EARLY IFNB-1a and Simvastatin Combination Therapy in Clinically Isolated Syndrome Suggestive of Multiple Sclerosis

• Status: Completed
• Trial end date: 2007-12-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to determine the safety, tolerability and efficacy of a combination therapy interferon beta-1a(Avonex) plus simvastatin (Zocor) vs. interferon beta-1a plus placebo in patients with clinically isolated syndrome suggestive of Multiple Sclerosis.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: University of North Carolina
• Treatments: Interferon beta-1a; Simvastatin

Criteria

Inclusion Criteria:

1. Subject has a diagnosis of CIS suggestive of MS involving optic nerve (unilateral optic neuritis), spinal cord (incomplete transverse myelitis), brain stem or cerebellum syndrome confirmed by ophthalmologic or neurological examinations. (Onset of CIS symptoms must occur within twelve months of randomization).

2. At baseline, subject will be between the ages of 18 and 60, inclusive.

3. Subject has a baseline EDSS score between 0.0 and 5.5, inclusive.

4. MRI findings on the brain scan should reveal at least three out the four following findings: one Gd-enhancing lesion or nine T2 hyperintense lesions; or at least one infratentorial lesion; or at least one juxtacortical lesion and or at least three periventricular lesions.

5. Subject has signed informed consent and HIPAA forms.

Exclusion Criteria:

1. Subject has a diagnosis of CD RRMS according to Poser criteria, definitive MS according McDonald criteria, secondary progressive, or primary progressive MS.

2. Subject has been treated with statins in the previous three months. Subject has history of severe side effects related to statin therapy.

3. Subject has had a clinically significant infectious illness (e.g., cellulitis, abscess, pneumonia, septicemia) within 30 days prior to randomization.

4. Subject has a history of, or abnormal laboratory results indicative of, any significant cardiac, endocrinologic, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, gastrointestinal, dermatologic, psychiatric, renal, and/or other major disease.

5. Subject has a history of severe allergic or anaphylactic reactions or known drug hypersensitivity.

6. Subject has an abnormal screening blood test, performed at the screening visit, exceeding any of the limits defined below:

• alanine transaminase (ALT) or aspartate transaminase (AST) > 1.5 times the upper limit of normal (1.5x ULN)

• total white blood cell count < 2,300/mm^3

• CPK level > 2 x ULN on two consecutive occasions tested at least one week apart.

• Platelets less than 150,00/mm3

• Creatinine > 1.5mg/dl.

• prothrombin time (PT) > ULN

7. Subject has history of treatment with either interferon-beta 1a or 1b, or glatiramer acetate.

8. Subject has had any prior treatment with any of the following medications:

• total lymphoid irradiation

• intravenous immunoglobulins IVIg, or plasma exchange

• natalizumab or any other therapeutic monoclonal antibody

9. Subject has had treatment with any of the following medications within 1 year prior to randomization:

• mitoxantrone

• cyclophosphamide

10. Subject has had treatment with any of the following medications:

• cyclosporine

• azathioprine

• methotrexate

• glatiramer acetate

• interferon beta-1b or INF beta-1a

• intravenous immunoglobulin (IVIG)

• plasmapheresis or cytapheresis

11. Subject has had treatment with any of the following medications within 50 days prior to randomization:

• intravenous corticosteroid treatment

• oral corticosteroid treatment

12. Subject has a history of alcohol abuse within 2 years prior to randomization.

13. Subject is a female who is not postmenopausal for at least one year, surgically sterile, or willing to practice effective contraception (as defined by the investigator) during the study. The rhythm method is not to be used as the sole method of contraception.

14. Subject is a nursing mother, pregnant woman, or planning to become pregnant while on study.

15. Subject has had participation in any other investigational study within 6 months prior to randomization.

16. Subject is unwilling or is unable to comply with the requirements of this protocol including the presence of any condition (physical, mental, or social) that is likely to affect the subject's ability to comply with the study protocol.

17. Subject is determined unsuitable for enrollment into this study for any other reason in the opinion of the Investigator and/or the Sponsor.