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Flavonoid
Fisetin for Frailty (AFFIRM-LITE Trial)
Phase 2
Waitlist Available
Led By Robert Pignolo, MD, PhD
Research Sponsored by Mayo Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Age ≥ 70 years
Be older than 65 years old
Must not have
Strong inhibitors of CYP3A4
New/active invasive cancer except non-melanoma skin cancers
Timeline
Screening 3 weeks
Treatment Varies
Follow Up seven days
Summary
This trial tests if Fisetin can reduce inflammation and frailty in elderly adults. Fisetin may help by lowering oxidative stress and improving overall health. The study focuses on older adults because they often face these health issues. Fisetin is a natural flavonoid found in many fruits and vegetables, known for its anti-inflammatory and antioxidant properties.
Who is the study for?
This trial is for people aged 70 or older who are experiencing frailty and inflammation. They must be able to take oral medication and not be on certain drugs that can't be stopped for the duration of the trial, including strong CYP3A4 inhibitors, proton pump inhibitors without a break, or senolytic agents used in the past year. Pregnant individuals, those with specific infections like hepatitis B/C or HIV, recent cancer except non-melanoma skin cancers, and those with certain lab abnormalities cannot join.
What is being tested?
The study is testing Fisetin's ability to reduce signs of aging such as frailty and inflammation compared to a placebo. Participants will receive either Fisetin capsules or a placebo (a capsule with no active drug) to see if there's an improvement in their condition.
What are the potential side effects?
Potential side effects from Fisetin may include allergic reactions for those sensitive to it. Since this is a pilot study assessing efficacy and safety, detailed side effect profiles will be determined during the trial.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 70 years old or older.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am not taking strong CYP3A4 inhibitors.
Select...
I have a new or active cancer that is not a non-melanoma skin cancer.
Select...
I cannot take medicine by mouth.
Select...
I have an invasive fungal or viral infection.
Select...
My vitamin D level is above 20 ng/ml.
Select...
I am currently on or have been treated with tyrosine kinase inhibitor therapy.
Select...
I am currently on medication that includes chemotherapy drugs.
Select...
I am not currently taking any antibiotics or antifungals listed.
Select...
I cannot or will not stop my proton pump inhibitor medication for 4 days during the Fisetin treatment.
Select...
My weight is over 150 kg or my BMI is over 50.
Select...
I cannot or do not want to give permission for treatment.
Select...
I have an active hepatitis B or C infection.
Select...
I am HIV positive.
Select...
I have unmanaged fluid buildup in my chest or abdomen.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ seven days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~seven days
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Decrease in blood inflammation markers
Side effects data
From 2023 Phase 1 & 2 trial • 75 Patients • NCT0421098638%
Arthralgia
15%
Pain in Extremity
12%
Lab Findings
12%
Nausea
9%
Fatigue
9%
Back Pain
9%
Headache
6%
Flatulence
6%
Muscle Cramp
6%
Dry Mouth
6%
Rash Maculo-Papular
3%
Neoplasms
3%
Covid 19
3%
Bladder Perforation
3%
Rotator Cuff Injury
100%
80%
60%
40%
20%
0%
Study treatment Arm
Fisetin
Placebo
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: TreatmentExperimental Treatment1 Intervention
Fisetin 20mg/kg/day, orally for 2 consecutive days
Group II: PlaceboPlacebo Group1 Intervention
Placebo capsules orally for 2 consecutive days
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Fisetin
2016
Completed Phase 2
~250
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Frailty Syndrome, such as anti-inflammatory agents like Fisetin, work by reducing systemic inflammation, which is a major contributor to the symptoms of frailty. These treatments target inflammatory pathways to decrease levels of inflammatory markers in the blood.
This reduction in inflammation can lead to improvements in muscle strength, reduced insulin resistance, and decreased bone resorption. By addressing these underlying issues, anti-inflammatory treatments can enhance physical function and quality of life for patients with Frailty Syndrome.
Find a Location
Who is running the clinical trial?
Mayo ClinicLead Sponsor
3,326 Previous Clinical Trials
3,059,442 Total Patients Enrolled
Robert Pignolo, MD, PhDPrincipal InvestigatorMayo Clinic
1 Previous Clinical Trials
61 Total Patients Enrolled
James L Kirkland, MD, PhDPrincipal InvestigatorMayo Clinic
4 Previous Clinical Trials
195 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I cannot or will not stop my proton pump inhibitor medication for 4 days during the Fisetin treatment.I am not taking strong CYP3A4 inhibitors.I have a new or active cancer that is not a non-melanoma skin cancer.I am on medication that interacts with specific liver enzymes.I cannot take medicine by mouth.I have taken quinolone antibiotics in the last 10 days.I haven't taken any senolytic agents like Fisetin or Dasatinib in the last year.I have an invasive fungal or viral infection.My vitamin D level is above 20 ng/ml.I am 70 years old or older.I am currently on or have been treated with tyrosine kinase inhibitor therapy.I am not willing to stop taking my H2-antagonist medication for 3 weeks.I am currently on medication that includes chemotherapy drugs.I am not currently taking any antibiotics or antifungals listed.I can stop my current medications for 2 days to take Fisetin.My weight is over 150 kg or my BMI is over 50.I cannot or do not want to give permission for treatment.I have an active hepatitis B or C infection.I am HIV positive.You have a known allergy or sensitivity to fisetin.I have unmanaged fluid buildup in my chest or abdomen.
Research Study Groups:
This trial has the following groups:- Group 1: Treatment
- Group 2: Placebo
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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