ECC5004
AstraZeneca's oral-peptide GLP-1 candidate (in-licensed from China-based Eccogene in 2023) — Phase 2b in obesity and T2DM; a peptide, not a small molecule, distinguishing it from orforglipron and danuglipron despite the oral route.
An oral GLP-1 receptor agonist peptide developed by Eccogene (Shanghai) and licensed by AstraZeneca in November 2023 in a deal potentially worth up to $2B; Phase 1 data demonstrated meaningful oral bioavailability and weight loss, with Phase 2b trials in obesity and T2DM ongoing — notably an actual peptide (not a small molecule like orforglipron).
Mechanism of action
Oral peptide GLP-1 receptor agonism. The peptide chemistry is designed for GI stability and enhanced oral bioavailability without the absorption-enhancer SNAC strategy used by oral semaglutide (Rybelsus). Distinct mechanistically from small-molecule oral GLP-1 agonists (orforglipron, danuglipron) in that it binds the orthosteric GLP-1 peptide site.
Primary uses
- Obesity (Phase 2)
- Type 2 diabetes mellitus (Phase 2)
Typical dosing
Phase 2 doses under evaluation; not publicly finalized.
Regulatory status
Not approved. AstraZeneca licensed ex-China global rights from Eccogene in November 2023. Phase 2b program in obesity and T2DM initiated 2024.
References
- [manufacturer] AstraZeneca. Press release: licensing agreement with Eccogene for ECC5004 (AZD5004), November 2023.
- [manufacturer] AstraZeneca pipeline page — AZD5004 Phase 2 status.
Related peptides
This entry is for educational purposes only and does not constitute medical advice. Dosing information reflects published regulatory or research data and is not a recommendation. Many compounds described here are not approved for human use in the United States. Consult a licensed medical professional before considering any peptide therapy.