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

NCT01476657 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 210

Last updated 2021-03-17

No results posted yet for this study

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.

Conditions

Interventions

DRUG

IPI-145 (duvelisib)

Oral Twice A Day (BID) Dosing

Sponsors & Collaborators

  • SecuraBio

    lead INDUSTRY

Principal Investigators

  • Hagop Youssoufian, MD · Verastem, Inc.

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-10-31
Primary Completion
2016-12-31
Completion
2017-01-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01476657 on ClinicalTrials.gov