Clinical Trials Directory

Trials / Completed

CompletedNCT00523432

A Phase I Study of CCI-779 (Temsirolimus) in Combination With Topotecan in Patients With Gynecologic Malignancies

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
15 (actual)
Sponsor
University of Chicago · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of the trial is to determine the recommended phase II dose of weekly intravenous topotecan in combination with a fixed dose (25 mg or 15 mg) of weekly intravenous temsirolimus in patients with and without prior pelvic radiation.

Conditions

Interventions

TypeNameDescription
DRUGTopotecanWeekly doses via IV infusion. Dose will be assigned based on time of study entry.
DRUGCCI-779 (temsirolimus)Weekly 25mg dose via IV infusion.

Timeline

Start date
2007-08-01
Primary completion
2009-09-01
Completion
2010-12-01
First posted
2007-08-31
Last updated
2013-09-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00523432. Inclusion in this directory is not an endorsement.