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Teduglutide

Aliases: Gattex · Revestive

Last verified: 2026-09-23

Approved drugStrong evidencePeptidesMedium interest

The short version

A GLP-2 analogue — approved for short-bowel syndrome: increases absorption and reduces parenteral-nutrition dependence.

Identity & type

Molecular type
analog
Origin
A GLP-2 analogue — approved for short-bowel syndrome: increases absorption and reduces parenteral-nutrition dependence.

Mechanism of action

GLP-2R agonism → villus/crypt growth, improved gut barrier and absorption.

Dosing & routes

Official / clinical context

Approved drug — indications, dosing and warnings are defined by the official label. 0.05 mg/kg SC daily.

Regulator-approved labeling and published study designs — never a recommendation.

Community-reported practice

0.05 mg/kg SC daily. Gattex: in short-bowel syndrome significantly reduces parenteral-nutrition needs — patients gain independence from infusions.

Unverified self-reports. Not medical advice. Not endorsement.

Expected effects (community)

Gattex: in short-bowel syndrome significantly reduces parenteral-nutrition needs — patients gain independence from infusions.

Protocol — official vs community

Official / label

Gattex/Revestive, for short-bowel syndrome with dependence on parenteral nutrition (adults; pediatric approval exists in some markets): 0.05 mg/kg SC once daily.

Duration: Chronic. STEPS program: ~63% of patients achieved ≥20% reduction in parenteral-nutrition volume, and some weaned off entirely.

GLP-2R agonism regrows villus mass and improves absorption. Colonoscopy before starting and periodically thereafter per label, because trophic gut signaling could accelerate occult neoplasia.

Community (anecdotal)

No meaningful community use — specialty intestinal-rehabilitation drug with REMS-style distribution in the US.

Cycle:
—
Break:
—

Off-label IBD interest exists in the literature but no self-directed protocol has formed around it.

Human evidence

STEPS program: 63% of patients cut PN ≥20%; off-label interest in IBD.

Preclinical evidence

The preclinical phase was completed and submitted to regulators as part of registration; pharmacology and toxicology details are part of the official label.

Known risks

  • Abdominal pain, stoma complications; risk of accelerating polyp/tumor growth (colonoscopy monitoring).characterized

Teal: characterized in clinical/labeling contexts. Amber: theoretical or reported outside controlled settings.

Unknowns & evidence gaps

  • Real-world data outside controlled trials

Frequently asked questions

References