Marlene Braz

Fundação Oswaldo Cruz
  •  62
    Ethical issues related to the access to orphan drugs in Brazil: the case of mucopolysaccharidosis type I
    with Raquel Boy, Ida V. D. Schwartz, Bárbara C. Krug, Luiz C. Santana-da-Silva, Carlos E. Steiner, Angelina X. Acosta, Erlane M. Ribeiro, Marcial F. Galera, and Paulo G. C. Leivas
    Journal of Medical Ethics 37 (4): 233-239. 2011.
    Mucopolysaccharidosis type I (MPS I) is a rare lysosomal storage disorder treated with bone marrow transplantation or enzyme replacement therapy with laronidase, a high-cost orphan drug. Laronidase was approved by the US Food and Drug Administration and the European Medicines Agency in 2003 and by the Brazilian National Health Surveillance Agency in 2005. Many Brazilian MPS I patients have been receiving laronidase despite the absence of a governmental policy regulating access to the drug. Epide…Read more