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FDA Approves Ado-Trastuzumab emtansine (Kadcyla)

16 May 2019 8:24 AM | Nathan Strunk (Administrator)

The U.S. Food and Drug Administration approved ado-trastuzumab emtansine (Kadcyla; Genentech) for the adjuvant treatment of patients with HER2-positive early breast cancer (EBC) who have residual invasive disease after neoadjuvant taxane and trastuzumab-based treatment. Read full press release. 

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