• The enrollment milestone represents a crucial step forward for the FLASH2 study, which builds upon the previous statistically significant Phase 3 FLASH study.
• The promising early results are further corroborated by an ongoing investigator-initiated study being conducted at the University of Pennsylvania.
• Soligenix is positioning itself to potentially deliver the first FDA-approved photodynamic therapy specifically indicated for CTCL.

In a pivotal advancement for patients suffering from a rare form of skin cancer, Soligenix (NASDAQ: SNGX) has achieved a critical clinical trial milestone that brings its investigational treatment significantly closer to potential FDA approval. The company announced that is has completed the planned enrollment of 50 patients necessary for the interim analysis in its 80-patient confirmatory Phase 3 clinical trial evaluating HyBryte(TM) (synthetic hypericin) for the treatment of cutaneous T-cell lymphoma (https://ibn.fm/ZeQoN).

The enrollment milestone represents a crucial step forward for the FLASH2 study, a randomized, double-blind, placebo-controlled clinical trial that builds upon the previous statistically significant Phase 3 FLASH study. What makes this announcement particularly noteworthy is not merely that the company has…

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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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