FDA accepts priority review for Replimune's melanoma treatment RP1, used with Nivolumab.

Replimune Group's application for its melanoma treatment RP1, used with Nivolumab, has been accepted by the FDA for priority review, with a decision expected by July 2025. This follows positive results from the IGNYTE trial and has boosted Replimune's stock by over 25%. The treatment aims to enhance the body's immune response against tumors.

2 months ago
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