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十一酸睾酮 - 先灵公司

Testosterone Undecanoate-Schering AG.

出版信息

Drugs R D. 2004;5(6):368-9. doi: 10.2165/00126839-200405060-00012.

Abstract

Schering AG is developing a formulation of testosterone undecanoate [Nebido] for the treatment of testosterone deficiency or hypogonadism. This deficiency can lead to decreased muscle mass, impaired muscle function, osteoporosis, reduced sexual function and mental degeneration. Schering claims that its new formulation provides superior control of blood levels of the drug and permits a longer period of application. Nebido requires only four injections per year, and represents a major improvement for men with testosterone deficiency. Schering AG received approval of its testosterone undecanoate formulation in its first European country, Finland, in November 2003 for the treatment of hypogonadism in men. In July 2004, Schering's testosterone undecanoate formulation completed approval of the European mutual recognition procedure. This approval clears the way for marketing the product (as Nebido) in the large pharmaceutical markets like Germany, France and the UK. The initial phase of the product launch will occur in Finland in October 2004, and in Germany in November 2004. Other European countries will follow in 2005, and following receipt of approval, it will be introduced in the first Latin American and Asian countries. In its 2002 Annual Report, Schering predicted that testosterone undecanoate has the potential to reach peak sales of euro 100 million, 3 years after launch-launch in Europe was at the time anticipated in 2004.

摘要

先灵公司正在研发一种十一酸睾酮制剂[耐必多],用于治疗睾酮缺乏或性腺功能减退。这种缺乏会导致肌肉量减少、肌肉功能受损、骨质疏松、性功能减退以及精神衰退。先灵公司宣称其新制剂能更好地控制药物的血药浓度,并允许更长的用药周期。耐必多每年只需注射四次,这对睾酮缺乏的男性来说是一项重大改进。2003年11月,先灵公司的十一酸睾酮制剂在其首个欧洲国家芬兰获批,用于治疗男性性腺功能减退。2004年7月,先灵公司的十一酸睾酮制剂完成了欧洲相互认可程序的审批。这一审批为该产品(以耐必多之名)在德国、法国和英国等大型制药市场的销售铺平了道路。产品上市的初始阶段将于2004年10月在芬兰进行,2004年11月在德国进行。其他欧洲国家将在2005年跟进,在获得批准后,它将被引入首批拉丁美洲和亚洲国家。在先灵公司2002年的年度报告中,该公司预测十一酸睾酮在上市三年后有可能达到1亿欧元的峰值销售额——当时预计在2004年在欧洲上市。

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