A Study of Xeloda (Capecitabine) in Patients With Advanced and/or Metastatic Colorectal Cancer
| Status: | Completed |
|---|---|
| Conditions: | Colorectal Cancer, Cancer |
| Therapuetic Areas: | Oncology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 8/3/2016 |
| Start Date: | July 2001 |
| End Date: | January 2005 |
An Open-label Study of the Effect of Continuous Xeloda Therapy in Combination With Irinotecan on Treatment Response in Patients With Advanced and/or Metastatic Colorectal Cancer
This study will assess the efficacy and safety of continuous oral Xeloda administration in
combination with intravenous irinotecan as a first-line treatment in patients with advanced
and/or metastatic colorectal cancer. The anticipated time on study treatment is 3-12 months
and the target sample size is <100 individuals.
combination with intravenous irinotecan as a first-line treatment in patients with advanced
and/or metastatic colorectal cancer. The anticipated time on study treatment is 3-12 months
and the target sample size is <100 individuals.
Inclusion Criteria:
- adult patients >=18 years of age;
- locally advanced and/or metastatic colorectal cancer;
- >=1 target lesion.
Exclusion Criteria:
- previous treatment with Xeloda or irinotecan;
- previous systemic therapy for metastatic disease;
- progressive disease during previous adjuvant therapy or within 6 months of
completion.
We found this trial at
10
sites
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