Efpeglenatide
Also known as: Eppe, HM11260C, LAPS-Exendin
Key Facts: Efpeglenatide
- Category
- Weight Loss
- FDA Status
- Not FDA Approved
- Clinical Status
- Approved in South Korea only (Eppe, MFDS, 7 October 2026) for chronic weight management in adults without diabetes (BMI 30 or more, or 27 or more with a weight-related condition). Hanmi has said a diabetes filing in Korea would come later. Not approved by the FDA or EMA; Sanofi exited the program in 2020.
- Banned in Sport (WADA)
- Not on the WADA Prohibited List (2026). Its approval in South Korea means the S0 catch-all does not apply.
- Administration
- Subcutaneous auto-injector once weekly
- Typical Dose
- 10 mg once weekly maintenance (Korean label)
- Frequency
- Once weekly
- Duration
- Long-term (chronic weight management); 40-64 weeks in the Korean phase 3
How does Efpeglenatide work?
Efpeglenatide activates the GLP-1 receptor, which raises insulin release after meals, lowers glucagon, slows stomach emptying and reduces appetite. The active part is an exendin-4 analog (the same parent peptide as exenatide and lixisenatide) attached through a small linker to a human IgG4 Fc fragment, using Hanmi's LAPSCOVERY platform. The Fc piece makes the molecule big enough to dodge kidney clearance and lets it recycle in the body, which stretches its half-life to weekly dosing. Hanmi argues its lower brain penetration explains the milder GI profile; that is a company argument rather than an independently proven fact.
What does the research show?
The strongest data come from Sanofi's AMPLITUDE-O trial (NEJM 2021), which enrolled people with type 2 diabetes and cardiovascular or kidney disease. Efpeglenatide 4 or 6 mg weekly cut major cardiovascular events by 27% versus placebo (7.0% vs 9.2%, hazard ratio 0.73) over a median of 1.8 years, and also reduced kidney outcomes. Sanofi still returned the rights in 2020 for business reasons. Hanmi then ran a Korean phase 3 obesity trial in 448 adults without diabetes (average BMI 32): at 40 weeks, weight loss was 9.02% versus 0.89% on placebo, and 75.1% lost at least 5%. That is less weight loss than semaglutide or tirzepatide in their pivotal trials, though trial designs differ, and GI side effects were somewhat lower (diarrhea 17.6%, nausea 16.6%, vomiting 11.6%). Korea's MFDS approved it for chronic weight management on 7 October 2026, with launch planned for late October. Bottom line: a solid, proven drug class member with real outcome data, but modest weight loss and no Western approval.
What doses have been studied?
Typical Dosingⓘ
Community experience
10 mg once weekly maintenance (Korean label)
2-10 mg weekly, escalated over 12 weeks
Once weekly
These doses come from the Korean approval and trials. Outside Korea it remains unapproved, and no other regulator has set a dose.
Research Dosingⓘ
Scientific studies
Korean label dosing for Eppe (prescription only in South Korea); other doses are trial doses
Doses from Studies
2 mg escalating to 10 mg weekly
MFDS approval (Korea) - Eppe approval and Korean phase 3 obesity trial ↗
Duration
Long-term (chronic weight management); 40-64 weeks in the Korean phase 3
Administration
Subcutaneous auto-injector once weekly
When and how is Efpeglenatide taken?
Best Time to Take
Same day each week
Once weekly subcutaneous injection
Food Recommendation
With or without food
Why This Timing?
The Fc-linked design gives it a long half-life, so weekly consistency matters more than time of day.
What are the side effects of Efpeglenatide?
Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.
- ●Diarrhea (about 18% in the Korean phase 3)
- ●Nausea (about 17%)
- ●Indigestion
- ●Constipation
- ●Vomiting (about 12%)
- ●Usual GLP-1 class risks: gallbladder disease, pancreatitis
- ●Long-term data in obesity limited to Korean trial population
References
- https://www.koreajoongangdaily.com/business/koreas-first-glp1-obesity-drug-wins-approval-with-less-weight-loss-but-fewer-side-effects/12910491
- https://www.koreabiomed.com/news/articleView.html?idxno=33584
- https://www.acc.org/latest-in-cardiology/clinical-trials/2021/07/12/18/03/amplitude-o
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11801804/
Research This Peptide Further
Frequently Asked Questions
What does Efpeglenatide do?
Efpeglenatide is a long-acting, once-weekly GLP-1 agonist from Hanmi Pharmaceutical, made by linking an exendin-4 analog to an antibody fragment so it lasts days instead of hours. Sanofi licensed it for diabetes in 2015 and handed it back in 2020 despite a positive heart outcomes trial. Hanmi relaunched it for obesity, and on 7 October 2026 South Korea approved it as Eppe, the country's first homegrown GLP-1 obesity drug. It is not approved by the FDA or EMA.
How does Efpeglenatide work?
Efpeglenatide activates the GLP-1 receptor, which raises insulin release after meals, lowers glucagon, slows stomach emptying and reduces appetite. The active part is an exendin-4 analog (the same parent peptide as exenatide and lixisenatide) attached through a small linker to a human IgG4 Fc fragment, using Hanmi's LAPSCOVERY platform. The Fc piece makes the molecule big enough to dodge kidney clearance and lets it recycle in the body, which stretches its half-life to weekly dosing. Hanmi argues its lower brain penetration explains the milder GI profile; that is a company argument rather than an independently proven fact.
Is Efpeglenatide FDA approved?
No, Efpeglenatide is not currently FDA approved. Current status: Approved in South Korea only (Eppe, MFDS, 7 October 2026) for chronic weight management in adults without diabetes (BMI 30 or more, or 27 or more with a weight-related condition). Hanmi has said a diabetes filing in Korea would come later. Not approved by the FDA or EMA; Sanofi exited the program in 2020.
Is Efpeglenatide banned in sport?
Not on the WADA Prohibited List (2026). Its approval in South Korea means the S0 catch-all does not apply.
What are the side effects of Efpeglenatide?
Reported side effects include: Diarrhea (about 18% in the Korean phase 3), Nausea (about 17%), Indigestion, Constipation, Vomiting (about 12%). Individual responses vary based on dosage, duration, and personal health factors.
What is the typical dose of Efpeglenatide?
Community-reported common dose: 10 mg once weekly maintenance (Korean label) (Once weekly). Range: 2-10 mg weekly, escalated over 12 weeks. Administration: Subcutaneous auto-injector once weekly. Community-reported doses. Not medical advice. Consult healthcare provider.
Related Peptides
Peptides commonly compared with Efpeglenatide or used in similar applications.
Tirzepatide
FDATirzepatide is a single peptide that activates two receptors at once: GIP and GLP-1, the two main incretin hormones your gut releases after eating. It is FDA-approved as Mounjaro for type 2 diabetes and as Zepbound for chronic weight management and obstructive sleep apnea, and it has produced the largest weight-loss numbers of any approved drug to date. Like semaglutide, this is a heavily trialed, fully approved medicine, not a gray-market research compound.
Weight LossCagriSema
Clinical TrialsCagriSema is a once-weekly injectable that pairs two drugs in one shot: semaglutide (a GLP-1 receptor agonist, the molecule behind Ozempic and Wegovy) and cagrilintide (a long-acting amylin analog). It is being developed by Novo Nordisk for obesity and type 2 diabetes, and in 2025 it cleared its phase 3 REDEFINE trials. It is not yet approved by the FDA, though regulatory filings are underway.
Weight LossLiraglutide
FDALiraglutide is a once-daily injectable GLP-1 receptor agonist, a synthetic peptide that shares about 97% of its sequence with the natural gut hormone GLP-1 but is engineered with a fatty acid chain so it survives in the body far longer. It is FDA-approved as Victoza for type 2 diabetes (2010) and as Saxenda for chronic weight management (2014), and is one of the most studied drugs in its class. As of 2024 a generic version is also FDA-approved.
Weight LossDulaglutide
FDADulaglutide (brand name Trulicity) is a once-weekly injectable GLP-1 receptor agonist made by fusing a modified GLP-1 peptide to a fragment of a human antibody, which is what lets it last a full week between shots. It is FDA-approved for type 2 diabetes and, notably, to reduce cardiovascular risk in adults with diabetes. The once-weekly dosing made it a major convenience step up from earlier daily and twice-daily agents.
Weight LossCagrilintide
Clinical TrialsCagrilintide (also called AM833) is a long-acting synthetic analog of amylin, the gut-brain satiety hormone co-secreted with insulin by pancreatic beta cells. It is an investigational once-weekly injectable being developed by Novo Nordisk for obesity, most prominently as the amylin half of CagriSema (cagrilintide plus semaglutide). It is not yet approved as a standalone drug, but it has cleared phase 2 trials and is in late-stage development.
Weight LossEloralintide
Clinical TrialsEloralintide (Eli Lilly code LY3841136) is an investigational, long-acting, selective amylin receptor agonist given as a once-weekly subcutaneous injection for obesity. Amylin is the satiety hormone your pancreas releases alongside insulin, and eloralintide is built to mimic it without the gut side effects that sink most appetite drugs. It is not approved anywhere yet, but it has cleared Phase 1 and a 263-person Phase 2 trial with weight loss up to roughly 20 percent, and Lilly has said it is moving into Phase 3.
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