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Safety and Effectiveness of Two Doses of ABT-874 as Compared to Placebo in Subjects with Multiple Sclerosis (MS)
This study is currently recruiting patients.
Sponsored by: | Abbott Laboratories |
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Information provided by: | Abbott Laboratories |
Purpose
The objective of the trial is to study the safety and effectiveness of ABT-874 administered weekly or every other week in patients with relapsing remitting and secondary progressive multiple sclerosis as compared to placebo. Effectiveness will be measured based on MRI scans done periodically thoughout the study.
Condition | Treatment or Intervention | Phase |
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Multiple Sclerosis Multiple Sclerosis, Relapsing Remitting Multiple Sclerosis, Secondary Progressive |
Drug: ABT-874/Human monoclonal antibody against IL-12 |
Phase II |
MedlinePlus related topics: Multiple Sclerosis
Study Type: Interventional
Study Design: Treatment, Safety/Efficacy Study
Study start: May 2004
Eligibility
Ages Eligible for Study: 18 Years - 55 Years, Genders Eligible for Study: Both
Criteria
Inclusion Criteria:
Exclusion Criteria:
Patients with the following conditions are not eligible to participate in the study:
Location and Contact Information
More Information
U.S. National Library of Medicine, Contact NLM Customer Service | ||||||||||||||
National Institutes of Health, Department of Health & Human Services | ||||||||||||||
Copyright, Privacy, Accessibility, Freedom of Information Act |