Cagrilintide

Also known as: Cagrilintide Tre; Long-Acting Acylated Amylin Analogue

Overview

Cagrilintide is a long-acting amylin analogue that regulates appetite, slows gastric emptying, and improves glucose control, making it effective for weight loss and glycemic management. When combined with GLP-1 receptor agonists like semaglutide, it enhances metabolic outcomes and supports sustained weight reduction. Cagrilintide is a synthetic, long-acting amylin analogue developed to enhance metabolic health and support weight management. It is structurally similar to natural amylin but includes key modifications, such as lipidation of the N-terminal lysine and specific amino acid substitutions (N14E, V17R, and P37Y), which improve stability and therapeutic efficacy. By activating amylin receptors and modulating hunger and energy expenditure, Cagrilintide has shown promise in obesity management and glycemic control, particularly when combined with GLP-1 receptor agonists like semaglutide.

Benefits

- Effective weight loss

- Improved glycemic control

- Sustained results

- Complementary therapy

Consider This Peptide If You Want To

- Support weight loss and appetite control by enhancing satiety and reducing food intake

- Regulate blood sugar levels and improve metabolic health

Dosage & Administration

Dosage Guidelines

Recommended Dosage

• Amount:300 mcg

• Frequency:weekly

• Duration:8 weeks

• Rest Period:8 weeks

• Time of Day:morning

• Ingestion:subcutaneous

Administration Routes:Subcutaneous

Research Findings on Dosage:

• Subcutaneous Injection:

◦ Commonly Reported Dosage: 300-450 mcg once weekly.

◦ Duration: Studied up to 32 weeks in clinical trials.

▪ Notes: Commonly combined with GLP-1 receptor agonists for enhanced efficacy.

Mechanism of Action

Mechanism of Action

How this peptide works in the body

Appetite Regulation:

Cagrilintide activates amylin receptors (AMYRs) in the area postrema and nucleus of the solitary tract (NTS) of the brainstem, reducing hunger and increasing satiety. This activation modulates neuropeptide signaling, including suppression of neuropeptide Y (NPY) (which promotes hunger) and stimulation of pro-opiomelanocortin (POMC)(which enhances satiety), leading to a sustained decrease in food intake.

Gastric Emptying Delay:

By modulating vagal nerve activity, Cagrilintide reduces gastrointestinal motility and slows gastric emptying, prolonging the sensation of fullness after meals. This occurs through amylin receptor activation in the dorsal vagal complex (DVC), which decreases cholinergic signaling to the stomach, resulting in delayed gastric emptying and prolonged nutrient absorption.

Glucose Control:

Cagrilintide enhances postprandial glucose regulation by suppressing glucagon secretion from pancreatic alpha cells, reducing hepatic glucose production. This leads to improved insulin sensitivity and more stable blood sugar levels, particularly in individuals with type 2 diabetes or insulin resistance.

Combination Benefits:

When used with GLP-1 receptor agonists like semaglutide, Cagrilintide amplifies weight loss and metabolic benefits by targeting complementary pathways. GLP-1 enhances insulin secretion and beta-cell function, while amylin receptor activation reduces appetite and delays gastric emptying, creating a synergistic effect for superior metabolic outcomes.

Consider Stacking With

- Semaglutide/Tirzepatide

- Any GHRP (Ipamorelin, GHRP-2)

- Any GHRH (CJC-1295, MOD-GRF-1295, Tesamorelin)

- AOD-9604

- MOTS-c

- 5-Amino-1MQ

- BPC-157

- TB-4

Side Effects & Cautions

Common Side Effects

- Gastrointestinal symptoms such as nausea, vomiting, and mild constipation

Research & References

Research Highlights

Clinical Efficacy:

Phase 2 trials demonstrated a 15.6% mean weight reduction with Cagrilintide and semaglutide combination therapy over 32 weeks.

Glycemic Improvements:

Significant reductions in HbA1c levels observed in type 2 diabetes patients.

Safety Profile:

Low incidence of adverse effects with sustained efficacy over prolonged periods.

References

Lutz, T.A. "Creating the Amylin Story." Appetite, 2022. https://doi.org/10.1016/j.appet.2022.105965

Novo Nordisk, "Phase 2 Clinical Trial Results of Cagrilintide," 2024

Jensen, J. et al., "Amylin Analogues in Obesity Management," Metabolism, 2023

Smith, P. et al., "Cagrilintide and GLP-1 Synergy," Obesity Reviews, 2024