CagriSema Blend (Cagrilintide 5mg + Semaglutide 5mg) — 10mg
Research-grade CagriSema Blend, a dual-pathway peptide complex combining cagrilintide (5mg) and semaglutide (5mg) studied for amylin/calcitonin and GLP-1 receptor co-activation in metabolic research. 10mg total lyophilized powder, 99%+ purity per component verified by Janoshik Analytical via HPLC and mass spectrometry.
For laboratory research use only.
Not for human or veterinary use.
Not intended for diagnosis, treatment, cure, or prevention of any disease.
Use only in controlled laboratory settings by qualified personnel following appropriate safety procedures.
CagriSema is the research designation for a fixed-dose combination of two synthetic peptides — cagrilintide (a long-acting amylin analog) and semaglutide (a GLP-1 receptor agonist). Originally developed by Novo Nordisk and currently progressing through Phase 3 clinical trials (REDEFINE 1, REDEFINE 2, REIMAGINE 2), this combination is among the most closely watched investigational compounds in modern metabolic research. Published Phase 3 data in the New England Journal of Medicine (2025) reported a 20.4% mean body weight reduction in the combination arm versus 3.0% with placebo over 68 weeks. Durham Peptides also carries Semaglutide and Tirzepatide individually for researchers interested in single-pathway or dual-agonist studies.
BENEFITS
Dual-pathway research — amylin/calcitonin (cagrilintide) + GLP-1 (semaglutide) co-activation in one vial
Investigational reference — corresponds to Novo Nordisk's CagriSema clinical program
Convenience — two compounds in a single vial, eliminating dual-vial reconstitution
Synergy modeling — published Phase 3 data demonstrates combination effects exceed monotherapy
Once-weekly profile — both components feature fatty-acid lipidation supporting extended half-life research
WHAT RESEARCHERS LOOK AT
Cagrilintide: amylin and calcitonin receptor activation, brainstem satiety pathways
Semaglutide: GLP-1 receptor agonism, hypothalamic appetite suppression
Combined vs. monotherapy comparisons in Phase 1-3 clinical research data
Glucagon suppression and gastric emptying delay (cagrilintide) vs. insulin secretion modulation (semaglutide)
Weight loss curves, lipid parameters, and cardiometabolic markers in published trials
