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Top News In Global Product Development At Genentech Today - Breaking & Trending Today

FDA Accepts Biologics License Application for Crovalimab for Paroxysmal Nocturnal Hemoglobinuria

Crovalimab achieved disease control and non-inferiority compared to eculizumab, which is the current standard-of-care for individuals with paroxysmal nocturnal hemoglobinuria. ....

Levi Garraway , Global Product Development At Genentech , European Hematology Association , Global Product Development ,

Tecentriq Indication for Previously Untreated Advanced Bladder Cancer Withdrawn

Genentech has voluntarily withdrawn the US indication for Tecentriq (atezolizumab) for previously untreated urothelial carcinoma. ....

Levi Garraway , Approval Program , Drug Administration , Global Product Development At Genentech , Global Product Development ,