Author:
Gallo Paul,Chen Joshua,Quan Hui,Menjoge Shailendra,Luo Xiaolong,Tanaka Yoko,Li Gang,Ouyang S. Peter,Binkowitz Bruce,Ibia Ekopimo,Talerico Steven,Ikeda Kimitoshi
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Public Health, Environmental and Occupational Health,Drug Guides,Pharmacology (nursing)
Reference15 articles.
1. Chen J, Quan H, Gallo P, Ouyang SP, Binkowitz B. An adaptive strategy for assessing regional consistency in multi-regional clinical trials. Technical Report #138, Merck Research Laboratories. March 2011.
2. US Food and Drug Administration. Draft guidance for industry: adaptive design clinical trials for drugs and biologics. February 2010.
3. Wang SJ, O’Neill RT, Hung HMJ. Approaches to evaluation of treatment effect in randomized clinical trials with genomic subset. Pharm Stat. 2007;6:227–244
4. Luo X, Shih WJ, Ouyang SP, Delap RJ. An optimal adaptive design to coordinate local regulations with simultaneous global development. Pharm Stat. 2010;9:179–189
5. O’Shea JC, DeMets DL. Statistical issues relating to international differences in clinical trials. Am Heart J. 2001;142:21–28
Cited by
16 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献