A Study To Investigate The Pharmacokinetics, Safety, And Tolerability Of Subcutaneous Ocrelizumab Administration In Participants With Multiple Sclerosis

PHASE1CompletedINTERVENTIONAL
Enrollment

134

Participants

Timeline

Start Date

August 12, 2019

Primary Completion Date

June 3, 2025

Study Completion Date

June 3, 2025

Conditions
Multiple Sclerosis (MS)
Interventions
DRUG

Ocrelizumab

Administered by subcutaneous Injection

DRUG

Ocrelizumab

Administered by Intravenous (IV) Injection

DRUG

rHuPH20

Administered in a 2-mL glass vial as a sterile, single-use, injectable liquid to be manually mixed with SC ocrelizumab

Trial Locations (18)

10032

Columbia University Medical Center, New York

15213

University of Pittsburgh, Pittsburgh

19104

University of Pennsylvania, Philadelphia

20007

Georgetown University Medical Center, Washington D.C.

21287

John Hopkins University School of Medicine, Baltimore

38018

Neurology Clinic PC, Cordova

44195

Cleveland Clinic Mellen Center, Cleveland

45417

UC Health Neurology, Dayton

48201

Wayne State University, Detroit

48867

Memorial Healthcare Institute for Neurosciences and Multiple Sclerosis, Owosso

63110

Washington Univ School of Med, St Louis

70121

Ochsner Clinic Foundation, New Orleans

71301

The NeuroMedical Clinic of Central Louisiana, Alexandria

77030

University of Texas at Houston, Houston

80045

University of Colorado, Aurora

98122

Swedish Neuroscience Institute, Seattle

98405

MultiCare Health System Institute for Research and Innovation, Tacoma

01655

University of Massachusetts Medical School, Worcester

All Listed Sponsors
lead

Hoffmann-La Roche

INDUSTRY

NCT03972306 - A Study To Investigate The Pharmacokinetics, Safety, And Tolerability Of Subcutaneous Ocrelizumab Administration In Participants With Multiple Sclerosis | Biotech Hunter | Biotech Hunter