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GABA receptor modulator

Brexanolone for Tinnitus

Phase 2
Waitlist Available
Research Sponsored by Sage Therapeutics
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, up to approximately 6 days from day 2 to day 7 after ip infusion given on day 1
Awards & highlights
No Placebo-Only Group

Summary

This trial is testing a medication called brexanolone to see if it is safe for people who have tinnitus, a condition where they hear ringing in their ears.

Who is the study for?
Adults with tinnitus for 6 months to less than 10 years, experiencing mild to severe distress but in good physical health. They must not have significant medical conditions or allergies related to the treatment, and be able to stop certain medications before and during the trial. A companion is required for clinic visits.
What is being tested?
The safety and tolerability of a single continuous intravenous infusion of brexanolone over 6 hours are being tested on adults with tinnitus to see if it can help reduce their symptoms.
What are the potential side effects?
While specific side effects aren't listed here, participants will be monitored for any adverse reactions due to brexanolone infusion which could include typical IV medication risks such as irritation at the injection site, allergic reactions, or systemic effects.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, up to approximately 6 days from day 2 to day 7 after ip infusion given on day 1
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, up to approximately 6 days from day 2 to day 7 after ip infusion given on day 1 for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Number of Participants With Treatment-Emergent Adverse Events (TEAE)
Secondary study objectives
Change From Baseline to Hour 6 of Infusion in Visual Analog Scale-Annoyance (VAS-A) Ratings
Change From Baseline to Hour 6 of Infusion in Visual Analog Scale-Loudness (VAS-L) Ratings
Change From Baseline to Post-infusion in VAS-A Ratings Measured via Daily Diary Over Multiple Days
+1 more

Side effects data

From 2021 Phase 3 trial • 28 Patients • NCT03665038
25%
Infusion site pain
13%
Sedation
13%
Nausea
13%
Upper respiratory tract infection
100%
80%
60%
40%
20%
0%
Study treatment Arm
Double-Blind Phase: Placebo
Double-Blind Phase: Brexanolone
Open-Label Phase: Brexanolone

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: BrexanoloneExperimental Treatment1 Intervention
Participants will receive a continuous, 6-hour IV infusion of Brexanolone on Day 1 of the Treatment Period.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Brexanolone
2018
Completed Phase 3
~50

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for tinnitus include cognitive behavioral therapy (CBT), sound therapy, and pharmacological treatments. Brexanolone, a GABA-A receptor modulator, is being studied for its potential to alleviate tinnitus symptoms by enhancing inhibitory neurotransmission in the brain. This is significant for tinnitus patients because it targets the neural hyperactivity believed to contribute to tinnitus perception. Understanding these mechanisms helps patients and clinicians make informed decisions about treatment options that may effectively reduce the distress and impact of tinnitus on daily life.

Find a Location

Who is running the clinical trial?

Sage TherapeuticsLead Sponsor
50 Previous Clinical Trials
11,123 Total Patients Enrolled

Media Library

Brexanolone (GABA receptor modulator) Clinical Trial Eligibility Overview. Trial Name: NCT05645432 — Phase 2
Tinnitus Research Study Groups: Brexanolone
Tinnitus Clinical Trial 2023: Brexanolone Highlights & Side Effects. Trial Name: NCT05645432 — Phase 2
Brexanolone (GABA receptor modulator) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05645432 — Phase 2
Tinnitus Patient Testimony for trial: Trial Name: NCT05645432 — Phase 2
~4 spots leftby Nov 2025