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Clinical Trial Summary

The purpose of this study is to evaluate the safety and efficacy of 40 mg pimavanserin compared to placebo in patients with Parkinson's disease psychosis (PDP).


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01174004
Study type Interventional
Source ACADIA Pharmaceuticals Inc.
Contact
Status Completed
Phase Phase 3
Start date July 2010
Completion date November 2012

See also
  Status Clinical Trial Phase
Recruiting NCT06068465 - A Study of the Safety and Efficacy of Pimavanserin in Patients With Parkinson's Disease Psychosis Phase 3
Recruiting NCT04373317 - Pimavanserin vs. Quetiapine for Treatment of Parkinson's Psychosis Phase 4
Completed NCT01518309 - An Open-label Safety Study of Pimavanserin in Parkinson's Disease Patients Phase 2
Completed NCT00658567 - A Study of Safety and Efficacy of Pimavanserin (ACP-103) in Patients With Parkinson's Disease Psychosis Phase 3
Completed NCT00477672 - A Study of the Safety and Efficacy of Pimavanserin (ACP-103) in Patients With Parkinson's Disease Psychosis Phase 3
Completed NCT00550238 - A Study of the Safety and Tolerability of Pimavanserin (ACP-103) in Patients With Parkinson's Disease Psychosis Phase 3
Recruiting NCT05590637 - Comparing Antipsychotic Medications in LBD Over Time Phase 4
Approved for marketing NCT02762591 - Expanded Access of Pimavanserin for Patients With PD Psychosis N/A