Clinical trial

Safety and Efficacy of Interferon-Beta-1a (Rebif®) for Treating Subjects With…

NCT00303381 · EMD Serono, Industry · Completed

Key facts

NCT number NCT00303381
Title Safety and Efficacy of Interferon-Beta-1a (Rebif®) for Treating Subjects With Acute Symptoms of Ulcerative Colitis
Official title A Multicentre, Randomised, Double-blind, Placebo-controlled, Dose-finding Phase II Study of Subcutaneously Administered IFN-beta-1a in the Treatment of Patients With Moderately Active Ulcerative Colitis
Lead sponsor EMD Serono, Industry
Collaborators Merck Serono International SA Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Ulcerative Colitis
Intervention type Drug
Interventions Interferon-beta-1a, 44 microgram, Placebo, 66 microgram
Enrollment 194
Start date Dec 1, 2001
Primary completion Jan 1, 2003
Completion Jan 1, 2003
First posted Mar 16, 2006
Last update posted Aug 6, 2013
Countries Germany, Israel, Netherlands, Singapore, Sweden, Switzerland, United Kingdom

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies