Clinical Study of Cinacalcet in Japan

被引:3
作者
Akizawa, Tadao [1 ]
Koshikawa, Shozo [1 ]
机构
[1] Showa Univ, Sch Med, Div Nephrol,Dept Med, Shinagawa Ku, Tokyo 1428666, Japan
关键词
Adverse events; Calcium phosphorus products; Cinacalcet hydrochloride; Parathyroid hormone; Secondary hyperparathyroidism;
D O I
10.1111/j.1744-9987.2008.00625.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
For the approval of cinacalcet hydrochloride, five clinical trials have been performed excluding pharmacokinetic studies for healthy volunteers and hemodialysis patients. An early phase II dose-finding study was started for regular hemodialysis patients with secondary hyperparathyroidistn from a daily dose of 12.5 mg cinacalcet and increasing 25 mg up to 50 mg for 9 weeks. A placebo-controlled double-blind three dose-finding study (late phase II study) was then conducted. By this trial, an adequate initial dose of cinacalcet was determined as 25 mg daily, and the placebo-controlled double-blind study (phase III study) was started using this initial dose. Two longterm (I year) phase III open trials were also conducted during and after these phase II and III studies. The results of two double-blind trials (phase II and phase III) and safety profiles of cinacalcet in all Japanese clinical trials for approval are summarized in this article.
引用
收藏
页码:S13 / S15
页数:3
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