Clinical trial
Veliparib (ABT888) and Topotecan (Hycamtin�) for Patients with Platinum-Resistant or Partially Platinum-Sensitive Relapse of Epithelial Ovarian Cancer with Negative or Unknown BRCA Status
Phase I:
To determine:
Maximum-tolerated dose (MTD)
Dose-limiting toxicities (DLT)
Recommended phase II dose
Phase II:
To investigate response rates (based on either CA125 GCIG or RECIST criteria) of combination topotecan and veliparib (ABT888) in relapsed ovarian cancer with negative or unknown BRCA status.
Category | Value |
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Study start date | 2012-06-19 |