Semaglutide is a GLP-1 receptor agonist that mimics a gut hormone released after eating. It can reduce appetite and slow gastric emptying. Your dose is set and adjusted by a licensed provider, only if treatment is appropriate.
Prescription required
GLP-1 receptor agonist: a single incretin pathway.
In STEP 1, brand semaglutide 2.4 mg weekly produced mean weight loss of 14.9% at 68 weeks vs 2.4% placebo. Those averages describe the studied brand regimen, not compounded therapy. Individual results vary.
Once weekly, titrated by your provider. Compounded after a valid prescription.
A licensed provider authorizes treatment only if it is medically appropriate, never as a cart-only purchase.
Dosing is increased gradually under clinical guidance so your body can adjust. Your exact schedule is set by your provider.
Dose adjustments and provider messaging are included so the plan can change with your response.
You typically begin at a low dose so your body can adjust. Many people notice appetite changes early on; others take longer. Side effects, if they occur, are often GI-related and may ease as titration continues.
Your provider may step the dose up on a schedule that fits you. Weight change, when it occurs, is gradual. Habits, starting weight, and adherence all matter. Individual results vary.
You may settle into a maintenance dose. Trial averages (such as STEP 1) describe research populations at specific brand doses, not a guarantee for compounded therapy or for any one person.
Your provider can review response and refine the plan. This is ongoing clinical care, not a one-time ship-and-forget order.
Every semaglutide prescription is written by a US-licensed provider who has reviewed your history, and who can decline when treatment is not appropriate.
The DirectGLP standardCompounded medications contain clinically studied active ingredients but are prepared for you by a state-licensed 503A pharmacy. They are not the same as FDA-approved brand products (for example Wegovy®) and are not FDA-approved finished drugs. Trial results apply to the studied brand regimens and populations.
GLP-1 therapy isn't appropriate for every patient. A licensed provider screens for these during your assessment, so please share your full history.
GLP-1 receptor agonists carry a boxed warning regarding thyroid C-cell tumors observed in rodents; it is unknown whether they cause medullary thyroid carcinoma (MTC) in humans. They are contraindicated in patients with a personal or family history of MTC or MEN 2. These medications are compounded by state-licensed 503A pharmacies and are not FDA-approved finished products. This page is educational and is not medical advice. Eligibility is always determined by a licensed provider after reviewing your full history.
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