drugset / Trial / NCT00322920

Efficacy Study of Weekly Topotecan With Cisplatin in Advanced Stage or Recurrent Cervical Cancer

NCT00322920 ↗

Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the maximum tolerated dose (MTD) of topotecan when given weekly with cisplatin in patients with persistent, recurrent, or advanced stage cervical cancer. Secondary purposes are to describe the toxicity profile in patients with persistent, recurrent, or advanced stage cervical cancer treated with the combination of topotecan when given weekly with cisplatin and to determine the response rate and time to progression in patients with persistent, recurrent, or advanced stage cervical cancer treated with the combination of topotecan when given weekly with cisplatin.

Timeline

Start
2005-07
Primary completion
—
Completion
—

Outcome

Outcome not reported

Stopped (Enrollment): “Low accrual”

Drugs

EvaluationDrugModalityDoseRoute
Subject Topotecan Small molecule 2 unknown —
Background Cisplatin Other / unclassified 50 mg/m2 —

Indications