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Early Tecentriq OK Gives Roche/Genentech Jump On PD-L1 Bladder Cancer Market

 
• By Donna Young

By granting an approval four months ahead of schedule of Roche AG's and Genentech Inc.'s anti-PD-LI cancer immunotherapy Tecentriq (atezolizumab), the FDA may have helped the companies secure a better lead in the bladder cancer marketplace than the firms otherwise would have held. But already established immunotherapies, Merck & Co. Inc.'s Keytruda (pembrolizumab) and Bristol-Myer Squibb Co.'s Opdivo (nivolumab), are in hot pursuit.

Roche AG and its US unit Genentech Inc. on May 18 gained an earlier-than-expected approval of Tecentriq (atezolizumab), the first and only anti-PD-L1 cancer immunotherapy approved by the FDA for locally advanced or metastatic urothelial carcinoma (mUC), the most common form of bladder cancer.

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