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WEIGHT LOSS

Cagrilintide

Cagrilintide (Long-Acting Amylin Analog)

Long-Acting Amylin Analog for Weight Loss

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The information on this page is compiled from peer-reviewed research and is provided for educational and research purposes only. It is not medical advice, a diagnosis, or a treatment recommendation. Peptides discussed here may not be approved for human use in your jurisdiction. Always consult a qualified healthcare provider before starting, stopping, or modifying any health protocol.

Overview

What is Cagrilintide?

Cagrilintide is a long-acting amylin analog developed by Novo Nordisk as a once-weekly injectable for the treatment of obesity. Amylin is a peptide hormone co-secreted with insulin from pancreatic beta cells; it plays a key role in regulating satiety by acting on homeostatic and hedonic regions of the brain, slowing gastric emptying, and suppressing glucagon release. Cagrilintide replicates and substantially extends these effects through modifications that increase its half-life and receptor binding stability compared to native amylin.

Phase 2 data published in The Lancet (2021) established the dose-ranging profile of cagrilintide as monotherapy, demonstrating up to 10.8% body weight reduction over 26 weeks compared to 3.0% with placebo [1]. Monotherapy results at 68 weeks showed an average body weight reduction of 11.8% versus 3.0% for placebo, establishing clinical meaningfulness even before combination therapy was explored.

The most compelling data comes from the CagriSema combination program, pairing cagrilintide with the GLP-1 receptor agonist semaglutide. The REDEFINE 1 trial, published in the New England Journal of Medicine, showed a mean body weight reduction of 20.4% over 68 weeks for the combination group [2] versus 3.0% for placebo. Sixty percent of participants achieved at least 20% weight loss, and 23% lost 30% or more of body weight. These results reflect an additive mechanism: cagrilintide acts on amylin receptors while semaglutide acts on GLP-1 receptors, producing complementary appetite suppression across different neural circuits.

Cagrilintide is not currently FDA-approved for any indication as of early 2026 and remains under investigation. Its use outside of clinical trials is considered off-label and investigational. All research and clinical interest is directed at understanding how amylin-pathway activation can complement existing GLP-1-based therapies for sustainable obesity management.

Research Supply

Source high-purity Cagrilintide for your research

Protocol

Dosage Guide

Route: Subcutaneous injection, once weekly

Dosing Schedule

PeriodDose
Weeks 1-40.25 mg once weekly
Weeks 5-80.5 mg once weekly
Weeks 9-121.0 mg once weekly
Weeks 13-161.7 mg once weekly
Week 17+ (maintenance)2.4 mg once weekly

Reconstitution

VIAL SIZEVaries by supplier
WATER VOLUMEBacteriostatic water (0.9% benzyl alcohol) per vial labeling
CONCENTRATIONPer vial-specific labeling
Varies by reconstitution volume

Injection Volumes

DoseVolumeSyringe Units

Administration Tips

  • Administer subcutaneously once weekly; the extended half-life supports once-weekly dosing without daily injections
  • The dose escalation protocol is designed to minimize gastrointestinal side effects during initiation
  • In the phase 2 monotherapy trial, the 2.4 mg dose was identified as the optimal balance of efficacy and tolerability
  • Reconstitute lyophilized powder with bacteriostatic water using standard aseptic technique; follow vial-specific labeling
Safety

Risks & Side Effects

Commonly Reported

Nausea (most common, particularly during dose escalation)VomitingDiarrheaConstipationAbdominal discomfort or painDecreased appetite (expected pharmacological effect)Injection site reactions (redness, bruising, local irritation)Fatigue, especially early in treatment

Serious Risks

Pancreatitis

Risk signal consistent with other amylin/GLP-1 class agents; discontinue if pancreatitis is suspected.

Severe dehydration

Can occur secondary to prolonged vomiting or diarrhea, particularly early in treatment.

Gallbladder disease

Cholelithiasis observed at higher rates in significant weight loss trials across the GLP-1 class.

Hypoglycemia

Particularly if combined with insulin secretagogues or insulin.

Related Research
Expert Voices

Experts Covering Cagrilintide

LEGAL DISCLAIMER

The information provided on this page is for educational and informational purposes only and is not intended as medical advice. Cagrilintide has not been approved by the FDA for any medical condition. Always consult with a qualified healthcare professional before starting any peptide therapy. Individual results may vary. Peptides Institute is not responsible for any adverse effects resulting from the use of information provided on this site.

Frequently Asked Questions

What is Cagrilintide and how does it work?
Cagrilintide is a long-acting amylin analog developed by Novo Nordisk as a once-weekly injectable for obesity treatment. Amylin is a hormone co-secreted with insulin that regulates satiety, slows gastric emptying, and suppresses glucagon. Cagrilintide extends these effects through modifications increasing its half-life and receptor stability.
How much weight can you lose with Cagrilintide?
Phase 2 monotherapy data showed up to 11.8% body weight reduction at 68 weeks [1]. Combined with semaglutide as CagriSema in the REDEFINE 1 trial, participants achieved a mean 20.4% body weight reduction over 68 weeks, with 60% achieving at least 20% weight loss and 23% losing 30% or more.
What is CagriSema?
CagriSema is the combination of cagrilintide (amylin analog) with semaglutide (GLP-1 receptor agonist). The two compounds produce complementary appetite suppression [2] through different neural circuits. The REDEFINE 1 trial demonstrated 20.4% average weight loss, significantly exceeding either compound alone.
What are Cagrilintide side effects?
The most common side effects are gastrointestinal: nausea (especially during dose escalation), vomiting, diarrhea, constipation, and abdominal discomfort. Decreased appetite is an expected pharmacological effect. Serious risks include pancreatitis, severe dehydration from prolonged vomiting, and gallbladder disease with significant weight loss.
Is Cagrilintide FDA approved?
Cagrilintide is not currently FDA-approved for any indication as of early 2026 and remains under investigation. The combination product CagriSema is in late-stage clinical development. All current use outside of clinical trials is considered off-label and investigational with limited safety characterization.
How is Cagrilintide dosed?
Cagrilintide follows a gradual dose escalation: 0.25 mg weekly for weeks 1 to 4, increasing through 0.5, 1.0, and 1.7 mg steps, reaching the maintenance dose of 2.4 mg weekly by week 17. This slow titration protocol minimizes gastrointestinal side effects during treatment initiation.

References

  1. Lau DCW, Erichsen L, Francisco-Ziller N, et al.. Once-weekly cagrilintide for weight management in people with overweight and obesity: a multicentre, randomised, double-blind, placebo-controlled and active-controlled, dose-finding phase 2 trial. Lancet. 2021. PMID 34798060
  2. Enebo LB, Berthelsen KK, Kankam M, et al.. Safety, tolerability, pharmacokinetics, and pharmacodynamics of concomitant administration of multiple doses of cagrilintide with semaglutide 2.4 mg for weight management: a randomised, controlled, phase 1b trial. Lancet. 2021. PMID 33894838
  3. Kruse T, Hansen JL, Dahl K, et al.. Development of Cagrilintide, a Long-Acting Amylin Analogue. J Med Chem. 2021. PMID 34288673

Regulatory & Official Sources