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Bristol’s Opdivo Joins Keytruda, Imfinzi In Perioperative NSCLC Treatment Space

 
• By Joseph Haas

PD-1 inhibitor Opdivo has obtained US FDA approval for pre- and post-surgical treatment in operable non-small cell lung cancer, but Merck and AstraZeneca got there first.

Bristol Myers Squibb office building in Brisbane, CA
BMS's Opdivo gets approval for perioperative therapy in resectable NSCLC • Source: Shutterstock

Bristol Myers Squibb Company has racked up another indication for its anti-PD-1 blockbuster Opdivo (nivolumab), joining Merck & Co., Inc.’s PD-1 inhibitor, Keytruda (pembrolizumab), and AstraZeneca PLC’s PD-L1 inhibitor, Imfinzi (durvalumab), with an approval for perioperative combination therapy in resectable non-small cell lung cancer on 4 October.

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Pipeline Watch: Eight Approvals And Three Phase III Readouts

Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.

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• By Sushmita Panda

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• By Neena Brizmohun

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Genentech To Try Repertoire’s Immune Synapse Technology In Autoimmune Disease

 
• By Joseph Haas

Deal snapshot: The Flagship portfolio firm will use its Decode platform to seek novel targets for an unspecified autoimmune disease, with Genentech holding license rights.

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• By Andrew McConaghie

The Swiss biotech firm could go public on the NASDAQ later this year, and points to other preclinical dealmaking in the space to back its strategy.