drugset / Trial / NCT03623321

Extension Study of Pimavanserin in Adult Subjects With Neuropsychiatric Symptoms Related to Neurodegenerative Disease

NCT03623321

Phase 3 Completed 595 enrolled ACADIA Pharmaceuticals Inc.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the long-term safety and tolerability of pimavanserin in adult and elderly subjects with neuropsychiatric symptoms related to neurodegenerative disease exposed to open-label pimavanserin for up to 52 weeks.

Timeline

Start
2018-07-17
Primary completion
2023-05-05
Completion
2023-05-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Pimavanserin Small molecule 20 mg Oral
Subject Pimavanserin Small molecule 34 mg Oral