Pharmacokinetic simulator
How the drug builds up, week by week
Every step up the ladder leaves more drug in you than the last, until what goes in and what clears out settle against each other. This traces that for injectable semaglutide and tirzepatide and for oral orforglipron — the climb, the plateau, the peaks and troughs between doses, and the dip that follows one you skip.
Select medication
Brand names: Wegovy · Half-life 168 h (7.0 d) · Once weekly
Standard titration schedule
Wk 1–4
0.25mg
Wk 5–8
0.5mg
Wk 9–12
1mg
Wk 13–16
1.7mg
Maintenance
2.4mg
target dose
The dashed violet line marks where the maintenance dose plateaus, which is what 100% means here. Each curve follows the standard titration ramp, and every value on the axis is relative and educational — not a blood level.
Half-life
7.0 d
168 h
Steady state
~5 weeks
4–5 half-lives at constant dose
Dosing interval
Weekly
Subcutaneous injection
Maintenance dose
2.4 mg
target after titration
Missed dose simulator
Pick a dose below and it disappears from the schedule, so you can watch what the curve does without it. The first 8 weekly doses of the titration ramp.
How this plotter works
What is drawn is a relative concentration curve run out over 24 weeks of titration. Behind it sits a one-compartment model with first-order absorption and elimination — the Bateman equation — and the doses are superposed on one another so that accumulation toward steady state appears. The plateau at the maintenance dose is set to 100%, which makes the axis relative buildup rather than a blood level anyone could measure.
Where the approved drugs are concerned the ladders come off their FDA labels [1, 2, 3, 4, 5]. For retatrutide, still investigational, the ladder comes from its phase 2 trial registry entry:
- Semaglutide (Wegovy injection): 0.25 mg → 0.5 mg → 1 mg → 1.7 mg → 2.4 mg, increased every 4 weeks. For adult weight reduction the label allows up to 7.2 mg once weekly after at least 4 weeks at 2.4 mg. Ozempic uses its own ladder (0.25 mg → 0.5 mg, then 1 mg or 2 mg; 2 mg maximum)
- Tirzepatide (Zepbound / Mounjaro): 2.5 mg → 5 mg → 7.5 mg → 10 mg → 12.5 mg → 15 mg, increased every 4 weeks
- Orforglipron (Foundayo): 0.8 mg → 2.5 mg → 5.5 mg → 9 mg → 14.5 mg → 17.2 mg, each step after at least 30 days; the steps above 5.5 mg depend on response and tolerability
- Retatrutide (LY3437943, investigational): 2 mg → 4 mg → 8 mg → 12 mg, the escalation used in the 12 mg arm of the phase 2 trial (NEJM 2023). The trial registry does not state how long each step lasted, so the chart assumes 4 weeks. Retatrutide is not yet FDA-approved; we include it for educational comparison only.
Half-life and steady state
One number explains more about how a GLP-1 feels over the weeks than any other, and it is the elimination half-life. Orforglipron taken by mouth sits at roughly 29 to 49 hours [5]; tirzepatide at about 5 days [8]; retatrutide, still investigational, near 6 [10]; and semaglutide longest of all, about 7 days [7]. After 4-5 half-lives of constant dosing the drug reaches steady state, which is the plateau the chart shows at the dashed reference line. The labels put that at 4 to 5 weeks for weekly semaglutide, about 4 weeks for weekly tirzepatide, and about 1 week for daily orforglipron [2, 4, 5].
The missed-dose simulator
Skip a weekly dose of semaglutide and, by the model, the level has roughly halved by the time the next dose is due; tirzepatide, with its shorter half-life, falls further. For Wegovy, take a missed dose as soon as possible if the next one is more than 2 days away, and otherwise skip it [1]. For Zepbound and Mounjaro the window is 4 days (96 hours) after the missed dose [3, 4].
The control beneath the chart will drop any single dose across those 24 weeks so you can watch the curve answer.
Important disclaimer
Educational only, and not medical advice. These curves are relative shapes drawn from published parameters; nobody should read them as the concentration in their own blood. What a real person carries varies a great deal with body weight, where the injection went, how the liver and kidneys are working, whatever else is being taken, and much besides. Decisions about dose belong with a qualified clinician. GLP Watchdog does not diagnose, does not treat, and does not tell you what to take.
References
- 1.Novo Nordisk Inc. WEGOVY (semaglutide) — US Prescribing Information, Sections 2.2, 2.4 and 12.3. DailyMed. 2026. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ee06186f-2aa3-4990-a760-757579d8f77b
- 2.Novo Nordisk Inc. OZEMPIC (semaglutide) injection — US Prescribing Information, Sections 2.2 and 12.3. DailyMed. 2026. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=adec4fd2-6858-4c99-91d4-531f5f2a2d79
- 3.Eli Lilly and Company. ZEPBOUND (tirzepatide) injection — US Prescribing Information, Sections 2.1-2.3 and 12.3. DailyMed. 2026. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=487cd7e7-434c-4925-99fa-aa80b1cc776b
- 4.Eli Lilly and Company. MOUNJARO (tirzepatide) injection — US Prescribing Information, Sections 2.1 and 12.3. DailyMed. 2026. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d2d7da5d-ad07-4228-955f-cf7e355c8cc0
- 5.Eli Lilly and Company. FOUNDAYO (orforglipron) tablets — US Prescribing Information, Sections 2.1 and 12.3. DailyMed. 2026. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8ac446c5-feba-474f-a103-23facb9b5c62
- 6.Ma X, Liu R, Pratt EJ, Benson CT, Bhattachar SN, Sloop KW. Effect of Food Consumption on the Pharmacokinetics, Safety, and Tolerability of Once-Daily Orally Administered Orforglipron (LY3502970), a Non-peptide GLP-1 Receptor Agonist. Diabetes Therapy. 2024. PMID: 38402332.
- 7.Hall S, Isaacs D, Clements JN. Pharmacokinetics and Clinical Implications of Semaglutide: A New Glucagon-Like Peptide (GLP)-1 Receptor Agonist. Clinical Pharmacokinetics. 2018. PMID: 29915923.
- 8.Urva S, Quinlan T, Landry J, Martin J, Loghin C. Effects of Renal Impairment on the Pharmacokinetics of the Dual GIP and GLP-1 Receptor Agonist Tirzepatide. Clinical Pharmacokinetics. 2021. PMID: 33778934.
- 9.Coskun T, Urva S, Roell WC, Qu H, Loghin C, Moyers JS, O'Farrell LS, Briere DA, Sloop KW, Thomas MK, Pirro V, Wainscott DB, Willard FS, Abernathy M, Morford L, Du Y, Benson C, Gimeno RE, Haupt A, Milicevic Z. LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss: From discovery to clinical proof of concept (retatrutide). Cell Metabolism. 2022. PMID: 35985340.
- 10.Urva S, Coskun T, Loh MT, Du Y, Thomas MK, Gurbuz S, Haupt A, Benson CT, Hernandez-Illas M, D'Alessio DA, Milicevic Z. LY3437943, a novel triple GIP, GLP-1, and glucagon receptor agonist in people with type 2 diabetes: a phase 1b, multicentre, double-blind, placebo-controlled, randomised, multiple-ascending dose trial. The Lancet. 2022. PMID: 36354040.
Related research
The trial evidence behind each of them:
The retatrutide curve rests on a phase 2 registry entry, and what its phase 3 trials found is written up in retatrutide's phase 3 and the gray market.
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