Treatment of Multiple Sclerosis With Copaxone and Albuterol

Condition(s) targeted: Autoimmune Diseases; Multiple Sclerosis

Intervention: Glatiramer acetate (Drug); Albuterol (Drug)

Phase: N/A

Status: Active, not recruiting

Sponsored by: National Institute of Allergy and Infectious Diseases (NIAID)

Official(s) and/or principal investigator(s):
Samia Khoury, Principal Investigator

The purpose of this study is to determine the effects of glatiramer acetate (Copaxone) alone compared to Copaxone plus albuterol in patients with Multiple Sclerosis (MS).

MS is thought to be an autoimmune disease of the central nervous system. Certain white blood cells of the immune system become abnormally active and mistakenly attack the myelin of nerve fibers. Myelin is a fatty sheath that surrounds nerve fibers and insulates the nerve like insulation around an electrical wire. Without proper myelin insulation, messages sent between the brain and other parts of the body may be confused or fail completely. Damage to myelin causes the symptoms of MS. The most common form of MS is known as relapsing-remitting (RR), where partial or total recovery occurs after attacks. Four therapies are currently approved for the treatment of MS. These therapies, however, are only moderately effective and can cause undesirable side effects. For this reason, there is a need to find new therapies that have minimal side effects and may stop the disease from getting worse.

Official title: Treatment of Multiple Sclerosis With Copaxone (Glatiramer Acetate) and Albuterol

Study design: Treatment, Double-Blind, Efficacy Study

Primary outcome:

Change in each participant's disease status, as measured by the Multiple Sclerosis Functional Composite score (MSFC)

glatiramer acetate-specific cytokine secretion at Months 3, 6 and 12, compared to baseline measurement of IL-13 cytokine secretion and IFN-gamma secretion by glatiramer acetate-reactive T-cell lines

Secondary outcome:

Change in IL-5 secretion in the supernatants of lines stimulated with glatiramer acetate

change in percentage of IL-12-producing monocytes by intracytoplasmic staining

time to first exacerbation

number and severity of exacerbations

MRI evidence at baseline and Months 12 and 24 of MS progression, as measured by T2 lesion volume, number of enhancing lesions on T1 weighted images, and measurements of atrophy (brain parenchymal fraction, atrophy index)

Expanded Disability Status Scale (EDSS), Ambulation Index (AI), and Disease Steps (DS) scores

Detailed description: MS is a chronic inflammatory disease of the central nervous system characterized by focal T cell and macrophage infiltrates that lead to demyelination and loss of neurologic function. Four therapies are currently approved for the treatment of MS. Three of these are approved for the treatment of patients with the relapsing-remitting (RR) form of MS, in which patients have clinical exacerbations followed by partial or complete recovery of function. These treatments are only modestly effective and are associated with significant toxicity, often causing patients to delay therapy for significant lengths of time. Thus, there is a need to find therapies with low toxicities that can be administered early during the disease course with the potential for arresting the disease.

During the pre-treatment phase, patients undergo neurological exams, including the extended disability status scale (EDSS), Ambulation Index (AI), disease steps (DS) scale MS functional composite score, PASAT, 9 hole peg test, and the 25 foot walking time. A 12-lead electrocardiogram (EKG) and chest x-ray are performed. Serum chemistry is assessed as well as electrolyte and thyroid stimulating hormone (TSH) levels. A brain MRI (with and without gadolinium), urinalysis, and urine pregnancy test (for women of reproductive potential) are performed. Blood is collected for mechanistic studies. In the treatment phase, patients are assigned randomly to 1 of 2 study arms:

Arm 1: Copaxone plus placebo. Arm 2: Copaxone plus albuterol. At the treatment visits, blood is collected and neurological exams and a brain MRI are performed. A pregnancy test is administered to women of reproductive potential. Neurological exams are performed every 6 months. MRIs are performed at baseline, Year 1, and Year 2. At the end of the study, patients have a complete physical exam, a neurological exam, and a brain MRI.

Minimum age: 18 Years. Maximum age: 55 Years. Gender(s): Both.

Criteria:

Inclusion Criteria

Patients may be eligible for this study if they:

- Have been diagnosed with RR-MS, within 2 years of diagnosis.

- Are 18-55 years old.

- Have RR-MS with evidence of demyelination on MRI scanning of the brain.

- Have extended disability status scale (EDSS) scores between 0 and 3. 5.

- Have not taken Copaxone or oral myelin.

- Have not had immunomodulating therapy for the past 3 months.

- Have not taken immunosuppressants.

- Have not had steroid treatment 1 month before entry.

- Have no evidence of active infection or cancer.

Exclusion Criteria

Patients may not be eligible for this study if they:

- Have a normal brain MRI.

- Are not willing to practice contraception (applies to women who are able to have

children).

- Are pregnant or breast-feeding.

- Are currently taking any of the following drugs: beta2-adrenergic agonist or

antagonist, diuretics, tricyclic antidepressants, or monoamine oxidase inhibitors.

- Have heart, blood, liver, or kidney problems.

- Have a disease that affects blood clotting or lung function.

- Have abnormalities that relate to the endocrine system.

- Have a history of alcohol or drug abuse within 6 months of enrollment.

- Have been diagnosed with primary progressive MS, in which the disease slowly worsens

without periods of recovery.

Brigham and Women's Hospital/Harvard Medical School, Boston, Massachusetts 02115, United States

Last updated: April 2, 2007