A PHASE II, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY EVALUATING THE ONGOING LUNG DECLINE WITH AGE INTENSIFIED RESPONSE (OLD AIR)
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Forced Vital Capacity (FVC)
研究概览
简要总结
This Phase II, randomized, double-blind, placebo-controlled pilot study will evaluate the effects of fisetin, a senolytic flavonoid compound, on lung function and biomarkers of cellular senescence in older adults aged 60 years and older. Participants will include individuals with a history of at least 10 pack-years of smoking as well as age-matched never-smokers. Forty participants will be randomized to receive either fisetin or placebo using a short-course "hit-and-run" dosing strategy (approximately 20 mg/kg/day orally for 2 consecutive days on Days 1-2 and Days 8-9).
详细描述
This Phase II, randomized, double-blind, placebo-controlled study is designed to evaluate the effects of fisetin, a naturally occurring flavonoid with senolytic properties, on pulmonary health in older adults. Aging and cigarette smoke exposure have both been associated with cellular senescence, a biological process characterized by the accumulation of dysfunctional cells that may contribute to progressive decline in organ function. The study investigates whether intermittent administration of fisetin can favorably influence lung physiology and biological markers associated with aging.
Participants will be randomized to receive either fisetin or placebo and will undergo a short-course treatment regimen using a "hit-and-run" approach intended to transiently target senescent cells. The study population includes older adults with and without a history of cigarette smoking to allow assessment across groups with differing risk for accelerated pulmonary aging.
Study procedures include clinical evaluations, pulmonary function testing, exercise-based assessments, electrocardiography, laboratory testing, and collection of blood and urine samples for analysis of biomarkers related to cellular senescence and aging. Participants will be followed over a two-week study period, during which safety, tolerability, and protocol feasibility will be assessed. The results of this pilot study are intended to inform the design of future trials evaluating senolytic therapies as potential interventions for age-related declines in lung function and health.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
盲法说明
This is a quadruple-masked (participant, care provider, investigator, outcomes assessor) study. Participants will be randomized to receive either fisetin or placebo. The investigational product and placebo will be prepared and dispensed by the Research Pharmacy according to a predetermined randomization schedule. Participants, investigators, study staff involved in participant assessments, and outcome assessors will remain blinded to treatment assignment throughout the study. Only designated unblinded pharmacy personnel responsible for investigational product preparation and dispensing will have access to treatment allocation information. Blinding will be maintained until completion of study procedures unless unblinding is required for participant safety.
入排标准
- 年龄范围
- 60 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Adults aged 60 years and older who are physically capable of participating in study procedures;
- •Willing to be randomized to fisetin or placebo; weight stable within the previous 2 months (<5-pound change);
- •No blood donation within 2 months before screening; absence of unstable chronic disease;
- •Willing to maintain baseline activity level throughout the study;
- •Body mass index <30 kg/m²;
- •Either a history of at least 10 pack-years of cigarette smoking or never-smoking status.
排除标准
- •Electrocardiogram (ECG) abnormalities, including prolonged QTc.
- •Use of fisetin, other flavonoid supplements, or known senolytic compounds within 6 months prior to screening.
- •Resting systolic blood pressure >160 mmHg or diastolic blood pressure >110 mmHg.
- •Known allergy or hypersensitivity to fisetin or any component of the study product.
- •Active malignancy, except non-melanoma skin cancer.
- •Clinically significant hepatic, renal, cardiovascular, endocrine, immunologic, metabolic, or other uncontrolled medical conditions that, in the opinion of the investigator, would interfere with study participation or interpretation of results.
- •Clinically significant laboratory abnormalities, including severe anemia, leukopenia, thrombocytopenia, uncontrolled diabetes, advanced kidney disease, significant liver dysfunction, or evidence of systemic inflammation.
- •Human immunodeficiency virus (HIV) infection, active hepatitis B or hepatitis C infection, or invasive fungal infection.
- •History of diverticulitis or diverticulosis with gastrointestinal bleeding.
- •Current use of systemic corticosteroids.
- •Current use of warfarin.
- •Current use of medications with significant interaction potential with fisetin, including selected CYP450 or transporter substrates, inhibitors, or inducers, unless such medications can be safely withheld according to protocol requirements.
- •Recent medication, supplement, or lifestyle changes that may affect study outcomes, in the opinion of the investigator.
- •Inability to perform required study procedures, including pulmonary function testing, exercise testing, or other protocol assessments.
- •Unwillingness or inability to provide informed consent.
- •Pregnancy or breastfeeding.
- •Any other condition that, in the opinion of the investigator, would make participation unsafe or compromise study integrity.
研究组 & 干预措施
Placebo
Participants receive matching placebo capsules administered on the same schedule as the fisetin arm (Days 1-2 and Days 8-9).
干预措施: Placebo (Drug)
Fisetin
Participants receive oral fisetin at approximately 20 mg/kg/day for 2 consecutive days on Days 1-2 and again on Days 8-9 using a senolytic "hit-and-run" dosing strategy.
干预措施: Fisetin (Drug)
结局指标
主要结局
Forced Vital Capacity (FVC)
时间窗: Baseline and Day 14
Forced vital capacity measured by spirometry to assess lung function following treatment with fisetin versus placebo.
Forced Expiratory Volume in 1 Second (FEV1)
时间窗: Baseline and Day 14
Forced expiratory volume in one second measured by spirometry following treatment with fisetin versus placebo.
FEV1/FVC Ratio
时间窗: Baseline and Day 14
Ratio of FEV1 to FVC measured by spirometry following treatment with fisetin versus placebo.
次要结局
- 6-Minute Walk Distance (6MWD)(Baseline and Day 14)
- Peak Oxygen Uptake (VO₂)(Baseline and Day 14)
- Biomarkers of Cellular Senescence(Baseline and Day 14)
研究者
Samuel Cohen, MD
Assistant Professor of Medicine
Cedars-Sinai Medical Center