Randomized trial of AT-1015 for treatment of intermittent claudication. A novel 5-hydroxytryptamine antagonist with no evidence of efficacy

被引:18
作者
Hiatt, WR
Hirsch, AT
Cooke, JP
Olin, JW
Brater, DC
Creager, MA
机构
[1] Univ Colorado, Hlth Sci Ctr, Colorado Prevent Ctr, Denver, CO 80203 USA
[2] Univ Colorado, Sch Med, Dept Med, Sect Vasc Med, Denver, CO USA
[3] Univ Minnesota, Sch Publ Hlth, Minneapolis Heart Inst, Vasc Med Program, Minneapolis, MN USA
[4] Univ Minnesota, Sch Publ Hlth, Div Epidemiol, Minneapolis, MN 55455 USA
[5] Stanford Univ, Sch Med, Vasc Med & Biol Program, Stanford, CA 94305 USA
[6] Mt Sinai Med Ctr, Zena & Michael A Wiener Cardiovasc Inst, New York, NY 10029 USA
[7] Indiana Univ, Sch Med, Dept Med, Div Clin Pharmacol, Indianapolis, IN USA
[8] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Cardiovasc, Boston, MA 02115 USA
关键词
intermittent claudication; peripheral vascular disease; randomized controlled trial; treatment;
D O I
10.1191/1358863x04vm520oa
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
AT-1015 is a novel selective 5-HT2A serotonin receptor antagonist that is known to impair platelet aggregation and vasoconstriction. Serotonin has been hypothesized to contribute to claudication symptoms in individuals with peripheral arterial disease ( PAD) via microvascular vasoconstrictor and thrombotic effects. AT-1015 was thus evaluated in 439 patients with claudication who were randomized in a double-blind, placebo-controlled trial comparing 10 mg, 20 mg, and 40 mg BID versus placebo for 24 weeks. Treadmill walking performance was assessed by peak walking time ( PWT) and pain-free walking time (PFWT). Quality of life (QoL) was measured by the Walking Impairment Questionnaire (WIQ) and the Health Status Survey SF-36. Limb hemodynamics was assessed with the ankle - brachial index (ABI). The 40 mg arm was terminated prematurely by recommendation of the Data Safety Monitoring Committee due to an excess number of non-fatal myocardial infarctions. At study conclusion, there were no statistically significant differences in the mean change of PWT, PFWT, ABI and QoL between the 10 mg and 20 mg BID treatment groups compared with placebo. The proportion of patients who experienced an adverse event (AE) was similar across all treatment groups. Antimuscarinic and gastrointestinal AEs were more common in the AT-1015 treatment groups. Two deaths occurred: one in the placebo group and the other in the AT-1015 20 mg group. Although a prolongation of the QTc interval was observed in all groups, this was not clinically significant (QTc > 500 ms). Mean supine pulse rates were significantly increased in all AT-1015 treatment groups, consistent with predicted antimuscarinic effects. Population pharmacokinetic analysis fit a one-compartment model with first-order absorption and elimination. These data indicate that selective serotonin receptor blockade does not improve exercise tolerance or quality of life in individuals with claudication.
引用
收藏
页码:18 / 25
页数:8
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