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    Eloralintide (LY3841136) molecular structure

    Eloralintide (LY3841136)

    Weight LossPhase 3

    Also known as: LY3841136, LY-3841136, AT53786, Eloralintida

    Eloralintide is an amylin analog developed by Eli Lilly and Company for weight management, given as a once-weekly subcutaneous injection. It is a 37 amino acid peptide containing three non-coded residues and a C20 fatty diacid that binds albumin, which is what stretches its action out to a week (PMID: 41109426).

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    Lowest price per mg

    $18.00/mg$179.99 for 10mg

    at Disguised Alpha

    Half-life: Terminal geometric mean half-life 310 to 366 hours, that is 1…Route: Subcutaneous injectionMW: 4526 g/molCAS: 2883634-40-8
    Last reviewed:

    Overview

    At A Glance

    Mechanism

    Eloralintide is a selective agonist at the amylin 1 receptor, a complex formed by the calcitonin receptor with receptor activity-modifying protein 1. Activating that receptor in the area postrema and related hindbrain circuits promotes satiation, slows gastric emptying and suppre…

    Half-Life
    Terminal geometric mean half-life 310 to 366 hours, that is 12.9 to 15.3 days, across the doses tested in the phase 1 single-ascending-dose study in humans (PMID: 41109426)
    Routes
    Subcutaneous injection
    Potential Benefits
    Mean body weight change from baseline of about 9 percent to 20 percent across dose groups at 48 weeks against 0.4 percent on placebo in a 263-patient phase 2 trial in adults with obesity or overweight (PMID: 41207310)Weight reduction of 2.6 percent to 11.3 percent across dose groups at 12 weeks in 100 adults with obesity or overweight in a phase 1 multiple-ascending-dose study (PMID: 41559929)Week 4 weight reduction of 2.5 percent and 4.4 percent after single doses in healthy participants against a 0.6 percent gain on placebo (PMID: 41109426)Dose-dependent reduction in food intake and body weight, mainly through fat mass loss, in diet-induced obese rats (PMID: 41109426)Significantly less conditioned taste avoidance than cagrilintide in lean rats, a marker of reduced aversive signaling (PMID: 41109426)

    Overview

    Eloralintide is an amylin analog developed by Eli Lilly and Company for weight management, given as a once-weekly subcutaneous injection. It is a 37 amino acid peptide containing three non-coded residues and a C20 fatty diacid that binds albumin, which is what stretches its action out to a week (PMID: 41109426). It is investigational everywhere. No regulator has approved it, and it is in phase 3 trials as of 2026. Amylin is a hormone released from pancreatic beta cells alongside insulin. It slows gastric emptying, suppresses glucagon after meals and signals meal termination through the brainstem. Pramlintide, the first approved amylin analog, proved the concept but was limited by frequent dosing and modest effect. The newer analogs split into two groups: dual amylin and calcitonin receptor agonists such as cagrilintide, and selective amylin receptor agonists. Eloralintide belongs to the second group. In cells expressing human receptors it activated the amylin 1 receptor about 12-fold more potently than the calcitonin receptor and about 11-fold more potently than the amylin 3 receptor (PMID: 41109426). That selectivity is the design idea, because calcitonin receptor engagement is thought to contribute to nausea. Preclinical results back this up. In lean rats, eloralintide produced significantly less conditioned taste avoidance than cagrilintide, a marker of aversive signaling. In diet-induced obese rats it reduced food intake and lowered body weight in a dose-dependent way, mostly through loss of fat mass, and pharmacokinetics in rats and monkeys supported weekly dosing (PMID: 41109426). The human data are what make this compound notable. A phase 1 single-ascending-dose study in 48 healthy participants reported mostly mild adverse events and week 4 weight reduction of 2.5 percent and 4.4 percent in the two highest single-dose groups against a 0.6 percent gain on placebo (NCT05295940, PMID: 41109426). A 12-week multiple-ascending-dose study in 100 participants with obesity or overweight, run without dose escalation, reported weight reduction across dose groups ranging from 2.6 percent to 11.3 percent, with decreased appetite in 19 percent, headache in 12 percent and fatigue in 11 percent, and infrequent gastrointestinal events: diarrhea in 10 percent, nausea in 8 percent and vomiting in 4 percent (PMID: 41559929). A 48-week phase 2 trial randomized 263 adults across six dose or dose-escalation arms and placebo and reported mean weight change from baseline of about 9 percent to 20 percent against 0.4 percent on placebo, with nausea and fatigue the most common adverse events (NCT06230523, PMID: 41207310). A network meta-analysis of six trials in 4642 adults ranked high-dose eloralintide second only to amycretin for percent body weight reduction, ahead of semaglutide, while noting that gastrointestinal adverse events rose with high doses of amylin-based therapies and that the evidence is still sparse and low certainty (PMID: 42175595). Anything sold outside a trial is not the studied product and has no verified identity or purity.

    Potential Research Fields

    Obesity pharmacotherapyAmylin receptor pharmacologyMetabolic diseaseAppetite regulation

    Chemical Information

    IUPAC Name

    Not yet available

    CAS Number

    2883634-40-8

    Molecular Formula

    C201H319N49O65S2

    Molecular Mass

    4526 g/mol

    Dosing & Protocols

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    Research

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    Interactions

    Contraindications

    No labeled contraindications exist, since the drug is not approved. Trial-based and mechanism-based: the phase 2 program enrolled adults with obesity or overweight and excluded people outside those criteria, so nothing is known about use in people at a healthy weight. Because amylin receptor agonists slow gastric emptying, pre-existing gastroparesis or severe gastrointestinal disease is a mechanism-based reason for caution, and the ongoing program includes dedicated hepatic and renal impairment pharmacokinetic studies precisely because those populations have not been characterized (NCT07401862, NCT07426380). Pregnancy and breastfeeding have not been studied.

    Research Disclaimer

    This interaction data is compiled from published research and community reports. It may not be exhaustive. Always consult a healthcare professional before combining compounds.

    Best Price

    $179.99

    Best $/mg

    $17.9990

    Vendors

    1

    Listings

    1

    vial

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    Eloralintide 10 mg vial 1 vial (10 mg)● In Stock $179.99BEST $18.00 —

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    Tracking since Sep 7, 2026 · 1 data point

    Vendors Selling Eloralintide (LY3841136)

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    Every supplier above is graded 0 to 100 on COA verification, payment transparency, shipping, reviews, and active listings. Methodology published, no pay-to-rank.

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    t½ No published human value. The first-in-human trial planned pharmacokinetic sampling at 10 minutes, 30 minutes, 1 hour and 4 hours after dosing but was terminated with no results posted (ClinicalTrials.gov NCT01262664). The monkey studies used daily subcutaneous dosing chosen by body surface area scaling rather than from a measured half-life (PMID: 22072637)
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    t½ Immediate-release (Byetta): terminal half-life about 2.4 hours, cleared mainly by the kidneys. Extended-release (Bydureon): the same peptide is released slowly from biodegradable microspheres over roughly 10 weeks, reaching steady-state plasma levels by about 6 to 7 weeks. 5 to 10 mcg twice daily (Byetta, immediate-release) or 2000 mcg (2 mg) once weekly (Bydureon, extended-release)
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    t½ Not applicable to the blend; the water-soluble components (choline, inositol, B-vitamins, carnitine) are cleared over hours to a few days, and excess is largely excreted. 1 mL of a compounded MIC blend intramuscularly, 1 to 2x per week. No standardized dose exists; concentrations vary by compounding pharmacy.
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    View Full Dosage Guide →

    Protocols, calculator & safety for Eloralintide (LY3841136)

    Lowest Price per mg

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    $179.99($18.00/mg)

    1 vendor · 1 listing

    Research Score

    30

    0 PubMed results

    Quality Indicators

    Data Completeness

    63%
    Description
    Mechanism of Action
    Chemical Data
    Dosing Protocols
    Safety Profile
    PubMed Results
    Interactions
    Vendor Listings

    COA Verification

    0

    Verified COAs

    1

    Vendors w/ COA

    Latest test: 9/16/2026

    Quick Facts

    Half-Life

    Terminal geometric mean half-life 310 to 366 hours, that is 12.9 to 15.3 days, across the doses tested in the phase 1 single-ascending-dose study in humans (PMID: 41109426)

    Molecular Weight

    4526 g/mol

    Administration

    Subcutaneous injection

    CAS Number

    2883634-40-8

    Trial Phase

    Phase 3

    Research Disclaimer

    This information is for educational and research purposes only. Not intended as medical advice. Consult a healthcare professional before use.

    Frequently Asked Questions

    What is Eloralintide (LY3841136) used for in research?

    Eloralintide is an amylin analog developed by Eli Lilly and Company for weight management, given as a once-weekly subcutaneous injection. It is a 37 amino acid peptide containing three non-coded residues and a C20 fatty diacid that binds albumin, which is what stretches its action out to a week (PMID: 41109426). It is investigational everywhere. No regulator has approved it, and it is in phase 3 trials as of 2026.

    Amylin is a hormone released from pancreatic beta cells alongside insulin. It slows gastric emptying, suppresses glucagon after meals and signals meal termination through the brainstem. Pramlintide, the first approved amylin analog, proved the concept but was limited by frequent dosing and modest effect. The newer analogs split into two groups: dual amylin and calcitonin receptor agonists such as cagrilintide, and selective amylin receptor agonists. Eloralintide belongs to the second group. In cells expressing human receptors it activated the amylin 1 receptor about 12-fold more potently than the calcitonin receptor and about 11-fold more potently than the amylin 3 receptor (PMID: 41109426). That selectivity is the design idea, because calcitonin receptor engagement is thought to contribute to nausea.

    Preclinical results back this up. In lean rats, eloralintide produced significantly less conditioned taste avoidance than cagrilintide, a marker of aversive signaling. In diet-induced obese rats it reduced food intake and lowered body weight in a dose-dependent way, mostly through loss of fat mass, and pharmacokinetics in rats and monkeys supported weekly dosing (PMID: 41109426).

    The human data are what make this compound notable. A phase 1 single-ascending-dose study in 48 healthy participants reported mostly mild adverse events and week 4 weight reduction of 2.5 percent and 4.4 percent in the two highest single-dose groups against a 0.6 percent gain on placebo (NCT05295940, PMID: 41109426). A 12-week multiple-ascending-dose study in 100 participants with obesity or overweight, run without dose escalation, reported weight reduction across dose groups ranging from 2.6 percent to 11.3 percent, with decreased appetite in 19 percent, headache in 12 percent and fatigue in 11 percent, and infrequent gastrointestinal events: diarrhea in 10 percent, nausea in 8 percent and vomiting in 4 percent (PMID: 41559929). A 48-week phase 2 trial randomized 263 adults across six dose or dose-escalation arms and placebo and reported mean weight change from baseline of about 9 percent to 20 percent against 0.4 percent on placebo, with nausea and fatigue the most common adverse events (NCT06230523, PMID: 41207310).

    A network meta-analysis of six trials in 4642 adults ranked high-dose eloralintide second only to amycretin for percent body weight reduction, ahead of semaglutide, while noting that gastrointestinal adverse events rose with high doses of amylin-based therapies and that the evidence is still sparse and low certainty (PMID: 42175595). Anything sold outside a trial is not the studied product and has no verified identity or purity.

    What forms does Eloralintide (LY3841136) come in?

    Eloralintide (LY3841136) is available in vial form.

    How do I compare Eloralintide (LY3841136) vendors?

    Compare prices, payment methods, shipping, and COA scores across 1 vendor.

    How many vendors sell Eloralintide (LY3841136), and what does it cost per mg?

    1 of the vendors BodyHackGuide tracks list Eloralintide (LY3841136) (1 listing). Among BodyHackGuide's Eloralintide (LY3841136) listings recorded as in stock with a milligram count, the lowest price per milligram is $18.00/mg at Disguised Alpha and the median is $18.00/mg. The Eloralintide (LY3841136) prices on BodyHackGuide are vendors' listed prices as BodyHackGuide last recorded them, not transactions; the most recent recorded change to a Eloralintide (LY3841136) listing is dated 7 September 2026.

    Which vendors have third-party COAs for Eloralintide (LY3841136) on file at BodyHackGuide?

    BodyHackGuide holds 4 third-party certificate records for Eloralintide (LY3841136), from . No editor has read any of BodyHackGuide's 4 certificate records for Eloralintide (LY3841136). The laboratory named on BodyHackGuide's Eloralintide (LY3841136) certificate records is Freedom Diagnostics Testing, and the newest test date on them is 29 September 2026. Each vendor page on BodyHackGuide shows how many certificate records BodyHackGuide holds for that vendor and links to each record that has its own page.

    Research Tools

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    5-Amino-1MQ

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    5-Amino-1MQ (5-amino-1-methylquinolinium iodide) is a small-molecule inhibitor of nicotinamide N-methyltransferase (NNMT), an enzyme that transfers a methyl group from S-adenosyl-L-methionine (SAM) to nicotinamide to form 1-methylnicotinamide (1-MNA) and S-adenosyl-L-homocysteine (SAH).

    t½ ~6–12 hours (oral) 50 mg - 150 mg daily (oral or injection)
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    Adipotide

    Weight LossPhase 1

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    t½ No published human value. The first-in-human trial planned pharmacokinetic sampling at 10 minutes, 30 minutes, 1 hour and 4 hours after dosing but was terminated with no results posted (ClinicalTrials.gov NCT01262664). The monkey studies used daily subcutaneous dosing chosen by body surface area scaling rather than from a measured half-life (PMID: 22072637)
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    Research compound — no established human doses. Animal studies use 10-100 mg/kg
    58 PubMedView Profile

    Exenatide

    Weight LossFDA-approved

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    t½ Immediate-release (Byetta): terminal half-life about 2.4 hours, cleared mainly by the kidneys. Extended-release (Bydureon): the same peptide is released slowly from biodegradable microspheres over roughly 10 weeks, reaching steady-state plasma levels by about 6 to 7 weeks. 5 to 10 mcg twice daily (Byetta, immediate-release) or 2000 mcg (2 mg) once weekly (Bydureon, extended-release)
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    500 mg - 2000 mg daily (oral or injection)
    4,002 PubMedView Profile

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    t½ Not applicable to the blend; the water-soluble components (choline, inositol, B-vitamins, carnitine) are cleared over hours to a few days, and excess is largely excreted. 1 mL of a compounded MIC blend intramuscularly, 1 to 2x per week. No standardized dose exists; concentrations vary by compounding pharmacy.
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