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Terminated Phase 2 Interventional

Tezacitabine and Oxaliplatin for the Treatment of Patients With Metastatic Colorectal Cancer

ClinicalTrials.gov ID: NCT00051688

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT00051688. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 12, 2026, 6:13 AM EST

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Brief summary

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

The primary purpose of this study is to determine the best dose of tezacitabine when combined with oxaliplatin in patients with metastatic colorectal cancer. This study will also evaluate tumor response to the combination of anti-cancer drugs.

Study identification

NCT ID
NCT00051688
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Chiron Corporation
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Jun 2003 (Type not available)
Primary completion
Not listed
Completion
Aug 2004 (Type not available)
Last update posted
Jul 11, 2006

2003 – 2004

United States locations

U.S. sites
8
U.S. states
6
U.S. cities
8
Facility City State ZIP Site status
ACRC/Arizona Clinical Research Center Tucson Arizona 85712 —
USC/Norris Comprehensive Cancer Center Los Angeles California 90033 —
Comprehensive Cancer Centers of the Desert Palm Springs California 92262 —
Cancer Institute Medical Group Santa Monica California 90404 —
Georgetown University Medical Center, Lombardi Cancer Center Washington D.C. District of Columbia 20007 —
H. Lee Moffitt Cancer Center & Research Institute Tampa Florida 33612-9497 —
Northwestern University Feinberg School of Medicine Chicago Illinois 60611 —
Kansas City Oncology and Hematology Group Kansas City Missouri 64111 —

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 NCT00051688, 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 Jul 11, 2006 · Synced Nov 12, 2026

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