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

CagrilintidevsSelank

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
BHuman-MechanisticAUTO-DRAFTED11/40 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
Selank
Anxiolytic + Cognitive · Russian Pharma
150–300 mcg/doseIntranasalZaderej 2014
~30 minOnset
Intranasal · 2–3×/day during stress / cognitive demand

01Mechanism of Action

Parameter
Cagrilintide
Selank
Primary target
Amylin receptor (AMYR) and calcitonin receptor (CTR) heterodimeric complexesBailey 2026
Monoamine system (serotonin / GABA modulation) + immunomodulation via tuftsin domainZaderej 2014
Pathway
AMYR/CTR agonism → Central satiety signaling → Reduced food intake, delayed gastric emptying, suppressed glucagonBailey 2026
Tuftsin-derived immune signaling + CNS monoamine modulation → reduced anxiety + improved mood / cognitionMedvedev 2007
Downstream effect
Central satiety induction, prandial glucagon suppression, reduced caloric intake, weight loss, improved glycemic controlBailey 2026Yamauchi 2026
Anxiolytic + cognitive enhancement; immunomodulation via increased IL-6 + IFN-γMedvedev 2007Zaderej 2014
Feedback intact?
Yes — acts via physiological amylin pathways
No GABA-receptor binding; no dependence reportedMedvedev 2007
Origin
Second-generation non-aggregating long-acting amylin analogue designed for once-weekly dosingBailey 2026
Synthetic 7-AA peptide derived from human tuftsin (immune-system tetrapeptide)Zaderej 2014
Antibody development

02Dosage Protocols

Parameter
Cagrilintide
Selank
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.
2–3× per day during stress
Evidence basis
Phase 3 RCT (REDEFINE 5), meta-analysis of 3 RCTs (n=3545)Yamauchi 2026Ahmed 2026
Human-mechanistic + Russian clinical trialsMedvedev 2007
Duration
26–52 weeks in trialsYamauchi 2026
10–14 day cycles, repeated as needed
Route
Subcutaneous injectionBailey 2026
Standard dose
150–300 mcg / dose intranasalZaderej 2014
Lower / starter dose
75 mcg / dose
Reconstitution
Pre-formulated nasal spray (commercial); research vial: bacteriostatic water
Timing
Morning + early afternoon preferred
Half-life
Short (minutes plasma); CNS effect lasts ~3 hr

03Metabolic / Fat Loss Evidence

Parameter
Cagrilintide
Selank
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
Selank
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.
Nasal irritation
Mild burning or congestion (transient)
Sedation
None — distinct from benzodiazepinesMedvedev 2007
Dependence / withdrawal
None reported in clinical useZaderej 2014
Cognitive impairment
None — opposite effect (enhancement)
Allergic reaction
Rare hypersensitivity
Long-term safety
Limited Western RCT data
Pregnancy / OB
Avoid — insufficient data
Absolute Contraindications
Cagrilintide
  • ·Hypersensitivity to cagrilintide or formulation components
Selank
  • ·Pregnancy / breastfeeding
  • ·Hypersensitivity to peptide
Relative Contraindications
Cagrilintide
  • ·Severe gastrointestinal disease
  • ·History of pancreatitis (incretin-based therapy consideration)
Selank
  • ·Active autoimmune disease (theoretical via immunomodulation)

05Administration Protocol

Parameter
Cagrilintide
Selank
1. Dosing frequency
Once-weekly subcutaneous injection. Long-acting formulation designed for weekly administration schedule.Bailey 2026
Pre-formulated nasal spray (commercial) or research vial reconstituted with bacteriostatic water.
2. Combination form
Co-formulated with semaglutide as CagriSema for single weekly injection combining amylin and GLP-1 receptor agonism.Yamauchi 2026Bailey 2026
Intranasal — 1–3 sprays per nostril per dose. Tilt head slightly back.
3. Injection site
Subcutaneous — typically abdomen, thigh, or upper arm. Rotate injection sites weekly to minimize local reactions.
Morning + early afternoon for cognitive demand; PRN for acute anxiety.
4. Storage
Refrigerate 2–8°C. Follow product-specific storage instructions for pre-filled pens or vials. Protect from light.
Refrigerate after reconstitution; ≤30 days. Light-protected.
5. Dietary considerations
Nutritional monitoring recommended during treatment. Dietary management strategies important for tolerability and outcomes.Pardali 2026
Avoid co-administration with strong sedatives or other anxiolytics initially.

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
Selank
— no documented stacks