
Safety data sheet
Standardized safety protocols and material specifications for professional use.
Certificate of Analysis
Purity verified via High-Performance Liquid Chromatography (HPLC) for #myo-semaglutide-plus-cagrilintide-5mg-5mg
Semaglutide + Cagrilintide (5mg + 5mg)
Research Grade >99.3% Purity
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Scientific Background
CagriSema is a precision dual-agonist research blend combining Semaglutide (GLP-1 receptor agonist) and Cagrilintide (long-acting amylin analog) — two complementary metabolic hormones that target appetite, satiety, and energy balance through distinct but synergistic receptor pathways.
Semaglutide suppresses appetite via central hypothalamic GLP-1 receptor signalling, slows gastric emptying, and improves insulin sensitivity. Its ~7-day half-life enables stable once-weekly dosing. Cagrilintide is a long-acting amylin analog that signals fullness through the area postrema and nucleus accumbens, further delays gastric emptying, and suppresses post-prandial glucagon secretion — mechanisms entirely complementary to GLP-1. Together they produce additive appetite suppression through two independent neural and peripheral circuits.
Phase 2 clinical trials of co-administered CagriSema demonstrated mean weight reduction of ~15–17% at 32 weeks — significantly superior to semaglutide monotherapy — with continued progression beyond. In type 2 diabetes cohorts, the combination achieved substantial HbA1c reductions alongside robust body weight reduction. The dual-pathway mechanism consistently outperforms either agent in isolation.
Intended Research Use
- Superior weight reduction research vs. GLP-1 monotherapy (dual amylin + GLP-1)
- Type 2 diabetes — combined glycaemic control and weight management
- Comparative metabolic agonist pharmacology (GLP-1 + amylin vs. GLP-1 + GIP)
- Appetite suppression and gastric emptying delay mechanism studies
- Body composition — fat mass reduction with lean mass preservation
- Long-acting dual agonist pharmacokinetics and tolerability research
menu_bookScientific Publications
Lancet (2023)
CagriSema vs. semaglutide and cagrilintide in weight management — Phase 2 trial
open_in_newhttps://pubmed.ncbi.nlm.nih.gov/37121257/
Diabetes Care (2023)
Dual amylin and GLP-1 receptor agonism with CagriSema in type 2 diabetes
open_in_newhttps://pubmed.ncbi.nlm.nih.gov/37490519/
New England Journal of Medicine (2021)
Once-Weekly Semaglutide in Adults with Overweight or Obesity — STEP 1
open_in_newhttps://pubmed.ncbi.nlm.nih.gov/33567185/
FOR RESEARCH USE ONLY. This product is intended for laboratory research purposes only and is not for human consumption, medical, or diagnostic use.
Possible stacks with other peptides
Synergistic combinations for enhanced research outcomes
CagriSema's dual GLP-1 + amylin mechanism can be further supported with metabolic and mitochondrial compounds for comprehensive weight and metabolic research.

Retatrutide 10mg (10mg vial)
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Triple-agonist comparison — retatrutide adds GIP receptor and glucagon activation to provide a research comparison point for triple vs. dual agonism in weight reduction and metabolic research.

MOTS-C (10mg vial)
arrow_forwardmyo-mots-c-10mg
Mitochondrial metabolic support — MOTS-C's AMPK activation supports cellular energy adaptation during caloric restriction achieved through CagriSema, preventing metabolic rate decline.

AICAR (50mg vial)
arrow_forwardmyo-aicar-50mg
Exercise-mimetic metabolic adjunct — AICAR's AMPK activation provides energy balance support alongside CagriSema's appetite suppression for comprehensive metabolic research protocols.

Cagrilintide 5mg (5mg vial)
arrow_forwardmyo-cagrilintide-5mg
The amylin analog component of this blend — standalone Cagrilintide for isolated amylin pathway research before combining with the full CagriSema protocol.
Cycling Note: CagriSema is not cycled — it is used as continuous once-weekly maintenance. Titrate to maximum tolerated dose and maintain for the full protocol duration.