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Abuse potential of mirogabalin in recreational polydrug users.


ABSTRACT: Mirogabalin is a selective calcium channel ?2? subunit ligand being developed to treat neuropathic pain. In accordance with US Food and Drug Administration (FDA) guidance, the human abuse potential of mirogabalin (15-105 mg) was examined, relative to placebo, diazepam (15 or 30?mg), and pregabalin (200 or 450?mg), in two single-dose, randomized, double-blind, placebo- and active-controlled crossover studies in recreational polydrug users who could discern between positive comparator and placebo. The primary endpoint was maximum observed effect (E max) for Drug Liking Visual Analog Scale. At therapeutic doses, mirogabalin Drug Liking E max did not differ significantly from placebo and was significantly lower than diazepam and pregabalin. This indicates therapeutic doses mirogabalin may have less abuse potential versus diazepam or pregabalin. At supratherapeutic doses (?4× therapeutic dose), mirogabalin had significantly higher Drug Liking E max than placebo, but lower E max than pregabalin. In both studies, therapeutic doses of mirogabalin demonstrated limited evidence of abuse potential.

SUBMITTER: Mendell J 

PROVIDER: S-EPMC6452577 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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Abuse potential of mirogabalin in recreational polydrug users.

Mendell Jeanne J   Levy-Cooperman Naama N   Sellers Ed E   Vince Bradley B   Kelsh Debra D   Lee James J   Warren Vance V   Zahir Hamim H  

Therapeutic advances in drug safety 20190405


Mirogabalin is a selective calcium channel α<sub>2</sub>δ subunit ligand being developed to treat neuropathic pain. In accordance with US Food and Drug Administration (FDA) guidance, the human abuse potential of mirogabalin (15-105 mg) was examined, relative to placebo, diazepam (15 or 30 mg), and pregabalin (200 or 450 mg), in two single-dose, randomized, double-blind, placebo- and active-controlled crossover studies in recreational polydrug users who could discern between positive comparator a  ...[more]

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