Therapeutic Response

FLT3 p.D835H status confers therapeutic sensitivity to Gilteritinib in patients with Acute Lymphoid Leukemia.

Statements

Source and description
Xospata (gilteritinib) [package insert]. FDA. The U.S. Food and Drug Administration granted approval to gilteritinib for the treatment of adult patients with relapsed or refractory acute myeloid leukemia (AML) with a FLT3 mutation, as detected by an FDA-approved test.