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Abuse potential of mirogabalin in recreational polydrug users.
Mendell, Jeanne; Levy-Cooperman, Naama; Sellers, Ed; Vince, Bradley; Kelsh, Debra; Lee, James; Warren, Vance; Zahir, Hamim.
Afiliação
  • Mendell J; Daiichi Sankyo, Inc., Basking Ridge, NJ, USA.
  • Levy-Cooperman N; Altreos Research Partners, Inc., Toronto, Ontario, Canada.
  • Sellers E; University of Toronto, Toronto, Ontario, Canada DL Global Partners Inc., Toronto, Ontario, Canada.
  • Vince B; Vince and Associates Clinical Research, Overland Park, KS, USA.
  • Kelsh D; Vince and Associates Clinical Research, Overland Park, KS, USA.
  • Lee J; Daiichi Sankyo, Inc., Basking Ridge, NJ, USA.
  • Warren V; Daiichi Sankyo, Inc., Basking Ridge, NJ, USA.
  • Zahir H; Daiichi Sankyo, Inc., 211 Mt. Airy Road, Basking Ridge, NJ 07920, USA.
Ther Adv Drug Saf ; 10: 2042098619836032, 2019.
Article em En | MEDLINE | ID: mdl-31057786
ABSTRACT
Mirogabalin is a selective calcium channel α2δ 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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article