| Literature DB >> 28206702 |
Sheila M Bird1, Rosemary A Bailey2, Andrew P Grieve3, Stephen Senn4.
Abstract
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.Entities:
Keywords: combined approvals; first-in-human; healthy volunteer; protocol; recommendations; study design
Mesh:
Substances:
Year: 2017 PMID: 28206702 PMCID: PMC5357061 DOI: 10.1002/pst.1801
Source DB: PubMed Journal: Pharm Stat ISSN: 1539-1604 Impact factor: 1.894