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Teduglutide

✓ FDA Approved
Teduglutide
Also known as: Gattex, Revestive, ALX-0600, GLP-2 Analog
Brand names: Gattex, Revestive
Page last reviewed

Quick Summary

Teduglutide (Gattex/Revestive) is a synthetic analog of glucagon-like peptide-2 (GLP-2), an endogenous intestinal growth factor produced by L-cells of the distal small intestine and colon. FDA-approved in 2012 for short bowel syndrome (SBS) in adults, it promotes intestinal adaptation by stimulating mucosal growth, increasing villus height, and reducing parenteral nutrition dependence.

GI Peptide / Trophic Factor FDA Approved
Teduglutide (Gattex/Revestive) is a synthetic analog of glucagon-like peptide-2 (GLP-2), an endogenous intestinal growth factor produced by L-cells of the distal small intestine and colon. FDA-approved in 2012 for short bowel syndrome (SBS) in adults, it promotes intestinal adaptation by stimulating mucosal growth, increasing villus height, and reducing parenteral nutrition dependence.
Storage Stability
Lyophilized
6–12 months (2–8°C)
Reconstituted
~30 days (2–8°C)
Room temp
Avoid

Mechanism of Action

GLP-2 Receptor Activation

Teduglutide binds the GLP-2 receptor expressed on intestinal enteroendocrine cells and subepithelial myofibroblasts. Receptor activation triggers downstream signaling through adenylate cyclase and PKA, promoting enterocyte proliferation, reducing apoptosis, and increasing crypt depth and villus height. These trophic effects enhance the absorptive surface area of the remaining intestine.

Intestinal Blood Flow and Barrier Function

Beyond epithelial growth, teduglutide increases intestinal blood flow and strengthens tight junction integrity. Improved barrier function reduces bacterial translocation and intestinal permeability. Enhanced mesenteric blood flow improves nutrient delivery and oxygen supply to intestinal epithelium, supporting adaptation.


Research Summary

Short Bowel Syndrome

FDA Approved

Phase 3 trials (STEPS) demonstrated that teduglutide 0.05 mg/kg/day significantly reduced parenteral nutrition requirements versus placebo over 24 weeks in SBS patients. Approximately 63% of teduglutide patients achieved a 20% reduction in parenteral nutrition versus 30% on placebo. Several patients achieved complete parenteral nutrition independence.

Pediatric SBS

FDA Approved

Teduglutide received approval for pediatric SBS patients aged 1 year and older based on the STEPS-2 trial. Pediatric patients showed similar reductions in parenteral nutrition requirements. Structural adaptations including increased villus height and crypt depth were confirmed on biopsy.


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Research Protocols

GoalDoseFrequencyRoute
Adult SBS treatment0.05 mg/kgOnce dailySubcutaneous injection
Pediatric SBS (1+ year)0.05 mg/kgOnce dailySubcutaneous injection

Requires colonoscopy before initiation and annually. Monitor for polyp development.


Interactions

Moderate
Oral medications
Increased intestinal absorption may alter bioavailability of orally administered drugs
Monitor
Benzodiazepines
Enhanced absorption may increase sedative effects; dose adjustment may be needed

Safety Profile

Most common adverse effects are abdominal pain, nausea, injection site reactions, and fluid retention. The trophic effect raises concern for accelerated neoplastic growth; colonoscopy is required before initiation and annually. Teduglutide is contraindicated in patients with active gastrointestinal malignancy. Fluid retention and cardiac decompensation have been reported in heart failure patients.


References

  • [1]Jeppesen PB et al. (2012). Teduglutide reduces need for parenteral support among patients with short bowel syndrome with intestinal failure. Gastroenterology, 143(6), 1473-1481.
  • [2]Schwartz LK et al. (2016). Long-term teduglutide for the treatment of patients with intestinal failure associated with short bowel syndrome. Clinical and Translational Gastroenterology, 7(2), e142.
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Verified Scientific Data Last audited:
Data Sources & External References
Source: peer-reviewed literature  ·  Domain: ascendpeptide.org

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