Therapeutic reversal of cellular senescence: A systematic review of senolytics, senomorphics and anti-ageing therapies in human clinical trials
What this study shows
A PRISMA-guided systematic review of six completed human clinical studies that met its eligibility criteria, testing drugs that clear or calm senescent ("zombie") cells -- senolytics such as dasatinib+quercetin, plus senomorphic and mTOR-targeting approaches. It reported limited and heterogeneous results, a mixture of biomarker and functional outcomes, with mostly mild side effects, and judged the evidence too thin (small samples, short follow-up) to call any of it an established therapy yet. Six INCLUDED studies is not a census of every completed human senotherapeutic trial: inclusion depends on the review's search date and eligibility criteria, and those have to be stated before any field-wide coverage conclusion is drawn. Useful mainly as a rare systematic look at where human senescence-targeting trials, mTOR inhibitors included, stand -- not as proof that any one drug works.
At a glance
| Evidence type | S Synthesis of human data Marked S because it synthesizes multiple human studies (a systematic review or meta-analysis); the code names the kind of study, not the quality of any single included study. |
| Study type | 1 - Systematic Review |
| Model system | Human clinical trials (PRISMA 2020 systematic review, 6 completed studies + 1 ongoing) |
| Journal | British Journal of Clinical Pharmacology |
| Year | 2026 |
| Peer reviewed | Yes |
| Record last updated | 2026-10-01 |
| Source | DOI 10.1002/bcp.70871 · PMID 42834340 |
In the Atlas
Related topics
Open questions that cite this study
- Cited as supporting evidence for the open question How much of rapamycin's healthspan benefit runs through fewer senescent cells?.
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- mTOR regulates the pro-tumorigenic senescence-associated secretory phenotype by promoting IL1A translation (2015)
- Spatial coupling of mTOR and autophagy augments secretory phenotypes (2011)
- mTOR regulation and therapeutic rejuvenation of aging hematopoietic stem cells (2009)
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