A Study of Xeloda (Capecitabine) in Patients With Advanced and/or Metastatic Colorectal Cancer
NCT ID: NCT00048126
Last Updated: 2016-11-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
57 participants
INTERVENTIONAL
2001-07-31
2005-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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1
Irinotecan
100mg/m2 iv on days 1, 8, 15 and 22 of each 6 week cycle.
capecitabine [Xeloda]
1000mg po bid
Interventions
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Irinotecan
100mg/m2 iv on days 1, 8, 15 and 22 of each 6 week cycle.
capecitabine [Xeloda]
1000mg po bid
Eligibility Criteria
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Inclusion Criteria
* locally advanced and/or metastatic colorectal cancer;
* \>=1 target lesion.
Exclusion Criteria
* previous systemic therapy for metastatic disease;
* progressive disease during previous adjuvant therapy or within 6 months of completion.
18 Years
ALL
No
Sponsors
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Hoffmann-La Roche
INDUSTRY
Responsible Party
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Principal Investigators
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Clinical Trials
Role: STUDY_DIRECTOR
Hoffmann-La Roche
Locations
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Hoover, Alabama, United States
La Jolla, California, United States
Miami, Florida, United States
Boston, Massachusetts, United States
Albuquerque, New Mexico, United States
New York, New York, United States
Charlotte, North Carolina, United States
Providence, Rhode Island, United States
Memphis, Tennessee, United States
Nashville, Tennessee, United States
Countries
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Other Identifiers
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MO16460
Identifier Type: -
Identifier Source: org_study_id