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

Multiple Sclerosis Clinical Trial

Official title:

A Phase I Trial of Immunotherapy With BHT-3009 Alone or Combined With Atorvastatin in Patients With Multiple Sclerosis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00103974
• Other study ID #: BHT-3009-01
• Status: Completed
• Phase: Phase 1
• First received: February 17, 2005
• Last updated: April 4, 2008
• Start date: July 2004
• Est. completion date: March 2007

Study information

• Verified date: February 2008
• Source: Bayhill Therapeutics
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

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).

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: March 2007
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

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.

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Multiple Sclerosis
• Sclerosis

Intervention

Biological:
• BHT-3009-01

Locations

Country	Name	City	State
Canada	Montreal Neurological Institute, Clinical Research Unit and MS clinic	Montreal	Quebec
Canada	University of British Columbia, MS Research	Vancouver	British Columbia
United States	USC, LAC & USC Medical Center	Los Angeles	California
United States	Barrow Neurology Clinics	Phoenix	Arizona

Sponsors (1)

Lead Sponsor	Collaborator
Bayhill Therapeutics

Countries where clinical trial is conducted

United States,  Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Evaluate safety of BHT-3009 alone and when combined with atorvastatin in patients with multiple sclerosis.
Primary	Determine dose of BHT-3009 and regimen for phase II testing.
Secondary	Describe effect of treatment on antibody and T cell responses to myelin basic protein (MBP).
Secondary	Describe clinical course of treated patients.
Secondary	Explore biomarkers of MS activity

External Links

•   Click here for more information about this study: BHT-3009-01