Comparison of Alemtuzumab and Rebif® Efficacy in Multiple Sclerosis, Study One
NCT00530348 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 581
Last updated 2014-11-24
Summary
The purpose of this study was to establish the efficacy and safety of alemtuzumab (Lemtrada™) as a treatment for relapsing-remitting multiple sclerosis (MS), in comparison with subcutaneous (SC) interferon beta-1a (Rebif®). The study had enrolled participants who had not previously received MS disease-modifying therapies. Participants had monthly laboratory tests and comprehensive testing every 3 months.
Conditions
- Multiple Sclerosis, Relapsing-Remitting
Interventions
- BIOLOGICAL
-
Alemtuzumab
Alemtuzumab 12 milligram (mg) per day intravenous (IV) infusion on 5 consecutive days at Month 0, followed by alemtuzumab 12 mg per day IV infusion on 3 consecutive days at Month 12.
- BIOLOGICAL
-
Interferon beta-1a
Interferon beta-1a 44 microgram (mcg) subcutaneously 3-times weekly for 24 months. Dose adjustment was done as per Investigator's discretion.
Sponsors & Collaborators
- collaborator INDUSTRY
-
Genzyme, a Sanofi Company
lead INDUSTRY
Principal Investigators
-
Medical Monitor · Genzyme, a Sanofi Company
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2007-08-31
- Primary Completion
- 2011-04-30
- Completion
- 2011-04-30
Countries
- United States
- Argentina
- Australia
- Brazil
- Canada
- Croatia
- Czechia
- France
- Germany
- Mexico
- Poland
- Russia
- Serbia
- Sweden
- Ukraine
- United Kingdom
Study Locations
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