Literature DB >> 25201661

The hidden cost of low prices: limited access to new drugs in India.

Ernst R Berndt1, Iain M Cockburn2.   

Abstract

The pricing and accessibility of patent-protected drugs in low- and middle-income countries is a contentious issue in the global context. But questions about price have little meaning if a drug is not available for purchase, and the extent to which patent policy affects when (and if) new drugs become available in these countries has largely been overlooked. We examined data on the sales of 184 drugs approved by the US Food and Drug Administration between 2000 and 2009. We found that 50 percent of those 184 drugs went on sale in India only after lags of more than five years from their first worldwide introduction. More than half of the drugs that became newly available in India during the study period were produced and sold by multiple manufacturers in the country within one year of their introduction. The presence of multiple manufacturers indicates sharp competition and weak patent protection--factors that are disincentives to manufacturers to incur the costs of gaining access to the market. We conclude that modest patent and regulatory reform could bring the faster availability of a wider range of new drugs in India with limited impact on prices--a trade-off that merits greater policy attention. Project HOPE—The People-to-People Health Foundation, Inc.

Keywords:  Developing World < International/global health studies; Health Economics; Legal/Regulatory Issues; Pharmaceuticals

Mesh:

Substances:

Year:  2014        PMID: 25201661     DOI: 10.1377/hlthaff.2013.1307

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


  6 in total

Review 1.  What is the impact of intellectual property rules on access to medicines? A systematic review.

Authors:  Brigitte Tenni; Hazel V J Moir; Belinda Townsend; Burcu Kilic; Anne-Maree Farrell; Tessa Keegel; Deborah Gleeson
Journal:  Global Health       Date:  2022-04-15       Impact factor: 10.401

2.  Evaluation of Drug Trials in High-, Middle-, and Low-Income Countries and Local Commercial Availability of Newly Approved Drugs.

Authors:  Jennifer E Miller; Michelle M Mello; Joshua D Wallach; Emily M Gudbranson; Blake Bohlig; Joseph S Ross; Cary P Gross; Peter B Bach
Journal:  JAMA Netw Open       Date:  2021-05-03

Review 3.  Addressing the challenge of high-priced prescription drugs in the era of precision medicine: A systematic review of drug life cycles, therapeutic drug markets and regulatory frameworks.

Authors:  Toon van der Gronde; Carin A Uyl-de Groot; Toine Pieters
Journal:  PLoS One       Date:  2017-08-16       Impact factor: 3.240

4.  An evaluation of drug lag for new drugs approved by the Indian regulator relative to the United States, European Union, and Japanese regulatory agencies: A 15-year analysis (2004-2018).

Authors:  Mahanjit Konwar; Mitesh R Maurya; Tushar B Nishandar; Urmila M Thatte; Nithya J Gogtay
Journal:  Perspect Clin Res       Date:  2021-01-08

5.  Indian pharmaceutical patent prosecution: The changing role of Section 3(d).

Authors:  Bhaven N Sampat; Kenneth C Shadlen
Journal:  PLoS One       Date:  2018-04-02       Impact factor: 3.240

6.  Impacts of intellectual property provisions in trade treaties on access to medicine in low and middle income countries: a systematic review.

Authors:  Md Deen Islam; Warren A Kaplan; Danielle Trachtenberg; Rachel Thrasher; Kevin P Gallagher; Veronika J Wirtz
Journal:  Global Health       Date:  2019-12-30       Impact factor: 10.401

  6 in total

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