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Completed Phase 3 Interventional Results available

A Study to Learn More About How Well Elinzanetant Works and How Safe it is for the Treatment of Vasomotor Symptoms (Hot Flashes) That Are Caused by Hormonal Changes Over 52 Weeks in Women Who Have Been Through the Menopause

ClinicalTrials.gov ID: NCT05030584

Public ClinicalTrials.gov record NCT05030584. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 30, 2026, 2:05 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-blind, Randomized, Placebo-controlled Multicenter Study to Investigate Efficacy and Safety of Elinzanetant for the Treatment of Vasomotor Symptoms Over 52 Weeks in Postmenopausal Women

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Researchers are looking for a better way to treat women who have hot flashes after they have been through the menopause. Hot flashes are caused by the hormonal changes that happen when a woman's body has been through the menopause. Menopause is when women stop having a menstrual cycle, also called a period. During the menopause, the ovaries increasingly produce less sex hormones as a result of the natural ageing process and related hormonal adjustments. The decline in hormone production can lead to various symptoms which, in some cases, can have a very adverse effect on a menopausal woman's quality of life. The study treatment, elinzanetant, was developed to treat symptoms caused by hormonal changes. It works by blocking a protein called neurokinin from sending signals to other parts of the body, which is thought to play a role in starting hot flashes. There are treatments for hot flashes in women who have been through the menopause, but may cause medical problems for some people. In this study, the researchers will learn how well elinzanetant works compared to a placebo in women who have been through the menopause and have hot flashes. A placebo is a treatment that looks like a medicine but does not have any medicine in it. To compare these study treatments, the participants will record information about their hot flashes in an electronic diary. The researchers will study the number of hot flashes the participants have and how severe they are. They will study the results from before treatment and after 12 weeks of treatment. The participants in this study will take two capsules of either elinzanetant or the placebo once a day. The participants will take the study treatments for 52 weeks. During the study, the participants will visit their study site approximately 11 times and perform 2 visits by phone. Each participant will be in the study for approximately 62 weeks. During the study, the participants will: * record information about their hot flashes in an electronic diary * answer questions about their symptoms The doctors will: * check the participants' health * take blood samples * ask the participants questions about what medicines they are taking and if they are having adverse events An adverse event is any medical problem that a participant has during a study. Doctors keep track of all adverse events that happen in studies, even if they do not think the adverse events might be related to the study treatments.

Study identification

NCT ID
NCT05030584
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bayer
Industry
Enrollment
628 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years to 65 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 27, 2021 (Actual)
Primary completion
Mar 29, 2023 (Actual)
Completion
Feb 12, 2024 (Actual)
Last update posted
Dec 1, 2025

2021 – 2024

United States locations

U.S. sites
36
U.S. states
19
U.S. cities
33
Facility City State ZIP Site status
Mobile ObGyn, P.C. | Mobile, AL Mobile Alabama 36608 —
Mesa Obstetricians and Gynecologists | Research Department Mesa Arizona 85206 —
National Institute of Clinical Research - Garden Grove Garden Grove California 92844 —
Marvel Clinical Research | Huntington Beach, CA Huntington Beach California 92647 —
Empire Clinical Research | Pomona, CA Pomona California 91767 —
Coastal Connecticut Research | New London, CT New London Connecticut 06320 —
IntimMedicine | Washington, DC Washington D.C. District of Columbia 20036 —
Boca Midwifery Boca Raton Florida 33486 —
Helix Biomedics LLC | Boynton Beach, FL Boynton Beach Florida 33435 —
UF Health Women's Specialists - Emerson Jacksonville Florida 32207 —
Suncoast Clinical Research - Palm Harbor Palm Harbor Florida 34684 —
Physician Care Clinical Research LLC | Sarasota, FL Sarasota Florida 34239 —
Suncoast Clinical Research - New Port Richey Trinity Florida 34655 —
Paramount Research Solutions | College Park Location College Park Georgia 30349 —
Investigators Research Group, LLC Brownsburg Indiana 46112 —
Southern Clinical Research Associates Metairie Louisiana 70001 —
Southern Clinical Research, LLC Zachary Louisiana 70791 —
Johns Hopkins Hospital - Gynecology and Obstetrics Baltimore Maryland 21287 —
Boeson Research | Great Falls, MT Great Falls Montana 59405 —
Boeson Research | Missoula, MT Missoula Montana 59804 —
Affiliated Clinical Research, Inc. | Las Vegas, NV Las Vegas Nevada 89113 —
AMR - Las Vegas Las Vegas Nevada 89119 —
Elite Clinical Network (ECN) | Las Vegas Clinical Trials, LLC North Las Vegas Nevada 89030 —
M3 Wake Research | Raleigh, NC Raleigh North Carolina 27612 —
ClinOhio Research Services, LLC. | Columbus, OH Columbus Ohio 43213 —
HWC Women's Research Center | Englewood, OH Englewood Ohio 45322 —
Clinical Research Philadelphia | Philadelphia, PA Philadelphia Pennsylvania 19114 —
Venus Gynecology, LLC | Myrtle Beach, SC Myrtle Beach South Carolina 29572 —
Advances in Health, INC. | Houston, TX Houston Texas 77030 —
UTHealth Womens Research Program | Memorial City Houston Texas 77054 —
Elligo Health Research | Medical Colleagues of Texas Hurst Texas 76054 —
Elligo Health Research | Protenium Clinical Research Katy Texas 77493 —
Maximos Ob/Gyn League City Texas 77573 —
Tidewater Clinical Research - Norfolk Norfolk Virginia 23502 —
Eastern Virginia Medical School | OB/GYN Clinical Research Center Norfolk Virginia 23507 —
Seattle Clinical Research Center Seattle Washington 98105 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 50 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05030584, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 1, 2025 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05030584 live on ClinicalTrials.gov.

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