A Study to Evaluate Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of Natalizumab (BG00002) Administered Subcutaneously to Japanese Participants With Relapsing-Remitting Multiple Sclerosis

PHASE3TerminatedINTERVENTIONAL
Enrollment

21

Participants

Timeline

Start Date

April 26, 2022

Primary Completion Date

January 18, 2024

Study Completion Date

May 27, 2024

Conditions
Multiple Sclerosis, Relapsing-Remitting
Interventions
DRUG

Natalizumab

Administered as specified in the treatment arm

Trial Locations (12)

113-8431

Juntendo University Hospital, Bunkyō City

260-8677

Chiba University Hospital, Chiba

216-8511

St.Marianna University Hospital, Kawasaki-shi

187-8551

National Center of Neurology and Psychiatry, Kodaira-shi

570-8507

Kansai Medical University Medical Center, Moriguchi-shi

145-0065

Tokyo Metropolitan Hospital Organization Tokyo Metropolitan Ebara Hospital, Ōta-ku

252-0375

The Kitasato Institute Kitasato University Hospital, Sagamihara-shi

063-0005

National Hospital Organization Hokkaido Medical Center, Sapporo

983-8512

Tohoku Medical and Pharmaceutical University Hospital, Sendai

565-0871

Osaka University Hospital, Suita-shi

305-8576

University of Tsukuba Hospital, Tsukuba

276-8524

Tokyo Women's Medical University Yachiyo Medical Center, Yachiyo-shi

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Biogen

INDUSTRY