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Article: The potential role of biosimilars in healthcare sustainability in Latin America

TitleThe potential role of biosimilars in healthcare sustainability in Latin America
Authors
KeywordsBiologic
biosimilar
cost saving
education
Latin America
policy
regulatory
Issue Date29-May-2025
PublisherTaylor and Francis Group
Citation
Expert Opinion on Biological Therapy, 2025, v. 25, n. 6, p. 633-647 How to Cite?
AbstractIntroduction: Latin American (LatAm) countries face significant increases in healthcare expenditure, driven largely by population growth and aging, and the rising prevalence of cancer and other chronic diseases. Growing demand and high costs of biologic medicines present barriers to patient access in this region. Biosimilars can improve the affordability and accessibility of biologics, supporting long-term healthcare sustainability. However, their uptake in LatAm has generally been slow. Areas covered: Challenges and barriers to the use of biosimilars and potential strategies to increase biosimilar uptake in LatAm, drawing on learnings from Europe and the U.S.A. Expert opinion: Potential initiatives to drive biosimilar uptake across LatAm include (1) harmonized regulatory processes for biosimilars, with reimbursement policies that prioritize their use and incentives to encourage prescribing; (2) education for key stakeholders to limit misinformation about biosimilars, provide reassurance about safety and efficacy, and increase understanding and acceptance; (3) simplified health technology assessment processes for biosimilars that expedite or adapt some aspects of the traditional approach; and (4) coordinated regional efforts to enable national healthcare systems to purchase medicines in the most cost-effective way, with value frameworks to support decision-making and the implementation of centralized purchasing, competition policies, and risk-sharing agreements.
Persistent Identifierhttp://hdl.handle.net/10722/364140
ISSN
2023 Impact Factor: 3.6
2023 SCImago Journal Rankings: 1.104

 

DC FieldValueLanguage
dc.contributor.authorSchaffel, Rony-
dc.contributor.authorCornes, Paul-
dc.contributor.authorEspinoza, Manuel A.-
dc.contributor.authorGómez-Almaguer, David-
dc.contributor.authorMaiolino, Angelo-
dc.contributor.authorFreire, Daniel-
dc.contributor.authorFoierl, Tobias-
dc.date.accessioned2025-10-23T00:35:13Z-
dc.date.available2025-10-23T00:35:13Z-
dc.date.issued2025-05-29-
dc.identifier.citationExpert Opinion on Biological Therapy, 2025, v. 25, n. 6, p. 633-647-
dc.identifier.issn1471-2598-
dc.identifier.urihttp://hdl.handle.net/10722/364140-
dc.description.abstractIntroduction: Latin American (LatAm) countries face significant increases in healthcare expenditure, driven largely by population growth and aging, and the rising prevalence of cancer and other chronic diseases. Growing demand and high costs of biologic medicines present barriers to patient access in this region. Biosimilars can improve the affordability and accessibility of biologics, supporting long-term healthcare sustainability. However, their uptake in LatAm has generally been slow. Areas covered: Challenges and barriers to the use of biosimilars and potential strategies to increase biosimilar uptake in LatAm, drawing on learnings from Europe and the U.S.A. Expert opinion: Potential initiatives to drive biosimilar uptake across LatAm include (1) harmonized regulatory processes for biosimilars, with reimbursement policies that prioritize their use and incentives to encourage prescribing; (2) education for key stakeholders to limit misinformation about biosimilars, provide reassurance about safety and efficacy, and increase understanding and acceptance; (3) simplified health technology assessment processes for biosimilars that expedite or adapt some aspects of the traditional approach; and (4) coordinated regional efforts to enable national healthcare systems to purchase medicines in the most cost-effective way, with value frameworks to support decision-making and the implementation of centralized purchasing, competition policies, and risk-sharing agreements.-
dc.languageeng-
dc.publisherTaylor and Francis Group-
dc.relation.ispartofExpert Opinion on Biological Therapy-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectBiologic-
dc.subjectbiosimilar-
dc.subjectcost saving-
dc.subjecteducation-
dc.subjectLatin America-
dc.subjectpolicy-
dc.subjectregulatory-
dc.titleThe potential role of biosimilars in healthcare sustainability in Latin America -
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1080/14712598.2025.2507173-
dc.identifier.pmid40374575-
dc.identifier.scopuseid_2-s2.0-105007162579-
dc.identifier.volume25-
dc.identifier.issue6-
dc.identifier.spage633-
dc.identifier.epage647-
dc.identifier.eissn1744-7682-
dc.identifier.issnl1471-2598-

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