Semaglutide
The established GLP-1.
- Lyophilised powderFormat
- 8–80 weeksVial coverage
- 2 mL BAC waterReconstitution
What it is, in plain language
Semaglutide is a long-acting GLP-1 receptor agonist, marketed clinically under the brand names Ozempic (diabetes) and Wegovy (obesity). It is the established benchmark in the incretin class and the most-studied weight-management compound of the past five years.
In the AEON line, Semaglutide is positioned alongside Retatrutide as a research-context metabolic compound — Semaglutide for protocols where the GLP-1-only mechanism is preferred, Retatrutide for the triple-agonist research frontier. AEON Semaglutide is supplied for in-vitro research only and is not approved by the TGA for human use.
Semaglutide is the benchmark of the incretin class — the broadest evidence base and the slowest tolerated titration.
How it works
Activates the GLP-1 receptor, producing dose-dependent appetite suppression, delayed gastric emptying, increased insulin secretion, and glucose-dependent suppression of glucagon. Weekly dosing is enabled by structural modifications (a C18 fatty-acid chain) that bind albumin and extend half-life to approximately 7 days.
What the literature shows
The clinical literature is extensive. Phase 3 trials report ~15% body-weight reduction at 68 weeks at the 2.4 mg/week dose (Wegovy STEP trial program), with consistent improvements in HbA1c, blood pressure, and cardiovascular risk markers.
The compound has the strongest real-world evidence base in its class. GI side-effects (nausea, fatigue) are dose-dependent across the entire titration ladder and the literature is unanimous that mandatory slow titration is the difference between tolerated and abandoned protocols.
Protocol reference
Common research-grade reference figures. Not medical advice — every protocol must be reviewed against the latest published literature and your study design.
Semaglutide is not cycled like the regenerative peptides. Same continuous-use pattern as Retatrutide: titration phase (16–20 weeks), active phase (6–18 months at maximum tolerated dose), maintenance step-down. Hard discontinuation is associated with rebound and weight regain. Pauses, if required, are tapered, not stopped.
2 mL BAC → 10 mg/mL. Draw 0.025 mL = 0.25 mg; 0.05 mL = 0.5 mg; 0.10 mL = 1 mg; 0.24 mL = 2.4 mg. Insulin syringes essential for the smaller doses.
Lyophilised vial: room temperature short-term, refrigerator long-term. Reconstituted: refrigerate; use within 28 days when reconstituted with bacteriostatic water.
Common questions
Semaglutide vs Retatrutide — when to choose which?
Detailed answer coming soon. In the meantime, see the mechanism and protocol sections above, or email hello@aeonco.com.au.
Why is titration so slow?
Detailed answer coming soon. In the meantime, see the mechanism and protocol sections above, or email hello@aeonco.com.au.
What does the Phase 3 data show?
Detailed answer coming soon. In the meantime, see the mechanism and protocol sections above, or email hello@aeonco.com.au.
Why is it not cycled?
Detailed answer coming soon. In the meantime, see the mechanism and protocol sections above, or email hello@aeonco.com.au.
What is the regulatory status in Australia?
Detailed answer coming soon. In the meantime, see the mechanism and protocol sections above, or email hello@aeonco.com.au.
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