Statistical issues in first-in-human studies on BIA 10=2474: Neglected comparison of protocol against practice

被引:11
作者
Bird, Sheila M. [1 ]
Bailey, Rosemary A. [2 ]
Grieve, Andrew P. [3 ]
Senn, Stephen [4 ]
机构
[1] Univ Cambridge, Sch Clin Med, MRC Biostat Unit, Cambridge, England
[2] Univ St Andrews, Sch Math & Stat, St Andrews, Fife, Scotland
[3] ICON plc, Marlow, Bucks, England
[4] Luxembourg Inst Hlth Strassen, Competence Ctr Methodol & Stat, Luxembourg, Luxembourg
关键词
combined approvals; first-in-human; healthy volunteer; protocol; recommendations; study design; CLINICAL-TRIALS;
D O I
10.1002/pst.1801
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
By setting the regulatory-approved protocol for a suite of first-in-human studies on BIA 10-2474 against the subsequent French investigations, we highlight 6 key design and statistical issues, which reinforce recommendations by a Royal Statistical Society Working Party, which were made in the aftermath of cytokine release storm in 6 healthy volunteers in the United Kingdom in 2006. The 6 issues are dose determination, availability of pharmacokinetic results, dosing interval, stopping rules, appraisal by safety committee, and clear algorithm required if combining approvals for single and multiple ascending dose studies.
引用
收藏
页码:100 / 106
页数:7
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