Saltar al contenido
República del Perú · Observatorio de la producción científica universitaria
OApol.org Observatorio de Inteligencia Científica Universitaria del Perú
OApol.org
Inicio Universidades Publicaciones Investigadores
Repositorios
Tesis y trabajos académicosRevistas
Indicadores
Ranking trimestralRanking por carreraObjetivos de Desarrollo SostenibleReporte OCDERed neuronal 3D
Acerca
MetodologíaPrivacidad

Biosimilars approvals by thirteen regulatory authorities: A cross-national comparison

Machado F.L.D.S.; Cañás M.; Doubova S.V.; Urtasun M.A.; Marín G.H.; Osorio-de-Castro C.G.S.; Albuquerque F.C.; Ribeiro T.B.; Pont L.; Crisóstomo Landeros J.; Roldán Saelzer J.; Sepúlveda Viveros D.; Acosta A.; Machado Beltrán M.A.; Gordillo Alas L.I.; Orellana Tablas L.A.; Benko R.; Convertino I.; Bonaso M.; Tuccori M.; Kirchmayer U.; Contreras Sánchez S.E.; Rodríguez-Tanta L.Y.; Gutierrez Aures Y.; Lin B.; Alipour-Haris G.; Eworuke E.; Lopes L.C. · Regulatory Toxicology and Pharmacology (2023) · DOI: 10.1016/j.yrtph.2023.105485

Resumen

Biosimilars are biological medicines highly similar to a previously licensed reference product and their licensing is expected to improve access to biological therapies. This study aims to present an overview of biosimilars approval by thirteen regulatory authorities (RA). The study is a cross-national comparison of regulatory decisions involving biosimilars in Argentina, Australia, Brazil, Chile, Canada, Colombia, Europe, Hungary, Guatemala, Italy, Mexico, Peru and United States. We examined publicly available documents containing information regarding the approval of biosimilars and investigated the publication of public assessment reports for registration applications, guidelines for biosimilars licensing, and products approved. Data extraction was conducted by a network of researchers and regulatory experts. All the RA had issued guidance documents establishing the requirements for the licensing of biosimilars. However, only three RA had published public assessment reports for registration applications. In total, the investigated jurisdictions had from 19 to 78 biosimilars approved, most of them licensed from 2018 to 2020. In spite of the advance in the number of products in recent years, some challenges still persist. Limited access to information regarding the assessment of biosimilars by RA can affect confidence, which may ultimately impact adoption of these products in practice.

Instituciones: Universidad Científica del Sur