Borison R L, Arvanitis L A, Miller B G
Psychiatry Service, Augusta Veterans Administration Medical Center, GA 30910, USA.
J Clin Psychopharmacol. 1996 Apr;16(2):158-69. doi: 10.1097/00004714-199604000-00008.
ICI 204,636 is a new, potentially atypical antipsychotic. In early phase II trials, the antipsychotic was well tolerated and results suggested efficacy in the treatment of the positive and negative symptoms of schizophrenia. The efficacy and safety of ICI 204,636 were evaluated on a larger scale in a 6-week, multicenter, double-blind trial. Hospitalized patients who met DSM-III-R criteria for chronic or subchronic schizophrenia with acute exacerbation, as well as other criteria, were randomized to ICI 204,636 (75 to 750 mg daily) (N = 54) or placebo (N = 55). Patients were assessed weekly by use of the Brief Psychiatric Rating Scale (BPRS), Scale for the Assessment of Negative Symptoms (SANS), and Clinical Global Impression Scale (CGI) for efficacy and the Simpson Scale and Abnormal Involuntary Movement Scale for extrapyramidal side effects (EPS). Significant differences (p < or = 0.05) between treatment groups, which favored ICI 204,636, were identified throughout the trial. Endpoint differences were significant (by analysis of covariance) for BPRS factor IV (activation) and SANS scores and were marginally significant for total BPRS, BPRS factor III (thought disturbance), BPRS positive-symptom cluster, and CGI Severity of Illness item scores (p = 0.07, 0.09, 0.06, and 0.09, respectively). ICI 204,636 was well tolerated, although it was associated with mild transient increases in alanine aminotransferase and a higher incidence of somnolence and anticholinergic effects compared with placebo. In the dose range studied, treatment with ICI 204,636 did not induce EPS as determined by analysis of Simpson Scale total scores and lack of treatment-emergent acute dystonic reactions. Furthermore, ICI 204,636 did not produce sustained levels of prolactin; the mean change from baseline at endpoint (-7.2 micrograms/L) was comparable (p = 0.44) to that for placebo (-8.2 micrograms/L). These findings distinguish ICI 204,636 from standard antipsychotics and confirm preclinical predictions that ICI 204,636 is an atypical antipsychotic.
ICI 204,636是一种新型的、可能属于非典型抗精神病药物。在II期早期试验中,该抗精神病药物耐受性良好,结果表明其在治疗精神分裂症的阳性和阴性症状方面具有疗效。在一项为期6周的多中心双盲试验中,对ICI 204,636的疗效和安全性进行了更大规模的评估。符合DSM-III-R标准的慢性或亚慢性精神分裂症急性加重患者以及其他标准的住院患者被随机分为ICI 204,636组(每日75至750毫克)(N = 54)或安慰剂组(N = 55)。每周使用简明精神病评定量表(BPRS)、阴性症状评定量表(SANS)和临床总体印象量表(CGI)评估疗效,使用辛普森量表和异常不自主运动量表评估锥体外系副作用(EPS)。在整个试验中发现治疗组之间存在显著差异(p≤0.05),ICI 204,636组更具优势。通过协方差分析,BPRS因子IV(激活)和SANS评分的终点差异具有显著性,总BPRS、BPRS因子III(思维紊乱)、BPRS阳性症状群和CGI疾病严重程度项目评分的差异接近显著(分别为p = 0.07、0.09、0.06和0.09)。ICI 204,636耐受性良好,尽管与安慰剂相比,它与丙氨酸转氨酶轻度短暂升高以及嗜睡和抗胆碱能作用的发生率较高有关。在所研究的剂量范围内,根据辛普森量表总分分析以及未出现治疗中突发的急性肌张力障碍反应确定,ICI 204,636治疗未诱发EPS。此外,ICI 204,636未产生持续的催乳素水平;终点时相对于基线的平均变化(-7.2微克/升)与安慰剂组(-8.2微克/升)相当(p = 0.44)。这些发现使ICI 204,636有别于标准抗精神病药物,并证实了临床前预测,即ICI 204,636是一种非典型抗精神病药物。