Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

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

17 de agosto de 2026 atualizado por: 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.

Visão geral do estudo

Status

Ainda não está recrutando

Descrição detalhada

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 de estudo

Intervencional

Inscrição (Estimado)

220

Estágio

  • Fase 3

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

  • Nome: Mollie B Bandy, BA
  • Número de telefone: 412-648-9088
  • E-mail: BandyMB@upmc.edu

Locais de estudo

    • Illinois
      • Chicago, Illinois, Estados Unidos, 60612
        • University of Illinois, Chicago
        • Contato:
        • Subinvestigador:
          • Pauline M Maki, PhD
    • Pennsylvania
      • Pittsburgh, Pennsylvania, Estados Unidos, 15260
        • University of Pittsburgh
        • Contato:
        • Contato:
        • Investigador principal:
          • Rebecca C Thurston, PhD

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

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.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Triplo

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador de 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).
Experimental: 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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Flow-Mediated Dilation
Prazo: 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
Prazo: Baseline and end of treatment at 12 weeks.
Verbal memory performance on the California Verbal Learning Test
Baseline and end of treatment at 12 weeks.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Endothelial Biomarkers
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: Baseline and end of treatment at 12 weeks.
Objective sleep monitoring.
Baseline and end of treatment at 12 weeks.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Investigadores

  • Investigador principal: Rebecca C Thurston, PhD, University of Pittsburgh

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

25 de setembro de 2026

Conclusão Primária (Estimado)

30 de novembro de 2029

Conclusão do estudo (Estimado)

30 de dezembro de 2029

Datas de inscrição no estudo

Enviado pela primeira vez

18 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

18 de maio de 2026

Primeira postagem (Real)

26 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

19 de agosto de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

17 de agosto de 2026

Última verificação

1 de agosto de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • STUDY25120039

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Sim

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

produto fabricado e exportado dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Se inscrever