drugset / Trial / NCT00407407

ABI-007 With Carboplatin as First-Line Therapy in Patients With Epithelial Ovarian, Primary Peritoneal, or Fallopian Tube Carcinoma

NCT00407407 ↗

Phase 1 Terminated 6 enrolled Celgene Corporation
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

EvaluationDrugModalityDoseRoute
Subject ABI-007 Unknown 80 mg/m2 Intravenous
Subject ABI-007 Unknown 150 mg/m2 Intravenous
Background Carboplatin Small molecule — Intravenous