Metabolic & weight
Ecnoglutide
Also called XW003, Xianyida (China, type 2 diabetes)
Ecnoglutide is a once-weekly GLP-1 injection made by Sciwind Biosciences in China. In 2026 China approved it for type 2 diabetes and for long-term weight management in adults with obesity or overweight. It is described as a 'biased' GLP-1 drug, meaning it is designed to switch on only part of the receptor's signaling. It is not approved in the US or Europe.
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Overview
Ecnoglutide is a once-weekly GLP-1 injection made by Sciwind Biosciences in China. In 2026 China approved it for type 2 diabetes and for long-term weight management in adults with obesity or overweight. It is described as a 'biased' GLP-1 drug, meaning it is designed to switch on only part of the receptor's signaling. It is not approved in the US or Europe.
How it works
Established: ecnoglutide activates the GLP-1 receptor, which lowers blood sugar and promotes fullness 8. Proposed: it is 'cAMP-biased' — in lab tests it strongly triggered the cAMP signal (EC50 0.018 nM) but did not cause the receptor to be pulled into the cell, and the company says it minimizes beta-arrestin recruitment 57. The idea is that avoiding receptor internalization may keep the drug working longer, but whether this bias gives a real advantage in people is still being studied 5. Its half-life in healthy volunteers was about 124–138 hours, which supports weekly dosing 5.
What research shows
- SLIMMER (human phase 3 RCT, n=664 Chinese adults with overweight or obesity and no diabetes): at week 40, weight fell 9.1%, 10.9% and 13.2% on 1.2, 1.8 and 2.4 mg vs a 0.1% gain on placebo; 77–87% lost at least 5% vs 16% on placebo 1. The company reports 15.4% average loss on 2.4 mg at week 48 (company press release, not peer reviewed) 7.
- EECOH-2 (human phase 3 RCT, n=621 adults with type 2 diabetes on metformin, open-label, 52 weeks): HbA1c fell 1.91% (0.6 mg) and 1.89% (1.2 mg) vs 1.65% on dulaglutide 1.5 mg at week 32, meeting non-inferiority; the 1.2 mg dose was statistically better than dulaglutide, but the authors judged the difference not clinically relevant 2.
- EECOH-1 (human phase 3 RCT, n=211 adults with type 2 diabetes, 24 weeks): HbA1c fell 1.96% (0.6 mg) and 2.43% (1.2 mg) vs 0.87% on placebo 3.
- Phase 2 (human RCT, n=145 adults with type 2 diabetes, 20 weeks): HbA1c fell 1.81–2.39% vs 0.55% on placebo 4.
- SLIMMER-UP-SWITCH (human phase 2, open-label, n=163, interim week-20 result presented at ADA 2026 and reported in trade press): weight fell 12.8% on ecnoglutide 2.4 mg vs 9.5% on semaglutide 2.4 mg; the trial is ongoing and not yet peer reviewed 11.
- Animal studies (db/db mice, obese rats): lowered blood sugar and caused more weight loss than semaglutide 5.
Doses studied in people
| Study or label | Dose used | Source |
|---|---|---|
| SLIMMER phase 3 RCT in overweight/obesity (n=664) | 1.2 mg, 1.8 mg or 2.4 mg once weekly, subcutaneous, vs placebo | 1 |
| EECOH-2 phase 3 RCT in type 2 diabetes on metformin (n=621) | 0.6 mg or 1.2 mg once weekly vs dulaglutide 1.5 mg once weekly | 2 |
| EECOH-1 phase 3 RCT in type 2 diabetes (n=211) | 0.6 mg or 1.2 mg once weekly vs placebo | 3 |
| Phase 2 RCT in type 2 diabetes (n=145, 20 weeks) | 0.4 mg, 0.8 mg or 1.2 mg once weekly by injection, vs placebo | 4 |
| Phase 1 study in healthy volunteers | Single doses 0.03–1.0 mg; multiple doses 0.2–0.6 mg once weekly for 6 weeks, subcutaneous | 5 |
Doses shown are from published human trials only and are reported, not recommended. The Chinese prescribing label was not available to review.
Read this first: these are the amounts given to participants in published studies or written on official prescribing labels, reported for reference. They are not recommendations. Trial doses were chosen for specific patients under medical supervision, and a dose that is safe in one person can be harmful in another.
Vial math
Many research vials hold 5 or 10 mg of powder. This table shows how much ends up in each mark on a U-100 insulin syringe for common amounts of added liquid. It is arithmetic only, not a dose.
| Vial | Liquid added | Concentration | Per unit (0.01 mL) | |
|---|---|---|---|---|
| 5 mg | 1 mL | 5 mg/mL | 50 mcg | Open in calculator |
| 5 mg | 2 mL | 2.5 mg/mL | 25 mcg | Open in calculator |
| 5 mg | 3 mL | 1.67 mg/mL | 16.7 mcg | Open in calculator |
| 10 mg | 1 mL | 10 mg/mL | 100 mcg | Open in calculator |
| 10 mg | 2 mL | 5 mg/mL | 50 mcg | Open in calculator |
| 10 mg | 3 mL | 3.33 mg/mL | 33.3 mcg | Open in calculator |
More sizes: all vial sizes · How this works: Syringes and units · Reconstitution guide.
Safety
- In SLIMMER, 93% in each ecnoglutide group reported a side effect vs 84% on placebo; most were mild-to-moderate stomach and gut problems, and 10 people on ecnoglutide stopped because of side effects 1.
- In EECOH-2, 3–4% stopped due to side effects, similar to dulaglutide (3%) 2.
- In the phase 1 study, reported effects included decreased appetite, nausea and headache 5.
- Long-term safety is unknown: published trials last up to about one year, and data come mostly from Chinese participants 12.
Report side effects of any drug or product to the FDA through MedWatch. For a possible poisoning in the US, call Poison Control at 1-800-222-1222.
Legal status
- FDA
- Not FDA-approved; no US marketing application was found in the sources reviewed.
- Compounding
- No FDA compounding listing or action specific to ecnoglutide was found in the sources reviewed.
- Sports (WADA)
- Not prohibited as of the 2026 list. GLP-1 receptor agonists are not listed and remain off the 2027 list 1314. Because it is approved in China, the S0 'non-approved substance' class does not appear to apply 13.
- Other
- Approved in China by the NMPA: type 2 diabetes in adults (January 2026, brand Xianyida) and chronic weight management in adults with obesity, or overweight plus a weight-related condition (March 2026) 678. Not covered by China's state insurance for diabetes at launch 8. Studies in adolescents, sleep apnea, knee osteoarthritis and an oral tablet form are under way 6.
Rules change often. See Legal status of peptides for how these categories work.
History
Discovered and developed by Hangzhou Sciwind Biosciences; its discovery and first-in-human study were published in 2023 5. A phase 2 trial in type 2 diabetes was published in 2024 4, and phase 3 trials in obesity (SLIMMER) and type 2 diabetes (EECOH-1 and EECOH-2) were published in 2025–2026 123. In January 2025 Sciwind licensed rights outside Greater China and South Korea for an oral form (XW004) to Verdiva Bio 10. China's NMPA approved the injection (brand Xianyida) for type 2 diabetes in January 2026 68 and for chronic weight management in March 2026 67. Pfizer China holds mainland China commercial rights, announced in February 2026 9.
Common questions
Is ecnoglutide approved?
How much weight loss did it cause in trials?
What does 'biased' GLP-1 agonist mean?
It means the drug was designed to trigger mainly one signal (cAMP) from the GLP-1 receptor while causing little receptor pull-in, which in lab tests may help it keep working 5. Whether this matters for patients is not yet proven.
What are the known risks?
Related compounds
Semaglutide
Wegovy · Ozempic
Semaglutide is a long-acting copy of the gut hormone GLP-1.
Dulaglutide
Trulicity · LY2189265
Dulaglutide (brand name Trulicity) is a once-weekly GLP-1 medicine for type 2 diabetes.
Liraglutide
Saxenda · Victoza
Liraglutide is an older, once-daily GLP-1 medicine.
Tirzepatide
Zepbound · Mounjaro
Tirzepatide is a weekly shot that acts on two gut-hormone receptors, GIP and GLP-1, at once.
Mazdutide
IBI362 · LY3305677
Mazdutide is a weekly shot that acts on both the GLP-1 and glucagon receptors.
Orforglipron
Foundayo · LY3502970
Orforglipron is a once-daily pill that activates the GLP-1 receptor, but it is a small molecule, not a peptide.
Sources
- Ji L et al. Efficacy and safety of a biased GLP-1 receptor agonist ecnoglutide in adults with overweight or obesity: a phase 3 trial (SLIMMER). Lancet Diabetes Endocrinol 2025;13(9):777-789 (PMID 40555243) Journal
- He Y et al. Ecnoglutide versus dulaglutide in type 2 diabetes on metformin (EECOH-2): a 52-week phase 3 trial. Lancet Diabetes Endocrinol 2025;13(10):863-873 (PMID 40854315) Journal
- Zhu D et al. Ecnoglutide monotherapy versus placebo in type 2 diabetes (EECOH-1): phase 3 trial. Nat Commun 2026;17:1420 (PMID 41501026) Journal
- Zhu D et al. Efficacy and safety of GLP-1 analog ecnoglutide in adults with type 2 diabetes: a phase 2 trial. Nat Commun 2024;15:8408 (PMID 39333121) Journal
- Guo W et al. Discovery of ecnoglutide – a novel, long-acting, cAMP-biased GLP-1 analog. Mol Metab 2023;75:101762 (PMID 37364710) Journal
- Shirley M. Ecnoglutide: First Approvals. Drugs 2026;86(9):1563-1570 (PMID 42412371) PubMed review
- Sciwind Biosciences press release: ecnoglutide injection approved by China's NMPA for chronic weight management (March 6, 2026) Regulatory
- The Standard (Reuters): Sciwind Biosciences diabetes drug approved in China (Jan 30, 2026) News
- BioPharm International: China approval of ecnoglutide expands competition in the GLP-1 obesity market (March 6, 2026) News
- Sciwind Biosciences press release: global licensing agreement with Verdiva Bio for metabolic portfolio (Jan 10, 2025) Regulatory
- HCPLive (trade press): Ecnoglutide delivers 35% greater weight loss than semaglutide in head-to-head trial (June 8, 2026) News
- PubChem: Ecnoglutide (CID 162625103) Database
- WADA 2026 Prohibited List (official PDF, mirrored by Asia Rugby) Regulatory
- WADA publishes 2027 Prohibited List (World Rugby summary) Regulatory
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Last reviewed 2026-10-29 · How we research · Found an error? See our corrections policy.