Developers of the top-selling checkpoint inhibitor therapies for cancer are competing to bring the first subcutaneous formulation to market and Genentech, Inc. announced a major step in that goal on 2 August, revealing that a pivotal study testing a subcutaneous formulation of its anti-PD-L1 therapy Tecentriq (atezolizumab) versus the current intravenous formula met the primary endpoints.
The Roche Holding AG subsidiary did not provide any numerical data from the Phase Ib/III IMscin001 trial, but said...







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