Clinical Trials Directory

Trials / Completed

CompletedNCT00004876

Carboplatin With or Without Thalidomide in Treating Patients With Ovarian Epithelial Cancer

A Randomized Study Comparing Carboplatin and Thalidomide With Carboplatin Alone in Patients With Stage Ic - IV Ovarian Cancer

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Cancer Research UK · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Thalidomide may stop the growth of ovarian cancer by stopping blood flow to the tumor. PURPOSE: This randomized phase II trial is studying how well giving carboplatin together with thalidomide works compared to carboplatin alone in treating patients with ovarian epithelial cancer.

Detailed description

OBJECTIVES: * Determine the safety of carboplatin and thalidomide in patients with stage IC-IV ovarian cancer. * Determine the antiangiogenic effect of thalidomide in this patient population. * Compare the efficacy of carboplatin with or without thalidomide in this patient population. OUTLINE: This is a randomized study. Patients are randomized to one of two treatment arms. * Arm I: Patients receive carboplatin IV over 1 hour. Treatment continues every 4 weeks for up to 6 courses in the absence of disease progression or unacceptable toxicity. * Arm II: Patients receive carboplatin as in arm I. Patients receive thalidomide orally once daily. Thalidomide treatment continues for up to 24 weeks commencing on the first day of carboplatin therapy and ceasing 4 weeks after the last course of carboplatin. PROJECTED ACCRUAL: Approximately 30 patients will be accrued for this study.

Conditions

Interventions

TypeNameDescription
DRUGcarboplatin
DRUGthalidomide

Timeline

Start date
1999-08-01
First posted
2003-01-27
Last updated
2013-08-26

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00004876. Inclusion in this directory is not an endorsement.