A Study of Guselkumab in Participants With Moderately to Severely Active Crohn's Disease

PHASE3CompletedINTERVENTIONAL
Enrollment

38

Participants

Timeline

Start Date

June 10, 2020

Primary Completion Date

February 29, 2024

Study Completion Date

September 12, 2025

Conditions
Crohns Disease
Interventions
DRUG

Guselkumab

Guselkumab will be administered intravenously for the first 3 doses and then subcutaneously for the subsequent doses.

Trial Locations (25)

5960042

Kishiwada Tokushukai Hospital, Kishiwada

9308550

Toyama Prefectural Central Hospital, Toyama

9810914

Sendai Kosei Hospital, Sendai Miyagi

270-1168

KOKIKAI Tokatsu Tsujinaka Hospital, Abiko

113 8519

Institute of Science Tokyo Hospital, Bunkyō City

317-0077

Hitachi General Hospital, Hitachi

078 8510

Asahikawa Medical University Hospital, Hokkaido

247-0056

Ofuna Chuo Hospital, Kamakura

860-8556

Kumamoto University Hospital, Kumamoto

861-8520

Japanese Red Cross Kumamoto Hospital, Kumamoto

181-8611

Kyorin University Hospital, Mitaka

635-0022

Kenseikai Dongo Hospital, Nara

663 8501

Hyogo Medical University Hospital, Nishinomiya Shi

700-8558

Okayama University Hospital, Okayama

870 0823

Ishida Clinic of IBD and Gastroenterology, Ōita

849-8501

Saga University Hospital, Saga

252-0375

Kitasato University Hospital, Sagamihara

350 8550

Saitama Medical Center, Saitama

004-0041

Sapporo Tokushukai Hospital, Sapporo

329-0498

Jichi Medical University Hospital, Shimotsuke

162-8655

National Center for Global Health and Medicine, Shinjuku

162-8666

Tokyo Women's Medical University Hospital, Shinjuku-ku

130 8575

Tokyo Metropolitan Bokutoh Hospital, Sumida Ku

569-8686

Osaka Medical and Pharmaceutical University Hospital, Takatsuki

441-8570

National Hospital Organization Toyohashi Medical Center, Toyohashi

Sponsors
All Listed Sponsors
lead

Janssen Pharmaceutical K.K.

INDUSTRY

NCT04397263 - A Study of Guselkumab in Participants With Moderately to Severely Active Crohn's Disease | Biotech Hunter | Biotech Hunter