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J&J goes after another FDA approval for a cancer bispecific

December 30, 2021


The latest to reach the regulatory stage is teclistamab, one of two bispecifics for multiple myeloma in the late-stage pipeline of J&J’s Janssen division stemming from its longstanding and fertile collaboration with Danish biotech Genmab.

That alliance also generated Darzalex (daratumumab) – Janssen’s $4.1 billion myeloma blockbuster – as well as Rybrevant (amivantamab), its first bispecific which has been approved to treat EGFR-mutated non-small cell lung cancer (NSCLC).

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