COCP

Cocrystal Pharma, Inc.
4 filings tracked
healthcarebiotechnologySMALL ($300M-2B)

Signal Magnitude Chart

BULLISH | 70% | 3/31/2026 | margin expansionBEARISH | 80% | 3/31/2026 | dilution riskNEUTRAL | 50% | 3/31/2026 | regulatory actionBULLISH | 40% | 3/31/2026 | capital raiseBULLISH | 80% | 5/15/2026 | regulatory actionBEARISH | 90% | 5/15/2026 | capital raiseBEARISH | 60% | 5/15/2026 | margin compressionBULLISH | 80% | 5/15/2026 | regulatory actionBEARISH | 90% | 5/15/2026 | capital raiseBEARISH | 60% | 5/15/2026 | margin compressionNEUTRAL | 30% | 5/26/2026 | management changeBEARISH | 60% | 5/26/2026 | capital raiseMar 26May 26HIGHLOW
bullish
bearish
neutral

Signal Timeline

neutralMay 26

Strategic update on antiviral pipeline issued by management.

management change
30%
bearishMay 26

Potential for dilution as company seeks partnerships to fund burn.

capital raise
60%
bullishMay 15

FDA granted Fast Track designation to lead candidate CDI-988.

regulatory action
80%
bearishMay 15

Company reports substantial doubt about ability to continue as a going concern due to low cash.

capital raise
90%
bearishMay 15

G&A expenses increased due to legal fees associated with CRO arbitration.

margin compression
60%
bullishMay 15

FDA granted Fast Track designation to lead candidate CDI-988.

regulatory action
80%
bearishMay 15

Company reports substantial doubt about ability to continue as a going concern due to low cash.

capital raise
90%
bearishMay 15

G&A expenses increased due to legal fees associated with CRO arbitration.

margin compression
60%
bullishMar 31

Net loss reduced by 50% through aggressive R&D and G&A cost cutting.

margin expansion
70%
bearishMar 31

Significant warrant overhang and history of ATM sales to fund operations.

dilution risk
80%
neutralMar 31

Commencement of Phase 1b human challenge study for CDI-988.

regulatory action
50%
bullishMar 31

Recent direct offering and private placement provided $5.2 million in liquidity.

capital raise
40%

Filing History

8-KMay 26, 2026

The May 26 filing serves as a strategic signal regarding Cocrystal's antiviral pipeline, though it leaves investors weighing promotional optimism against a lack of hard data. While the company claims to be de-risking its development pathway through novel mechanisms of action, the market remains cautious due to the absence of disclosed Phase I results. The ultimate impact of this filing will depend on whether the company can convert these 'strategic optionality triggers' into tangible partnerships or clinical wins before its cash runway necessitates further capital raises.

10-QMay 15, 2026

The latest 10-Q presents a stark dichotomy between clinical potential and financial instability. On one hand, the FDA's Fast Track designation for CDI-988 provides a clear regulatory pathway and addresses a massive unmet medical need, positioning the company as a potential acquisition target if the Phase 1b data is positive. The ability to secure NIH funding further suggests that the underlying science remains attractive to institutional bodies. However, the immediate reality is a liquidity crisis. The company is operating on a razor-thin margin of error, where any delay in clinical readouts or failure to secure immediate financing could lead to a cessation of operations. Investors are essentially weighing a high-risk binary event: the potential for a blockbuster antiviral breakthrough against the very real possibility of corporate insolvency. The outcome of the Emory University challenge study will likely determine if Cocrystal survives to see its candidates reach the market.

10-KMar 31, 2026

The 10-K filing reveals a company at a crossroads, balancing cutting-edge structural biology against a critical lack of capital. While the operational lean-out is a positive signal for management's ability to extend the runway, the fundamental risk remains the binary nature of its clinical pipeline. The shift in focus toward CDI-988 and the use of human challenge models are attempts to compress the time to value, but these efforts are happening against a backdrop of severe financial distress. For investors, the trade-off is clear: the potential for a breakthrough in the norovirus market versus the very real possibility of a liquidity crisis. The outcome of the Phase 1b study at Emory University will likely determine the company's survival. Until then, the stock remains a highly speculative venture, where the scientific pedigree of the leadership is the only counterbalance to a balance sheet that suggests a precarious future.