Your browser doesn't support javascript.
loading
The Impact of the Priority Review Voucher on Research and Development for Tropical Diseases.
Aerts, Celine; Barrenho, Eliana; Miraldo, Marisa; Sicuri, Elisa.
Afiliação
  • Aerts C; ISGlobal, Hospital Clínic, Universitat de Barcelona, Carrer Rosselló 132, 08036, Barcelona, Spain. celine.aerts24@gmail.com.
  • Barrenho E; Business School, Imperial College London, London, UK.
  • Miraldo M; Organisation of Economic Co-operation and Development, Employment, Labour and Social Affairs Directorate, Health Division, Paris, France.
  • Sicuri E; Business School, Imperial College London, London, UK.
Pharmaceut Med ; 36(3): 189-197, 2022 06.
Article em En | MEDLINE | ID: mdl-35588350
BACKGROUND: In 2007, the priority review voucher (PRV) was implemented in the US to incentivize research and development (R&D) for tropical diseases. The PRV is issued by the US FDA and grants a quicker review to manufacturers upon successful development of a product for a disease eligible for the program. OBJECTIVE: The objective of this analysis was to assess whether the PRV has incentivized R&D (measured as clinical trial activity) for the intended tropical diseases. METHOD: We used a difference-in-difference-in-differences (DDD) strategy by exploiting variation in its implementation across diseases and registries around the world. Clinical trials were retrieved from the World Health Organization International Clinical Trials Registry Platform for the years 2005-2019. RESULTS: We found a positive, but not statistically significant, effect of the PRV on stimulating R&D activity. Delayed effects of the policy could not be found. CONCLUSION: Our findings, which were robust across a series of robustness tests, suggest that the PRV program is not associated with a trigger in innovation for neglected diseases and therefore should not be considered as a stand-alone solution. It should be supplemented with other government measures to incentivize R&D activity. To increase the value of the program, we recommend that the PRV only be awarded to novel products and not to products that have already been licensed outside the US. Doing so would restrict the number of vouchers awarded and slow down their ongoing market depreciation. Finally, we propose that product sponsors be required to submit an access plan for PRV-awarded products.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Limite: Humans País/Região como assunto: America do norte Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Limite: Humans País/Região como assunto: America do norte Idioma: En Ano de publicação: 2022 Tipo de documento: Article