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)

Last updated:
2026-07-18
Language and content disclaimer

The content and search results on this site are collected from or provided by third parties. As such some of the information may only be available in the language originally submitted by the sponsor of the trial. Learn more about the information on the search portal.

Linking to Non-Government of Canada Websites

Links to websites not under the control of the Government of Canada, including those to our social media accounts, and to clinical trial records in international registries are provided solely for the convenience of our website visitors. We are not responsible for the accuracy, currency or reliability of the content of such websites. The Government of Canada does not offer any guarantee in that regard and is not responsible for the information found through these links, nor does it endorse the sites and their content.

Visitors should also be aware that information offered by non-Government of Canada sites to which this website links is not subject to the Privacy Act or the Official Languages Act and may not be accessible to persons with disabilities. The information offered may be available only in the language(s) used by the sites in question. With respect to privacy, visitors should research the privacy policies of these non-government websites before providing personal information.

View trial details

Overview

Official protocol 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

Intervention/treatment:
ELINZANETANT (BAY 3427080)
Medical condition:
POST-MENOPAUSAL VASOMOTOR SYMPTOMS
Protocol code:
21652
Control number:
257036
Status:
Closed
Approved:
November 26, 2021
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT05099159
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: FEMALE
Age
40 Years to 65 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Therapeutic Area Head
Organization
Bayer AG
Phone:
(+)1-888-84 22937
Sponsor
BAYER INC

Locations

Alpha Recherche Clinique | Lebourgneuf
Québec, G2J 0C4

Alberta

Alta Clinical Research Inc | Edmonton, Canada
Edmonton, Alberta, T5A 4L8
Diex Recherche Quebec Inc.
Québec, Alberta, G1V 4T3

Nova Scotia

IWK Health Centre | Department of Obstetrics and Gynaecology
Halifax, Nova Scotia, B3K 6R8

Quebec

Alpha Recherche Clinique | Val-Belair
Val-Bélair, Quebec, G3K 2P8
Clinique Ovo | R&D Department
Montreal, Quebec, H4P 2S4
Diex Recherche Sherbrooke Inc.
Sherbrooke, Quebec, J1L 0H8
Diex Recherche Victoriaville Inc.
Victoriaville, Quebec, G6P 6P6
Ecogene 21
Chicoutimi, Quebec, G7H 0S7
GCP Research | Montreal, Canada
Montreal, Quebec, H1M 1B1

Results

See the results from the trial NCT05099159. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
Did you find what you were looking for?