Drug evidence profileInvestigational - not FDA approved

Zenagamtide (formerly Amycretin): trials, results, and current status.

Also searched as amycretin · NNC0487-0111 · AMAZE 7

Zenagamtide, formerly called amycretin, is Novo Nordisk’s investigational single-molecule GLP-1 and amylin receptor agonist. Both a once-daily tablet and a once-weekly injection are in development, so calling it only “the pill” misses half the program.

Name and formulation

Is Amycretin now Zenagamtide, and is it a pill?

Yes, Zenagamtide is the current name for the molecule formerly called Amycretin. A once-daily oral tablet and a once-weekly injection are both in development, so it is not only a pill. Both formulations remain investigational, and the small 12-week oral Phase 1 result is not an approved product claim.

Live decision workspace

Compare Amycretin / Zenagamtide with Retatrutide, without losing the country context.

Put evidence status, ClinicalTrials.gov coverage, official United States records, and qualified US research prices in one view. Blank fields stay blank when the underlying dataset does not support a number.

AIdentity record
Amycretin / Zenagamtide

Investigational clinical program

No linked research price board
Destination fixedUnited StatesNorth America

Official product and seller records attached

BComparison record
Retatrutide

Investigational clinical program

No linked research price board
01 · Status02 · Trials03 · Country04 · Price
Current program snapshot

What can you conclude about Zenagamtide today?

These are dated program facts, not a cross-trial ranking, approval forecast, personal treatment recommendation, or proof that a same-name online product is the sponsor's medicine.

Current nameZenagamtide

Novo Nordisk now uses zenagamtide for the asset formerly called amycretin.

Oral Phase 113.1% at 12 weeks

Exploratory mean weight change in a small early cohort of 16 participants, versus 1.1% with placebo.

Two formulationsTablet + injection

Once-daily oral and once-weekly subcutaneous programs are being developed separately.

Current Phase 3 recordAMAZE 7

A not-yet-recruiting trial plans to compare weekly zenagamtide with weekly semaglutide in 650 adults with obesity.

Marketing and authorization statusInvestigational - not FDA approved
Evidence checked July 20, 2026Open lead source
Program identity

Know which molecule the result belongs to.

Sponsor
Novo Nordisk
Mechanism
GLP-1 + amylin receptor agonist
Route being studied
Once-daily oral or once-weekly subcutaneous
Current stage
Phase 3 development underway
Featured trial anchors
NCT06049329 · NCT07503210 · NCT07668414
Evidence checked
July 20, 2026
Sourced weight-loss trial results

Zenagamtide weight-loss results, with the trial attached.

This visual shows one selected result, not every dose or endpoint in the program. The percentage remains attached to its duration, population, comparator, analysis method, and source.

Evidence checked July 21, 2026
Phase 1Daily oral
NCT05369390
13.1%Active-arm mean
First-in-human oral multiple-dose cohort12 weeks

Zenagamtide reported 13.1% mean reduction at 12 weeks under the sponsor-reported exploratory phase 1 mean. The comparator recorded 1.1% mean reduction.

Zenagamtide reported mean13.1%
Comparator mean1.1% mean reduction

Bar lengths share a 0 to 30% visual scale. They describe this selected record and do not make separate trials head-to-head.

Population
Adults with obesity or overweight
Participants
16 Active oral cohort only
Dose
Oral dose reported in the 12-week cohort
Primary analysis
Sponsor-reported exploratory Phase 1 mean
Regulatory status
Investigational; not FDA approved
ClinicalTrials.gov program landscape

Zenagamtide clinical trials by status, phase, and location.

The current exact-intervention snapshot matches 24 unique NCT records. This chart describes registry coverage and current study fields. It does not compare efficacy, safety, approval probability, eligibility, or treatment access.

Snapshot 2026-07-24
24matched NCT records
10overall Recruiting
0registry results posted
935recruiting site observations
28countries with recruiting sites
Registry phase mix3 phase labels
Phase labels come from ClinicalTrials.gov. A larger phase count is not stronger evidence or a better program.
2026 pipeline guide

What comes after Retatrutide?

Compare Zenagamtide/Amycretin, MariTide, CagriSema, standalone cagrilintide, and survodutide by route, evidence maturity, trial result, and approval status without ranking unrelated studies as one race.

Open the upcoming weight-loss drugs guide →
Worldwide status map

Amycretin / Zenagamtide across 42 countries.

This profile establishes the program identity and its cited clinical or regulatory record. It does not turn a same-name seller listing into the sponsor’s asset or prove authorization, availability, or lawful supply in another destination.

Compare Amycretin / Zenagamtide by country →Compare Amycretin / Zenagamtide by US state →Browse the global peptide country dataset →
Country-specific status checks

Is Zenagamtide approved or available in your country?

Start with the United States FDA record, then check the destination that matters to you. Each country page separates drug identity, authorization, product records, seller claims, and supply rules. Directory checked July 20, 2026.

Evidence ledger

What the record shows - and what it doesn’t.

Trial percentages are kept beside the design details that make them interpretable. Unknowns stay visible instead of being filled with launch speculation.

Supported
01

The 13.1% result was an early signal

Novo Nordisk’s 2024 investor material reported 13.1% mean weight loss after 12 weeks with oral amycretin versus 1.1% with placebo. The active cohort included 16 participants, so the result is useful for explaining why development continued, not for declaring a market winner.

02

Later Phase 2 data broadened the picture

In 262 adults with type 2 diabetes, Novo Nordisk reported 14.6% observed mean weight reduction with weekly subcutaneous zenagamtide 40 mg at 36 weeks versus 2.1% with pooled placebo. Its dose-response model estimated 14.5%. The dose-finding trial was not a head-to-head comparison against retatrutide or an approved obesity medicine.

03

AMAZE 7 creates a direct semaglutide question, not an answer

The Phase 3 AMAZE 7 record plans to randomize 650 adults with obesity to weekly zenagamtide or weekly semaglutide, with body-weight change measured through week 84. The record was not yet recruiting when posted on June 25, 2026 and estimates an October 2028 primary completion. A comparative design does not produce a result before the trial is conducted and reported.

Not established
01

“Strongest pill” is not established

The early oral result came from a small Phase 1 cohort and was not a direct comparison with retatrutide, CagriSema, or approved medicines. Cross-trial speed and percentage comparisons are unreliable.

02

No approved dose or launch date

The oral and injectable formulations remain investigational. A commercial formulation, final dose, FDA decision, price, and insurance coverage are not established.

03

Tolerability needs Phase 3 context

Novo Nordisk says the safety profile was consistent with incretin and amylin-based therapies, with gastrointestinal events most common. Larger and longer trials are needed to characterize benefits and harms more completely.

Direct answers

The questions behind the search.

Concise answers based on the dated sponsor and trial records below. This is educational reporting, not medical advice.

01

Are zenagamtide and amycretin the same drug?

Yes. Zenagamtide is the current name for the Novo Nordisk molecule previously called amycretin, also identified in early records as NNC0487-0111. It is a single, long-acting peptide designed to activate both GLP-1 and amylin receptors. Older trial results and references still use amycretin, while newer sponsor announcements and Phase 3 records increasingly use zenagamtide. Following both names prevents older evidence and newer development updates from becoming disconnected.

02

Is zenagamtide an oral weight-loss pill?

An oral tablet is one part of the program, but zenagamtide is not only a pill. Novo Nordisk is developing once-daily oral and once-weekly subcutaneous versions. Both remain investigational. The often-cited 13.1% result came from a small, 12-week Phase 1 oral cohort. Later studies have evaluated both routes, and Phase 3 programs are intended to determine whether either formulation has a benefit-risk profile that supports regulatory approval.

03

Did zenagamtide cause 13.1% weight loss in 12 weeks?

Novo Nordisk reported a 13.1% mean reduction after 12 weeks in an exploratory oral Phase 1 cohort, compared with 1.1% for placebo. The active group had 16 participants. That is a promising early signal, but it is not proof that every patient would lose that amount, that the effect is faster or stronger than another drug, or that the same result will hold in larger Phase 3 populations.

04

What is the zenagamtide AMAZE 7 trial?

AMAZE 7 is a Phase 3 randomized trial designed to compare once-weekly subcutaneous zenagamtide with once-weekly subcutaneous semaglutide in an estimated 650 adults with obesity. The ClinicalTrials.gov record was not yet recruiting on June 25, 2026, listed an estimated September 2026 start, and measures relative body-weight change through week 84. It has no efficacy or safety results yet and does not establish that zenagamtide is better than semaglutide.

Important boundaryApproval status is jurisdiction-specific.

Do not use an investigational name, trial dose, or online research listing as a substitute for approved care. This page does not recommend treatment, sourcing, or participation in a clinical trial.

Understand the product-category boundary →
Primary referencesResearch and early development presentationOral Phase 1 cohort size and 13.1% 12-week resultNovo Nordisk · March 2024Phase 2 amycretin results in type 2 diabetesOral and subcutaneous schedules, Phase 2 weight results, and safety summaryNovo Nordisk · November 25, 2025Zenagamtide Phase 2 results presented at ADA 2026Current name, unimolecular peptide identity, 262-participant design, observed 14.6% result, modeled 14.5% estimate, placebo result, and Phase 3 planNovo Nordisk · June 6, 2026AMAZE 7 zenagamtide versus semaglutide Phase 3 study - NCT07668414Not-yet-recruiting status, randomized comparator, estimated enrollment, schedule, week-84 outcome, and completion timingClinicalTrials.gov · Record posted June 25, 2026Innovation and therapeutic focus - Annual Report 2025Zenagamtide rename, mechanism, formulations, and Phase 3 statusNovo Nordisk · February 2026