Skip to content
New: free dose calculator with 14 peptide presets. No signup.
Peptides Academy
Ecnoglutide
GLP-1 Analogs

Ecnoglutide

Research-Grade

Ecnoglutide (development code XW003) is a long-acting GLP-1 receptor agonist notable for its biased-agonism design. GLP-1 receptor activation can signal through multiple downstream routes, principally the cAMP/PKA second-messenger pathway and beta-arrestin recruitment. Ecnoglutide is engineered to preferentially activate cAMP signaling while minimizing beta-arrestin-mediated receptor internalization. The rationale is that cAMP signaling drives the metabolically beneficial effects — glucose-dependent insulin secretion and appetite regulation — while reduced receptor internalization may sustain surface receptor availability and improve the durability of the response. Structurally it is a modified human-GLP-1-based peptide with a fatty-acid modification for albumin binding and half-life extension, supporting once-weekly subcutaneous dosing. An oral formulation has also been pursued, positioning ecnoglutide among the agents attempting to broaden GLP-1 access beyond injectables. Ecnoglutide has been developed primarily in China, where it has progressed through Phase 2 and Phase 3 trials in type 2 diabetes and obesity. Reported results include dose-dependent HbA1c reductions and clinically meaningful weight loss, with a gastrointestinal tolerability profile typical of the class. It is not approved by the FDA, EMA, or MHRA and outside of clinical programs is treated as a research compound.

Specifications

Origin / ManufacturerSynthetic (cAMP-biased GLP-1 agonist)
Active Components
Ecnoglutide
StorageStore at 2–8°C; protect from light.
Shelf Life24 months (lyophilized, refrigerated)
Form FactorSolution for subcutaneous injection (clinical); oral formulation investigational

Clinical Evidence

Phase 2 and Phase 3 trials in China evaluated ecnoglutide in type 2 diabetes and in obesity

Clinical report reference

Reported dose-dependent reductions in HbA1c in diabetes trials

Clinical report reference

Reported clinically meaningful weight loss in obesity trials

Clinical report reference

Gastrointestinal effects (nausea, diarrhea) were the predominant adverse events, consistent with the GLP-1 class

Clinical report reference

Not approved by the FDA, EMA, or MHRA as of 2026

Clinical report reference

Frequently Asked Questions

Reviewed by

Clinical Research Review Board

Metabolic & Endocrine Peptide Review

All clinical claims cross-checked against primary sources. Read our editorial policy →

Related Peptides

Reviewed by Clinical Research Review BoardMetabolic & Endocrine Peptide Review

Search

Search across products, blog posts, wiki articles, and more.