drugset / Trial / NCT01131039

Safety and Efficacy Study of Gemcitabine Plus Bevacizumab in Patients With Platinum-Resistant Ovarian, Primary Peritoneal or Fallopian Tube Cancer

NCT01131039 ↗

NaSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to determine whether the administration of bevacizumab and gemcitabine given by IV infusion can prolong survival, delay tumor growth, and/or shrink tumors in patients with ovarian cancer, primary peritoneal, or fallopian tube cancer.

Timeline

Start
2011-01
Primary completion
2011-09
Completion
2011-09

Outcome

Outcome not reported

Stopped: “PI left Emory”

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody — Intravenous
Subject Gemcitabine Small molecule — Intravenous