On Tuesday, July 11, 2017, the Oncologic Drugs Advisory Committee (ODAC) supported, by a vote of 6-Yes to 1-No, with no abstentions, the safety and efficacy of Mylotarg (gemtuzumab ozogamicin) by Wyeth Pharmaceuticals Inc. (Wyeth), a subsidiary of Pfizer Inc., for the treatment of certain patients with acute myeloid leukemia (AML).
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Earlier Event: June 26
Science Board to FDA
Later Event: July 12
Oncologic Drugs Advisory Committee