Immunotherapy With BHT-3009 Alone or Combined With Atorvastatin in Patients With Multiple Sclerosis

Bayhill Therapeutics

Status and phase

Completed

Phase 1

Conditions

Multiple Sclerosis

Treatments

Biological: BHT-3009-01

Study type

Interventional

Funder types

Industry

Identifiers

NCT00103974

BHT-3009-01

Details and patient eligibility

About

This research study is being done to evaluate the safety of BHT-3009 alone and when combined with atorvastatin (Lipitor) in patients with multiple sclerosis (MS).

Full description

This research study is being done to evaluate the safety of BHT-3009 alone and when combined with atorvastatin (Lipitor) in patients with multiple sclerosis (MS).

Patients with MS are thought to have an immune response that attacks certain proteins in the brain, including myelin basic protein. (Myelin basic protein is a protein that makes up part of the outside layer of nerve cells.) BHT-3009 is an investigational immunotherapy product that is designed to alter the immune response to myelin basic protein and make the response less harmful. BHT-3009 contains the DNA (gene) for myelin basic protein.

Three different doses of BHT-3009 will be tested to determine if there are any differences in safety or effects on immunity. This is the first clinical research study of BHT-3009. Laboratory studies have shown that BHT-3009 and atorvastatin given together alters the immune response to myelin basic protein and makes the response less harmful.

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Definite diagnosis of multiple sclerosis by the McDonald criteria.
Patients with relapsing remitting MS or secondary progressive MS are eligible.
1-5 gadolinium enhancing (Gd+) lesions on the first Screening MRI or relapse in the previous 2 years, or disease worsening in the previous 2 years
Clinically stable for > 1 month before screening evaluation and during screening. Patients who are stable on approved therapy are eligible only if they have intolerable side effects or other medical reasons for discontinuing approved therapy.
Off interferon for > 1 month before screening evaluation.
Off immunosuppressive and cytotoxic therapy (e.g. mitoxantrone, cladrabine) >12 months or > 6 months with CD4 count > 400.
EDSS ≥ 2.5 and < 7.0.
Female or male, age > 18 years.
Able to give informed consent.
WBC and platelets in normal range, hemoglobin > 10.0 g/dl.
AST, ALT, bilirubin < upper limit of normal.
Creatinine < upper limit of normal.
CPK < upper limit of normal.

Exclusion criteria

High-dose corticosteroids (e.g. >500 mg methylprednisolone or equivalent) within previous month.
>5 Gd+ lesions on the first Screening MRI.
Previous vaccine therapy, stem cell transplantation or total lymphoid radiation.
Glatiramer within previous 12 months.
Treatment with any statin in the previous 6 months or elevated cholesterol that requires treatment with a statin.
Pregnant or lactating women.
Unwilling to use a medically acceptable form of birth control.
History of positive test for HIV, hepatitis B or hepatitis C.
Clinically significant ECG abnormalities.
Medical condition or social circumstances that would in the opinion of the investigator prevent full participation in the trial or evaluation of study endpoints.
Implanted pacemakers, defibrillators or other metallic objects on or inside the body that limit performing MRI scans.
History of intolerable adverse events with statin therapy.