| Literature DB >> 32489520 |
Abstract
Regulatory science comprises the tools, standards, and approaches that regulators use to assess safety, efficacy, quality, and performance of drugs and medical devices. A major focus of regulatory science is the design and analysis of clinical trials. Clinical trials are an essential part of clinical research programs that aim to improve therapies and reduce the burden of disease. These clinical experiments help us learn about what works clinically and what does not work. The results of clinical trials support therapeutic and policy decisions. When designing clinical trials, investigators make many decisions regarding various aspects of how they will carry out the study, such as the primary objective of the study, primary and secondary endpoints, methods of analysis, sample size, etc. This paper provides a brief review of the clinical development of new treatments and argues for the use of Bayesian methods and decision theory in clinical research.Entities:
Keywords: Clinical trials; Decision theory; Study design
Year: 2019 PMID: 32489520 PMCID: PMC7265656 DOI: 10.1080/19466315.2019.1668843
Source DB: PubMed Journal: Stat Biopharm Res ISSN: 1946-6315 Impact factor: 1.452