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fezolinetant

Generic: FEZOLINETANT·Brand: VEOZAH, Veozah

fezolinetant: 4 clinical trials tracked.

fezolinetant evidence translation

What we can confirm

4 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about fezolinetant, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 1 study sponsors
Clinical Trials (4)

A Phase 2, Randomized, Placebo-controlled, 12-week, Double-blind Study to Assess the Efficacy and Safety of Fezolinetant 45 mg in Chinese Women Suffering From Moderate to Severe Vasomotor Symptoms (Hot Flashes) Associated With Menopause

NCT06812754·Phase 2
Completed

Primary endpoint: Mean change in the frequency of moderate to severe Vasomotor Symptoms (VMS) from baseline to week 12

InterventionalRandomizedtriple150 enrolledStarted 2025-03Completion 2026-0326 sites · ChinaAstellas Pharma Global Development, Inc.

A Randomized, Placebo-controlled, Double-blind, Phase 3 Clinical Study to Investigate the Efficacy and Safety of Fezolinetant for Treatment of Moderate to Severe Vasomotor Symptoms (Hot Flashes) in Women With Stage 0 to 3 Hormone Receptor-positive Breast Cancer Who Are Receiving Adjuvant Endocrine Therapy

NCT06440967·Phase 3·CRNX
Recruiting

Primary endpoint: Mean change from Baseline to Week 4 in the frequency of moderate to severe VMS

InterventionalRandomizeddouble540 targetStarted 2024-07Completion 2027-0650 sites · Canada, Czechia, Denmark, France…Astellas Pharma Global Development, Inc.

A Phase 3, Randomized, Placebo-controlled, Double-blind Study to Investigate the Long Term Safety of Fezolinetant in Japanese Women Suffering From Vasomotor Symptoms (Hot Flashes) Associated With Menopause

NCT06206421·Phase 3·CRNX
Active, not recruiting

Primary endpoint: Number of participants with Adverse Events (AEs)

InterventionalRandomizedtriple277 targetStarted 2024-02Completion 2026-0324 sites · JapanAstellas Pharma Inc

A Phase IV, Longitudinal, Observational Study Examining Real-World Outcomes of Non-Hormonal Pharmacotherapies Among Individuals Treated for Bothersome Vasomotor Symptoms

Completed

Primary endpoint: Mean change from baseline to week 12 in symptom bother measured by the Menopause-Specific Quality of Life Domain (MENQoL) 1-week recall VMS domain score

Observational999 enrolledStarted 2023-11Completion 2026-0548 sites · United StatesAstellas Pharma Global Development, Inc.