drugset / Trial / NCT01061996

Basiliximab Maintenance in Ulcerative Colitis

NCT01061996

Phase 2 Terminated 88 enrolled Cerimon Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

Primary Objective Safety: assess the safety of basiliximab 40 mg, given every 4 weeks, in subjects with ulcerative colitis who completed previous basiliximab studies. Secondary Objectives: evaluate the efficacy and assess the immunogenicity of this multiple-dose maintenance regimen in this population

Timeline

Start
2007-07
Primary completion
2008-12
Completion
2008-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Basiliximab Monoclonal antibody 40 mg Intravenous

Indications