The U.S. Food and Drug Administration (FDA) has approved Tecentriq (atezolizumab) in combination with Avastin (bevacizumab) for the treatment of newly diagnosed patients with advanced hepatocellular carcinoma (HCC), the most common form of liver cancer. Genentech, a Roche subsidiary developing Tecentriq, submitted a supplemental biologics license application to the FDA earlier this year requesting approval for this indication. With the new approval, the combination therapy of Tecentriq-Avastin has become the first and only FDA-approved cancer immunotherapy…
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