Retatrutide is dosed from a titration schedule, not from a range. This calculator gives the syringe units for every step of that schedule at your vial size and water volume, and shows the week each step opens.
Below the calculator: the full titration schedule, a reconstitution chart built from its steps, the supplies it takes to reach maintenance, the health conditions that change the answer, and the references. Every dose figure is read from the Klarovel engine's own titration constant, never typed into the page.
How many milligrams are in your Retatrutide vial?
How much bacteriostatic water are you adding?
Syringe size
Which step of the titration are you on?
Each chip is a rung on the published titration schedule, in the order it is climbed. The full schedule with the week each rung opens is below.
No experience, weight or age input here
Retatrutide is dosed from a titration schedule rather than an experience envelope, and the schedule is not individualised by age, sex, body mass, kidney function or liver function. The other calculators on this site offer those inputs because the compounds they cover genuinely use them. Offering them here would imply a personalisation the published schedule does not have.
Step 1 dose, from week 1
20.0 units
2 mg
Frequency: once weekly. Timing: Any time. Route: subcutaneous.
Schedule note: Investigational. Dosing per the phase 2 trial protocol.
Every rung of the published schedule, the week it opens, and the unit mark it works out to at 20 mg in 2 ml. Change the vial or the water above and the whole table recomputes. The schedule itself does not change: it is the same for every reader, which is the point of a titration ladder.
| Step | Opens | Dose | Draw | Doses per vial |
|---|---|---|---|---|
| Step 1 | Week 1-4 | 2 mg | 20.0 units | 10 |
| Step 2 | Week 5-8 | 4 mg | 40.0 units | 5 |
| Step 3 | Week 9-12 | 8 mg | 80.0 units | 2 |
| Maintenance | Week 13 onward | 12 mg | 120.0 units | 1 |
If a rung is not tolerated the schedule holds it for a further 4 weeks rather than advancing. If it is still not tolerated after that, the schedule drops back one rung for up to 4 weeks before re-attempting. Reaching maintenance takes 12 weeks when every rung is tolerated first time, and longer when one is not.
Rungs, durations and tolerance rules read verbatim from GLP1_TITRATION_LADDERS, the engine's label-driven titration constant. ADR-046 puts that ahead of the engine's experience-tier dose table for this class, so the tier envelope is deliberately not published on this page: two dose stories on one page is worse than one. Unit marks are arithmetic over your vial size and water volume.
Pre-calculated syringe units for every water volume against the dose figures this compound actually uses, at your selected vial size of 20 mg. A cell reading "n/a" means the draw exceeds a 100-unit syringe at that concentration.
| BAC water | Conc. | Step 12 mg | Step 24 mg | Step 38 mg | Maintenance12 mg |
|---|---|---|---|---|---|
| 1 ml | 20 mg/ml | 10 | 20 | 40 | 60 |
| 1.5 ml | 13.33 mg/ml | 15 | 30 | 60 | 90 |
| 2 ml | 10 mg/ml | 20 | 40 | 80 | n/a |
| 2.5 ml | 8 mg/ml | 25 | 50 | 100 | n/a |
| 3 ml | 6.67 mg/ml | 30 | 60 | n/a | n/a |
| 4 ml | 5 mg/ml | 40 | 80 | n/a | n/a |
| 5 ml | 4 mg/ml | 50 | 100 | n/a | n/a |
Column doses are the rungs of the titration schedule in GLP1_TITRATION_LADDERS. Unit marks are arithmetic.
Climbing every rung without a hold takes 12 weeks at one administration per week. Multiplied out at your selected step and your mix, that is what reaching maintenance costs in consumables. A held or dropped-back rung lengthens it, and the schedule has no off-period to end on: the engine catalog marks this compound continuous use.
| Weeks to maintenance | 12 weeks, no off-period |
|---|---|
| Administrations per week | 1 |
| Total administrations | 12 |
| Vials of 20 mg | 2 |
| Insulin syringes | 12 (30-unit holds the draw) |
| Bacteriostatic water | 4 ml, 1 bottle of 10 ml |
Weeks to maintenance and the weekly cadence read from GLP1_TITRATION_LADDERS. Continuous use read from PEPTIDE_CATALOG. Counts are arithmetic.
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Retatrutide, developed as LY3437943, is a single molecule that agonises three receptors at once: the glucose-dependent insulinotropic polypeptide receptor, the glucagon-like peptide 1 receptor and the glucagon receptor. The third is what separates it from semaglutide and tirzepatide, and a 2024 structural study in Cell Discovery mapped how one peptide manages all three. It is investigational. It is not approved by the FDA, and the dose figures on this page come from a trial protocol rather than from a label.
The phase 2 obesity trial, published in the New England Journal of Medicine in 2023 and registered as NCT04881760, is the study most readers are thinking of. At forty-eight weeks the least-squares mean change in body weight was 24.2 per cent below baseline in the highest dose group, against 2.1 per cent in the placebo group. A phase 2 trial in type 2 diabetes appeared in the Lancet the same year, and a randomised trial in metabolic dysfunction-associated steatotic liver disease in Nature Medicine the year after.
The phase 3 programme is registered and running. TRIUMPH-1 through TRIUMPH-4 (NCT05929066, NCT05929079, NCT05882045 and NCT05931367) have completed, and further TRIUMPH trials remain active. That is the honest state of the evidence: a large, well-registered programme that has not yet produced an approval, which is a different thing from either a proven drug or an unstudied one.
| Route | subcutaneous |
|---|---|
| Timing | Any time |
| Catalog frequency | once weekly |
| Cycle | 52 weeks on, 0 weeks off |
| Taper before the off period | Not specified |
| Loading phase | None |
| Weight sensitive | No |
Catalog note: Triple agonist at the GIP, GLP-1 and glucagon receptors. Dosing follows the phase 2 trial protocol. Not FDA-approved, and requires experienced guidance.
Every row above is read from PEPTIDE_CATALOG, the engine catalog, and the note is quoted verbatim rather than paraphrased.
Klarovel holds dose data for Retatrutide in more than one place, and they do not all say the same thing. The engine's experience-tier dose table carries a span per experience level. The older research row carries a single conservative figure. The titration schedule carries a fixed sequence of rungs with a duration on each.
For this class the schedule is the one that binds, and that precedence is written down rather than improvised: it is the first rule in the source order the dosing hub, the dose guard and the engine all follow. The reason is that a titration schedule is not a range someone picks a point inside. It is a sequence, and the sequence is the dose. Publishing an experience envelope next to it would invite exactly the thing the schedule exists to prevent, which is starting somewhere in the middle.
So the experience-level, body-weight and age inputs the other calculators on this site offer are absent here. They are absent because the published schedule is not adjusted for any of them, not because the page ran out of room.
A public page cannot know your health data, so it cannot tell you whether a compound is appropriate. What it can do is list the conditions the engine's contraindication matrix associates with this compound, and what the engine does about each. In a generated protocol these resolve automatically and the reason is shown alongside the exclusion.
| Condition | Engine action | Reason |
|---|---|---|
| Diabetes type1 | Caution | GLP-1 agonists affect insulin secretion and require careful adjustment of insulin doses with type 1 diabetes. Only under diabetologist supervision. |
| Kidney | Monitored | GLP-1 agonists may affect kidney function. Monitor eGFR and creatinine with existing kidney disease. |
| Liver | Monitored | GLP-1 agonists are partially hepatically metabolized. Monitor ALT/AST with liver disease. Tesamorelin may actually improve liver fat. |
Conditions, severities and reasons read verbatim from CONTRAINDICATION_RULES, the engine's contraindication matrix. This is not the full set of things worth raising with a clinician; it is the set the engine acts on.
These papers cover retatrutide from receptor pharmacology through the phase 2 programme: the structural work on triple agonism, the phase 2 obesity and type 2 diabetes trials, the steatotic liver disease trial, body composition substudies, and the systematic reviews and meta-analyses of the trials to date. They are not the source of the dose figures on this page, which come from the engine's titration constant.
The dose figures on this page are not sourced from these papers. They are read from the Klarovel engine's own dose table, which is cited inline wherever a number appears. These references cover mechanism, pharmacology and clinical context.
12 references, every identifier resolved against NCBI on 2026-08-03. Per peptide, a relevance-sorted esearch was run and every returned id was resolved through esummary. Any id esummary could not resolve was dropped, and any record carrying the 'Retracted Publication' pubtype was dropped. Titles, journals, years and first authors below are the values esummary returned, not authored text. One retracted record was dropped: PMID 37696839 (thymosin beta 4 query). Regenerated 2026-08-03 for cjc1295_no_dac, ipamorelin, pt141, retatrutide, aod9604 and sermorelin using the same esearch + esummary procedure; no record was added whose esummary payload lacked a title, journal or first author.
Beyond the arithmetic
A calculator converts a dose into syringe units. The Klarovel engine decides the dose: it reads your health data, resolves contraindications, sets the envelope by experience level, removes incompatible pairs and builds the cycling and monitoring schedule. Blood work is optional and sharpens the result. It is never required.