A Phase I/II, Open-Label Pilot Trial to Evaluate the Safety of Rapamune (Sirolimus) in Patients With Multiple Sclerosis
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Multiple Sclerosis (MS) - Relapsing-remitting
- Sponsor
- National Institute of Allergy and Infectious Diseases (NIAID)
- Enrollment
- 14
- Locations
- 1
- Primary Endpoint
- Mean number of new and overall total number of gadolinium-enhancing lesions reported on sequential brain MRIs
- Status
- Terminated
- Last Updated
- 9 years ago
Overview
Brief Summary
The purpose of this study is to determine the safety and tolerability of the drug sirolimus in patients with multiple sclerosis (MS) who have failed other treatments.
Detailed Description
MS is a chronic autoimmune disease of the central nervous system in which myelin, the protein sheath that protects nerve cells, is degraded by T cells and macrophages, leading to an eventual loss of neurologic function. MS can be classified as either relapsing-remitting, in which patients experience worsening in symptoms followed by partial or complete recovery of function; or progressive, in which patients have a gradual increase in symptoms, with or without relapses. Standard treatments used to treat relapsing-remitting MS are only modestly effective and may be associated with significant toxicity. There is a need to develop therapies with lower toxicities that can be administered early during the course of disease and have the potential to stop disease progression altogether. Sirolimus has been demonstrated to provide potent immunosuppression in recent clinical trials involving kidney transplantation, and may help people with autoimmune diseases like MS. This study will determine the benefit of sirolimus in MS patients. Blood and urine collection will occur at screening. Participants will take daily doses of sirolimus for 6 months. There will be nine study visits; they will occur at Days 14, 28, 42, 56, 90, 120, 150, 180, and 225. Medication adverse events, concomitant medications, and vital signs will be recorded at Visits 1 through 8. At all visits, patient compliance to the sirolimus regimen will be measured, and blood and urine collection will occur. Physical and neurological exams, magnetic resonance imaging (MRI) brain scans, MS status tests, and a chest x-ray will be conducted at selected times throughout the study.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Relapsing-remitting MS
- •Evidence of demyelination on magnetic resonance imaging (MRI) scan
- •Expanded Disability Status Scale (EDSS) score between 0 and 6
- •Nonresponsive to beta-interferon or Glatiramer acetate therapy
- •Discontinuation of beta-interferon or Glatiramer acetate therapy within 1 month prior to study entry
- •Willing to use acceptable methods of contraception
Exclusion Criteria
- •Primary progressive MS
- •Prior treatment with immunosuppressants
- •Steroid therapy within 1 month prior to study entry
- •Evidence of active infection or cancer
- •Heart or hematologic dysfunction
- •High levels of lipids in the blood
- •Use of lipid-lowering agents
- •History of cirrhosis or liver disease requiring treatment
- •History of hepatitis B or C
- •Active cytomegalovirus infection
Outcomes
Primary Outcomes
Mean number of new and overall total number of gadolinium-enhancing lesions reported on sequential brain MRIs
Safety of sirolimus, including number of lesions detected by brain MRI
Tolerability of sirolimus
Secondary Outcomes
- Effect of sirolimus therapy on the immune function of patients with relapsing-remitting multiple sclerosis (RRMS)
- Efficacy, as measured by change in the mean number of new and overall total number of gadolinium-enhancing lesions on pre-treatment brain MRIs, compared to post-treatment