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Clinical Trial Details

Overview

Research Study Summary

New Investigational Medication for Relapsing Remitting Multiple Sclerosis (RRMS) who have had a documented relapse in the last year

Purpose

This is a 12 month study to compare the safety and efficacy of 2 doses of Fingolimod (0.25mg and 0.5mg) every day vs Copaxone 20mg SC every day for patients with RRMS.

Patient Inclusion Criteria:

  • 18-65
  • 1 documented relapse in the last year
  • NO monoclonal antibodies within 6 months prior to start of study medication
  • NO varicella zoster
  • Heartrate must be greater than 45/bpm
  • NO uncontrolled diabetes with HbA1c >7%
  • Cannot have positive Hepatitis A, B, C and E

To Learn more

CW ID:182097
Date Last Changed: July 18, 2013

Clinical Trial Snapshot

Gender
Both Male and Female
Age
18 to 65 Years
Overall Status
Recruiting
Duration
12 Months
Facility Type
N/A

Contact

Alpine Clinical Research Center
1000 Alpine Avenue , Suite 200
Boulder, CO 80304
Phone: 303-443-7229

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Research Center Information: Alpine Clinical Research Center

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