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A Study of Teduglutide in Japanese People With Short Bowel Syndrome
Sponsor: Takeda
Summary
The main aims of this study are to check for side effects from treatment with teduglutide (Revestive) and how well teduglutide controls symptoms of short bowel syndrome. The study sponsor will not be involved in how the participants are treated but will provide instructions on how the clinics will record what happens during the study. During the study, participants with short bowel syndrome will receive an injection of teduglutide just under the skin (subcutaneous) according to their clinic's standard practice. The study doctors will check for side effects from teduglutide for 36 months.
Official title: Special Drug Use Investigation of Revestive Subcutaneous Injection 3.8 mg (All-case Surveillance)
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
120
Start Date
2021-09-01
Completion Date
2026-02-28
Last Updated
2025-05-11
Healthy Volunteers
No
Conditions
Interventions
Teduglutide
Teduglutide 0.05 mg/kg SC injection
Locations (2)
Takeda Selected Site
Tokyo, Tokyo, Japan
Takeda selected site
Tokyo, Tokyo, Japan