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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 (OASIS-2)

ClinicalTrials.gov ID: NCT05099159

Public ClinicalTrials.gov record NCT05099159. 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 Sep 3, 2026, 12:34 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
NCT05099159
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bayer
Industry
Enrollment
400 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
Oct 28, 2021
Primary completion
Jun 12, 2023
Completion
Oct 9, 2023
Last update posted
Feb 11, 2026

2021 – 2023

United States locations

U.S. sites
48
U.S. states
25
U.S. cities
46
Facility City State ZIP Site status
Accel Research Sites | Cahaba Medical Care - Birmingham, AL Birmingham Alabama 35218
Women's Health Alliance of Mobile Mobile Alabama 36604
Onyx Clinical Research - Peoria Peoria Arizona 85381
Lynn Institute of the Ozarks Little Rock Arkansas 72204
National Institute of Clinical Research - Garden Grove Garden Grove California 92844
Clinical Trials Research - Lincoln Lincoln California 95648
Torrance Clinical Research Institute, Inc. | Lomita, CA Lomita California 90717
Women's Health Care Research | San Diego, CA San Diego California 92111
Advanced Women's Health Institute | Denver Office, Greenwood Village, CO Greenwood Village Colorado 80111
Physicians' Research Options, LLC | Red Rocks OBGYN Lakewood Colorado 80228
Helix Biomedics, LLC Boynton Beach Florida 33435
Clinical Research of West Florida | Clearwater, FL Clearwater Florida 33765
Sweet Hope Research Specialty, Inc. - Miami Lakes Hialeah Florida 33016
Ocean Blue Medical Research Center, Inc | Miami Springs, FL Miami Springs Florida 33166
Suncoast Clinical Research Inc. | Pasco New Port Richey Florida 34652
Sensible Healthcare, LLC Ocoee Florida 34761
Clinical Research of West Florida | Tampa, FL Tampa Florida 33606
Fellows Research Alliance, Inc | Savannah, GA Savannah Georgia 31406
Family Care Research | Boise, ID Boise Idaho 83713
Leavitt Clinical Research | Idaho Falls, ID Idaho Falls Idaho 83404
University of Chicago | Laboratory of Dr. Al-Hendy Chicago Illinois 60637
AMR - Chicago Oak Brook Illinois 60523
Clinical Trials Management | Northshore Office Covington Louisiana 70433
Tandem Clinical Research | Marrero, LA Marrero Louisiana 70072
Ob and Gyn Physicians MidAtlantic - SKYCRNG Oxon Hill Maryland 20705
Genesis Clinical Research and Consulting, LLC Fall River Massachusetts 02723
Saginaw Valley Medical Research Group, LLC | Saginaw, MI Saginaw Michigan 48604
Metro Jackson OBGYN | Jackson, MS Jackson Mississippi 39202
R. Garn Mabey Jr. M.D. Gynecology Las Vegas Nevada 89128
Capital Health | Capital Health OBGYN Lawrenceville Lawrenceville New Jersey 08648
Columbia University Medical Center New York New York 10032
Eastern Carolina Women's Center | New Bern, NC New Bern North Carolina 28562
Unified Women's Clinical Research | Raleigh, NC Raleigh North Carolina 27607
OHSU Hospital - OB-GYN - Women's Health Research Unit Portland Oregon 97239
UPMC Magee-Women's Hospital - Gynecology Pittsburgh Pennsylvania 15213
Tribe clinical Research LLC | Greenville, SC Greenville South Carolina 29607
Medical Research Center of Memphis | Memphis, TN Memphis Tennessee 38120
Research Memphis Associates, LLC | Memphis, TN Memphis Tennessee 38120
Austin Regional Clinic | ARC Kelly Lane Austin Texas 78731
DiscoveResearch, Inc. Bryan Texas 77802
South Texas Clinical Research Corpus Christi Texas 78404
Sig Gyn Services (Dr. John A. Whitfield, MD) | Fort Worth, TX Fort Worth Texas 76104-4145
Advances in Health, INC. | Houston, TX Houston Texas 77030
UTHealth Womens Research Program | Memorial City Houston Texas 77054
ClinRx Research, LLC Plano Texas 75024
The Woman's Place - Midlife Health Charlottesville Virginia 22903
Tidewater Clinical Research, Inc. Norfolk Virginia 23456
Northwest Clinical Research Center | Bellevue, WA Bellevue Washington 98007

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 65 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05099159, 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 11, 2026 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05099159 live on ClinicalTrials.gov.

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