drugset / Trial / NCT02158507
Pilot Study of Veliparib (ABT-888) and Lapatinib (Tykerb) in Patients With Metastatic, Triple Negative Breast Cancer
Completed
20 enrolled
University of Alabama at Birmingham
AbbVie · collabBreast Cancer Research Foundation of Alabama · collabGlaxoSmithKline · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Lapatinib | Small molecule | 1250 mg | — |
| Subject | Veliparib | Small molecule | 200 mg | — |