2015
DOI: 10.1517/13543784.2015.1029573
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Valbenazine granted breakthrough drug status for treating tardive dyskinesia

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Cited by 42 publications
(33 citation statements)
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“…VMAT2 inhibitors, such as tetrabenazine, which act primarily by depleting presynaptic dopamine rather than by blocking postsynaptic dopamine receptors, have not been documented to cause TD 26. Indeed, tetrabenazine and novel VMAT2 inhibitors, such as deutetrabenazine and NBI-98854,27,28 are currently under clinical investigation for the treatment of TD.…”
Section: Discussionmentioning
confidence: 99%
“…VMAT2 inhibitors, such as tetrabenazine, which act primarily by depleting presynaptic dopamine rather than by blocking postsynaptic dopamine receptors, have not been documented to cause TD 26. Indeed, tetrabenazine and novel VMAT2 inhibitors, such as deutetrabenazine and NBI-98854,27,28 are currently under clinical investigation for the treatment of TD.…”
Section: Discussionmentioning
confidence: 99%
“…However, valbenazine appears to have fewer side effects and a more favorable once-daily dosing regimen for the treatment of TD. Tardive dyskinesia (TD) is an involuntary movement disorder induced by prolonged exposure to dopamine receptor blocking agents (DRBAs), including antipsychotics and antiemetics [1,2]. Research shows that the prescription of antipsychotics alone increased more than threefold over 10 years; conservative estimates thus indicate that approximately 5 million patients have been exposed to antipsychotics in the United States (US) [3].…”
mentioning
confidence: 99%
“…Recognizing that TD was an important unmet medical need and that a proven TD treatment would be an important pharmacological development, the US FDA granted breakthrough status to valbenazine in 2015 and approval as a treatment for TD in 2017 [2,25]. Valbenazine is a novel and highly selective VMAT2 inhibitor that is rapidly absorbed but more slowly metabolized, with a half-life of approximately 20 h that supports oncedaily dosing [22,26].…”
mentioning
confidence: 99%
“…Erkenntnisse aus der arti ziellen Studienwelt sind dazu nicht geeignet [1,2]. Da Valbenazin nicht zu β-Dihydrotetrabenazinderivaten metabolisiert wird [3], stellt sich die Frage, ob Valbenazin nicht langfristig die bessere Alternative zu SD809 ist.…”
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