Clinical Trials Directory

Trials / Completed

CompletedNCT01560104

A Clinical Study Conducted in Multiple Centers Comparing Veliparib in Combination With Carboplatin and Paclitaxel Versus a Placebo in Combination With Carboplatin and Paclitaxel in Patients With Advanced Non-small Cell Lung Cancer

Randomized, Double-Blind, Multicenter, Phase 2 Trial Comparing Veliparib Plus Carboplatin and Paclitaxel Versus Placebo Plus Carboplatin and Paclitaxel in Previously Untreated Metastatic or Advanced Non-Small Cell Lung Cancer (NSCLC)

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
160 (actual)
Sponsor
AbbVie (prior sponsor, Abbott) · Industry
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

A Randomized, Double-Blind, Multicenter, Phase 2 Trial Comparing Veliparib Plus Carboplatin and Paclitaxel Versus Placebo Plus Carboplatin and Paclitaxel in Previously Untreated Metastatic or Advanced Non-Small-Cell Lung Cancer (NSCLC).

Detailed description

Subjects will be randomized in a 2:1 ratio to one of the two treatment groups. The safety of each treatment group will be assessed by evaluating study drug exposure, adverse events, serious adverse events, all deaths, changes in laboratory determinations and vital sign parameters. Progression -Free Survival (PFS) using Response Evaluation Criteria in Solid Tumors (RECIST) (version 1.1) will be assessed as well as Overall Survival (OS) and the Objective Response Rate (ORR). Study visits will be conducted according to the protocol schedule. Study visits will include physical examination, laboratory blood sample collection, and assessment of vital signs, medical history and urinalysis. 12-lead Electrocardiogram (ECG) will be performed at protocol specified visits.

Conditions

Interventions

TypeNameDescription
DRUGVeliparib
DRUGCarboplatin
DRUGpaclitaxel
DRUGplacebo

Timeline

Start date
2012-02-01
Primary completion
2014-09-01
Completion
2014-09-01
First posted
2012-03-22
Last updated
2015-10-21

Source: ClinicalTrials.gov record NCT01560104. Inclusion in this directory is not an endorsement.