Wålinder J, Holm A C
Department of Psychiatry, Linköping University, Sweden.
Acta Psychiatr Scand Suppl. 1990;358:158-63. doi: 10.1111/j.1600-0447.1990.tb05310.x.
An international clinical trial programme was undertaken to evaluate the clinical safety and tolerability of remoxipride during a 12 month long-term study and to evaluate safety, tolerability and efficacy of remoxipride for up to 6 months in a double-blind comparison with haloperidol. A total of 145 patients were treated with remoxipride for at least 12 months. In the double-blind evaluation 106 patients on remoxipride and 50 on haloperidol were included. The doses of remoxipride ranged between 90-600 mg daily and of haloperidol between 5-45 mg daily. The therapeutic efficacy of remoxipride obtained in short-term studies was maintained during long-term treatment in most patients and was similar to that of haloperidol. Remoxipride had a clear cut advantage concerning extrapyramidal symptoms and anticholinergic drugs were needed less frequently with remoxipride than with haloperidol. The tolerability and safety showed no clinically significant differences compared to the data from short-term studies. This indicates that remoxipride can be used safely and with maintained efficacy for long-term treatment.
开展了一项国际临床试验项目,以评估瑞莫必利在为期12个月的长期研究中的临床安全性和耐受性,并在与氟哌啶醇的双盲比较中评估瑞莫必利长达6个月的安全性、耐受性和疗效。共有145名患者接受了至少12个月的瑞莫必利治疗。在双盲评估中,纳入了106名接受瑞莫必利治疗的患者和50名接受氟哌啶醇治疗的患者。瑞莫必利的剂量为每日90 - 600毫克,氟哌啶醇的剂量为每日5 - 45毫克。在大多数患者的长期治疗中,瑞莫必利在短期研究中获得的治疗效果得以维持,且与氟哌啶醇相似。瑞莫必利在外周锥体外系症状方面具有明显优势,与氟哌啶醇相比,使用瑞莫必利时需要抗胆碱能药物的频率更低。与短期研究的数据相比,耐受性和安全性没有临床显著差异。这表明瑞莫必利可安全用于长期治疗,且疗效得以维持。