Clinical trials in cystic fibrosis

被引:37
作者
Doering, Gerd
Elborn, J. Stuart
Johannesson, Marie
de Jonge, Hugo
Griese, Matthias
Smyth, Alan
Heijerman, Harry
机构
[1] Univ Tubingen, Inst Med Microbiol & Hyg, Univ Klinikum, D-72074 Tubingen, Germany
[2] Queens Univ, Belfast, Antrim, North Ireland
[3] Childrens Univ Hosp, Uppsala, Sweden
[4] Erasmus Univ, Med Ctr, Rotterdam, Netherlands
[5] Univ Munich, Munich, Germany
[6] Univ Nottingham, Nottingham NG7 2RD, England
[7] Haga Teaching Hosp, The Hague, Netherlands
关键词
drug development; pre-clinical drug testing; animal models; surrogate end points; safety issues; drug licensing; European clinical trial network for CF;
D O I
10.1016/j.jcf.2007.02.001
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
In patients with cystic fibrosis (CF), clinical trials are of paramount importance. Here, the current status of drug development in CF is discussed and future directions highlighted. Methods for pre-clinical testing of drugs with potential activity in CF patients including relevant animal models are described. Study design options for phase II and phase III studies involving CF patients are provided, including required patient numbers, safety issues and surrogate end point parameters for drugs, tested for different disease manifestations. Finally, regulatory issues for licensing new therapies for CF patients are discussed, including new directives of the European Union and the structure of a European clinical trial network for clinical studies involving CF patients is proposed.
引用
收藏
页码:85 / 99
页数:15
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