Literature DB >> 28784733

Drugs Cleared Through The FDA's Expedited Review Offer Greater Gains Than Drugs Approved By Conventional Process.

James D Chambers1, Teja Thorat2, Colby L Wilkinson3, Peter J Neumann4.   

Abstract

We investigated whether drugs approved by the Food and Drug Administration (FDA) through expedited review have offered larger health gains, compared to drugs approved through conventional review processes. We identified published estimates of additional health gains (measured in quality-adjusted life-years, or QALYs) associated with drugs approved in the period 1999-2012 through expedited (seventy-six drugs) versus conventional (fifty-nine) review processes. We found that drugs in at least one expedited review program offered greater gains than drugs reviewed through conventional processes (0.182 versus 0.003 QALYs). We also found that, compared to drugs not included in the same program, greater gains were provided by drugs in the priority review (0.175 versus 0.007 QALYs), accelerated approval (0.370 versus 0.031 QALYs), and fast track (0.254 versus 0.014 QALYs) programs. Our analysis suggests that the FDA has prioritized drugs that offer the largest health gains. Project HOPE—The People-to-People Health Foundation, Inc.

Keywords:  Pharmaceuticals; innovation

Mesh:

Year:  2017        PMID: 28784733     DOI: 10.1377/hlthaff.2016.1541

Source DB:  PubMed          Journal:  Health Aff (Millwood)        ISSN: 0278-2715            Impact factor:   6.301


  4 in total

1.  Orphan Drugs Offer Larger Health Gains but Less Favorable Cost-effectiveness than Non-orphan Drugs.

Authors:  James D Chambers; Madison C Silver; Flora C Berklein; Joshua T Cohen; Peter J Neumann
Journal:  J Gen Intern Med       Date:  2020-04-13       Impact factor: 5.128

2.  The use of validated and nonvalidated surrogate endpoints in two European Medicines Agency expedited approval pathways: A cross-sectional study of products authorised 2011-2018.

Authors:  Catherine Schuster Bruce; Petra Brhlikova; Joseph Heath; Patricia McGettigan
Journal:  PLoS Med       Date:  2019-09-10       Impact factor: 11.069

3.  The Potential Benefit of Expedited Development and Approval Programs in Precision Medicine.

Authors:  Ariel Kantor; Susanne B Haga
Journal:  J Pers Med       Date:  2021-01-14

4.  Unpacking the effects of adverse regulatory events: Evidence from pharmaceutical relabeling.

Authors:  Matthew J Higgins; Xin Yan; Chirantan Chatterjee
Journal:  Res Policy       Date:  2020-09-12
  4 in total

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