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Research compound · not FDA-approved

Zenagamtide

Also called Amycretin.

Zenagamtide, once called Amycretin, is an experimental weight-loss drug being tested as an injection and a pill. It acts on GLP-1 and amylin signals.

What matters first

Why people look it up
Sellers offer unapproved versions to people seeking weight loss, often under the older Amycretin name.
What the evidence shows
Early trials reported average weight loss with injected and oral forms. Phase 3 trials are registered, but no phase 3 result is available.
Dose status
Zenagamtide is not FDA-approved, so no dosing label exists for it. The sections below explain what researchers tested and what remains unknown.

Evidence snapshot

Published human trial

The fastest way to see what kind of evidence this page is built on.

Regulation
Not FDA-approvedNo US prescribing label
Dose source
Human study7 reported dose rows
Safety evidence
2 listed safety findingsCommon and serious effects shown apart
Sources
6 cited sourcesMedical review complete · 2026-08-17
Zenagamtide at a glance: published human trial, dosing basis, regulatory status, safety coverage, and cited-source count. These details summarize the available sources; they are not treatment recommendations.

Further down: research and dosing details · how it works · how good the evidence is · questions

Medically reviewed by Jennifer Montecillo, MD · non-practicing medical reviewerReviewed 2026-08-17open the primary sources

What is known about Zenagamtide

Zenagamtide, once called Amycretin, is an experimental shot and pill that acts on GLP-1 and amylin signals. An early shot study tested four doses for 20, 28 or 36 weeks. The 60 mg group lost an average of 24.3% at week 36, versus 1.1% with placebo. A later company update reported up to 14.6% in people with diabetes. No phase 3 result exists yet.

Zenagamtide research and regulatory details: evidence quality, approval status, doses, handling, and presentation.
TopicValue
Strongest sourceHuman trial
FDA approvalNot FDA-approved
Studied dosing1–25 mg one dose in phase 1 (1, 3, 6, 12, 18 or 25 mg) from clinical trials
Studied dosing3–12 mg daily for 10 days in phase 1 (3, 6 or 12 mg) from clinical trials
Studied dosing50–100 mg daily for 12 weeks after trial-set titration to a 50 or 100 mg target from clinical trials
Studied dosing1.25 mg once weekly for 20 weeks in phase 1b/2a from clinical trials
Studied dosing5 mg once weekly for 28 weeks in phase 1b/2a from clinical trials
Studied dosing20–60 mg once weekly for 36 weeks in phase 1b/2a (20 or 60 mg targets) from clinical trials
Studied dosing0.4–40 mg once weekly for 36 weeks in a company-announced phase 2b diabetes study from clinical trials
PresentationZenagamtide has no approved vial or reconstitution instructions; its trials study prepared oral and subcutaneous formulations.

Every row links back to a source listed below. These facts are for reference, not a personal recommendation.

How Zenagamtide works

Zenagamtide acts at GLP-1 + amylin. Here is what that means.

This design puts two meal-ending signals into one peptide. GLP-1 is released by the gut after eating. Amylin is released by the pancreas alongside insulin. Both can reduce how much someone eats, but they reach that outcome through different receptor systems.

◆ Receptor targets2 of 4 · GLP-1 + amylin
4What each receptor does 4 rows in the data table
Receptors targeted by Zenagamtide, and what each receptor does
ReceptorZenagamtideWhat it does
GLP-1targetedpancreas, gut and brainSupports insulin release while blood sugar is rising, slows stomach emptying and acts on brain circuits involved in appetite. The same stomach effect can also produce nausea and early fullness.
GIPnot targeted
Glucagonnot targeted
Amylintargetedarea postrema and hindbrainAdds a separate fullness signal from the brainstem and also slows how quickly food leaves the stomach. It is not a second GLP-1 signal, even when the visible effects overlap.

The same four receptor groups are shown for every drug, so the differences are easy to compare. Targets come from the drug class. Any result specific to Zenagamtide comes from the cited sources.

The pairing reaches fullness through two pathways. One milligram on either pathway does not mean the same thing. Trials still need to show whether that balance improves long-term results or how well people handle the drug. Early weight-loss results cannot answer that on their own.

What the evidence for Zenagamtide is

These numbers come from a study in people that was published in a peer-reviewed journal. The drug or dose may still be experimental and may not have FDA approval.

Human trial
What it establishes
The study gave known doses to a defined group, monitored what happened and compared the results with another group.
What it does not establish
One trial cannot prove long-term safety or show that the result applies to everyone. The highest dose tested is a study dose, not a target for personal use.

Read each result with the study length, dose and number of participants. Results from separate trials are not a direct comparison because the people and study designs differ.

Where Zenagamtide is in clinical trials

3 registered studies; the program has reached phase 3. Studies are running, but none is taking new participants.

The soonest a running study expects to finish measuring people is June 2028. That is when the sponsor expects to finish collecting the main measurement. It is not a results date, and not a date anything goes on sale.

  • Phase 3Not yet recruiting

    AMAZE 13: A Research Study Investigating How Well the Medicine Zenagamtide Helps People in Asia With Excess Body Weight Lose Weight

    Novo Nordisk A/S · Obesity, Overweight · 400 participants planned · started January 2027

    Main measurement due January 2029 (sponsor estimate)

    NCT07668401 on ClinicalTrials.gov

  • Phase 3Not yet recruiting

    A Research Study Investigating How Well the Medicine Zenagamtide Helps People With Excess Body Weight Lose Weight Compared to Semaglutide

    Novo Nordisk A/S · Overweight, Obesity · 650 participants planned · started September 2026

    Main measurement due October 2028 (sponsor estimate)

    NCT07668414 on ClinicalTrials.gov

  • Phase 3Not yet recruiting

    AMAZE 9: A Research Study Investigating How Well Zenagamtide Tablets Help People With Excess Body Weight Lose Weight

    Novo Nordisk A/S · Overweight, Obesity · 950 participants planned · started September 2026

    Main measurement due June 2028 (sponsor estimate)

    NCT07720271 on ClinicalTrials.gov

A registered study means a sponsor filed a plan and started enrolling. It is not evidence the drug works, and most drugs tested in people never reach a pharmacy. Sponsors write and update these sources themselves; the National Library of Medicine publishes them without checking them.

ClinicalTrials.gov · retrieved 2026-08-23

Every compound we track, and what stage each one has reached →

Regulatory status

Zenagamtide is not FDA-approved and has no approved dose.

The pill and shot use different study schedules. A listed trial shows what researchers plan to test; it does not prove that the drug works.

Full regulatory tracker →

Where to go next on Zenagamtide

The schedule, the side effects and the mixing math each have their own page.

Safety notes

  • Investigational compound — no approved dose or prescribing label exists
  • Oral and subcutaneous study quantities are not interchangeable
  • The phase 3 registrations have no results yet

Questions about Zenagamtide

Is Zenagamtide FDA-approved?

No. There is no prescribing label for it, so no approved dose exists — the regulatory status section above has the detail.

How is Zenagamtide taken?

Trials study it both by mouth and by injection under the skin. The table above keeps each route and schedule separate.

How does Zenagamtide differ from the other compounds in this class?

It acts at GLP-1 + amylin. The nearest alternatives act elsewhere: Tirzepatide (GIP + GLP-1), Semaglutide (GLP-1 alone), Liraglutide (GLP-1 alone), Retatrutide (GIP + GLP-1 + glucagon), Cagrilintide (amylin), Survodutide (glucagon + GLP-1), Mazdutide (glucagon + GLP-1), VK2735 (GIP + GLP-1), Pemvidutide (glucagon + GLP-1). Adding or removing a receptor changes both the effect and how much of it people can tolerate, so these molecules are not swappable at the same number of milligrams. Comparing them milligram for milligram is the most common mistake in this category.

What is not known about Zenagamtide?

One trial cannot prove long-term safety or show that the result applies to everyone. The highest dose tested is a study dose, not a target for personal use.

6primary sources, each with the day we read it — open the documents used on this page