Glasdegib plus intensive/nonintensive chemotherapy in untreated acute myeloid leukemia: BRIGHT AML 1019 Phase III trials

Author:

Cortes Jorge E1,Dombret Hervé2,Merchant Akil3,Tauchi Tetsuzo4,DiRienzo Christine G5,Sleight Barbara5,Zhang Xiaoxi5,Leip Eric P5,Shaik Naveed5,Bell Timothy5,Chan Geoffrey5,Sekeres Mikkael A6

Affiliation:

1. Georgia Cancer Center, Augusta University, Augusta, GA 30912, USA.

2. Institut de Recherche Saint-Louis, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris Institut Universitaire d`Hematologie Hopital Saint Louis, Paris, France

3. Department of Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA

4. Department of Hematology, Shin-Yurigaoka General Hospital, Kawasaki, Japan

5. Pfizer Oncology, Pfizer Inc., New York, NY 10017, USA

6. Leukemia Program, Cleveland Clinic, Cleveland, OH 44195, USA

Abstract

Glasdegib, an oral Hedgehog pathway inhibitor, has been associated with significantly improved survival when combined with low-dose cytarabine in patients with untreated acute myeloid leukemia (AML) who were unsuitable for intensive chemotherapy, when compared with low-dose cytarabine alone. BRIGHT AML 1019 (NCT03416179) comprises two independently powered Phase III, randomized (1:1), double-blind global trials evaluating oral glasdegib 100 mg once daily or placebo plus one of two standard chemotherapy regimens in adults with untreated AML. The intensive trial combines glasdegib/placebo with cytarabine and daunorubicin (7 + 3), while the nonintensive trial combines glasdegib/placebo with azacitidine. The primary end point of both studies is overall survival. Secondary end points include response, time to and duration of response, event-free survival, safety, patient-reported outcomes and pharmacokinetics. Trial registration number: ClinicalTrials.gov identifier: NCT03416179

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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