drugset / Trial / NCT00461786

A Study of Single Agent Pemetrexed Disodium in Treating Patients With Recurrent or Persistent Ovarian or Primary Peritoneal Cancer

NCT00461786 ↗

Non-randomizedSingle-groupOpen-labelTreatment

Summary

The primary purpose of this trial is to estimate the drug effect on tumors in patients with ovarian or primary peritoneal cancers. Patients will receive Pemetrexed every 21 days until disease progression or unacceptable toxicity. This medication will be given over 10 minutes and may be administered intravenously (IV), through a vein in your arm. Vitamin supplementation is a required part of this study.

Timeline

Start
2004-09
Primary completion
2007-10
Completion
2008-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Pemetrexed Small molecule 900 mg/m2 Intravenous