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:October 2001
End Date:June 2005

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An Open-label Study of the Effect of Intermittent Xeloda 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 intermittent oral Xeloda administration in
combination with 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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Houston, TX
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Albuquerque, NM
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Buffalo, NY
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from
Denver, CO
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Fountain Valley, California 92708
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from
Fountain Valley, CA
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from
Hutchinson, KS
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La Jolla, CA
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Las Vegas, NV
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Phoenix, AZ
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from
Santa Rosa, CA
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