Replimune Group, Inc.
PDUFA AI-extracted
RP1 (vusolimogene oderparepvec)
advanced melanoma
Resolved
102days ago
FDA decision Β· Mar 27, 2026
What's at stake The FDA's approval decision on RP1 (vusolimogene oderparepvec) for advanced melanoma is due Mar 27, 2026. A green light opens the market; a complete response letter (CRL) usually sinks the stock.
β€œthe FDA has set a PDUFA action date of March 27, 2026”

Provenance

2 sources on file.

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