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氯卡色林(一种5-羟色胺2C受体激动剂)用于大麻使用障碍的开放标签试验

Open Label Pilot of Lorcaserin (a serotonin 2C-receptor agonist) for Cannabis Use Disorder.

作者信息

Brezing Christina A, Sibai Mohammad, Choi C Jean, Mitra Souparno, Mariani John J, Naqvi Nasir, Mahony Amy L, Brooks Daniel, Pavlicova Martina, Levin Frances R

机构信息

New York State Psychiatric Institute, Division on Substance Use Disorders, 1051 Riverside Drive, New York, NY 10032, USA.

Columbia University Irving Medical Center, Department of Psychiatry, 630 West 168 Street, New York, NY 10032, USA.

出版信息

J Subst Use. 2024;29(4):487-494. doi: 10.1080/14659891.2023.2202760. Epub 2023 May 10.

Abstract

BACKGROUND AND OBJECTIVE

Cannabis Use Disorder (CUD) has no FDA approved treatment. Serotonin-2c (5HT2c) agonists have preclinical and human laboratory evidence for potential efficacy for CUD. We assessed the tolerability and effects of lorcaserin (5HT2c agonist) on CUD.

METHODS

In a 10-week, open label, uncontrolled trial, the tolerability of lorcaserin was tested in outpatients with CUD. Adverse events (AE) were assessed weekly. Cannabis use was assessed twice weekly by the Timeline follow-back and quantitative urine metabolites.

RESULTS

17 participants enrolled, and 14 received medication. Participants' average age was 35 years; majority were male (N=12). The medication was well tolerated in males. There were no serious adverse events (SAE). The most common AE's were headache/migraine (N=4, all females), anorexia (N=3), and irritability (N=2). Participants decreased their frequency of cannabis use significantly (p < 0.001), adjusted for baseline use. By the end of the trial, participants decreased by 1.76 (SE=0.47) cannabis using days/week. Average daily amount of cannabis and urine THC metabolite levels did not change significantly.

CONCLUSIONS

Lorcaserin was well tolerated in males but not females suggesting possible sex differences. Future trials of other 5HT2c agonists (lorcaserin was withdrawn at the request of the FDA) should consider longer dose titration phases.

TRIAL REGISTRATION

NCT02932215.

摘要

背景与目的

大麻使用障碍(CUD)尚无美国食品药品监督管理局(FDA)批准的治疗方法。血清素-2c(5HT2c)激动剂在临床前和人体实验室研究中有证据表明对CUD可能有效。我们评估了洛卡塞林(5HT2c激动剂)对CUD的耐受性和疗效。

方法

在一项为期10周的开放标签、非对照试验中,对患有CUD的门诊患者进行了洛卡塞林耐受性测试。每周评估不良事件(AE)。通过时间线追溯法和尿液定量代谢物每周两次评估大麻使用情况。

结果

17名参与者入组,14名接受了药物治疗。参与者的平均年龄为35岁;大多数为男性(N = 12)。该药物在男性中耐受性良好。无严重不良事件(SAE)。最常见的不良事件为头痛/偏头痛(N = 4,均为女性)、厌食(N = 3)和易怒(N = 2)。根据基线使用情况进行调整后,参与者的大麻使用频率显著降低(p < 0.001)。到试验结束时,参与者每周使用大麻的天数减少了1.76天(标准误 = 0.47)。大麻的日均使用量和尿液中四氢大麻酚(THC)代谢物水平无显著变化。

结论

洛卡塞林在男性中耐受性良好,但在女性中并非如此,提示可能存在性别差异。未来其他5HT2c激动剂的试验(应FDA要求,洛卡塞林已撤市)应考虑更长的剂量滴定阶段。

试验注册号

NCT02932215。

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