Literature DB >> 27187789

Conceptual clarifications regarding Chilean Act 20850 on public funding of high-cost diseases.

Miguel Hugo Kottow Lang1.   

Abstract

In 2015, Chile enacted the 20850 law, providing public funds for rare and costly diseases that demanded high diagnostic and therapeutic expenditures. The law modifies the Chilean Sanitary Code regulation of research with human beings, aiming at the protection of subjects by securing post-investigational medical benefits and insurance coverage for damage imputable to the research they participated in. Due to ambiguous phrasing, a polemic rose for fear that these protective measures applied to all clinical research, although a careful reading of the law in its context clearly suggests that it refers to phase I therapeutic trials. This paper stresses the distinction between compassionate use and genuine phase I/II therapeutic trials aimed at both pharmacodynamics and an intended therapeutic effect for severe and progressive diseases that are therapeutically orphaned, emphasizing the ethical and medical duty of providing post-trial beneficial medication.

Entities:  

Keywords:  clinical trials; compassionate use; rare diseases

Mesh:

Year:  2016        PMID: 27187789     DOI: 10.5867/medwave.2016.03.6436

Source DB:  PubMed          Journal:  Medwave        ISSN: 0717-6384


  1 in total

Review 1.  A civil society view of rare disease public policy in six Latin American countries.

Authors:  Mo Mayrides; Eva Maria Ruiz de Castilla; Silvina Szelepski
Journal:  Orphanet J Rare Dis       Date:  2020-02-27       Impact factor: 4.123

  1 in total

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