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Clinical Trial Summary

A Study to Evaluate NYX-458 in Subjects With Mild Cognitive Impairment or Mild Dementia Associated With Parkinson's Disease or Prodromal or Manifest Lewy Body Dementia


Clinical Trial Description

The study will be a 16 to 18-week study, including a 2 to 4-week screening period, followed by a 12-week double-blind, randomized, placebo-controlled treatment Period, and a 2-week follow-up period. Subjects eligible for the study will be randomized to receive either NYX-458 or placebo. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04148391
Study type Interventional
Source Aptinyx
Contact
Status Active, not recruiting
Phase Phase 2
Start date November 14, 2019
Completion date December 30, 2022

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