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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 26 Weeks in Women Who Have Been Through the Menopause

ClinicalTrials.gov ID: NCT05042362

Public ClinicalTrials.gov record NCT05042362. 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 20, 2026, 8:01 AM 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 26 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 women 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 looks like a treatment but does not have any medicine in it. To compare these study treatments, the doctors will ask the participants to record information about the participants' hot flashes in an electronic diary. The researchers will study the number of hot flashes the participants have and how severe the hot flashes are. The researchers will look at the results from before treatment, after 4 weeks, 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 who take elinzanetant will take it for 26 weeks. The participants who take the placebo will take it for 12 weeks and then take elinzanetant for the next 14 weeks. During the study, the participants will visit the site approximately 9 times and perform 1 visit by phone. Each participant will be in the study for approximately 36 weeks. The treatment duration will be 26 weeks. During the study, the participants will: * record information about the participants' hot flashes in an electronic diary * answer questions about the participants' symptoms The doctors will: * check the participants' health * take blood samples * ask the participants questions about what medicines the participants are taking and if the participants 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 doctors do not think the adverse events might be related to the study treatments.

Study identification

NCT ID
NCT05042362
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bayer
Industry
Enrollment
396 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
Jul 25, 2023 (Actual)
Completion
Nov 27, 2023 (Actual)
Last update posted
Feb 12, 2026

2021 – 2023

United States locations

U.S. sites
55
U.S. states
25
U.S. cities
50
Facility City State ZIP Site status
Alabama Clinical Therapeutics | Birmingham, AL Birmingham Alabama 35205 —
Central Research Associates | Birmingham, AL Birmingham Alabama 35205 —
Mesa Obstetricians and Gynecologists | Research Department Mesa Arizona 85206 —
MomDoc Women's Health Research | Scottsdale, AZ Scottsdale Arizona 85251 —
Noble Clinical Research | Tucson, AZ Tucson Arizona 85704 —
Del Sol Research | Women Health studies Tucson Arizona 85715 —
Applied Research Center of Arkansas Little Rock Arkansas 72205 —
Alliance Research Institute | Bell Gardens, CA Bell Gardens California 90201 —
Diagnamics | Encinitas, CA Encinitas California 92024 —
Om Research LLC | Lancaster, CA Lancaster California 93534 —
Northern California Research | Sacramento Sacramento California 95821 —
IntimMedicine | Washington, DC Washington D.C. District of Columbia 20036 —
AMR - Fort Myers, FL Fort Myers Florida 33912 —
Suncoast Clinical Research Inc | Pinellas Palm Harbor Florida 34684 —
Physician Care Clinical Research LLC | Sarasota, FL Sarasota Florida 34239 —
Medisense Inc. | Atlanta, GA Atlanta Georgia 30363 —
Paramount Research Solutions | College Park Location College Park Georgia 30349 —
Soapstone Center for Clinical Research, Inc. | Decatur, GA Decatur Georgia 30033-3500 —
Drug Studies America Marietta Georgia 30060 —
M3 Wake Research Atlanta Sandy Springs Georgia 30126 —
Clinical Research Prime Idaho Falls Idaho 83404 —
Investigators Research Group, LLC Brownsburg Indiana 46112 —
The Iowa Clinic - Ankeny Ankeny Iowa 50023 —
Southern Clinical Research Associates | Metairie, LA Metairie Louisiana 70001 —
Continental Clinical Solutions | Towson, MD Towson Maryland 21204 —
Revive Research Institute, Inc. - Women's Health Dearborn Heights Michigan 48127 —
Valley OBGYN Saginaw Michigan 48602 —
Women's Clinic of Lincoln, P.C. | Lincoln, NE Lincoln Nebraska 68510 —
Jubilee Clinical Research Inc | Las Vegas, NV Las Vegas Nevada 89106 —
Affiliated Clinical Research, Inc. | Las Vegas, NV Las Vegas Nevada 89113 —
M3 Wake Research - Clinical Research Center of Nevada Las Vegas Nevada 89123 —
The Center for Womens Health & Wellness, LLC | Lawrenceville, NJ Lawrenceville New Jersey 08648 —
Rutgers Robert Wood Johnson Medical School New Brunswick New Jersey 08901 —
Velocity Clinical Research - Albuquerque Albuquerque New Mexico 87107 —
Bosque Women's Care | Albuquerque, NM Albuquerque New Mexico 87109 —
Circuit Clinical | OB GYN Associates of WNY West Seneca New York 14224 —
OnSite Clinical Solutions - Charlotte Charlotte North Carolina 28277 —
M3 Wake Research | Raleigh, NC Raleigh North Carolina 27612 —
Unified Women's Clinical Research | Lyndhurst Clinical Research, Winston-Salem, NC Winston-Salem North Carolina 27103 —
Axia Women's Health - Anderson Township Cincinnati Ohio 45242 —
Centricity Research - Women's Health - Dublin, OH Dublin Ohio 43016 —
HWC Women's Research Center | Englewood, OH Englewood Ohio 45322 —
Hilltop Obstetrics & Gynecolofy Franklin Ohio 45005 —
Women's Care Research Institute/Marion OBGYN, Inc. Marion Ohio 43302 —
University Hospitals | UH Cleveland Medical Center - MacDonald Clinical Trials Unit Mayfield Heights Ohio 44124 —
Clinical Research Philadelphia | Philadelphia, PA Philadelphia Pennsylvania 19114 —
MUSC Women's Health - Cannon St. Charleston South Carolina 29425 —
Venus Gynecology, LLC | Myrtle Beach, SC Myrtle Beach South Carolina 29572 —
Coastal Carolina Research Center North Charleston South Carolina 29405 —
Chattanooga Medical Research, LLC. | Chattanooga, TN Chattanooga Tennessee 37404 —
Elligo Health Research | Women Partners in Health PLLC Austin Texas 78705 —
Cedar Health Research, LLC. | DFW-East Clinical Site Dallas Texas 75251 —
Maximos Ob/Gyn League City Texas 77573 —
Northeast Clinical Research of San Antonio, LLC San Antonio Texas 78233 —
Seattle Women's | Seattle, WA 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 44 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05042362, 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 Feb 12, 2026 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05042362 live on ClinicalTrials.gov.

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