drugset / Trial / NCT00856180
Sequential Angiogenic Blockade for the Treatment of Recurrent Mullerian Malignancies
Phase 2
Completed
20 enrolled
Dana-Farber Cancer Institute
Brigham and Women's Hospital · collabGenentech, Inc. · collabMassachusetts General Hospital · collab
NaSingle-groupOpen-labelTreatment
Summary
The goals of this study were to evaluate the efficacy and safety of sequentially blocking the angiogenesis pathway via known antiangiogenic mechanisms, first with bevacizumab and then addition of oral cyclophosphamide upon progression of cancer through bevacizumab. The drugs used in this study were chosen because of their known antiangiogenic properties, tolerability, and anti-ovarian cancer effects.
Timeline
- Start
- 2009-02
- Primary completion
- 2010-04
- Completion
- 2014-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bevacizumab | Monoclonal antibody | 15 mg/kg | Intravenous |
| Subject | Cyclophosphamide | Other / unclassified | 50 mg | Oral |