A Study of Xeloda (Capecitabine) in Patients With Metastatic Colorectal Cancer



Status:Completed
Conditions:Colorectal Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:July 2003
End Date:August 2006

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An Open-Label Randomized Phase III Study of Intermittent Oral Capecitabine in Combination With Intravenous Oxaliplatin (Q3W) ("XELOX") Versus Bolus and Continuous Infusion Fluorouracil/ Intravenous Leucovorin With Intravenous Oxaliplatin (Q2W) ("FOLFOX4") as Treatment for Patients With Metastatic Colorectal Cancer Who Have Received Prior Treatment With CPT-11 in Combination With 5-FU/LV as First Line Therapy

This 2 arm study will assess the efficacy and safety of intermittent oral Xeloda, or iv
fluorouracil/leucovorin, in combination with intravenous Eloxatin (oxaliplatin) in patients
previously treated for metastatic colorectal cancer. Patients will be randomized to receive
either 1)XELOX (Xeloda 1000mg/m2 po bid on days 1-15 + oxaliplatin) in 3 week cycles or 2)
FOLFOX-4 (oxaliplatin + leucovorin + 5-FU in 2 week cycles. The anticipated time on study
treatment is until disease progression, and the target sample size is 500+ individuals.


Inclusion Criteria:

- adult patients >=18 years of age;

- metastatic colorectal cancer;

- >=1 target lesion;

- failed first-line chemotherapy with 5-fluorouracil and irinotecan.

Exclusion Criteria:

- previous treatment with oxaliplatin;

- progressive or recurrent disease during or within 6 months of completion of
first-line chemotherapy;

- >=1 previous chemotherapeutic agent or systemic anticancer regimen for metastatic
disease.
We found this trial at
9
sites
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Billings, MT
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Bakersfield, CA
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Bruxelles,
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Colorado Springs, Colorado 80910
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Colorado Springs, CO
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Dallas, TX
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Nyack, NY
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St Louis, MO
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Terre Haute, IN
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from
Washington,
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