drugset / Trial / NCT02158507

Pilot Study of Veliparib (ABT-888) and Lapatinib (Tykerb) in Patients With Metastatic, Triple Negative Breast Cancer

NCT02158507

NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the effectiveness and safety of the combination of two drugs, Veliparib and Lapatinib, given to participants with metastatic triple negative breast cancer that have undergone previous treatment. Veliparib is an investigational drug and has not been approved by the FDA while Lapatinib has been approved by the FDA for another type of breast cancer. All eligible participants will receive the study medications and not a placebo.

Timeline

Start
2014-09-04
Primary completion
2021-07-22
Completion
2021-07-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Lapatinib Small molecule 1250 mg
Subject Veliparib Small molecule 200 mg