Literature DB >> 30235525

Comparison of Stakeholder Metrics for Traditional and Adaptive Development and Licensing Approaches to Drug Development.

Lynn G Baird1,2, Mark R Trusheim3,2, Hans-Georg Eichler4, Ernst R Berndt4, Gigi Hirsch1.   

Abstract

This study evaluates whether an adaptive development and licensing approach to drug development, compared with approaches widely used today, might have tangible advantages across stakeholder groups, thereby facilitating the future adoption. Details involving actual and modeled clinical development and licensing programs for 3 case studies were used as inputs into a discounted cash flow spreadsheet model. Outputs included net present value and expected net present value, which are metrics considered as key incentives for pharmaceutical developers, and change in patient access over the product life and numbers of appropriately and inappropriately treated patients, which are metrics considered as key incentives for regulators, patients, and prescribers. Actual and modeled development programs were compared using an "adaptiveness" scoring algorithm. Generally, the more adaptive programs correlated with more favorable stakeholder outcomes. However, favorable outcomes may be overwhelmed in some cases, and the causative conditions and stakeholder reactions need to be defined.

Entities:  

Keywords:  adaptive licensing; adaptiveness score; clinical development; net present value; regulatory policy; stakeholder metrics

Year:  2013        PMID: 30235525     DOI: 10.1177/2168479013487355

Source DB:  PubMed          Journal:  Ther Innov Regul Sci        ISSN: 2168-4790            Impact factor:   1.778


  4 in total

1.  PIPELINEs: Creating Comparable Clinical Knowledge Efficiently by Linking Trial Platforms.

Authors:  M R Trusheim; A A Shrier; Z Antonijevic; R A Beckman; R K Campbell; C Chen; K T Flaherty; J Loewy; D Lacombe; S Madhavan; H P Selker; L J Esserman
Journal:  Clin Pharmacol Ther       Date:  2016-10-19       Impact factor: 6.875

2.  Social pharmaceutical innovation and alternative forms of research, development and deployment for drugs for rare diseases.

Authors:  Conor M W Douglas; Fernando Aith; Wouter Boon; Marina de Neiva Borba; Liliana Doganova; Shir Grunebaum; Rob Hagendijk; Larry Lynd; Alexandre Mallard; Faisal Ali Mohamed; Ellen Moors; Claudio Cordovil Oliveira; Florence Paterson; Vanessa Scanga; Julino Soares; Vololona Raberharisoa; Tineke Kleinhout-Vliek
Journal:  Orphanet J Rare Dis       Date:  2022-09-05       Impact factor: 4.303

3.  Adaptive Biomedical Innovation: Evolving Our Global System to Sustainably and Safely Bring New Medicines to Patients in Need.

Authors:  G Hirsch; M Trusheim; E Cobbs; M Bala; S Garner; D Hartman; K Isaacs; M Lumpkin; R Lim; K Oye; E Pezalla; P Saltonstall; H Selker
Journal:  Clin Pharmacol Ther       Date:  2016-10-22       Impact factor: 6.875

Review 4.  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
  4 in total

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