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Apraglutide
Healing & Body-Protection

Apraglutide

Ironwood Pharmaceuticals

Apraglutide is a synthetic analog of glucagon-like peptide-2 (GLP-2), a hormone released by the gut that promotes growth and repair of the intestinal lining. It belongs to the same intestinotrophic class as teduglutide, the first approved GLP-2 analog, but is engineered for a longer half-life that supports once-weekly subcutaneous dosing rather than daily injection — a meaningful practical difference for a chronic condition. The target indication is short bowel syndrome with intestinal failure (SBS-IF), a serious condition in which surgical loss of much of the small intestine leaves patients unable to absorb enough nutrients and fluid, often requiring lifelong parenteral (intravenous) nutrition. By stimulating the GLP-2 receptor, apraglutide is intended to increase the absorptive surface and function of the remaining bowel, with the clinical goal of reducing dependence on parenteral support — the amount of intravenous nutrition and fluid a patient needs each week. Apraglutide has advanced through late-stage clinical trials in SBS-IF, including studies in both patients with and without a remaining colon in continuity. As of this writing it is investigational and not yet a broadly approved commercial product across all major markets; regulatory review has been ongoing. This entry is an educational reference on an emerging GLP-2 therapy for a rare, serious condition — not a product available for self-administration, which would in any case be inappropriate given the specialized medical management SBS-IF requires.

Specifications

Origin / ManufacturerSynthetic GLP-2 analog
Active Components
Apraglutide
StorageInvestigational — formulation-dependent (refrigerated expected)
Shelf LifeNot established (investigational)
Form FactorSubcutaneous injection (designed for once-weekly dosing)

Clinical Evidence

Apraglutide has been evaluated in phase 2 and phase 3 clinical programs in short bowel syndrome with intestinal failure, with the primary aim of reducing dependence on parenteral support. Reported trial work includes patients both with and without colon-in-continuity, a clinically important distinction because colonic anatomy influences the response to GLP-2 therapy. As with teduglutide, the class shares characteristic considerations such as the need to monitor for intestinal and other effects of sustained trophic stimulation. Specific trial magnitudes should be read from the primary publications and regulatory documents; this entry summarizes the class rationale and development status rather than asserting precise figures. Apraglutide remains investigational and is managed only within specialist care.

Clinical report reference

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