Fezolinetant and Vascular Health and Brain Health (FAVES-B)
The goal of this clinical trial is to learn whether a study drug called fezolinetant impacts cardiovascular and cognitive health in women who have moderate to severe menopausal hot flashes and night sweats.
Researchers will compare fezolinetant to a placebo. A placebo is a pill that looks like the study drug but does not contain any active medicine. This comparison helps researchers understand whether fezolinetant works better than no treatment.
Participants will:
Be randomly assigned to take either fezolinetant (45 mg) or a placebo once a day for 12 weeks.
Visit the research clinic for regular checkups and tests during the study. Complete tests that measure blood vessel function and cognition.
Participants and study staff will not know which treatment each participant receives during the study.
研究概览
详细说明
研究类型
注册 (估计的)
阶段
- 第三阶段
联系人和位置
学习联系方式
- 姓名:Sarah M Conklin, PhD
- 电话号码:878-261-6899
- 邮箱:conklinsm2@upmc.edu
研究联系人备份
- 姓名:Mollie B Bandy, BA
- 电话号码:412-648-9088
- 邮箱:BandyMB@upmc.edu
学习地点
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Illinois
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Chicago、Illinois、美国、60612
- University of Illinois, Chicago
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接触:
- Ece K Weishaar, MS
- 电话号码:312-996-1623
- 邮箱:EceKilic@UIC.Edu
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副研究员:
- Pauline M Maki, PhD
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Pennsylvania
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Pittsburgh、Pennsylvania、美国、15260
- University of Pittsburgh
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接触:
- Sarah M Conklin, PhD
- 电话号码:8782616899
- 邮箱:conklinsm2@upmc.edu
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接触:
- Mollie B Bandy, BA
- 电话号码:8782616899
- 邮箱:BANDYMB@upmc.edu
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首席研究员:
- Rebecca C Thurston, PhD
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Born female
- Age ≥40 - ≤65 years at the time of the screening visit
- Body Mass Index (BMI) ≥18 to ≤38 kg/m2
- Seeking treatment or relief for moderate to severe VMS associated with menopause
- Confirmed menopausal as per one of the following criteria at the time of screening: Reporting spontaneous amenorrhea for ≥12 consecutive months; spontaneous amenorrhea for ≥6 and < 12 months with follicle-stimulating hormone >40 IU/L
- Negative urine pregnancy test at screening (if <12 months of amenorrhea)
- A minimum average of 7-8 moderate to severe VMS per day, or 50-60 per week prior to randomization as reported in the 7-day hot flash diary
- Agrees to not participate in another interventional study (pharmaceutical or device) while participating in this current study
Exclusion Criteria:
- Pregnancy/lactation (past 6 months)
- Any treatment for hot flashes with demonstrated efficacy for hot flashes
- Currently using systemic sex-hormone medications.
- Currently using cytochrome P450 1A2 (CYP1A2) inhibitors (as listed according to the FDA).
- Severely elevated blood pressure [systolic blood pressure (SBP) >180 and/or diastolic blood pressure (DBP) >110]
- A medical condition or chronic disease (including history of hepatic, renal, cardiovascular, gastrointestinal, pulmonary [e.g., moderate asthma], endocrine or gynecological disease) or malignancy that could confound interpretation of the study in the opinion of the investigator or study physician
- Self-reported narcolepsy
- Previous/current history of a malignant tumor, except for basal cell carcinoma
- Participants with known cirrhosis, active liver disease, jaundice, or elevated liver aminotransferases or total bilirubin (ALT, AST, and total bilirubin), should not be enrolled if ALT or AST is ≥ 2 x ULN or if the total bilirubin is ≥ 2 x ULN for the evaluating laboratory. Participants with ALP > 1.5 × ULN and judged clinically significant by the study physician.
- Severe renal impairment [estimated glomerular filtration rate (eGFR) 15 to <30 mL/min per 1.73 m2] or end-stage renal disease (ESRD) (eGFR < 15 mL/min/1.73 m2) at screening as per USPI
- Positive Hepatitis C virus antibody, Hepatitis B surface antigen, and/or human immunodeficiency virus antibody screen at screening
- History within the last 6 months of undiagnosed uterine bleeding
- Key medical conditions (history of cardiovascular disease, stroke/cerebrovascular accident, brain injury with loss of consciousness for more than 60 seconds within the last five years, cognitive disorders, brain tumor, dementia, Parkinson's disease, chemotherapy, psychotic disorders)
- Metal in the body, claustrophobia, or cannot undergo 3T magnetic resonance imaging (MRI); Inability to meet MRI eligibility criteria
- Lymph node removal on both sides of the body, mastectomy, or dialysis
- Hysterectomy; levonorgestrel-releasing intrauterine systems initiated before 12 months of spontaneous amenorrhea (Not exclusionary if placed after 12 months of spontaneous amenorrhea), or history of endometrial ablation will be excluded due to inability to stage menopause; Bilateral oophorectomy if completed prior to 12 months of spontaneous amenorrhea
- Cardiovascular medication use.
- Prior exposure to fezolinetant or elinzanetant
- Current participation in another interventional study or participated in an interventional study or received any investigational drug within 3 months
- Illicit substance use reported in the past week or detected by urine toxicology screen.
- Subject has any condition, which in the investigator's or study physician's opinion, makes the subject unsuitable for study participation.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:三倍
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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安慰剂比较:Placebo Arm
The placebo tablet will be an identical tablet appearing to active medication.
The placebo tablets contain the following inactive ingredients: ferric oxide, hydroxypropyl cellulose, hypromellose, low-substituted hydroxypropyl cellulose, magnesium stearate, mannitol, microcrystalline cellulose, polyethylene glycol, talc, and titanium dioxide.
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The placebo tablet will be an identical tablet appearing to active medication.
The placebo tablets contain the following inactive ingredients: ferric oxide, hydroxypropyl cellulose, hypromellose, low-substituted hydroxypropyl cellulose, magnesium stearate, mannitol, microcrystalline cellulose, polyethylene glycol, talc, and titanium dioxide).
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实验性的:Active Study Drug
Fezolinetant is a white powder.
It is very slightly soluble in water (0.29 mg/mL).
Fezolinetant tablets that will be used in this study are round, light red film-coated tablets with no marking on the tablets.
Each fezolinetant tablet for oral use contains 45 mg of fezolinetant and the following inactive ingredients: ferric oxide, hydroxypropyl cellulose, hypromellose, low-substituted hydroxypropyl cellulose, magnesium stearate, mannitol, microcrystalline cellulose, polyethylene glycol, talc, and titanium dioxide.
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Fezolinetant is a white powder.
It is very slightly soluble in water (0.29 mg/mL).
Fezolinetant tablets that will be used in this study are round, light red film-coated tablets with no marking on the tablets.
Each fezolinetant tablet for oral use contains 45 mg of fezolinetant and the following inactive ingredients: ferric oxide, hydroxypropyl cellulose, hypromellose, low-substituted hydroxypropyl cellulose, magnesium stearate, mannitol, microcrystalline cellulose, polyethylene glycol, talc, and titanium dioxide.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Flow-Mediated Dilation
大体时间:Baseline and end of treatment at 12 weeks.
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Endothelial function assessed by flow-mediated dilation
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Baseline and end of treatment at 12 weeks.
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Verbal Memory Performance
大体时间:Baseline and end of treatment at 12 weeks.
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Verbal memory performance on the California Verbal Learning Test
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Baseline and end of treatment at 12 weeks.
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Endothelial Biomarkers
大体时间:Baseline and end of treatment at 12 weeks.
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Blood-based endothelial function biomarkers
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Baseline and end of treatment at 12 weeks.
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Brain Activation during Verbal Encoding
大体时间:Baseline and end of treatment at 12 weeks.
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Memory circuitry as measured by changes in brain activation during performance of a functional magnetic resonance imaging (fMRI) task of verbal encoding
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Baseline and end of treatment at 12 weeks.
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Functional Connectivity during recall
大体时间:Baseline and end of treatment at 12 weeks.
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Memory circuitry as measured by changes in functional connectivity during performance of a functional magnetic resonance imaging (fMRI) task of verbal recall
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Baseline and end of treatment at 12 weeks.
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Subjective Vasomotor Hot Flash Diary
大体时间:Baseline and end of treatment at 12 weeks.
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frequency of subjectively assessed VMS using a digital hot flash diary
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Baseline and end of treatment at 12 weeks.
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Objective Vasomotor Monitoring
大体时间:Baseline and end of treatment at 12 weeks.
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Frequency of objectively measured VMS using 24-hour skin conductance monitoring
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Baseline and end of treatment at 12 weeks.
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Sleep Monitoring
大体时间:Baseline and end of treatment at 12 weeks.
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Objective sleep monitoring.
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Baseline and end of treatment at 12 weeks.
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合作者和调查者
调查人员
- 首席研究员:Rebecca C Thurston, PhD、University of Pittsburgh
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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