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A Study to Learn More About How the Study Treatment Elinzanetant (or BAY3427080) Moves Into, Through and Out of the Body, How Safe it is and How it Affects the Body After Taking Single and Multiple Doses in Healthy Women Aged 40 to 65 Years

Primary Purpose

Vasomotor Symptoms as a Sex Hormone-dependent Disorder in Women and Men, Hot Flashes, Healthy Volunteers

Status
Completed
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
Elinzanetant (BAY3427080)
Placebo
Sponsored by
Bayer
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Vasomotor Symptoms as a Sex Hormone-dependent Disorder in Women and Men

Eligibility Criteria

40 Years - 65 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Participant must be 40 to 65 years of age inclusive, at the time of signing the informed consent.
  • Participants who are overtly healthy as determined by medical evaluation including medical history, physical examination, vital signs, laboratory tests and electrocardiogram (ECG).
  • Race: Chinese in China mainland.
  • Body weight of at least 40 kg and body mass index (BMI) within the range 18.0 and 30.0 kg/m^2 (inclusive) at screening.
  • Female:

    • Women of childbearing potential will have to use highly effective non-hormonal contraception when having sexual intercourse with a male partner from signing the informed consent form until 5 days after last dose of the study intervention.
    • Women of non-childbearing potential are not required to use contraception.
  • Capable of giving signed informed consent.

Exclusion Criteria:

  • Any clinically relevant abnormal findings in medical history and physical examination at screening or Day -1 which in the opinion of the investigators, may put the participant at risk because of her participation in the trial or provide difficulties in interpreting the trial data.
  • History or evidence of any clinically relevant cardiovascular, gastrointestinal, endocrine, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, neurologic, dermatologic, psychiatric, renal and/or other clinically relevant disease, as judged by the investigator.
  • Known hypersensitivity to the study interventions (active substances, or excipients of the preparations).
  • Use of any systemic or topical medicine or substance which oppose the study objectives, or which might influence them within 4 weeks before first administration of study intervention. This includes but is not limited to CYP P450 inducers/inhibitors, OATP substrates or P-gp substrates with narrow therapeutic range (e.g. digoxin, dabigatran etc).
  • Regular use of therapeutic drugs or supplements, e.g., carnitine products, anabolics, high dose vitamins.
  • Use of herbal drugs or natural remedies, e.g. St. John's wort within 4 weeks before first study intervention administration.

Sites / Locations

  • The First Affiliated Hospital of Guangzhou University of TCM

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Elinzanetant (BAY3427080)

Placebo

Arm Description

Healthy female participants who meet all of the inclusion criteria and do not meet any of the exclusion criteria will be randomized to treatment with elinzanetant.

Healthy female participants who meet all of the inclusion criteria and do not meet any of the exclusion criteria will be randomized and assigned to treatment with placebo.

Outcomes

Primary Outcome Measures

Cmax: maximum observed drug concentration in measured matrix after single dose administration
AUC: area under the concentration vs. time curve from zero to infinity after single dose
AUC(0-tlast) will be used as the main parameter if AUC cannot be reliably determined
Cmax,md: maximum observed drug concentration in measured matrix after multiple dose administration
AUC(0-24)md: AUC from time 0 to 24 hours for multiple dosing

Secondary Outcome Measures

Number of participants with and severity of treatment-emergent adverse events (TEAEs)

Full Information

First Posted
April 29, 2022
Last Updated
July 25, 2022
Sponsor
Bayer
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1. Study Identification

Unique Protocol Identification Number
NCT05381142
Brief Title
A Study to Learn More About How the Study Treatment Elinzanetant (or BAY3427080) Moves Into, Through and Out of the Body, How Safe it is and How it Affects the Body After Taking Single and Multiple Doses in Healthy Women Aged 40 to 65 Years
Official Title
A Randomized, Single-blind, Placebo-controlled Study to Investigate the Pharmacokinetics, Safety and Tolerability of Single and Multiple Doses of Elinzanetant in Chinese Healthy Female Participants 40 to 65 Years of Age
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
May 23, 2022 (Actual)
Primary Completion Date
July 11, 2022 (Actual)
Study Completion Date
July 11, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Bayer

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Researchers are looking for a better way to treat men and women with vasomotor symptoms, a condition of having hot flashes caused by hormonal changes. In women, these hormonal changes happen in the time around their menopause, the last period (menstrual cycle) a woman has. After the menopause, the ovaries produce less and less sex hormones as a result of the natural ageing process and related hormonal adaptations. The decrease in hormones produced can lead to various symptoms that may be troublesome. Vasomotor symptoms are also seen in men. The study treatment, elinzanetant, is under development to treat symptoms caused by hormonal changes. It works by blocking a substance called neurokinin, which is thought to play a role in starting hot flashes. Previous studies have been done. This study will provide information on how to use elinzanetant in Chinese people. The main purpose of this study is to learn how much of the study treatment elinzanetant gets into the participants' blood when a single dose is taken in healthy Chinese women. To answer this question, the researchers will measure: The (average) total level of elinzanetant in the blood (also called AUC) The (average) highest level of elinzanetant in the blood (also called Cmax) The researchers also want to learn how much elinzanetant gets into the blood when taken for 6 days in a row. Dependent on the treatment group, the participants will either take elinzanetant or placebo. First, a single dose of two capsules is taken by mouth and later multiple doses once a day for another 6 days in a row are taken. Each participant will be in the study for approximately 22 days including 7 treatment days in total. Participants will stay in-house for 16 days. In addition, one visit to the study site prior start and four visits after the in-house period are planned. During the study, the study team will: Do physical examinations Take blood and urine samples Check vital signs Examine the participants' heart health using electrocardiogram (ECG) Ask the participants questions about how they are feeling and what adverse events they are having. 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 they do not think the adverse events might be related to the study treatments.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vasomotor Symptoms as a Sex Hormone-dependent Disorder in Women and Men, Hot Flashes, Healthy Volunteers

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
Participant
Masking Description
The study will be performed with a participant-blinded design.
Allocation
Randomized
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Elinzanetant (BAY3427080)
Arm Type
Experimental
Arm Description
Healthy female participants who meet all of the inclusion criteria and do not meet any of the exclusion criteria will be randomized to treatment with elinzanetant.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Healthy female participants who meet all of the inclusion criteria and do not meet any of the exclusion criteria will be randomized and assigned to treatment with placebo.
Intervention Type
Drug
Intervention Name(s)
Elinzanetant (BAY3427080)
Other Intervention Name(s)
NT-814
Intervention Description
Elinzanetant will be administered as a single dose on Study Day 1 and a multiple dose once daily for another 6 consecutive days on Study Day 8 to Study Day 13.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Matching placebo will be administered the same as Elinzanetant (BAY3427080)
Primary Outcome Measure Information:
Title
Cmax: maximum observed drug concentration in measured matrix after single dose administration
Time Frame
From pre-dose up to 168 hours after first dosing
Title
AUC: area under the concentration vs. time curve from zero to infinity after single dose
Description
AUC(0-tlast) will be used as the main parameter if AUC cannot be reliably determined
Time Frame
From pre-dose up to 168 hours after first dosing
Title
Cmax,md: maximum observed drug concentration in measured matrix after multiple dose administration
Time Frame
From pre-dose up to 180 hours after last dosing
Title
AUC(0-24)md: AUC from time 0 to 24 hours for multiple dosing
Time Frame
From pre-dose up to 180 hours after last dosing
Secondary Outcome Measure Information:
Title
Number of participants with and severity of treatment-emergent adverse events (TEAEs)
Time Frame
From first dose of study intervention until follow-up visit on day 21

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Participant must be 40 to 65 years of age inclusive, at the time of signing the informed consent. Participants who are overtly healthy as determined by medical evaluation including medical history, physical examination, vital signs, laboratory tests and electrocardiogram (ECG). Race: Chinese in China mainland. Body weight of at least 40 kg and body mass index (BMI) within the range 18.0 and 30.0 kg/m^2 (inclusive) at screening. Female: Women of childbearing potential will have to use highly effective non-hormonal contraception when having sexual intercourse with a male partner from signing the informed consent form until 5 days after last dose of the study intervention. Women of non-childbearing potential are not required to use contraception. Capable of giving signed informed consent. Exclusion Criteria: Any clinically relevant abnormal findings in medical history and physical examination at screening or Day -1 which in the opinion of the investigators, may put the participant at risk because of her participation in the trial or provide difficulties in interpreting the trial data. History or evidence of any clinically relevant cardiovascular, gastrointestinal, endocrine, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, neurologic, dermatologic, psychiatric, renal and/or other clinically relevant disease, as judged by the investigator. Known hypersensitivity to the study interventions (active substances, or excipients of the preparations). Use of any systemic or topical medicine or substance which oppose the study objectives, or which might influence them within 4 weeks before first administration of study intervention. This includes but is not limited to CYP P450 inducers/inhibitors, OATP substrates or P-gp substrates with narrow therapeutic range (e.g. digoxin, dabigatran etc). Regular use of therapeutic drugs or supplements, e.g., carnitine products, anabolics, high dose vitamins. Use of herbal drugs or natural remedies, e.g. St. John's wort within 4 weeks before first study intervention administration.
Facility Information:
Facility Name
The First Affiliated Hospital of Guangzhou University of TCM
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510405
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Availability of this study's data will later be determined according to Bayer's commitment to the EFPIA/PhRMA "Principles for responsible clinical trial data sharing". This pertains to scope, timepoint and process of data access. As such, Bayer commits to sharing upon request from qualified researchers patient-level clinical trial data, study-level clinical trial data, and protocols from clinical trials in patients for medicines and indications approved in the US and EU as necessary for conducting legitimate research. This applies to data on new medicines and indications that have been approved by the EU and US regulatory agencies on or after January 01, 2014. Interested researchers can use www.clinicalstudydatarequest.com to request access to anonymized patient-level data and supporting documents from clinical studies to conduct research. Information on the Bayer criteria for listing studies and other relevant information is provided in the Study sponsors section of the portal.
Links:
URL
https://clinicaltrials.bayer.com/
Description
Click here to find information for studies related to Bayer products. To find this study enter the NCT number or Bayer Study ID in the search field.

Learn more about this trial

A Study to Learn More About How the Study Treatment Elinzanetant (or BAY3427080) Moves Into, Through and Out of the Body, How Safe it is and How it Affects the Body After Taking Single and Multiple Doses in Healthy Women Aged 40 to 65 Years

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