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Clinical Trial Summary

This study seeks to evaluate the long-term safety and effectiveness of nelotanserin for the treatment of visual hallucinations (VHs) and Rapid Eye Movement (REM) Sleep Behavior Disorder (RBD) in subjects with Lewy body dementia (LBD).


Clinical Trial Description

This is a multi-center open-label, long-term study in LBD subjects with RBD and/or VHs. Eligible subjects who completed a previous nelotanserin VH or RBD study and choose to participate in this open-label study will receive 20, 40, 60, or 80 mg nelotanserin once daily for 24 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02871427
Study type Interventional
Source Axovant Sciences Ltd.
Contact
Status Terminated
Phase Phase 2
Start date October 20, 2016
Completion date January 17, 2019

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