drugset / Trial / NCT00502294

A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Visilizumab in Subjects With Intravenous Steroid-Refractory Ulcerative Colitis

NCT00502294

Phase 3 Withdrawn 150 enrolled Facet Biotech PDL BioPharma, Inc. · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

To compare the efficacy of visilizumab at 5 mcg/kg/day administered intravenously (IV) on Days 1 and 2 to placebo in subjects with IVSR-UC.

Timeline

Start
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Visilizumab Monoclonal antibody 5 ug/kg Intravenous

Indications

No indication recorded.