Weight Loss

Cagrilintide

Also known as: AM833, NN9838, CagriSema (combination)

Clinical Trials
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Key Facts: Cagrilintide

Category
Weight Loss
FDA Status
Not FDA Approved
Clinical Status
Phase 3 Trials - Primary path via CagriSema combo (cagrilintide + semaglutide). NDA submitted Dec 2025, FDA decision expected Q4 2026.
Administration
Subcutaneous injection once weekly
Typical Dose
2.4 mg weekly
Frequency
Once weekly
Duration
Long-term / chronic use expected
Also Known As
AM833, NN9838, CagriSema (combination)

Mechanism of Action

Cagrilintide is a non-selective agonist of the amylin and calcitonin receptor family. It activates amylin receptors (which are calcitonin receptors paired with RAMP accessory proteins) to signal satiety in the brain, slow gastric emptying, and blunt the post-meal glucagon rise. Mechanistic work in mice shows it reduces body weight mainly through amylin receptors AMY1R and AMY3R acting in the hindbrain, with the area postrema as a key entry point and downstream signaling through the nucleus of the solitary tract and parabrachial nucleus. Notably, weight loss in those studies persisted even after the acute appetite-suppressing effect faded, hinting at effects on energy balance beyond simple food-intake reduction. Chemically it is built on a pramlintide-like 37-amino-acid backbone with substitutions and a fatty-diacid chain attached to extend its half-life to roughly a week, enabling once-weekly dosing.

Research Summary

Cagrilintide has real human data, which sets it apart from most peptides in this category. In a 2021 Lancet phase 2 dose-finding trial (Lau et al.), once-weekly cagrilintide at 4.5 mg produced about 10.8% mean body weight loss over 26 weeks, beating both placebo (around 3%) and liraglutide 3.0 mg (around 9%), establishing that amylin agonism alone can drive clinically meaningful weight loss. Its bigger story is combination therapy: paired with semaglutide as CagriSema, it advanced into phase 3 REDEFINE trials for obesity and type 2 diabetes, with reported weight loss in the low 20% range, though final results came in somewhat below the most optimistic expectations. Side effects are dominated by the expected gastrointestinal effects (nausea, vomiting) common to gut-hormone drugs. As of 2026 cagrilintide is investigational and not FDA-approved on its own. The evidence is genuinely human and well-controlled here, which is rare, but it is still a drug under regulatory review rather than an approved therapy.

Trial Progress:Phase III
Pre
I
II
III
IV
FDA

Dosing Information

Human Trials·Phase 3 clinical trials completed, awaiting FDA approval

Typical Dosing

Community experience

Common Dose

2.4 mg weekly

Range

1.0-2.4 mg weekly (dose escalation)

Frequency

Once weekly

Most effective when combined with semaglutide (CagriSema). Works through amylin pathway which is complementary to GLP-1 mechanism. Dose escalation typically used to minimize GI side effects. Not yet commercially available - still in clinical trials.

Research Dosing

Scientific studies

Doses from clinical trials - not yet approved

Duration

Long-term / chronic use expected

Administration

Subcutaneous injection once weekly

Timing & Administration

Best Time to Take

Any consistent time weekly

Once weekly

Food Recommendation

With or without food

Why This Timing?

Once-weekly injection provides sustained amylin receptor activation. Timing is flexible but should be consistent week to week.

Possible Side Effects

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

  • Nausea (common, usually transient)
  • Vomiting
  • Diarrhea
  • Constipation
  • Abdominal pain
  • Injection site reactions
  • Decreased appetite
  • Headache
  • Dyspepsia
  • GI events affected 79.6% in CagriSema trials (mostly mild-moderate)
  • Limited long-term safety data - still in trials

References

Research This Peptide Further

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Cagrilintide from $108/kit

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Frequently Asked Questions

What does Cagrilintide do?

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.

How does Cagrilintide work?

Cagrilintide is a non-selective agonist of the amylin and calcitonin receptor family. It activates amylin receptors (which are calcitonin receptors paired with RAMP accessory proteins) to signal satiety in the brain, slow gastric emptying, and blunt the post-meal glucagon rise. Mechanistic work in mice shows it reduces body weight mainly through amylin receptors AMY1R and AMY3R acting in the hindbrain, with the area postrema as a key entry point and downstream signaling through the nucleus of the solitary tract and parabrachial nucleus. Notably, weight loss in those studies persisted even after the acute appetite-suppressing effect faded, hinting at effects on energy balance beyond simple food-intake reduction. Chemically it is built on a pramlintide-like 37-amino-acid backbone with substitutions and a fatty-diacid chain attached to extend its half-life to roughly a week, enabling once-weekly dosing.

Is Cagrilintide FDA approved?

No, Cagrilintide is not currently FDA approved. Current status: Phase 3 Trials - Primary path via CagriSema combo (cagrilintide + semaglutide). NDA submitted Dec 2025, FDA decision expected Q4 2026.

What are the side effects of Cagrilintide?

Reported side effects include: Nausea (common, usually transient), Vomiting, Diarrhea, Constipation, Abdominal pain. Individual responses vary based on dosage, duration, and personal health factors.

What is the typical dose of Cagrilintide?

Community-reported common dose: 2.4 mg weekly (Once weekly). Range: 1.0-2.4 mg weekly (dose escalation). Administration: Subcutaneous injection once weekly. Investigational drug - not yet approved. Clinical trial doses shown. Not medical advice.

Related Peptides

Peptides commonly compared with Cagrilintide or used in similar applications.

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

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

Dulaglutide

FDA

Dulaglutide (brand name Trulicity) is a once-weekly injectable GLP-1 receptor agonist made by fusing a modified GLP-1 peptide to a fragment of a human antibody, which is what lets it last a full week between shots. It is FDA-approved for type 2 diabetes and, notably, to reduce cardiovascular risk in adults with diabetes. The once-weekly dosing made it a major convenience step up from earlier daily and twice-daily agents.

Weight Loss

Retatrutide

Clinical Trials

Retatrutide is the heavy hitter of the new weight-loss drugs: a once-weekly injectable peptide that hits three receptors at once - GIP, GLP-1, and glucagon - earning it the nickname triple-G agonist. In a phase 2 trial it produced some of the largest weight loss ever recorded for a drug, up to roughly 24 percent of body weight at the top dose. It is investigational, made by Eli Lilly, and not yet FDA approved as of 2026.

Weight Loss

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