Eloralintide
Also known as: GSBR-1290, Structure GSBR-1290
Key Facts: Eloralintide
- Category
- Weight Loss
- FDA Status
- Not FDA Approved
- Clinical Status
- Phase 2 - Actively enrolling Phase 3 trials for obesity
- Administration
- Oral tablet
- Typical Dose
- 120-240mg once daily (oral)
- Frequency
- Once daily
- Duration
- 36 weeks in Phase 2 trials
Mechanism of Action
Amylin (also called IAPP) is a hormone co-secreted with insulin after you eat, and it tells your brain you are full and slows how fast your stomach empties. Eloralintide is engineered to selectively switch on the amylin receptor, which is the calcitonin receptor paired with a receptor-activity-modifying protein (RAMP), in appetite-control regions of the brainstem and hypothalamus. The result is reduced food intake and earlier satiety. The reason this class is interesting is that, unlike GLP-1 drugs such as semaglutide and tirzepatide, amylin agonists seem to drive weight loss with much less nausea and vomiting, which is what the eloralintide trials reported. Whether it preserves more lean mass than GLP-1 drugs is a real hypothesis being tested, not a settled fact.
Research Summary
This is one of the few research peptides on this site with genuinely strong, recent human data. The Phase 1 proof-of-concept study (Eli Lilly, published 2026) randomized 100 adults with obesity across five ascending dose cohorts and reported dose-proportional pharmacokinetics and least-squares mean weight reductions of 2.6 to 11.3 percent by week 12, with notably low gastrointestinal side effects (nausea 8 percent, vomiting 4 percent). In November 2025 Lilly announced topline Phase 2 results in 263 adults with obesity or overweight: at 48 weeks all dose arms beat placebo, with mean weight loss from about 9.5 percent at the lowest dose up to 20.1 percent at 9 mg, versus 0.4 percent on placebo, plus improvements in waist circumference, blood pressure, lipids, and glycemic markers. The most common adverse events were mild-to-moderate nausea and fatigue. The honest caveat: full peer-reviewed Phase 2 data and any head-to-head against tirzepatide are still pending, and there are no long-term safety or cardiovascular outcome results yet because Phase 3 is only just beginning. So the early efficacy signal is impressive, but durability and long-term safety are unproven.
Dosing Information
Typical Dosingⓘ
Community experience
120-240mg once daily (oral)
120-240mg per day
Once daily
Oral small-molecule GLP-1 agonist. No injection required. Phase 2 trial doses only. Longer half-life may support less frequent dosing in future formulations.
Research Dosingⓘ
Scientific studies
Doses from clinical trials only - not yet approved
Doses from Studies
Duration
36 weeks in Phase 2 trials
Administration
Oral tablet
Possible Side Effects
Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.
- ●Nausea (lower incidence than injectable GLP-1s)
- ●Diarrhea
- ●Vomiting
- ●Constipation
- ●Decreased appetite
- ●Abdominal discomfort
- ●Limited long-term safety data (Phase 2 only)
References
- https://pubmed.ncbi.nlm.nih.gov/41559929/
- https://www.prnewswire.com/news-releases/lillys-selective-amylin-agonist-eloralintide-demonstrated-meaningful-weight-loss-and-favorable-tolerability-in-a-phase-2-study-of-adults-with-obesity-or-overweight-302607061.html
- https://investor.lilly.com/news-releases/news-release-details/lillys-selective-amylin-agonist-eloralintide-demonstrated
- https://www.lilly.com/news/stories/what-to-know-about-eloralintide
Research This Peptide Further
Frequently Asked Questions
What does Eloralintide do?
Eloralintide (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.
How does Eloralintide work?
Amylin (also called IAPP) is a hormone co-secreted with insulin after you eat, and it tells your brain you are full and slows how fast your stomach empties. Eloralintide is engineered to selectively switch on the amylin receptor, which is the calcitonin receptor paired with a receptor-activity-modifying protein (RAMP), in appetite-control regions of the brainstem and hypothalamus. The result is reduced food intake and earlier satiety. The reason this class is interesting is that, unlike GLP-1 drugs such as semaglutide and tirzepatide, amylin agonists seem to drive weight loss with much less nausea and vomiting, which is what the eloralintide trials reported. Whether it preserves more lean mass than GLP-1 drugs is a real hypothesis being tested, not a settled fact.
Is Eloralintide FDA approved?
No, Eloralintide is not currently FDA approved. Current status: Phase 2 - Actively enrolling Phase 3 trials for obesity
What are the side effects of Eloralintide?
Reported side effects include: Nausea (lower incidence than injectable GLP-1s), Diarrhea, Vomiting, Constipation, Decreased appetite. Individual responses vary based on dosage, duration, and personal health factors.
What is the typical dose of Eloralintide?
Community-reported common dose: 120-240mg once daily (oral) (Once daily). Range: 120-240mg per day. Administration: Oral tablet. Clinical trial doses only. Not yet approved. Not medical advice.
Related Peptides
Peptides commonly compared with Eloralintide or used in similar applications.
Cagrilintide
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 LossTirzepatide
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 LossRetatrutide
Clinical TrialsRetatrutide is the heavy hitter of the new weight-loss drugs: a once-weekly injectable peptide that hits three receptors at once - GIP, GLP-1, and glucagon - earning it the nickname triple-G agonist. In a phase 2 trial it produced some of the largest weight loss ever recorded for a drug, up to roughly 24 percent of body weight at the top dose. It is investigational, made by Eli Lilly, and not yet FDA approved as of 2026.
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