All therapiesEvidence snapshot 2026-10-02
Weight & glucose

EloraTZP

Eloralintide activates amylin receptors; tirzepatide activates GLP-1 and GIP receptors. The phase 2b study used separate injections. A co-formulated product is planned for phase 3; minimal calcitonin-receptor activity is not presented as an equal therapeutic target.

At a glance

Selected evidence in this atlas
Studied use & population

Adults with obesity or overweight and type 2 diabetes

Study context
Approval & development

Investigational; co-formulated AMPLIFY phase 3 planned for Q4 2026, not confirmed started.

Status & indications
Selected efficacy evidence

2.91 percentage-point HbA1c decrease · 2.41 pp decrease with Tirzepatide 15 mg weekly · 48 weeks

EloraTZP phase 2b · Phase 2b · sponsor · Eloralintide 9 mg + tirzepatide 15 mg once weekly, separate injections · Assuming continued treatment

Evidence & limitations
Important safety context

At eloralintide 9 mg + tirzepatide 15 mg: nausea 49%, diarrhea 30%, vomiting 24%; 27% discontinued because of adverse events. Comparator discontinuation was 2.9% with tirzepatide and 16.7% with placebo (slides round to 3% and 17%). Across combination arms, discontinuation ranged from 10.8% to 27.0%.

Safety context
Next milestone

Q4 2026 · EloraTZP co-formulated AMPLIFY phase 3 initiation.

Sponsor forecast

Milestone details

Study results apply to their own population, dose and analysis. They do not establish a ranking between therapies.

Evidence in the atlas

1 result

Each result belongs to its own study population, dose and analysis. Open a result for its chart, comparator, safety findings and limitations.

Glucose control

EloraTZP phase 2b

2.91 percentage-point HbA1c decrease · 2.41 pp decrease with Tirzepatide 15 mg weekly · 48 weeks

Eloralintide 9 mg + tirzepatide 15 mg once weekly, separate injections

Adults with obesity or overweight and type 2 diabetes

Model-based efficacy estimand: assumes all randomized participants remained on intervention through week 48, allowing dose interruptions/modifications. The modeled endpoint is separate from observed-visit means. Investigational; co-formulated AMPLIFY phase 3 planned for Q4 2026, not confirmed started.

Safety context

At eloralintide 9 mg + tirzepatide 15 mg: nausea 49%, diarrhea 30%, vomiting 24%; 27% discontinued because of adverse events. Comparator discontinuation was 2.9% with tirzepatide and 16.7% with placebo (slides round to 3% and 17%). Across combination arms, discontinuation ranged from 10.8% to 27.0%.

Safety source

Limitations: Small phase 2b arms; sponsor-reported efficacy estimand assumes continued intervention despite the substantial discontinuation rate. Primary comparison was weight change versus placebo; HbA1c and tirzepatide comparisons were secondary. Placebo HbA1c decrease was 0.29 pp. Weight loss was 23.3% versus 14.8% with tirzepatide and 3.0% with placebo. No co-formulated phase 3 result or approval.

Biology & identity

Status in this atlas: Investigational; co-formulated AMPLIFY phase 3 planned for Q4 2026, not confirmed started.

Hormone activity

Eloralintide activates amylin receptors; tirzepatide activates GLP-1 and GIP receptors. The phase 2b study used separate injections. A co-formulated product is planned for phase 3; minimal calcitonin-receptor activity is not presented as an equal therapeutic target.

EloraTZP is an investigational combination name, not an approved commercial brand. Zepbound and Mounjaro are brands of the tirzepatide component, not brands or approvals for this combination.

Eli Lilly and Company · Developer and clinical-trial sponsor of the eloralintide–tirzepatide combination.

Uses, doses and availability depend on the formulation, indication and country. Study doses below describe research; they are not prescribing instructions.

The molecule

An exact molecular structure has not yet been added for this therapy.

Development timeline

Next milestone

Q4 2026 · EloraTZP co-formulated AMPLIFY phase 3 initiation.

Sponsor forecast

Milestone calendar
Development history1 selected milestones

EloraTZP · compound history across indications

Selected combination-specific milestones. Earlier development of each component is recorded under eloralintide and tirzepatide; this is not a complete development history.

  1. Announcement

    Phase 2b results and phase 3 plan announced

    In 367 adults with obesity/overweight and T2D, the 9 mg + 15 mg combination achieved 23.3% weight loss and 2.91 pp HbA1c reduction at 48 weeks (efficacy estimand). Tirzepatide achieved 14.8% and 2.41 pp; placebo 3.0% and 0.29 pp. AE discontinuation was 27% at this combination dose. Co-formulated AMPLIFY phase 3 is forecast for Q4 2026, not a confirmed start.

    Source

Selected sources checked Oct 2, 2026. This is not an exhaustive history.