Amgen wins FDA approval for Kanjinti injection for treatment of breast cancer, gastro-esophageal junction adenocarcinoma

Reuters

13 June 2019 - U.S. FDA says Kanjinti (trastuzumab-anns) is biosimilar to Herceptin (trastuzumab).

U.S. FDA says Kanjinti comes with a boxed warning for cardiomyopathy, infusion reactions, embryo-fetal toxicity, pulmonary toxicity.

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Michael Wonder

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Michael Wonder

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Outcome , Medicine , US , Biosimilar