CagriSema (Cagrilintide + Semaglutide)Metabolic CombinationBlendSafety Rating 7/10

Primary research areaMetabolic / weight research

Research-literature reference data, NOT patient instructions. Not for human use. Consult a licensed clinician for any human application.

Research dose range2.4 mg cagrilintide + 2.4 mg semaglutide SC weeklysource ↗
AdministrationSubcutaneous injection
Half-life~7 days (semaglutide arm)
Safety7/10 · Phase III (not yet approved)
NCAA D1Not listed

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Overview

About CagriSema

Mechanism of action

Combination of cagrilintide (amylin agonist) and semaglutide (GLP-1 agonist); dual mechanism targets appetite, gastric emptying, and satiety via complementary central and peripheral pathways; demonstrated greater weight loss than either alone.

Safety profile

Nausea, vomiting, diarrhea (additive GI effects vs. either alone); injection site reactions; constipation. Profile similar to GLP-1 class. · Strong Phase III data; GI side effects similar to semaglutide; regulatory review ongoing

Storage

Stability & handling

❄️Lyophilized (powder)−20°Clong-term stable
💉Reconstituted2–8°Cwithin 30 days
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Research

Studies & key findings

  • Fixed-ratio combination of cagrilintide (amylin analogue) + semaglutide (GLP-1 agonist) in a once-weekly subcutaneous injection — dual complementary mechanisms targeting satiety, gastric emptying, and energy expenditure.
  • REIMAGINE Phase 2/3 trials demonstrated ~25% mean body weight loss at 68 weeks, with significant improvements in HbA1c, waist circumference, and blood pressure.

4 peer-reviewed sources cited — clinical, preclinical, and regulatory.

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