PTX-100 receives US FDA Fast Track Designation for the treatment of adults with R/R mycosis fungoides, the most common subtype of CTCL
Prescient Therapeutics CEO, James McDonnell commented: “Getting Fast-Track designation is a critical milestone towards our goal of advancing PTX-100 into a registration-enabling trial designed to support potential accelerated approval and, from there, commercialisation. As we progress our Phase 2 trials, we will be engaging closely with the FDA to ensure alignment on endpoints and study scope.”
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