Effect of Interferon Beta-1a (Avonex®) on Changes of Non-Conventional MRI Measures in Patients With MS

This study has been completed.
Information provided by:
State University of New York at Buffalo
ClinicalTrials.gov Identifier:
First received: April 19, 2007
Last updated: NA
Last verified: April 2007
History: No changes posted
Phase IV open label, single-blind study, post-marketing, 1-year MRI observational study evaluating effect of Avonex® monotherapy (6.0 MIU administered i.m. each week) on the year-to-year changes in two annual measures—magnetization transfer imaging and diffusion-weighted imaging in patients with either relapsing-remitting (RR) or secondary-progressive (SP) multiple sclerosis (MS). One hundred fifty (150) patients with RR and SP MS—followed at the Jacobs Neurological Institute, University at Buffalo, Buffalo NY—who satisfy both inclusion and exclusion criteria will be included. They will be assessed at baseline and at 12 months with MRI and clinical examinations.

Condition Intervention Phase
Multiple Sclerosis
Drug: Avonex® monotherapy (6.0 MIU administered i.m. each week)
Phase 4

Study Type: Observational
Study Design: Observational Model: Defined Population
Time Perspective: Longitudinal
Official Title: Effect of Interferon Beta-1a (Avonex®) on Changes of Non-Conventional MRI Measures in Patients With Relapsing-Remitting and Secondary-Progressive Multiple Sclerosis

Resource links provided by NLM:

Further study details as provided by State University of New York at Buffalo:

Estimated Enrollment: 150
Study Start Date: June 2005
Study Completion Date: September 2006
  Show Detailed Description


Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Patient diagnosed with clinical definite MS according to the McDonald criteria
  • Age 18-65
  • Have a RR or SP disease course
  • Have EDSS scores less than or equal to 6.5
  • Have disease duration 6 months to 20 years
  • Be on intramuscular 6 MIU of Avonex® for a minimum of 3-6 months before the study entry
  • Signed informed consent
  • None of the exclusion criteria

Exclusion Criteria:

  • Previous treatment 3 months prior to study entry with immunosuppressant agents, e.g., mitoxantrone, cyclophosphamide, cladribine, fludarabine, cyclosporine or total body irradiation or any other concomitant immunomodulatory therapies besides Avonex® (e.g., Azathioprine, methotrexate, IVIG, cellcept, natalizumab, etc).
  • Patients who received steroid therapy during the 3 months prior to study entry or patients who received steroid treatment 30-60 days prior to the follow-up MRI scan date.
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00463710

United States, New York
The Jacobs Neurological Institute
Buffalo, New York, United States, 14127
Sponsors and Collaborators
State University of New York at Buffalo
Principal Investigator: Robert Zivadinov, MD, PhD SUNY Buffalo
  More Information

ClinicalTrials.gov Identifier: NCT00463710     History of Changes
Other Study ID Numbers: 003-05-AVX 
Study First Received: April 19, 2007
Last Updated: April 19, 2007
Health Authority: United States: Institutional Review Board

Keywords provided by State University of New York at Buffalo:
MTI, DWI, Avonex, MRI

Additional relevant MeSH terms:
Multiple Sclerosis
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Demyelinating Autoimmune Diseases, CNS
Demyelinating Diseases
Immune System Diseases
Nervous System Diseases
Pathologic Processes
Interferon beta 1a
Adjuvants, Immunologic
Anti-Infective Agents
Antineoplastic Agents
Antiviral Agents
Immunologic Factors
Pharmacologic Actions
Physiological Effects of Drugs
Therapeutic Uses

ClinicalTrials.gov processed this record on May 01, 2016