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Clinical Trial Summary

To determine if PT intervention will be improved while in the "on" motor state vs. the "end-of-dose-off" motor state during the PT Intervention Visit in subjects with PD.


Clinical Trial Description

Multicenter, outpatient trial to evaluate PT outcomes in subjects diagnosed with PD and currently using APOKYN. Those subjects who satisfy all eligibility criteria will be randomized to 2 treatment groups: 1. "APO+" (APOKYN treatment before the PT Intervention Visit) and; 2. "APO-" (APOKYN treatment withheld before the PT Intervention Visit). The study will have: - Baseline Assessment Visit(s) - 1 day at Investigator's clinic and PT clinic - APOKYN Response Verification Visit - 1 day - PT Intervention Visits - for 6 weeks - End-of-study Assessment Visit(s) - 1 day at Investigator's clinic and PT clinic All subjects will participate in a standardized PT intervention. In both treatment groups, ALL subjects will arrive for the PT Intervention Visit in an "end-of-dose-off" motor state. The "end-of-dose-off" motor state will be achieved by the subject withholding his/her carbidopa/levodopa dose and APOKYN dose for at least 3 hours before the PT Intervention Visit. It is hypothesized that the outcome of PT will be improved when subjects are in the "on" motor state during PT Intervention visits compared with being in the "end-of-dose-off" motor state during PT Intervention visits. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02549573
Study type Interventional
Source Supernus Pharmaceuticals, Inc.
Contact
Status Terminated
Phase Phase 4
Start date January 2016
Completion date December 2016

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