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Teduglutide (Gattex)

Teduglutide is a recombinant analog of glucagon-like peptide-2 (GLP-2) with a Gly2 substitution that resists DPP-4 degradation, extending its activity relative to native GLP-2. It acts on GLP-2 receptors in the gut to increase villus height, crypt depth, and mucosal blood flow, which enhances fluid and nutrient absorption. This reduces the volume of parenteral support needed in short bowel syndrome. Because it is trophic to intestinal tissue, the label advises surveillance for neoplasia.

Molecular Profile
linear
33 AA Sequence
Evidence grade (Strong): Multiple randomized controlled trials in humans. This grade reflects the overall quality of available research on this compound and does not constitute a clinical recommendation.
CAS
197922-42-2
Formula
33-aa GLP-2 analog (Gly2 substitution)
Chain length
33 aa
Sequence
33-amino-acid GLP-2 (Gly2) analog
Onset and duration

Metabolic effects build over days to weeks of consistent use.

Storage and reconstitution

Store the lyophilized powder refrigerated (2 to 8 C), or frozen for long-term storage, protected from light. After reconstitution with bacteriostatic water, keep refrigerated and use within about 4 weeks.

Clinical Evidence

What the literature says

Scientific Overview

According to PubMed, a population-PK and exposure-response analysis across 219 patients found teduglutide 0.05 mg/kg daily produced a maximum reduction in parenteral support of about 5.76 L/week, with an elimination half-life near 1.47 hours in short bowel syndrome (Marier JF et al., Clin Transl Sci 2021). It is FDA-approved (Gattex/Revestive) and well characterized by its label.

Pharmacokinetics

Half-life (t½)
1.5 h
Approximate plasma half-life
Routes
Subcutaneous

Last reviewed: 2026-06-15

Research Guide

How users approach this compound

The following reflects patterns observed in research literature and community protocols. This is not medical advice and does not constitute a clinical recommendation.

Typical Dose Range Observed

0.05 mg
0.05 mg/kg once daily subcutaneous

Research Protocols

Common Dosages

Short bowel syndrome (label)

0.05 mg/kg
Once daily SC

Per FDA labeling; rotate injection sites

Dosages listed are common research protocols found in peer-reviewed literature and clinical trials. Individual results and requirements may vary significantly in a research context.

Reported Uses

  • Short bowel syndrome dependent on parenteral support (approved)
  • Investigational interest in other malabsorptive states

Key Research Benefits

  • Increases intestinal villus height and crypt depth, improving absorption
  • Reduces dependence on parenteral nutrition and IV fluids in short bowel syndrome
  • Approved for both adult and pediatric short bowel syndrome

Potential Side Effects

Abdominal pain
Nausea
Injection-site reactions
Fluid overload
Stoma-related complications

Considerations and Cautions

  • Active or suspected gastrointestinal malignancy
  • History of GI cancer within the past 5 years (label caution)
  • Hypersensitivity to teduglutide

Labs to monitor

Educational context only, not a testing mandate. Any bloodwork decisions belong with your clinician.

Dose Calculator

Peptide Reconstitution Calculator

mg

Total amount of peptide in the vial.

mL

Volume of water used to mix.

mcg

Draw to this mark

10 Units

or 0.10 mL on a U-100 syringe

Concentration:2.50 mg/mL
Peptide per Unit:25.00 mcg/unit
*Always double-check your calculations. This tool is for educational purposes only.

Teduglutide (Gattex) by goal

Read Teduglutide (Gattex)'s profile filtered through specific research goals.

Related Tools

Not medical advice

Information on DoseVault is for educational purposes only and is not a substitute for medical advice, diagnosis, or treatment from a qualified healthcare provider.