drugset / Trial / NCT00207662

A Safety and Efficacy Study of Infliximab (Remicade) in Patients With Moderate to Severe Active Crohn's Disease

NCT00207662

Phase 3 Completed 580 enrolled Centocor, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a study of infliximab (Remicade) in subjects with Crohn's disease

Timeline

Start
2000-07
Primary completion
Completion
2005-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Infliximab Monoclonal antibody 5 mg/kg Intravenous
Subject Infliximab Monoclonal antibody 10 mg/kg Intravenous

Indications