Learn languages naturally with fresh, real content!

Popular Topics
Explore By Region
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.
6 Articles
La FDA acepta la revisión prioritaria del tratamiento con melanoma RP1 de Reclimune, utilizado con Nivolumab.