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Ideaya Biosciences

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Replimune Tudriqev FDA approval and subsequent legal action

5 clusters · 20 sources · last updated

Latest: Replimune faces lawsuits following TUDRIQEV approval

On 6 August 2026, the FDA granted accelerated approval to Replimune’s oncolytic herpes-virus therapy RP1, marketed as Tudriqev, for use with Bristol Myers Squibb’s Opdivo (nivolumab) in adults with unresectable or metast

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