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Johnson & Johnson Says FDA Grants Priority Review To Subcutaneous Amivantamab For Recurrent Or Metastatic Head And Neck Cancer, Citing 42% Overall Response Rate In OrigAMI-4 Study

Jul 30, 2026 · 08:39 AM ET· updated 2h ago

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Why It Matters

Johnson & Johnson's new cancer medicine got fast-track approval from health officials because it helped 42% of patients with serious head and neck cancer. When a company gets this kind of speed-up, it shows their medicine might work well, which investors watch as a sign the company could grow.

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Source: Benzinga · Read the original report at the publisher. Headline and figures shown for context; data may be delayed.

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