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A Study of Teduglutide in Japanese People With Short Bowel Syndrome

StatusCompleted
PhaseNot specified
SponsorTakeda
Started2021-09-01
View on ClinicalTrials.gov ↗
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.

Amendment history 1 change detected by DataLookout

2026-08-08
notable
Trial completed
Trial Details
NCT Number NCT05023382
Lead Sponsor Takeda
Conditions Short Bowel Syndrome
Enrollment 250 participants
Start Date 2021-09-01
Primary Completion 2026-07-31 (estimated)
Study Completion 2026-07-31 (estimated)
Updated on ClinicalTrials.gov 2026-08-07