Literature DB >> 25730094

The future of comparative effectiveness and relative efficacy of drugs: an international perspective.

Donna A Messner1, Adrian Towse2, Penny Mohr3, Martina Garau2.   

Abstract

Drug development takes place in a global marketplace, albeit with the USA and EU markets currently dominating. In the USA, demands for comparative effectiveness research have gained traction against a backdrop of health delivery reform, while European stakeholders deliberate the role of relative effectiveness in health technology assessment, trying to reduce the duplication of effort by regulators and health technology assessment bodies. In both arenas, drug-makers are faced with mounting drug development costs, and uncertainty over the types of evidence acceptable for a growing list of stakeholders. This article reports and compares future scenarios for evidence expectations for drugs for the USA and EU in 2020. The similarities, differences, and joint implications of the scenarios are considered to create an view of future evidence generation for drugs developed for these markets.

Keywords:  EMA; FDA; HTA; PCORI; adaptive licensing; comparative effectiveness research; drug development; effectiveness; efficacy; postauthorization efficacy studies; relative effectiveness; relative efficacy

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Year:  2015        PMID: 25730094     DOI: 10.2217/cer.15.8

Source DB:  PubMed          Journal:  J Comp Eff Res        ISSN: 2042-6305            Impact factor:   1.744


  3 in total

Review 1.  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

2.  Bridging the gap: Can International Consortium of Health Outcomes Measurement standard sets align outcomes accepted for regulatory and health technology assessment decision-making of oncology medicines.

Authors:  Rachel R J Kalf; Rick A Vreman; Diana M J Delnoij; Marcel L Bouvy; Wim G Goettsch
Journal:  Pharmacol Res Perspect       Date:  2021-04

Review 3.  Improving Interactions Between Health Technology Assessment Bodies and Regulatory Agencies: A Systematic Review and Cross-Sectional Survey on Processes, Progress, Outcomes, and Challenges.

Authors:  Richard Ofori-Asenso; Christine E Hallgreen; Marie Louise De Bruin
Journal:  Front Med (Lausanne)       Date:  2020-10-16
  3 in total

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