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Clinical Trial Summary

Following screening visit and verification of inclusion/exclusion criteria and informed consent, participants will undergo a multiple sleep latency test (MSLT) and polysomnogram (PSG) assessments to confirm eligibility for randomization. Participants will be randomized to two groups: placebo or XW10172 MR. The drug will be taken orally at bedtime for 6 weeks of treatment that will consist of a 2-week dose escalation/titration period and a 4-week stable-dose maintenance period. There will be a 2-week safety period following dosing.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05056194
Study type Interventional
Source XWPharma
Contact Beth Zib
Phone 650-885-9682
Email Beth.Zib@XWPharma.com
Status Not yet recruiting
Phase Phase 2
Start date November 1, 2021
Completion date November 1, 2022

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