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Drugs. 2015 Jul;75(11):1293-303. doi: 10.1007/s40265-015-0438-2.
Full-length recombinant human parathyroid hormone [rhPTH (1-84); Natpara(®)] is approved in the USA as an adjunct to calcium and vitamin D therapy for control of hypocalcaemia in patients with hypoparathyroidism. This article reviews the clinical efficacy and tolerability of rhPTH (1-84) in hypoparathyroidism and summarizes its pharmacological properties. In a pivotal phase III trial, subcutaneous rhPTH (1-84) was effective in maintaining albumin-corrected total serum calcium levels while reducing/eliminating the need for oral calcium and active vitamin D. rhPTH (1-84) had a generally acceptable tolerability profile in this trial, with <3% of patients discontinuing treatment because of adverse events. Commonly occurring adverse reactions included hypocalcaemia, hypercalcaemia and hypercalciuria. As the first PTH replacement therapy for hypoparathyroid patients with hypocalcaemia, rhPTH (1-84) is an effective regimen, has generally acceptable tolerability and represents an important advance for the management of hypoparathyroidism.
全长重组人甲状旁腺激素[rhPTH(1-84);Natpara®]在美国被批准作为钙和维生素 D 治疗的辅助手段,用于控制甲状旁腺功能减退症患者的低钙血症。本文综述了 rhPTH(1-84)在甲状旁腺功能减退症中的临床疗效和耐受性,并总结了其药理学特性。在一项关键的 III 期试验中,皮下注射 rhPTH(1-84)可有效维持白蛋白校正的总血清钙水平,同时减少/消除对口服钙和活性维生素 D 的需求。在这项试验中,rhPTH(1-84)具有一般可接受的耐受性,不到 3%的患者因不良反应而停止治疗。常见的不良反应包括低钙血症、高钙血症和高钙尿症。作为首个用于低钙血症甲状旁腺功能减退症患者的甲状旁腺激素替代治疗药物,rhPTH(1-84)是一种有效的治疗方案,具有一般可接受的耐受性,代表了甲状旁腺功能减退症治疗的重要进展。