[What can we expect from clinical trials in psychiatry?]

Encephale. 2016 Dec;42(6S):S2-S6. doi: 10.1016/S0013-7006(17)30046-5.
[Article in French]

Abstract

Clinical trials in psychiatry allow to build the regulatory dossiers for market authorization but also to document the mechanism of action of new drugs, to build pharmacodynamics models, evaluate the treatment effects, propose prognosis, efficacy or tolerability biomarkers and altogether to assess the impact of drugs for patient, caregiver and society. However, clinical trials have shown some limitations. Number of recent dossiers failed to convince the regulators. The clinical and biological heterogeneity of psychiatric disorders, the pharmacokinetic and pharmacodynamics properties of the compounds, the lack of translatable biomarkers possibly explain these difficulties. Several breakthrough options are now available: quantitative system pharmacology analysis of drug effects variability, pharmacometry and pharmacoepidemiology, Big Data analysis, brain modelling. In addition to more classical approaches, these opportunities lead to a paradigm change for clinical trials in psychiatry.

Keywords: Cerveau virtuel; Clinical trials; Essais cliniques; Pharmacoepidemiology; Pharmacogenetics; Pharmacogenétique; Pharmacologie quantitative des systèmes; Pharmacoépidémiologie; Quantitative system pharmacologie; Virtual brain.

MeSH terms

  • Brain / pathology
  • Clinical Trials as Topic* / methods
  • Clinical Trials as Topic* / organization & administration
  • Clinical Trials as Topic* / standards
  • Computer Simulation
  • Humans
  • Mental Disorders / epidemiology
  • Mental Disorders / therapy*
  • Pharmacoepidemiology
  • Pharmacogenomic Testing / methods
  • Pharmacogenomic Testing / trends
  • Psychiatry / methods*
  • Psychiatry / trends*
  • Research Design / standards
  • User-Computer Interface