COVID-FISETIN: Pilot in SARS-CoV-2 of Fisetin to Alleviate Dysfunction and Inflammation

• ClinicalTrials.gov Identifier: NCT04476953
• Recruitment Status: Enrolling by invitation
• First Posted: July 20, 2020
• Last Update Posted: January 25, 2023
• Sponsor: Mayo Clinic
• Information provided by (Responsible Party): James L. Kirkland, MD, PhD, Mayo Clinic

Study Description

Brief Summary:

The purpose of this study is to test whether Fisetin, a senolytic drug, can assist in preventing an increase in the disease's progression and alleviate complications of coronavirus due to an excessive inflammatory reaction.

Condition or disease	Intervention/treatment	Phase
Covid19	Drug: Placebo; Drug: Fisetin	Phase 2

Detailed Description:

To determine if Fisetin treatment can prevent deterioration of oxygenation status as measured by S/F ratio: SpO2/ FiO2, as well as prevent deterioration in physical function (frailty) and hyper-inflammation, other measures of oxygenation status (progression to supplemental oxygen requirement, assisted breathing/ ventilation), and progression from mild/ moderate to severe/ critical proven SARS-CoV-2 infection in hospitalized patients and to evaluate the safety and tolerability of Fisetin in this patient population.

Study Design

• Study Type: Interventional (Clinical Trial)
• Estimated Enrollment: 80 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Double (Participant, Investigator)
• Primary Purpose: Treatment
• Official Title: COVID-FISETIN: A Phase 2 Placebo-Controlled Pilot Study in SARS-CoV-2 of Fisetin to Alleviate Dysfunction and Excessive Inflammatory Response in Hospitalized Adults
• Actual Study Start Date: August 3, 2020
• Estimated Primary Completion Date: September 2023
• Estimated Study Completion Date: September 2023

Arms and Interventions

Arm	Intervention/treatment
Experimental: Treatment Group; Subjects will receive treatment drug Fisetin	Drug: Fisetin; ~20 mg/kg/day oral, NG or D tube course for 2 consecutive days; Other Name: 3,3',4',7-tetrahydroxyflavone
Placebo Comparator: Placebo Group; Subjects will receive placebo	Drug: Placebo; Placebo looks exactly like the study drug, but it contains no active ingredient.

Outcome Measures

Primary Outcome Measures :

1. Serious Adverse Events [ Time Frame: 6 months ]
   Number of participants to experience serious adverse events and hypersensitivity reactions.
2. Change in oxygenation status [ Time Frame: baseline, Day 3, 7, 10, 14, 17 and 30; Months 3 and 6 ]
   change in oxygenation levels as measured by S/F ratio (SPO2/FiO2)

Secondary Outcome Measures :

1. CoV Severity Category [ Time Frame: 6 months ]
   Number of participants to progress to severe or critical classification CoV

Eligibility Criteria

• Ages Eligible for Study: 18 Years and older (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria - Patients must meet all of the following inclusion criteria to be enrolled in this study.

1. Men or women 60 years of age or older

   OR

   Age 18 - 59 years WITH at least one of the following comorbidities:

   • BMI greater than or equal to 35
   • Diabetes
   • Asthma/ Chronic Obstructive Pulmonary Disease (COPD)
   • Previous Myocardial Infarction
   • Previous Stroke/ Cerebrovascular Accident (CVA)
   • Hypertension/ Atherosclerosis/ Peripheral Vascular Disease
   • Smoking and/or vaping
   • Other conditions associated with senescent cell accumulation (i.e. previous chemotherapy or radiation)
2. SpO2 greater than or equal to 85% (on room air or less than or equal to 2 L of supplemental oxygen)
3. Willing and able to provide written informed consent or have a legally authorized representative (LAR) who will provide informed consent
4. SARS-CoV-2 infection confirmed by PCR test at Mayo Clinic (or other CLIA certified) laboratory within 10 days prior to randomization.

Exclusion Criteria - Patients who meet any of the following exclusion criteria are not to be enrolled in this study.

General Exclusion Criteria

1. Presence of any condition that the Investigator or the subject's attending physician believes would put the subject at risk or would preclude the patient from successfully completing the trial
2. Pregnant and/or lactating. Women of childbearing potential (WCBP) must have a negative pregnancy test within 72 hours prior to randomization
3. WCBP who are unwilling to abstain from sex or use an adequate method of contraception from the time of the first IP administration through 48 hours after the last IP administration

4. Men who are unwilling to abstain from sex with WCBP or use an adequate method of contraception from the time of the first IP administration through 48 hours after the last IP administration

   Laboratory Exclusion Criteria

5. Total bilirubin >3X upper limit of normal or as per clinical judgment.
6. Serum aspartate transaminase (AST) or alanine aminotransferase (ALT) >4x the upper limits of normal or as per clinical judgment.
7. Hemoglobin <7 g/dL; white blood cell count ≤ 2,000/mm3 (< or = 2.0 x 109/L) or > or = 20,000/mm3 (> or = 20 x 109/L); platelet count < or = 40,000/µL (< or = 40 x 109/L); absolute neutrophil count < or = 1 x 109/L; lymphocyte count <0.3 x 109/L at screening or as per clinical judgment.
8. Unstable (as per clinical judgment) major cardiovascular, renal, endocrine, immunological, or hepatic disorder.
9. eGFR <25 ml/ min/ 1.73 m2 or as per clinical judgment.

10. Plasma and/or serum glucose >300 or as per clinical judgment.

    Clinical History Exclusion Criteria

11. Human immunodeficiency virus infection.
12. Known active hepatitis B or C infection.
13. Invasive fungal infection.
14. Uncontrolled (as per clinical judgement) pleural/pericardial effusions or ascites.

15. New/active invasive cancer except non-melanoma skin cancers.

    Medication Exclusion Criteria (See Appendices 1-3 for additional information)

16. Known hypersensitivity or allergy to Fisetin.
17. Patients currently using medications which utilize CYP450 2C9 for metabolism. These medications include: Fosphenytoin, Phenytoin, Warfarin, Glimepiride, Diclofenac, Bosentan, and Glyburide. Patients taking any of these medications may participate if the medications can be held immediately before the 1st IP administration until at least 10 hours after the last (2nd) IP administration and the patient is otherwise eligible.
18. Patients currently using medications which utilize CYP2C9, CYP2C19, CYP1A2, OATP1B1. These medications include: Olanzapine, Clozapine, Theophylline, Tizanidine, Warfarin, Rameltoen, Tacrine, Duloxetine, Mexiletine, Riluzole, and Atomoxetine. Patients taking any of these medications may participate if the medications can be held immediately before the 1st IP administration until at least 10 hours after the last (2nd) IP administration and the patient is otherwise eligible.
19. Patients currently using medications which are strong inhibitors of CYP3A4. These medications include: Atazanavir, Ceritinib, Clarithromycin, Darunavir, Idelalisib, Indinavir, Itraconazole, Ketoconazole, Lopinavir, Mefipristone, Nefazodone, Nelfinavir, Ombitasivir-paritaprevir-ritonivir, Ombitasivir-paritaprevir-ritonivir-plus dasabuvir, Posaconazole, Saquinavir, Telithromycin, Tucatinib, and Voriconazole. Patients taking any of these medications may participate if the medications can be held immediately before the 1st IP administration until at least 10 hours after the last (2nd) IP administration and the patient is otherwise eligible.
20. Patients currently using antifungals. If antifungals are absolutely necessary from an infectious disease perspective, then they will be allowed only if the levels are subtherapeutic or therapeutic.

21. Patients taking any of these medications may participate if the medications can be held immediately before the 1st IP administration until at least 10 hours after the last (2nd) IP administration and the patient is otherwise eligible:

    • Cardiac: digoxin, flecainide, amiodarone
    • Psychiatric: lithium, thioridazine
    • Neurologic: carbamazepine, phenobarbital
    • Antimicrobial/fungal: aminoglycosides (e.g. amikacin, gentamicin, kanamycin, neomycin, netilmicin, paromomysin, streptomycin, tobramycin), rifampin
    • Anticoagulants/ Antiplatelets: warfarin
    • Others: methotrexate, nitroglycerin, St. John's wort, tyrosine kinase inhibitors, tacrine, diclofenac
22. Participation in other clinical trials involving treatment for SARS-CoV-2. (unless reviewed and approved by the Principal Investigator). Note that institutional standard of care treatment of SARS-CoV-2 including glucocorticoids, hydroxychloroquine, azithromycin, remdesivir, anti-spike antibodies, and/or convalescent plasma are not excluded from the study.

Contacts and Locations

Locations

United States, Minnesota

Mayo Clinic in Rochester

Rochester, Minnesota, United States, 55905

Sponsors and Collaborators

Mayo Clinic

Investigators

• Principal Investigator: James L Kirkland, MD, PhD; Mayo Clinic

More Information

Additional Information:

Mayo Clinic Clinical Trials 

• Responsible Party: James L. Kirkland, MD, PhD, Principal Investigator, Mayo Clinic
• ClinicalTrials.gov Identifier: NCT04476953
• Other Study ID Numbers: 20-003936
• First Posted: July 20, 2020
• Last Update Posted: January 25, 2023
• Last Verified: January 2023

Individual Participant Data (IPD) Sharing Statement:

• Plan to Share IPD: No

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No

Keywords provided by James L. Kirkland, MD, PhD, Mayo Clinic:

SARS-CoV-2