▲ Human lifespan evidence: no lifespan RCT — human evidence is open-label pilot only (senescent-cell biomarker reduction and feasibility)

What it is

Class: Combination senolytic (tyrosine-kinase inhibitor + flavonoid; SCAP-disabling)

Also known as: D+Q, dasatinib and quercetin

Relationship to senescence: Transiently disables senescent-cell anti-apoptotic pathways (SCAPs). Dasatinib targets tyrosine-kinase-dependent survival signals; quercetin affects Bcl-2-family and PI3K/SERPINE nodes. The combination clears a broader range of senescent cell types than either alone in preclinical work.

Regulatory status

Dasatinib is an FDA-approved prescription tyrosine-kinase inhibitor (chronic myeloid leukaemia / Ph+ ALL); quercetin is a dietary flavonoid sold as a supplement. Neither is approved as a senolytic or for any anti-aging, longevity, or healthspan indication. No 'senolytic dose' or cycling schedule is an established clinical regimen.

Mechanism

Intermittent ('hit-and-run') dosing transiently inhibits the pro-survival networks senescent cells depend on, tipping them into apoptosis while sparing normal cells. See /bcl2-bclxl-scaps and /senolytics-vs-senomorphics.

Evidence — Human (open-label pilots)

Species / populationSmall open-label pilots: idiopathic pulmonary fibrosis (n=14); diabetic kidney disease (n=9); early-stage Alzheimer's disease (n=5).
Exposure, route, scheduleIntermittent oral D+Q, e.g. dasatinib 100 mg/day + quercetin 1000-1250 mg/day for 3 consecutive days (regimen varied by trial).
Comparator / durationMostly single-arm/open-label; the IPF pilot was described as single-blind placebo-controlled for feasibility.
Endpoint / numeric resultFeasibility/tolerability; physical function (IPF); senescent-cell and SASP markers in adipose/skin (DKD); CNS penetration of the drugs (Alzheimer's).
What it did NOT establishNo lifespan outcome, no disease-modification proof, no randomized hard clinical endpoint. Pilots are not powered for efficacy.

Negative or null findings

  • The Alzheimer's pilot found cognitive and neuroimaging measures did not significantly change from baseline; quercetin was not detected in cerebrospinal fluid.
  • No pilot demonstrated a clinical-outcome benefit; all were explicitly feasibility/biomarker studies.