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

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00051688
Enrollment
Unknown
Registered
2003-01-16
Start date
2003-06-30
Completion date
2004-08-31
Last updated
2006-07-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Neoplasms

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.

Interventions

DRUGoxaliplatin

Sponsors

Chiron Corporation
Lead SponsorINDUSTRY

Study design

Primary purpose
TREATMENT

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026