Approved

Teduglutide (Gattex): Uses, Evidence, and Side Effects

Molecular formulaC164H252N44O55S
Molecular weight3752.1 g/mol
Registered trials50
PubChem CID16139605
Drug classGLP-2 Analog [EPC]
Brand namesGattex

Mechanism of Action

12.1 Mechanism of Action Teduglutide is an analog of naturally occurring human glucagon-like peptide-2 (GLP-2), a peptide secreted by L-cells of the distal intestine. GLP-2 is known to increase intestinal and portal blood flow and inhibit gastric acid secretion. Teduglutide binds to the glucagon-like peptide-2 receptors located in intestinal subpopulations of enteroendocrine cells, subepithelial myofibroblasts and enteric neurons of the submucosal and myenteric plexus. Activation of these recept

Source: FDA label

Living with short bowel syndrome often means relying on parenteral nutrition just to meet daily needs. Teduglutide is a lab-made version of a gut hormone designed to help reduce that dependence.

Key takeaways

  • Teduglutide is a GLP-2 analog sold under the brand name Gattex.
  • It is approved for adults and children 1 year and older with short bowel syndrome who depend on parenteral support.
  • More than 50 trials have registered teduglutide, including completed phase 3 work in short bowel syndrome.
  • The most reported issues involve weight changes, gastrointestinal symptoms, and vascular device infections.
  • FAERS counts reflect submitted reports, not confirmed rates of occurrence.

What Teduglutide Is

Teduglutide is a synthetic analog of glucagon-like peptide-2 (GLP-2), a hormone normally released by cells in the lower intestine. Natural GLP-2 helps regulate blood flow to the gut and limits stomach acid production. Teduglutide works by binding to GLP-2 receptors found on cells throughout the intestinal lining and surrounding tissue, including enteroendocrine cells, myofibroblasts, and enteric neurons. Activating these receptors supports the intestine's ability to absorb nutrients and fluids.

What Teduglutide Is Approved For

Teduglutide, marketed as Gattex, is approved to treat short bowel syndrome in adults and pediatric patients age 1 and older. It is specifically indicated for those who still need parenteral support to sustain adequate nutrition and hydration. The label does not carry a boxed warning.

What the Evidence Shows

Teduglutide has been studied across more than 50 registered clinical trials. A completed phase 3 trial followed subjects with short bowel syndrome who had finished an earlier teduglutide protocol, evaluating longer-term safety and efficacy. Separately, a completed phase 1 study examined how teduglutide behaves pharmacokinetically in people with moderately impaired liver function compared with healthy participants.

Reported Side Effects

Reports submitted to FAERS for teduglutide most often involve changes in body weight, with both weight decreased and weight increased appearing among the top reactions. Gastrointestinal symptoms are also common, including nausea, abdominal pain, and diarrhoea, each with over a thousand reports. Vascular device infection and dehydration were reported frequently as well, along with issues related to missed doses. These figures represent counts of submitted reports, not confirmed rates or proof that teduglutide caused the reaction.

FAQ

What is teduglutide used for?
Teduglutide, sold as Gattex, is approved to treat short bowel syndrome in adults and children age 1 and older. It is specifically for patients who still depend on parenteral support for nutrition or hydration. It works by mimicking a natural gut hormone called GLP-2.
How does teduglutide work in the body?
Teduglutide is a synthetic version of glucagon-like peptide-2 (GLP-2), a hormone the intestine naturally produces. It binds to GLP-2 receptors on various intestinal cells, which supports blood flow to the gut and helps the intestine absorb nutrients more effectively.
Does teduglutide carry a boxed warning?
No, the current label for teduglutide (Gattex) does not include a boxed warning.
What are the most commonly reported side effects of teduglutide?
The most frequently reported issues in adverse event data include weight changes, nausea, abdominal pain, diarrhoea, vascular device infections, and dehydration. These are counts of submitted reports rather than confirmed side effect rates, so they do not prove teduglutide caused each reaction.
Has teduglutide been studied in clinical trials?
Yes, teduglutide has been registered in more than 50 clinical trials. This includes a completed phase 3 study following short bowel syndrome patients long-term and a phase 1 study looking at how the drug is processed in people with liver impairment.
This page is an editorial information resource. It does not sell, prescribe, or recommend any medication. Content is editorial information, not medical advice. Talk to your doctor before any treatment decision.

Sources: FDA label (Gattex) ClinicalTrials.gov FDA FAERS PubChem

Updated 2026-09-19