Roche Holding AG’s PD-L1 inhibitor Tecentriq (atezolizumab) is losing one of its US Food and Drug Administration approvals as the Swiss drug maker is withdrawing its indication for first-line metastatic urothelial carcinoma. The move is one of multiple setbacks that PD-1 and PD-L1 checkpoint inhibitors have experienced in that setting and leaves Merck & Co., Inc.’s Keytruda (pembrolizumab) as the major player.
Roche’s Genentech division said 28 November that it would voluntarily withdraw the indication for Tecentriq in adults with locally advanced...
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