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FDA Approves Amgen and Allergan’s Kanjinti, a Biosimilar to Herceptin

10:04 EDT 14 Jun 2019 | Speciality Pharma Journal

THOUSAND OAKS, Calif., June 13, 2019 /PRNewswire/ — Amgen (NASDAQ:AMGN) and Allergan plc (NYSE:AGN) today announced that the U.S. Food and Drug Administration (FDA) has approved KANJINTI™ (trastuzumab-anns) for all approved indications of the reference product, Herceptin® (trastuzumab):  for the treatment of HER2-overexpressing adjuvant and metastatic breast cancer and HER2-overexpressing metastatic gastric or gastroesophageal junction adenocarcinoma. “The FDA approval of KANJINTI is an important milestone for our …

Original Article: FDA Approves Amgen and Allergan’s Kanjinti, a Biosimilar to Herceptin

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