drugset / Trial / NCT04091425

Study of TAK-925 in Participants With Obstructive Sleep Apnea (OSA) Who Are Experiencing Excessive Daytime Sleepiness (EDS) Despite Adequate Use of Continuous Positive Airway Pressure (CPAP)

NCT04091425

Phase 1 Completed 25 enrolled Millennium Pharmaceuticals, Inc.
RandomizedCrossoverQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of administering a single intravenous (IV) infusion dose of TAK-925 to adults with obstructive sleep apnea (OSA) who are experiencing excessive daytime sleepiness (EDS) despite adequate use of CPAP as the primary OSA therapy.

Timeline

Start
2019-11-21
Primary completion
2020-04-02
Completion
2020-04-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Danavorexton Small molecule Intravenous