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Monday, June 7, 2021

Just how sadly misguided is the FDA on aducanumab? - Endpoints News

Over the past two and a half years, J&J scientists have rolled up their sleeves alongside partners at argenx to get a closer look at the anti-CD70 antibody cusatuzumab, chasing what a top exec considered “an important target in the biology of select cancers,” starting with acute myeloid leukemia.

The pharma giant decided it’s time to call it quits.

Cilag — the Janssen subsidiary in charge of the program — is cutting off the collaboration and returning the worldwide commercial rights to cusatuzumab. With interim Phase Ib data in hand, argenx says it will “evaluate all alternatives to advance” the drug while preparing for the launch of its lead candidate, efgartigimod, currently under FDA review.

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Just how sadly misguided is the FDA on aducanumab? - Endpoints News
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[unable to retrieve full-text content] Regional Bank Stocks Fall After New York Community Bancorp Cuts Dividend, Posts Loss    The Wall St...