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.
調査の概要
詳細な説明
研究の種類
入学 (推定)
段階
- フェーズ 3
連絡先と場所
研究連絡先
- 名前:Sarah M Conklin, PhD
- 電話番号:878-261-6899
- メール:conklinsm2@upmc.edu
研究連絡先のバックアップ
- 名前:Mollie B Bandy, BA
- 電話番号:412-648-9088
- メール:BandyMB@upmc.edu
研究場所
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Illinois
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Chicago、Illinois、アメリカ、60612
- University of Illinois, Chicago
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コンタクト:
- Ece K Weishaar, MS
- 電話番号:312-996-1623
- メール:EceKilic@UIC.Edu
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副調査官:
- Pauline M Maki, PhD
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Pennsylvania
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Pittsburgh、Pennsylvania、アメリカ、15260
- University of Pittsburgh
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コンタクト:
- Sarah M Conklin, PhD
- 電話番号:8782616899
- メール:conklinsm2@upmc.edu
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コンタクト:
- Mollie B Bandy, BA
- 電話番号:8782616899
- メール:BANDYMB@upmc.edu
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主任研究者:
- Rebecca C Thurston, PhD
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:トリプル
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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プラセボコンパレーター: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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実験的: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.
|
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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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Flow-Mediated Dilation
時間枠: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
時間枠: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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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Endothelial Biomarkers
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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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協力者と研究者
スポンサー
捜査官
- 主任研究者:Rebecca C Thurston, PhD、University of Pittsburgh
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
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