Weight LossNot FDA ApprovedClinical Trials

CagriSema

Also known as Semaglutide + Cagrilintide

Investigational combination therapy demonstrating 22.7% body weight reduction at 68 weeks in Phase 3 trials, outperforming semaglutide monotherapy.

NDA Submitted - Expected approval late 2026/early 2027

Regulatory Pathway

Preclinical
Phase I
Phase II
Phase III
Phase IV
Approved

Dosing Protocol

Typical Dose

Semaglutide 2.4mg + Cagrilintide 2.4mg weekly

Frequency

Weekly

Duration

Long-term use expected

Community-reported dosing. Individual results vary. Not a medical recommendation.
Typical community protocol: Semaglutide 2.4mg + Cagrilintide 2.4mg weekly via Subcutaneous injection, Weekly. Dose range: 2.4 mg each component weekly. Duration: Long-term use expected.

Timing & Administration

Administer via Subcutaneous injection. Frequency: Weekly.

Mechanism of Action

Combines GLP-1 receptor agonism (semaglutide) with amylin receptor agonism (cagrilintide) for enhanced satiety and gastric control through complementary pathways.

Research Summary

Evidence level: clinical trials. Clinical status: NDA Submitted - Expected approval late 2026/early 2027.

Side Effects & Safety

Important Warnings

  • Higher gastrointestinal effects than semaglutide alone
Nausea
vomiting
diarrhea
constipation
GI events (72-80% vs 34-40% placebo)

References

No references available.