RecruitingPhase 1Phase 2NCT06431932

Pilot Trial of Fisetin in Healthy Volunteers and Older Patients With Multimorbidity

Pharmacokinetics, Safety, and Efficacy of Fisetin - A Phase I and Pilot Phase IIa Study


Sponsor

Ove Andersen

Enrollment

60 participants

Start Date

Mar 24, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The accumulation of senescent cells with age is a central mechanism that contributes to the development of chronic diseases, primarily by driving systemic chronic inflammation. Senolytic compounds such as fisetin can selectively target senescent cells for elimination and reduce multiple age-related pathologies in animal models. We will conduct a clinical trial in healthy volunteers and older patients with multiple chronic diseases. The participants will receive fisetin or placebo for two days, after which they will be examined at regular intervals for up to three months. We will investigate how fisetin is absorbed and metabolized by the body, and whether fisetin is safe. We will also identify methods to best measure the effect of fisetin on chronic inflammation, senescent cells, and general health.


Eligibility

Min Age: 20 Years

Inclusion Criteria15

  • Healthy volunteers:
  • Aged 20-35 years
  • suPAR levels \<3.5 ng/mL (± 15% corresponding to assay variation)
  • Able to cooperate cognitively
  • Able to read and understand Danish
  • Women of childbearing potential must use effective contraception
  • At screening #1 during hospital admission:
  • Acutely hospitalized medical patient
  • Age ≥65 years
  • suPAR \>5 ng/mL (± 15% corresponding to assay variation)
  • Multimorbidity (≥2 chronic diagnoses)
  • Able to cooperate cognitively
  • Able to read and understand Danish
  • At screening #2 28 days after hospital discharge:
  • suPAR \>5 ng/mL (± 15% corresponding to assay variation)

Exclusion Criteria39

  • Body weight \>100 kg
  • Inability to swallow pills
  • Pregnant and/or lactating
  • Known hypersensitivity or allergy to fisetin or excipients in the placebo capsules
  • Presence of any condition that the investigator believes would put the subject at risk or would preclude the participant from successfully completing all aspects of the trial
  • Presence of known chronic diagnosis
  • Active acute illness
  • Prescribed medication, except contraceptives
  • Previous cancer diagnosis or treatment
  • Use of senolytic and other "anti-aging" supplements
  • Older patients with multimorbidity:
  • At screening #1 during hospital admission:
  • Body weight \>100 kg
  • Inability to swallow pills
  • Known human immunodeficiency virus infection, active hepatitis B or C infection, invasive fungal infection
  • Uncontrolled (as per clinical judgment) pleural/pericardial effusions or ascites
  • New/active invasive cancer except non-melanoma skin cancers
  • Active cancer treatment or disseminated cancer
  • Known condition associated with major immunodeficiency
  • Known hypersensitivity or allergy to fisetin or excipients in the placebo capsules
  • Use of senolytic and other "anti-aging" supplements
  • At screening #2 28 days after hospital discharge:
  • Body weight \>100 kg
  • CRP \>30 mg/L (± 15% corresponding to assay variation)
  • Inability to swallow pills
  • Presence of any condition, or abnormal routine biochemistry test, that the investigator believes would put the subject at risk or would preclude the patient from successfully completing all aspects of the trial
  • Unstable (as per clinical judgment) major disorders, e.g., cardiovascular, renal, endocrine, immunological, hepatic disorder, or cancer
  • Estimated glomerular filtration rate (eGFR) \<15 ml/min/1.73 m2 or as per clinical judgment (e.g., risk of acute kidney injury)
  • Human immunodeficiency virus infection, known active hepatitis B or C infection, invasive fungal infection
  • Uncontrolled (as per clinical judgment) pleural/pericardial effusions or ascites
  • New/active invasive cancer except non-melanoma skin cancers
  • Active cancer treatment or disseminated cancer
  • Known condition associated with major immunodeficiency
  • Known hypersensitivity or allergy to fisetin or excipients in the placebo capsules
  • Subjects taking strong inhibitors or inducers of CYP3A4 or as per clinical judgment
  • Subjects taking specified substrates with a narrow therapeutic range for CYP3A4 or as per clinical judgment
  • Subjects taking specified inhibitors, inducers, or substrates of CYP2D6, CYP2C9, or CYP2C8, or as per clinical judgment
  • Subjects regularly using drug classes or specific medications or as per clinical judgment
  • Use of senolytic and other "anti-aging" supplements

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Interventions

DRUGFisetin

Subjects will receive fisetin corresponding to 20 mg/kg/day for two consecutive days.

DRUGPlacebo

Subjects will receive a corresponding number of placebo capsules for two consecutive days.


Locations(1)

Department of Clinical Research, Copenhagen University Hospital Amager & Hvidovre

Hvidovre, Denmark

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NCT06431932


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