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Weight Loss

Amycretin

Also known as: Zenagamtide, NNC0487-0111, GLP-1/amylin co-agonist

Clinical Trials
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Key Facts: Amycretin

Category
Weight Loss
FDA Status
Not FDA Approved
Clinical Status
Phase 3 (investigational) - Novo Nordisk began the AMAZE phase 3 program in 2026 for weekly subcutaneous amycretin in obesity (AMAZE 1, NCT07339423) and in obesity with type 2 diabetes (AMAZE 2), with oral amycretin also slated for phase 3. Not approved by FDA, EMA or any other regulator.
Banned in Sport (WADA)
Not named on the WADA list, but WADA's S0 catch-all bans any substance without human therapeutic approval, which covers it until it is approved. Prohibited at all times.
Administration
Subcutaneous injection once weekly, or oral tablet once daily (separate formulations)
Typical Dose
Trial doses of 1.25-40 mg once weekly (injection)
Frequency
Once weekly (injection) or once daily (tablet)
Duration
20-36 weeks in published trials; phase 3 runs longer
Also Known As
Zenagamtide, NNC0487-0111, GLP-1/amylin co-agonist

How does Amycretin work?

Amycretin hits two appetite systems at once. The GLP-1 side slows stomach emptying, boosts insulin release after meals, and dampens appetite in the brain, the same biology behind semaglutide. The amylin side mimics a hormone your pancreas releases alongside insulin, which acts on the brainstem to make you feel full sooner and also curbs glucagon after eating. Novo combined these two signals in one molecule rather than mixing two drugs (which is what its CagriSema combination does). The bet is that the two pathways add together, giving more weight loss than either alone. That idea fits the early data, but it has not yet been tested head-to-head against semaglutide or tirzepatide in a large trial.

What does the research show?

Two early trials were published in The Lancet in June 2025. In the subcutaneous phase 1b/2a trial (125 adults with overweight or obesity), the estimated weight loss assuming full adherence was 24.3% at 60 mg over 36 weeks and 22.0% at 20 mg over 36 weeks, versus roughly flat weight on placebo, with no plateau by the end of treatment. A separate phase 1 trial of the oral tablet (144 people, 12 weeks) showed up to 13.1% loss at the highest dose. In November 2025 Novo reported a 36-week phase 2 trial in 448 adults with type 2 diabetes: up to 14.5% weight loss with weekly injections (2.6% on placebo), up to 10.1% with the daily pill, and HbA1c drops of up to 1.8 points. Side effects were mostly gastrointestinal, dose-related, and mild to moderate. Novo moved both forms into phase 3; AMAZE 1 (weekly injection at 1.25, 5, 20 or 40 mg versus placebo, about 1,150 people without diabetes) is registered as NCT07339423 with completion expected in 2029. Honest caveats: the headline numbers come from small trials using an efficacy estimand that assumes everyone stayed on drug, and long-term safety is unknown.

Trial Progress:Phase III
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FDA

What doses have been studied?

Human Trials·Phase 1-2 trials published, phase 3 AMAZE program underway since 2026

Typical Dosingⓘ

Community experience

Common Dose

Trial doses of 1.25-40 mg once weekly (injection)

Range

0.4-60 mg weekly in trials; 6-100 mg daily for the oral form

Frequency

Once weekly (injection) or once daily (tablet)

These are trial doses, reached by gradual escalation over weeks to months to limit nausea. No dose has been approved, and the oral and injectable forms are not interchangeable mg for mg.

Research Dosingⓘ

Scientific studies

Trial doses only (investigational drug, no approved dose)

Duration

20-36 weeks in published trials; phase 3 runs longer

Administration

Subcutaneous injection once weekly, or oral tablet once daily (separate formulations)

When and how is Amycretin taken?

Best Time to Take

Same day each week (injection); trial protocols set timing for the tablet

Once weekly injection, or once daily tablet in oral trials

Food Recommendation

With or without food

Why This Timing?

The injectable form is long-acting and dosed weekly, so consistency matters more than time of day. Oral peptide tablets usually have strict fasting rules, but amycretin's final label instructions do not exist yet.

What are the side effects of Amycretin?

Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.

  • ●Nausea
  • ●Vomiting
  • ●Diarrhea and constipation
  • ●Reduced appetite
  • ●GI effects rise with dose and are most common during escalation
  • ●Expected GLP-1 class risks (gallbladder issues, pancreatitis) not yet characterized in large trials
  • ●No long-term human safety data

References

Research This Peptide Further

Frequently Asked Questions

What does Amycretin do?

Amycretin is Novo Nordisk's single-molecule agonist of both the GLP-1 and amylin receptors, developed as a once-weekly injection and a once-daily pill. Early trials produced some of the biggest weight-loss numbers seen with any obesity drug so far, and the injectable version entered phase 3 (the AMAZE program) in 2026. It is not approved anywhere, and everything known about it comes from company-run trials of up to 36 weeks.

How does Amycretin work?

Amycretin hits two appetite systems at once. The GLP-1 side slows stomach emptying, boosts insulin release after meals, and dampens appetite in the brain, the same biology behind semaglutide. The amylin side mimics a hormone your pancreas releases alongside insulin, which acts on the brainstem to make you feel full sooner and also curbs glucagon after eating. Novo combined these two signals in one molecule rather than mixing two drugs (which is what its CagriSema combination does). The bet is that the two pathways add together, giving more weight loss than either alone. That idea fits the early data, but it has not yet been tested head-to-head against semaglutide or tirzepatide in a large trial.

Is Amycretin FDA approved?

No, Amycretin is not currently FDA approved. Current status: Phase 3 (investigational) - Novo Nordisk began the AMAZE phase 3 program in 2026 for weekly subcutaneous amycretin in obesity (AMAZE 1, NCT07339423) and in obesity with type 2 diabetes (AMAZE 2), with oral amycretin also slated for phase 3. Not approved by FDA, EMA or any other regulator.

Is Amycretin banned in sport?

Not named on the WADA list, but WADA's S0 catch-all bans any substance without human therapeutic approval, which covers it until it is approved. Prohibited at all times.

What are the side effects of Amycretin?

Reported side effects include: Nausea, Vomiting, Diarrhea and constipation, Reduced appetite, GI effects rise with dose and are most common during escalation. Individual responses vary based on dosage, duration, and personal health factors.

What is the typical dose of Amycretin?

Community-reported common dose: Trial doses of 1.25-40 mg once weekly (injection) (Once weekly (injection) or once daily (tablet)). Range: 0.4-60 mg weekly in trials; 6-100 mg daily for the oral form. Administration: Subcutaneous injection once weekly, or oral tablet once daily (separate formulations). Community-reported doses. Not medical advice. Consult healthcare provider.

Related Peptides

Peptides commonly compared with Amycretin or used in similar applications.

Cagrilintide

Clinical Trials

Cagrilintide (also called AM833) is a long-acting synthetic analog of amylin, the gut-brain satiety hormone co-secreted with insulin by pancreatic beta cells. It is an investigational once-weekly injectable being developed by Novo Nordisk for obesity, most prominently as the amylin half of CagriSema (cagrilintide plus semaglutide). It is not yet approved as a standalone drug, but it has cleared phase 2 trials and is in late-stage development.

Weight Loss

Eloralintide

Clinical Trials

Eloralintide (Eli Lilly code LY3841136) is an investigational, long-acting, selective amylin receptor agonist given as a once-weekly subcutaneous injection for obesity. Amylin is the satiety hormone your pancreas releases alongside insulin, and eloralintide is built to mimic it without the gut side effects that sink most appetite drugs. It is not approved anywhere yet, but it has cleared Phase 1 and a 263-person Phase 2 trial with weight loss up to roughly 20 percent, and Lilly has said it is moving into Phase 3.

Weight Loss

Petrelintide

Clinical Trials

Petrelintide is a long-acting amylin analog from Zealand Pharma, co-developed with Roche, designed as a once-weekly injection for obesity. The pitch is gentler weight loss than GLP-1 drugs but with far less nausea and vomiting. Two phase 2 trials read out positively in 2026 (up to 10.7% weight loss at 42 weeks), and a roughly 7,000-person phase 3 program has started. It is not approved anywhere.

Weight Loss

Tirzepatide

FDA

Tirzepatide is a single peptide that activates two receptors at once: GIP and GLP-1, the two main incretin hormones your gut releases after eating. It is FDA-approved as Mounjaro for type 2 diabetes and as Zepbound for chronic weight management and obstructive sleep apnea, and it has produced the largest weight-loss numbers of any approved drug to date. Like semaglutide, this is a heavily trialed, fully approved medicine, not a gray-market research compound.

Weight Loss

CagriSema

Clinical Trials

CagriSema is a once-weekly injectable that pairs two drugs in one shot: semaglutide (a GLP-1 receptor agonist, the molecule behind Ozempic and Wegovy) and cagrilintide (a long-acting amylin analog). It is being developed by Novo Nordisk for obesity and type 2 diabetes, and in 2025 it cleared its phase 3 REDEFINE trials. It is not yet approved by the FDA, though regulatory filings are underway.

Weight Loss

Liraglutide

FDA

Liraglutide is a once-daily injectable GLP-1 receptor agonist, a synthetic peptide that shares about 97% of its sequence with the natural gut hormone GLP-1 but is engineered with a fatty acid chain so it survives in the body far longer. It is FDA-approved as Victoza for type 2 diabetes (2010) and as Saxenda for chronic weight management (2014), and is one of the most studied drugs in its class. As of 2024 a generic version is also FDA-approved.

Weight Loss

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