A Study to Confirm if Fezolinetant Helps Reduce Hot Flashes in Women With Breast Cancer Who Are Having Hormone Therapy (NCT06440967)
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
🩺 Plain-English Summary (8th-Grade Level)
One of the standard treatments for women with breast cancer is hormone therapy, but this treatment can cause hot flashes. Hormone replacement therapy, or HRT, is most often prescribed for hot flashes for women in menopause but cannot be given to women on hormone therapy for breast cancer. Fezolinetant, an alternative to HRT, treats hot flashes for women in menopause. As hot flashes happen in the same way for women on hormone therapy for breast cancer, fezolinetant could help these women. In this study, women on hormone therapy for breast cancer who have moderate to severe hot flashes will take part. They will either take fezolinetant or a placebo to treat their hot flashes. The placebo looks like fezolinetant but doesn't have any medicine in it. The main aim of this study is to confirm if women who take fezolinetant have fewer hot flashes that are less severe compared to women who take the placebo. Women 18 years or older seeking treatment for hot flashes. They can take part in the study if they have an average of 7 or more moderate to severe hot flashes each day. They are having hormone therapy for breast cancer from stage 0 (cancer cells that have not spread to nearby tissue) up to stage 3+ (the cancer has spread from the breast to the lymph nodes near the breast or the chest wall). The women will be assigned 1 of 2 study treatments (fezolinetant or placebo) by chance alone. Treatment will be double-blinded. That means that the women in the study and the study doctors will not know who takes which of the study treatments (fezolinetant or placebo). Women who take part in the study will take 1 tablet every day for 52 weeks (1 year). Each woman will be given an electronic handheld device with an app to track their hot flashes on a daily basis. Some women may be able to use the app on their own smartphone. They will also use another device to answer questions about how hot flashes affect their daily life. During the study, the women will visit their study clinic about every 4 weeks for a health check. The last clinic visit will be 3 weeks after the women take their last tablet of study treatment (fezolinetant or placebo). After this visit the women will be called twice to check their health. The women will be in the study for about 2 years.
Who can join: Review the eligibility criteria below.
Location: Site CA15019 — Sarnia, Ontario
Age range: 18 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (110 Sites)
Showing the first 25 of 110 sites.
- Site CA15019 — Sarnia, Ontario
- Site CA15016 — Sault Ste. Marie, Ontario
- Site CA15002 — Montreal, Quebec
- Site CA15001 — Québec, Quebec
- Site CA15004 — Québec, Quebec
- Site CA15003 — Sherbrooke, Quebec
- Site CA15020 — Victoriaville, Quebec
- Site CA15007 — Trois-Rivières,
- Site CZ42006 — České Budějovice,
- Site CZ42003 — Hořovice,
- Site CZ42002 — Hradec Králové,
- Site CZ42011 — Nový Jičín,
- Site CZ42001 — Olomouc,
- Site CZ42005 — Prague,
- Site CZ42008 — Prague,
- Site CZ42013 — Prague,
- Site CZ42004 — Tábor,
- Site CZ42007 — Vodňany,
- Site CZ42009 — Vsetín,
- Site DK45007 — Aalborg,
- Site DE45003 — Esbjerg,
- Site DK45009 — Hillerød,
- Site DK45002 — Næstved,
- Site DE45008 — Sønderborg,
- Site FR33003 — Angers,
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Hot Flashes
- Solifenacin Compared to Clonidine for Reducing Hot Flashes Among Breast Cancer Patients — Little Rock, Arkansas
- The Cardiovascular Impact of Hot Flushes — Minneapolis, Minnesota
- Hot Flashes and Neurovascular Function in Women — Rochester, Minnesota
- A Study in Canada to Follow Outcomes of Women in Menopause Treated With Fezolinetant for Hot Flashes, When Given in Clinical Practice — Montreal,
- Men With Prostate Cancer: Optimizing Wellness by Enhanced Relief From Hot Flashes With Acupuncture — Fairfax, Virginia
Explore by condition: All Hot Flashes clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.