Safety and Efficacy of THN102 in Patients With Parkinson's Disease and Excessive Daytime Sleepiness

Safety and Efficacy of THN102 in Patients With Parkinson's Disease and Excessive Daytime Sleepiness

Recruitment Information:

Seeking volunteers with following diagnosis: PD Study Type: Interventional
Eligible Ages: 18 - 80 Status: Active, not recruiting
Time Since Diagnosis: Any may be eligible Study Focus:

Study Purpose:

This is a randomized, placebo-controlled, 3-way cross-over phase IIa trial comparing two dose levels of THN102 to placebo in patients suffering from Parkinson's disease associated with excessive daytime sleepiness.

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More Details

The treatment duration is 2 weeks per period. Each treatment period is followed by a one-week washout period.

Phase: Phase 2 Lead Sponsor: Theranexus
Trial ID: 005338 Sponsor Type: Industry
Primary Country: United States Additional Collaborators or Sponsors:
Estimated Enrollment: 60 Study Start Date:
Estimated Study Completion Date: December 2019 Source: ClinicalTrials.gov
Study Website: www.theranexus.com/en/platform-and-products/thn102.html

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