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Schedule tool

Titration Schedule Builder

Generate a research-stage stepwise titration plan for any incretin-class peptide — or any peptide on the site. Set your starting dose, target maintenance, step size and step duration; the builder lays out the week-by-week schedule, totals the cumulative peptide required, and surfaces the right bloodwork checkpoints for the peptide class.

Inputs

Modelled on the published Semaglutide STEP trial: 0.25 → 0.5 → 1.0 → 1.7 → 2.4 mg weekly, stepping every 4 weeks until the maintenance dose.

Peptide

Filtered to the Metabolic / GLP-1 class — stepwise titration matters most for incretin-receptor agonists.

mcg
mcg
mcg
weeks
weeks
mg

Common: 3, 5, 10, 15 mg

Summary

Titration phase

20 wk

Maintenance phase

12 wk

Total duration

32 wk

Total peptide

53.8 mg

Vials

18 × 3 mg

Weekly admins

1

Dose-over-time stepped profile

630mcg1.26mg1.89mg2.52mgwk 8wk 16wk 24wk 32target 2.40 mgweeks

Calculations run entirely in your browser. Schedule patterns are research-stage models, not clinical recommendations.

Week-by-week schedule

Click any row to open the Dosage Calculator pre-filled for that step.

WeeksPhaseDose / adminWeekly totalCumulative mg
Weeks 1–4titration250 mcg0.25 mg1.0 mgOpen dosage
Weeks 5–8titration750 mcg0.75 mg4.0 mgOpen dosage
Weeks 9–12titration1.25 mg1.25 mg9.0 mgOpen dosage
Weeks 13–16titration1.75 mg1.75 mg16.0 mgOpen dosage
Weeks 17–20titration2.25 mg2.25 mg25.0 mgOpen dosage
Weeks 21–32maintenance2.40 mg2.40 mg53.8 mgOpen dosage

Suggested bloodwork checkpoints

Markers below are typical for the Metabolic / GLP-1 class. Use as a starting point, not a clinical prescription.

HbA1cfasting glucoselipid panelweightblood pressureliver enzymes
  1. Checkpoint 1

    Week 1

    Baseline panel before week 1

  2. Checkpoint 2

    Week 4

    Tolerability check after the first titration step

  3. Checkpoint 3

    Week 16

    Mid-protocol panel at the start of maintenance

  4. Checkpoint 4

    Week 32

    End-of-cycle panel two weeks after the final administration

Why titration matters for GLP-1 / GIP / glucagon agonists

Every published research-stage protocol for Semaglutide, Tirzepatide and Retatrutide uses a multi-step dose escalation rather than starting at the maintenance level. The stated rationale is identical across the literature: stepping the dose lets the gut adapt to slowed gastric emptying and reduces the rate of nausea, dyspepsia and vomiting — the dominant tolerability-failure modes at the therapeutic plateau.

The builder above implements the three canonical trial ramps as one-click presets, plus conservative and aggressive variants. The custom mode lets you specify every parameter independently — useful when your research design calls for a non-standard target or step size.

How the maths works

Starting at the start dose, the builder adds stepMcg every stepWeeks weeks until the running dose reaches the target maintenance level. The maintenance phase then runs at the target level for the duration you choose. Cumulative peptide is summed across both phases as dose × administrations-per-week (taken from the peptide's default frequency) times the number of weeks at that dose.

Bloodwork checkpoints

Suggested markers are tied to the peptide class:

  • Metabolic / GLP-1: HbA1c, fasting glucose, lipid panel, weight, blood pressure, liver enzymes.
  • Growth Hormone: IGF-1, fasting glucose, lipid panel, thyroid panel.
  • Healing & Repair: hs-CRP, full blood count, fibrinogen.
  • Mitochondrial: fasting glucose, lactate, lipid panel.
  • Longevity: hs-CRP, IGF-1, lipid panel, fasting glucose.

Click any week to open the dosage calculator

Every row in the schedule table includes an “Open dosage” link that takes you to the Dosage Calculator pre-filled with that week's dose, the selected peptide, and the chosen vial size. Use it to get the exact draw volume and syringe-tick count for any step.

Related tools

Frequently asked questions

What is a titration schedule and why does it matter?
For incretin-class peptides (Semaglutide, Tirzepatide, Retatrutide) the published research protocols escalate the dose stepwise rather than starting at the maintenance level. Stepwise titration drastically reduces nausea and gastric side effects, which are the dominant tolerability issues at full dose.
What is the STEP-style preset based on?
It mirrors the published Semaglutide STEP weight-management trial: 0.25 → 0.5 → 1.0 → 1.7 → 2.4 mg weekly with each level held for 4 weeks before stepping up. The maintenance phase then runs at 2.4 mg weekly for the duration you choose.
How does the SURMOUNT-style preset differ?
It mirrors the Tirzepatide SURMOUNT obesity trial: 2.5 → 5 → 7.5 → 10 → 12.5 → 15 mg weekly with 4 weeks per step. Tirzepatide's dual receptor agonism allows a slightly longer ramp because the full-dose tolerability bar is higher.
What does the "conservative" preset do?
Half-size steps versus STEP, holding 4 weeks at each level. Useful when prior data suggests the research subject has gastric-tolerability concerns, when sample size is small, or when the protocol prioritises low adverse-event rates over time-to-target.
Why does "aggressive" come with a caveat?
Doubling step size at half the step duration produces gastric tolerability problems in the published literature. It reaches target in a third of the time but with much higher early-cycle adverse-event rates. Use only when the research target requires fast onset and tolerability is not the primary endpoint.
How accurate are the bloodwork checkpoint suggestions?
They are derived from the marker patterns reported in the corresponding published trials and reviews for each peptide class. The week numbers (baseline / tolerability / mid / final) are timing conventions, not clinical recommendations — adjust to your laboratory protocol and ethics-board guidance.
Can I share my titration schedule?
"Copy share link" encodes every input (preset, peptide, dose levels, step size, durations, vial size) into the URL hash. Bookmark or share that URL to restore the exact schedule. Nothing is stored on the server.