Abstract
Abstract
Background
The objective of this paper is to analyze the prices of biological drugs in the treatment of Rheumatoid Arthritis (RA) in three Latin American countries (Brazil, Colombia and Mexico), as well as in Spain and the United States of America (US), from the point of market entry of biosimilars.
Methods
We analyzed products authorized for commercialization in the last 20 years, in Brazil, Colombia, and Mexico, comparing them to the United States of America (USA) and Spain. For this analysis, we sought the prices and registries of drugs marketed between 1999 and October 1, 2019, in the regulatory agencies’ databases. The pricing between countries was based on purchasing power parity (PPP).
Results
The US authorized the commercialization of 13 distinct biologicals and four biosimilars in the period. Spain and Brazil marketed 14 biopharmaceuticals for RA, ten original, four biosimilars. Colombia and Mexico have authorized three biosimilars in addition to the ten biological ones. For biological drug prices, the US is the most expensive country. Spain’s price behavior seems intermediate when compared to the three LA countries. Brazil has the highest LA prices, followed by Mexico and Colombia, which has the lowest prices. Spain has the lowest values in PPP, compared to LA countries, while the US has the highest prices.
Conclusion
The economic effort that LA countries make to access these medicines is much higher than the US and Spain. The use of the PPP ensured a better understanding of the actual access to these inputs in the countries analyzed.
Publisher
Springer Science and Business Media LLC
Reference35 articles.
1. Burgos-Vargas R, Catoggio LJ, Galarza-Maldonado C, Ostojich K, Cardiel MH. Current therapies in rheumatoid arthritis: a Latin American perspective. Reumatol Clínica English Ed. 2013;9(2):106–12. https://doi.org/10.1016/j.reumae.2013.01.007.
2. Brasil. Ministério da Saúde. Coordenação de Gestão de Protocolos Clínicos e Diretrizes Terapêuticas. Protocolo Clínico e Diretrizes Terapêuticas da Artrite Reumatoide . Brasilia; 2020 [access 2020 Nov 19]. p. 171. Available from: http://conitec.gov.br/images/Consultas/Relatorios/2020/Relatrio_Artrite_Reumatoide_CP_21_2020.pdf
3. Zozaya N, Pérez-Camarero S, Martínez-Galdeano L. La regulación y financiación de los medicamentos biosimilares en la OCDE. Madrid: Weber.Org.Es.; 2017. Report No.: 01/2017. Available from: http://weber.org.es/wp-content/uploads/2018/04/La_Regulacion_y_financiacion_de_los-biosimilares_en_la-OCDE_weber.pdf
4. Castañeda-Hernández G, Szekanecz Z, Mysler E, Azevedo VF, Guzman R, Gutierrez M, et al. Biopharmaceuticals for rheumatic diseases in Latin America, Europe, Russia, and India: innovators, biosimilars, and intended copies. Jt Bone Spine. 2014;81(6):471–7 Available from: https://linkinghub.elsevier.com/retrieve/pii/S1297319X14000992.
5. Levenhagen K, Davies C, Perdomo M, Ryans K, Gilchrist L. United Rheumatology Clinical Practice Guideline. Vol. 97; 2019.
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