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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 company relationship

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 · 0 study sponsors

Related indications

Study sponsors

No additional listed-company sponsor is linked.

Clinical Trial Registry Records (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

NCT06812754Registry updated 2026-03-19·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

NCT06440967Registry updated 2026-02-19·Phase 3
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

NCT06206421Registry updated 2026-02-18·Phase 3
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

NCT06049797Registry updated 2026-06-05
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.