Triple Negative Metastatic Breast Cancer Clinical Trial
Official title:
Phase I Study to Evaluate the Tolerability, Safety and Efficacy of BMN-673 in Combination With Carboplatin and Paclitaxel in Patients With Advanced Solid Tumor Malignancies That Have BRCA Mutations or Triple Negative Metastatic Breast Cancer
Open label, non-randomized, dose escalation and expansion Phase Ia/b trial to evaluate the safety of the combination of BMN 673 and carboplatin, and subsequently BMN 673 in combination with paclitaxel and carboplatin to determine the recommended Phase II dose of the combination.
Poly adenosine diphosphate-ribose polymerase (PARP) 1/2 inhibitors are a novel class of
anticancer agents that have shown activity in tumors with defects in DNA repair and may
induce synthetic lethality in combination with agents that induce DNA damage by preventing
DNA repair.
The rationale of this study is to determine whether a DNA damaging agent can potentiate the
cell death induced by PARP inhibitors in individuals with tumor that are more susceptible to
chemotherapy.
The study will evaluate the potential benefits of BMN 673 in combination with weekly
carboplatin in patients with metastatic tumors associated with BRCA germ line mutations or
patients with triple negative breast cancer with no known BRCA mutation, subsequently if
tolerated, an additional cohort will examine the feasibility of adding paclitaxel to this
combination for any solid tumor malignancies with potential benefit to this combination.
This is the first study to evaluate the safety and efficacy of BMN 673 in combination with
carboplatin in patients with either BRCA mutations or TNBC. If tolerable paclitaxel will be
added to the combination in any solid tumor malignancies with potential benefit to this
combination.
;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT00516724 -
Study to Assess the Safety and Tolerability of a PARP Inhibitor in Combination With Carboplatin and/or Paclitaxel
|
Phase 1 | |
| Completed |
NCT01576666 -
Phase Ib, Dose Escalation Study of Oral LDE225 in Combination With BKM120 in Patients With Advanced Solid Tumors
|
Phase 1 | |
| Terminated |
NCT01069796 -
Bevacizumab + Paclitaxel + Capecitabine in Triple Negative Metastatic Breast Cancer
|
Phase 2 |