Clinical evaluation of a new hypolipidemic drug, CIBA 13,437-Su

G Hartmann, G. Forster
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引用次数: 16

Abstract

The first clinical trials with a new aryloxy-type of hypolipidemic compound, the tetralin-derivative CIBA 13,437-Su, are reported. Various hyperlipidemic syndromes were treated in a total of 88 patients for periods up to 22 months.

With daily doses of 4–10 mg/kg, i.e. 300-600 mg per day, serum triglycerides and cholesterol were markedly lowered. The most pronounced effect was observed in hyperlipidemias of Types III, IV, and V of the Fredrickson-Lees classification. The pre-β-fraction appeared to be more readily lowered than the β-fraction, although the rather resistant hypercholesterolemia of Type II responded in all cases, yet to a lesser degree, and these patients received the higher doses. Slight transient increases in serum transaminases were observed in 7 out of 88 patients. The compound was very well tolerated subjectively. The results demonstrate that 13,437-Su is a very potent hypolipidemic agent.

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降血脂新药ciba13437 - su的临床评价
报道了一种新的芳氧基型降血脂化合物——四联素衍生物CIBA 13437 - su的首次临床试验。共有88名患者接受了各种高脂血症的治疗,疗程长达22个月。每日剂量为4-10毫克/公斤,即每天300-600毫克,血清甘油三酯和胆固醇明显降低。在Fredrickson-Lees分类的III型、IV型和V型高脂血症中观察到最明显的效果。β前部分似乎比β部分更容易降低,尽管II型高胆固醇血症在所有病例中都有反应,但程度较低,这些患者接受较高的剂量。88例患者中有7例血清转氨酶轻微短暂升高。这种化合物的主观耐受性很好。结果表明,13437 - su是一种非常有效的降血脂剂。
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