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临床试验/JPRN-jRCT2080223628
JPRN-jRCT2080223628已完成3 期

An Intra-Subject Dose-Adjustment Study of KHK7580 for the Treatment of Hypercalcemia in Patients with Parathyroid Carcinoma or Primary Hyperparathyroidism who are Unable to Undergo Parathyroidectomy or Relapse after Parathyroidectomy

Kyowa Kirin Co., Ltd.0 个研究点目标入组 18 人开始时间: 2017年8月25日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
18

研究概览

简要总结

Evocalcet demonstrated long-term effectiveness in reducing serum cCa concentrations and safety without any unexpected drug related TEAEs in PHPT patients.

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • Personally submitted written voluntary informed consent to participate in the study
  • - Patients with a diagnosis of parathyroid carcinoma or primary hyperparathyroidism who are unable to undergo parathyroidectomy or relapse after parathyroidectomy.
  • - Corrected serum calcium level is > 11.3 mg/dL at screening.

排除标准

  • - Patients receiving cinacalcet hydrochloride within 2 weeks before screening
  • - Patients diagnosed with hypercalcemia associated with malignant tumors other than parathyroid carcinoma.

研究者

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