Biotech News

Replimune Announces FDA Acceptance of BLA Resubmission of RP1 for the Treatment of Advanced Melanoma

Replimune Group (REPL)Replimune Group2026-06-25 13:46 ESTFDA / regulatory

Prescription Drug User Fee Act (PDUFA) target action date set for April 10, 2026 WOBURN, Mass. , Oct. 20, 2025 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (NASDAQ: REPL), a clinical stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today announced that the

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Replimune Group

Replimune Group is a biopharmaceutical company focused on advancing a pipeline of therapeutic programs. Investors usually track how clinical data, regulatory milestones, and launch execution change the story over time.

Recent company news

REPLReplimune Group2026-06-26 10:48 EST

Replimune Presents Final First-in-Human Data for RP2 in Advanced Solid Tumors During Oral Presentation at the 2026 American Society of Clinical Oncology Annual Meeting

REPLReplimune Group2026-06-26 10:48 EST

Replimune Presents 3-Year Landmark Overall Survival Analysis from IGNYTE Clinical Trial During Oral Presentation at the 2026 American Society of Clinical Oncology Annual Meeting

REPLReplimune Group2026-06-26 10:48 EST

Replimune Announces Planned RP1 BLA Resubmission Following Productive Discussion with FDA

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Replimune Provides Update Following Type A Meeting with FDA

REPLReplimune Group2026-06-26 10:48 EST

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