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Clinical Trial Summary

The purpose of this study is to evaluate the safety and efficacy of 34 mg pimavanserin compared to placebo in patients with Parkinson's disease psychosis (PDP).


Clinical Trial Description

Not provided ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06068465
Study type Interventional
Source Tasly Pharmaceutical Group Co., Ltd
Contact Rui Liu
Phone 022-86343626
Email liurui2@tasly.com
Status Recruiting
Phase Phase 3
Start date September 27, 2023
Completion date January 1, 2026

See also
  Status Clinical Trial Phase
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 NCT01174004 - A Study of the Safety and Efficacy of Pimavanserin 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