ArticlesSeptember 16, 2026·7 min read

EloraTZP: Eloralintide + Tirzepatide Hits 17% Loss

Lilly's eloraTZP — eloralintide plus tirzepatide — hit 17% weight loss in 16 weeks vs 10% on tirzepatide alone. Phase 2 data lands at EASD Sept 30.

Two luminous ribbons of light braiding into a single brighter strand, representing the eloralintide and tirzepatide combination

Eli Lilly announced on September 15, 2026 that it will unveil Phase 2 data for eloraTZP — a combination of the selective amylin receptor agonist eloralintide and the GIP/GLP-1 agonist tirzepatide — at the 62nd EASD Annual Meeting in Milan later this month. It is the first Phase 2 readout for the compound, and it arrives alongside Phase 3 retatrutide data at the same conference.

The number that has circulated so far comes from Phase 1b: adding eloralintide 3 mg to tirzepatide 5 mg produced 17% weight loss over 16 weeks, against 10% for tirzepatide 5 mg alone. That is a 7-point gap at a low tirzepatide dose and a short duration, which is why the Phase 2 readout is drawing attention.

Research-context information only. EloraTZP and eloralintide are investigational compounds not approved by the FDA, and neither is available through research-peptide vendors. Doses and outcomes described below come from published clinical trial disclosures. This article reports what has been documented, not what should be done. Possession or use of investigational drugs outside an authorized clinical trial may be illegal in your jurisdiction. Consult a licensed physician for personal medical decisions.

What Lilly Is Presenting

The EASD meeting runs September 28 to October 2, 2026. Lilly's cardiometabolic slate spans four compounds, with three EASD-sponsored symposia stacked on September 30 and October 1:

Session Date (CEST) Compound Data
Amylins in diabetes symposium Sept 30, 4:30–5:30 p.m. eloraTZP Phase 2, obesity/overweight + type 2 diabetes
Retatrutide symposium Sept 30, 8:30–9:30 a.m. Retatrutide Phase 3 (TRIUMPH-2)
Tirzepatide symposium Sept 30, 8:30–9:30 a.m. Tirzepatide SURPASS-CVOT
Orforglipron symposium Oct 1, 8:30–9:15 a.m. Orforglipron Phase 3 (ACHIEVE program)

EloraTZP is the only genuinely new entry on that list. The others extend programs with published readouts: TRIUMPH-2 reported 20.8% weight loss and a 1.6-point A1C reduction at 80 weeks in adults with obesity and type 2 diabetes, and SURPASS-CVOT reported an 8% lower risk of three-point major adverse cardiovascular events for tirzepatide versus dulaglutide (HR 0.92; 95.3% CI 0.83–1.01).

Lilly calls eloraTZP "triple-acting," which is worth unpacking. Retatrutide is a single peptide that binds GIP, GLP-1, and glucagon receptors. EloraTZP reaches three receptor systems too, but through two separate molecules and with amylin replacing glucagon as the third arm. Glucagon agonism raises energy expenditure; amylin agonism works on satiety and gastric signaling. Same headline count, different biology.

The Phase 1b Data Behind the Headline

The 17%-versus-10% figure comes from a dose-ranging Phase 1b package that ran several parallel cohorts. The fuller picture reported from those cohorts:

16-week cohort (eloralintide added to tirzepatide 5 mg):

Arm Mean Weight Change
Placebo + tirzepatide 5 mg −10.0%
Eloralintide 3 mg + tirzepatide 5 mg −17.0%
Eloralintide 6 mg + tirzepatide 5 mg −18.2%
Eloralintide 9 mg + tirzepatide 5 mg −20.5%

24-week cohort (monotherapy arms versus combination):

Arm Mean Weight Change
Double placebo −0.5%
Eloralintide 9 mg alone −14.2%
Tirzepatide 15 mg alone −16.4%
Eloralintide 9 mg + tirzepatide 15 mg −25.5%

The 24-week cohort is the more informative one, because it carries both monotherapy comparators. Eloralintide alone reached −14.2% and tirzepatide alone −16.4%, while the combination reached −25.5% — more than either arm, though less than their arithmetic sum. A longer 32-week cohort layered eloralintide onto tirzepatide 15 mg and reported up to −29.0%, but that arm is the weakest evidence in the package: only a handful of participants completed it, and small-completer arms routinely overstate effect size.

Reported tolerability followed the class pattern. Adverse events were predominantly gastrointestinal and characterized as mild to moderate. Dropouts clustered in the higher eloralintide arms and in the longer cohorts, which is the signal worth watching when the Phase 2 numbers land — a combination that adds 7 points of weight loss but loses a third of participants is a different product than one that holds them.

These are Phase 1b cohorts of roughly 12 to 16 participants per arm with baseline BMIs of 32.8 and 30.5. Phase 2 exists precisely to test whether those numbers survive larger, longer, more heterogeneous enrollment. The preclinical groundwork was presented at ADA 2026, where eloralintide combined with tirzepatide produced greater weight loss than either agent alone in diet-induced obese rats (abstract 3082-LB).

Four columns of light at increasing heights representing escalating weight-loss results across combination dose arms

What This Means for the Research Market

EloraTZP itself changes nothing about availability. Eloralintide is an investigational Lilly molecule with no approval and — unlike retatrutide — no established gray-market supply. It is not stocked by research-peptide vendors, and a fixed combination product is further out still. Nobody is sourcing eloraTZP.

What the data does is validate a thesis the research market has already been acting on: pairing an amylin agonist with an incretin agonist produces more weight loss than either class alone. Lilly's own 24-week cohort is the cleanest published demonstration of that — two monotherapy arms and a combination arm in the same trial, with the combination clearly ahead of both.

That same pairing already exists in the research market in a different form. Cagrilintide is the amylin analog that research vendors actually stock, and it is the compound the amylin-plus-incretin stacking discussion has centered on. Our retatrutide + cagrilintide stack cluster documents how that combination has been reported and dosed, and the cagrilintide dosing guide covers the amylin side on its own.

For readers comparing vendor sourcing on the compounds that are actually listed, Best Tirzepatide Vendors and Best Cagrilintide Vendors rank in-stock sources on price per milligram, third-party certificate-of-analysis testing, and reputation. Current vendor discounts across the recommended list are aggregated on the deals page.

This article contains affiliate links; The Peptide Catalog may earn a commission if you purchase through them. Compounds referenced are sold for research use only and are not FDA-approved for human use.

Where EloraTZP Sits in the Amylin Race

Amylin has become the most crowded mechanism in obesity drug development, and eloraTZP is Lilly's entry in the combination lane specifically. The field it joins:

  • Cagrilintide — Novo Nordisk's amylin analog, tested both alone and paired with semaglutide.
  • Petrelintide — Zealand's long-acting amylin analog, with ZUPREME-1 data reported at ADA 2026.
  • Eloralintide monotherapy — reached 20% weight loss at 48 weeks in Phase 2 without touching GLP-1 at all (published in The Lancet, PMID 41207310).
  • VK3019 — Viking's dual amylin and calcitonin receptor agonist.

The eloralintide monotherapy result is the important context for eloraTZP. A drug that reaches 20% on its own is not a minor add-on to tirzepatide — it is a second full-strength agent, which is part of why the combination arms climb into the 25%+ range and why tolerability is the open question rather than efficacy.

The strategic read is that Lilly now has two distinct paths past tirzepatide: retatrutide's single-molecule triple agonism, and eloraTZP's two-molecule amylin pairing. Retatrutide is far ahead on development timeline — Lilly has said it plans to file a Biologics License Application in Q1 2027, placing a possible approval in late 2027 or 2028. EloraTZP is only now producing Phase 2 data, so a Phase 3 program would follow, and approval sits well beyond retatrutide's window.

For head-to-head framing on the compounds already circulating, the retatrutide vs tirzepatide comparison covers the efficacy gap, and switching from tirzepatide to retatrutide documents how that transition has been reported.

Two glowing node clusters bridged by a filament of light, representing amylin and incretin receptor pathways acting together

Bottom Line

EloraTZP's Phase 1b numbers are strong — 17% at 16 weeks on a low tirzepatide dose, 25.5% at 24 weeks against monotherapy comparators of 14.2% and 16.4%. The Phase 2 readout on September 30 will show whether that separation holds in a larger type 2 diabetes population and, more importantly, what it costs in dropouts.

Nothing about access changes. Eloralintide has no research-market supply and eloraTZP is a combination product years from any approval decision. The transferable finding is mechanistic: amylin plus incretin beats either alone, which is the same logic behind the amylin stacking already documented in the research market.

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Frequently Asked Questions

What is eloraTZP?
EloraTZP is Eli Lilly's investigational fixed combination of eloralintide, a selective amylin receptor agonist, and tirzepatide, a GIP/GLP-1 receptor agonist. Lilly describes it as a triple-acting medicine because it engages three receptor systems — amylin, GIP, and GLP-1 — through two molecules rather than one.
How much weight loss did eloraTZP produce?
In the Phase 1b data Lilly has disclosed, adding eloralintide 3 mg to tirzepatide 5 mg produced 17% weight loss over 16 weeks, versus 10% for tirzepatide 5 mg alone. Higher eloralintide doses in the same cohort reported 18.2% at 6 mg and 20.5% at 9 mg. Phase 2 results are scheduled for presentation on September 30, 2026.
When will eloraTZP Phase 2 data be released?
Lilly will present Phase 2 results for eloraTZP at an EASD-sponsored symposium on amylins in diabetes on Wednesday, September 30, 2026, from 4:30 to 5:30 p.m. CEST, at the 62nd EASD Annual Meeting in Milan. The trial enrolled adults with obesity or overweight and type 2 diabetes.
How does eloraTZP differ from retatrutide?
Retatrutide is a single molecule hitting GIP, GLP-1, and glucagon receptors. EloraTZP pairs two molecules and swaps the glucagon arm for amylin. Both are described as triple-acting, but the third mechanism is different — glucagon drives energy expenditure, while amylin acts on satiety signaling.
Can you buy eloraTZP or eloralintide?
No. Neither eloralintide nor eloraTZP is FDA-approved, and neither is currently stocked by research-peptide vendors — eloralintide has no established gray-market supply. The amylin analog that is available in the research market is cagrilintide, and tirzepatide is widely listed. Both are sold for research use only and are not approved for human use.

References

  • Eli Lilly and Company. "Lilly to present new data on Foundayo, retatrutide, and eloraTZP at EASD 2026, as it strives to change the course of cardiometabolic health." Investor news release, September 15, 2026.
  • PR Newswire. "Lilly to present new data on Foundayo, retatrutide, and eloraTZP at EASD 2026." September 15, 2026.
  • RTTNews. "Eli Lilly To Showcase Retatrutide, Foundayo & EloraTZP Data At EASD 2026." September 15, 2026.
  • BioSpace. "Lilly to present new data on Foundayo, retatrutide, and eloraTZP at EASD 2026." September 15, 2026.
  • American Diabetes Association. "3082-LB: The Selective Amylin Analog Eloralintide Enhanced Weight-Loss Efficacy when Combined with Tirzepatide in DIO Rats." Diabetes 75 (Supplement 1), ADA 2026.
  • European Association for the Study of Diabetes. 62nd EASD Annual Meeting programme, Milan, September 28 – October 2, 2026.