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Teduglutide

Also referenced as: Gattex

A GLP-2 analogue used in short bowel syndrome with dependence on parenteral support.

Evidence grade
AStrong Clinical Evidence

Strong Clinical Evidence

Regulatory status
FDA Approved for Specific Indication

Gattex is FDA-approved for parenteral-support-dependent short bowel syndrome in adults and children aged 1 year and older.

Human data
Yes

Registered clinical trials exist

Last reviewed
October 27, 2026

Overview

A GLP-2 analogue used in short bowel syndrome with dependence on parenteral support.

Gattex is FDA-approved for parenteral-support-dependent short bowel syndrome in adults and children aged 1 year and older.

Benefits apply to short bowel syndrome, not ordinary digestive discomfort, gut optimization or weight-loss goals.

Why It's Being Studied

  • Short bowel syndrome
  • Intestinal absorption
  • Parenteral-support reduction

Mechanism of Action

In plain language

GLP-2 receptor signalling enhances intestinal absorptive capacity rather than acting as a GLP-1 appetite suppressant.

Technical detail

GLP-2 receptor signalling enhances intestinal absorptive capacity rather than acting as a GLP-1 appetite suppressant. Benefits apply to short bowel syndrome, not ordinary digestive discomfort, gut optimization or weight-loss goals.

Interactive diagram

From molecular target to clinical evidence

Tap each stage to see what happens.

Molecular target: Identify the receptor, enzyme, microbial membrane or binding site for the particular compound.

Background: Clinical Peptide Medicines

Clinical peptide medicines include endocrine treatments, antimicrobial drugs, receptor blockers and targeted diagnostic or cancer agents. They do not share one mechanism or one set of indications.

An approval belongs to a specific medicine and indication. A diagnostic tracer, an antibiotic and a hormone are not interchangeable wellness products; read each profile's own mechanism and prescribing source.

Research Areas & Routes Studied

Areas studied
  • Short bowel syndrome
  • Intestinal absorption
  • Parenteral-support reduction
Routes used in research
  • Subcutaneous approved medicine

Evidence Summary

Randomized studies demonstrate reduced parenteral-support requirements, with some participants achieving independence.

Evidence pyramid

Higher tiers carry more weight. Filled tiers have evidence for Teduglutide; tap to read it.

Human clinical trials
  • Randomized studies demonstrate reduced parenteral-support requirements, with some participants achieving independence.
Source breakdown

1 cited sources.

  • Prescribing label1

Human clinical evidence

  • Randomized studies demonstrate reduced parenteral-support requirements, with some participants achieving independence.

Reported Adverse Events in Research

  • Intestinal growth can accelerate neoplastic processes; polyps, obstruction, biliary or pancreatic disease and fluid overload require surveillance.

Limitations of Current Evidence

  • Benefits apply to short bowel syndrome, not ordinary digestive discomfort, gut optimization or weight-loss goals.
  • Findings apply to the product, route and population studied; they do not establish benefits or safety for unrelated wellness uses or research-vial products.

How to Read This Research

Questions to ask
  • Is this a single molecule or a family of medicines?
  • Is the use diagnostic, therapeutic or investigational?
  • Does the quoted outcome match the exact product, formulation and population?
Reading tips
  • Use the compound-specific mechanism above; this diagram describes drug development, not a shared biological pathway.
  • Historical approval, present availability and off-label use are distinct questions.
  • For radiopharmaceuticals and hospital medicines, specialist handling is part of the treatment context.
Indication
The condition and population for which a medicine is approved.
Antagonist
A compound that blocks activity at a receptor.
Radiopharmaceutical
A medicine containing a radioactive isotope for imaging or treatment.

Compare With Other Compounds

Compare side by side
TeduglutideTrofinetide
Evidence gradeA — Strong Clinical EvidenceB — Moderate Human Evidence
Regulatory statusFDA Approved for Specific IndicationFDA Approved for Specific Indication
Human dataYesYes
Clinical trialsRegistered trials existRegistered trials exist
Research routesSubcutaneous approved medicineOral approved medicine
Cited sources12
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Frequently Asked Questions

Research References

  • Prescribing label

    Teduglutide — prescribing label

    View Source
This page is an educational research summary. It is not medical advice, does not recommend human use, and does not provide individualised dosing. Many compounds discussed here are research use only and are not approved medicines.