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Assessing the safety of stem cell therapeutics
Authors:Goldring Chris E P  Duffy Paul A  Benvenisty Nissim  Andrews Peter W  Ben-David Uri  Eakins Rowena  French Neil  Hanley Neil A  Kelly Lorna  Kitteringham Neil R  Kurth Jens  Ladenheim Deborah  Laverty Hugh  McBlane James  Narayanan Gopalan  Patel Sara  Reinhardt Jens  Rossi Annamaria  Sharpe Michaela  Park B Kevin
Affiliation:MRC Centre for Drug Safety Science, Division of Molecular & Clinical Pharmacology, The Institute of Translational Medicine, The University of Liverpool, Liverpool L69 3GE, UK. C.E.P.Goldring@liverpool.ac.uk
Abstract:Unprecedented developments in stem cell research herald a new era of hope and expectation for novel therapies. However, they also present a major challenge for regulators since safety assessment criteria, designed for conventional agents, are largely inappropriate for cell-based therapies. This article aims to set out the safety issues pertaining to novel stem cell-derived treatments, to identify knowledge gaps that require further research, and to suggest a roadmap for developing safety assessment criteria. It is essential that regulators, pharmaceutical providers, and safety scientists work together to frame new safety guidelines, based on "acceptable risk," so that patients are adequately protected but the safety "bar" is not set so high that exciting new treatments are lost.
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