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

Phase 3
Withdrawn
Conditions
Intravenous Steroid-Refractory Ulcerative Colitis
Registration Number
NCT00502294
Lead Sponsor
Facet Biotech
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
150
Inclusion Criteria
  • Males and females, 18 years of age or older.
  • Diagnosis of UC verified by endoscopy within 60 months prior to consent.
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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