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Replimune Receives FDA Accelerated Approval For TUDRIQEVTM In Combination With Nivolumab For Treatment Of Adults With Unresectable Advanced Cutaneous Melanoma

BenzingaBenzinga Newsdesk

Replimune Group, Inc. (NASDAQ:REPL), a commercial stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today announced that the U.S. Food and Drug Administration (FDA) has granted

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  1. SEC EDGARSEC EDGAR

    8-K filing — Replimune Group, Inc. (REPL)

    Filed: 2026-08-14 AccNo: 0001104659-26-096483 Size: 266 KB Item 2.02: Results of Operations and Financial Condition Item 9.01: Financial Statements and Exhibits

  2. BenzingaBenzinga Newsdesk

    Replimune Group Q1 EPS $(0.72) Beats $(0.73) Estimate

    Replimune Group (NASDAQ:REPL) reported quarterly losses of $(0.72) per share which beat the analyst consensus estimate of $(0.73) by 1.37 percent. This is a 24.21 percent increase over losses of $(0.95) per share from