Cagrilintide
What is Cagrilintide?
Cagrilintide is a long-acting amylin analog developed by Novo Nordisk as a next-generation obesity treatment. Amylin is a naturally occurring hormone co-secreted with insulin from pancreatic beta cells that regulates satiety and gastric emptying. Cagrilintide is a stabilized, long-acting version (half-life ~7 days) that provides sustained amylin receptor activation. It works through multiple complementary mechanisms: slows gastric emptying to prolong fullness, activates satiety centers in the brainstem (area postrema), reduces food intake by enhancing meal-induced satiety, and suppresses glucagon secretion to improve glucose control. The peptide has shown remarkable efficacy in clinical trials, particularly when combined with semaglutide (GLP-1 agonist) in the CagriSema formulation. The REDEFINE trials demonstrated that cagrilintide + semaglutide produced up to 17.1% body weight loss over 32 weeks - significantly superior to semaglutide alone (9.8%). Cagrilintide addresses a different pathway than GLP-1 agonists, making the combination synergistic rather than redundant. Monotherapy studies show cagrilintide alone produces 6-10% weight loss. The peptide is administered via weekly subcutaneous injection and has an improved side effect profile compared to earlier amylin analogs like pramlintide, with less nausea and GI distress. Currently in Phase 3 trials with expected FDA submission for CagriSema combination therapy.
Benefits
- Superior Weight Loss (15-17% body weight reduction in trials)
- Powerful Appetite Suppression and Satiety
- Slowed Gastric Emptying (Prolonged Fullness)
- Reduced Food Intake and Cravings
- Improved Glycemic Control in Type 2 Diabetes
- Synergistic Effects with GLP-1 Agonists
- Reduced Nausea vs Traditional Amylin Analogs
- Preserved Lean Muscle Mass During Weight Loss
Typical Dosage
- Monotherapy: 2.4mg weekly (final dose)
- Combination (CagriSema): 2.4mg cagrilintide + 2.4mg semaglutide weekly
- Titration required over 16-20 weeks
- Subcutaneous injection, once weekly
Side Effects
- Nausea (common, dose-dependent, improves over time)
- Vomiting (especially during titration)
- Diarrhea or constipation
- Decreased appetite (intended effect)
- Injection site reactions
- Fatigue (transient)
- Abdominal discomfort
- Significantly better tolerated than pramlintide
Dosage Protocol
Cagrilintide requires slow titration to minimize gastrointestinal side effects. Clinical trial protocol: Start at 0.3mg weekly for 4 weeks, increase to 0.6mg for 4 weeks, then 1.2mg for 4 weeks, then 1.8mg for 4 weeks, and finally 2.4mg maintenance dose. Each dose increase should be made only if the previous dose is well-tolerated. If combining with semaglutide (CagriSema), both peptides are titrated simultaneously but may require slower escalation. Administer on the same day each week, with or without food. Injection sites: abdomen, thigh, or upper arm - rotate sites to prevent lipohypertrophy. If a dose is missed and it's been less than 5 days since scheduled dose, take immediately. If more than 5 days, skip and resume normal schedule.
Reconstitution
Dosing Schedule
Standard Protocol
- •Weeks 1-4: 0.3mg weekly
- •Weeks 5-8: 0.6mg weekly
- •Weeks 9-12: 1.2mg weekly
- •Weeks 13-16: 1.8mg weekly
- •Week 17+: 2.4mg weekly (maintenance)
Negative Interactions
- Other amylin analogs (redundant mechanism)
- Medications that slow gastric emptying
- History of pancreatitis (caution)
- Severe gastroparesis
- Type 1 diabetes (limited data)
- Pregnancy/breastfeeding
Cagrilintide is currently in Phase 3 clinical trials and NOT yet FDA approved. The CagriSema combination (cagrilintide + semaglutide) has shown exceptional results in trials with 15-17% weight loss. Data suggests superior efficacy and tolerability compared to earlier amylin analogs. Expected regulatory approval 2024-2025. Use only in clinical trial settings or under specialized medical supervision. NOT recommended for competitive athletes (WADA status pending). Monitor for signs of pancreatitis, severe GI distress, or hypoglycemia if combined with insulin or sulfonylureas.