drugset / Trial / NCT01063816

A Study of ABT-888 in Combination With Carboplatin and Gemcitabine in Subjects With Advanced Solid Tumors

NCT01063816

Phase 1 Completed 79 enrolled AbbVie
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the maximum tolerated dose of veliparib (ABT-888)and to establish the recommended Phase 2 dose of veliparib (ABT-888) when administered in combination with carboplatin and gemcitabine in subjects with advanced solid tumors.

Timeline

Start
2010-01
Primary completion
2016-08
Completion
2016-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Veliparib Small molecule Oral
Background Carboplatin Small molecule Intravenous
Background Gemcitabine Small molecule Intravenous

Indications