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A Study of Guselkumab in Participants With Moderately to Severely Active Crohn's Disease
Sponsor: Janssen Pharmaceutical K.K.
Summary
The purpose of this study is to evaluate the safety of Guselkumab in participants with Crohn's disease.
Official title: A Phase 3, Open-label, Multicenter Study to Evaluate the Safety and Efficacy of Guselkumab in Participants With Moderately to Severely Active Crohn's Disease
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
38
Start Date
2020-06-10
Completion Date
2025-09-12
Last Updated
2026-10-07
Healthy Volunteers
No
Conditions
Interventions
Guselkumab
Guselkumab will be administered intravenously for the first 3 doses and then subcutaneously for the subsequent doses.
Locations (25)
KOKIKAI Tokatsu Tsujinaka Hospital
Abiko, Japan
Institute of Science Tokyo Hospital
Bunkyō City, Japan
Hitachi General Hospital
Hitachi, Japan
Asahikawa Medical University Hospital
Hokkaido, Japan
Ofuna Chuo Hospital
Kamakura, Japan
Kishiwada Tokushukai Hospital
Kishiwada, Japan
Kumamoto University Hospital
Kumamoto, Japan
Japanese Red Cross Kumamoto Hospital
Kumamoto, Japan
Kyorin University Hospital
Mitaka, Japan
Kenseikai Dongo Hospital
Nara, Japan
Hyogo Medical University Hospital
Nishinomiya Shi, Japan
Okayama University Hospital
Okayama, Japan
Ishida Clinic of IBD and Gastroenterology
Ōita, Japan
Saga University Hospital
Saga, Japan
Kitasato University Hospital
Sagamihara, Japan
Saitama Medical Center
Saitama, Japan
Sapporo Tokushukai Hospital
Sapporo, Japan
Sendai Kosei Hospital
Sendai Miyagi, Japan
Jichi Medical University Hospital
Shimotsuke, Japan
National Center for Global Health and Medicine
Shinjuku- Ku, Japan
Tokyo Women's Medical University Hospital
Shinjuku-ku, Japan
Tokyo Metropolitan Bokutoh Hospital
Sumida Ku, Japan
Osaka Medical and Pharmaceutical University Hospital
Takatsuki, Japan
Toyama Prefectural Central Hospital
Toyama, Japan
National Hospital Organization Toyohashi Medical Center
Toyohashi, Japan