Cagrilintide 10 mg
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Cagrilintide 10 mg

Drug Class: Amylin Analog
Composition: Cagrilintide Acetate
Dosage: 10 mg/vial
Form: Lyophilized Powder
Unit: 2 mL Vial
Brand: Peptide Hubs
For Research and Laboratory Use Only

Out of stock

Peptide Hubs Cagrilintide: The Next-Generation Research Peptide for Metabolic Science

For researchers at the forefront of metabolic science and weight management, Peptide Hubs introduces its premium Cagrilintide 10 mg. This long-acting amylin analogue represents a significant leap forward in the study of appetite regulation and energy expenditure. Sourced and stocked within the USA, our Cagrilintide is supplied as a highly pure, lyophilized powder in a sterile 2 mL vial, ensuring stability and precise dosing for advanced research protocols.

As a trusted leader in research compounds, Peptide Hubs guarantees the highest standards of purity and product integrity. When you buy Cagrilintide USA from us, you are investing in a reliable, potent, and consistent research chemical backed by our commitment to excellence and fast, discreet domestic shipping.

What is Cagrilintide?

Cagrilintide is a novel, long-acting acylated amylin analogue that mimics the activity of the naturally occurring hormone amylin. Amylin is co-secreted with insulin by the pancreas and plays a crucial role in regulating blood glucose, satiety, and gastric emptying. A study published in The Lancet highlighted cagrilintide's potent weight-loss effects in clinical trials, demonstrating its potential as a powerful tool for metabolic research. Its engineered structure provides a significantly extended half-life compared to the native hormone, allowing for sustained research effects with less frequent administration.

Mechanism of Action

Understanding how Cagrilintide works is key to its research application. Its primary mechanisms are multifaceted and potent:

  • Appetite Suppression: It acts centrally on amylin receptors in the brain's appetite control centers, particularly the area postrema, to powerfully reduce hunger and increase feelings of fullness (satiety).
  • Slowed Gastric Emptying: Cagrilintide delays the emptying of the stomach's contents into the small intestine. This prolongs the sensation of stomach fullness after eating and helps blunt post-meal blood glucose spikes.
  • Glucagon Suppression: It inhibits the secretion of glucagon, a hormone that raises blood sugar, thereby contributing to better overall glycemic control.
  • Energy Expenditure: Some research suggests that amylin analogues may have a modest effect on increasing energy expenditure, contributing to a negative energy balance.

Effects of Cagrilintide

In research settings, the effects of Cagrilintide are profound and directly target the mechanisms of weight management. Key observed outcomes include:

  • Significant and Sustained Weight Loss: Research data indicates dose-dependent, substantial reductions in body weight, making it a compound of high interest for obesity and metabolic syndrome studies.
  • Marked Reduction in Caloric Intake: Through its potent appetite-suppressing effects, subjects consistently demonstrate a lower voluntary calorie consumption.
  • Improved Glycemic Control: By modulating gastric emptying and glucagon secretion, it contributes to stabilized blood glucose levels.
  • Reduction in Body Fat Percentage: The weight loss driven by Cagrilintide is characterized by a significant loss of adipose tissue, which is a primary focus in body composition research.

Dosage and Administration

Important: The following information is based on emerging research protocols and is provided for educational purposes only. Researchers must consult current scientific literature to determine appropriate dosages for their specific models.

Cagrilintide is administered via subcutaneous injection. Due to its long half-life of approximately 7-8 days, it is typically administered once weekly. Research dosages are still being defined, but clinical trials have explored a range from 0.5 mg to 4.5 mg administered once weekly.

Reconstitution: The lyophilized powder must be reconstituted with Bacteriostatic Water (Bac Water). Reconstituting a 10 mg vial with 2 mL of Bac Water yields a concentration of 5 mg per mL. A 0.1 mL injection would then deliver a 0.5 mg dose. Proper aseptic technique is crucial. Peptide Hubs offers pharmaceutical-grade Bac Water for this purpose.

Cycle and Research Stacking

Research cycles with Cagrilintide are typically long-term, reflecting its use in chronic weight management studies. Cycles often range from 12 to 24 weeks to observe significant and sustained metabolic changes. Its unique mechanism makes it an excellent candidate for powerful combination research.

Here are advanced research stacks involving Peptide Hubs Cagrilintide:

  • For Maximum Appetite Suppression and Fat Loss: Stack Cagrilintide with Semaglutide 5 mg. This combination of an amylin analogue and a GLP-1 agonist targets multiple satiety pathways simultaneously for potentially synergistic effects.
  • For Enhanced Lipolysis and Metabolic Rate: Combine with AOD 9604 5 mg to research the effects of targeted fat breakdown alongside powerful appetite control.
  • For Body Recomposition and Muscle Preservation: Add Tesamorelin/Ipamorelin to a Cagrilintide protocol to investigate the preservation of lean muscle mass during significant caloric deficit.
  • For Comprehensive Metabolic and Anti-Aging Research: Research the systemic effects by stacking with NAD+ 100 mg to support cellular energy and metabolism while managing weight.
  • For Post-Cycle Weight Management: Utilize Cagrilintide after a research phase with growth-promoting compounds to manage rebound weight gain, potentially stacking it with Gonadorelin 10 mg for endocrine system support.

Possible Side Effects

Based on clinical research, the side effects of Cagrilintide are primarily related to its mechanism of action on the GI tract and are generally mild to moderate, often subsiding with continued use. Researchers should monitor for:

  • Gastrointestinal Discomfort: This is the most common category and can include nausea, vomiting, diarrhea, and constipation, especially during the initial dose-titration phase.
  • Decreased Appetite: While this is a desired research effect, it can be pronounced and must be managed to ensure adequate nutrient intake in research models.
  • Injection Site Reactions: As with any subcutaneous injection, there is a potential for minor redness, swelling, or itching at the administration site.
  • Mild Hypoglycemia: In models where insulin or other glucose-lowering agents are used, the combined effect with Cagrilintide could potentially increase the risk of low blood sugar.

Notably, Cagrilintide does not exhibit androgenic, estrogenic, or progestogenic activity and has no known impact on the HPTA axis.

Why Choose Peptide Hubs Cagrilintide?

Choosing to buy Cagrilintide USA from Peptide Hubs means securing a cutting-edge research compound of uncompromising quality. We understand the critical nature of consistency and purity in metabolic research. Our products are manufactured to the highest standards, and our direct USA distribution ensures your research is never delayed. Trust Peptide Hubs to be your source for the most advanced peptides in the scientific landscape.

Cagrilintide Profile

Name: Cagrilintide
Drug Class: Long-Acting Amylin Analogue
Other common names and terms: AM-833
Active Life: 7-8 days
Detection Time: Not well-established; estimated 2-3 weeks
Chemical Structure: Acylated Amylin Analogue
Common Doses: 0.5 mg - 4.5 mg, administered once weekly
Blood pressure: May cause a slight decrease
Acne: No significant effect reported
Water retention: No significant effect reported
Aromatisation: Does not aromatize
Liver toxicity: No liver toxicity reported
Decrease HPTA function: No significant suppression of the HPTA axis

How is Cagrilintide different from Semaglutide or Tirzepatide?

Cagrilintide, Semaglutide, and Tirzepatide all promote weight loss but through different primary pathways. Semaglutide is a GLP-1 receptor agonist, primarily reducing appetite and food intake. Tirzepatide is a dual GIP and GLP-1 receptor agonist. Cagrilintide, however, is an amylin analogue. It mimics the natural hormone amylin, suppressing appetite, slowing gastric emptying, and suppressing glucagon. This unique mechanism offers a different pathway for research, and early studies on its combination with Semaglutide show potentially synergistic, powerful effects.

How often is Cagrilintide administered?

Due to its engineered long-acting structure, Cagrilintide has a half-life of approximately one week. This allows for a convenient once-weekly administration schedule in research protocols. This less frequent dosing can be advantageous for long-term studies on weight management and metabolic health compared to daily-administered compounds.

What are the most common side effects in research?

The most frequently observed side effects are gastrointestinal in nature and are a direct extension of its pharmacological action. These include nausea, vomiting, diarrhea, and constipation. These effects are typically dose-dependent and are most common during the initial phase of research. They often diminish as the research subject adapts to the compound.

Can Cagrilintide be stacked with other weight loss peptides?

Yes, Cagrilintide is an excellent candidate for combination research. Its most powerful stack appears to be with GLP-1 agonists like Semaglutide, targeting multiple satiety pathways. It can also be stacked with peptides that enhance fat oxidation, like AOD 9604, or with growth hormone secretagogues like Tesamorelin/Ipamorelin to study the preservation of lean mass during significant weight loss.

How should Cagrilintide be stored?

Before reconstitution, the lyophilized powder should be stored refrigerated between 2°C and 8°C (36°F and 46°F) and protected from light. After reconstitution with Bacteriostatic Water, the solution must be refrigerated and is typically stable for several weeks (refer to specific laboratory guidelines). Always use aseptic techniques to prevent microbial contamination.

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