drugset / Trial / NCT00343044
Ph II Study of Wkly Topotecan + Bevacizumab in Plat. Resistant/Recurrent Gyn Cancers
Phase 2
Completed
40 enrolled
Benaroya Research Institute
Genentech, Inc. · collabGlaxoSmithKline · collab
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to evaluate the clinical safety and toxicity of intravenous bevacizumab (Days 1 and 15 of a 28 day cycle) in combination with weekly topotecan (Days 1, 8, 15 of a 28 day cycle) in patients with platinum resistant recurrent ovarian, fallopian tube and primary peritoneal cancer.
Timeline
- Start
- 2006-06
- Primary completion
- 2010-01
- Completion
- 2011-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bevacizumab | Monoclonal antibody | 10 mg/kg | Intravenous |
| Subject | Topotecan | Small molecule | 4 mg/m2 | Intravenous |