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Oncolytic virotherapy stories

Jul 31, 2026

FDA Advisory Committee Votes 10-3 in Favor of Replimune's RP1 Efficacy Data from Ignyte Study

The FDA's Cellular, Tissue, and Gene Therapies Advisory Committee determined that efficacy data from Replimune's Ignyte study for RP1 is evaluable and clinically meaningful, voting 10 to 3 in favor.

Jul 31, 2026·1 source
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Top claims

  • ▪Replimune's stock surged over 120%, nearly doubling, following the FDA advisory committee's favorable vote on the Ignyte study results on July 30, 2026
  • ▪RP1, or vusolimogene oderparepvec, is Replimune's lead product candidate built on a proprietary strain of herpes simplex virus
  • ▪RP1 is genetically engineered and armed with a fusogenic protein, GALV-GP R-, and GM-CSF to maximize tumor killing potency and activate a systemic anti-tumor immune response

Subtopics

Cancer immunotherapy1Cancer treatment breakthroughs1Drug Approval and Clinical Trials1

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