Abstract
Valbenazine (Ingrezza®) is an orally bioavailable, selective and reversible vesicular monoamine transporter 2 (VMAT2) inhibitor that is indicated for the once-daily treatment of adults with tardive dyskinesia (TD) in the USA. By inhibiting VMAT2, thereby interfering with the presynaptic uptake and storage of dopamine and other monoamines, valbenazine is thought to counteract the heightened postsynaptic dopaminergic activity that is believed to cause TD. In adults with dopamine-receptor blocking agent-induced TD and underlying schizophrenia, schizoaffective disorder or mood disorder, valbenazine was associated with rapid, significant and sustained on-treatment improvements in TD severity relative to placebo. Somnolence is the most common treatment-emergent adverse event associated with valbenazine and, importantly, depression and extrapyramidal symptoms have not been associated with its use.
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Acknowledgements
The manuscript was updated from Drugs 2017;77(10):1123–29 [8], and was reviewed by: L.J. Cloud, Department of Neurology, School of Medicine, Virginia Commonwealth University, Richmond (VA), USA; J.H. Friedman, Movement Disorders Program, Butler Hospital, and Department of Neurology, Warren Alpert Medical School of Brown University, Providence (RI), USA; R.C. Josiassen, Translational Neuroscience LCC, Conshohocken (PA),USA; M. Solmi, Psychiatry Unit, Neurosciences Department, University of Padua, Padua, Italy. During the peer review process, the manufacturer of valbenazine was also offered an opportunity to review this article. Changes resulting from comments received were made on the basis of scientific and editorial merit.
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E.S. Kim and K.A. Lyseng-Williamson are employees of Adis/Springer, are responsible for the article content and declare no conflicts of interest.
Additional information about this Adis Drug Review can be found here http://www.medengine.com/Redeem/C9ECF060386A50C9.
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Kim, E.S., Lyseng-Williamson, K.A. Valbenazine in tardive dyskinesia: a profile of its use. Drugs Ther Perspect 34, 99–104 (2018). https://doi.org/10.1007/s40267-018-0479-1
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DOI: https://doi.org/10.1007/s40267-018-0479-1