,176)
(566)
7
—
—
—
—
4,735
—
—

Signifi cant components of the Company’s deferred tax assets as of December 31, 2018 and 2017 are shown below. A valuation 
allowance has been recognized to off set the net deferred tax assets as realization of such deferred tax assets have not met the 
more likely than not threshold.

F-23

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

14. Income Taxes (cont.)

Deferred tax assets:

Deferred Rent . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Federal and State Net Operating Loss Carryovers  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Stock Based Compensation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Compensation Accruals and Other . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total deferred tax assets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Valuation Allowance for deferred tax assets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Deferred tax assets, net of valuation allowance  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

Deferred tax liabilities:

Depreciation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total deferred tax liabilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

12/31/18

12/31/17

4
12,964
448
187
13,603
(13,550)
53

(53)
(53)

—

29
17,013
9,234
(5)
26,271
(26,222)
49

(49)
(49)

—

At December 31, 2018, the Company has federal and state net operating loss carryforwards of approximately $51.1 million 
and  $37.6  million,  respectively,  not  considering  the  IRC  Section  382  annual  limitation  discussed  below.  The  federal  loss 
carryforwards begin to expire in 2023, unless previously utilized.

Additionally,  the  utilization  of  the  net  operating  loss  carryforwards  are  subject  to  an  annual  limitation  under  Section  382 
and  383  of  the  Internal  Revenue  Code  of  1986,  and  similar  state  tax  provisions  due  to  ownership  change  limitations  that 
have occurred previously or that could occur in the future. These ownership changes limit the amount of net operating loss 
carryforwards and other deferred tax assets that can be utilized to off set future taxable income and tax, respectively. In general, 
an ownership change, as defi ned by Section 382 and 383, results from transactions increasing ownership of certain stockholders 
or public groups in the stock of the corporation by more than 50 percent points over a three-year period. The Company has 
not conducted an analysis of an ownership change under section 382. To the extent that a study is completed and an ownership 
change is deemed to occur, the Company’s net operating losses could be limited.

The following table summarizes the activity related to the Company’s gross unrecognized tax benefi ts at the beginning and end 
of the years ended December 31, 2018 and 2017 (in thousands):

Gross unrecognized tax benefits at the beginning of the year . . . . . . . . . . . . . . . . . . . . . . . 
Increases related to current year positions  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Increases related to prior year positions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Decreases related to prior year positions  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Expiration of unrecognized tax benefits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Gross unrecognized tax benefits at the end of the year . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

12/31/18

12/31/17

—
—
—
—
—
—
—

—
—
—
—
—
—
—

None of the unrecognized tax benefi ts would aff ect the Company’s annual eff ective tax rate.

The Company does not expect a signifi cant change in unrecognized tax benefi ts over the next 12 months.

The Company fi les income tax returns in the United States and Arizona with general statutes of limitations of 3 and 4 years, 
respectively. Due to net operating losses incurred, the Company’s tax returns from inception to date are subject to examination 
by taxing authorities. The Company’s policy is to recognize interest expense and penalties related to income tax matters as a 
component of income tax expense. As of Dec 31, 2018, the Company had no interest or penalties accrued for uncertain tax 
positions.

F-24

 
 
SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

14. Income Taxes (cont.)

Tax Cuts and Jobs Act Disclosures:

On December 20, 2017 the United States House of Representatives and the Senate passed the “Tax Cuts and Jobs Act” (the “Tax 
Act”), which was signed into law on December 22, 2017.

Due to the complexity of the Tax Act, the SEC issued guidance in ASU 2018-05 which clarifi ed the accounting for income 
taxes under ASC 740 if certain information was not yet available, prepared or analyzed in reasonable detail to complete the 
accounting for income tax eff ects of the Tax Act. ASU 2018-05 provided for a measurement period of up to one year after the 
enactment of the Tax Act, during which time the required analyses and accounting must have been completed.

During the measurement period (i) income tax eff ects of the Tax Act must have been reported if the accounting was completed; 
(ii) provisional amounts must have been reported for income tax eff ects of the Tax Act for which the accounting was incomplete 
but a reasonable estimate could be determined; and (iii) provisional amounts were not required to be reported for income tax 
eff ects of the Tax Act for which a reasonable estimate could not be determined.

The Tax Act did not have a material impact on the Company’s net deferred tax balances or its provision for income taxes due to 
the Company’s full valuation allowance since inception.

The  determination  of  the Tax Act’s  income  tax  eff ects  may  change  following  future  legislation  or  further  interpretation  of 
the Tax Act based on the publication of recently proposed U.S. Treasury regulations and guidance from the Internal Revenue 
Service and state tax authorities.

15. Commitments and Contingencies

Legal Proceedings

The Company may be subject to legal proceedings and claims arising from contracts or other matters from time to time in the 
ordinary course of business. Management is not aware of any pending or threatened litigation where the ultimate disposition or 
resolution could have a material adverse eff ect on its fi nancial position, results of operations or liquidity.

On February 20, 2018, New Enterprises, Ltd. (“New Enterprises”), fi led lawsuit against the Company and Roth Capital Partners, 
LLC (“Roth”) in the U.S. District Court for the District of Arizona (the “Court”). The complaint alleges nine counts against 
the Company, including that: the Company engaged in common law fraud and securities fraud to induce the chairman of New 
Enterprises into investing in the Company; failed to register New Enterprises’ requested transfer; breached stock certifi cates 
and the lock-up contract; tortuously interfered with prospective business advantage; and conversion. New Enterprises is seeking 
monetary damages, including compensatory damages, punitive damages, and attorney’s fees. On April 23, 2018, the Company 
moved to dismiss each of the claims alleged against the Company, and on May 18, 2-18, Roth moved to dismiss each of the 
claims alleged against it. The motions to dismiss were fully briefed, the Court issued an order granting the motions to dismiss, 
dismissing  each  of  the  claims  alleged  in  the  Complaint  but  allowed  New  Enterprises  to  fi le  a  motion  for  leave  to  fi le  an 
Amended Complaint seeking to cure the defi ciencies in its claims. On January 25, 2019, New Enterprises moved for leave to fi le 
an amended complaint, alleging similar claims against the Company and Roth. The Company and Roth have fi led oppositions to 
New Enterprises’ motion, New Enterprises fi led its reply, and the motion is currently under advisement with the Court. Roth has 
made a claim for indemnifi cation to the Company based on contractual indemnifi cation agreements, but to date, the Company 
has not accepted Roth’s indemnifi cation demand.

On April 20, 2018, the Company’s former Executive Vice President and Chief Operating Offi  cer Andrew Altman fi led a charge 
of employment discrimination with the Equal Employment Opportunity Commission (EEOC) against the Company. Mr. Altman 
claimed that he was terminated after he expressed opposition to an email Cheryl Dyer, Chief Research Offi  cer, had sent out 
to the management team, in which she criticized a Mormon newspaper. The Company fi led a position statement on May 21, 
2018. No substantive action has been taken since then, and the Company has not heard anything further either from the EEOC 
or Mr. Altman’s attorneys.

F-25

SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

15. Commitments and Contingencies (cont.)

Lease Commitments

The  Company  is  obligated  under  capital  leases  for  certain  research  and  computer  equipment  that  expire  on  various  dates 
through May 2020. At December 31, 2018, the gross amount of offi  ce and computer equipment, and research equipment and 
the related accumulated amortization recorded under the capital leases was $521 and $200, respectively.

In February 2012, the Company entered into an operating lease for its corporate headquarters. The lease was due to expire 
in January 2015. In December 2013, the Company amended its lease to expand into the remaining area in the building and 
extended the term to December 31, 2019. In February 2014, the Company further amended the lease to expand into an adjacent 
building. The lease requires escalating rental payments over the lease term. Minimum rental payments under the operating lease 
are recognized on a straight-line basis over the term of the lease and accordingly, the Company records the diff erence between 
the cash rent payments and the recognition of rent expense as a deferred rent liability. The lease is guaranteed by the President 
of the Company. We are in current discussions to extend the current lease.

On November 16, 2016, we leased an additional 1,954 square feet of research and development space, also in Flagstaff . This 
lease expired on November 15, 2018 but was extended for an additional 24 months, through November 2020. A subsequent 
amendment to the lease allows for the Company to cancel the lease at any time through the lease term with 30 days notice.

The lease extension requires fi xed rental payments over the lease term. Minimum rental payments under the operating lease are 
recognized on a straight-line basis over the term of the lease as expense, and accordingly, the Company recorded no deferred 
rent liability under this lease.

Rent expense was $242 and $312 for the year ended December 31, 2018 and 2017, respectively. The future minimum lease 
payments  under  non-cancellable  operating  lease  and  future  minimum  capital  lease  payments  as  of  December  31,  2018  are 
follows:

Capital 
Leases

Operating 
Lease

Years Ending December 31,
2019. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
2020. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
2021. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
2022. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
2023. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 
Total minimum lease payments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  $ 

99
78
63
33
3
276 $ 

Less: amounts representing interest (ranging from 7.75% to 11.58%) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . $ 

Present value of minimum lease payments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Less: current installments under capital lease obligations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Total long-term portion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . $ 

271
45
—
—

316

Capital 
Leases

43

233

77

156

F-26

 
SENESTECH, INC.
NOTES TO THE FINANCIAL STATEMENTS
(In thousands, except share and per share data)

16. Subsequent Events

In January 2019, the Company net issued 18,474 shares of common stock for a cashless exercise of vested common share 
options.

Also in January 2019, the Company issued 38,580 shares of common stock to certain employees in net settlement of bonus 
compensation of $49 accrued at December 31, 2018.

In March 2019, the Company issued an aggregate of 31,811 shares of common stock for the exercise of certain warrants. The 
net proceeds to the company for this exercise was $37.

On March 20, 2019 we received notice from the listing qualifi cations staff  of the Nasdaq Stock Market, notifying us that the 
closing bid price of our common stock was greater than $1.00 per share for ten consecutive business days and that we had 
regained compliance with the minimum bid price requirement of the Nasdaq Stock Market.

F-27

Item 9.  Changes in and Disagreements with Accountants on Accounting and Financial Disclosure.

None.

Item 9A.  Controls and Procedures.

Evaluation of Disclosure Controls and Procedures

We maintain disclosure controls and procedures that are designed to ensure that the information required to be disclosed in the 
reports that we fi le or submit under the Securities Exchange Act of 1934 (“Exchange Act”) is recorded, processed, summarized 
and reported within the time periods specifi ed in the SEC’s rules and forms, and that such information is accumulated and 
communicated to our management, including our Chief Executive Offi  cer and Chief Financial Offi  cer, as appropriate, to allow 
timely decisions regarding required disclosure.

In connection with the preparation of this Annual Report on Form 10-K, our management carried out an evaluation, under 
the  supervision  and  with  the  participation  of  our  Chief  Executive  Offi  cer  and  Chief  Financial  Offi  cer,  as  of  December  31, 
2018, of the eff ectiveness of the design and operation of our disclosure controls and procedures, as such term is defi ned under 
Rule  13a-15(e)  and  15d-15(e)  under  the  Exchange Act.  Based  upon  this  evaluation,  our  Chief  Executive  Offi  cer  and  Chief 
Financial Offi  cer concluded that our disclosure controls and procedures were eff ective as of December 31, 2018.

Management’s Report on Internal Control Over Financial Reporting

Management is responsible for establishing and maintaining adequate internal control over fi nancial reporting as defi ned in 
Rules 13a-15(f) or 15d-15(f) under the Exchange Act of 1934. Our internal control over fi nancial reporting is a process designed 
to provide reasonable assurance regarding the reliability of fi nancial reporting and the preparation of fi nancial statements for 
external purposes in accordance with U.S. GAAP. All internal control systems, no matter how well designed, have inherent 
limitations.  Even  those  systems  determined  to  be  eff ective  can  provide  only  reasonable  assurance  with  respect  to  fi nancial 
statement preparation and presentation. Management is committed to continue monitoring our internal controls over fi nancial 
reporting and will modify or implement additional controls and procedures that may be required to ensure the ongoing integrity 
of our consolidated fi nancial statements.

With the participation of our Chief Executive Offi  cer and Chief Financial Offi  cer, management conducted an evaluation of the 
eff ectiveness of internal control over fi nancial reporting as of December 31, 2018. In making this assessment, the Company 
used the framework established in Internal Control — Integrated Framework (2013) issued by the Committee of Sponsoring 
Organizations  of  the Treadway  Commission,  (COSO).  Based  on  this  assessment,  management  has  concluded  that  internal 
control over fi nancial reporting was eff ective as of December 31, 2018 based on those criteria.

This annual report does not include an attestation report of the company’s registered public accounting fi rm due to a transition 
period established by rules of the Securities and Exchange Commission for smaller reporting companies and emerging growth 
companies.

Changes in Internal Control over Financial Reporting

There was no change in our internal control over fi nancial reporting that occurred during the quarter ended December 31, 2018, 
that has materially aff ected, or is reasonably likely to materially aff ect, our internal control over fi nancial reporting.

Item 9B.  Other Information.

None.

37

Item 10.  Directors, Executive Offi  cers and Corporate Governance.

PART III

Certain information required by this Item regarding our directors and executive offi  cers is set forth in Part I of this report 
under Item 1, “Business — Directors and Executive Offi  cers of the Registrant” and will be included in our defi nitive proxy 
statement for our 2019 Annual Meeting of Stockholders to be fi led with the SEC under the captions “Nominees and Continuing 
Directors” and “Executive Offi  cers” and is incorporated herein by this reference.

The information required by this Item regarding compliance by our directors, executive offi  cers and holders of ten percent 
of a registered class of our equity securities with Section 16(a) of the Securities Exchange Act of 1934 will be included in our 
defi nitive proxy statement for our 2019 Annual Meeting of Stockholders to be fi led with the SEC under the caption “Stock 
Ownership” and is incorporated herein by this reference.

The remaining information required by this Item will be included in our defi nitive proxy statement for our 2019 Annual 
Meeting of Stockholders to be fi led with the SEC under the caption “Corporate Governance” and is incorporated herein by this 
reference.

Item 11.  Executive Compensation.

The information required by this Item will be included in our defi nitive proxy statement for our 2019 Annual Meeting of 
Stockholders to be fi led with the SEC under the captions “Corporate Governance” and “Executive Offi  cer Compensation” and 
is incorporated herein by this reference.

Item 12.  Security Ownership of Certain Benefi cial Owners and Management and Related Stockholder Matters.

The information required by this Item regarding equity compensation plan information will be included in our defi nitive 
proxy statement for our 2019 Annual Meeting of Stockholders to be fi led with the SEC under the caption “Equity Compensation 
Plan Information” and is incorporated herein by this reference.

The  information  required  by  this  Item  regarding  security  ownership  will  be  included  in  our  defi nitive  proxy  statement 
for our 2019 Annual Meeting of Stockholders to be fi led with the SEC under the caption “Security Ownership of Principal 
Stockholders, Directors and Management” and is incorporated herein by this reference.

Item 13.  Certain Relationships and Related Transactions, and Director Independence.

The information required by this Item will be included in our defi nitive proxy statement for our 2019 Annual Meeting 
of Stockholders to be fi led with the SEC under the captions “Corporate Governance” and “Certain Relationships and Related 
Transactions” and is incorporated herein by this reference.

Item 14.  Principal Accounting Fees and Services.

The  information  required  by  this  Item  with  respect  to  principal  accounting  fees  and  services  will  be  included  in  our 
defi nitive proxy statement for our 2019 Annual Meeting of Stockholders to be fi led with the SEC under the caption “Ratify 
Appointment of Independent Registered Public Accounting Firm” and is incorporated herein by this reference.

38

PART IV

Item 15.  Exhibits, Financial Statement Schedules.

(a)  Financial Statements and Schedules

1.  Financial Statements.

The following consolidated fi nancial statements are fi led as part of this report under Item 8 of Part II, “Financial Statements 

and Supplementary Data.”

A.  Balance Sheets as of December 31, 2018 and 2017.

B.  Statements of Operations and Comprehensive Income (Loss) for the years ended December 31, 2018 and 2017.

C.  Statements of Stockholders’ Equity for the years ended December 31, 2018 and 2017.

D.  Statements of Cash Flows for the years ended December 31, 2018 and 2017.

2.  Financial Statement Schedules.

Financial statement schedules not included herein have been omitted because they are either not required, not applicable, 

or the information is otherwise included herein.

3.  Exhibits.

Exhibits are incorporated herein by reference or are fi led with this report as indicated below (numbered in accordance with 

Item 601 of Regulation S-K).

(b)  Exhibits

The exhibits listed in the accompanying Index to Exhibits are fi led with this report or incorporated herein by reference.

39

SENESTECH, INC.
INDEX TO EXHIBITS

Incorporated by Reference

Form

Filing Date

Exhibit

File No.

S-1/A
S-1

10/20/2016
9/21/2016

3.3
3.5

333-213736
333-213736

S-1

S-1

8-K
S-1

9/21/2016

10.1

333-213736

9/21/2016

10.2

333-213736

12/21/2016
9/21/2016

4.1
10.2

001-37941
333-213736

S-1

9/21/2016

10.7

333-213736

S-1

9/21/2016

10.8

333-213736

S-1

9/21/2016

10.9

333-213736

S-1

9/21/2016

10.5

333-213736

S-1

9/21/2016

10.10

333-213736

S-1

9/21/2016

10.11

333-213736

8-K

1/23/2017

1.1

001-37941

Exhibit 
Number

Description

Filed or 
Furnished 
Herewith

3.1

3.2
10.1(1)

10.2(1)

10.3(1)

10.4(1)
10.5(1)

10.6(1)

10.7(1)

10.8

10.9(2)

10.10(2)

10.11

21.1
23.1

31.1

31.2

Amended and Restated Certificate of 
Incorporation
Amended and Restated Bylaws
SenesTech, Inc. 2008 – 2009 
Non-Qualified Stock Option Plan and 
form of agreement thereunder
SenesTech, Inc. 2015 Equity Incentive 
Plan and forms of agreement thereunder
Form of Restricted Stock Unit 
Agreement
Form of Indemnification Agreement
Employment Letter Agreement by and 
between the Registrant and Loretta P. 
Mayer, Ph.D. dated June 30, 2016
Employment Letter Agreement by and 
between the Registrant and Cheryl A. 
Dyer, Ph.D. dated June 30, 2016
Employment Offer Letter by and 
between the Registrant and Thomas 
Chesterman dated November 20, 2015.
Lease by and between the Registrant 
and Caden Court, LLC, dated as of 
December 20, 2011 and amendments 
thereto dated December 6, 2013 and 
February 27, 2014.
Agency Agreement by and between the 
Registrant, Inmet S.A. and Bioceres, 
Inc. dated January 21, 2016.
Services Agreement by and between the 
Registrant, Inmet S.A. and Bioceres, 
Inc. dated January 21, 2016.
Settlement Agreement and Release 
dated January 23, 2017 by and between 
Neogen Corporation and the Registrant.
Subsidiaries of the Registrant
Consent of Independent Registered 
Public Accounting Firm
Certification of Chief Executive 
Officer pursuant to Exchange Act Rule 
13a-14(a) under the Securities and 
Exchange Act of 1934
Certification of Chief Financial 
Officer pursuant to Exchange Act Rule 
13a-14(a) under the Securities and 
Exchange Act of 1934

X

X

X

X

40

Exhibit 
Number

32.1

32.2

Description

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
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

101.INS XBRL Instance Document
101.
SCH
101.
CAL
101.
DEF
101.
LAB
101.
PRE

XBRL Taxonomy Extension Schema 
Document
XBRL Taxonomy Extension 
Calculation Linkbase Document
XBRL Taxonomy Extension Definition 
Linkbase
XBRL Taxonomy Extension Label 
Linkbase Document
XBRL Taxonomy Extension 
Presentation Linkbase Document

Incorporated by Reference

Filed or 
Furnished 
Herewith

Form

Filing Date

Exhibit

File No.

X

X
X

X

X

X

X

X

Indicates a management contract or compensatory plan or arrangement.

(1) 
(2)  Confi dential treatment has previously been granted by the SEC for certain portions of the referenced exhibit.

(c) Financial Statement Schedules

None

Item 16.  Form 10-K Summary.

Not applicable.

41

Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this 
report to be signed on its behalf by the undersigned, thereunto duly authorized.

SIGNATURES

Date: March 29, 2019 

Date: March 29, 2019 

SENESTECH, INC.

By:

By:

/s/ Loretta P. Mayer, Ph.D.
Loretta P. Mayer
Chair of the Board, Chief Executive Officer 
and Chief Scientific Officer

/s/ Thomas C. Chesterman
Thomas C. Chesterman
Chief Financial Officer and Treasurer

Pursuant to the requirements of the Securities Exchange Act of 1934, this report has been signed below by the following persons 
on March 29, 2019, on behalf of the registrant and in the capacities indicated.

Signature

Title

/s/ Loretta P. Mayer, Ph.D.

Loretta P. Mayer, Ph.D.

/s/ Thomas C. Chesterman
Thomas C. Chesterman

/S/ Delphine Francois Chiavarini
Delphine Francois Chiavarini

/S/ Marc Dumont
Marc Dumont

/S/ Jamie Bechtel
Jamie Bechtel

/S/ Matthew K. Szot
Matthew K. Szot

/S/ Julia Williams, M.D.
Julia Williams, M.D.

 /S/ Ken Siegel
Ken Siegel

Chair of the Board, Chief Executive Officer and 
Chief Scientific Officer
(Principal Executive Officer)

Chief Financial Officer and Treasurer
(Principal Financial and Accounting Officer)

Director

Director

Director

Director

Director

Director

42

[This page intentionally left blank] 

Directors, Officers and Corporate Information

Headquarters

3140 N. Caden Court, Suite 1, Flagstaff, Arizona 86004

Corporate Counsel

Perkins Coie, Phoenix, Arizona

Independent Registered Public Accountants

M&K CPAS, PLLC, Houston, Texas

Transfer Agent and Registrar

Transfer Online, Inc., Portland, Oregon

Investor Relations

Lytham Partners, LLC, Phoenix, Arizona

Directors
•  Loretta P. Mayer, Ph.D. – Chair of the Board, CEO and Chief Scienti c Of cer, SenesTech, Inc.
•  Jamie Bechtel – Co-founder and board member of New Course, Founder and managing partner  of Kito Global 
•  Marc Dumont – Owner, Chairman and CEO of Chateau de Messey Wineries, Meursault, France
•  Kenneth Siegel – President, Diamond Resorts International, Inc., Retired
•  Matthew K. Szot – CFO and Executive Vice President, S&W Seed Company
•  Julia Williams, M.D. – Physician, Founder and President of Humanitarian Efforts Reaching Out (HERO) 

Of cers 
•  Loretta P. Mayer, Ph.D. – Chair of the Board, CEO and Chief Scienti c Of cer, SenesTech, Inc.
•  Cheryl A. Dyer, Ph.D. – Director, President and Chief Research Of cer, SenesTech, Inc.
•  Thomas C. Chesterman – Executive Vice President, CFO, Treasurer and Assistant Secretary, SenesTech, Inc.
•  Kim Wolin – Executive Vice President Operations, SenesTech, Inc.
•  Edward Albe – Senior Vice President of Commercialization, SenesTech, Inc.

Annual Meeting
Our annual meeting of stockholders will be held on June 18, 2019 at 10:00 a.m., local time, at the Holiday Inn & Suites Phoenix 
Airport North, 1515 North 44th Street, Phoenix, AZ 85008.

Form 10-K
We  le an Annual Report on Form 10-K with the Securities and Exchange Commission. Copies are available without charge 
upon request. Requests should be sent to inquiries@senestech.com.

Stock Exchange Listing
Our common stock is traded on the NASDAQ Capital Market under the symbol SNES.

Dividends
We have never declared or paid cash dividends on our common stock. We currently intend to 
retain all available funds and any future earnings to support our operations and  nance the growth and development of our 
business and, therefore, do not intend to pay cash dividends on our common stock for the foreseeable future.

Forward-Looking Statements 
This annual report contains forward-looking statements based on current expectations, estimates and projections about 
our industry and management’s beliefs and assumptions. These forward-looking statements are not guarantees of future 
performance and are subject to risks and uncertainties that are dif cult to predict. Please refer to the information set forth 
under the captions “Risk Factors” and “Cautionary Note Regarding Forward-Looking Statements” in our Annual Report on Form 
10-K and other reports or documents we  le from time to time with the Securities and Exchange Commission. Readers are 
cautioned not to place undue reliance on the forward-looking statements, which speak only as of the date made, and except as 
required by law, we undertake no obligation to update any forward-looking statement.

 
 
 
 
 
SenesTech, Inc.
(Nasdaq: SNES)
3140 N. Caden Court, Suite 1
Flagstaff, Arizona 86004

(928) 779-4143
info@senestech.com
www.senestech.com

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