Purpose

This is a 2-arm, Phase 3 study to evaluate the safety and efficacy of veliparib plus carboplatin and paclitaxel versus the Investigator's choice of standard chemotherapy in Lung Subtype Panel (LSP) positive subjects with metastatic or advanced non-squamous non-small cell lung cancer.

Category

IRB Number
20140210HU
NCT Number
-
Open to Enrollment
Yes
Sponsor
AbbVie -



Study Contact

Principal Investigator
Subrata Debnath

Subrata Debnath
(210) 508-2889
nath@uthscsa.edu



Eligibility

Eligible Ages
Between 18 Years and 99 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

    Exclusion Criteria


      Study Design

      Arm Groups