drugset / Trial / NCT02298166

Study of Crenolanib in Combination With Chemotherapy in Patients With Relapsed or Refractory Acute Myeloid Leukemia and Activating FLT3 Mutations

NCT02298166

Phase 3 Terminated 9 enrolled University of Ulm
RandomizedParallel-groupTriple-blindTreatment

Summary

The main trial is a double-blinded, placebo-controlled, randomized, phase III, multi-center trial in adult patients with relapsed or refractory AML harboring an activating FLT3 mutation as defined in the inclusion /exclusion criteria. An initial open label dose-finding run-in phase I of the study will be performed administering the study drug crenolanib with salvage chemotherapy consisting of mitoxantrone and cytarabine (MC) in 18 patients according to the experimental arm of the study. After completion of this dose-finding run-in phase I, toxicity and response data will be provided to the external Data and Safety Monitoring Board (DSMB) and the Trial Committee by the Coordinating Investigator. The Trial Committee will decide on the basis of these data and the recommendation of the DSMB on dose modification and the further conduct of the study with regard to the double-blinded, placebo-controlled, randomized phase of the study. The double-blinded, placebo-controlled randomized portion will start after the completion of the dose-finding run-in phase I and positive opinion of the Trial Committee. Crenolanib starts on day 7 of MC and is given continuously until 48 hours prior to the next chemotherapy; if receiving allogeneic HCT, crenolanib is held 48 hours prior to conditioning and restarts no sooner than 30 days and not later than day 100 after transplant. Sample size randomized phase: 276 patients Primary objective: To evaluate the impact of crenolanib given in combination with salvage chemotherapy and consolidation including allogeneic hematopoietic cell transplantation and ongoing single agent maintenance therapy with crenolanib on event-free (EFS) and overall survival (OS) in adult patients with relapsed or refractory AML harboring FLT3 activating mutations.

Timeline

Start
2016-11-17
Primary completion
2020-03-09
Completion
2020-03-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Crenolanib Small molecule Oral
Background Cytarabine Small molecule 500 mg/m2 Intravenous
Background Cytarabine Small molecule 1000 mg/m2 Intravenous
Background Cytarabine Small molecule 1500 mg/m2 Intravenous
Background Mitoxantrone Small molecule 8 mg/m2 Intravenous
Background Mitoxantrone Small molecule 10 mg/m2 Intravenous