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GLP-1 Foundation

Stack: Semaglutide · the licensed entry to the incretin class
"Unusually for this catalogue, the foundation here is a fully approved, clinically-proven medicine — not a research compound. The honest issue isn't whether it works; it's that it's prescription-only, and a large grey market runs it without supervision."
GoalWeight loss / glycaemic control
Compounds1 · Semaglutide
Human evidenceStrong — large RCTs (STEP / SUSTAIN)
StatusMHRA (UK): licensed medicine — prescription only (Wegovy / Ozempic / Rybelsus) · FDA (US): approved. Buying or possessing without a prescription, or sourcing research-grade, is outside the licensed supply chain
In this stack — snapshot; tap through for the full molecule file
Provenance & evidence layers — of the combination, not the parts
Where / who
Licensed and prescribed worldwide for type-2 diabetes and chronic weight management — Ozempic/Rybelsus (diabetes) and Wegovy (weight).
Status
A fully approved medicine with marketing authorisation, an SmPC and active pharmacovigilance — the opposite of a research compound.
Evidence it adds
Regulator-grade efficacy and safety — for the licensed product, used as directed.
Basis: MHRA / EMA / FDA marketing authorisations
Weight
The STEP programme: roughly 15% mean body-weight reduction at 68 weeks vs placebo in adults with obesity.
Glycaemic / CV
SUSTAIN (HbA1c) and SELECT (cardiovascular outcomes) — large, randomised, published in major journals.
Evidence it adds
Controlled human efficacy and safety data at scale — the strongest tier in this catalogue.
Basis: STEP, SUSTAIN, SELECT — peer-reviewed RCTs
Where / who
Large numbers source semaglutide outside prescription — research-grade vials, overseas pharmacies, peer reconstitution.
What changes
The molecule is the same; the supervision, dose titration, sterility and product identity are not. Mis-dosing and counterfeit/under-dosed product are the documented real-world harms.
Evidence it adds
None on efficacy — this layer is about how unsupervised use diverges from the trials.
Basis: real-world sourcing patterns — not a trial tier
MHRA (UK)
Licensed medicine — prescription only (POM). Legal to be prescribed and to possess with a prescription; supplying or buying outside that route is not lawful supply.
FDA (US)
Approved. Compounded semaglutide is only permitted under specific shortage/clinical conditions.
What it means
"Proven and licensed" is exactly why the supervised route matters — the safety record belongs to the prescribed product.
Basis: MHRA POM classification · FDA approval
Why this is the foundation

Semaglutide sits at the base of the incretin class because it's the most-studied, most-prescribed GLP-1 receptor agonist with the deepest outcome data behind it. Everything heavier in this section — dual and triple agonists — is measured against it. The honest framing here is unusual for the catalogue: the question isn't whether it works, it's whether it's being run the way the evidence was generated — prescribed, titrated and supervised — or sourced and self-administered outside that.

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Cycle shape — how it's typically structured, not a schedule to follow
Titration
step up slowly
Maintenance
effective dose
Review
continue / adjust
GLP-1s are titrated up gradually to manage GI side-effects — this mirrors the licensed schedule, not a prescription to follow.
What's worth monitoring

Unlike most of this catalogue, semaglutide has a defined clinical monitoring picture: GI tolerance during titration, and — for some — pancreatitis symptoms, gallbladder issues and significant muscle-mass loss alongside fat loss. The licensed product is monitored by a prescriber; outside that route, no one is. Baseline bloods and a clinician conversation are the sensible floor. General information, not medical advice.