Pimavanserin: A Truly Effective Treatment for Parkinson's Disease Psychosis? A Review of Interventions
- PMID: 37274140
- PMCID: PMC10239266
- DOI: 10.2147/NDT.S371641
Pimavanserin: A Truly Effective Treatment for Parkinson's Disease Psychosis? A Review of Interventions
Abstract
Parkinson's disease (PD) is the second-most common neurodegenerative disorder with a long-term 60% cumulative prevalence of PD psychosis. Medical treatment is limited to few atypical antipsychotic drugs with low affinity to dopamine D2 receptors. In 2016, pimavanserin, a selective 5-HT2A inverse agonist/antagonist, was approved by the US Food and Drug Administration (FDA) as the only treatment for PD psychosis (PDP). This article provides an overview of the epidemiology, pathophysiology, and treatment options for PDP and illuminates the mode of action and therapy options with pimavanserin and the current study data.
Keywords: Parkinson’s disease; pimavanserin; psychosis.
© 2023 Heim et al.
Conflict of interest statement
Dr Beatrice Heim reports grants from from Austrian Science Fund (FWF), personal fees from AbbVie and Novartis, outside the submitted work; Dr Florian Krismer reports grants from National Institutes of Health, grants from Austrian Science Fund (FWF), grants from MSA Coalition, personal fees from Servier, personal fees from Sanofi-Aventis, personal fees from Servier, personal fees from Takeda, outside the submitted work; Dr Atbin Djamshidian reports Honoriaria from Novo Nordisk, Roche, Biogen, and BIAL, outside the submitted work; Dr Klaus Seppi reports personal fees from Ono Pharma UK Ltd, personal fees from Teva, personal fees from UCB Pharma, personal fees from Lundbeck, grants, personal fees from AOP Orphan Pharmaceuticals AG, personal fees from Roche Pharma, personal fees from Grünenthal, personal fees from Stada, personal fees from AbbVie, personal fees from Ever Pharma, personal fees from Licher Pharma, personal fees from Biogen, personal fees from BIAL, grants, personal fees from International Parkinson and Movement Disorders Society, grants from Michael J. Fox Foundation, grants from FWF Austrian Science Fund, outside the submitted work. The authors report no conflicts of interest in this work.
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