FDA approves Hedgehog pathway inhibitor for AML
The US Food and Drug Administration Wednesday approved Daurismo (glasdegib) tablets to be used in combination with low-dose cytarabine (LDAC), a type of chemotherapy, for the treatment of newly-diagnosed acute myeloid leukemia (AML) in adults who are 75 years of age or older or who have other chronic health conditions or diseases (co-morbidities) that may preclude the use of intensive chemotherapy.
US pharma giant Pfizer’s INSE: PFE) Daurismo is claimed to be the first and only FDA-approved Hedgehog pathway inhibitor for AML.
“As our second medicine approved in the last 14 months for patients with acute myeloid leukemia, Daurismo reinforces our commitment to delivering new medicines to patients living with some of the most difficult-to-treat cancers, especially those for which there are limited treatment options available, commented Andy Schmeltz, global president Pfizer Oncology.
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