A Study of Xeloda (Capecitabine) in Combination With Avastin + Short Course Chemotherapy in Patients With Metastatic Colorectal Cancer

Stopped early · Phase 2

Conditions studied: Colorectal Cancer

In brief

This 2-arm study was designed to evaluate the efficacy and safety of 2 treatment regimens of Xeloda and Avastin, with either irinotecan or oxaliplatin administered for the first 12 cycles, as first line treatment in patients with metastatic colorectal cancer. Patients were randomized to receive 2-weekly cycles of treatment with either: 1) Xeloda, Avastin and oxaliplatin; or 2) Xeloda, Avastin and irinotecan. After 9 cycles, patients continued to receive maintenance treatment with Xeloda + Avastin. The anticipated time on study treatment was until disease progression, and the target sample size was 100-500 individuals.

Key facts

Study ID

NCT00642603

Run by

Hoffmann-La Roche

People needed

41

Starts

2008-05-01

Expected to finish

2009-03-01

Last updated by the study team

2018-03-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adult patients, ≥18 years of age
• Histologically confirmed adenocarcinoma of colon or rectum, with unresectable metastatic or locally advanced disease
• ≥1 measurable target lesion
• Ambulatory, with an Eastern Cooperative Oncology Group (ECOG) performance status of ≤1

You may not qualify if…

• Prior systemic therapy for advanced or metastatic disease
• History of another malignancy within last 5 years, except cured basal cell cancer of skin or cured cancer in situ of the cervix
• Clinically significant cardiovascular disease
• Current or recent use of full dose oral warfarin or full dose parenteral anticoagulants or thrombolytic agents
• Chronic daily treatment with >325 mg/day aspirin

Where it is running

• Study site — Sedona, Arizona, United States
• Study site — Tucson, Arizona, United States
• Study site — Anaheim, California, United States
• Study site — Colton, California, United States
• Study site — Greenbrae, California, United States
• Study site — Loma Linda, California, United States
• Study site — Modesto, California, United States
• Study site — Montebello, California, United States
• Study site — Pomona, California, United States
• Study site — Sacramento, California, United States
• Study site — Norwich, Connecticut, United States
• Study site — Waterbury, Connecticut, United States
• Study site — Lake Worth, Florida, United States
• Study site — Miami Shores, Florida, United States
• Study site — New Port Richey, Florida, United States
• Study site — Ocala, Florida, United States
• Study site — Ocoee, Florida, United States
• Study site — Marietta, Georgia, United States
• Study site — Niles, Illinois, United States
• Study site — Paducah, Kentucky, United States
• Study site — Alexandria, Louisiana, United States
• Study site — Baltimore, Maryland, United States
• Study site — Baltimore, Maryland, United States
• Study site — Westminster, Maryland, United States
• Study site — PARK Springs, Arizona, United States

Full record on ClinicalTrials.gov

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