Cagrilintide + Semaglutide 10 mg Blend
Metabolic & weight Investigational (in clinical trials)
Amylin analog + GLP-1 receptor agonist blend · also known as CagriSema, Cagrilintide/Semaglutide
For reference only — not medical advice. Figures are commonly reported values compiled from published sources and may be wrong or out of date. Many compounds listed are not approved for human use. Talk to a licensed clinician before using any compound.
This 10 mg vial holds 5 mg each of cagrilintide and semaglutide. The pairing follows the combination that has been studied in registered trials for weight management and type 2 diabetes, where both agents are escalated together in equal amounts. Escalation in published schedules is stepwise rather than starting at the target.
Commonly reported dosing (10 mg vial)
| Phase | Dose | Volume | U-100 units |
|---|---|---|---|
| Starting | 500 mcg | 0.15 mL | 15 |
| Standard | 2 mg | 0.6 mL | 60 |
Commonly reported dose escalation
| Weeks | Dose | Volume | U-100 units |
|---|---|---|---|
| Weeks 1-4 | 500 mcg | 0.15 mL | 15 |
| Weeks 5-8 | 1 mg | 0.3 mL | 30 |
| Weeks 9-12 | 2 mg | 0.6 mL | 60 |
| Weeks 13-16 | 3.4 mg | 1.02 mL | 102 (warning) |
| Week 17+ | 4.8 mg | 1.44 mL | 144 (warning) |
Commonly reported reconstitution steps
- Vials are usually brought to room temperature (about 15-20 minutes) first.
- 3 mL of bacteriostatic water is added slowly down the inside wall of the 10 mg vial.
- The vial is swirled gently until clear, not shaken.
- This gives 3.33 mg/mL. Mixed vials are typically labeled with the date and refrigerated.
Storage
Before mixing: Sealed vials are commonly stored refrigerated (2-8 °C) and protected from light, or frozen for long-term storage.
After mixing: Reconstituted solution is commonly kept refrigerated (2-8 °C), protected from light, and not frozen.
How it works
Semaglutide activates GLP-1 receptors, supporting glucose-dependent insulin release, slower gastric emptying and reduced appetite. Cagrilintide mimics amylin, a pancreatic hormone, and engages satiety circuits through a separate receptor family, so the pair is studied as complementary.
Researched for
- Studied in clinical trials of co-administered cagrilintide and semaglutide for weight management and type 2 diabetes.
- Investigated for additive satiety effects compared with either agent alone.
Notes
- Because it is a blend, each weekly amount covers both peptides together; chart figures split it equally.
- Gastrointestinal effects such as nausea are the most commonly reported early adverse events in trials, and they track the escalation schedule.
- Semaglutide is FDA-approved as single-agent products; cagrilintide and the fixed combination are investigational in the US.
- Approved semaglutide products are pre-filled pens and no combined product is approved; the reconstitution figures here apply to research vials.
- The top step (4.8 mg total, about 2.4 mg of each) is about 1.44 mL at 3 mL reconstitution, beyond a 1 mL syringe; it appears in the escalation table only.
Sources
- PubMed — Frias et al., co-administered cagrilintide 2.4 mg with semaglutide 2.4 mg in type 2 diabetes (Lancet 2023)
- The Lancet — Once-weekly cagrilintide for weight management: dose-finding phase 2 trial (Lau et al., 2021)
- DailyMed — Wegovy (semaglutide) FDA prescribing information
- PeptideDosages.com — Cagrilintide + Semaglutide 10 mg blend dosage chart (figures cross-check)
Related
Cagrilintide
Long-acting amylin analogueCagrilintide is an acylated analogue of the hormone amylin, studied as a once-weekly appetite-regulating agent.
Semaglutide
GLP-1 receptor agonistSemaglutide is a GLP-1 receptor agonist widely studied for glucose regulation and appetite.
Tirzepatide
GIP/GLP-1 dual receptor agonistTirzepatide is a dual agonist that activates both the GIP and GLP-1 receptors.
Retatrutide
GLP-1 / GIP / glucagon triple agonistRetatrutide is an investigational triple agonist targeting the GLP-1, GIP, and glucagon receptors.
Survodutide
Glucagon/GLP-1 dual receptor agonistSurvodutide is an investigational dual glucagon and GLP-1 receptor agonist being developed for obesity and fatty liver disease.
Mazdutide
GLP-1/glucagon dual receptor agonistMazdutide activates both the GLP-1 and glucagon receptors; it is approved in China and still investigational in the US.