drugset / Trial / NCT00407407
ABI-007 With Carboplatin as First-Line Therapy in Patients With Epithelial Ovarian, Primary Peritoneal, or Fallopian Tube Carcinoma
Non-randomizedParallel-groupOpen-labelTreatment
Summary
The primary purpose of this study is to determine the maximum tolerated dose and dose-limiting toxicities (DLTs) of weekly and every 3-weeks ABI-007 in combination with carboplatin (area under the curve \[AUC\]=6) in patients with ovarian cancer, primary peritoneal cancer, or fallopian tube cancer.
Timeline
- Start
- 2006-11-01
- Primary completion
- 2008-02-01
- Completion
- 2008-02-01
Outcome
Outcome not reported
Stopped: “MTD not determined”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | ABI-007 | Unknown | 80 mg/m2 | Intravenous |
| Subject | ABI-007 | Unknown | 150 mg/m2 | Intravenous |
| Background | Carboplatin | Small molecule | — | Intravenous |