Cagrilintide manufacturers
- Cagrilintide
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- $1.00 / 1g
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2024-07-29
- CAS:1415456-99-3
- Min. Order: 1g
- Purity: 99%
- Supply Ability: 100kg
- Cagrilintide
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- $70.00 / 1box
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2024-07-26
- CAS:1415456-99-3
- Min. Order: 1box
- Purity: 99.9%
- Supply Ability: 2000box
- Cagrilintide
-
- $70.00 / 1box
-
2024-07-26
- CAS:1415456-99-3
- Min. Order: 1box
- Purity: 99+
- Supply Ability: 200t
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| | Cagrilintide Basic information |
| | Cagrilintide Chemical Properties |
| form | Solid | | color | White to off-white |
| | Cagrilintide Usage And Synthesis |
| Description |
Cagrilintide is an amylin-analog, now being developed in combination with the GLP-1 agonist semaglutide to achieve sustained weight loss in persons with overweight and obesity. This drug is an investigational therapy that reduced body weight in a phase 2 trial when administered as monotherapy in participants without diabetes and with a BMI of at least 30 kg/m2 or at least 27 kg/m2 with hypertension or dyslipidaemia[1-2].
| | Mechanism of action |
Cagrilintide, a non-selective agonist, is designed for weekly subcutaneous injection at low pH. It is based on the h-amylin backbone, drawing inspiration from calcitonin, and exhibits a prolonged action profile, likely attributed to reversible albumin binding similar to semaglutide. This amylin analog is currently under development in combination with the GLP-1 agonist semaglutide to achieve sustained weight loss in individuals with overweight and obesity. Amylin, co-secreted with insulin from pancreatic beta cells, exerts its satiating effect through both the homoeostatic and hedonic brain regions. On the other hand, semaglutide, a GLP-1 receptor agonist, reduces appetite by acting on GLP-1 receptors in the hypothalamus, increases insulin production, and decreases glucagon secretion, thus delaying gastric emptying. These distinct yet interconnected mechanisms of action of an amylin analog and a GLP-1 receptor agonist appear to synergistically reduce appetite[3-4].
| | Side effects | The most frequent adverse events were gastrointestinal disorders (e.g., nausea, constipation, and diarrhoea) and administration-site reactions. More participants receiving cagrilintide 0·3-4·5 mg had gastrointestinal adverse events compared with placebo (41%-63% vs 32%), primarily nausea (20%-47% vs 18%)[5]. | | References |
[1] Antonella M D’Ascanio, William H Frishman, & Jamie A Mullally. “Cagrilintide: A Long-Acting Amylin Analog for the Treatment of Obesity.” Cardiology in Review (2024): 83–90.
[2] Juan P Frias. “Efficacy and safety of co-administered once-weekly cagrilintide 2·4 mg with once-weekly semaglutide 2·4 mg in type 2 diabetes: a multicentre, randomised, double-blind, active-controlled, phase 2 trial.” Lancet 402 10403 (2023): 720–730.
[3] Antonella M D’Ascanio, William H Frishman, Jamie A Mullally. “Cagrilintide: A Long-Acting Amylin Analog for the Treatment of Obesity.” Cardiology in Review (2024): 83–90.
[4] Thomas Kruse*. “Development of Cagrilintide, a Long-Acting Amylin Analogue.” Journal of Medicinal Chemistry 64 15 (2021): 11183–11194.
[5] David C W Lau. “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): 2160–2172.
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| | Cagrilintide Preparation Products And Raw materials |
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