drugset / Trial / NCT00804856

Phase I/IIa Trial to Investigate BI 6727 (Volasertib) as Monotherapy or in Combination With Cytarabine in Acute Myeloid Leukaemia

NCT00804856

Phase 2 Completed 180 enrolled Boehringer Ingelheim
RandomizedParallel-groupOpen-labelTreatment

Summary

The trial will be performed in two parts, a phase I part and a phase IIa part. In the phase I part of the trial, BI 6727 will be investigated as monotherapy and in combination with low dose cytarabine (LD-Ara-C) in patients with relapsed/refractory AML that are not eligible for intensive treatment. The dose of BI 6727 will be escalated to determine the maximum tolerated dose (MTD) of BI 6727 monotherapy and BI 6727 in combination with LD-Ara-C in AML patients. In the phase IIa part, the combination of BI 6727 at MTD with LD-Ara-C and LD-Ara-C monotherapy will be investigated to explore the efficacy of the combination schedule in comparison to LD-Ara-C monotherapy in previously untreated AML patients that are not eligible for intensive treatment.

Timeline

Start
2008-11-27
Primary completion
2012-03-09
Completion
2021-04-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Cytarabine Small molecule 20 mg Subcutaneous
Subject Volasertib Small molecule 150 mg Intravenous
Subject Volasertib Small molecule 200 mg Intravenous
Subject Volasertib Small molecule 250 mg Intravenous
Subject Volasertib Small molecule 300 mg Intravenous
Subject Volasertib Small molecule 350 mg Intravenous
Subject Volasertib Small molecule 400 mg Intravenous
Subject Volasertib Small molecule 450 mg Intravenous
Subject Volasertib Small molecule 500 mg Intravenous
Subject Volasertib Small molecule 550 mg Intravenous