Clinical trial

A Phase II Study Comparing Low- and High-Dose Alemtuzumab and High-Dose Rebif®…

NCT00050778 · Genzyme, a Sanofi Company, Industry · Completed

Key facts

NCT number NCT00050778
Title A Phase II Study Comparing Low- and High-Dose Alemtuzumab and High-Dose Rebif® in Patients With Early, Active Relapsing-Remitting Multiple Sclerosis
Official title A Phase II, Randomized, Open-Label, Three-Arm Study Comparing Low- and High-Dose Alemtuzumab and High-Dose Subcutaneous Interferon Beta-1a (Rebif®) in Patients With Early, Active Relapsing-Remitting Multiple Sclerosis
Lead sponsor Genzyme, a Sanofi Company, Industry
Collaborators Bayer Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Multiple Sclerosis, Relapsing-Remitting
Intervention type Biological
Interventions Interferon beta-1a, Alemtuzumab 12 mg, Alemtuzumab 24 mg
Enrollment 334
Start date Dec 1, 2002
Primary completion Sep 1, 2007
Completion Jan 1, 2010
First posted Dec 23, 2002
Last update posted Jan 8, 2015
Countries Croatia, Poland, Russia, United Kingdom, United States

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

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

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

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