Soligenix Announces Formation of European Medical Advisory Board for Cutaneous T-Cell Lymphoma

19/11/2024 - 20:30

Phase 3 clinical study of HyBryte™ in CTCL initiating in 2024

PRINCETON, N.J., Nov. 19, 2024 /PRNewswire/ -- Soligenix, Inc. (Nasdaq: SNGX) (Soligenix or the Company), a late-stage biopharmaceutical company focused on developing and commercializing products to treat rare diseases where there is an unmet medical need, announced today the formation of a European Medical Advisory Board (MAB) to provide additional medical/clinical strategic guidance to the Company as it advances its confirmatory Phase 3 multicenter, double-blind, placebo-controlled study evaluating the safety and efficacy of HyBryte™ (synthetic hypericin) in the treatment of cutaneous T-cell lymphoma (CTCL) patients with early-stage disease. This confirmatory, 18-week study is expected to enroll approximately 80 patients in the United States (U.S.) and Europe, and is targeted to begin patient enrollment by the end of 2024 with top-line results anticipated in the second half of 2026.
Soligenix Forms Expert European Board for Phase 3 CTCL Treatment Study | SNGX Stock News