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AMG 416(维立西呱)是一种新型肽类药物,在单次给药的血液透析患者中进行的研究中用于治疗继发性甲状旁腺功能亢进症。

AMG 416 (velcalcetide) is a novel peptide for the treatment of secondary hyperparathyroidism in a single-dose study in hemodialysis patients.

机构信息

Division of Nephrology, Saint Louis University School of Medicine, Saint Louis, Missouri, USA.

Amgen, Inc, Thousand Oaks, California, USA.

出版信息

Kidney Int. 2014 Jan;85(1):191-7. doi: 10.1038/ki.2013.289. Epub 2013 Jul 31.

DOI:10.1038/ki.2013.289
PMID:23903371
Abstract

AMG 416 (velcalcetide), a novel peptide agonist of the calcium-sensing receptor, lowers plasma parathyroid hormone in preclinical uremic animal models and in normal healthy individuals. Here, we studied its efficacy in hemodialysis patients suffering from secondary hyperparathyroidism. Major inclusion criteria were hemodialysis for at least 3 months, serum parathyroid hormone over 300 pg/ml, a corrected serum calcium of 9.0 mg/dl or more, and stable doses of vitamin D analogs for at least 3 weeks prior to screening. Twenty-eight patients were enrolled in one of five cohorts (5, 10, 20, 40, 60 mg). Cohorts 1-3 (four patients each) were treated in a two-period crossover design, while cohorts 4 and 5 (eight patients each) were randomized 1:1 to AMG 416 or placebo. Patients were admitted to a clinical research unit following hemodialysis and studied for 3 days prior to discharge for hemodialysis. Single intravenous doses of AMG 416 from 5 to 60 mg were well tolerated, and plasma levels increased in a dose-related manner. AMG 416 treatment was associated with significant, dose-dependent reductions in serum parathyroid hormone and fibroblast growth factor 23. Compared with placebo, all dose groups of 10 mg or more were associated with attenuation in the rise in serum phosphate during the interdialytic period. Dose-dependent reductions in serum calcium were observed and were well tolerated. Thus, AMG 416 represents a novel therapeutic approach for the treatment of secondary hyperparathyroidism in hemodialysis patients.

摘要

AMG 416(钙敏感受体肽激动剂)是一种新型的钙敏感受体肽激动剂,可降低临床前尿毒症动物模型和正常健康个体的血浆甲状旁腺激素水平。在此,我们研究了其在继发性甲状旁腺功能亢进的血液透析患者中的疗效。主要纳入标准为血液透析至少 3 个月、甲状旁腺激素超过 300pg/ml、校正血清钙 9.0mg/dl 或更高、以及在筛选前至少 3 周稳定使用维生素 D 类似物。28 例患者入组了五个队列之一(5、10、20、40、60mg)。队列 1-3(每组 4 例)采用两周期交叉设计治疗,而队列 4 和 5(每组 8 例)随机分为 AMG 416 或安慰剂组。患者在血液透析后入住临床研究单位,并在出院前进行 3 天的研究。5 至 60mg 的 AMG 416 单剂量静脉给药耐受性良好,且血浆水平呈剂量相关性增加。AMG 416 治疗与血清甲状旁腺激素和成纤维细胞生长因子 23 的显著、剂量依赖性降低相关。与安慰剂相比,10mg 或更高剂量的所有剂量组在透析间期血清磷酸盐升高方面均有减轻。观察到剂量依赖性的血清钙降低,且耐受性良好。因此,AMG 416 为血液透析患者的继发性甲状旁腺功能亢进症提供了一种新的治疗方法。

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