drugset / Trial / NCT00082212

A Study in Patients With Persistent or Recurrent Epithelial Ovarian or Primary Peritoneal Carcinoma

NCT00082212 ↗

Phase 2 Terminated 25 enrolled Eli Lilly and Company Bristol-Myers Squibb · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the overall response rate, time to progression, and 1 yr survival with cetuximab in patients with ovarian or primary peritoneal carcinoma.

Timeline

Start
2004-11
Primary completion
2007-06
Completion
2007-06

Outcome

Outcome not reported

Stopped: “Due to lack of sufficient efficacy.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Cetuximab Monoclonal antibody 250 mg/m2 —

Indications