drugset / Trial / NCT01476657

A Phase 1 Study of Duvelisib in Patients With Advanced Hematologic Malignancies

NCT01476657

Phase 1 Terminated 210 enrolled SecuraBio
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety, maximum tolerated dose and pharmacokinetics of IPI-145 in patients with advanced hematologic malignancies.

Timeline

Start
2011-10
Primary completion
2016-12
Completion
2017-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Duvelisib Small molecule 8 mg Oral
Subject Duvelisib Small molecule 25 mg Oral
Subject Duvelisib Small molecule 75 mg Oral
Subject Duvelisib Small molecule 100 mg Oral