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Biochemical markers and the FDA critical Path: How biomarkers may contribute to the understanding of pathophysiology and provide unique and necessary tools for drug development

  • M. A. Karsdal
  • , K. Henriksen
  • , D. J. Leeming
  • , P B Mitchell
  • , K. Duffin
  • , N. Barascuk
  • , L. Klickstein
  • , Pramod K Aggarwal
  • , O. Nemirovskiy
  • , I. Byrjalsen
  • , P. Qvist
  • , A. C. Bay-Jensen
  • , E. B. Dam
  • , S. H. Madsen
  • , C. Christiansen

Publikation: Bidrag til tidsskrift › Review › peer review

Abstract

The aim of this review is to discuss the potential usefulness of a novel class of biochemical markers, neoepitopes, in the context of the US Food and Drug Administration (FDA) Critical Path Initiative, which emphasizes biomarkers of safety and efficacy as areas of pivotal interest. Examples of protein degradation fragments neoepitopes that have proven useful for research on bone and cartilage are collagen type I and collagen type II degradation products, respectively. These markers have utility in the translational approach, as they can be used to estimate safety and efficacy in both preclinical models and clinical settings. Biochemical markers of tissue degradation may provide optimal tools, which in combination with other techniques, prove essential to drug discovery and development.

OriginalsprogEngelsk
TidsskriftBiomarkers
Vol/bind14
Udgave nummer3
Sider (fra-til)181-202
ISSN1354-750X
DOI
StatusUdgivet - maj 2009
Udgivet eksterntJa

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