Vol. IV · No. 19
Tuesday, June 23, 2026
Issue: Spring · 2026
Established · MMXXVI
— The evidence base for longevity medicine —
Indexed by PubMed · CTG · Cochrane
Editorial team · geroevidence.com
Subscription · app.geroevidence.com
Senolytic · Senescence

D + Q dasatinib + quercetin

Senolytic ·Senescence pathway

D + Q (dasatinib + quercetin) functions as a senolytic by selectively inducing apoptosis in senescent cells through dasatinib's inhibition of SRC family kinases and quercetin's broad tyrosine kinase inhibition, while simultaneously blocking anti-apoptotic pathways in cells that have exited the cell cycle. This combination targets the senescence-associated secretory phenotype (SASP) pathway, reducing chronic low-grade inflammation driven by accumulated senescent cells with age. Preclinical evidence in murine models demonstrates improved physical function, reduced frailty markers, and extended healthspan following senolytic treatment; human clinical trials remain limited, with preliminary data from small cohorts suggesting improvements in physical function and reduced senescence markers in osteoarthritis and idiopathic pulmonary fibrosis patients, though robust longevity outcomes in humans remain to be established.

Last reviewed: May 19, 2026
Evidence strength
Emerging
— for healthspan endpoints
Strong Ph. III
Moderate ≥2 RCTs
Emerging 1 RCT
Insufficient pre-clin
Single RCT or pooled small-trial signal. Promising but limited.
Key outcome
No pooled HR
Kirkland 2023 · Phase II
Evidence tier
Emerging
Updated May 19, 2026
Active trials
from ClinicalTrials.gov
Drug class
Senolytic
Senescence

Recent papers — reviewed before publication

48 indexed
Mechanism
Jun 1, 2026
Combined Senolytics Induce Varied Phenotypic and Functional Responses on Senescent Phenotypes of Mesenchymal Stromal Cell Populations.
Heinrichs et al. · Biochimie
Review
Jun 1, 2026
Biomarkers and therapies Associated with Hutchinson-Gilford Syndrome.
Ali et al. · Ageing research reviews
More papers available — with plain language summaries
Subscribers see all papers with summaries, daily new publications, evidence alerts, and trial updates.
Start free trial →

Active trials — from ClinicalTrials.gov

0 tracked
Full trial tracking
Active trials, phase, enrollment, primary endpoints, and completion dates — available to subscribers.
Start free trial →

Frequently asked

What are senolytics and are they FDA-approved?

Senolytics (e.g., dasatinib + quercetin, fisetin) are compounds studied for their ability to selectively eliminate senescent cells. They are not FDA-approved for any senolytic or longevity indication; dasatinib itself is approved for certain leukemias.

What human trial data exists for dasatinib + quercetin (D+Q)?

Early-phase human trials (e.g., Kirkland 2023, Phase II) have evaluated D+Q in small cohorts. No pooled hazard ratio for hard clinical outcomes currently exists — see the full profile for available trial-level detail.

Why is the evidence tier for senolytics graded Emerging?

This reflects single-trial or small pooled-trial signal in humans, per Geroevidence's four-tier methodology, rather than the larger concordant RCT base required for a Moderate or Strong classification.

What are the known risks of dasatinib + quercetin (D+Q)?

Dasatinib carries known risks from its approved leukemia indication, including myelosuppression and fluid retention, typically at doses higher than senolytic protocols studied. Quercetin's safety profile as a supplement is generally considered favorable, though drug-interaction data is limited.

How does D+Q compare to fisetin as a senolytic approach?

Both are studied as senolytics with distinct proposed mechanisms. D+Q has more published human trial data; fisetin's human evidence base is currently under editorial review on Geroevidence. See the fisetin profile for comparison.

This information is provided for educational reference only and does not constitute medical advice or a treatment recommendation.
Evidence profiles are reviewed by the Geroevidence editorial team. Key outcomes are from published meta-analyses or landmark RCTs. No clinical recommendations are made. Full evidence dossiers with paper summaries and weekly updates are available to subscribers.