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Genentech’s Tecentriq Stakes New Claim With FDA Lung Cancer Approval

 
• By Mandy Jackson

Genentech’s PD-L1 inhibitor Tecentriq could steal market share from the PD-1 inhibitors Opdivo and Keytruda in its new indication, but the Roche subsidiary’s drug is a year behind competitors from Bristol-Myers and Merck in NSCLC with seven Phase III trials under way to expand its reach in lung cancer.

US FDA approval for Tecentriq (atezolizumab) as a second-line treatment for non-small cell lung cancer (NSCLC) allows Genentech Inc. to stake its claim in an indication where its predecessors have been approved for a year or more – and where the Roche subsidiary believes it can win market share.

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