drugset / Trial / NCT01757535

Efficacy of Oral Azacitidine Plus Best Supportive Care as Maintenance Therapy in Subjects With Acute Myeloid Leukemia (AML) in Complete Remission

NCT01757535 ↗

Phase 3 Completed 472 enrolled Celgene Corporation
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study enrolled 472 participants, aged 55 or older, with a diagnosis of de novo acute myeloid leukemia (AML) or AML secondary to prior myelodysplastic disease or chronic myelomonocytic leukemia (CMML), and who have achieved first complete remission (CR)/ complete remission with incomplete blood count recovery (CRi) following induction with or without consolidation chemotherapy. The study is amended to include an extension phase (EP). The EP allows participants who are currently receiving oral azacitidine and who are demonstrating clinical benefit as assessed by the investigator, to continue receiving oral azacitidine after unblinding by sponsor until the participant meets the criteria for study discontinuation or until oral azacitidine becomes commercially available and reimbursed. In addition, all participants in the placebo arm and participants who had been discontinued from the treatment phase (irrespective of randomization arm) and continuing in the follow-up phase will be followed for survival in the EP.

Timeline

Start
2013-04-24
Primary completion
2019-07-15
Completion
2024-06-18

Outcome

Met primary endpoint

registry analysis (superiority test); Oral Azacitidine Plus Best Supportive Care vs Placebo Plus Best Supportive Care; p = 0.0009; Hazard Ratio (HR) 0.69 NCT01757535 ↗

paper Median overall survival from the time of randomization was significantly longer with CC-486 than with placebo (24.7 months and 14.8 months, respectively; P<0.001). PMID 33369355 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Azacitidine Other / unclassified 300 mg Oral