Literature DB >> 33216976

The Evidence REVEAL Study: Exploring the Use of Real-World Evidence and Complex Clinical Trial Design by the European Pharmaceutical Industry.

Peter Varnai1, Anoushka Davé1, Kristine Farla1, Anke Nooijen2, Liana Petrosova2.   

Abstract

The rapid evolution of science and technology allows innovative approaches to generate new types of evidence about the effectiveness of medical product development so as to speed up patients' access to better diagnostics and treatment. Our study explored how two emerging approaches, the use of real-world evidence (RWE) and complex clinical trial (CCT) design, are currently being used by the pharmaceutical industry to support premarketing authorization of medical product development and reviewed the international landscape for regulatory acceptance of such novel approaches. Combining evidence from a literature review, company survey, and interviews with international regulators and experts, we found that 80% of Europe-based pharmaceutical companies have used RWE and 50% have used CCTs, in some capacity. Further, we present case examples of how companies are using these approaches and how international regulators are preparing for such developments. To conclude, we provide a set of recommendations for European industry and regulators to consider so that these novel approaches achieve their full potential within the EU regulatory system.
© 2020 The Authors. Clinical Pharmacology & Therapeutics published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.

Entities:  

Year:  2020        PMID: 33216976     DOI: 10.1002/cpt.2103

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


  4 in total

Review 1.  Pharmacokinetic and Pharmacodynamic Modeling of siRNA Therapeutics - a Minireview.

Authors:  Jae Yoon Jeon; Vivaswath S Ayyar; Amitava Mitra
Journal:  Pharm Res       Date:  2022-07-12       Impact factor: 4.580

Review 2.  Computational drug repurposing based on electronic health records: a scoping review.

Authors:  Nansu Zong; Andrew Wen; Sungrim Moon; Sunyang Fu; Liwei Wang; Yiqing Zhao; Yue Yu; Ming Huang; Yanshan Wang; Gang Zheng; Michelle M Mielke; James R Cerhan; Hongfang Liu
Journal:  NPJ Digit Med       Date:  2022-06-14

3.  Use of Real-World Data and Evidence in Drug Development of Medicinal Products Centrally Authorized in Europe in 2018-2019.

Authors:  Sini Marika Eskola; Hubertus Gerardus Maria Leufkens; Andrew Bate; Marie Louise De Bruin; Helga Gardarsdottir
Journal:  Clin Pharmacol Ther       Date:  2021-11-16       Impact factor: 6.903

4.  The effect of adding real-world evidence to regulatory submissions on the breadth of population indicated for rare disease medicine treatment by the European Medicines Agency.

Authors:  Ravi Jandhyala
Journal:  J Pharm Policy Pract       Date:  2022-05-04
  4 in total

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