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Brief Title: A Study of Xeloda (Capecitabine) in Patients With Advanced and/or Metastatic Colorectal Cancer
Official Title: 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
Study ID: NCT00048126
Brief Summary: 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.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
, 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
Name: Clinical Trials
Affiliation: Hoffmann-La Roche
Role: STUDY_DIRECTOR