Clavulanic Acid Attenuated Cocaine Craving in Individuals with Cocaine Use Disorder.

Mary F Morrison, Ronan Cunningham, M Ingre Walters, Daohai Yu, Xiaoning Lu, Joya Maser, Kyle M Kampman
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Abstract

This randomized, controlled trial examined the safety of clavulanic acid (CLAV), a GLT-1 (astrocytic glutamate transporter) modulator, in combination with intravenous cocaine to determine whether CLAV can be safely studied in outpatients with cocaine use disorder who may continue to use cocaine. Participants were adults with moderate to severe cocaine use disorder planning to continue regular cocaine use. In a placebo controlled, crossover, inpatient study, the safety of 3 doses of oral CLAV (250 mg/day, 500 mg/day, and added later 750 mg/day) were studied in combination with 40 mg intravenous cocaine on a medical unit with close cardiac monitoring and pharmacokinetic sampling. Ten participants, 8 men and 2 women with cocaine use disorder, were studied with all participants receiving CLAV (250 mg, 500 mg, and placebo) and 5 participants receiving the additional 750 mg dose, in combination with cocaine. There were no clinically significant drug or dose related changes in vital signs, electrocardiogram intervals, pupillary diameters between CLAV and placebo. CLAV 500 mg decreased cocaine craving, using the 10 item Cocaine Craving Questionnaire-Brief, with a large effect size (Cohen's d = 1.25). Thirty-two mild to moderate adverse events were recorded, with most drug related events being gastrointestinal. CLAV, at the doses of 250 mg, 500 mg, and 750 mg was reasonably well tolerated and safe in combination with intravenous cocaine. Associated adverse events were mild to moderate and resolved. CLAV 500 mg was associated with decreased craving for cocaine in people with cocaine use disorder.

克拉维酸可减轻可卡因使用障碍患者的可卡因渴求。
这项随机对照试验检查了clavulanic acid (clavulanic acid, GLT-1(星形细胞谷氨酸转运体)调节剂)与静脉注射可卡因联合使用的安全性,以确定clavulanic acid是否可以安全地用于可能继续使用可卡因的门诊可卡因使用障碍患者。参与者是中度至重度可卡因使用障碍的成年人,计划继续定期使用可卡因。在一项安慰剂对照、交叉、住院研究中,研究了3种剂量的口服clv (250 mg/天、500 mg/天,随后添加750 mg/天)与40 mg静脉注射可卡因联合使用的安全性,并进行了密切的心脏监测和药代动力学采样。10名参与者,8名男性和2名女性,有可卡因使用障碍,所有参与者接受clv(250毫克,500毫克和安慰剂),5名参与者接受额外的750毫克剂量,与可卡因联合使用。clv组和安慰剂组在生命体征、心电图间隔、瞳孔直径方面没有临床显著的药物或剂量相关变化。clv 500毫克降低可卡因渴望,使用10项可卡因渴望问卷-简要,具有大效应量(科恩d = 1.25)。记录了32例轻中度不良事件,大多数与药物相关的事件发生在胃肠道。250毫克、500毫克和750毫克剂量的clv与静脉注射可卡因联合使用,耐受性相当好,也很安全。相关不良事件为轻度至中度且已消退。clv 500毫克与可卡因使用障碍患者对可卡因的渴望减少有关。
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