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Fezolinetant and Vascular Health and Brain Health (FAVES-B)

18 maggio 2026 aggiornato da: Rebecca Thurston

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.

Panoramica dello studio

Stato

Non ancora reclutamento

Descrizione dettagliata

Double-blind, placebo-controlled randomized trial to determine whether 12 weeks of 45 mg of fezolinetant, a non-hormonal treatment for hot flashes associated with menopause, improves vascular and brain health in participants with moderate to severe menopausal hot flashes. Participants will be randomized to either 12 weeks of fezolinetant 45 mg or placebo. Primary endpoints include change from baseline in endothelial function and verbal memory.

Tipo di studio

Interventistico

Iscrizione (Stimato)

220

Fase

  • Fase 3

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

  • Nome: Mollie B Bandy, BA
  • Numero di telefono: 412-648-9088
  • Email: BandyMB@upmc.edu

Luoghi di studio

    • Illinois
      • Chicago, Illinois, Stati Uniti, 60612
        • University of Illinois, Chicago
        • Contatto:
        • Sub-investigatore:
          • Pauline M Maki, PhD
    • Pennsylvania
      • Pittsburgh, Pennsylvania, Stati Uniti, 15260
        • University of Pittsburgh
        • Contatto:
        • Contatto:
        • Investigatore principale:
          • Rebecca C Thurston, PhD

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Triplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore placebo: 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.
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).
Sperimentale: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Flow-Mediated Dilation
Lasso di tempo: Baseline and end of treatment at 12 weeks.
Endothelial function assessed by flow-mediated dilation
Baseline and end of treatment at 12 weeks.
Verbal Memory Performance
Lasso di tempo: Baseline and end of treatment at 12 weeks.
Verbal memory neuropsychological test performance
Baseline and end of treatment at 12 weeks.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Endothelial Biomarkers
Lasso di tempo: Baseline and end of treatment at 12 weeks.
Blood-based endothelial function biomarkers
Baseline and end of treatment at 12 weeks.
Brain Activation during Verbal Encoding
Lasso di tempo: Baseline and end of treatment at 12 weeks.
Memory circuitry as measured by changes in brain activation during performance of a functional magnetic resonance imaging (fMRI) task of verbal encoding
Baseline and end of treatment at 12 weeks.
Functional Connectivity during recall
Lasso di tempo: Baseline and end of treatment at 12 weeks.
Memory circuitry as measured by changes in functional connectivity during performance of a functional magnetic resonance imaging (fMRI) task of verbal recall
Baseline and end of treatment at 12 weeks.
Subjective Vasomotor Hot Flash Diary
Lasso di tempo: Baseline and end of treatment at 12 weeks.
frequency of subjectively assessed VMS using a digital hot flash diary
Baseline and end of treatment at 12 weeks.
Objective Vasomotor Monitoring
Lasso di tempo: Baseline and end of treatment at 12 weeks.
Frequency of objectively measured VMS using 24-hour skin conductance monitoring
Baseline and end of treatment at 12 weeks.
Sleep Monitoring
Lasso di tempo: Baseline and end of treatment at 12 weeks.
Objective sleep monitoring.
Baseline and end of treatment at 12 weeks.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Rebecca C Thurston, PhD, University of Pittsburgh

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

25 settembre 2026

Completamento primario (Stimato)

30 novembre 2029

Completamento dello studio (Stimato)

30 dicembre 2029

Date di iscrizione allo studio

Primo inviato

18 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

18 maggio 2026

Primo Inserito (Effettivo)

26 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

26 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

18 maggio 2026

Ultimo verificato

1 aprile 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • STUDY25120039

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

prodotto fabbricato ed esportato dagli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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