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)
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.
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
- 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.