ARTICLE | Company News
FDA approves Opdivo for bladder cancer
February 2, 2017 11:35 PM UTC
FDA granted accelerated approval to Opdivo nivolumab from Bristol-Myers Squibb Co. (NYSE:BMY) to treat locally advanced or metastatic urothelial carcinoma that has progressed on or after platinum-containing chemotherapy.
Opdivo is the second checkpoint inhibitor to receive FDA approval for the indication. In May, FDA granted accelerated approval to rival PD-L1 inhibitor Tecentriq atezolizumab from the Genentech Inc. unit of Roche (SIX:ROG; OTCQX:RHHBY) (see BioCentury Extra, May 18, 2016)...
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