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

This study has been terminated.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00051688
First Posted: January 16, 2003
Last Update Posted: July 11, 2006
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Chiron Corporation
January 15, 2003
January 16, 2003
July 11, 2006
June 2003
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Complete list of historical versions of study NCT00051688 on ClinicalTrials.gov Archive Site
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Tezacitabine and Oxaliplatin for the Treatment of Patients With Metastatic Colorectal Cancer
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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.
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Interventional
Phase 2
Primary Purpose: Treatment
Colorectal Neoplasms
  • Drug: tezacitabine
  • Drug: oxaliplatin
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
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August 2004
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  • Patients with metastatic colorectal adenocarcinoma who have failed one prior course of chemotherapy.
  • Patients must have at least one measurable tumor.
  • Patients may not have received prior treatment with oxaliplatin.
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00051688
TEZ101
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Chiron Corporation
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Chiron Corporation
July 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP