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Completed Phase 2 Interventional

Phase II CT-2103/Carboplatin in Ovarian Cancer

ClinicalTrials.gov ID: NCT00069901

Public ClinicalTrials.gov record NCT00069901. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 28, 2026, 1:05 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

CT-2103/Carboplatin for Patients With Newly Diagnosed Stage III or IV Ovarian or Primary Peritoneal Cancer: A Phase 2 Study

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the safety and efficacy of CT-2103 (poly(L)glutamate-paclitaxel) in combination with carboplatin for the treatment of patients with Stage III or IV ovarian or primary peritoneal cancer.

Study identification

NCT ID
NCT00069901
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
CTI BioPharma
Industry
Enrollment
82 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 2003 (Type not available)
Primary completion
Nov 2005 (Actual)
Completion
Sep 2006 (Actual)
Last update posted
Sep 22, 2008

2003 – 2006

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
California Cancer Care Greenbrae California 94904 —
Gynecology Oncology Associates Greenbrae California — —
Stockton Hematology Oncology Medical Stockton California 95204 —
Raben and Fldman Research Associates South Miami Florida 33143 —
University of Louisville Louisville Kentucky 40202 —
Resource Center for Gynecology/ Oncology Kansas City Missouri 64132 —
Upstate New York Cancer Research and Education Foundation Rochester New York 98104 —
Gynecology, Oncology, and Pelvic Surgery Associates, Inc. Columbus Ohio 43222 —
Albert Einstein Cancer Center Philadelphia Pennsylvania 19141 —
Guthrie Foundation for Education and Research Sayre Pennsylvania 18840 —
South Carolina Oncology Assoicates Columbia South Carolina 29203 —
Chattanooga GYN-Oncology Chattanooga Tennessee 37403 —
Baptist Regional Cancer Center Knoxville Tennessee 37920 —
Arlington Fairfax Hematology Oncology Arlington Virginia 22205 —
Pacific Gynecology Specialists Seattle Washington 98104 —
Swedish Cancer Institute Seattle Washington 98104 —
Aurora Health Care, Inc. Milwaukee Wisconsin 53201 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00069901, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 22, 2008 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00069901 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →