
Long-Acting Amylin Analog
Cagrilintide is a long-acting amylin analog designed for once-weekly subcutaneous administration. It acts on amylin receptors in the brain to reduce food intake and body weight. When combined with semaglutide (CagriSema), it has shown synergistic weight loss effects in clinical research. Our cagrilintide is produced with fatty acid conjugation for extended half-life.
B2B Wholesale Only · For Research Use Only · COA Provided with Every Order
Cagrilintide is a long-acting amylin analog designed for once-weekly subcutaneous administration. It acts on amylin receptors in the brain to reduce food intake and body weight. When combined with semaglutide (CagriSema), it has shown synergistic weight loss effects in clinical research. Our cagrilintide is produced with fatty acid conjugation for extended half-life.
Lys-Cys-Asn-Thr-Ala-Thr-Cys-Ala-Thr-Gln-Arg-Leu-Ala-Asn-Phe-Leu-Val-His-Ser-Ser-Asn-Asn-Phe-Gly-Pro-Ile-Leu-Pro-Pro-Thr-Asn-Val-Gly-Ser-Asn-Thr-Tyr-NH₂
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Peer-reviewed scientific literature on Cagrilintide from PubMed, NEJM, The Lancet, and other authoritative sources.
Research Use Only. The following citations are provided for informational purposes and represent independent scientific research. These studies do not constitute medical advice or claims about our products. All products are sold for research purposes only and are not intended for human use.
Enebo LB, Berthelsen KK, Kankam M, et al.
The Lancet, 397: 1736–1748 (2021)
Cagrilintide 2.4 mg produced a mean weight loss of 10.8% over 26 weeks vs. 3.0% with placebo (p<0.001), with a favorable safety profile and no dose-limiting adverse events.
Lau DCW, Erichsen L, Francisco AM, et al.
New England Journal of Medicine, 391: 2053–2065 (2024)
CagriSema produced a mean weight loss of 22.7% vs. 8.1% for semaglutide alone and 11.8% for cagrilintide alone (p<0.001 for all comparisons), demonstrating significant synergistic efficacy.
Citations sourced from PubMed / NCBI, New England Journal of Medicine, The Lancet, Nature, and other peer-reviewed publications. DOI links lead to original publisher pages.

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