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首页> 外文期刊>Osteoporosis international: a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA >Recommendations for an update of the current (2001) regulatory requirements for registration of drugs to be used in the treatment of osteoporosis in postmenopausal women and in men.
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Recommendations for an update of the current (2001) regulatory requirements for registration of drugs to be used in the treatment of osteoporosis in postmenopausal women and in men.

机译:建议更新有关绝经后女性和男性中用于治疗骨质疏松症的药物的当前(2001年)法规要求。

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摘要

Recent advances in the understanding of the epidemiology of osteoporosis suggest that certain parts of the current European guidelines for the registration of drugs in osteoporosis might be no longer substantiated. The object of this review is to provide the European regulatory authorities with an evidence-based working document providing suggestions for the revision of the "Note for guidance for the approval of drugs to be used in postmenopausal osteoporosis" (CPMP/EWP/552/95). Following an extensive review of the literature (1990-2004), the Group for the Respect of Ethics and Excellence in Science (GREES) organized a workshop including European regulators, academic scientists and representatives of the pharmaceutical industry. The outcomes of this meeting reflect the personal views of those who attended and should not, in any case, be seen as an official position paper of any regulatory agency. The group identified a certain number of points that deserve discussion. They mainly relate to the nature of the indication being granted to new chemical entities (treatment of osteoporosis in women at high risk of fracture instead of prevention and treatment of osteoporosis), the requirements of showing an anti-fracture efficacy on all or on major nonvertebral fractures (instead of the hip), the duration of pivotal trials (2 years instead of 3) and the possibility of considering bridging studies for new routes of administration, new doses or new regimens of previously approved drugs. The group also recommends that an indication could be granted for the treatment of osteoporosis in males on the basis of a placebo-controlled study, with bone mineral density changes after 1 year as the primary endpoint, for medications approved in the treatment of osteoporosis in women at high risk of fractures. cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA.
机译:对骨质疏松症流行病学认识的最新进展表明,目前欧洲骨质疏松症药物注册指南的某些部分可能不再得到证实。审查的目的是向欧洲监管机构提供基于证据的工作文件,该文件为修订“绝经后骨质疏松症所用药物批准指南的注意事项”(CPMP / EWP / 552/95)提出了建议。 )。在对文献进行了广泛回顾之后(1990年至2004年),尊重道德和科学卓越小组(GREES)组织了一个由欧洲监管机构,学术科学家和制药行业代表组成的研讨会。本次会议的结果反映了与会人员的个人观点,在任何情况下均不应被视为任何监管机构的正式立场文件。该小组确定了一些值得讨论的观点。它们主要涉及给予新化学实体的适应症的性质(治疗高骨折风险女性的骨质疏松症,而不是预防和治疗骨质疏松症),对所有或主要非椎骨显示抗骨折功效的要求骨折(而不是髋部),关键试验的持续时间(从2年而不是3年)以及考虑对先前批准的药物的新给药途径,新剂量或新方案进行桥接研究的可能性。该小组还建议,可以在安慰剂对照研究的基础上给予男性骨质疏松症治疗的适应症,以1年后骨矿物质密度的变化为主要终点,以治疗女性骨质疏松症的药物被批准极易发生骨折。欧洲骨质疏松基金会和美国国家骨质疏松基金会之间的合作。

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