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奥氮平加萨米多弗(ALKS 3831)治疗精神分裂症合并共病酒精使用障碍的 2 期随机临床试验。

Olanzapine Plus Samidorphan (ALKS 3831) in Schizophrenia and Comorbid Alcohol Use Disorder: A Phase 2, Randomized Clinical Trial.

机构信息

Geisel School of Medicine at Dartmouth, Dartmouth-Hitchcock Medical Center, One Medical Center Drive, Lebanon, NH 03756.

Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire, USA.

出版信息

J Clin Psychiatry. 2020 Mar 10;81(2):19m12786. doi: 10.4088/JCP.19m12786.

Abstract

OBJECTIVE

Alcohol use disorder (AUD) is a common comorbidity of schizophrenia. No effective pharmacologic treatment is available for both disorders to date.

METHODS

In a phase 2, double-blind study, patients with schizophrenia and AUD experiencing ≥ 10 drinking and ≥ 2 heavy-drinking days in the previous month and recent (≤ 6 mo) disease symptom exacerbation were recruited between June 2014 and March 2017. DSM-IV-TR and DSM-5 criteria were used to assign the diagnoses of schizophrenia and AUD, respectively. After a 6-week lead-in period, 234 eligible patients were randomized (1:1) to olanzapine + 10 mg samidorphan tablets (OLZ/SAM) or olanzapine + placebo tablets (olanzapine) for 36-60 weeks of treatment. The primary outcome of time to the first event of exacerbation of disease symptoms (EEDS) was evaluated using the log rank test for treatment comparison, and the Cox proportional-hazards model was used to estimate hazard ratio. Safety was assessed as adverse events and laboratory measures.

RESULTS

No significant difference was observed between groups in the time to first EEDS (hazard ratio = 0.91; 95% CI, 0.53-1.56; P = .746). Patients treated with OLZ/SAM vs olanzapine had numerically lower rates in 6 of 8 criteria to evaluate EEDS. Change from baseline in percentage of heavy-drinking days during the double-blind treatment period was similar in OLZ/SAM- vs olanzapine-treated patients. OLZ/SAM was generally well tolerated with a safety profile similar to olanzapine.

CONCLUSIONS

OLZ/SAM was not superior to olanzapine in the time to EEDS and was well tolerated in patients with schizophrenia and AUD. Further research is needed to identify effective treatments for this difficult-to-treat population.

TRIAL REGISTRATIONS

ClinicalTrials.gov identifier: NCT02161718; EudraCT number: 2014-001211-39 ​.

摘要

目的

酒精使用障碍(AUD)是精神分裂症的常见合并症。迄今为止,尚无针对这两种疾病的有效药物治疗方法。

方法

在一项 2 期、双盲研究中,招募了 2014 年 6 月至 2017 年 3 月期间患有精神分裂症和 AUD、过去一个月有≥10 次饮酒和≥2 次重度饮酒日且近期(≤6 个月)疾病症状加重的患者。DSM-IV-TR 和 DSM-5 标准分别用于诊断精神分裂症和 AUD。在 6 周导入期后,234 名符合条件的患者被随机(1:1)分为奥氮平+10mg 萨米多芬片(OLZ/SAM)或奥氮平+安慰剂片(奥氮平)治疗 36-60 周。使用对数秩检验比较治疗组的疾病症状加重的首次事件时间(EEDS)的主要结局,并使用 Cox 比例风险模型估计风险比。安全性评估为不良事件和实验室指标。

结果

两组在首次 EEDS 时间上无显著差异(风险比=0.91;95%CI,0.53-1.56;P=0.746)。与奥氮平治疗组相比,OLZ/SAM 治疗组有 8 项评估 EEDS 的标准中有 6 项的发生率较低。在双盲治疗期间,从基线变化的重度饮酒天数百分比在 OLZ/SAM-和奥氮平治疗组相似。OLZ/SAM 总体耐受性良好,安全性与奥氮平相似。

结论

OLZ/SAM 在 EEDS 时间上并不优于奥氮平,且在患有精神分裂症和 AUD 的患者中耐受性良好。需要进一步研究以确定针对这一治疗困难人群的有效治疗方法。

试验注册

ClinicalTrials.gov 标识符:NCT02161718;EudraCT 编号:2014-001211-39。

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