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Securities registered pursuant to Section 12(g) of
the Act: Common Stock, $.001 par value
Indicate by check mark if the registrant is a well-known seasoned issuer,
as defined in Rule 405 of the Securities Act. Yes ☐ No ☒
Indicate by check mark if the registrant is not required to file reports
pursuant to Section 13 or Section 15(d) of the Exchange Act. Yes ☐ No ☒
Indicate by check mark whether the registrant (1) has filed all reports
required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter
period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes ☒ No ☐
Indicate by check mark whether the registrant has submitted electronically
every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T during the preceding 12 months (or for such
shorter period that the registrant was required to submit such files). Yes ☒ No ☐
Indicate by check mark whether the registrant is a large accelerated
filer, an accelerated filer, a non-accelerated filer, smaller reporting company, or an emerging growth company. See the definitions of
“large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth
company” in Rule 12b-2 of the Exchange Act.
If an emerging growth company, indicate by checkmark if the registrant
has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant
to Section 13(a) of the Exchange Act. ☐
Indicate by check mark whether the registrant has filed a report on and
attestation to its management’s assessment of the effectiveness of its internal control over financial reporting under Section 404(b)
of the Sarbanes-Oxley Act (15 U.S.C. 7262(b)) by the registered public accounting firm that prepared or issued its audit report. ☐
Indicate by check mark whether the registrant is a shell company (as defined
in Rule 12b-2 of the Act). ☐ Yes ☒ No
The aggregate market value of common stock held by non-affiliates of the
Registrant as of June 30, 2022 was $3,137,627 based on the closing price on the last day of trading prior to June 30, 2022.
This report includes “forward-looking statements” that are
subject to risks, uncertainties and other factors. All statements other than statements of historical fact are statements that could be
deemed forward-looking statements including continued compliance with government regulations, changing legislation or regulatory environments;
any statements of expectation or belief and any statements of assumptions underlying any of the foregoing. These risks, uncertainties
and other factors, and the general risks associated with the businesses of the Company described in the reports and other documents filed
with the SEC, could cause actual results to differ materially from those referred to in the forward-looking statements. The Company cautions
readers not to rely on these forward-looking statements. All forward-looking statements are based on information currently available to
the Company and are qualified in their entirety by this cautionary statement. The Company anticipates that subsequent events and developments
may cause its views to change. The information contained in this report speaks as of the date hereof and the Company has or undertakes
no obligation to update or revise these forward-looking statements, whether as a result of new information, future events or otherwise
unless required by law.
PART I
ITEM 1. BUSINESS
Evolutionary Genomics, Inc. (the "registrant" or "Company")
was incorporated under the laws of the state of Minnesota in November 1990 under the name Fonahome Corporation. On March 24, 2009, the
Company reincorporated in the state of Nevada and merged with its wholly-owned subsidiary, Fona, Inc., adopting the surviving company’s
name, Fona, Inc. and simultaneously adopted the capital structure of Fona Inc., which includes total authorized capital stock of 800,000,000
shares, of which 780,000,000 are common stock and 20,000,000 are blank check preferred stock. The preferred stock may be issued from time
to time in one or more series with such designations, preferences and relative participating, optional or other special rights and qualifications,
limitations or restrictions thereof, as shall be stated in the resolutions adopted by the Corporation’s Board providing for the
issuance of such preferred stock or series thereof.
On June 6, 2014, Evolutionary Genomics, Inc., a Delaware corporation merged
with Fona, Inc. treated as a reverse acquisition with Evolutionary Genomics, Inc. as the acquirer and Fona as the acquired party. Subsequent
to the Merger, Fona, Inc. was renamed Evolutionary Genomics, Inc. and our subsidiary was renamed from Evolutionary Genomics, Inc. to EG
Crop Science, Inc. On May 9, 2016, we formed ICAM Therapeutics, Inc. (a Delaware corporation) as a wholly owned subsidiary of Evolutionary
Genomics, Inc. We have not incurred any transactions in this company nor have we established any business plan for the future.
The Company maintains headquarters at the office of its Chief Executive
Officer. The Company maintains a website at www.evolgen.com. The Company is not required to deliver an annual report to security holders
and at this time does not anticipate the distribution of such a report. The Company will file reports with the SEC.
On August 14, 2000, the Company was issued patent number 6274319, titled
“Methods to identify evolutionarily significant changes in polynucleotide and polypeptide sequences in domestic plants and animals”.
On June 1, 2004, the Company was issued patent number 6743580, titled “Methods for producing transgenic plants containing evolutionarily
significant polynucleotides”. These patents are for the core Adapted Traits Platform that we use for the discovery of genes in humans,
animals and commercial crops. The Company has applied the Adapted Traits Platform in research projects including identifying genes believed
to be responsible for increases in yield in corn, increases in yield in rice, salt tolerance and sugar content in tomatoes and pest/disease
resistance in soybeans, bananas and multiple other crops.
Advances in genetic research and modification of crop species have led
to increased yield, drought tolerance and disease/pest resistance. In addition, mergers and consolidation within the industry has led
to fewer competitors among the seed and production companies. The largest companies control much of the implementation of new plant varieties
through patents and licensing agreements. Genetic traits providers, like Evolutionary Genomics, identify and develop genes that impact
traits of interest to the industry and market those genes to these companies.
EG Technology – The Adapted Traits Platform (“ATP’)
Genomics research generates vast amounts
of sequence data for thousands of genes. Some companies use this sequence data to try to predict the function of each gene and its potential
to impact key traits. Others try to match the thousands of random deoxyribonucleic acid
(“DNA”) changes between individuals with differences in traits. Evolutionary Genomics’
approach is to first narrow the search to genes that have undergone adaptive evolution (positively selected genes) in an organism that
has an adapted trait of potential commercial value. To identify genes with impact on commercially desirable traits, Evolutionary Genomics
screens first for positively selected genes. Evolutionary Genomics then focuses functional genomics efforts on demonstrating the effects
of these genes on the desired traits.
Evolutionary Genomics uses the Adapted Traits Platform to perform high
throughput molecular evolution analysis to identify positively selected genes based on Ka/Ks analysis (as defined below). Ka/Ks analysis
was developed to document the role of positive selection on known protein coding genes. Molecular-level adaptive evolution is indicated
when comparisons of homologous protein coding sequences from closely related species show that the number of amino acid differences fixed
due to selection exceeds what can be expected by neutral evolution. Molecular-level positive selection can be detected in protein-coding
genes by pairwise comparisons of the ratios of non-synonymous nucleotide substitutions per non-synonymous site (Ka) to synonymous substitutions
per synonymous site (Ks). The algorithm, by comparing substitutions per site, takes into account, in rigorous fashion, the effect of bias
and degeneracy in the genetic code, and also compensates for the effects of multiple hits at the same site. Ka/Ks ratios significantly
greater than unity strongly suggest that positive selection has fixed greater numbers of amino acid replacements than can be expected
as a result of chance alone.
Dr. Walter Messier, a Company founder and our Chief Science Officer, published
a seminal paper in the field: Messier and Stewart (1997) “Episodic adaptive evolution of primate lysozymes” Nature 385:151-154.
The work described in this publication demonstrated that a known lysozyme gene that had been recruited for a new function to aid in digestion
of leaves as a food source in certain monkeys had the kind of adaptive genetic changes indicating that the lysozyme gene had evolved more
rapidly than the neutral substitution rate, indicating Darwinian positive selection. Many groups have used such methods to document Darwinian
positive selection in other proteins. It was Dr. Messier’s insight that genes controlling a trait of interest could be identified
by using molecular evolution analysis as a screen, comparing genes in a species with a trait to genes of a closely related species lacking
the trait. The adapted genes found in such a screen could then be validated to determine their role in the presence or absence of the
trait of interest.
Business Model
Evolutionary Genomics’ primary source of revenue through March 31,
2020 had been contract services revenue for research performed by Evolutionary Genomics on behalf of other commercial entities and grant
income received from governmental agencies, industry associations and grant making foundations for research performed. Ownership of the
intellectual property in these projects varies from Evolutionary Genomics retaining all intellectual property rights to retaining none
of the developed intellectual property for the crop that is the subject of the project. In addition to contract services revenue for research,
Evolutionary Genomics intends to continue to pursue grant funding from governmental agencies, industry associations and grant making foundations.
These sources of funding are often subject to limitations in available funds, funding priorities in areas other than our area of focus,
political uncertainties, long approval processes and competition with other research proposals.
The single most valuable step in the process of crop improvement is the
identification of the key genes among the 30,000 or more in the genome that have the desired impact. The Company has identified pest/disease
resistance genes in bananas, soybeans and other commercially valuable crops. If validation testing of these genes is successful, we will
market them to the industry. This strategy requires Evolutionary Genomics to incur significant research costs prior to any confirmation
of commercial viability and there can be no guarantee that the desired results can be achieved or that commercialization can be reached.
The goal of the grant funded research projects was to discover genetic
intellectual properties with commercial value. Evolutionary Genomics’ soybean pest resistance project is a multiple year illustration
of the evolution of a project from concept through marketing to seed companies. The project has yielded identified genes for pest resistance
in soybeans with partial validation complete. Evolutionary Genomics has partially completed two generation, whole plant validation testing
but has decided to postpone further testing indefinitely to focus resources on our banana project. The Company has extended this soybean
pest resistance research to other crops including beans, tomatoes, cotton and maize and has identified candidate genes. Further research
on these crops is dependent on revenue from our banana project or additional capital funding. If we are able to complete additional validation
testing, we intend to market these genes to the seed industry.
Our banana pest resistance project is another project illustration. We
identified a gene (FusR1) in bananas that appears to confer resistance to Fusarium Fungus which leads to Panama Disease. We marketed the
gene to banana companies and, in August 2020, executed a Development and Commercialization Agreement (“DCA”) with Dole Food
Company (“Dole”) which includes development work funded by Dole and the framework for a long-term licensing relationship.
While Dole is supplying significant funding for the development of this banana gene in the form of promissory notes, there can be no assurance
that this development work will lead to licensing revenue as there are many risks involved in genetic trait development.
Licensing revenue can be lump sum payments, milestone payments upon achievement
of defined goals and/or percentages of revenue for products sold by licensee. These payments are often many years after completion of
gene identification project as licensees engage in significant additional testing including field trials prior to integration into licensee
commercial germplasm lines. There can be no guarantee that these licensing agreements will result in any additional revenue for Evolutionary
Genomics as further development of licensed intellectual property is mostly controlled by the licensee.
Evolutionary Genomics’ Banana Project
During the 1950s the global banana industry was devastated by a disease
(caused by Fusarium fungus) that effectively wiped out the predominate variety of commercial bananas know as Gros Michel leading to the
development of the Cavendish banana, which makes up well over 90% of the commercial banana market today. Cavendish was resistant to the
strain of Fusarium that wiped out the Gros Michel variety but, in recent years, is being challenged by a new race of Fusarium that threatens
to, once again, devastate the global banana industry. The recent emergence of TR4 Panama Disease in the Western Hemisphere makes a swift
solution to the crisis even more urgent. A substantial part of the banana market consists of exports from Central and South America to
the United States.
In 2018, the Company began a project to identify genes in wild banana relatives
that are resistant to Fusarium. We have previously used our technology to identify genes in common beans and, in our project for the Bill
and Melinda Gates Foundation in common beans, proved that these genes provided increased resistance to Fusarium fungus. We used our platform
to isolate a banana gene that controls Fusarium Wilt (FW), aka Panama Disease, Tropical Race 4. The gene, which we have named FusR1 (Fusarium
Resistance 1), is a native gene in Musa species, including cultivated bananas. We have found that, for all FW-resistant banana cultivars/species
that we have tested, one version of our gene exists while, in all FW-sensitive banana cultivars/species that we have tested, there is
a different version of FusR1. And notably, a third version exists in semi-resistant varieties that has allowed us to identify the particular
nucleotide changes that are crucial for resistance to Fusarium Wilt.
We have successfully introduced FusR1 into cultivated bananas using a gene
transformation approach in a project at the University of Wisconsin – Madison. Of the transformed events that were produced in the
transformation stage, roughly half survived to the testable stage and we have been testing those events for Fusarium resistance over the
last several months. Through the date of this report roughly half of those testable events remain untested, one-quarter were discarded
as being susceptible and one-quarter have shown some resistance to Fusarium. We expect to receive additional test results over the next
three months that may eliminate some of the events that have shown promise and/or may reveal additional events with promise.
The testing to date has included one to six plants per event which is not
enough to advance to commercial production. We have begun replication of the promising events for field trials which will likely take
2-1/2 to 3 years to complete. In addition to testing for Fusarium resistance, plants will be observed for any changes in other traits
such as fruit yield or taste. Many others are working on potential genetic and/or traditional breeding solutions. There can be no assurance
that any of these events will result in plants that can be advanced for commercial production or that we can be competitive with solutions
provided by others.
We believe that, given the threat of possible extinction for Cavendish,
rapid approaches are not only warranted but essential and minimally genetically edited bananas will be accepted depending upon how the
gene transfer is accomplished. Transfer of this native banana gene to cultivated bananas can also be accomplished with CRISPR technology,
which allows a targeted, gene transfer and which, as compared to more traditional genetic editing techniques, minimizes potential side
effects. We believe that Cavendish bananas can be rendered Fusarium Wilt resistant by changing only a few base pairs. These sorts of minimal
changes have been allowed by the USDA and FDA in several crops. Even in Europe, use of CRISPR technology has gained some traction. To
date, we have not used the CRISPR approach to produce resistant plants.
On June 26, 2019, we filed a United States patent application titled IDENTIFICATION
AND RESISTANCE GENES FROM WILD RELATIVES OF BANANA AND THEIR USES IN CONTROLLING PANAMA DISEASE. We are awaiting review of these patents
by the United States Patent Office. During 2021 and 2022, we filed patents in Europe, Africa, South and Central America, Australia and
Asia and are awaiting review of those as well.
On August 19, 2020, the Company entered into a Development and Commercialization
Agreement (“DCA”) with Dole Food Company for the development of plant varieties within the Musa genus of the Musaceae family
(including the Cavendish variety of banana) that exhibit resistance to Fusarium Wilt Tropical Race 4 (popularly known as Panama Disease).
Subject to compliance with various provisions of the agreement, the agreement includes partial working capital funding from Dole to the
Company through 2024. In addition to working capital funding, Dole reimburses the Company for the development of banana plants and Dole
will incur additional costs for the commercialization of plants upon successful completion of the development portion of this project.
From the effective date of the agreement, the Company has received $1,600,000 of working capital funding and $1,943,747 of development
costs pursuant to this agreement in the form of promissory notes. Per the Agreement, 50% of future royalties may be offset with the research
funding provided by Dole. In the event that Dole terminates the agreement for material breach by the Company or the Company’s bankruptcy,
the Company must repay all funding provided by Dole within six months of termination. The parties have agreed to negotiate the terms of
the long-term license agreement upon successful completion of the development portion of this project.
Upon successful completion of validation testing and field trials by Dole,
under the terms of the agreement with Dole, we expect to negotiate a long-term royalty contract for the commercialization of banana plants
using our genes. This licensing arrangement will likely be exclusively with Dole and contain royalty payments based on the number of plants
and/or hectares of plants. Even if EG’s genes are proven to be effective, it is difficult to predict the future revenue stream that
any licensing arrangement can generate and will be heavily dependent upon the speed with which Panama Disease spreads throughout the world
necessitating a solution and any changes in the price of bananas based on supply and demand. Many articles are available in the public
realm detailing the significance of the disease and the spread throughout the world.
Since bananas are seedless, they are propagated by clones which allows
for very rapid production of plants. An initial batch of 100 successful plants can generate a secondary propagation of over 15,000 plants
in one year (enough for 10 hectares) and 15 million in the next generation. There are over 400,000 hectares of banana production in Latin
America from Mexico to Peru. Adoption of the new variety will be dependent upon its effectiveness and the infection rate of Panama disease.
There are many risks associated with achieving these desired results including
but not limited to:
| - | We may not be able to adequately establish patent protection for our intellectual property or others may have competing claims. |
| - | Others may develop competitive approaches to compete with our genes. |
| - | Our genes may cause unforeseen and undesirable changes beyond the pest resistance such as yield degradation or changes in the appearance
or taste of the fruit. |
| - | Our genes may fail to deliver the desired results of resistance to Fusarium. |
| - | Global regulations and/or consumer preference may prevent the successful commercial launch of bananas with genetics changed using
our methods. |
| - | We will be dependent on others for the successful production and marketing of bananas with our genes and many factors will be outside
of our control. |
| - | Our expected future royalty revenue will be highly dependent upon the successful execution of the banana development project in the
DCA with Dole and the negotiation of a long-term royalty licensing agreement. |
While Panama Disease 1) is potentially existential to the banana industry,
2) has no known treatment and 3) is not yet widespread, Black Sigatoka Disease is a different disease that is very wide-spread and is
treated with toxins at a cost of up to $2,300 per hectare per year. We spent the last two years researching wild banana plants to identify
a gene that could potentially be used to develop plants that are resistant to Black Sigatoka with no or reduced use of toxins. We are
in the early stages of developing this gene and others are working on competing approaches. There is no guarantee that this will lead
to commercial success. Like our FusR1 project, transformation and validation can be very expensive and, if we do not receive licensing
revenue from our FusR1 gene, we will need funding from either grants or potential customers or additional capital from investors, none
of which can be assured.
Evolutionary Genomics’ Soybean Project
On April 29, 2014, the United States Patent and Trademark Office issued
patent 8,710,300 titled EXPRESSION OF DIRIGENT GENE EG261 AND ITS ORTHOLOGS AND PARALOGS ENHANCES PATHOGEN RESISTANCE IN PLANTS. On December
5, 2017 and March 3, 2020, the United States Patent and Trademark Office issued additional patents which extended the previous patent
to include additional variations of the gene. We have filed additional patents in multiple countries that are at various stages of processing.
On January 18, 2022, the Company filed a patent application on its second soybean pest/disease resistance gene, EG19, and has included
that gene in its ongoing two generation, whole plant validation research. The Company has also discovered additional candidate genes that
may impact pathogen resistance. There can be no assurance that any of these genes will be proven effective in validation testing or lead
to licensing agreements or revenue.
We entered into a Service Agreement with the Wisconsin Crop Innovation
Center (“WCIC”) under which they have transformed soybeans using our genes and helped to establish the right combinations
to achieve a range of expression. WCIC grew events from seven constructs of EG261 and EG19 in their greenhouses. The testing of these
T2 generation seedlings at the University of Missouri is partially complete but we have indefinitely suspended work on these genes to
focus our resources on our banana projects. If we resume these projects and results from the whole plant validation trials confirm the
findings of the University of Wisconsin-Madison for EG261 and the effectiveness of the new gene, EG19, the Company intends to enter negotiations
for a long-term research collaboration and licensing agreement with seed companies. The testing phase includes field trials which may
proceed for several years prior to generating licensing revenue. There are many risks in this process including some that are outside
of Evolutionary Genomics’ control and there can be no guarantee that we will ever generate any revenue from these potential agreements.
Competition
Evolutionary Genomics’ competition is very broad from the largest
seed companies and producing companies to the smallest grower who is successful in breeding new, improved varieties. These same competitors
are also Evolutionary Genomics customers as we seek to license intellectual property for commercialization into their production lines.
Many of these companies are exponentially larger with many more resources at their disposal and there can be no assurance that EG can
continue to compete with them or interest them in licensing our intellectual property.
Patents
Evolutionary Genomics is the owner of the following issued patents:
Patent/App Serial # |
Jurisdiction |
Title |
Filing Date |
Issue Date |
Expire Date |
8710300 / 13949035 |
United States |
EXPRESSION OF DIRIGENT GENE EG261 AND ITS ORTHOLOGS AND PARALOGS ENHANCES PATHOGEN RESISTANCE IN PLANTS |
7/23/2013 |
4/29/2014 |
7/23/2033 |
9834783/ 13901071 |
United States |
DIRIGENT GENE EG261 AND ITS ORTHOLOGS AND PARALOGS AND THEIR USES FOR PATHOGEN RESISTANCE IN PLANTS |
5/23/2013 |
12/5/2017 |
5/23/2033 |
10577625/ 15800179 |
United States |
DIRIGENT GENE EG261 AND ITS ORTHOLOGS AND PARALOGS AND THEIR USES FOR PATHOGEN RESISTANCE IN PLANTS |
11/1/2017 |
3/3/2020 |
11/1/2037 |
9,605,274 / 14/479,550 |
United States |
DIRIGENT GENE EG261 AND ITS ORTHOLOGS AND PARALOGS AND THEIR USES FOR PATHOGEN RESISTANCE IN PLANTS |
9/8/2014 |
3/28/2017 |
9/8/2034 |
AR091160B1 / P130101827 |
Argentina |
DIRIGENT GENE EG261 AND ITS ORTHOLOGS AND PARALOGS AND THEIR USES FOR PATHOGEN RESISTANCE IN PLANTS |
5/24/2013 |
6/8/2021 |
5/24/2033 |
2872128 |
Canada |
DIRIGENT GENE EG261 AND ITS ORTHOLOGS AND PARALOGS AND THEIR USES FOR PATHOGEN RESISTANCE IN PLANTS |
5/23/2013 |
9/19/2017 |
5/23/2033 |
112014029381-3 |
Brazil |
DIRIGENT GENE EG261 AND ITS ORTHOLOGS AND PARALOGS AND THEIR USES FOR PATHOGEN RESISTANCE IN PLANTS |
5/23/2013 |
9/19/2017 |
5/23/2033 |
ZL201380039727.4 |
China |
DIRIGENT GENE EG261 AND ITS ORTHOLOGS AND PARALOGS AND THEIR USES FOR PATHOGEN RESISTANCE IN PLANTS |
5/23/2013 |
7/25/2017 |
5/23/2033 |
Material Agreements
Effective March 1, 2012, Evolutionary Genomics entered into an Agreement
for Contract Services with Smith Bucklin Corporation (the “Contractor”) on behalf of the United Soybean Board. The contract
includes the payment of certain royalties, as defined in the Agreement. Evolutionary Genomics retains all ownership of patents and intellectual
property developed in the project and is obligated to pay royalties to the United Soybean Board of ten percent of the sale of products
derived from the soybean genes that were the subject of the research performed or from royalties received from the sale of products by
a third party not to exceed 150% of the total amount paid to Evolutionary Genomics under this Agreement. Evolutionary Genomics recognized
revenue of $262,400 from this contract, thus limiting any future royalties to a total of $393,600. The project term has expired but the
royalty provisions remain in perpetuity.
On February 21, 2015 the Company entered into the Sponsored Research Contract
with The Curators of the University of Missouri for phenotyping of transgenic soybean samples on a per unit basis. We expect to continue
this contract and will likely have additional amounts payable but the amount is indeterminable. Evolutionary Genomics retains sole ownership
of all patents and intellectual property, royalty free for all materials (including previously identified genes) related to this project.
On August 19, 2020, the Company entered into the DCA with Dole for the
development of our banana genes. The DCA provides for payments from Dole to the Company of $800,000 upon execution, $800,000 by the twelve-month
anniversary, $250,000 by the thirty-six month anniversary and $250,000 by the forty-eight month anniversary. Dole will also reimburse
the Company for costs incurred at the University of Wisconsin-Madison (“UW”) not to exceed $2,200,000 in coordination with
the Standard Research Agreement that the Company entered into with UW on September 18, 2020 which includes payments from the Company to
UW in the amount of $2,159,719 over the two-year expected term of the project. If the UW research is successful, Dole expects to incur
costs of $750,000 to perform field trials.
The DCA also specifies that the Company will execute notes payable to Dole
for the funding that Dole is providing up to $5,050,000. Through December 31, 2021, the Company executed notes
for $800,000, $800,000, $1,295,831 and $647,916 under this DCA and recorded them as a long-term notes payable for financial statement
purposes. There were no new notes in the year ended December 31, 2022. The notes are non-interest bearing and allow Dole to offset fifty
percent of future royalty payments to the Company by reducing the amount of principal due on these notes. Other than this offset of future
royalty payments, repayment of principal and interest is only required in the case of termination of the DCA by Dole for cause.
On September 18, 2020, the Company entered into a Standard Research Agreement
with WCIC for the development of our banana genes. The agreement includes payments from the Company in the amount of $2,159,719 over the
two-year expected term of the project. These costs will be reimbursed, in the form of notes payable by Dole in accordance with our DCA.
The Company entered into a Service Agreement with WCIC for the maintenance
and shipment of banana plants which includes unit pricing for services rendered and is expected to be completed by March 31, 2023. During
the year ended December 31, 2022, $59,330 of cost was incurred under this contract and was reimbursed by Dole.
On April 18, 2022, the Company entered into a Service Agreement with the
University of Wisconsin-Madison for the testing of banana plants which includes payments of $143,124 of which $128,811 were paid in the
year ended December 31, 2022 and reimbursed by Dole.
Trademarks
Evolutionary Genomics has no registered trademarks.
Employees
Evolutionary Genomics had two full time employees and two part time employees
as of December 31, 2022.
Facilities
The Company leases its operating facility on a month-to-month basis, with
monthly rental installments of $2,378. Renewals are by mutual agreement.
Legal Proceedings
Evolutionary Genomics is not currently involved in or aware of any threatened
or actual legal proceedings.
Capitalization
The Company is authorized to issue up to 780,000,000
shares of Common Stock and up to 20,000,000 shares of preferred stock. As of December 31, 2022, the Company had 6,655,232 shares of Common
Stock outstanding, 577,063 shares of Series A-1 Preferred Stock (“Series A-1”) outstanding and 189,337 shares of Series A-2
Preferred Stock (“Series A-2”) outstanding. Both Series A-1 and Series A-2 are convertible into shares of Common Stock on
a one share for one share basis. 1,400,000 shares of common stock have been reserved for issuance pursuant to the Company’s 2015
Stock Incentive Plan. Option grants have been issued for 340,000 shares of common stock at an exercise price of $0.55 per share, 133,333
shares of common stock at an exercise price of $0.83 per share, 490,000 shares of common stock at an exercise price of $1.50 per share,
150,000 shares of common stock at an exercise price of $1.65 per share, 180,000 shares of common stock at an exercise price of $3.00 per
share, 100,000 shares of common stock at an exercise price of $3.30 per share and 100,000 shares of common stock at an exercise price
of $3.50 per share. Options for 306,667 shares have been exercised, 158,333 have been cancelled and option grants of 1,028,333 shares
remain outstanding as of December 31, 2022.
Liquidation: Upon any liquidation, dissolution or winding-up of the Company,
whether voluntary or involuntary, the holders of the Series A-1 and Series A-2 shall be entitled to receive out of the assets of the Company
for each share of Series A-1 and Series A-2 an amount equal to its stated value, $5.25 per share plus any accrued but unpaid dividends
before any distribution or payment shall be made to the holders of any other class or series of stock of the Company that ranks junior
to the Series A-1 and Series A-2. The holders shall be entitled to convert their shares of Series A-1 and Series A-2 into Common Stock
at any time prior to the consummation of a Liquidation.
The Corporation is required to establish a segregated non-interest bearing
trust account (the “Sinking Fund Account”) for the benefit of the Holders. 50% of all licensing fees received by the Corporation
shall be deposited in the Sinking Fund Account within five (5) Business Days of receipt of any such fees by the Corporation. In the event
that the amount of cash in the Sinking Fund Account exceeds the liquidation preference of all issued and outstanding shares of Series
A-1 and Series A-2 Preferred Stock not previously redeemed or converted pursuant to the terms hereof, the Corporation shall deliver a
notice to the Holders (the “Mandatory Redemption Notice” and the date such notice is deemed delivered hereunder, the “Mandatory
Redemption Notice Date”) of its obligation to redeem all of the then outstanding shares of Series A-1 and Series A-2 Preferred Stock
(i) for cash in an amount equal to the liquidation preference per share and (ii) by issuing such number of fully paid and nonassessable
whole shares of Common Stock as is obtained by multiplying (x) the number of shares of Series A-1 and Series A-2 Preferred Stock so to
be redeemed by (y) the liquidation preference per share of the Series A-1 and Series A-2 Preferred Stock, and then by dividing such product
by (z) the conversion price per share, payable and issuable, respectively, in full on the 5th Trading Day following the Mandatory Redemption
Notice Date. This is considered a contingent redemption feature.
Conversion: The holders of Series A-1 and Series A-2 may convert their
shares at any time into shares of Common Stock at any time prior to the consummation of a liquidation, at the option of the holder, on
a one-share-for-one-share basis and shall be subject to certain adjustments.
Optional Redemption; Sinking Fund Account: The Company may elect to redeem
some or all of the then outstanding shares of Series A-1 and Series A-2, (i) for cash in an amount equal to the liquidation preference
per share, $5.25 per share as of December 31, 2022, subject to adjustment and (ii) by issuing one share, subject to adjustment, of Common
Stock for each share of Series A-1 and Series A-2 outstanding being redeemed. 50% of all licensing fees received by the Company will be
deposited into a separate sinking fund for use in an optional redemption. As of December 31, 2022, no licensing revenue has been received
under these provisions and no sinking fund account has been established.
Dividends: The Company shall pay to the holders of the Series A-1 and Series
A-2 dividends at the rate of 8% per annum multiplied by the amount invested. The dividend amount shall accrue and shall be payable in
shares of Common Stock upon the conversion of the Series A-1 and Series A-2, or upon the redemption of the Series A-1 and Series A-2.
No dividends shall be paid on any Common Stock of the Company or any capital stock of the Company that ranks junior to the Series A-1
and Series A-2 until dividends of Series A-1 and Series A-2 has been paid. As of December 31, 2022, there were $1,835,089 in accrued preferred
stock dividends.
Voting: The holders of the Series A-1 and Series A-2 are entitled to vote
on all matters submitted to the stockholders for a vote on an as-if-converted to Common Stock basis, with all stockholders voting as a
single class.
ITEM 1A. RISK FACTORS
We may require substantial additional funding and may be unable to
raise capital when needed, which could force us to delay, reduce or eliminate planned activities or result in our inability to continue
as a going concern.
As of December 31, 2022, the Company had $577,066 in operating cash and
expects that operating cash flow net of contractual reimbursements and notes payable funding from Dole for the year ending December 31,
2023 will be approximately $546,000. Management believes that there may not be enough cash to pay our expenses for one year beyond the
date of this report. Marketing of additional genes may lead to additional revenue and we have some flexibility to reduce operating costs
but we may require additional capital. These factors create substantial doubt as to our ability to continue as a going concern. The accompanying
consolidated financial statements do not include any adjustments that may result if the Company is unable to continue as a going concern.
Our future capital requirements will depend on, and could increase significantly
as a result of, many factors, including:
| · | the duration and results of the research projects; |
| · | unexpected delays or costs incurred in the acquisition of plant materials needed in these research projects and with subcontracts
that perform various parts of these projects; |
| · | the time and cost in preparing, filing, prosecuting, maintaining and enforcing patent claims; |
| · | other unexpected developments encountered in implementing our business development, research development and commercialization strategies;
and |
| · | further arrangements, if any, with collaborators. |
We may attempt to raise additional funds through public or private financings,
collaborations with other companies or financing from other sources. Additional funding may not be available on terms which are acceptable
to us or at all. If adequate funding is not available to us on reasonable terms, we may need to delay, reduce or eliminate one or more
of our research and development projects or obtain funds on terms less favorable than we would otherwise accept. To the extent that additional
capital is raised through the sale of equity securities or securities convertible into or exchangeable for equity securities, the issuance
of those securities could result in dilution to our stockholders. Moreover, the incurrence of debt financing could result in a substantial
portion of our future operating cash flow, if any, being dedicated to the payment of principal and interest on such indebtedness and could
impose restrictions on our operations. This could render us more vulnerable to competitive pressures and economic downturns.
In addition, if we do not meet our payment obligations to third parties
as they come due, we may be subject to litigation claims. Even if we are successful in defending against these claims, litigation could
result in substantial costs and be a distraction to management and may result in unfavorable results that could further adversely impact
our financial condition.
We have relied on the availability of grant funding to fund some
of our research efforts and our inability to compete successfully for these limited grant funding opportunities may significantly affect
our results of operations and our ability to complete research projects.
We have traditionally funded many of our research projects, partially or
wholly, using grant funding provided by government programs, industry associations and grant making institutions. The availability of
these funds is impacted by many factors including changing political priorities, fiscal budget issues, agency priorities, availability
of funds and competition from other grant seekers. Our ability to present proposals that fit within grant making guidelines and which
are attractive relative to other proposals submitted may significantly impact our ability to fund our research projects.
Efforts to protect our intellectual property rights and to defend
claims against us can increase our costs and will not always succeed; any failures could adversely affect profitability or restrict our
ability to do business.
Intellectual property rights are crucial to our business. We endeavor to
obtain and protect our intellectual property rights in jurisdictions in which products are produced from the biotechnology that we produce
and in jurisdictions into which those products are imported. Different nations may provide limited rights and inconsistent duration of
protection for our intellectual property. We may be unable to obtain protection for our intellectual property in key jurisdictions. Even
if protection is obtained, competitors, farmers or others may raise legal challenges to our rights or illegally infringe on our rights,
including through means that may be difficult to prevent or detect. In addition, because of the rapid pace of technological change, and
the confidentiality of patent applications in some jurisdictions, competitors may be issued patents from applications that were unknown
to us prior to issuance. These patents could reduce the value of our commercial or pipeline biotechnology or, to the extent they cover
key technologies on which we have unknowingly relied, require that we seek to obtain licenses or cease using the technology, no matter
how valuable to our business. We cannot assure we would be able to obtain such a license on acceptable terms. In addition, patent laws
are subject to change and any change in our ability to protect the intellectual property that we develop may impact our ability to commercialize
that intellectual property. The extent to which we succeed or fail in our efforts to protect our intellectual property will affect our
costs, sales and other results of operations.
Genes that we have discovered and may discover in the future with
expected desirable impact on traits may, upon further research and field trials, be revealed to also have undesirable impact on traits.
Evolutionary Genomics’ gene discovery process focuses on the identification
of positively selected genes that impact the trait of interest that we are working on. When we further test them in lab validation, we
are again focused on whether they have the desired impact on the trait of interest and we are specifically testing for that outcome. Laboratory
experiments are under more ideal circumstances than field trials and use in production and there can be no guarantee that the lab result
will be repeated under those conditions. Additional field trials and use in production may also reveal undesirable impacts on other traits
that were not a focused part of our research. For example, the soybean or banana genes that we have discovered may be found to have a
negative impact on yield. These may impact our ability to realize revenue from the commercialization of our biotechnology and may expose
us to liability for undesirable outcomes that we don’t anticipate.
Undesirable results from our ongoing research may result in expensing
of our acquired research in progress.
We currently carry $4,016,596 (gross) of acquired research in progress
on our balance sheet as an intangible asset subject to amortization. Upon executing our DCA with Dole, we began amortization of this asset
in the year ended December 31, 2020. If this project produces undesirable results, we may need to expense the intangible asset.
Others may find additional genes or other methods of accomplishing
the same desired outcome that our biotechnology does, rendering our biotechnology less valuable or commercializable.
There are many other companies pursuing similar gene discovery programs
and other approaches to solving the same issues that we are addressing and many of these companies have vastly more resources than we
do. Even when we identify genes that impact desired traits, there may be other genes that have a similar or greater effect on these traits.
For example, one or more of the other genes in soybeans and bananas may have an impact on pest/disease resistance similar to our genes
or there may be other orthologs of the genes that we have discovered in other varieties that have a greater impact. In addition, other
companies may develop commercial chemicals that compete with genetic changes to solve the issues that we are addressing. Any of these
may impact our ability to realize revenue from the commercialization of our biotechnology.
The successful development of our research efforts and commercialization
of our biotechnology will be necessary for our growth and profitability.
We intend to use recent successes in which we have identified genes that
may have an impact on pest/disease resistance in soybeans and bananas and look for similar genes in other crops. This research may result
in significant costs incurred without any commercial value produced. We also intend to attempt to improve the potential pest/disease resistance
genes we have identified. Even if we find effective genes, we may not be able to find a commercial market for them. There can be no assurance
we will be able to achieve any improvement and performing this research may also result in significant costs incurred without any commercial
value produced. The processes of breeding, biotechnology trait discovery and development and trait integration are lengthy and a very
small percentage of the genes identified in research are selected for commercialization. The length of time and the risk associated with
the breeding and biotech pipelines are interlinked because both are required as a package for commercial success in markets where biotech
traits are approved for growers. Commercial success frequently depends on being the first company to the market, and many of our competitors
are also making considerable investments in similar new biotechnology. Consequently, if we are not able to fund extensive research and
development activities and deliver new products to the markets we serve on a timely basis, our growth and operations will be harmed including,
but not limited to, the possible impairment of our intangible assets.
We rely heavily on our founder, Walter Messier, our current Chief
Science Officer. The loss of his services would have a material adverse effect upon us and our business and prospects.
Our success depends, to a significant extent, upon the continued services
of Walter Messier, who is a founder of Evolutionary Genomics and our current Chief Science Officer. Since inception, we have been dependent
upon Dr. Messier, who is the inventor on most of our patents and responsible for the development of our core Adapted Traits Platform.
If Dr. Messier or any key management personnel resign to join a competitor or form a competing company, the loss of such personnel, together
with the loss of any customers or potential customers due to such executive’s departure, could materially and adversely affect our
business and results of operations.
We are dependent on a technically trained workforce and an inability
to retain or effectively recruit such employees could have a material adverse effect on our business, financial condition and results
of operations.
Our ability to compete effectively depends largely on our ability to attract
and retain certain key personnel, including additional researchers that we intend to hire in order to pursue our planned research projects.
Industry demand for such skilled employees, however, exceeds the number of personnel available, and the competition for attracting and
retaining these employees is intense. Because of this intense competition for skilled employees, we may be unable to retain our existing
personnel or attract additional qualified employees to keep up with future business needs. If this should happen, our business, operating
results and financial condition could be adversely affected.
In addition, we intend to hire business development and marketing personnel
and advisors to promote and market the biotechnology that we develop. We cannot assure you that we will be able to recruit and retain
qualified personnel and advisors to perform these functions. Our inability to hire and then retain such personnel, advisors and scientists
could have a materially adverse effect on our business and our projects.
We may not obtain the
necessary permits and authorizations to operate our business.
We may not be able to obtain or maintain the necessary licenses, permits,
authorizations or accreditations, or may only be able to do so at great cost. In addition, we may not be able to comply fully with the
wide variety of laws and regulations applicable to the agricultural industry. Failure to comply with or to obtain the necessary licenses,
permits, authorizations or accreditations could result in restrictions on our ability to operate our business, which could have a material
adverse effect on our business.
Competition in agricultural biotechnology has significantly affected
and will continue to affect our revenue and results of operations.
Many companies engage in research and development of plant biotechnology
and breeding and speed in getting a new product to market can be a significant competitive advantage. Our competitors’ success could
render the biotechnology that we identify as less competitive, resulting in reduced sales compared to our expectations or past results.
We expect to see increasing competition from agricultural biotechnology firms and from major agrichemical, seed and food companies. The
extent to which we can realize cash and profit from our business will depend on our ability to control research costs, predict and respond
effectively to competitor products and marketing; and develop new products and services attractive to our customers.
Our customers are subject to extensive regulation affecting their
use of our biotechnology, which may affect our revenue and profitability.
Regulatory and legislative requirements affect the development and distribution
of products made from the biotechnology that we produce, including the testing and planting of seeds containing our biotechnology traits
and the import of crops grown from those seeds, and non-compliance can harm our revenue and profitability. Obtaining testing, planting
and import approvals for seeds or biotechnology traits can be time-consuming and costly, with no guarantee of success. The failure to
receive necessary permits or approvals could have near- and long-term effects on our ability to sell some current and future biotechnology.
Concern about unintended but unavoidable trace amounts (sometimes called “adventitious presence”) of commercial biotechnology
traits in conventional (non-biotechnology) seed, or in the grain or products produced from conventional or organic crops, among other
things, could lead to increased regulation or legislation, which may include: liability transfer mechanisms that may include financial
protection insurance; possible restrictions or moratoria on testing, planting or use of biotechnology traits; and requirements for labeling
and traceability, which requirements may cause food processors and food companies to avoid biotechnology and select non-biotechnology
crop sources and can affect farmer seed purchase decisions and, ultimately the sale and use of the biotechnology that we produce. Legislation
encouraging or discouraging the planting of specific crops can also harm our sales.
The degree of public acceptance or perceived public acceptance of
products made from our biotechnology can affect our sales and results of operations by affecting planting approvals, regulatory requirements
and farmer purchase decisions.
Some opponents of the use of biotechnology in agriculture raise public
concern about the potential for adverse effects of products produced using genetic information that we provide to our customers on human
or animal health, other plants and the environment. The potential for adventitious presence of commercial biotechnology traits in conventional
seed, or in the grain or products produced from conventional or organic crops, is another factor that can affect general public acceptance
of these traits. Public concern can affect the timing of, and whether our customers are able to obtain, government approvals. Even after
approvals are granted, public concern may lead to increased regulation or legislation or litigation concerning prior regulatory approvals,
which could affect our sales and results of operations by affecting planting approvals and may adversely affect sales of our customers’
products to farmers, due to their concerns about available markets for the sale of crops or other products derived from biotechnology
which may lead to less demand from our customers. In addition, opponents of agricultural biotechnology have attacked farmers’ fields
and facilities used by agricultural biotechnology companies and may launch future attacks against farmers’ fields and our field
testing sites and research, production, or other facilities, which could affect our sales and our costs.
We are dependent upon other companies to integrate biotechnology
that we have licensed to them into their breeding operations for our future license revenue.
We perform research for other entities under grant and research agreements
that provide service revenue. In addition to the service revenue, our long-term profitability depends on the commercialization of the
biotechnology that we provide to other companies for their commercial breeding lines. The extent to which our biotechnology is integrated
into these breeding lines is largely outside of our control and can take many years. If our biotechnology is not integrated into breeding
lines, we may not realize license revenue which may affect our results of operations.
The biotechnology industry is subject to rapid technological change,
and if we fail to keep up with such change, our results of operations and financial condition could be adversely impacted.
Biotechnology has undergone and is subject to rapid and significant change.
We expect that the technologies associated with biotechnology research and development will continue to develop rapidly. Our failure to
keep pace with such rapid change could result in our products becoming obsolete and we may be unable to recoup any expenses incurred with
developing such products, which may adversely affect our future revenues and financial condition.
The Company may be required to expend substantial sums in order to
bring it into compliance with the various reporting requirements applicable to public companies and/or to prepare required financial statements,
and such efforts may harm operating results or be unsuccessful altogether.
We are subject to many of the requirements applicable to public companies,
including Section 404 of the Sarbanes-Oxley Act of 2002, or the Sarbanes-Oxley Act, which requires that the Company evaluate and report
on its system of internal controls. If the Company’s finance and accounting staff or internal controls over financial reporting
are inadequate, it may be required to hire additional staff and incur substantial legal and accounting costs to address such inadequacies.
Moreover, the Company cannot be certain that its remedial measures to correct current material weaknesses will be effective. Any failure
to implement required or improved controls, or difficulties encountered in their implementation, could harm the Company’s operating
results or increase its risk of material weaknesses in internal controls.
Members of our management team have significant influence over us.
Our officers and directors own, directly or indirectly approximately 29.3%
of the outstanding shares of common and preferred stock, excluding options. Including options and warrants, our officers and directors
own, directly or indirectly, approximately 36.4% of the outstanding shares of common stock. These stockholders, therefore, have a controlling
influence in determining the outcome of any corporate transaction or other matters submitted to our stockholders for approval, including
Mergers, consolidations and the sale of all or substantially all of our assets, election of directors, and other significant corporate
actions. The interests of these stockholders may differ from the interests of our other stockholders.
Our certificate of incorporation and bylaws and Nevada law may have
anti-takeover effects that could discourage, delay or prevent a change in control, which may cause our stock price to decline.
Our certificate of incorporation and bylaws and law could make it more
difficult for a third party to acquire us, even if closing such a transaction would be beneficial to our stockholders. We are authorized
to issue up to 20,000,000 shares of preferred stock. This preferred stock may be issued in one or more series, the terms of which may
be determined at the time of issuance by our board of directors without further action by stockholders. The terms of any series of preferred
stock may include voting rights (including the right to vote as a series on particular matters), preferences as to dividend, liquidation,
conversion and redemption rights and sinking fund provisions. We currently have 577,063 shares of Series A-1 preferred stock issued and
outstanding and 189,337 shares of Series A-2 preferred stock issued and outstanding. The issuance of any preferred stock could materially
adversely affect the rights of the holders of our common stock and existing holders of preferred stock, and therefore, reduce the value
of those securities. In particular, specific rights granted to future holders of preferred stock could be used to restrict our ability
to merge with, or sell our assets to, a third party and thereby preserve control by the present management.
Provisions of our certificate of incorporation and bylaws and law also
could have the effect of discouraging potential acquisition proposals or making a tender offer or delaying or preventing a change in control,
including changes a stockholder might consider favorable. Such provisions may also prevent or frustrate attempts by our stockholders to
replace or remove our management. In particular, the certificate of incorporation and bylaws and law, as applicable, among other things:
| · | provide the board of directors with the ability to alter the bylaws without stockholder approval; |
| · | place limitations on the removal of directors; |
| · | provide that the Board of Directors may change the size of the Board; and |
| · | provide that vacancies on the board of directors may be filled by a majority of directors in office, although less than a quorum. |
These provisions may delay or prevent someone from acquiring or merging
with us, which may cause the market price of our common stock to decline.
We do not foresee paying cash dividends in the foreseeable future
and, as a result, our investors’ sole source of gain, if any, will depend on capital appreciation, if any.
We do not plan to declare or pay any cash dividends on our shares of common
stock in the foreseeable future and currently intend to retain any future earnings for funding growth. As a result, investors should not
rely on an investment in our securities if they require the investment to produce dividend income. Capital appreciation, if any after
payments due to preferred shareholders, of our shares may be investors’ sole source of gain for the foreseeable future. Moreover,
investors may not be able to resell their shares of our common stock at or above the price they paid for them.
Our ability to use our net operating loss
carry-forwards and certain other tax attributes is limited by Sections 382 and 383 of the Internal Revenue Code.
Subject to certain limitations, a corporation may offset a net operating
loss carryforward against profit earned in a future year to determine its U.S. federal income tax expenses for such year. Sections 382
and 383 of the Internal Revenue Code of 1986 limit a corporation’s ability to utilize its net operating loss carryforwards and certain
other tax attributes (including research credits) to offset future federal taxable income or tax if, in general, the corporation experiences
a cumulative ownership change of more than 50% over any rolling three-year period. State net operating loss carryforwards (and certain
other tax attributes) may be similarly limited. For the year ended December 31, 2022, we recorded no state tax liability. An ownership
change can therefore result in significantly greater tax liabilities than a corporation would incur in the absence of such a change and
any increased liabilities could adversely affect the corporation’s business, results of operations, financial condition and cash
flow.
As of December 31, 2022, we had available total federal and state
net operating loss carryforwards of approximately $11,965,000 plus additional net operating losses generated in the year ending December
31, 2022. These NOL’s expire at various intervals through the year 2037 except for the NOL’s for the years ending after December
31, 2017 which have no expiration date.
Additional ownership changes may occur in the future as a result of additional
equity offerings or events over which we will have little or no control, including purchases and sales of our equity by our five-percent
security holders, the emergence of new five-percent security holders, redemptions of our securities or certain changes in the ownership
of any of our five percent security holders.
If securities or industry analysts do not publish research or publish
inaccurate or unfavorable research about our business, our stock price and trading volume could decline.
The trading market for our common stock depends in part on the research
and reports that securities or industry analysts publish about us or our business. We do not currently have and may never obtain research
coverage by securities and industry analysts. If no securities or industry analysts commence coverage of our company, the trading price
for our stock would be negatively impacted. If we obtain securities or industry analyst coverage and if one or more of the analysts who
covers us downgrades our stock, or publishes unfavorable research about our business, our stock price would likely decline. If one or
more of these analysts ceases coverage of us or fails to publish reports on us regularly, demand for our stock could decrease, which could
cause our stock price and trading volume to decline.
ITEM 1B. UNRESOLVED STAFF COMMENTS
Not applicable.
ITEM 2. PROPERTIES
The Company has no owned properties and at this time has no agreements
to acquire any properties. The Company currently maintains a rent-free mailing address at 4220 Morning Star Drive, Castle Rock, CO 80108,
which is the address of the office of its Chief Executive Officer and lab facilities on lease at 1801 Sunset Place, Unit C, Longmont CO
80501. The Company leases its operating facility on a month-to-month basis, with monthly rental installments of $2,378.
ITEM 3. LEGAL PROCEEDINGS
The Company is not a party to any pending legal proceedings, and no such
proceedings are known to be contemplated.
ITEM 4. MINE SAFETY DISCLOSURES
Not applicable.
PART III.
ITEM 10. DIRECTORS, EXECUTIVE OFFICERS AND CORPORATE GOVERNANCE
Officers and Directors
The following table sets forth certain information concerning each of the
Company’s directors and executive officers:
Name |
|
Age |
|
Position |
Steve B. Warnecke |
|
66 |
|
Chairman of the Board, President, CEO, CFO |
Walter Messier |
|
67 |
|
Treasurer, Secretary |
Virginia Orndorff |
|
72 |
|
Director |
Mark Boggess |
|
62 |
|
Director |
Compliance with Section 16 (a) of the Exchange Act
Section 16(a) of the Exchange Act requires our officers, directors
and persons who beneficially own more than ten percent of our ordinary shares to file reports of ownership and changes in ownership with
the SEC. These reporting persons are also required to furnish us with copies of all Section 16(a) forms they file. Based solely upon a
review of such Forms, we believe that during the year ended December 31, 2022 there were no delinquent filers.
Code of Conduct
Committees
We have not formed an Audit Committee, Compensation Committee or Nominating
and Corporate Governance Committee as of the filing of this report. Our Board of Directors performs the principal functions of an Audit
Committee. We currently do not have an audit committee financial expert on our Board of Directors. We believe that an audit committee
financial expert is not required because the cost of hiring an audit committee financial expert to act as one of our directors and to
be a member of an Audit Committee outweighs the benefits of having an audit committee financial expert at this time. However, we intend
to implement a comprehensive corporate governance program, including establishing various board committees in the future.
There are no agreements or understandings for any officer or director
to resign at the request of another person and none of the above-named officers and directors are acting on behalf of or will act at the
direction of any other person.
There is no family relationship between any director or executive
officer of the Company.
The board of directors presently has no committees.
Set forth below are the names of all directors and executive officers
of the Company, all positions and offices with the Company held by each such person, the period during which he has served as such, and
the business experience of such persons during at least the last five years:
Steve B. Warnecke was appointed Chief Financial Officer, Treasurer,
Secretary and member of the board of directors of the Company on June 6, 2014, and became its principal executive officer as President,
Chief Executive Officer and Chairman of the Board on October 1, 2014. Mr. Warnecke has served as a member of the board of directors of
Evolutionary Genomics since September 2010 and was appointed as Chief Executive Officer in November 2010. Mr. Warnecke has served part-time
roles as Chairman of the Board of Directors and Chief Financial Officer for VetDC, Inc. since November 2012, President of CereScan Corp
from November 2016 to August 2018 and Chairman of the Pink Lightning Foundation (supporting Children’s Hospitals and cystic fibrosis
research) since November 2011. He has also served as Senior Vice-President of Children’s Hospital Colorado Foundation from 2003
through January 2017 and been a member of the Board of Directors of CereScan from 2014 to 2019. Previously, Mr. Warnecke served as Lead
Independent Director and Audit Committee Chair for Evolving Systems, Inc. (NASDAQ: EVOL, an international telecom software company) from
2003 to 2011, as Chief Financial Officer of Targeted Medical Pharma, Inc. in 2011, as Chief Financial Officer and member of the Board
of Directors for Bacterin International, Inc. (NASDAQ: BONE), a biologics and medical device company from 2008 to 2010, member of the
Board of Directors of Emmaus Life Sciences, Inc. in 2011, member of the Board of Directors of Boppy Company from 2005 to 2008, Senior
Vice-President of Strategic Planning for First Data/Western Union (NYSE: FDC) from 2001 to 2002 and Chief Financial Officer for Frontier
Airlines (former NASDAQ company acquired by Republic Airways) from 1999 to 2001. Mr. Warnecke graduated from the University of Iowa with
a BBA in Accounting, Finance and Management and passed the Certified Public Accountant exam in 1979.
Virginia Orndorff was appointed as a director
of the Company on October 1, 2014. She has served as a member of the Evolutionary Genomics board of directors since 2000. She served as
Chief Executive Officer and President of Evolutionary Genomics from 2000 to November 2010. She is a founder and CEO of Sieyax, LLC, an
early-stage oncology company. From February 2015 to February 2017, Ms. Orndorff served as Executive Director, Chief Executive Officer
and Director of the Colorado Institute for Drug, Device and Diagnostic Development. She has served on Colorado’s State Board of
Pharmacy from March 2012 to March 2015. 1997 to 2000, Ms. Orndorff served as Vice President then President and Chief Executive Officer
of GenoPlex, Inc. of Denver and served as Director of Technology/Business Development of NeXstar Pharmaceuticals, Inc. of Boulder, Colorado,
from 1993 to 1997. From 1989 to 1993 she served as the Director of Biotechnology Programs for the Colorado Advanced Technology Institute
in Denver. Ms. Orndorff was employed by the Georgia Institute of Technology as Manager of a biotechnology start-up incubator (the Health
Science Technology Center) from 1987 to 1989; prior to that for eight years by Genex Corporation of Gaithersburg, Maryland, first as a
Laboratory Supervisor then as Manager of Technology Assessment. From 1975 to 1979, Ms. Orndorff had served as a Microbiologist at Stanford
Research Institute. She received a BA in Biology from the University of California at Santa Cruz, an MA in Microbiology from California
State University at San Jose, and an MBA from Loyola College (where she graduated second in her class).
Mark Boggess, Ph.D. was appointed as a director of the Company on
October 1, 2014. He has served as a director of Evolutionary Genomics since 2010. Dr. Boggess has a diverse background in the animal sciences
and animal industries. Born and raised on a traditional Iowa farm, he served as a swine and beef cattle extension specialist with the
University of Idaho in Twin Falls from 1990 to 1994 where he was responsible for all swine extension and educational programming and served
as the animal breeding resource specialist for the University beef extension team. From 1994 to 2004, Dr. Boggess served as President
of Salmon Creek Farms, LLC where he was responsible for development of the Salmon Creek Farms Natural Pork program and branded product
line, at Independent Meat Company in Twin Falls, ID. From 2004 to 2009, Dr. Boggess assumed the position of Director of Animal Science
for the National Pork Board where he was responsible for program direction and industry funding coordination for research in pork quality;
nutritional efficiency; sow lifetime productivity; genomics-genetics; alternatives to antimicrobials; production-management systems and
biotechnology. Dr. Boggess also served as the National Pork Board liaison for animal science to producers, academia, media, regulators
and the National Pork Producers Council and directed numerous pork industry based advisory groups. From 2009 to 2014, Dr. Boggess served
as the National Program Leader for Food Animal Production and the National Program Leader for Pasture, Forage and Rangeland Systems for
the USDA Agriculture Research Service in Beltsville, Maryland. In this role, he directed ARS research for diverse programs in genetics
and genomics, nutrition, reproductive physiology, animal welfare and meat quality. Dr. Boggess also directed research to improve pasture
and rangeland management practices and land-use strategies, improve and restore the ecology of western rangelands and improve the capacity
and efficiency of forage-based food animal production systems. From 2014 to 2018, Dr. Boggess served as the Director of the U.S. Dairy
Forage Research Center in Madison, WI. In this role Dr. Boggess directed the research programs for 21 scientists and 75 support staff.
The USDFRC includes two research farms in rural Wisconsin as well as offices and laboratories on the campus of the University of Wisconsin.
Currently, Dr. Boggess serves as the Director of the US Meat Animal Research Center, the largest meat animal-based research Center in
the world. USMARC spans 34,000 acres and houses 25,000 head of beef, sheep and swine. The research programs include 45 scientists in five
research units conducting research focused on genetics, genomics, physiology, nutrition, reproduction, food safety, meat quality, animal
health, precision agriculture, and environmental quality. Dr. Boggess attended Iowa State University receiving a BS degree in Animal Science
in 1983. After receiving an MS degree from Cornell University with a major in Animal Breeding in 1985, Dr. Boggess returned to Iowa State
University, receiving his PhD in 1990, also in Animal Breeding.
Walter Messier, Ph.D. was appointed Secretary and Treasurer of the
Company on October 1, 2014. He is a Founder of Evolutionary Genomics and has served as its Chief Technology Officer since 2000 and has
served as its Secretary since 2007. Dr. Messier has published in such prestigious scientific journals as Nature, Nature Medicine, Current
Biology, and Science. Dr. Messier is recognized as an authority on the use and interpretation of Ka/Ks algorithms. Dr. Messier’s
research on the detection of molecular-level positive selection in the primates is well known. In addition to the research programs Dr.
Messier developed and spearheads at Evolutionary Genomics, he is currently collaborating with colleagues in several areas, including identification
and validation of novel targets for breast cancer therapeutics, identification and validation of novel targets for HIV/AIDS therapeutics,
the role of molecular Darwinian selection in human speciation, and creation of more powerful algorithms for the detection of molecular
Darwinian selection. Dr. Messier received his Masters of Science from the State University of New York at New Paltz, and his Ph.D. from
the University of Albany (State University of New York).
CONFLICTS OF INTEREST
The Company’s officers and directors have in the past and may in
the future be officers and directors of other companies. Consequently, they may have potential inherent conflicts of interest in serving
as officers and directors of the Company. Insofar as the officers and directors are engaged in other business activities, management anticipates
it will not devote all of its time to the Company’s affairs. The officers and directors of the Company may in the future become
shareholders, officers or directors of other companies which may be formed for the purpose of engaging in business activities similar
to those conducted by the Company. The Company does not currently have a right of first refusal pertaining to opportunities that come
to management’s attention even if the opportunities relate to the Company’s proposed business operations.
The officers and directors are under no obligation to make any opportunities
that come to their attention in the performance of their duties for any other companies or in any other manner available to the Company.
Except as set forth above, the Company has not adopted any other conflict of interest policy with respect to such transactions.
ITEM 11. EXECUTIVE COMPENSATION
The following table summarizes compensation of our executive officers:
| |
| | |
| | |
| | |
Option | | |
| | |
| |
Name and Position | |
Year | | |
Salary | | |
Bonus | | |
Awards | | |
Other | | |
Total | |
Steve B. Warnecke | |
| 2022 | | |
$ | 130,100 | | |
$ | — | | |
$ | 93,025 | | |
$ | 10,000 | | |
$ | 233,125 | |
Chief Executive Officer | |
| 2021 | | |
$ | 150,000 | | |
$ | — | | |
$ | — | | |
$ | 10,000 | | |
$ | 160,000 | |
Chairman of the Board | |
| 2020 | | |
$ | 150,000 | | |
$ | 50,000 | | |
$ | 151,846 | | |
$ | 10,000 | | |
$ | 361,846 | |
| |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Walter Messier | |
| 2022 | | |
$ | 150,000 | | |
$ | — | | |
$ | — | | |
$ | — | | |
$ | 150,000 | |
Chief Technology Officer | |
| 2021 | | |
$ | 150,000 | | |
$ | — | | |
$ | — | | |
$ | — | | |
$ | 150,000 | |
Secretary | |
| 2020 | | |
$ | 150,000 | | |
$ | 50,000 | | |
$ | 310,598 | | |
$ | — | | |
$ | 510,598 | |
| |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Virginia Orndorff | |
| 2022 | | |
$ | — | | |
$ | — | | |
$ | — | | |
$ | 10,000 | | |
$ | 10,000 | |
Director | |
| 2021 | | |
$ | — | | |
$ | — | | |
$ | — | | |
$ | 10,000 | | |
$ | 10,000 | |
| |
| 2020 | | |
$ | — | | |
$ | — | | |
$ | 46,590 | | |
$ | 10,000 | | |
$ | 56,590 | |
| |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Mark Boggess | |
| 2022 | | |
$ | — | | |
$ | — | | |
$ | — | | |
$ | 10,000 | | |
$ | 10,000 | |
Director | |
| 2021 | | |
$ | — | | |
$ | — | | |
$ | — | | |
$ | 10,000 | | |
$ | 10,000 | |
| |
| 2020 | | |
$ | — | | |
$ | — | | |
$ | 46,590 | | |
$ | 10,000 | | |
$ | 56,590 | |
The Company had no employment agreements as of December 31, 2022 and paid
cash compensation to each to its directors of $10,000 during the years ended December 31, 2022 and 2021. During the year ended December
31, 2022, Evolutionary Genomics issued option grants for 133,333 shares to Steve Warnecke. The amounts reported under “Option Awards”
in the above table reflect the grant date fair value of these awards as determined in accordance with the Financial Accounting Standards
Board’s Accounting Standards Codification Topic 718, Compensation – Stock Compensation, rather than amounts paid to or realized
by the named individual. The value of the option awards was estimated using the Black-Scholes option pricing model. The
valuation assumptions used in the valuation of options granted may be found in the Notes to our financial statements included in this
annual report on Form 10-K.
ITEM 12. SECURITY OWNERSHIP OF CERTAIN BENEFICIAL
OWNERS AND MANAGEMENT AND RELATED STOCKHOLDER MATTERS
Principal Stockholders
The following table sets forth certain information as of December 31, 2022
regarding the beneficial ownership of the Company’s common stock by (i) each stockholder known by the Company to be the beneficial
owner of more than 5% of our common stock, (ii) by each director and executive officer of the Company and (iii) by all executive officers
and directors of the Company as a group. Each of the persons named in the table has sole voting and investment power with respect to common
stock beneficially owned. The percentage ownership is the number of shares of common stock owned compared to the combined number of shares
of common and preferred stock outstanding. None of the officers or directors own any shares of preferred stock.
| |
Number of | | |
Percentage | |
| |
Shares Owned | | |
of Shares | |
Name and Address | |
or Controlled | | |
Owned | |
| |
| | |
| |
Steve B. Warnecke | |
| 1,841,374 | (1) | |
| 24.81 | % |
4220 Morning Star Dr | |
| | | |
| | |
Castle Rock, CO 80108 | |
| | | |
| | |
| |
| | | |
| | |
Virginia Orndorff | |
| 123,490 | (2) | |
| 1.66 | % |
4220 Morning Star Dr | |
| | | |
| | |
Castle Rock, CO 80108 | |
| | | |
| | |
| |
| | | |
| | |
Mark Boggess | |
| 26,000 | (3) | |
| 0.35 | % |
4220 Morning Star Dr | |
| | | |
| | |
Castle Rock, CO 80108 | |
| | | |
| | |
| |
| | | |
| | |
Walter Messier | |
| 182,044 | (4) | |
| 2.45 | % |
4220 Morning Star Dr | |
| | | |
| | |
Castle Rock, CO 80108 | |
| | | |
| | |
| |
| | | |
| | |
All Officers and Directors as a Group (1) | |
| 2,172,908 | | |
| 29.28 | % |
———————
| (1) | Mr. Warnecke is Chief Executive Officer and Chairman of the Board of the Company. Mr. Warnecke holds options for 100,000 shares exercisable
at $3.30 per share, 150,000 shares execisable at $1.65 per share and 133,333 shares exercisable at $.83 per share. |
| (2) | Ms. Orndorff is a Director of the Company. Ms. Orndorff holds options for 15,000 shares exercisable at $3.00 per share and 45,000
shares exercisable at $1.50 per share. |
| (3) | Mark Boggess is a Director of the Company. Mr. Boggess holds options for 15,000 shares exercisable at $3.00 per share and 45,000 shares
exercisable at $1.50 per share. |
| (4) | Dr. Messier is the Company’s Treasurer and Secretary. Dr. Messier holds options for 100,000 shares exercisable at $3.00 per
share and 300,000 shares exercisable at $1.50 per share.. |
ITEMS 13. CERTAIN RELATIONSHIPS, RELATED TRANSACTIONS AND DIRECTOR INDEPENDENCE
We maintain a mailing address at the offices of our president, Steve B.
Warnecke, located at 4220 Morning Star Drive, Castle Rock, CO 80108 for which we pay no rent. There have been no transactions or proposed
transactions in which the amount involved exceeds $120,000 for the last two completed fiscal years in which any of our directors, executive
officers of beneficial holders of more than 5% of the outstanding shares of common stock, or any of their respective relatives, spouses,
associates or affiliates has had or will have any direct or material indirect interest.
ITEM 14. PRINCIPAL ACCOUNTANT FEES AND SERVICES
Audit Fees
The aggregate fees billed during the years ended December 31, 2022 and
2021 for professional services rendered by our principal accountant, Plante & Moran PLLC, Denver, Colorado (PCAOB ID No. 166) for
the audit of our annual financial statements and quarterly reviews were $65,000 and $65,000, respectively.
Audit Related Fees
The Company incurred no fees for the years ended December 31, 2022 and
2021 for audit related services by our principal accountant that were reasonably related to the performance of the audit or review of
our financial statements, and not reported under Audit Fees above.
Tax Fees
For the years ended December 31, 2022 and 2021, fees for professional services
rendered by our principal accountant for tax preparation were $7,200 and $0, respectively.
All Other Fees
We did not incur any fees for other professional services rendered by our
principal accountant during the fiscal years ended December 31, 2022 and 2021.
Notes to Consolidated Financial Statements
December 31, 2022 and 2021
Note 1: Business Activity
Evolutionary
Genomics, Inc. (the “Company,” “We,” or “Our”) has developed
a technology platform, the Adapted Traits Platform (“ATP”), to identify commercially
valuable genes that control important traits in animals and plants. We are using the ATP
to identify genes to improve crop plant traits such as yield, sugar content, biomass, drought
tolerance, and pest/disease resistance. Our platform identifies key genes that have changed
successfully to impart new or improved traits.
In the past, the Company performed research
on behalf of governmental organizations, non-profit foundations and commercial entities and received revenue from grants and commercial
research contracts. We have not received any revenue from these grant arrangements since early 2020. The Company now focuses on research
projects that may lead to long-term licensing arrangements with agricultural seed companies and crop producers as with our soybean and
banana projects. These projects take several years to develop, and successful commercialization may take many years to produce license
royalty payments. Our banana project, in cooperation with Dole Food Company is an example that has resulted in notes payable funding
for the development phase of our banana genes and may result in a long-term royalty bearing license once the development phase is complete.
During 2014, the Company purchased 75.16%
of the outstanding stock of Fona, Inc., (“Fona”) a public shell company. Since Fona was a public shell company which did
not constitute a business and the purchase was done in contemplation of a reverse merger, the Company accounted for the payment as a
distribution to Fona shareholders. The Company also entered into an Agreement and Plan of Merger (the “Merger”), which was
consummated on October 19, 2015. As a result of the Merger, Evolutionary Genomics, Inc. became a wholly owned subsidiary of Fona. For
accounting purposes, the merger was treated as a reverse acquisition with Evolutionary Genomics, Inc. as the acquirer and Fona as the
acquired party. Subsequent to the Merger, Fona was renamed Evolutionary Genomics, Inc. and our subsidiary was renamed from Evolutionary
Genomics, Inc. to EG Crop Science, Inc.
Note 2: Summary of Significant Accounting
Policies
Principals of Consolidation: These
consolidated financial statements include the accounts of Evolutionary Genomics, Inc. and its wholly owned subsidiaries. All material
intercompany transactions and balances have been eliminated.
Use of Estimates: The preparation
of consolidated financial statements in conformity with accounting principles generally accepted in the United States of America requires
management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent
assets and liabilities at the date of the consolidated financial statements and the reported amounts of revenues and expenses during
the reporting period. Actual results could differ materially from those estimates.
These consolidated financial statements
have been prepared on the basis of going concern. Management’s plans to address the Company’s liquidity are discussed further
in Note 13.
Cash: The Company considers all highly
liquid investments purchased with an original or remaining maturity of three months or less when purchased to be cash.
Employee Retention Credit: During
the year ended December 31, 2022, the Company filed forms 941-X for the quarters ending December 31, 2020, March 31, 2021, June 30, 2021
and September 30, 2021 and expects to receive refunds totaling $78,000. Subsequent to December 31, 2022, the Company received a $21,000
refund for the quarter ended September 30, 2021.
Property and Equipment: Property
and equipment are stated at cost, net of accumulated depreciation. Depreciation is provided for by the straight-line method over three-
to seven-year estimated useful lives of software, furniture and fixtures and equipment. Maintenance and repairs are expensed as incurred;
major renewals and betterments that extend the useful lives of property and equipment are capitalized. When property and equipment are
sold or retired, the related cost and accumulated depreciation are removed from the accounts and any gain or loss is recognized.
Evolutionary Genomics, Inc. and Subsidiaries Notes to Consolidated Financial Statements December 31, 2022 and 2021 |
Long-Lived Assets: The long-lived
assets held and used by the Company are reviewed for impairment whenever events or changes in circumstances indicate that the carrying
amount of an asset may not be recoverable. In the event that facts and circumstances indicate that the cost of any long-lived assets
may be impaired, an evaluation of recoverability is performed. An impairment is considered to exist if the total estimated undiscounted
cash flows are less than the carrying amount of the asset. An impairment loss is measured and recorded to the extent that the carrying
amount of the asset exceeds its estimated fair value. No asset impairment was recorded during the years ended December 31, 2022 and 2021.
Intangible Assets: Intangible assets
include acquired research in progress and patents on the Company’s core technology for gene identification. Previously acquired
patents were capitalized and are amortized over their expected useful life of 20 years using the straight-line method. Acquired research
in progress was placed into service on August 19, 2020 in conjunction with the Development and Commercialization Agreement and is being
amortized over four years consistent with the term of the Dole agreement using the straight-line method. Costs incurred to renew intangible
assets and to file new patent applications are expensed in the period incurred, while costs incurred to extend the lives of patents are
capitalized and amortized over the remaining useful life of the asset. Intangible assets held and used by the Company are reviewed for
impairment whenever events or changes in circumstances indicate that the carrying amount of an asset may not be recoverable. In the event
that facts and circumstances indicate that the cost of any intangible assets may be impaired, an evaluation of recoverability is performed.
An impairment is considered to exist if the total estimated undiscounted cash flows are less than the carrying amount of the asset. No
impairment was recorded during the years ended December 31, 2022 and 2021.
Income Taxes: Deferred tax assets
and liabilities are recognized for the expected tax consequences of temporary differences between the tax bases of assets and liabilities
and their reported amounts. Management regularly assesses the likelihood that deferred tax assets will be recovered from future taxable
income, and to the extent management believes that it is more likely than not that a deferred tax asset will not be realized, a valuation
allowance is established. When a valuation allowance is established, increased or decreased, an income tax charge or benefit is included
in the consolidated financial statements and net deferred tax assets are adjusted accordingly. As of December 31, 2022 and 2021, a full
valuation allowance has been established on the net deferred tax asset.
Under the Income Tax topic of the ASC, in
order to recognize an uncertain tax benefit, the taxpayer must be more likely than not of sustaining the position, and the measurement
of the benefit is calculated as the largest amount that is more than 50% likely to be realized upon resolution of the benefit. The Company
has no accruals for uncertain tax benefits.
Stock-Based Compensation: The Company
accounts for stock option awards in accordance with ASC 718. The estimated grant-date fair value of stock-based awards is expensed over
the requisite service period, which is typically equivalent to the vesting term of the award.
The Company’s accounting policy for
equity instruments issued to consultants and vendors in exchange for goods and services received follows the provisions of ASC Topic
718. Accordingly, the measurement date for the fair value of the equity instruments issued is determined at the earlier of (i) the date
at which a commitment for performance by the consultant or vendor is reached or (ii) the date at which the consultant or vendor’s
performance is complete.
Research
and Development: Research and development costs are expensed as incurred. In instances where we enter into agreements with third
parties for research and development activities, we may prepay for services at the initiation of the contract. We record the prepayment
as a prepaid asset and amortize the asset into research and development expense over the period of time the contracted research and development
services are performed.
Net Loss Per Common Share: Basic
net (loss) income per common share excludes any dilutive effects of equity instruments. We compute basic net (loss) income per common
share using the weighted average number of common shares outstanding during the period. We compute diluted net (loss) income per common
share using the weighted average number of common shares and common stock equivalents outstanding during the period. For the year ended
December 31, 2022, common stock equivalents including 766,400 shares of convertible preferred stock and options for 1,028,333 shares
of common stock and for the year ended December 31, 2021, common stock equivalents including 679,923 shares of convertible preferred
stock and options for 1,081,667 shares of common stock were excluded because their effect was anti-dilutive.
Evolutionary Genomics, Inc. and Subsidiaries Notes to Consolidated Financial Statements December 31, 2022 and 2021 |
Note 3: New Accounting Standards
Recently Issued Accounting Standards
In June 2016, the FASB issued ASU 2016-13,
“Financial Instruments – Credit Losses: Measurement of Credit Losses on Financial Instruments,” which requires entities
to estimate all expected credit losses for certain types of financial instruments, including trade receivables, held at the reporting
date based on historical experience, current conditions, and reasonable and supportable forecasts. The updated guidance also expands
the disclosure requirements to enable users of financial statements to understand the entity’s assumptions, models and methods
for estimating expected credit losses over the entire contractual term of the instrument from the date of initial recognition of that
instrument. This guidance is effective for fiscal years beginning after December 15, 2022, including interim periods within that reporting
period and is not expected to have an impact on the Company’s consolidated financial statements.
Note 4: Property and Equipment
Property and equipment is comprised of the
following:
Schedule of Property and Equipment | |
| | | |
| | |
| |
December 31, | | |
December 31, | |
| |
2022 | | |
2021 | |
Equipment | |
$ | 432,499 | | |
$ | 432,499 | |
Software | |
| 63,179 | | |
| 63,179 | |
Furniture and fixtures | |
| 7,987 | | |
| 7,987 | |
| |
| 503,665 | | |
| 503,665 | |
Accumulated depreciation | |
| (499,709 | ) | |
| (484,967 | ) |
Property and equipment, net | |
$ | 3,956 | | |
$ | 18,698 | |
Depreciation expense for the years ended
December 31, 2022 and 2021 was $14,742 and $32,065, respectively.
Note 5: Intangible Assets
Intangible assets are comprised of the following:
Schedule of Intangible Assets | |
| | | |
| | |
| |
December 31, | | |
December 31, | |
| |
2022 | | |
2021 | |
Acquired research in progress - definite lived | |
$ | 4,016,596 | | |
$ | 4,016,596 | |
Patents | |
| 52,045 | | |
| 52,045 | |
Accumulated amortization | |
| (2,417,800 | ) | |
| (1,411,049 | ) |
Intangible assets, net | |
$ | 1,650,841 | | |
$ | 2,657,592 | |
Evolutionary Genomics, Inc. and Subsidiaries Notes to Consolidated Financial Statements December 31, 2022 and 2021 |
The Company expects
to recognize amortization expense related to its acquired research in progress and patents according to the following:
Schedule of Intangible Assets Amortization | | |
| | |
Year Ending | | |
Amortization | |
December 31, 2023 | | |
| 1,006,751 | |
December 31, 2024 | | |
| 638,105 | |
December 31, 2025 | | |
| 2,602 | |
December 31, 2026 | | |
| 2,602 | |
December 31, 2027 | | |
| 781 | |
Total | | |
$ | 1,650,841 | |
Amortization
expense for the acquired research in progress and patents during the years ended December 31, 2022 and 2021 was $1,006,751.
In its merger completed
on October 19, 2015, the Company acquired research in progress. The value of the acquired research in progress was based upon several
factors including, evaluation of other intangible assets, the purchase price, estimated future cash flows, and the amounts expended on
the research to date. The research in progress was the identification and validation of genes to provide pest and disease resistance
to plants performed by EG I. With the banana development project contract in place, the Company placed this asset in service on August
19, 2020. Additional costs to complete the soybean research are expected to be approximately $33,000, which will be expensed as incurred.
The timing and cost of additional research may vary from these estimates as the success of the research is subject to many factors outside
of the Company’s control.
Note 6: Income
Taxes
For the years ended December 31, 2022 and
2021, the Company did not recognize any current or deferred income tax benefit or expense. For the years ended December 31, 2022 and
2021, the reconciliation between the income tax benefit computed by applying the statutory U.S. federal income tax rate of 21.0% to the
pre-tax loss before income taxes, and total income tax benefit (expense) recognized in the financial statements is as follows
Schedule of income tax rate reconciliation | |
| | | |
|
| |
| |
2022 | | |
2021 | |
Income tax benefit at statutory U.S. federal rate | |
$ | 406,343 | | |
$ |
586,728 | |
Income tax benefit attributable to U.S. states | |
| 67,259 | | |
|
99,325 | |
Research and development credits | |
| (66,000 | ) | |
|
137,728 | |
Non-taxable forgiveness of PPP and EIDL loans | |
| — | | |
|
20,478 | |
Non-deductible expenses | |
| (299 | ) | |
|
(300 | ) |
Stock- based compensation related to incentive stock options | |
| (47,290 | ) | |
|
(53,952 | ) |
Other changes | |
| (7,439 | ) | |
|
(15,182 | ) |
Change in valuation allowance | |
| (352,574 | ) | |
|
(774,825 | |
Total income tax expense (benefit) | |
$ | — | | |
$ |
— | |
As of December 31, 2022 and 2021, the components
of deferred income tax assets and liabilities were as follows:
Schedule of deferred tax assets and liabilities | |
| | | |
|
| |
| |
2022 | | |
2021 | |
Deferred income tax assets: | |
| | | |
|
| |
Net operating loss carryforwards | |
$ | 2,928,442 | | |
$ |
2,876,543 | |
Research and development credits | |
| 449,981 | | |
|
515,982 | |
Accrued Compensation | |
| 23,667 | | |
|
— | |
Long-term capital loss carryforward | |
| 94,445 | | |
|
94,728 | |
Valuation allowance for deferred income tax assets | |
| (3,187,682 | ) | |
|
(2,835,108 | ) |
Net deferred income tax assets | |
| 308,853 | | |
|
652,145 | |
Deferred income tax liabilities: | |
| | | |
|
| |
Intangible assets | |
| (307,885 | ) | |
|
(647,554 | ) |
Property, equipment and other | |
| (968 | ) | |
|
(4,591 | ) |
Total deferred income tax liabilities | |
| (308,853 | ) | |
|
(652,145 | ) |
Net deferred income tax assets | |
$ | — | | |
$ |
— | |
The Company uses
the asset and liability method of accounting for income taxes. Under this method, deferred tax assets and liabilities are recognized
for the future tax consequences attributable to differences between the financial statement carrying amounts of existing assets and liabilities
and their respective tax basis. Deferred tax assets and liabilities are measured using enacted tax rates expected to apply to taxable
income in the years in which those temporary differences are expected to reverse.
Evolutionary Genomics, Inc. and Subsidiaries Notes to Consolidated Financial Statements December 31, 2022 and 2021 |
The Company records a valuation allowance
for certain temporary differences for which it is more likely than not that a future tax benefit will be received. The Company assesses
its past earnings history and trends and projections of future net income. The Company recorded a valuation allowance for the entire
amount of the net deferred tax asset as of December 31, 2022 and 2021. As of December 31, 2022, the Company had a total valuation allowance
of approximately $3,188,000 for its deferred tax assets. The Company will continue to review this valuation allowance and make adjustments
as appropriate.
As of December 31, 2022, the Company had
net operating loss (“NOL”) carryforwards of approximately $11,965,000, consisting of $5,545,000 that have an indefinite carryover
period and $6,420,000 that expire at various intervals through 2037. Use of NOL carryforwards is limited by the provisions of Section
382 of the Internal Revenue Code. At this point, the Company has not performed an analysis to determine whether an ownership change (as
defined under Section 382) occurred during this year or preceding years. A determination of the potential impact these provisions might
have on the utilization of net operating losses will be made when the net operating loss is projected to be utilized. As of December
31, 2022, the Company also has a capital loss carryforward of approximately $386,000 that expires in 2025, and a research and development
credit carryforward of approximately $450,000 that will expire at various intervals from 2030 through 2040.
The calculation of the Company’s tax
liabilities involves dealing with uncertainties in the application of complex tax laws and regulations. ASC 740 states that a tax benefit
from an uncertain tax position may be recognized when it is more likely than not that the position will be sustained upon examination,
including resolutions of any related appeals or litigation processes, on the basis of the technical merits. At this time, the Company
does not have any uncertain tax positions to assess.
Note 7: Notes
Payable
Small Business Administration
(“SBA”) Paycheck Protection Program: On February 22, 2021, the Company received $76,395 in proceeds from the PPP, which
was created under the Coronavirus Aid, Relief and Economic Security Act (CARES). Under the program, the Company applied for and received
forgiveness of the debt in the year ended December 31, 2021. The forgiveness was recorded as loan forgiveness in other income on the
consolidated statements of operations in the year ended December 31, 2021.
SBA Economic Injury
Disaster Loan: On June 5, 2020, the Company received $150,000 in proceeds from the SBA’s EIDL Program. On July 20, 2021, the
Company received an additional $7,000 SBA EIDL Advance which has been forgiven and, on July 14, 2021, the Company received a $50,000
increase in the SBA EIDL Loan. Installment payments, including interest at the rate of 3.75% per annum, of $1,019 monthly over thirty
years from the date of the original promissory note began on December 13, 2022. The Company granted to the SBA a continuing security
interest in all tangible and intangible personal property. The Company may not make any distribution of assets of the Company to any
shareholder without the written consent of the SBA. As of December 31, 2022, the Company recognized $16,128 of accrued interest on the
note.
Dole Food Company:
On August 19, 2020,
the Company entered into a Development and Commercialization Agreement (“DCA”) with Dole Food Company (“Dole”)
for the development of our banana genes. The DCA provides for payments from Dole to the Company of $800,000 upon execution, $800,000
by the twelve-month anniversary, $250,000 by the thirty-six month anniversary and $250,000 by the forty-eight month anniversary. Dole
also reimburses the Company for costs incurred at the University of Wisconsin-Madison (“UW”) not to exceed $2,200,000 in
coordination with the Standard Research Agreement that the Company entered into with UW on September 18, 2020. The agreement with UW
includes payments from the Company to UW in the amount of $2,159,719 over the two-year expected term of the project. If the UW research
is successful, Dole expects to incur costs of approximately $750,000 to perform field trials.
The DCA also specifies
that the Company will execute notes payable to Dole for the funding that Dole is providing up to $5,050,000. Upon receipt of $800,000
on August 26, 2020, $800,000 on July 28, 2021, $1,295,831 on December 29, 2020 and $647,916 on September 29, 2021, the Company executed
the notes under this DCA and recorded them as long-term notes payable for financial statement purposes. The notes are non-interest bearing
and allow Dole to offset fifty percent of future royalty payments to the Company by reducing the amount of principal due on these notes.
Other than this offset of future royalty payments, repayment of principal and interest is only required in the case of termination of
the DCA by Dole for cause.
Evolutionary Genomics, Inc. and Subsidiaries Notes to Consolidated Financial Statements December 31, 2022 and 2021 |
Note 8: Stockholders’
Equity
The Amended and Restated
Certificate of Incorporation of the Company dated October 19, 2015 authorized the issuance of 800,000,000 shares of all classes of stock
including 780,000,000 shares of Common Stock having a par value of $0.001 per share and 20,000,000 shares of Preferred Stock having a
par value of $0.001 per share, 600,000 of which were designated as Series A-1 Convertible Preferred Stock (“Series A-1”)
and 200,000 of which were designated as Series A-2 Convertible Preferred Stock (“Series A-2”). The Board of Directors, without
a vote of the shareholders, is authorized to issue additional shares of Preferred Stock in series and to establish the characteristics
thereof.
Liquidation:
Upon any liquidation, dissolution or winding-up of the Company, whether voluntary or involuntary, the holders of the Series A-1 and Series
A-2 shall be entitled to receive out of the assets of the Company for each share of Series A-1 and Series A-2 an amount equal to its
stated value, $5.25 per share as of December 31, 2022 and 2021, plus any accrued but unpaid dividends before any distribution or payment
shall be made to the holders of any other class or series of stock of the Company that ranks junior to the Series A-1 and Series A-2.
The holders shall be entitled to convert their shares of Series A-1 and Series A-2 into Common Stock at any time prior to the consummation
of a Liquidation. This is considered a contingent redemption feature.
Conversion:
The holders of Series A-1 and Series A-2 may convert their shares into shares of Common Stock, at the option of the holder, on a one-share-for-one-share
basis and shall be subject to certain adjustments at any time.
Optional Redemption;
Sinking Fund Account: The Company may elect to redeem some or all of the then outstanding shares of Series A-1, (i) for cash in an
amount equal to the liquidation preference per share, $5.25 per share as of December 31, 2022, subject to adjustment and (ii) by issuing
one share, subject to adjustment, of Common Stock for each share of Series A-1 and Series A-2 outstanding being redeemed. 50% of all
licensing fees received by the Company will be deposited into a separate sinking fund for use in an optional redemption. As of December
31, 2022, no licensing revenue has been received under these provisions and no sinking fund account has been established.
Dividends: The
Company shall pay to the holders of the Series A-1 and Series A-2 dividends at the rate of 8% per annum and the Company has accrued these
dividends since issuance of the Series A-1 and Series A-2. The dividend amount shall accrue and shall be payable in shares of Common
Stock upon the conversion of the Series A-1 and Series A-2, or upon the redemption of the Series A-1 and Series A-2. No dividends shall
be paid on any Common Stock of the Company or any capital stock of the Company that ranks junior to the Series A-1 and Series A-2 until
dividends of Series A-1 and Series A-2 been paid. As of December 31, 2022, there were $1,835,089 in accrued stock dividends.
Voting: The
holders of the Series A-1 and Series A-2 are entitled to vote on all matters submitted to the stockholders for a vote on an as-if-converted
to Common Stock basis, with all stockholders voting as a single class.
Note 9: Stock-Based Compensation
The Company grants stock-based instruments
under the 2015 Stock Incentive Plan (“Plan”) for which 1,400,000 shares of the Company’s Common Stock has been reserved.
The Plan allows for the issuance of incentive stock options and non-qualified stock options with a maximum contractual term of 10 years.
Shares and options that are cancelled are available for reissuance under the Plan. For years ended December 31, 2022 and 2021, the Company
recorded compensation costs for stock options of $193,208 and $219,718, respectively. Stock options are generally issued with an exercise
price at or above the estimated per-share value of the Company’s Common Stock. The Company granted options for 133,333 shares of
common stock during the year ended December 31, 2022 and none in the year ended December 31, 2021.
Management has valued the options at their
date of grant utilizing the Black-Scholes option pricing model. Volatility of the underlying common shares was determined based on the
historical volatility for the Company’s stock for a term consistent with the expected life of the options. The risk-free interest
rate used in the calculations is based on the implied yield available on U.S. Treasury issues with an equivalent term approximating the
expected life of the options on the date of the grant. Due to the lack of sufficient historical activity, the expected term of the options
was estimated using the formula set forth in Securities and Exchange Commission SAB 107.
Evolutionary Genomics, Inc. and Subsidiaries Notes to Consolidated Financial Statements December 31, 2022 and 2021 |
The fair value of the share option awards
was estimated using the Black-Scholes method based on the following weighted-average assumptions:
Schedule Weighted Average Assumptions |
|
Volatility |
154% |
Expected Term |
5.5
years |
Dividend Rate |
0% |
Risk Free Rate |
2.56% |
The following table summarizes the status
of the Company’s aggregate stock options granted:
Schedule of Stock Option Activity | | |
| | | |
| | | |
| | | |
| | |
| | |
Number of Options | | |
Weighted Average Exercise Price | | |
Weighted Average Remaining Term (Years) | | |
Total Intrinsic Value | |
| | |
| | |
| | |
| | |
| |
Balance, January 1, 2021 | | |
| 1,081,667 | | |
$ | 1.74 | | |
| 6.67 | | |
| | |
Granted | | |
| — | | |
| — | | |
| — | | |
| | |
Exercised | | |
| — | | |
| — | | |
| — | | |
| | |
Cancelled | | |
| — | | |
| — | | |
| — | | |
| | |
| | |
| | | |
| | | |
| | | |
| | |
Balance, December 31, 2021 | | |
| 1,081,667 | | |
$ | 1.74 | | |
| 5.67 | | |
| | |
| | |
| | | |
| | | |
| | | |
| | |
Balance, January 1, 2022 | | |
| 1,081,667 | | |
$ | 1.74 | | |
| 5.67 | | |
| | |
Granted | | |
| 133,333 | | |
$ | 0.83 | | |
| 9.23 | | |
| | |
Exercised | | |
| (186,667 | ) | |
$ | 0.55 | | |
| — | | |
| | |
Cancelled | | |
| — | | |
| — | | |
| — | | |
| | |
| | |
| | | |
| | | |
| | | |
| | |
Balance, December 31, 2022 | | |
| 1,028,333 | | |
$ | 1.84 | | |
| 6.22 | | |
$ | — | |
| | |
| | | |
| | | |
| | | |
| | |
Exercisable at December 31, 2022 | | |
| 861,664 | | |
$ | 2.00 | | |
| 5.73 | | |
$ | — | |
During the years ended December 31, 2022
and 2021, options for 179,999 and 180,000 shares vested, respectively. As of December 31, 2022, there was $85,548 unrecognized compensation
cost related to share-based compensation arrangements that will be recognized through the year ending December 31, 2023.
Evolutionary Genomics, Inc. and Subsidiaries Notes to Consolidated Financial Statements December 31, 2022 and 2021 |
Note 10: Commitments and Contingencies
Officer Indemnification: Under the
Company’s organizational documents, the Company’s officers, employees, and directors are indemnified against certain liabilities
arising out of the performance of their duties. The Company’s maximum exposure under these arrangements is unknown, as this would
involve future claims that may be made against the Company that have not yet occurred. However, based on experience, the Company expects
any risk of loss to be remote. The Company also has an insurance policy for its directors and officers to insure them against liabilities
arising from their performance in their positions with the Company.
Lease Commitments: The Company leases
its operating facility and pays its rent in monthly installments. The lease was renewed in June 2016 for a period of twelve months and
monthly rentals for the period of July 1, 2016 through December 31, 2022 are $2,378 per month which continues on a month-to-month basis.
There is no minimum lease commitment as of December 31, 2022. Renewals after June 30, 2017 are by mutual agreement. The Company’s
rent expense for the years ended December 31, 2022 and 2021 was $26,157 and $28,535, respectively.
Royalty: Effective March 1, 2012,
the Company entered into an Agreement for Contract Services with SmithBucklin Corporation (the “Contractor”) on behalf of
the United Soybean Board. The contract includes the payment of certain royalties, as defined in the Agreement.
The Company is
obligated to pay royalties to the United Soybean Board of 10% of the sale of products derived from the soybean genes that were the subject
of the research performed by the Contractor or from royalties received by the Company from the sale of products by a third party not
to exceed 150% of the total amount paid to the Contractor under this Agreement. The Company has recognized to date grant revenue from
the contract of $262,400 as of December 31, 2022, thus limiting any future royalties as of December 31, 2022 to a total of $393,600.
The Company has not accrued or paid any royalties under the terms of the Agreement as of and during the years ended December 31, 2022
and 2021 because it has not received any revenue from the sale of products to date.
Other
Commitments: On September 18, 2020, the Company entered into a Standard Research Agreement with WCIC for the development of
our banana genes. The agreement includes payments from the Company in the amount of $2,159,719
over the 2 two-year expected term of the project. These costs will be reimbursed, in the form of notes payable by Dole in accordance
with our DCA.
The Company entered into a Service Agreement
with WCIC for the maintenance and shipment of banana plants which includes unit pricing for services rendered and is expected to be completed
by March 31, 2023. During the year ended December 31, 2022, $59,330 of cost was incurred under this contract and was reimbursed by Dole.
On April 18, 2022, the Company entered into
a Service Agreement with the University of Wisconsin-Madison for the testing of banana plants which includes payments of $143,124 of
which $128,811 were paid in the year ended December 31, 2022 and reimbursed by Dole.
Note 11: Related Parties and Transactions
Steve B. Warnecke: Mr. Warnecke is
the Company’s Chief Executive Officer and Chairman of the Board and owns, directly or indirectly, 1,841,374 shares or 24.8% of
the Common Stock outstanding as of December 31, 2022.
Note 12: Concentrations
Considerations of Credit Risk: Financial
instruments that potentially subject the Company to concentrations of credit risk consist principally of cash. The Company maintains
its cash balances at high-credit, quality financial institutions. The balances, at times, may exceed federally insured limits. The Company
routinely monitors the credit quality of its customers.
Evolutionary Genomics, Inc. and Subsidiaries Notes to Consolidated Financial Statements December 31, 2022 and 2021 |
Note 13: Liquidity and Going Concern
The Company has historically financed operations
through cash flows from operations and equity transactions. Net cash used in operating activities was $640,947 for the year ended December
31, 2022 compared to $1,583,138 for the year ended December 31, 2021. The $942,191, or 59.5%, decrease was primarily due to the decreased
net operating loss. Net cash provided from financing activities was $550,000 of proceeds from the issuance of common stock and $454,004
from the issuance of preferred stock compared to $1,447,916 in proceeds from notes payable from Dole and $133,395 in proceeds from the
PPP loan and the EIDL in the year ended December 31, 2021.
As of December 31, 2022, the Company had
$577,066 in operating cash and expects that operating cash flow net of contractual reimbursements and notes payable funding from Dole
for the year ending December 31, 2023 will be approximately $546,000. Management believes that there may not be enough cash to pay our
expenses for one year beyond the date of this report. Marketing of additional genes may lead to additional revenue and we have some flexibility
to reduce operating costs but we may require additional capital. These factors create substantial doubt as to our ability to continue
as a going concern. The accompanying consolidated financial statements do not include any adjustments that may result if the Company
is unable to continue as a going concern.
Note 14: Subsequent Event
During the year ended December 31, 2022,
the Company filed forms 941-X for the quarters ending December 31, 2020, March 31, 2021, June 30, 2021 and September 30, 2021 and expects
to receive refunds totaling $78,000. Subsequent to December 31, 2022, the Company received a $21,000 refund for the quarter ended September
30, 2021.
F-16