Prescription Drug Safety and Effectiveness in Multiple Sclerosis

CompletedOBSERVATIONAL
Enrollment

35,000

Participants

Timeline

Start Date

January 1, 1996

Primary Completion Date

March 31, 2018

Study Completion Date

March 31, 2018

Conditions
Multiple Sclerosis
Interventions
DRUG

Exposure to one or more disease-modifying drug(s)(DMDs) used to treat MS

Individuals with MS exposed to one or more DMDs (beta-interferon, glatiramer acetate, natalizumab, fingolimod, dimethyl fumarate, teriflunomide, alemtuzumab, daclizumab or ocrelizumab; regardless of dose, frequency or duration of treatment) between 1st January 1996 and 31st March 2018 in five Canadian provinces.

All Listed Sponsors
collaborator

University of Manitoba

OTHER

collaborator

Dalhousie University

OTHER

collaborator

University of Saskatchewan

OTHER

collaborator

Alberta Health services

OTHER

collaborator

University of Alberta

OTHER

lead

University of British Columbia

OTHER

NCT04472975 - Prescription Drug Safety and Effectiveness in Multiple Sclerosis | Biotech Hunter | Biotech Hunter