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Study identifier: NCT06973304 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study of Teduglutide in Chinese Adults With Short Bowel Syndrome

Condition: Short Bowel Syndrome  ·  Sponsor: Takeda

PhasePhase 3
Planned participants13
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Takeda Contact  ·  +1-877-825-3327  ·  medinfoUS@takeda.com

Always discuss trial participation with your own doctor first.

Locations (4)

Beijing Tsinghua Changgung HospitalChangping, Beijing Municipality, ChinaRecruiting
Peking Union Medical College HospitalDongcheng, Beijing Municipality, ChinaRecruiting
Affiliated Jinling Hospital, Medical School of Nanjing UniversityNanjing, Jiangsu, ChinaRecruiting
Zhongshan Hospital, Xiamen UniversitySiming, Xiamen, ChinaCompleted

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Source record: clinicaltrials.gov/study/NCT06973304