Pharmacokinetic simulator

GLP-1 Dose & Concentration Plotter

Visualize how injectable semaglutide, injectable tirzepatide, and oral orforglipron build up in the body across the standard titration ramp. See steady-state convergence, peak and trough patterns, and what happens when a dose is missed.

Select medication

Brand names: Wegovy, Ozempic · 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

0%25%50%75%100%125%Wk 0Wk 4Wk 8Wk 12Wk 16Wk 20Wk 24Weeks of therapyRelative concentration

Dashed violet line = steady-state peak of the maintenance dose (defined as 100%). Curves show the standard titration ramp; all values are educational and relative, not absolute blood levels.

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

Tap a dose number below to skip that injection and see how the concentration curve responds. Showing the first 8 weekly doses of the titration ramp.

How this plotter works

The chart shows a relative plasma concentration curve for the selected GLP-1 drug across a 24-week titration timeline. The underlying math is a one-compartment pharmacokinetic model with first-order absorption and elimination — the standard Bateman equation — with linear superposition across repeated doses to capture accumulation toward steady state. The maintenance-dose steady-state peak is normalized to 100% so the chart shows relative buildup, not absolute blood levels.

The titration schedules are taken directly from each drug's FDA prescribing information for the approved drugs [1, 2, 3, 4, 5] and from the published phase 2 / phase 3 trial protocols for investigational drugs:

  • Semaglutide (Wegovy / Ozempic): 0.25 mg → 0.5 mg → 1 mg → 1.7 mg → 2.4 mg, increased every 4 weeks
  • 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, increased every 4 weeks
  • Retatrutide (LY3437943, investigational): 2 mg → 4 mg → 6 mg → 8 mg → 10 mg → 12 mg, increased every 4 weeks. Sourced from the Jastreboff phase 2 trial (NEJM 2023) and the TRIUMPH phase 3 program protocol. Retatrutide is not yet FDA-approved; we include it for educational comparison only.

Half-life and steady state

The single most important number for understanding how a GLP-1 dose “feels” over time is the elimination half-life. For semaglutide it's about 7 days [7]. For tirzepatide, about 5 days [8]. For oral orforglipron, about 36 hours [6]. For investigational retatrutide, about 6 days [9]. 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. This is why GLP-1 prescribers tell patients it can take 4-5 weeks at each dose level for the full effect to be felt.

The missed-dose simulator

For weekly drugs (semaglutide, tirzepatide), missing one dose causes plasma concentrations to drop by approximately 50% at the would-be next dose, and it usually takes 2-3 subsequent doses for levels to recover. The general FDA label guidance is: if your missed dose is less than 5 days late, take it as soon as you remember. If more than 5 days late, skip it and resume on your normal schedule [1, 3].

The missed-dose simulator below the chart lets you skip any single dose across the full 24-week window and see how the concentration curve responds.

Important disclaimer

This tool is for educational purposes only and does not constitute medical advice. The concentration curves show relative pharmacokinetic patterns based on published parameters and should not be interpreted as actual blood levels in any individual patient. Real plasma concentrations vary substantially between patients based on body weight, injection site, hepatic and renal function, drug interactions, and many other factors. Dosing decisions should always be made with a qualified healthcare provider. Weight Loss Rankings does not provide medical advice, diagnosis, or treatment recommendations.

Related research

For the clinical trial evidence behind each drug:

References

  1. 1.Novo Nordisk Inc. WEGOVY (semaglutide) injection — US Prescribing Information. FDA Approved Labeling. 2025. https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/215256s024lbl.pdf
  2. 2.Novo Nordisk Inc. OZEMPIC (semaglutide) injection — US Prescribing Information. FDA Approved Labeling. 2025. https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/209637s029lbl.pdf
  3. 3.Eli Lilly and Company. ZEPBOUND (tirzepatide) injection — US Prescribing Information. FDA Approved Labeling. 2025. https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/217806s016lbl.pdf
  4. 4.Eli Lilly and Company. MOUNJARO (tirzepatide) injection — US Prescribing Information. FDA Approved Labeling. 2025. https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/215866s019lbl.pdf
  5. 5.Eli Lilly and Company. FOUNDAYO (orforglipron) tablets — US Prescribing Information. FDA Approved Labeling. 2026. https://www.accessdata.fda.gov/drugsatfda_docs/label/2026/foundayo-pi.pdf
  6. 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. 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. 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: 33704694.
  9. 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 glycaemic control and weight loss: from discovery to clinical proof of concept (retatrutide). Cell Metabolism. 2022. PMID: 36240769.