A Six-Week Study of the Safety and Efficacy of JZP-110 in the Treatment of Excessive Sleepiness in Subjects with Obstructive Sleep Apnea (OSA)

Brief Description Of Study

Medication trial for the treatment of excessive sleepiness in adult subjects with treated or untreated obstructive sleep apnea (OSA).

Clinical Study Identifier: TX1038

Detailed Study Description

This trial is testing a drug for adult subjects with sleep apnea to see if it can help treat excessive sleepiness and improve patients’ ability to stay awake. We are looking for subjects who have been diagnosed with sleep apnea and are either currently being treated for sleep apnea, or have tried treatment in the past (either with CPAP, oral appliance, or surgery). Subjects do not need to be currently treated for sleep apnea. Subjects will undergo overnight sleep studies and daytime sleepiness tests to determine level of sleepiness. If subjects qualify for the study, they will be given the study medication and will take it for up to 6 weeks. Subjects will be asked to come in for periodic monitoring visits to assess changes in sleepiness (including overnight sleep studies and daytime sleepiness tests). All tests are covered by the sponsor (no tests are billed to insurance) and compensation is provided for time and travel for the study.

Contact research investigator to learn more about this study by filling out the form below.


To: Research Study Investigator
Subject: I am interested in participating in your Research Study
Dear Investigator,
I'm interested in learning more about and participating in your research study named: A Six-Week Study of the Safety and Efficacy of JZP-110 in the Treatment of Excessive Sleepiness in Subjects with Obstructive Sleep Apnea (OSA)
I am hoping to hear back from you and discuss details of the study

By clicking "Contact Research Team", your contact information will be sent directly to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.