A Study of Suboptimally Controlled Participants Previously Taking Injectable DMDs for RMS (CLICK-MS)

CompletedOBSERVATIONAL
Enrollment

100

Participants

Timeline

Start Date

May 21, 2019

Primary Completion Date

March 30, 2024

Study Completion Date

March 30, 2024

Conditions
Multiple Sclerosis
Interventions
DRUG

Cladribine

Participants received cladribine tablets as per investigator discretion and as per United States approved label: 3.5 milligram/kilogram (mg/kg) body weight over 2 years, administered as 1 treatment course of 1.75 mg/kg per year.

Trial Locations (18)

23229

Neurological Associates, Richmond

23456

Sentara Ambulatory Care Center, Virginia Beach

24073

Blacksburg Neurology, PC, Christiansburg

27405

Guilford Neurologic Associates, Greensboro

46804

Fort Wayne Neurological Center, Fort Wayne

48202

Henry Ford Health System, Detroit

48867

Memorial Healthcare, Owosso

55422

Minneapolis Clinic of Neurology - Neurology, Minneapolis

62702

Prairie Education & Research, Springfield

66212

College Park Family Care Center, Overland Park

72205

University of Arkansas for Medical Sciences, Little Rock

78258

Neurology Center of San Antonio, San Antonio

80113

HCA Research Institute, Englewood

80528

Advanced Neurosciences Research, Fort Collins

98034

MS Center of Evergreen, Kirkland

02481

The Elliot Lewis Center for Multiple Sclerosis Care, LLC, Wellesley

01655

UMASS - Neurology, Worcester

23298-0211

VCU Medical Center - Pediatric Neurology, Richmond

All Listed Sponsors
collaborator

Merck KGaA, Darmstadt, Germany

INDUSTRY

lead

EMD Serono Research & Development Institute, Inc.

INDUSTRY

NCT03933215 - A Study of Suboptimally Controlled Participants Previously Taking Injectable DMDs for RMS (CLICK-MS) | Biotech Hunter | Biotech Hunter