Clinical Trial

A Study of Teduglutide in Chinese Adults With Short Bowel Syndrome

Recruiting Phase 3
View on ClinicalTrials.gov →
Summary
The main aim of the study is to assess how well teduglutide works over 24 weeks in Chinese adult participants with short bowel syndrome (SBS) who need parenteral support and to see how much it can reduce the amount of parenteral support and understand how the body absorbs, processes, and gets rid of teduglutide. Participants will receive a daily injection of teduglutide under the skin for 24 weeks. Safety of teduglutide will be checked for 24 weeks after treatment. Participants will be in the study for about 65 weeks.
Trial Details
NCT Number NCT06973304
Lead Sponsor Takeda
Conditions Short Bowel Syndrome
Enrollment 13 participants
Start Date 2025-06-26
Primary Completion 2027-02-10 (estimated)
Study Completion 2027-07-28 (estimated)
Updated on ClinicalTrials.gov 2026-06-24