Donati G, Spinazzè R
Divisione di Medicina, Ospedale De Gironcoli di Conegliano.
Clin Ter. 1993 Jan;142(1 Pt 2):19-28.
A study was performed with 60 patients, affected by acute phase rheumatological pathology, in order to determine the optimum posology of ST-679 administered orally. The 60 patients were divided into 4 groups: 3 treated with ST-679 at different dosages (group 1 = 600 mg/die; group 2 = 1200 mg/die; group 3 = 1800 mg/die) and one with placebo (group 4 = 600 mg/die). The highest dosage employed (1800 mg/die) performs an excellent therapeutical activity which is equivalent to that at the 1200 mg in reducing pain symptomatology, but on the average less tolerated. The 600 mg dosage was less efficacious with respect to the two higher doses.
对60例患有急性期风湿性疾病的患者进行了一项研究,以确定口服ST-679的最佳剂量。这60名患者被分为4组:3组接受不同剂量的ST-679治疗(第1组 = 600毫克/天;第2组 = 1200毫克/天;第3组 = 1800毫克/天),一组接受安慰剂治疗(第4组 = 600毫克/天)。所采用的最高剂量(1800毫克/天)具有出色的治疗活性,在减轻疼痛症状方面与1200毫克剂量相当,但平均耐受性较差。600毫克剂量相对于两个较高剂量效果较差。