Webster J, Petrie J C, Robb O J, Jamieson M, Verschueren J
Br J Clin Pharmacol. 1985 Oct;20(4):393-400. doi: 10.1111/j.1365-2125.1985.tb05083.x.
Single doses of bucindolol 50, 100 and 200 mg were compared to placebo and single doses of oxprenolol 40, 80 and 160 mg in seven patients with mild hypertension, in a double-blind randomized study. Both bucindolol and oxprenolol inhibited exercise induced tachycardia. The mean maximum inhibition of exercise heart rate was similar after each dose of both drugs (20%, P less than 0.001). Bucindolol produced a significantly greater reduction in blood pressure than either oxprenolol or placebo. This was most apparent in standing systolic and diastolic and post-exercise systolic blood pressures between 1 and 2 h after dosing and was dose-related. All seven patients experienced adverse effects related to hypotension within the first 2 h after ingestion of bucindolol 200 mg. Plasma concentrations of oxprenolol, bucindolol or 5-hydroxy-bucindolol, sampled 2 h after dosing, could not be related to either the changes in blood pressure or to the occurrence of symptoms. The results emphasise the need for careful dose-finding of new drugs prior to their more widespread evaluation in phase 3 studies.
在一项双盲随机研究中,将50毫克、100毫克和200毫克的单次剂量布新洛尔与安慰剂以及40毫克、80毫克和160毫克的单次剂量氧烯洛尔在7名轻度高血压患者中进行了比较。布新洛尔和氧烯洛尔均能抑制运动诱发的心动过速。两种药物各剂量后运动心率的平均最大抑制率相似(20%,P<0.001)。布新洛尔使血压降低的幅度明显大于氧烯洛尔或安慰剂。这在给药后1至2小时的站立收缩压和舒张压以及运动后收缩压中最为明显,且与剂量相关。所有7名患者在摄入200毫克布新洛尔后的头2小时内均出现了与低血压相关的不良反应。给药2小时后采集的氧烯洛尔、布新洛尔或5-羟基布新洛尔的血浆浓度与血压变化或症状出现均无关联。结果强调了在新药进行更广泛的3期研究评估之前,需要仔细确定其剂量。