- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07606664
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.
연구 개요
상세 설명
연구 유형
등록 (추정된)
단계
- 3단계
연락처 및 위치
연구 연락처
- 이름: Sarah M Conklin, PhD
- 전화번호: 878-261-6899
- 이메일: conklinsm2@upmc.edu
연구 연락처 백업
- 이름: Mollie B Bandy, BA
- 전화번호: 412-648-9088
- 이메일: BandyMB@upmc.edu
연구 장소
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Illinois
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Chicago, Illinois, 미국, 60612
- University of Illinois, Chicago
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연락하다:
- Ece K Weishaar, MS
- 전화번호: 312-996-1623
- 이메일: EceKilic@UIC.Edu
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부수사관:
- Pauline M Maki, PhD
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Pennsylvania
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Pittsburgh, Pennsylvania, 미국, 15260
- University of Pittsburgh
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연락하다:
- Sarah M Conklin, PhD
- 전화번호: 8782616899
- 이메일: conklinsm2@upmc.edu
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연락하다:
- Mollie B Bandy, BA
- 전화번호: 8782616899
- 이메일: BANDYMB@upmc.edu
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수석 연구원:
- Rebecca C Thurston, PhD
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참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
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.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 삼루타
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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위약 비교기: 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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실험적: 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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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Flow-Mediated Dilation
기간: 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
기간: 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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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Endothelial Biomarkers
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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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공동 작업자 및 조사자
스폰서
수사관
- 수석 연구원: Rebecca C Thurston, PhD, University of Pittsburgh
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- STUDY25120039
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
미국에서 제조되어 미국에서 수출되는 제품
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