Irinotecan
Drug250mg/m2 iv on day 1 of each 3 week cycle
NCT Number: NCT00048139
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.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Phoenix, Arizona, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
250mg/m2 iv on day 1 of each 3 week cycle
1000mg/m2 po bid on days 1-15 of each 3 week cycle
Time frame: Event driven
Time frame: Event driven
Hoffmann-La Roche
Industry
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
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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