Current partner codePEPTIDESDE
NCT07319832·Not applicable·OBSERVATIONAL

A Study of Teduglutide in Chinese Children and Teenagers With Short Bowel Syndrome

Status

Recruiting

Phase

Not applicable

Enrollment

12

Locations

4

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

Short Bowel Syndrome (SBS) is a rare condition that happens when a large part of the bowel (also called intestine) is missing or has been removed because of illness or surgery. In children, SBS means that the intestine cannot absorb enough food, water and important part of food the body needs (called nutrients) because a big part of it has been removed, bypassed or did not develop normally at birth and the children need support through a vein (parenteral support or PS) for more than 42 days to stay healthy and keep their energy. SBS in children is defined mainly by how well the intestine works and how long the children need this support, not just by how long the intestine is. The main aim of the study is to learn how well the teduglutide works in children and teenagers with SBS and who need PS. Another aim is to find out how well teduglutide works for participants to lower the amount of PS needed. Also, the study wants to learn more about how safe teduglutide is in children and teenagers with SBS who need PS. The study will review data already existing in the medical records of participants as well as collect new data during the study.

Interventions

Treatment arms and agents.

OTHER

No Intervention

No Intervention

Timeline

From registration to results.

  1. First posted

    Jan 6, 2026

  2. Study start

    Mar 5, 2026

  3. Primary completion

    Apr 30, 2027

  4. Study completion

    Sep 30, 2027

  5. Results posted

    Not reported

  6. Registry updated

    Mar 13, 2026

Outcomes

What the study measures.

Primary outcomes

Percentage of Participants Who Achieve at Least a 20% Reduction from Baseline in Weekly Parenteral Support (PS) Volume at Week 24

Time frame · At Week 24

Percentage of participants who achieve at least a 20 percent (%) reduction from baseline in weekly PS volume at Week 24 will be reported.

Secondary outcomes

Number of Participants Able to Completely Wean off PS Support at Week 24

Time frame · At Week 24

Number of participants who are able to completely wean off PS support at Week 24 will be reported.

Absolute Change from Baseline in PN/Intravenous (IV) Support Volume

Time frame · Baseline up to Week 24

Absolute change from baseline in PN/IV support volume will be reported.

Percent Change From Baseline in PN/IV Support Volume

Time frame · Baseline up to Week 24

Percent change from baseline in PN/IV support volume will be reported.

Absolute Change From Baseline in PN/IV Support Calories

Time frame · Baseline up to Week 24

Absolute change from baseline in PN/IV support calories will be reported.

Percent Change From Baseline in PN/IV Support Calories

Time frame · Baseline up to Week 24

Percent change from baseline in PN/IV support calories will be reported.

Absolute Change From Baseline in Plasma Citrulline

Time frame · Baseline, Week 24

Absolute change from baseline in plasma citrulline will be reported.

Percent Change From Baseline in Plasma Citrulline

Time frame · Baseline, Week 24

Percent change from baseline in plasma citrulline will be reported.

Absolute Change From Baseline in Enteral Nutrition (EN) Support Volume

Time frame · Baseline up to Week 24

Absolute change from baseline in EN support volume will be reported.

Percent Change From Baseline in EN Support Volume

Time frame · Baseline up to Week 24

Percent change from baseline in EN support volume will be reported.

Absolute Change From Baseline in EN Support Calories

Time frame · Baseline up to Week 24

Absolute change from baseline in EN support calories will be reported.

Eligibility

Who can take part.

Minimum age
1 Year
Maximum age
17 Years
Sex
ALL
Healthy volunteers
No

Inclusion criteria * Children and adolescents greater than or equal to (\>=)1 through 17 years of age at Day 1 (D1). * Documented diagnosis of SBS. * Received or plan to receive Teduglutide treatment for a minimum of 24 weeks. * Stable PN/IV support, defined as inability to significantly reduce PN/IV support, usually associated with minimal or no advance in enteral feeds (i.e., 10% or less change in PN or advance in feeds) for at least 3 months prior to D1, as assessed by the investigator. Transient instability for events such as interruption of central access or treatment for sepsis is allowed if the PN/IV support returns to within 10% of baseline prior to the event. * Informed consent obtained from the patient aged 8 to 17 years and their guardians, while informed consent from the guardians for participants under 8 years old, unless waived by the Institution's Ethics Committee. Exclusion criteria * Participants who are not expected to be able to advance oral or tube feeding regimens. * Serial Transverse Enteroplasty (STEP) or any other bowel lengthening procedure performed within 3 months prior to baseline. * Known clinically significant untreated intestinal obstruction contributing to feeding intolerance and inability to reduce PS. * Evidence of clinically significant obstruction on upper GI series done within 6 months prior to baseline. * Previous use of octreotide or Dipeptidyl peptidase-4 (DPP-4) inhibitors within 3 months prior to baseline. * Signs of active, severe, or unstable clinically significant hepatic impairment during the screening or baseline period, indicative by any of the following laboratory test results: 1. Total Bilirubin Level (TBL) \>= 2 × upper limit of normal (ULN) 2. Aspartate Aminotransferase (AST) \>=7 × ULN 3. Alanine Aminotransferase (ALT) \>=7 × ULN For Participants with Gilbert's disease: 4. Indirect (unconjugated) bilirubin \>=2 × ULN * Signs of known continuous active or unstable, clinically significant renal dysfunction shown by results of an estimated glomerular filtration rate (eGFR) below 50 millilitres per minutes per 1.73 meter square (mL/min/1.73 m\^2). * Known hypersensitivity of the active substance or excipient of teduglutide. * Body weight less than (\<) 10 kg at baseline. * Previous use of teduglutide or native/synthetic Glucagon-like Peptide-2 (GLP-2). * Previous use of GLP-1 analog or human growth hormone within 3 months prior to baseline. * Any condition, disease, illness, or circumstance that in the investigator's opinion puts the patient at any undue risk, prevents completion of the study, or interferes with analysis of the study results.

Study locations

4 registered sites.

China. Showing up to 24 locations stored in the fast local snapshot.

Guangzhou Women And Children's Medical Center

Guangzhou, Guangdong, China

Shanghai Children's Hospital

Shanghai, Shanghai Municipality, China

Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

Shanghai, Shanghai Municipality, China

Children's Hospital Zhejiang University School of Medicine

Hangzhou, Zhejiang, China

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Teduglutide.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.