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

Phase 2
Terminated
Conditions
Colorectal Neoplasms
Registration Number
NCT00051688
Lead Sponsor
Chiron Corporation
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (8)

Cancer Institute Medical Group

🇺🇸

Santa Monica, California, United States

ACRC/Arizona Clinical Research Center

🇺🇸

Tucson, Arizona, United States

USC/Norris Comprehensive Cancer Center

🇺🇸

Los Angeles, California, United States

Kansas City Oncology and Hematology Group

🇺🇸

Kansas City, Missouri, United States

Northwestern University Feinberg School of Medicine

🇺🇸

Chicago, Illinois, United States

Comprehensive Cancer Centers of the Desert

🇺🇸

Palm Springs, California, United States

Georgetown University Medical Center, Lombardi Cancer Center

🇺🇸

Washington, District of Columbia, United States

H. Lee Moffitt Cancer Center & Research Institute

🇺🇸

Tampa, Florida, United States

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