A Safety Study of Pimavanserin in Adult and Elderly Subjects Experiencing Neuropsychiatric Symptoms Related to Neurodegenerative Disease

  • STATUS
    Recruiting
  • End date
    Aug 24, 2022
  • participants needed
    750
  • sponsor
    ACADIA Pharmaceuticals Inc.
Updated on 24 September 2021
Investigator
Brian Raether
Primary Contact
Boston Center Memory (4.7 mi away) Contact
+125 other location

Summary

The purpose of this study is to assess the safety and tolerability of pimavanserin compared to placebo in adult and elderly subjects with neuropsychiatric symptoms related to neurodegenerative disease.

Details
Condition Neuropsychiatric Symptoms Related to Neurodegenerative Disease
Treatment Placebo, Pimavanserin
Clinical Study IdentifierNCT03575052
SponsorACADIA Pharmaceuticals Inc.
Last Modified on24 September 2021

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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