drugset / Trial / NCT00303381

Safety and Efficacy of Interferon-Beta-1a (Rebif®) for Treating Subjects With Acute Symptoms of Ulcerative Colitis

NCT00303381

Phase 2 Completed 194 enrolled EMD Serono Merck Serono International SA · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to determine the safety and efficacy of interferon-beta-1a in subjects with active ulcerative colitis (UC).

Timeline

Start
2001-12
Primary completion
2003-01
Completion
2003-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Interferon beta-1a Protein / enzyme biologic 44 ug Subcutaneous
Subject Interferon beta-1a Protein / enzyme biologic 66 ug Subcutaneous

Indications