- The original FLASH study enrolled 169 patients across three treatment cycles.
- The ongoing FLASH 2 trial builds on findings found in the first study while addressing regulatory requirements for confirmatory evidence.
- For Soligenix, the FLASH studies represent more than clinical milestones. These studies are key steps in the company’s regulatory and commercial journey.
Soligenix (NASDAQ: SNGX) is continuing to build momentum in its mission to advance HyBryte(TM), a first-in-class treatment for early-stage cutaneous T-cell lymphoma (“CTCL”). That progress is supported by results from its pivotal FLASH trial and its ongoing FLASH 2 confirmatory study. Together, the studies highlight not only the efficacy of synthetic hypericin activated by safe fluorescent light but also the company’s broader strategy to establish HyBryte as a new standard of care in a field where therapeutic innovation has lagged (https://www.ibn.fm/G18Hp). With statistically significant data already achieved and confirmatory enrollment well underway, Soligenix is taking important steps toward potential regulatory approvals Worldwide.
The original FLASH study, the largest double-blind, randomized, placebo-controlled trial ever conducted in CTCL, enrolled 169 patients across three treatment cycles. Patients receiving HyBryte showed compelling results, with statistically significant improvements observed as early as…
NOTE TO INVESTORS: The latest news and updates relating to SNGX are available in the company’s newsroom at https://ibn.fm/SNGX
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