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

18. maj 2026 opdateret af: 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.

Studieoversigt

Status

Ikke rekrutterer endnu

Detaljeret beskrivelse

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.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

220

Fase

  • Fase 3

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Studiesteder

    • Illinois
      • Chicago, Illinois, Forenede Stater, 60612
        • University of Illinois, Chicago
        • Kontakt:
        • Underforsker:
          • Pauline M Maki, PhD
    • Pennsylvania
      • Pittsburgh, Pennsylvania, Forenede Stater, 15260
        • University of Pittsburgh
        • Kontakt:
        • Kontakt:
        • Ledende efterforsker:
          • Rebecca C Thurston, PhD

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

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.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Tredobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Placebo komparator: 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).
Eksperimentel: 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.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Flow-Mediated Dilation
Tidsramme: 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
Tidsramme: Baseline and end of treatment at 12 weeks.
Verbal memory neuropsychological test performance
Baseline and end of treatment at 12 weeks.

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Endothelial Biomarkers
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: Baseline and end of treatment at 12 weeks.
Objective sleep monitoring.
Baseline and end of treatment at 12 weeks.

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Rebecca C Thurston, PhD, University of Pittsburgh

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

25. september 2026

Primær færdiggørelse (Anslået)

30. november 2029

Studieafslutning (Anslået)

30. december 2029

Datoer for studieregistrering

Først indsendt

18. maj 2026

Først indsendt, der opfyldte QC-kriterier

18. maj 2026

Først opslået (Faktiske)

26. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

26. maj 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

18. maj 2026

Sidst verificeret

1. april 2026

Mere information

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