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PEPTIDESUNCENSORED

Semaglutide

/sem-ah-GLOO-tide/aka Ozempic, Wegovy, Wegovy HD

Long-acting GLP-1 receptor agonist that lowers appetite and blood sugar. An FDA-approved prescription drug, not a research peptide.

SubcutaneousOralWeeklyDaily

Semaglutide: educational research discussion. Not medical advice. Not a protocol for you.Details

Reported range
0.25–2.4 mg weekly (7.2 mg HD)
Frequency
Weekly injection or daily tablet
Cycle length
16-week titration, then continuous
Half-life
≈ 1 week
Route
SC or oral

Reported figures describe what is published or discussed. None of them is a dose for you.

Mechanism

What it is proposed to do

Semaglutide is a modified copy of the gut hormone GLP-1. A fatty-acid side chain lets it bind albumin in the blood, which stretches its half-life to about a week. It activates GLP-1 receptors in the brain, pancreas and gut. Appetite drops, the stomach empties more slowly, and insulin release rises only when glucose is high. Most of the weight loss comes from eating less.

  1. 01

    Semaglutide

    GLP-1 analog with a fatty-acid chain; ~1-week half-life

    established
  2. 02

    GLP-1 receptors

    Brain, pancreas and gut

    established
  3. 03

    Appetite ↓ · gastric emptying ↓ · insulin ↑

    Insulin release is glucose-dependent

    established
  4. 04

    Weight loss · fewer CV events

    Shown in STEP and SELECT RCTs

    established
EstablishedProposed from animal or cell data

Half-life. About 1 week per the label, so the drug stays in circulation for roughly 5 to 7 weeks after the last injection.

Dosing & cycles

What is reported, and where it comes from

Numbers below are labeled FDA label, clinical trial range or commonly reported range. They describe the published and discussed landscape. They are not instructions and not a protocol for you.

Dosing studio

Every figure is labeled by where it comes from.

This is not your dose

Scale view: Wegovy injection label (weight management)

0
1
2
3
4

Probe at 1.32 mg: inside the reported band (0.25–2.4 mg). Drag it to read the scale. It does not pick a number for you.

Typical cycle, as a calendar

Wegovy label titration

16 weeks of steps, then continuous

The FDA label schedule: one injection a week, stepping up every 4 weeks to the 2.4 mg maintenance dose. There is no built-in end, because weight returns after stopping.

OffLow / startMid / loadingHigh / maintenance

Cycle patterns

Wegovy label titration

16 weeks of steps, then continuous

The FDA label schedule: one injection a week, stepping up every 4 weeks to the 2.4 mg maintenance dose. There is no built-in end, because weight returns after stopping.

0.25 mg
0.5 mg
1 mg
1.7 mg
2.4 mg maintenance
Week 1Week 24

Stacks

What it gets combined with

Why people pair things, and what nobody has tested.

GLP + anything

3 compounds
Why people combine these
People add repair or GH-axis peptides hoping to ease GI side effects or protect lean mass.
Caution
Semaglutide is the only tested drug in the mix. No interaction data exist, and if something goes wrong there is no way to tell which compound caused it.
What is unknown
No published human data on this combination: dosing, interactions and long-term effects are all unstudied.

Fat-loss layering

3 compounds
Why people combine these
Pitched as adding a "metabolic" compound to a GLP-1 drug to break a plateau.
Caution
The GLP-1 drug has the trials. The add-ons have mouse data or a failed human trial. Layering them adds unknowns, not evidence.
What is unknown
No published human data on this combination: dosing, interactions and long-term effects are all unstudied.

Evidence

How much of this is known

Evidence grade

A

Strong human evidence

Multiple adequate human RCTs and/or FDA approval for a defined indication.

How we grade

Graded A on the strength of multiple large RCTs and FDA approval for weight management, type 2 diabetes and cardiovascular risk reduction. The evidence belongs to the approved product, not to compounded or gray-market copies.

Human trial status

STEP 1 (1,961 adults, 68 weeks): 14.9% mean weight loss on 2.4 mg vs 2.4% on placebo. SELECT (17,604 adults with cardiovascular disease and no diabetes): 20% relative reduction in major adverse cardiovascular events. STEP UP (72 weeks): 18.7% on 7.2 mg vs 15.6% on 2.4 mg and 3.9% on placebo. OASIS 4 (64 weeks): 13.6% on oral 25 mg vs 2.2% on placebo.

Limitations

  • Benefits last only while treatment continues. In the STEP 1 extension, weight and cardiometabolic gains largely reversed within a year of stopping.
  • Trials used the branded product. Compounded and gray-market versions were not tested.
  • Part of the weight lost is lean mass, as with any large weight loss.
  • The 7.2 mg dose adds about 3 percentage points of weight loss over 2.4 mg, with more GI effects and far more dysesthesia.

Sources to read

Links open PubMed, DailyMed, FDA or trial-registry searches. We do not cite what we have not described accurately.

Safety

Side effects, cautions, status

Commonly reported effects

  • GI effects dominate: nausea, diarrhea, vomiting and constipation, mostly during dose escalation.
  • Boxed warning: thyroid C-cell tumors in rodents, human risk unknown. Contraindicated with a personal or family history of medullary thyroid carcinoma or MEN 2.
  • Label warnings include pancreatitis, gallbladder disease, kidney injury from dehydration, hypoglycemia with insulin or sulfonylureas, diabetic retinopathy complications and heart-rate increase.
  • At 7.2 mg, dysesthesia (tingling, burning or altered skin sensation) affected 22% of patients vs 6% at 2.4 mg in label data.
  • Weight regain after stopping: one year after STEP 1 treatment ended, participants had regained about two-thirds of the weight they lost.
NauseaGI upsetAppetite suppressionHeart rate increaseNumbness / tinglingFatigue

Who should be extra cautious

  • Medullary thyroid cancer or MEN 2 history. Contraindicated (boxed warning).
  • Pregnancy or planning one. The Wegovy label advises stopping at least 2 months before a planned pregnancy because of the long half-life.
  • Insulin or sulfonylurea users. Hypoglycemia risk rises in combination. The label addresses this directly.
  • Pancreatitis or gallbladder history. Both are label warnings.
  • Compounded or gray-market "sema". Not the approved product, and not what STEP or SELECT tested.

Legal & regulatory status

FDA-approved prescription drug, not a research peptide. Ozempic (2017) treats type 2 diabetes. Wegovy injection (2021) is approved for weight management, cardiovascular risk reduction and, under accelerated approval, MASH with liver fibrosis. Oral Wegovy 25 mg was approved December 22, 2025, and Wegovy HD 7.2 mg on March 19, 2026.

2026 compounding context. FDA declared the semaglutide shortage resolved in February 2025. Mass compounding of copies is no longer permitted, and "personalized" compounded versions are legally contested. A compounded product is not the drug tested in STEP or SELECT.

WADA. Not on the WADA Prohibited List. WADA has tracked it in its Monitoring Program since 2024 (tracked, not banned). Confirm with your federation.

Storage & handling, high level

Storage rules differ by product. Ozempic pens, for example, are refrigerated before first use and allowed up to 56 days once in use. Follow the label for the specific product, not a forum.

Reconstitution and injection technique are clinical skills. The reconstitution calculator does arithmetic only.

FAQ

Questions people ask about Semaglutide

Is semaglutide a research peptide?
No. It is an FDA-approved prescription drug sold as Ozempic, Wegovy and Rybelsus. It shows up in peptide circles because compounded and gray-market copies exist. Those copies are not the product that was tested.
What happens after stopping?
In the STEP 1 extension, people regained about two-thirds of their lost weight within a year, and blood pressure and other markers drifted back toward baseline. The trials support it as a long-term treatment, not a course.
Is 7.2 mg just more of the same?
Same molecule, three times the dose. In STEP UP it added about 3 percentage points of weight loss over 2.4 mg, with more GI effects and much more dysesthesia.
Can pharmacies still compound it?
FDA declared the shortage over in February 2025, which ended mass compounding of copies. "Personalized" compounded versions are legally contested.
Is it banned in sport?
No. It is not on the WADA Prohibited List, though WADA monitors its use. Confirm with your federation.

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