Sirolimus Rx

FDA-approved drug

Rapamycin has the best longevity data in pharmacology. None of it is human.

Both halves are true and we publish them together. The NIH's replicated mouse program extended lifespan in both sexes at three independent sites, even starting in late life. Humans have an approved transplant drug with a boxed warning, immune trials that mostly tested a different molecule (everolimus, labeled as such in our table), and one completed longevity trial that missed its primary endpoint. Every study row names its species and its compound; every number links to its source.

  • 23studies in the graded evidence table, species labeled on every row
  • 11of those rows are human studies, and 3 of the human rows tested a different rapalog, labeled in the compound column
  • 0completed human trials with a lifespan or disease-outcome primary endpoint. We print the zero instead of hiding it
  • 33fetch-verified sources, every one peer-reviewed or government

Online care, from intake to delivery

Sirolimus care, made simple

Choose your plan, complete a private medical intake, and connect with a licensed provider. If prescribed, treatment ships discreetly to your door.

Sirolimus care catalog product image
Compounded oral treatmentPrepared after approval
Catalog image. Dispensed product and packaging may vary by pharmacy.

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  1. 01
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  2. 02
    Complete your intakeShare your health history in our private, secure flow.
  3. 03
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Prescription treatment requires an online medical evaluation. A provider will determine whether treatment is medically appropriate; approval is not guaranteed.

Key facts

  • StatusFDA-approved drug
  • Tmax noteBlood levels in real-world longevity users peaked about 2 days after a weekly dose (observational data)
  • BioavailabilityAbout 14% (oral solution); tablets about 27% higher than solution; the two are not bioequivalent (clinically equivalent at 2 mg)
  • DistributionBlood-to-plasma ratio 36 +/- 18 (sequestered in red cells); Vss/F 12 +/- 8 L/kg; about 92% protein bound
  • MetabolismSubstrate of CYP3A4 and P-glycoprotein; extensive intestinal and hepatic metabolism
  • Steady state noteDerived: with a 62-hour half-life, steady state arrives in roughly 11 to 13 days (4 to 5 half-lives)
  • RouteOral (solution or tablets), once daily per label
  • Drug classmTOR inhibitor immunosuppressantFDA labelsource
  • Longevity statusOff-label; zero completed lifespan-outcome trialsAbsence of evidencesource
  • Half-lifeAbout 62 +/- 16 hoursFDA labelsource
  • Boxed warningImmunosuppression: infection, lymphoma/malignancy riskFDA labelsource
  • MonitoringWhole-blood troughs; label recommends TDM for all patientsFDA labelsource
  • Key interactionCYP3A4/P-gp substrate; grapefruit prohibited by labelFDA labelsource
  • Approved doses2 mg/day (renal, LAM start); 5 mg/day high-riskFDA labelsource
  • Best animal resultITP mice: +14% (F) / +9% (M) at 90th percentile, late-life startAnimalsource
  • Human evidence caveatFamous elderly immune RCTs used everolimus, not sirolimusDerived from cited datasource

Read the full Rapamycin (sirolimus) monograph

Browse by topic

Everything on Sirolimus (rapamycin), organized the way you research it.

All guides

56 in-depth, individually cited guides.

Evidence 17 guides

Safety 12 guides

Sourcing 11 guides

Dosing 11 guides

Get the two-column brief: what the mice proved, what humans have not

One email: the ITP results at species grade, the compound-labeled human trial table, the label's monitoring checklist, and the studied-doses table, all cited. Updates only when a label or trial changes something. No dosing advice by email. Unsubscribe anytime.

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