Cagrilintide

Batch #449021Batch #449021
Report #53443Report #53443
Tested at 10.53mgTested at 10.53mg
Size: 10mg
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RESEARCH USE ONLY
These compounds are NOT intended for human consumption, clinical use, or veterinary applications. We are not affiliated with any pharmaceutical companies or their commercial medications. By placing an order, you certify these materials will be used exclusively for in vitro testing and laboratory experimentation only. Bodily introduction of any kind into humans or animals is strictly forbidden by law. This product should only be handled by licensed, qualified professionals. This product is not a drug, food, or cosmetic and may not be misbranded, misused or mislabeled as a drug, food or cosmetic.

About Cagrilintide

Cagrilintide is a long-acting analogue of amylin a naturally occurring peptide that is co-released with insulin. It has been studied for its role in metabolic processes and its potential effects on liver function cardiovascular systems and cellular mechanisms. Research has also explored its use in combination with other compounds for enhancing metabolic pathways with ongoing investigations into its broader biological functions.

Product Specifications

Cagrilintide Lyophilized Powder in 3ml vial.

Application

Amylin receptor agonist research

Appearance

Solid, white powder in 3mL glass ampule

Chemical Formula
PubChem CID

171397054

Molecular Weight

4409 g/mol

Synonyms

Cagrilintide

Cagrilintide 10mg Storage

Store at ≤25°C, sealed, away from heat, light, and moisture.

Cagrilintide Research

1. Cagrilintide and Obesity 

Cagrilintide is a longer acting form of the natural hormone amylin, prepared to help people lose weight by reducing their appetite and making them feel full for longer. It acts directly with the brain cells to help control appetite and food intake.

Figure: Mean percent change in body weight over 26 weeks by treatment group (cagrilintide doses vs placebo).

In a Phase 2 clinical trial of adults who were overweight or obese, participants received weekly injections of cagrilintide for 26 weeks. The trials found that individuals taking cagrilintide lost more weight substantially, achieving an average reduction of 9.7% by week 26 compared to those in the placebo group, highest dose group lost, on average 10.8 kg, compared to 3.0 kg in the placebo group.

Further evidence came from a large Phase 3 trial involving more than 3,400 overweight or obese adults. In one group of this study, participants were given Cagrilintide alone (2.4 mg per week) for 68 weeks. Cagrilintide users lost significantly more weight than those who received a placebo, and had healthier waist measurements and metabolic profiles over all. This data indicates that Cagrilintide is safe and effective for long-term weight management on its own.

(Source: The New England Journal of Medicine, 2025; REDEFINE 1 ClinicalTrials.gov Identifier: NCT05567796)

These findings demonstrate that when combined with a balanced diet and lifestyle changes, cagrilintide can support durable, sustained weight-loss.

 

2. Mechanism of Action 

Cagrilintide is an imitator of endogenous amylin, which is a peptide that is co-secreted with insulin by pancreatic beta cells. By engaging amylin and calcitonin receptors inside the brain, it slows down stomach emptying, induces satiety and diminishes hunger.

Unlike other anti-obesity drugs, cagrilintide works mainly via central appetite suppression rather than metabolic stimulation, which helps in maintaining the right amount of caloric deficit without changing energy expenditure. In both animals and people, this system promotes a gradual, sustained decrease in food consumption and body weight.

 

3. Metabolic and Cardiovascular Effects 

Cagrilintide has also been shown to have positive effects on markers of metabolic health, such as fasting glucose, insulin resistance and lipids profile. These results suggest that cagrilintide is also able to decrease obesity-related cardiometabolic risks, though dedicated long-term outcomes studies are still needed.

Importantly, decrease in visceral fat mass have also been seen, which theoretically may lead to improved cardiovascular outcomes and increased insulin sensitivity (both major aims of overall obesity management).

 

4. Safety and Tolerability 

Cagrilintide has demonstrated a good safety profile in clinical trials. Gastrointestinal symptoms including nausea, vomiting and constipation were the most common adverse effects — mostly mild to moderate and transient. These reactions were generally mild in severity and most commonly arose during the dosage increase; but went away after some time as treatment continued.

No clinically significant safety concerns were identified in the studies. Laboratory tests, cardiovascular results and findings of electrocardiograms did not change over the treatment period, and no dose-limiting toxicities were seen.

 

5. Pharmacokinetics and Administration 

Cagrilintide has been developed for a single weekly subcutaneous administration because of it’s prolonged half-life, enabling for safe and stable plasma concentrations with weekly dosing. It shows high selectivity to receptors, good bioavailability and low accumulation.

In clinical trials, cagrilintide was administered as an escalating dose of 0.3 to 4.5 mg per week. Gradually raising the dosage might help in reducing stomach-related issues and makes it easier for patients to stay on treatment.


REFERENCES

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