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Specimen Atlas of Research Peptides81 plates · MIT
Side-by-side · Research reference

CagrilintidevsCortagen

Side-by-side comparison across mechanism, dosage, evidence, side effects, administration, and stack synergies. Citations on every claim where available.

APhase 3HUMAN-REVIEWED35/64 cited
BAnimal-MechanisticHUMAN-REVIEWED11/35 cited
Cagrilintide
Long-Acting Amylin Analogue · Phase 3
7.5%Additional weight loss vs semaglutideAhmed 2026
Once weeklyDosing frequencyBailey 2026
Dual AMYR/CTRReceptor agonismBailey 2026
SQ · Once WeeklyBailey 2026
Cortagen
Bioregulatory Tetrapeptide · Khavinson-School
TetrapeptideStructure
↓ LPO productsAntioxidant effectKozina 2007
AnimalEvidence level
Injectable · Animal models

01Mechanism of Action

Parameter
Cagrilintide
Cortagen
Primary target
Amylin receptor (AMYR) and calcitonin receptor (CTR) heterodimeric complexesBailey 2026
Cerebral cortex tissue — molecular targets under investigation
Pathway
AMYR/CTR agonism → Central satiety signaling → Reduced food intake, delayed gastric emptying, suppressed glucagonBailey 2026
Antioxidant pathway modulation — suppression of LPO cascade, reduction of protein oxidative modificationKozina 2007
Downstream effect
Central satiety induction, prandial glucagon suppression, reduced caloric intake, weight loss, improved glycemic controlBailey 2026Yamauchi 2026
Decreased lipid peroxidation products, reduced oxidative protein damage, altered gene expression in cardiac tissueKozina 2007Anisimov 2004
Feedback intact?
Yes — acts via physiological amylin pathways
Origin
Second-generation non-aggregating long-acting amylin analogue designed for once-weekly dosingBailey 2026
Synthetic tetrapeptide derived from amino acid analysis of natural brain cortex peptide preparation CortexinAnisimov 2004
Antibody development

02Dosage Protocols

Parameter
Cagrilintide
Cortagen
Standard dose (combination)
Cagrilintide 2.4 mg + Semaglutide 2.4 mg (CagriSema)Yamauchi 2026
Phase 3 REDEFINE 5 trial dosing.
Monotherapy dosing
Dose-dependent, under investigation
Monotherapy trials reported in meta-analysis.
Frequency
Once weekly (subcutaneous)Bailey 2026
Long-acting formulation.
Evidence basis
Phase 3 RCT (REDEFINE 5), meta-analysis of 3 RCTs (n=3545)Yamauchi 2026Ahmed 2026
Animal mechanistic studies
Duration
26–52 weeks in trialsYamauchi 2026
Route
Subcutaneous injectionBailey 2026
Injectable (inferred from animal protocols)
Animal model dose (rat)
Injection protocol (dose not specified in abstracts)
Multiple injections over study period.
Avian model dose (chicken)
40-day injection courseKuznik 2008
Compared to epithalon in hypophysectomized and aged birds.
Human peripheral nerve study
Therapeutic course (protocol details not provided)
Posttraumatic recovery context — reference cited but not detailed.

03Metabolic / Fat Loss Evidence

Parameter
Cagrilintide
Cortagen
Weight loss vs semaglutide
7.47% greater percentage weight lossAhmed 2026
CagriSema combination vs semaglutide monotherapy (meta-analysis).
Absolute weight change
Significantly greater absolute weight reductionAhmed 2026
Mean difference favoring combination therapy.
Mechanism
Central satiety inductionBailey 2026
BMI reduction
Significant BMI reduction vs comparatorAhmed 2026
Glycemic benefit
Reduced fasting glucose and HbA1cAhmed 2026
Synergistic effect with semaglutide in combination.
Lipid effects
Improvements in total cholesterol, LDL-C, HDL-C, VLDL-C, triglyceridesAhmed 2026
Body composition
Predominant fat loss with weight reduction
Mitochondrial function
In vitro effects on skeletal muscle mitochondria under metabolic stress conditionsOld 2026
C2C12 myotube study; clinical relevance under investigation.
Combination rationale
Multi-pathway approach: amylin (satiety) + GLP-1 (incretin)Lempesis 2026
Key publications
REDEFINE 5 (Yamauchi 2026) · Ahmed meta-analysis 2026 · Bailey review 2026Yamauchi 2026Ahmed 2026Bailey 2026

04Side Effects & Safety

Parameter
Cagrilintide
Cortagen
Gastrointestinal
Nausea, diarrhea (common with incretin-based therapies)Pardali 2026
Dietary management and nutritional monitoring recommended.
Injection site reactions
Local reactions possible with subcutaneous administration
Safety profile
Generally consistent with incretin-based therapies
Phase 3 and meta-analysis safety data.
Tolerability
Tolerability considerations similar to GLP-1RAs
Muscle preservation
Lean mass considerations during weight loss
In vitro mitochondrial effects observed; clinical impact under investigation.
Antioxidant suppression
Suppression of antioxidant activity noted alongside LPO reductionKozina 2007
Mechanism unclear — possible homeostatic adaptation.
Immune/hemostasis effects
No effect on immunity or hemostasis parameters in avian hypophysectomy model (unlike epithalon)Kuznik 2008
Epithalon reversed deficits; cortagen did not.
Human safety data
No adverse events reported in peripheral nerve recovery context
Limited detail in available abstracts.
Absolute Contraindications
Cagrilintide
  • ·Hypersensitivity to cagrilintide or formulation components
Cortagen
Relative Contraindications
Cagrilintide
  • ·Severe gastrointestinal disease
  • ·History of pancreatitis (incretin-based therapy consideration)
Cortagen

05Administration Protocol

Parameter
Cagrilintide
Cortagen
1. Dosing frequency
Once-weekly subcutaneous injection. Long-acting formulation designed for weekly administration schedule.Bailey 2026
Reconstitute lyophilised peptide with bacteriostatic water per supplier protocol. Exact volumes depend on concentration supplied.
2. Combination form
Co-formulated with semaglutide as CagriSema for single weekly injection combining amylin and GLP-1 receptor agonism.Yamauchi 2026Bailey 2026
Subcutaneous injection typical for bioregulatory peptides — abdomen or thigh. Rotate sites.
3. Injection site
Subcutaneous — typically abdomen, thigh, or upper arm. Rotate injection sites weekly to minimize local reactions.
Animal protocols used repeated dosing over weeks. Human timing not established — evening administration common in Khavinson tradition.
4. Storage
Refrigerate 2–8°C. Follow product-specific storage instructions for pre-filled pens or vials. Protect from light.
Lyophilised: refrigerate or freeze per supplier. Reconstituted: refrigerate 2–8 °C, use within guideline window.
5. Dietary considerations
Nutritional monitoring recommended during treatment. Dietary management strategies important for tolerability and outcomes.Pardali 2026

06Stack Synergy

Cagrilintide
+ Semaglutide
Strong
View Semaglutide

Cagrilintide (amylin receptor agonist) and semaglutide (GLP-1 receptor agonist) act on distinct receptor systems to produce synergistic weight loss through complementary mechanisms — central satiety via amylin pathways plus incretin-mediated glucose control and appetite suppression via GLP-1. Co-formulated as CagriSema, this combination demonstrates 7.5% greater weight loss versus semaglutide monotherapy in Phase 3 trials with additional benefits on glycemic control and lipid parameters.

CagriSema
Cagrilintide 2.4 mg + Semaglutide 2.4 mg
Frequency
Once weekly subcutaneous
Duration
26–52 weeks (trial data)
Primary benefit
Enhanced weight loss, improved glycemic control, multi-pathway metabolic modulation
Cortagen
— no documented stacks