Head-to-head
Tirzepatide vs Retatrutide
Side by side from the same data: half-life, evidence tier, research amounts, common schedule, and every decay curve on one chart.
How they differ
A plain-language read of what actually sets them apart. Reference only, not medical advice.
Both are weekly shots that copy more than one gut-hormone signal: tirzepatide copies two (GLP-1 and GIP), retatrutide three (adding glucagon). They last a similar time in the body, about five to six days. Tirzepatide is a licensed medicine taken up to 15 mg; retatrutide is still investigational and was studied up to 12 mg.
Side by side
Every figure is drawn from this site's own compound data — the same numbers on each compound's page.
| Measure | Tirzepatide | Retatrutide |
|---|---|---|
| Category | Metabolic | Metabolic |
| Evidence | A · Tested in people | A · Tested in people |
| Route | Subcutaneous | Subcutaneous |
| Half-life | 120 h | 144 h |
| Typical vial | 5 / 10 / 15 mg | 5 / 10 mg |
| Research amount | 2.5–15 mg | 0.5–12 mg |
| Common schedule | Once a week | Once a week |
| Cycle / break | Titrated | Titrated |
| Studied for | Metabolism and weight | Metabolism and weight |
These amounts and schedules are figures discussed in research and community reports, shared for learning — not a recommendation and not medical advice. A step-by-step dosing schedule exists only where a human trial backs it; the evidence tier tells you which.
Decay curves, overlaid
Every compound on one chart — something the single-compound pages cannot show.
Each line is scaled to that compound's own first dose, so the chart shows how each one builds up over time — not how the compounds' doses compare to one another, which these different molecules share no common unit for.
How they combine
Where two of these have a documented pairing in this reference.
Educational reference on commonly-discussed combinations, not medical advice. Combining compounds can change how each behaves — read this as a prompt to research, not a clearance.
- Tirzepatide + RetatrutideOverlapping GLP-1 receptor agonism; stacking incretin agonists compounds gastrointestinal load without adding a mechanism in research reports.Avoid combination