drugset / Trial / NCT02014558

Dose Escalation Study Investigating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics of ASP2215 in Patients With Relapsed or Refractory Acute Myeloid Leukemia

NCT02014558

Phase 1/2 Completed 265 enrolled Astellas Pharma Global Development, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The objective of this study was to assess the safety and tolerability, including the maximum tolerated dose, of gilteritinib in participants with relapsed or treatment-refractory acute myeloid leukemia (AML). This study also determined the pharmacokinetic (PK) parameters of gilteritinib.

Timeline

Start
2013-10-09
Primary completion
2017-08-04
Completion
2018-03-07

Drugs

EvaluationDrugModalityDoseRoute
Subject CEPHALEXIN ANHYDROUS Small molecule 500 mg Oral
Subject Gilteritinib Small molecule 20 mg Oral
Subject Gilteritinib Small molecule 40 mg Oral
Subject Gilteritinib Small molecule 80 mg Oral
Subject Gilteritinib Small molecule 120 mg Oral
Subject Gilteritinib Small molecule 200 mg Oral
Subject Gilteritinib Small molecule 300 mg Oral
Subject Gilteritinib Small molecule 450 mg Oral
Subject Midazolam Small molecule 2 mg Oral
Subject Voriconazole Small molecule 200 mg Oral