Soligenix announces second quarter 2026 financial results and pipeline updates
Net loss narrowed to $2.0 million, with $9.8 million cash. The company discontinued its HyBryte program and continues advancing SGX945 and ThermoVax.
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Late-stage biopharmaceutical company for rare diseases
soligenix.comLast updated
In short: Soligenix terminated its HyBryte Phase 3 trial for lymphoma due to futility and shifted focus to its pipeline and vaccine platform.
Net loss narrowed to $2.0 million, with $9.8 million cash. The company discontinued its HyBryte program and continues advancing SGX945 and ThermoVax.
The company plans to submit an application to CEPI by June 12, 2026, leveraging its ThermoVax platform and prior filovirus vaccine data.
The platform could enable rapid development of a thermostable subunit vaccine for the ongoing Ebola outbreak in Congo.
Net loss was $2.8 million; cash $6.0 million; FLASH2 trial halted for futility; strategic options including M&A to be evaluated.
Soligenix has terminated the late-stage development programme for its topical cutaneous T-cell lymphoma (CTCL) therapy, HyBryte, after the drug failed to show early signs of...
Soligenix, Inc. (Nasdaq: SNGX) (Soligenix or the Company), a biopharmaceutical company focused on developing and commercializing products to treat rare diseases where there is an...
Soligenix ( (SNGX)) has shared an announcement. On June 26, 2026, Soligenix, Inc. increased the maximum aggregate amount of common stock it may issue under...
The score is primarily constrained by weak financial performance (no revenue, persistent net losses, and significant cash burn) despite improved leverage. Technicals also remain negative...
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