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首页> 外文期刊>Clinical nephrology >A 12-week dose-escalating study of etelcalcetide (ONO-5163/AMG 416), a novel intravenous calcimimetic, for secondary hyperparathyroidism in Japanese hemodialysis patients
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A 12-week dose-escalating study of etelcalcetide (ONO-5163/AMG 416), a novel intravenous calcimimetic, for secondary hyperparathyroidism in Japanese hemodialysis patients

机译:一种12周的剂量升级的精体升级(ONO-5163 / AMG 416),一种新的静脉内钙化,用于日本血液透析患者的继发性甲状旁腺功能亢进症

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摘要

Aims: To evaluate doseescalation of etelcalcetide (ONO-5163/ AMG 416), a novel, intravenous (IV), longacting calcium-sensing receptor agonist, for treatment of secondary hyperparathyroidism (SHPT) in Japanese hemodialysis patients. Materials and methods: In this multicenter study, IV injections of etelcalcetide (3 times a week for 12 weeks) were administered, with dose escalation every 4 weeks depending on changes in serum intact parathyroid hormone (iPTH) and corrected calcium (cCa). A total of 24 patients participated in this study. Results: Serum iPTH was reduced in a time-and dose-dependent manner, with reductions (in pg/mL) at 12 weeks of -226.1 +/- 125.3, -362.5 +/- 161.5, and -412.4 +/- 130.2, respectively, for maximum doses of 5, 10, and 15 mg. At the end of the treatment, 50% of patients had serum iPTH levels within the target range (60 - 240 pg/mL). Serum cCa and phosphorus were reduced in parallel with iPTH. Adverse events (AEs) occurred in 20 patients (83.3%). The most frequently observed AEs (> 10%) were either mild or moderate nasopharyngitis (29.2%), decreased serum calcium (16.7%), and vomiting (12.5%). Conclusions: Dose-escalated triweekly etelcalcetide was effective for SHPT in Japanese hemodialysis patients and was satisfactorily tolerated.
机译:目的:评价物氟甲酸酯(ONO-5163 / AMG 416),一种新颖的静脉内(IV),纵向钙传感受体激动剂,用于治疗日本血液透析患者的继发性甲状旁腺功能亢进症(SHPT)的剂量。材料和方法:在该多中心研究中,施用IV的Etelcaletide(每周3次,每周3次),每4周给药,取决于血清完整甲状旁腺激素(IPTH)和矫正钙(CCA)的变化。共有24名患者参加了这项研究。结果:血清IPTH以时间和剂量依赖性的方式减少,在-226.1 +/- 125.3,-362.5 +/- 161.5和-412.4 +/-130.2的12周内减少(pg / ml),分别为5,10和15mg的最大剂量。在治疗结束时,50%的患者在目标范围内具有血清IPTH水平(60-240pg / ml)。血清CCA和磷与IPTH平行降低。 20名患者发生不良事件(AES)(83.3%)。最常观察到的AES(> 10%)是轻度或中度的鼻咽炎(29.2%),血清钙(16.7%)降低(16.7%)和呕吐(12.5%)。结论:剂量升级的三周地甘露出剂对日本血液透析患者的SHPT有效,令人满意地耐受。

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