Literature DB >> 22336591

Adaptive licensing: taking the next step in the evolution of drug approval.

H-G Eichler1, K Oye, L G Baird, E Abadie, J Brown, C L Drum, J Ferguson, S Garner, P Honig, M Hukkelhoven, J C W Lim, R Lim, M M Lumpkin, G Neil, B O'Rourke, E Pezalla, D Shoda, V Seyfert-Margolis, E V Sigal, J Sobotka, D Tan, T F Unger, G Hirsch.   

Abstract

Traditional drug licensing approaches are based on binary decisions. At the moment of licensing, an experimental therapy is presumptively transformed into a fully vetted, safe, efficacious therapy. By contrast, adaptive licensing (AL) approaches are based on stepwise learning under conditions of acknowledged uncertainty, with iterative phases of data gathering and regulatory evaluation. This approach allows approval to align more closely with patient needs for timely access to new technologies and for data to inform medical decisions. The concept of AL embraces a range of perspectives. Some see AL as an evolutionary step, extending elements that are now in place. Others envision a transformative framework that may require legislative action before implementation. This article summarizes recent AL proposals; discusses how proposals might be translated into practice, with illustrations in different therapeutic areas; and identifies unresolved issues to inform decisions on the design and implementation of AL.

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Year:  2012        PMID: 22336591     DOI: 10.1038/clpt.2011.345

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  59 in total

1.  Appropriate evidence for adaptive marketing authorization.

Authors:  Jean Philippe de Jong; Diederick E Grobbee; Bruno Flamion; Susan R Forda; Hubert G M Leufkens
Journal:  Nat Rev Drug Discov       Date:  2013-09       Impact factor: 84.694

2.  European regulatory experience with drugs for central nervous system disorders.

Authors:  Florence Butlen-Ducuing; Malgorzata Zienowicz; Frank Pétavy; Manuel Haas; Tomas Salmonson; Hans-Georg Eichler; Guido Rasi
Journal:  Nat Rev Drug Discov       Date:  2014-12-19       Impact factor: 84.694

3.  Observations on Three Endpoint Properties and Their Relationship to Regulatory Outcomes of European Oncology Marketing Applications.

Authors:  Lawrence Liberti; Pieter Stolk; James Neil McAuslane; Jan Schellens; Alasdair M Breckenridge; Hubert Leufkens
Journal:  Oncologist       Date:  2015-05-06

4.  Regulatory review time and post-market safety events for novel medicines approved by the EMA between 2001 and 2010: a cross-sectional study.

Authors:  Jean-David Zeitoun; Jérémie H Lefèvre; Nicholas S Downing; Henri Bergeron; Joseph S Ross
Journal:  Br J Clin Pharmacol       Date:  2015-05-28       Impact factor: 4.335

5.  The evolution of adaptiveness: balancing speed and evidence.

Authors:  Hans-Georg Eichler; Richard Barker; Nicola Bedlington; Jacoline C Bouvy; André W Broekmans; Anna Bucsics; Francesca Cerreta; Solange Corriol-Rohou; Alicia Granados; Yann Le Cam; Ad Schuurman
Journal:  Nat Rev Drug Discov       Date:  2018-07-06       Impact factor: 84.694

Review 6.  Considerations for the governance of gene drive organisms.

Authors:  Larisa Rudenko; Megan J Palmer; Kenneth Oye
Journal:  Pathog Glob Health       Date:  2018-07-05       Impact factor: 2.894

Review 7.  Biomarkers and sustainable innovation in cardiovascular drug development: lessons from near and far afield.

Authors:  Russell M Medford; T Forcht Dagi; Robert S Rosenson; Margaret K Offermann
Journal:  Curr Atheroscler Rep       Date:  2013-05       Impact factor: 5.113

Review 8.  Assessment of benefits and risks in development of targeted therapies for cancer--The view of regulatory authorities.

Authors:  Francesco Pignatti; Bertil Jonsson; Gideon Blumenthal; Robert Justice
Journal:  Mol Oncol       Date:  2014-10-16       Impact factor: 6.603

Review 9.  [Orphan drugs : New opportunities for the treatment of rare diseases].

Authors:  M Beck
Journal:  Internist (Berl)       Date:  2016-11       Impact factor: 0.743

Review 10.  European perspective for effective cancer drug development.

Authors:  Denis Lacombe; Sabine Tejpar; Roberto Salgado; Fatima Cardoso; Vassilis Golfinopoulos; Daniela Aust; Gunnar Folprecht; Arnaud Roth; Roger Stupp
Journal:  Nat Rev Clin Oncol       Date:  2014-06-17       Impact factor: 66.675

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