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FDA, Tudriqev and Replimune

FDA approves Replimune's Tudriqev melanoma drug on third try

The agency had twice rejected the engineered viral therapy over concerns about the design of Replimune's clinical trial

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· 9h · on MSN

Replimune wins FDA skin cancer drug approval on third try. Why the stock is tumbling.

Fierce Pharma · 1d

UPDATED: Replimune secures FDA approval for melanoma therapy Tudriqev after long regulatory battle

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REPL Stock Slumps 11% After-Hours — What’s Driving The Selloff?

Replimune said the U.S. Food and Drug Administration granted accelerated approval for TUDRIQEV, previously known as RP1, in ...

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Replimune Announces FDA Accelerated Approval of TUDRIQEVTM in Combination with Nivolumab for Unresectable Advanced Cutaneous Melanoma After Progression on an anti-PD-1 Based ...

Broad label to address high unmet need in advanced melanomaReplimune will host conference call on August 6, 2026 at 4:30 p.m. ET. WOBURN, ...

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