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Study identifier: NCT07602530 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study in Canada to Follow Outcomes of Women in Menopause Treated With Fezolinetant for Hot Flashes, When Given in Clinical Practice

Condition: Hot Flashes  ·  Sponsor: Astellas Pharma Europe Ltd.

PhaseN/A
Planned participants238
Who can joinFemale, N/A to no upper limit
Healthy volunteersNo

About this study

This study is for women in Canada who are in menopause. They have symptoms including hot flashes and night sweats (also known as vasomotor symptoms or VMS). Their own doctor has prescribed fezolinetant for hot flashes and night sweats, as part of routine health care in Canada. In this study, women will be taking tablets of fezolinetant. This study is about recording information only. The women's own doctor decides on treatment, not the study sponsor (Astellas). Women are taking fezolinetant every day for up to 52 weeks (1 year). The main aim is to learn if fezolinetant improves hot flashes and night sweats after 12 weeks. Other aims are to learn if fezolinetant improves hot flashes and night sweats throughout the study. This includes improved sleep and the women's wellbeing. Details are recorded on how satisfied the women are with fezolinetant and if they completed their treatment. This includes reasons for stopping treatment. Any safety issues are recorded. Details about other treatments taken before or with fezolinetant are also recorded.

This description comes directly from the study's public registry record.

Talk to the study team

Astellas Pharma Europe Ltd.  ·  +1-800-888-7704  ·  astellas.registration@astellas.com

Always discuss trial participation with your own doctor first.

Locations (2)

Site CA15002Montreal, CanadaRecruiting
Site CA15001Prince Albert, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT07602530