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Semaglutide (GLP-1 agonist)
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Reconstitution
Semaglutide is a GLP-1 receptor agonist used for type 2 diabetes management and chronic weight management. It mimics the incretin hormone GLP-1 to regulate appetite and glucose metabolism.
Binds to and activates GLP-1 receptors, leading to enhanced insulin secretion, reduced glucagon secretion, delayed gastric emptying, and reduced appetite through central nervous system effects.
The STEP clinical trial program demonstrated average weight loss of 15–17% body weight over 68 weeks. The SELECT trial showed a 20% reduction in major adverse cardiovascular events. Oral semaglutide (Rybelsus) is also FDA-approved for type 2 diabetes.
Typical Dose
0.25-2.4mg
Range
0.25-2.4mg (titrated)
Frequency
1x/week (subcutaneous)
Route
SubQ or Oral
Duration
12+ weeks (ongoing)
Reconstitution
Pre-filled pen or compounded vial
Notes
SubQ dosing follows a titration schedule: 0.25 mg for 4 weeks, then 0.5 mg, escalating to target dose. Oral form must be taken on an empty stomach with no more than 4 oz of water.
These biomarkers are commonly tracked to assess response and safety. Run baseline labs before starting, mid-cycle labs halfway through, and post-cycle labs 1–2 weeks after the final dose.
Build a protocol with Semaglutide, schedule blood work for key biomarkers, and track your results.
Build Protocol with SemaglutideThis platform provides informational tools only, not medical advice. This information is for educational purposes only. Consult a licensed provider.