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ZIIHERA® (Zanidatamab-hrii)

December 8, 2024December 8, 2024 RR FDA Approvals
Bile Duct Cancer

The FDA on November 20, 2024, granted accelerated approval to ZIIHERA®, a bispecific HER2-directed antibody, for previously treated, unresectable or metastatic HER2-positive (IHC 3+) biliary tract cancer (BTC), as detected by an FDA-approved test. ZIIHERA® is a product of Jazz Pharmaceuticals, Inc.

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