Opicapone for the Treatment of Parkinson’s Disease "Off" Episodes: Pharmacology and Clinical Considerations

• Published in: Clinical drug investigation Vol. 42; no. 2; pp. 127 - 135
• Main Authors: Berger, Amnon A., Robinson, Christopher, Winnick, Ariel, Izygon, Jonathan, Jacob, Binil M., Noonan, Mackenzie J., Kaye, Alan D., Kaye, Jessica S., Kaye, Adam M., Cornett, Elyse M., Shah, Rutvij J., Viswanath, Omar, Urits, Ivan
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 01.02.2022; Springer Nature B.V
• Subjects: Aerobics; Antiparkinson Agents - therapeutic use; Catechol O-Methyltransferase; Catechol O-Methyltransferase Inhibitors; Dopamine; Drug dosages; Enzymes; Exercise; FDA approval; Humans; Internal Medicine; Liver; Medicine; Medicine & Public Health; Nervous system; Oxadiazoles; Parkinson Disease - diagnosis; Parkinson Disease - drug therapy; Parkinson's disease; Patients; Pharmacology/Toxicology; Pharmacotherapy; Physical fitness; Quality of life; Review Article; United States > US
• ISSN: 1173-2563; 1179-1918
• DOI: 10.1007/s40261-021-01109-3

Parkinson's disease (PD) is a common neurodegenerative disorder. It is also the fastest-growing neurodegenerative disorder and has more than doubled between 1990 and 2016. Parkinson’s disease causes significant morbidity and disability from motor dysfunction, sleep disturbances, and cognitive and psychiatric symptoms. This paper reviews recent evidence in the treatment of PD “off” episodes with the novel drug opicapone, including its efficacy, safety, and clinical indications. Opicapone is a novel, peripherally acting catechol- O -methyl transferase (COMT) inhibitor used as adjunctive therapy to carbidopa/levodopa for treatment and prevention of "off” episodes. It has been approved for use as an adjunct to levodopa since 2016 in Europe and has recently (April 2020) gained FDA approval for use in the USA. By inhibiting COMT, opicapone slows levodopa metabolism and increases its availability. Several clinical studies demonstrated significant improvement in treatment efficacy and reduction in the duration of "off” episodes The main side effect demonstrated was dyskinesia, mostly with the 100 mg dose, which is higher than the approved, effective dose of 50 mg.