EconPapers    
Economics at your fingertips  
 

Restraining High and Rising Cancer Drug Prices: Need for Accelerating R&D Productivity and Aligning Prices with Value

Ramesh Bhardwaj

MPRA Paper from University Library of Munich, Germany

Abstract: ABSTRACT The high price of cancer drugs has become a world-wide phenomenon. In recent decades, studies have produced ample evidence of rising research and clinical testing costs underlying pharmaceutical innovations. There is a general concurrence that the current model of drug development needs a thorough streamlining. It is also alleged that the prices of new anticancer agents seem to be decided by pharmaceutical companies, according to what the market will bear, in a producer-dominated market. Studies have noted with concern that there is a little correlation between the actual efficacy of a new drug (in terms of prolonging a patient’s life in years, or quality-adjusted life-years (QALYs) and its price. The present study is an attempt to address some major challenges which are: (i) how to increase the overall pace of innovation (R&D productivity); (ii) how to control the costs and prices of new innovative drugs; (iii) how to direct more innovation to areas where social returns are highest; and (iv) how to improve patients’ timely access to innovative medicines while balancing ‘safety’ concerns. Primary proposals suggested in recent literature to deal with the above challenges include, among others, (a) modernization of the drug development process through ‘open models’ of strategic partnerships (between government, academia, and industry), (b) adoption of a value-based pricing system, (c) promotion of ‘Personalized/targeted Medicine’, (d) introduction of evidence-based decision making by stakeholders based upon ‘comparative effectiveness research’(CER) analysis, and (e) implantation of regulatory reforms in drugs’ evaluation and approval practices. The present study makes an attempt to shed light on the above challenges and proposals.

Keywords: Cancer Drugs Prices; R&D Productivity; Oncology; Drugs Development; Comparative Effectiveness Research; Personalized/targeted Medicine’; Evidence-based Decision Making; Regulatory Reforms; Drugs Approval; Adaptive licensing; R&D Effectiveness; Attrition Rates; Clinical Trial Designs; Value Based Pricing (search for similar items in EconPapers)
JEL-codes: I1 I10 I11 I13 I15 I18 I19 (search for similar items in EconPapers)
Date: 2015-04-01
New Economics Papers: this item is included in nep-ino
References: View references in EconPapers View complete reference list from CitEc
Citations:

Downloads: (external link)
https://mpra.ub.uni-muenchen.de/63405/1/MPRA_paper_63405.pdf original version (application/pdf)

Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.

Export reference: BibTeX RIS (EndNote, ProCite, RefMan) HTML/Text

Persistent link: https://EconPapers.repec.org/RePEc:pra:mprapa:63405

Access Statistics for this paper

More papers in MPRA Paper from University Library of Munich, Germany Ludwigstraße 33, D-80539 Munich, Germany. Contact information at EDIRC.
Bibliographic data for series maintained by Joachim Winter ().

 
Page updated 2025-03-19
Handle: RePEc:pra:mprapa:63405