drugset / Trial / NCT05645432

An Open-Label Study Evaluating Brexanolone in Adults With Tinnitus

NCT05645432 ↗

Phase 2 Completed 10 enrolled Supernus Pharmaceuticals, Inc.
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this study is to evaluate the safety and tolerability of brexanolone in participants with tinnitus following a single 6-hour continuous intravenous (IV) infusion.

Timeline

Start
2023-05-10
Primary completion
2023-11-21
Completion
2023-11-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Brexanolone Unknown 90 ug/kg —

Indications