Dyadic Announces First Quarter 2024 Financial Results and Highlights Recent Company Progress
Dyadic International (NASDAQ: DYAI) released its Q1 2024 results, reporting a net loss of $2.01 million or $(0.07) per share, compared to a net loss of $0.96 million or $(0.03) per share a year ago. Revenue for the quarter decreased to $335,000 from $934,000 in Q1 2023. Cash and equivalents stood at $12.1 million as of March 31, 2024.
Key advancements include positive Phase 1 results for DYAI-100, a COVID-19 booster vaccine, and multiple collaborations on vaccine and antibody projects. The company also expanded its work in animal health and alternative proteins sectors.
Strategic partnerships were formed to develop rabies vaccines and alternative proteins. The financial standing was bolstered by a $6.0 million convertible note. Leadership changes include Patrick Lucy as Board Chairman and Joe Hazelton as COO.
- Cash position of $12.1 million as of March 31, 2024.
- Successful issuance of $6.0 million in convertible notes at a conversion price of $1.79.
- Positive Phase 1 trial results for DYAI-100 COVID-19 booster vaccine.
- Entered fully funded vaccine and antibody projects covering over twelve targets.
- Expressed H1N1 influenza antigen in collaboration with Vaccine and Immunotherapy Center.
- Strong immune response in animal studies for H5N1 'Bird Flu' vaccine candidate.
- Advanced partnerships in the development of rabies vaccines and bio-threat solutions.
- Published preclinical studies in Nature Communications.
- Net loss increased to $2.01 million compared to $0.96 million in Q1 2023.
- Revenue decreased to $335,000 from $934,000 year-over-year.
- Research and development revenue fell due to winding down of large collaborations.
- General and administrative expenses rose by 20.9% to $1.79 million.
- Research and development expenses dropped by 35.5%.
Insights
Dyadic's first quarter financial results reveal a complex picture. While the company reported a significant increase in
The cost of revenue also decreased from
Despite the increased cash reserves, the net loss for Q1 2024 widened to
The successful completion of the DYAI-100 Phase 1 clinical trial is a significant milestone for Dyadic. The trial demonstrated the safety and antibody response of their recombinant protein receptor binding domain booster vaccine candidate for COVID-19. This achievement not only validates the C1 platform's capability to produce safe proteins but also lays a solid foundation for future human and animal vaccine applications.
The collaboration with the Vaccine and Immunotherapy Center at Massachusetts General Hospital, the strategic partnership with Rabian BV for rabies vaccines and the advancements in the H5N1 bird flu vaccine candidate demonstrate Dyadic's versatility in addressing diverse infectious diseases. The manuscript publication in Nature Communications further enhances the credibility of their C1-produced monoclonal antibodies.
However, the next steps involve securing regulatory approvals for further clinical trials, which can be lengthy and uncertain. Investors should monitor progress closely, especially any advancements toward Phase 2 trials or commercial applications. Overall, these developments indicate a promising trajectory for Dyadic's therapeutic and vaccine pipeline, but the journey to market approval and commercialization remains challenging.
Dyadic's entry into various funded research collaborations and strategic partnerships with major pharmaceutical companies and institutions such as the Israel Institute for Biological Research and the European Union’s Horizon Europe program highlights the growing industry interest in their microbial protein production platforms.
The company's efforts to diversify into non-pharmaceutical applications, including alternative proteins and non-animal dairy products, signify an astute business strategy aimed at reducing dependence on the pharmaceutical sector. The term sheet to develop recombinant serum albumin and the co-promotion agreement with Biftek Co. for cell culture growth media indicate potential new revenue streams in the rapidly growing alternative protein market.
However, it is essential to note that the commercialization of these non-pharmaceutical applications will require significant time and investment. The success of these ventures will depend on achieving target yield levels, securing commercialization agreements and navigating regulatory landscapes. Nevertheless, Dyadic's proactive approach in developing a robust and diversified pipeline positions them well for long-term growth, provided they can manage execution risks effectively.
Human Health Sector
- Final Clinical Study Report has been issued for the First-In-Human Phase 1 clinical trial demonstrating safety and antibody response for DYAI-100, a recombinant protein receptor binding domain booster vaccine candidate for protection against COVID-19 infection
- Entered into several fully funded vaccine and antibody projects covering more than twelve targets, five of which are funded by two of the top ten pharmaceutical companies
- Successfully expressed a H1N1 influenza antigen in our collaboration with the Vaccine and Immunotherapy Center (“VIC”) at Massachusetts General Hospital
- Announced strategic partnership to develop affordable rabies prophylactics and vaccines using C1-cell protein production platform
- Published a manuscript of preclinical studies on C1 produced monoclonal antibody in non-human primates and hamsters in prestigious peer-reviewed journal Nature Communications
- Advanced collaboration with Israel Institute for Biological Research (IIBR) targeting bio-threats and emerging disease solutions
- C1 produced adjuvanted recombinant ferritin nanoparticle H5N1 “Bird Flu” human vaccine candidate demonstrated a strong immune response in animal studies
Animal Health Sector
- C1 produced adjuvanted recombinant ferritin nanoparticle H5N1 “Bird Flu” human vaccine candidate demonstrated a strong immune response in animal studies for potential use in poultry, cattle and other animals
- Expanded collaboration with Phibro/Abic to develop vaccines and treatments for companion and livestock animal diseases
Alternative Proteins Sector
- Executed a term sheet to utilize our microbial protein production platforms to develop production strains for the production of recombinant serum albumin
- Advanced development of 6 product candidates for non-pharmaceutical applications utilizing the Dapibus™ platform technology
Corporate
- Closed a
$6.0 million convertible note in a private placement, with a conversion price of$1.79 and no warrants - Appointed Mr. Patrick Lucy as Board Chairman and Mr. Joe Hazelton as Chief Operating Officer
- Cash and investment grade securities of
$12.1 million as of March 31, 2024 - Financial results and business update conference call scheduled for 5:00 p.m. ET today
JUPITER, Fla., May 14, 2024 (GLOBE NEWSWIRE) -- Dyadic International, Inc. (“Dyadic”, “we”, “us”, “our”, or the “Company”) (NASDAQ: DYAI), a biotechnology company focused on the efficient large-scale manufacture of proteins for use in human and animal vaccines and therapeutics, as well as non-pharmaceutical applications including food, nutrition, and wellness, today announced its financial results for the first quarter of 2024 and highlighted recent Company progress.
“We continue to execute our business strategy to focus on near-term pharmaceutical and non-pharmaceutical applications for our proprietary and patented C1 and Dapibus™ protein production platforms and pipeline products,” said Mr. Mark Emalfarb, President and CEO of Dyadic. “One of our key highlights was the successful completion of a Phase 1 clinical trial that met its primary endpoint of safety and reactogenicity affirming the safety of proteins produced by Dyadic's C1 platform in humans. We believe this milestone not only establishes the safety of our platform but also provides a solid foundation for C1 technology’s future applications in human and animal vaccines and therapeutics. With the H5N1 ('Bird Flu') virus outbreaks in poultry and U.S. dairy cows, along with one recent human case, we are seeing an increasing interest in our H5N1 'Bird Flu' ferritin nanoparticle human vaccine candidate, developed with ViroVax. Additional animal studies indicate that the vaccine candidate has the potential to generate high neutralizing antibodies for use in cattle. Our Q1 2024 achievements demonstrate our ongoing commitment to enhancing our microbial platforms for diverse applications, and our dedication to improving health for humans and animals, while tackling the challenges of sustainable food production.”
Mr. Emalfarb continued, “As we progress into the second quarter, our Company continues to focus on enhancing the Dapibus™ platform, designed specifically for non- pharmaceutical uses in industries such as food, nutrition, health, and other bioproducts. To accomplish this goal, we have honed our business development strategy, focusing on key areas where our technologies can deliver the greatest impact with shorter commercialization timelines. Our strategy includes simultaneously targeting multiple offtakes for a single product in several corresponding business segments and seeking out new opportunities that are in line with our strategy.”
Joe Hazelton, Dyadic’s Chief Operating Officer, elaborated, “In addition to operational advancements, we also strengthened our financial position with the issuance of
Recent Company Progress
Corporate Events:
- On March 8, 2024, the Company issued an aggregate principal amount of
$6.0 million of its8.0% Senior Secured Convertible Promissory Notes due March 8, 2027 (the “Convertible Notes”) in a private placement in reliance on the exemption from registration provided by Section 4(a)(2) of the Securities Act of 1933, as amended. The purchasers of the Convertible Notes include immediate family members and family trusts related to Mark Emalfarb, our President and Chief Executive Officer and a member of our Board of Directors, including The Francisco Trust, an existing holder of more than5% of the Company’s outstanding common stock. - On March 28, 2024, the Company announced changes in the leadership roles of the Board and senior management team: the appointment of Mr. Patrick Lucy as Chairman of Board of Directors and promotion of Mr. Joe Hazelton to Chief Operating Officer.
Human Health Sector
DYAI-100 Phase 1 Clinical Trial
DYAI-100, a C1-SARS-CoV-2 recombinant protein RBD vaccine candidate, is the first C1-expressed protein tested in humans. The Phase 1 randomized, double-blind, placebo-controlled trial was designed as a first-in-human trial to assess the clinical safety and antibody response of DYAI-100, produced using the C1 platform and administered as a booster vaccine at two single dose levels in healthy volunteers. Following regulatory clearance from the South African Health Products Regulatory Authority (SAHPRA), the trial was initiated in 1Q 2023, with the last patient visit occurring in 3Q 2023. On November 29, 2023, the Company announced the top-line safety results, indicating that the study has met its primary endpoint that both the low and high dose levels of the vaccine are safe and well tolerated among participants. Additionally, the vaccine has been shown to induce immune responses at both dose levels, suggesting its potential efficacy in generating protective immunity against the target virus. The study has been finalized, and the final Clinical Study Report has been issued, demonstrating that the DYAI-100 vaccine met its primary endpoint of safety and reactogenicity.
- In April 2024, Dyadic and its development partner ViroVax reported pre-clinical animal testing on a ferritin nanoparticle H5N1 bird flu recombinant protein human vaccine candidate that demonstrated a strong immune response in rabbits. The potential vaccine combines Dyadic’s C1 single step ferritin nanoparticle H5N1 antigen production with a novel adjuvant from ViroVax. Additional animal studies are being carried out that preliminarily show that this H5N1 bird flu vaccine has the potential to be used in humans.
- Successfully expressed H1N1 influenza antigen in the fully funded research collaboration with the Vaccine and Immunotherapy Center (“VIC”) at Massachusetts General Hospital to express vaccine antigens for influenza A and other infectious diseases, as part of a US
$5.88 million award from the Department of Defense (“DoD”). - On March 25, 2024, the Company entered a funded research collaboration with a top ten pharmaceutical company to develop a vaccine antigen and a monoclonal antibody produced from the C1 technology.
- In March 2024, a manuscript of preclinical studies on C1-produced monoclonal antibody in non-human primates and hamsters was published in the prestigious peer-reviewed journal Nature Communications. A non-human primate challenge study completed dosing of a C1-produced COVID-19 monoclonal antibody (mAb) that had previously demonstrated broad neutralization and protection against Omicron (BA.1 and BA.2) and the other earlier variants of concern in hamsters. Preliminary results obtained from the challenge study with the SARS-CoV-2 Delta virus on non-human primates demonstrated potential high protection. This was the first time a C1-produced monoclonal antibody was used in a non-human primate study validating the safety and efficacy of a C1 produced antibody for infectious diseases.
- On February 28, 2024, the Company’s Dutch subsidiary, Dyadic Nederland BV, entered into a strategic partnership agreement and collaboration with Rabian BV (“Rabian”), a Dutch innovative SME founded by experienced entrepreneurs and vaccine scientists. Awarded by Eurostars for the AVATAR project, a part of the European Partnership on Innovative SMEs (small and medium-sized enterprises), and co-funded by the European Union through Horizon Europe. Rabian will use the total funding of approximately Є1.7 million leveraging its expertise in virology to develop a rabies vaccine using Dyadic’s C1 protein production platform to tackle the challenges posed by rabies, particularly in lower- and middle-income countries. Dyadic is expected to receive an equity stake in Rabian, fully funded research and development costs, and specified product milestones and royalties upon commercialization.
- On February 21, 2024, the Company announced it has advanced its collaboration with the IIBR and its commercial arm Life Science Research Israel (LSRI), to target emerging disease solutions. This partnership aims to leverage Dyadic’s expertise in microbial platforms for flexible scale protein bioproduction and the IIBR’s antibodies and antigens discovery capabilities to develop and manufacture innovative solutions for addressing emerging diseases and potential bio-threats. Through this collaboration, both parties are working towards the development of effective treatments and vaccines to combat global health challenges with the intention of future commercialization (to date, the framework is non-binding and subject to the execution of a binding agreement to be negotiated by the parties) through collaborative out-licensing initiatives.
- On February 13, 2024, the Company announced a strategic partnership with Cygnus Technologies®, part of Maravai LifeSciences®, who have developed the C1 Host Cell Protein ELISA Kit for the quality release of products produced using Dyadic’s protein expression platforms. The C1 Host Cell Protein ELISA Kit is now available for purchase on Cygnus Technologies website under Fungal HCP ELISA kits tab.
- On February 6, 2024, the Company announced it signed a fully funded evaluation agreement including a commercial option with an undisclosed leading global biopharmaceutical company to design and produce recombinant proteins using Dyadic’s C1 microbial protein production platform.
Animal Health Sector
- On March 15, 2024, the Company expanded its collaboration with Phibro Animal Health/Abic Biological Laboratories Ltd to develop vaccines and treatments for companion and livestock animal diseases.
- C1 produced adjuvanted recombinant ferritin nanoparticle H5N1 “Bird Flu” human vaccine candidate demonstrated a strong immune response in animal studies for potential use in poultry, cattle and other animals.
- The H5N1 C1 produced bird flu ferritin nanoparticle vaccine elicits high neutralizing antibodies against all three virus isolates (including Texas) of the H5 virus in livestock.
- The H5N1 C1 produced bird flu ferritin nanoparticle vaccine elicits high neutralizing antibodies against all three virus isolates (including Texas) of the H5 virus in livestock.
Alternative Proteins Sector
Dyadic is advancing a pipeline of differentiated product candidates that leverage its microbial protein production platforms, including Dapibus™ which have demonstrated the ability and efficiency to enable the rapid development and large-scale manufacture of proteins at low cost in a wide range of non-pharmaceutical applications and commercial use.
Cell Culture Media Products
- In March 2024, the Company executed a term sheet with a large global albumin manufacturer and distributor to develop and license Dyadic’s recombinant serum albumin. The Company’s animal-free recombinant serum albumin projects were initiated in late 2022 using Dyadic pharmaceutical cell lines for use in potential therapeutic, product development, research, and/or diagnostic human and animal pharmaceutical applications. The Company has completed the initial analysis of its recombinant albumin products and has Certificates of Analysis for recombinant human and bovine albumin that demonstrate comparability to reference standards used in the testing.
- In March 2024, the Company entered into a co-promotion agreement with Biftek Co. for the promotion of growth media supplement for cell culture.
- The Company is undergoing a project to produce recombinant transferrin for use in cell culture media for the alternative protein industry.
- The Company is currently sampling recombinant bovine albumin for application testing as growth media for the cultured meat industry.
Non-animal Dairy Products
- As previously announced, in September 2023, the Company entered into a development and exclusive license agreement to commercialize certain non-animal dairy enzymes used in the production of food products using Dapibus™ and received an upfront payment of
$0.6 million in October 2023. The Company believes it has achieved the specified target yield level required for a milestone payment upon verification by its partner, and the development of a second enzyme is progressing as planned. - The Company has developed a highly productive strain and is actively sampling recombinant alpha-lactalbumin, a whey protein, and is currently negotiating several development and commercialization agreements.
- The Company is undergoing a beta-lactoglobulin animal-free recombinant whey protein project, expected to begin sampling in the late third quarter.
- The Company is undergoing a recombinant lactoferrin project, expected to begin sampling the product in the late second or early third quarter.
Bio Industrial Products
- The Company has developed three enzymes, with plans for two additional enzymes, that have the potential for use in multiple industries, such as dairy, nutrition, biogas, biofuels and biorefining. Several initial targets are under evaluation with interested parties.
Financial Highlights
Cash Position: As of March 31, 2024, cash, cash equivalents, and the carrying value of investment-grade securities, including accrued interest, were approximately
Revenue: Research and development revenue and license revenue for the three months ended March 31, 2024, decreased to approximately
Cost of Revenue: Cost of research and development revenue for the three months ended March 31, 2024, decreased to approximately
R&D Expenses: Research and development expenses for the three months ended March 31, 2024, decreased by
G&A Expenses: General and administrative expenses for the three months ended March 31, 2024, increased by
Loss from Operations: Loss from operations for the three months ended March 31, 2024, slightly increased to
Net Loss: Net loss for the three months ended March 31, 2024, was
Conference Call Information:
Date: Tuesday, May 14, 2024
Time: 5:00 p.m. Eastern Time
Dial-in numbers: Toll Free 877-407-0784 International +1-201-689-8560
Conference ID: 13743568
Webcast link: https://viavid.webcasts.com/starthere.jsp?ei=1650831&tp_key=0f89478e24
An archive of the webcast will be available within 24 hours after completion of the live event and will be accessible on the Investor Relations section of the Company’s website at www.dyadic.com. To access the replay of the webcast, please follow the webcast link above.
About Dyadic International, Inc.
Dyadic International, Inc. is a biotechnology company focused on the efficient large-scale manufacture of proteins for use in human and animal vaccines and therapeutics, as well as non-pharmaceutical applications including food, nutrition, and wellness.
Dyadic’s gene expression and protein production platforms are based on the highly productive and scalable fungus Thermothelomyces heterothallica (formerly Myceliophthora thermophila). Our lead technology, C1-cell protein production platform, is based on an industrially proven microorganism (named C1), which is currently used to speed development, lower production costs, and improve performance of biologic vaccines and drugs at flexible commercial scales for the human and animal health markets. Dyadic has also developed the Dapibus™ filamentous fungal based microbial protein production platform to enable the rapid development and large-scale manufacture of low-cost proteins, metabolites, and other biologic products for use in non-pharmaceutical applications, such as food, nutrition, and wellness.
With a passion to enable our partners and collaborators to develop effective preventative and therapeutic treatments in both developed and emerging countries, Dyadic is building an active pipeline by advancing its proprietary microbial platform technologies, including our lead asset DYAI-100 COVID-19 vaccine candidate, as well as other biologic vaccines, antibodies, and other biological products.
To learn more about Dyadic and our commitment to helping bring vaccines and other biologic products to market faster, in greater volumes and at lower cost, please visit http://www.dyadic.com.
Safe Harbor Regarding Forward-Looking Statements
This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act and Section 21E of the Exchange Act, including those regarding Dyadic International’s expectations, intentions, strategies, and beliefs pertaining to future events or future financial performance, such as the success of our clinical trial and interest in our protein production platforms, our research projects and third-party collaborations, as well as the availability of necessary funding. Forward-looking statements generally can be identified by use of the words “expect,” “should,” “intend,” “anticipate,” “will,” “project,” “may,” “might,” “potential,” or “continue” and other similar terms or variations of them or similar terminology. Forward-looking statements involve many risks, uncertainties or other factors beyond Dyadic’s control. These factors include, but are not limited to, the following: (i) our history of net losses; (ii) market and regulatory acceptance of our microbial protein production platforms and other technologies; (iii) competition, including from alternative technologies; (iv) the results of nonclinical studies and clinical trials; (v) our capital needs; (vi) changes in global economic and financial conditions; (vii) our reliance on information technology; (viii) our dependence on third parties; (ix) government regulations and environmental, social and governance issues; and (x) intellectual property risks. For a more complete description of the risks that could cause our actual results to differ from our current expectations, please see the section entitled “Risk Factors” in Dyadic’s annual reports on Form 10-K and quarterly reports on Form 10-Q filed with the SEC, as such factors may be updated from time to time in Dyadic’s periodic filings with the SEC, which are accessible on the SEC’s website and at www.dyadic.com. All forward-looking statements speak only as of the date made, and except as required by applicable law, Dyadic assumes no obligation to publicly update any such forward-looking statements for any reason after the date of this press release to conform these statements to actual results or to changes in our expectations.
Contact:
Dyadic International, Inc.
Ping W. Rawson, Chief Financial Officer
Phone: 561-743-8333 Email: ir@dyadic.com
| DYADIC INTERNATIONAL, INC. AND SUBSIDIARIES CONSOLIDATED STATEMENTS OF OPERATIONS | |||||||
| Three Months Ended March 31, | |||||||
| 2024 | 2023 | ||||||
| Revenues: | |||||||
| Research and development revenue | $ | 334,617 | $ | 933,934 | |||
| License revenue | — | 44,118 | |||||
| Total revenue | 334,617 | 978,052 | |||||
| Costs and expenses: | |||||||
| Costs of research and development revenue | 143,955 | 726,918 | |||||
| Research and development | 522,723 | 810,566 | |||||
| General and administrative | 1,788,594 | 1,480,040 | |||||
| Foreign currency exchange loss | 4,903 | 11,022 | |||||
| Total costs and expenses | 2,460,175 | 3,028,546 | |||||
| Loss from operations | (2,125,558 | ) | (2,050,494 | ) | |||
| Other income (expense): | |||||||
| Interest income | 87,443 | 104,731 | |||||
| Gain on sale of Alphazyme | 60,977 | 989,319 | |||||
| Interest expense | (21,639 | ) | — | ||||
| Interest expense-related party | (10,819 | ) | — | ||||
| Total other income (expense), net | 115,962 | 1,094,050 | |||||
| Net loss | $ | (2,009,596 | ) | $ | (956,444 | ) | |
| Basic and diluted net loss per common share | $ | (0.07 | ) | $ | (0.03 | ) | |
| Basic and diluted weighted-average common shares outstanding | 28,828,282 | 28,761,469 | |||||
See Notes to Consolidated Financial Statements in Item 1 of Dyadic’s Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission on May 14, 2024.
| DYADIC INTERNATIONAL, INC. AND SUBSIDIARIES CONSOLIDATED BALANCE SHEETS | |||||||
| March 31, 2024 | December 31, 2023 | ||||||
| (Unaudited) | (Audited) | ||||||
| Assets | |||||||
| Current assets: | |||||||
| Cash and cash equivalents | $ | 10,569,814 | $ | 6,515,028 | |||
| Short-term investment securities | 1,468,002 | 748,290 | |||||
| Interest receivable | 15,227 | 10,083 | |||||
| Accounts receivable | 246,138 | 466,159 | |||||
| Prepaid expenses and other current assets | 242,131 | 327,775 | |||||
| Total current assets | 12,541,312 | 8,067,335 | |||||
| Non-current assets: | |||||||
| Operating lease right-of-use asset, net | 129,519 | 141,439 | |||||
| Other assets | 10,435 | 10,462 | |||||
| Total assets | $ | 12,681,266 | $ | 8,219,236 | |||
| Liabilities and stockholders’ equity | |||||||
| Current liabilities: | |||||||
| Accounts payable | $ | 661,243 | $ | 656,445 | |||
| Accrued expenses | 987,973 | 1,057,164 | |||||
| Deferred research and development obligations | 534,018 | 490,113 | |||||
| Operating lease liability, current portion | 49,551 | 48,059 | |||||
| Accrued interest | 19,556 | — | |||||
| Accrued interest -related party | 9,778 | — | |||||
| Total current liabilities | 2,262,119 | 2,251,781 | |||||
| Non-current liabilities: | |||||||
| Convertible notes, net of issuance costs | 3,884,967 | — | |||||
| Convertible notes, net of issuance costs -related party | 1,942,484 | — | |||||
| Operating lease liability, net of current portion | 75,894 | 88,870 | |||||
| Total liabilities | 8,165,464 | 2,340,651 | |||||
| Commitments and contingencies (Note 5) | |||||||
| Stockholders’ equity: | |||||||
| Preferred stock, $.0001 par value: | |||||||
| Authorized shares - 5,000,000; none issued and outstanding | — | — | |||||
| Common stock, $.001 par value: | |||||||
| Authorized shares - 100,000,000; issued shares - 41,440,316 and 41,064,563, outstanding shares - 29,186,814 and 28,811,061 as of March 31, 2024, and December 31, 2023, respectively | 41,441 | 41,065 | |||||
| Additional paid-in capital | 105,691,193 | 105,044,756 | |||||
| Treasury stock, shares held at cost - 12,253,502 | (18,929,915 | ) | (18,929,915 | ) | |||
| Accumulated deficit | (82,286,917 | ) | (80,277,321 | ) | |||
| Total stockholders’ equity | 4,515,802 | 5,878,585 | |||||
| Total liabilities and stockholders’ equity | $ | 12,681,266 | $ | 8,219,236 | |||
See Notes to Consolidated Financial Statements in Item 1 of Dyadic’s Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission on May 14, 2024.
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