A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Efficacy, Pharmacokinetics, and Pharmacodynamics of a Single Intravenous Infusion of Danavorexton in Participants With Moderate to Severe Obstructive Sleep

Protocol No

ANES-TAKEDA-TAK-925-1501

Phase

Summary

This project is being done to assess the safety and tolerability of danavorexton when administered to participants with moderate to severe OSA undergoing general anesthesia for abdominal surgery.

Description

Intravenous Danavorexton v Placebo in Moderate to Severe Sleep Apnea

Participating Institutions

Froedtert Hospital

Status

OPEN TO ACCRUAL