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Can a 3-Day drug cocktail rejuvenate kidney patients?

NCT ID NCT02848131

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only This study
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether a short course of two drugs, dasatinib and quercetin, can clear senescent (aging) cells in people with chronic kidney disease. The goal is to see if this reduces frailty and improves stem cell function. Thirty participants aged 40-80 with moderate-to-severe kidney disease will take the drugs for 3 days and be monitored for changes in cell health and physical ability.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Dasatinib and Quercetin
What this could lead to
If it works, this could point toward a treatment that reduces frailty and improves physical function in people with chronic kidney disease.
What could go wrong
This is a small, early-phase study with only 30 participants, so results may not apply broadly. The drugs are taken for just 3 days, so any benefits may be short-lived or not occur at all.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

About 30 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jul 2016

Expected to finish

Apr 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

40 to 80 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Age 40-80 years 2. Chronic kidney disease estimated glomerular filtration rate (eGFR) 15-45 ml/min/1.73m2 3. Diabetes mellitus and taking diabetes medications Exclusion Criteria: 1. Concomitant glomerulonephritis, 2. Nephrotic syndrome, 3. Solid organ transplantation, 4. Autosomal dominant or recessive polycystic kidney disease, 5. Known renovascular disease, 6. Pregnancy, 7. Active immunosuppression therapy, 8. Hemoglobin A1c≥10% at screening, 9. History of active substance abuse (including alcohol) within the past 2 years, 10. Current alcohol abuse (\>3 alcoholic beverages/day or \>21 per week), 11. Body weight \>150 kg or body mass index\>50 12. Human immunodeficiency virus infection 13. Active hepatitis B or C infection 14. Tyrosine kinase inhibitor therapy 15. Known hypersensitivity or allergy to dasatinib or quercetin 16. Inability to give informed consent 17. Uncontrolled systemic lupus erythematosus 18. Uncontrolled pleural/pericardial effusions or ascites 19. New invasive cancer except non-melanoma skin cancers 20. Invasive fungal or viral infection 21. Inability to tolerate oral medications 22. Total bilirubin\>2x upper limit of normal 23. Subjects taking medications that are sensitive to substrates or substrates with a narrow therapeutic range for CYP3A4, CYP2C8, CYP2C9, or CYP2D6 or strong inhibitors or inducers of CYP3A4 (e.g. cyclosporine, tacrolimus or sirolimus). If antifungals are absolutely necessary from an infectious disease perspective, then they will be allowed only if the levels are therapeutic. 24. Subjects on strong inhibitors of CYP3A4. 25. Subjects on therapeutic doses of anticoagulants (Warfarin (Coumadin);Rivaroxaban (Xarleto); Apixaban (Eliquis); Dabigatran (Pradaxa, Prazaxa) or Other). 26. Subjects on antiplatelet agents ((Clopidogrel (Plavix); Dipyridamole + Asprin (Aggrenox); Ticagrelor (Brilinta); Prasugrel (Effient); Ticlopidine (Ticlid) or Other) who are unable or unwilling to reduce or hold therapy prior to and during the 3-day drug dosing. Subjects may continue their previous regimen on day 4. 27. Subjects on quinolone antibiotic therapy for treatment or for prevention of infections within 10 days 28. Subjects taking H2-antagonists or proton pump inhibitors and unwilling to discontinue therapy 1 week prior and 2 weeks following enrollment. 29. Corrected QT interval (QTc)\>450 msec 30. Presence of any condition that the Investigator believes would put the subject at risk or would preclude the patient from successfully completing all aspects of the trial.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Mayo Clinic Florida

    Jacksonville, Florida, 32224, United States

  • Mayo Clinic in Rochester

    Rochester, Minnesota, 55905, United States

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