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Teduglutide

Teduglutide is the GLP-2 analogue in GATTEX, used in short bowel syndrome when patients depend on intravenous nutrition or fluids.

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At a glance

Evidence stage
Approved use
Regulatory status
GATTEX is US-approved for adults and children aged 1 year and older with short bowel syndrome who depend on parenteral support.
Research context
Teduglutide is the GLP-2 analogue in GATTEX, used in short bowel syndrome when patients depend on intravenous nutrition or fluids.

What this is

  • Teduglutide is the GLP-2 analogue in GATTEX, used in short bowel syndrome when patients depend on intravenous nutrition or fluids.

What this isn't

  • A recommendation to use, prepare, combine, or administer a product
  • Evidence that a related molecule or a differently formulated product has the same effects

Teduglutide is the GLP-2 analogue in GATTEX, used in short bowel syndrome when patients depend on intravenous nutrition or fluids.

Teduglutide activates GLP-2 receptors involved in intestinal adaptation, promoting pathways that support the absorptive lining and fluid uptake. This aims to help the remaining bowel absorb more in short bowel syndrome. It is a different receptor system and clinical purpose from GLP-1 medicines used in diabetes; the similar names should not obscure that distinction. Product label.

Evidence limits

How to read the evidence

Trial participants had established intestinal failure and structured assessment of fluid and nutritional requirements. This evidence does not support use for nonspecific bloating, ordinary gastrointestinal discomfort, or general intestinal wellness. Responses differ with remaining anatomy and clinical circumstances, and reduction of support must be distinguished from permanent recovery after treatment stops. Product-specific scope.

Sources appraised 2026-10-28. Educational information; not medical advice. Study findings apply to the populations, preparations and outcomes described.

External sources and citations

  1. Teduglutide — product label (DailyMed)
  2. Teduglutide STEPS randomized trial
  3. FDA application NDA203441 — approval and marketing records

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