Trial Information
Summary: Combination Rebif and Oral Cladribine Therapy for Multiple Sclerosis
MS patients who are currently taking Rebif are invited to
participate in this study if they have had a relapse within the
past year. Eligible patients will have either oral cladribine or
placebo tablets added to their Rebif treatment. The study duration
is 96 weeks and all medication and study related procedures are
provided at no cost to the patient.
Patient Inclusion Criteria
- Must have a diagnosis of a relapsing form of Multiple
Sclerosis
- Be between 18 and 55 years old
- Have been taking Rebif for at least the last 48 weeks
- Must have had at least one relapse in the past year
Patient Exclusion Criteria
- Not eligible if you have received immunosupressive or cytotoxic
agents in the past
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Contact:
Sarah Zacharias, Research Nurse/Coordinator
Alpine Clinical Research Center
1000 Alpine Avenue, Suite 200
Boulder, CO 80304
Telephone: 303-443-7229
Email:
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If you would like to learn more about participating in this study, please send an e-mail message using the form below.
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Trial listings updated: June 1, 2008 at 6:31:35 AM