A Study of BAY3427080 (NT-814) in the Treatment of Moderate to Severe Post-menopausal Vasomotor Symptoms

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A DOUBLE-BLIND, RANDOMISED, PLACEBO CONTROLLED, ADAPTIVE DESIGN STUDY OF THE EFFICACY, SAFETY AND PHARMACOKINETICS OF NT-814 IN FEMALE SUBJECTS WITH MODERATE TO SEVERE VASOMOTOR SYMPTOMS ASSOCIATED WITH THE MENOPAUSE

Intervention/treatment:
NT-814
Medical condition:
POST-MENOPAUSAL VASOMOTOR SYMPTOMS
Protocol code:
814-PM-02
Control number:
221424
Status:
Closed
Approved:
November 21, 2018
Date Completed:
Trial phase:
Phase 2
For more information:
ClinicalTrials.gov - NCT03596762
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:
1-888-8422937
Sponsor
NERRE THERAPEUTICS LTD

Locations

Alberta

Study Site 50
Red Deer, Alberta

British Columbia

Study Site 51
Mission, British Columbia

Ontario

Study Site 52
Scarborough Village, Ontario
Study Site 53
Toronto, Ontario
Study Site 54
Guelph, Ontario

Results

See the results from the trial NCT03596762. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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