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Gut & Digestive
Clinical

Teduglutide

Also known as: Gattex, Revestive, ALX-0600

A GLP-2 analog that boosts intestinal absorption in short bowel syndrome. FDA-approved as Gattex since 2012. Prescription medication.

Last updated

Mechanism of Action

Teduglutide is a 33-amino-acid analog of glucagon-like peptide-2 (GLP-2) with a single glycine-for-alanine substitution at position 2 that slows breakdown by dipeptidyl peptidase-4. It activates GLP-2 receptors on enteroendocrine cells and subepithelial myofibroblasts, which release mediators such as IGF-1 and keratinocyte growth factor. The result is increased villus height and crypt depth, greater intestinal blood flow and slower gastric emptying, improving fluid and nutrient absorption in the remaining bowel.

Half-life
~2 hours (subcutaneous, healthy adults); ~1.3 hours in short bowel syndrome
Administration Routes
Subcutaneous
Research Status
Clinical

Reported Benefits

  • Reduces parenteral support volume in adults with short bowel syndrome
  • Allows some patients to reduce days on parenteral support
  • Approved for children 1 year and older with short bowel syndrome dependent on parenteral support

Potential Side Effects

  • Abdominal pain and distension
  • Injection-site reactions
  • Nausea
  • Warnings for accelerated growth of intestinal polyps or neoplasms
  • Intestinal obstruction, gallbladder, bile duct and pancreatic disease, and fluid overload

Common Dosing

Labeled dosing is 0.05 mg/kg by subcutaneous injection once daily, with colonoscopy and polyp surveillance before and during treatment and ongoing adjustment of parenteral support. Dosing is set and supervised by the prescribing clinician.

The dosing information above is aggregated from research literature and anecdotal community reports for educational purposes only. It is not a recommendation, prescription, or medical advice. Peptides are sold as research chemicals only and are not intended for human use.

Contraindications

  • Active gastrointestinal malignancy (label warning: discontinue)
  • Intestinal obstruction
  • Known hypersensitivity to teduglutide

No documented stacking partners for Teduglutide yet.

  • Randomised placebo-controlled trial of teduglutide in reducing parenteral nutrition and/or intravenous fluid requirements in patients with short bowel syndrome

    2011

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  • Teduglutide reduces need for parenteral support among patients with short bowel syndrome with intestinal failure

    2012

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  • Safety and Efficacy of Teduglutide in Pediatric Patients With Intestinal Failure due to Short Bowel Syndrome: A 24-Week, Phase III Study

    2020

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Yes. The FDA approved teduglutide as Gattex in December 2012 for adults with short bowel syndrome who depend on parenteral support, and extended approval to children 1 year and older in 2019. In Europe it is sold as Revestive.

All three are GLP-2 analogs for short bowel syndrome. Teduglutide is the approved, once-daily option; apraglutide and glepaglutide are longer-acting analogs designed for weekly or twice-weekly dosing and are not FDA-approved as of 2026.

PeptideChat is for educational and research purposes only. Nothing on this site constitutes medical advice. Peptides are sold as research chemicals only and are not intended for human use. These statements have not been evaluated by the FDA and are not intended to diagnose, treat, cure, or prevent any disease. PeptideChat is an independent educational resource — not a pharmacy, compounding, or 503A/503B outsourcing facility — and does not sell products or provide medical advice.