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Neurokinin Antagonist
Elinzanetant for Hot Flashes (OASIS-1 Trial)
Phase 3
Waitlist Available
Research Sponsored by Bayer
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline to week 26
Awards & highlights
Pivotal Trial
Summary
This trial is testing a new medication called elinzanetant to help women who have hot flashes after menopause. The medication works by blocking signals that cause hot flashes. Researchers will track the number and severity of hot flashes over time.
Eligible Conditions
- Hot flashes
- Hot Flush
- Hot Flashes
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline to week 26
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to week 26
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Secondary study objectives
Mean change in BDI-II total score from baseline to Week 26
Mean change in Beck depression inventory (BDI-II) total score from baseline to Week 12
Mean change in menopause specific quality of life scale (MENQOL) total score from baseline to Week 12
+1 moreSide effects data
From 2019 Phase 2 trial • 199 Patients • NCT0359676212%
Diarrhoea
12%
Nausea
12%
Herpes zoster
12%
Headache
6%
Bradycardia
6%
Fatigue
6%
Nephrolithiasis
6%
Abdominal pain upper
6%
Aspartate aminotransferase increased
6%
Rash
6%
Haematuria
6%
Flatulence
6%
Non-cardiac chest pain
6%
Viral upper respiratory tract infection
6%
Viral sinusitis
6%
Blood creatine phosphokinase increased
6%
Electrocardiogram QT prolonged
6%
Liver function test increased
6%
Joint swelling
6%
Somnolence
6%
Depressed mood
6%
Insomnia
6%
Breast tenderness
6%
Cough
100%
80%
60%
40%
20%
0%
Study treatment Arm
80 mg Elinzanetant (BAY3427080)
120 mg Elinzanetant (BAY3427080)
Placebo
40 mg Elinzanetant (BAY3427080)
160 mg Elinzanetant (BAY3427080)
Awards & Highlights
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Elinzanetant (BAY3427080)Experimental Treatment1 Intervention
Participants will receive 120 mg elinzanetant orally once daily for 26 weeks.
Group II: Placebo + elinzanetantPlacebo Group2 Interventions
Participants will receive matching placebo orally once daily for 12 weeks, followed by elinzanetant 120 mg for 14 weeks.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Elinzanetant (BAY3427080)
2022
Completed Phase 3
~1940
Find a Location
Who is running the clinical trial?
BayerLead Sponsor
2,274 Previous Clinical Trials
25,514,405 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You are experiencing moderate to severe menopause-related hot flashes and want treatment for them.You have an untreated thyroid problem, either an overactive thyroid or an underactive thyroid.You have a medical condition that could make it hard to understand hot flashes or other symptoms related to blood vessel function, such as an ongoing infection with high fever, pheochromocytoma, or carcinoid syndrome.If you experience any unexpected vaginal bleeding after menopause.You are experiencing strong and frequent hot flashes due to menopause and are actively looking for treatment.The participant has completed the Hot Flash Daily Diary for at least 11 days during the two weeks preceding the baseline visit, and they have recorded at least 50 moderate or severe hot flashes over the last 7 days that the HFDD was completed.
Research Study Groups:
This trial has the following groups:- Group 1: Elinzanetant (BAY3427080)
- Group 2: Placebo + elinzanetant
Awards:
This trial has 1 awards, including:- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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