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Norovirus drug CDI-988 to be presented at ICAR2026 by Cocrystal (NASDAQ: COCP)

Filing Impact
(Moderate)
Filing Sentiment
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

Cocrystal Pharma filed a Form 8-K to share a press release about its oral norovirus protease inhibitor CDI-988. Initial progress from a Phase 1b norovirus challenge study will be presented at the 39th International Conference on Antiviral Research (ICAR2026) in Prague.

CDI-988 is described as the first oral antiviral drug candidate under development for prevention and treatment of acute norovirus gastroenteritis and is designed as a pan-viral 3CL protease inhibitor with potential activity against both noroviruses and coronaviruses. The company highlights the lack of approved antiviral therapies or vaccines for norovirus, which causes an estimated 200,000 deaths worldwide each year and significant economic burden, underscoring the potential medical need targeted by this program.

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Insights

Cocrystal is advancing an early-stage oral norovirus drug and showcasing initial Phase 1b data at a major antiviral conference.

Cocrystal Pharma is developing CDI-988, a direct-acting oral protease inhibitor targeting 3CL viral proteases. The program is in Phase 1/1b, with a norovirus challenge study evaluating both prophylactic and therapeutic use for acute norovirus gastroenteritis. Early-stage status means safety and proof-of-concept data are still emerging.

The company positions CDI-988 as a pan-viral candidate with potential applicability to noroviruses and coronaviruses, addressing an area with no approved antivirals or vaccines. That unmet need, along with high global disease and economic burden, frames a sizable theoretical opportunity but depends on successful clinical outcomes and regulatory pathways.

Presenting initial progress at ICAR2026 gives scientific visibility among antiviral experts but does not by itself change commercial prospects. Future data from the ongoing Phase 1b study at Emory University School of Medicine and any subsequent trials will be key to understanding CDI-988’s risk–benefit profile and potential positioning within norovirus and broader antiviral treatment landscapes.

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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

 

Pursuant to Section 13 or 15(d) of The Securities Exchange Act of 1934

 

Date of Report (Date of earliest event reported): February 19, 2026

 

Cocrystal Pharma, Inc.

(Exact name of registrant as specified in its charter)

 

Delaware   001-38418   35-2528215

(State or other Jurisdiction

of Incorporation)

 

(Commission

File Number)

 

(IRS Employer

Identification No.)

 

19805 N. Creek Parkway

Bothell, WA

  98011
(Address of principal executive offices)   (Zip Code)

 

Registrant’s telephone number, including area code: (877) 262-7123

 

(Former name or former address, if changed since last report.): n/a

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

 

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
   
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
   
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
   
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

 

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (17 CFR §230.405) or Rule 12b-2 of the Securities Exchange Act of 1934 (17 CFR §240.12b-2).

 

Emerging growth company

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

 

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

 

Title of Each Class   Trading Symbol(s)   Name of each exchange on which registered
Common Stock   COCP   The Nasdaq Stock Market, LLC
(The Nasdaq Capital Market)

 

 

 

 
 

 

Item 7.01 Regulation FD Disclosure.

 

On February 19, 2026, Cocrystal Pharma, Inc. (the “Company”) issued a press release announcing the Company’s first oral norovirus protease inhibitor CDI-988 to be featured at the International Society for Antiviral Research Conference (ICAR) 2026 being held April 27–May 1, 2026 in Prague, Czech Republic. A copy of the press release is furnished as Exhibit 99.1.

 

The information in this Item 7.01 (including Exhibit 99.1) shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934 (the “Exchange Act”) or otherwise subject to the liabilities under such section, and shall not be deemed to be incorporated by reference into any filing of the Company under the Securities Act of 1933 or the Exchange Act.

 

Item 9.01 Financial Statements and Exhibits.

 

(d) Exhibits

 

Exhibit   Description
99.1   Press Release dated February 19, 2026
104   Cover Page Interactive Data File (embedded within the Inline XBRL document)

 

 
 

 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

  Cocrystal Pharma, Inc.
     
Date: February 19, 2026 By: /s/ James Martin
  Name: James Martin
  Title: Co-Chief Executive Officer and Chief Financial Officer

 

 

 

Exhibit 99.1

 

 

Cocrystal Pharma’s First Oral Norovirus Protease Inhibitor CDI-988 to be Featured at the International Society for Antiviral Research Conference (ICAR) 2026

 

CDI-988 is the first oral antiviral drug candidate being developed for prevention and treatment of norovirus infections
  
Company to present Phase 1 data and updates from ongoing Phase 1b study conducted at Emory University School of Medicine
  
No approved antiviral therapies or vaccines for norovirus infections demonstrate an immediate market need

 

BOTHELL, Wash. (February 19, 2026) – Cocrystal Pharma, Inc. (Nasdaq: COCP) (“Cocrystal” or the “Company”) announces that initial progress of a norovirus challenge study with its direct-acting, oral protease inhibitor CDI-988 will be presented at the 39th International Conference on Antiviral Research (ICAR2026), being held April 27–May 1 in Prague, Czech Republic. CDI-988 is the first oral antiviral drug candidate under development for the prevention and treatment of acute norovirus gastroenteritis.

 

Sam Lee, Ph.D., Cocrystal President and co-CEO, will discuss the ongoing Phase 1b challenge study evaluating CDI-988 as both a potential prophylactic and therapeutic option for norovirus infection. CDI-988 was designed and developed using the Company’s proprietary structure-based drug discovery platform technology as a pan-viral protease inhibitor, targeting 3CL viral proteases. Based on its novel mechanism of action and superior broad-spectrum antiviral activity, CDI-988 represents a potential oral treatment for both noroviruses and coronaviruses.

 

“ICAR is widely regarded as the premier international conference for antiviral research, and it is a privilege to be selected to present our work to this antiviral research community,” said Dr. Lee. “We are excited to further advance CDI-988 into a Phase 1b norovirus challenge study at Emory University School of Medicine. CDI-988 is our first pan-viral protease inhibitor developed for the treatment of acute norovirus gastroenteritis and also represents a significant step toward a potential treatment for patients suffering from chronic norovirus infection.”

 

About ICAR2026

 

The International Society for Antiviral Research (ISAR) is an internationally recognized organization of scientists working across the basic, applied, translational and clinical aspects of antiviral research. The annual International Conference on Antiviral Research (ICAR), the Society’s main event, brings together virologists, chemists, clinicians, pharmacologists, biologists and regulatory representatives focused on antiviral agents and therapies. Topics include novel and broad-spectrum antivirals, host-targeted approaches, vaccines, pandemic preparedness and emerging or re-emerging viral threats, with a strong emphasis on interdisciplinary collaboration among academia, industry, government and non-profit organizations.

 

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About Norovirus

 

Norovirus is a common and highly contagious virus that afflicts people of all ages and causes symptoms of acute gastroenteritis including nausea, vomiting, stomach pain and diarrhea, as well as fatigue, fever and dehydration. This infection spreads rapidly in semi-closed and crowded settings such as hospitals, nursing homes, cruise ships, schools, disaster-relief shelters and military facilities, where close contact makes outbreaks especially difficult to control. Norovirus causes an estimated 200,000 deaths worldwide each year at a societal cost of approximately $60 billion. In the U.S., norovirus is responsible for about 21 million cases of acute gastroenteritis annually, including 109,000 hospitalizations, 465,000 emergency department visits and nearly 900 deaths, with an estimated annual economic burden of $10.6 billion.

 

About Cocrystal Pharma, Inc.

 

Cocrystal Pharma, Inc. is a clinical-stage biotechnology company discovering and developing novel antiviral therapeutics that target the replication process of influenza viruses, coronaviruses (including SARS-CoV-2), noroviruses and hepatitis C viruses. Cocrystal employs unique structure-based technologies to create viable antiviral drugs. For further information about Cocrystal, please visit www.cocrystalpharma.com.

 

Cautionary Note Regarding Forward-Looking Statements

 

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding the potential of CDI-988 as an oral treatment for both norovirus and coronavirus infections. The words “believe,” “may,” “estimate,” “continue,” “anticipate,” “intend,” “should,” “plan,” “could,” “target,” “potential,” “is likely,” “will,” “expect” and similar expressions, as they relate to us, are intended to identify forward-looking statements. We have based these forward-looking statements largely on our current expectations and projections about future events. Some or all of the events anticipated by these forward-looking statements may not occur. Important factors that could cause actual results to differ from those in the forward-looking statements include, but are not limited to, the risks and uncertainties arising from inflation, affordability, the possibility of a recession, the impact of future interest rate changes on the economy, tariffs and the resulting litigation, and geopolitical conflicts including those in Ukraine, Latin America and Middle East on our Company, our collaboration partners, and on the U.S. and global economies, including manufacturing and research delays arising from raw materials and labor shortages, supply chain disruptions and other business interruptions including any adverse impacts on our ability to obtain raw materials for and otherwise proceed with the planned norovirus study or subsequent studies as well as similar problems with our vendors and our current and any future clinical research organizations (CROs) and contract manufacturing organizations (CMOs), the progress and results of the studies including any adverse findings or delays, the ability of us and our CROs to recruit volunteers for, and to otherwise proceed with, clinical studies, our and our collaboration partners’ technology and software performing as expected, financial difficulties experienced by certain partners, the results of any current and future preclinical and clinical studies, general risks arising from clinical studies, receipt of regulatory approvals, regulatory changes and any adverse developments which may arise therefrom, potential mutations in a virus we are targeting that may result in variants that are resistant to a product candidate we develop, the potential for the development of effective treatments by competitors which could reduce or eliminate a prospective future market share commercializing any product candidates we may develop in the future, and our ability to meet our future liquidity needs. Further information on our risk factors is contained in our filings with the SEC, including the “Risk Factors” in Item 1A of our Annual Report on Form 10-K for the year ended December 31, 2024 and the Prospectus dated September 25, 2025. Any forward-looking statement made by us herein speaks only as of the date on which it is made. Factors or events that could cause our actual results to differ may emerge from time to time, and it is not possible for us to predict all of them. We undertake no obligation to publicly update any forward-looking statement, whether as a result of new information, future developments or otherwise, except as may be required by law.

 

Contact:

 

Alliance Advisors IR

Jody Cain

310-691-7100

jcain@allianceadvisors.com

 

# # #

 

2

FAQ

What did Cocrystal Pharma (COCP) disclose about CDI-988 in this 8-K?

Cocrystal Pharma disclosed that its oral norovirus protease inhibitor CDI-988 will have initial progress from a Phase 1b challenge study presented at ICAR2026 in Prague, highlighting its development as a potential prophylactic and therapeutic option for acute norovirus gastroenteritis.

What is CDI-988 in Cocrystal Pharma’s antiviral pipeline?

CDI-988 is Cocrystal Pharma’s first oral antiviral drug candidate under development for preventing and treating acute norovirus gastroenteritis. It is a direct-acting pan-viral 3CL protease inhibitor, designed using the company’s structure-based drug discovery platform and positioned for potential activity against noroviruses and coronaviruses.

Why is Cocrystal’s CDI-988 targeting norovirus considered important?

Norovirus currently has no approved antiviral therapies or vaccines, yet causes an estimated 200,000 deaths worldwide each year and about 21 million U.S. cases annually. Cocrystal’s CDI-988 targets this large unmet need, aiming to provide both prevention and treatment for acute norovirus gastroenteritis.

What clinical data on CDI-988 will be presented at ICAR2026?

Cocrystal plans to present Phase 1 data and updates from an ongoing Phase 1b norovirus challenge study of CDI-988 at ICAR2026. The study, conducted at Emory University School of Medicine, evaluates CDI-988 as a potential prophylactic and therapeutic option for norovirus infection in humans.

How does CDI-988 fit into Cocrystal Pharma’s broader antiviral strategy?

CDI-988 extends Cocrystal’s focus on structure-based antiviral discovery, targeting viral replication in influenza, coronaviruses, noroviruses and hepatitis C. As a pan-viral 3CL protease inhibitor, it aligns with the company’s strategy to develop broad-spectrum antivirals that may address multiple high-burden viral infections.

What market opportunity does Cocrystal see for CDI-988 against norovirus?

Cocrystal highlights norovirus’s significant global burden, including about 200,000 deaths and an estimated worldwide societal cost of $60 billion annually. In the U.S., it notes 21 million cases and $10.6 billion yearly economic burden, indicating a potentially large market if CDI-988 proves safe and effective.

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