Overview

CP-461 for the Treatment of Crohn's Disease

Status:
Completed
Trial end date:
2003-09-01
Target enrollment:
Participant gender:
Summary
Patients with moderately to severely active Crohn's disease will be treated with oral CP-461 200 mg (2 x 100 mg capsules) twice-daily for 8 weeks. The purpose of this study is to see if CP-461 improves the symptoms of Crohn's disease and/or the patient's quality of life. Patient's safety will be monitored throughout the study.
Phase:
Phase 2
Details
Lead Sponsor:
Astellas Pharma Inc
Collaborators:
Cell Pathways
OSI Pharmaceuticals