Atorvastatin (Lipitor) Therapy in Patients With Clinically Isolated Syndrome (CIS) at Risk for Multiple Sclerosis

PHASE2CompletedINTERVENTIONAL
Enrollment

82

Participants

Timeline

Start Date

May 31, 2005

Primary Completion Date

May 31, 2009

Study Completion Date

May 31, 2009

Conditions
Multiple Sclerosis
Interventions
DRUG

Atorvastatin

atorvastatin at the dose of 80 mg/day. Participants will be allowed to decrease the daily dose to 40 mg/day if the higher dose is not well-tolerated

DRUG

Placebo

tablet form

Trial Locations (14)

10029

Mount Sinai School of Medicine, New York

14203

Jacobs Neurological Institute, Buffalo

14642

University of Rochester, Rochester

21287

Johns Hopkins, Baltimore

44195

Cleveland Clinic Foundation, Cleveland

63110

Washington University Multiple Sclerosis Center, St Louis

75930

University of Texas Southwestern Medical Center, Dallas

85013

Barrow Neurological Institute, Phoenix

90033

Keck School of Medicine, Los Angeles

94143

University of California, San Francisco, San Francisco

97201

Oregon Health Sciences University, Portland

98111

Virginia Mason MS Center, Seattle

06510

Yale MS Research Center, New Haven

H3A 2B4

Montreal Neurological Institute, Montreal

All Listed Sponsors
collaborator

Immune Tolerance Network (ITN)

NETWORK

lead

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

NCT00094172 - Atorvastatin (Lipitor) Therapy in Patients With Clinically Isolated Syndrome (CIS) at Risk for Multiple Sclerosis | Biotech Hunter | Biotech Hunter