Beaver W T, Feise G A
J Clin Pharmacol. 1977 Aug-Sep;17(8-9):480-9. doi: 10.1002/j.1552-4604.1977.tb05640.x.
Using the twin crossover, balanced incomplete block design described in the previous paper, a double-blind determination of the relative analgesic potency of graded intramuscular doses of Win 20,836 (8-methoxycyclazocine) and morphine was carried out in patients with postoperative pain. Although no preliminary data at all on the human analgesic activity of Win 20,836 were available, the sequential decision-making process designed to choose the doses of the test medication most closely equianalgesic with the standard functioned efficiently to establish doses of Win 20,836 that had analgesic activity. Unfortunately, the occurrence of psychotomimetic side effects prevented the administration of doses of Win 20,836 equieffective with the morphine standard, and this necessitated substantal extrapolation of the dose-response curve of the test drug to arrive at a relative potency estimate. However, our relative potency estimate, which indicated that Win 20,836 is three to six times as potent as morphine, was dependable enough to predict with reasonable certainty that doses of Win 20,836 equieffective to the usual doses of morphine would produce an unacceptable level of psychotomimetic side effects. Clinical investigation of the drug was therefore terminated.
采用前一篇论文中描述的双交叉、平衡不完全区组设计,对术后疼痛患者进行了双盲测定,以确定不同肌内注射剂量的Win 20836(8-甲氧基环唑辛)和吗啡的相对镇痛效力。尽管当时完全没有关于Win 20836人体镇痛活性的初步数据,但旨在选择与标准药物镇痛效果最接近的等镇痛剂量的试验药物的序贯决策过程有效地发挥了作用,确定了具有镇痛活性的Win 20836剂量。不幸的是,拟精神病副作用的出现使得无法给予与吗啡标准等效的Win 20836剂量,因此有必要对试验药物的剂量反应曲线进行大量外推,以得出相对效力估计值。然而,我们的相对效力估计表明,Win 20836的效力是吗啡的三到六倍,这足以可靠地预测,与通常吗啡剂量等效的Win 20836剂量会产生不可接受的拟精神病副作用水平。因此,该药物的临床研究终止。