Mendell Jeanne, Levy-Cooperman Naama, Sellers Ed, Vince Bradley, Kelsh Debra, Lee James, Warren Vance, Zahir Hamim
Daiichi Sankyo, Inc., Basking Ridge, NJ, USA.
Altreos Research Partners, Inc., Toronto, Ontario, Canada.
Ther Adv Drug Saf. 2019 Apr 5;10:2042098619836032. doi: 10.1177/2042098619836032. eCollection 2019.
Mirogabalin is a selective calcium channel αδ 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 ( ) for Drug Liking Visual Analog Scale. At therapeutic doses, mirogabalin Drug Liking did not differ significantly from placebo and was significantly lower than diazepam and pregabalin. This indicates therapeutic doses mirogabalin may have less abuse potential diazepam or pregabalin. At supratherapeutic doses (⩾4× therapeutic dose), mirogabalin had significantly higher Drug Liking than placebo, but lower than pregabalin. In both studies, therapeutic doses of mirogabalin demonstrated limited evidence of abuse potential.
米罗加巴林是一种正在研发用于治疗神经性疼痛的选择性钙通道αδ亚基配体。根据美国食品药品监督管理局(FDA)的指导原则,在两项单剂量、随机、双盲、安慰剂和活性对照交叉研究中,对米罗加巴林(15 - 105毫克)相对于安慰剂、地西泮(15或30毫克)和普瑞巴林(200或450毫克)的人体滥用潜力进行了研究,研究对象为能够区分阳性对照药和安慰剂的多药滥用者。主要终点是药物喜好视觉模拟量表的最大观察效应( )。在治疗剂量下,米罗加巴林的药物喜好与安慰剂无显著差异,且显著低于地西泮和普瑞巴林。这表明治疗剂量的米罗加巴林可能比地西泮或普瑞巴林具有更低的滥用潜力。在超治疗剂量(≥4倍治疗剂量)下,米罗加巴林的药物喜好显著高于安慰剂,但低于普瑞巴林。在两项研究中,治疗剂量的米罗加巴林显示出有限的滥用潜力证据。