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1.
Clin Transl Sci ; 13(3): 451-461, 2020 05.
Artigo em Inglês | MEDLINE | ID: mdl-31909876

RESUMO

Developing a novel drug, including discovery, nonclinical toxicology studies, initial clinical trials, and thorough pivotal studies, may take many years. Once an applicant has generated this comprehensive body of data, the final step prior to regulatory approval is Health Authority review of the marketing authorization application. Review by regulatory authorities to evaluate whether the data support a positive benefit/risk profile takes many months, adding additional time before patients may access therapy. In this paper, we discuss the various opportunities the US Food and Drug Administration and the European Medicines Agency offer to expedite the drug development and regulatory approval timelines for drugs intended to treat serious diseases and unmet medical needs.


Assuntos
Aprovação de Drogas/legislação & jurisprudência , União Europeia , United States Food and Drug Administration/legislação & jurisprudência , Estados Unidos
2.
Clin Transl Sci ; 12(4): 334-342, 2019 07.
Artigo em Inglês | MEDLINE | ID: mdl-30884199

RESUMO

Testing novel drugs on fellow human beings is fraught with potential ethical concerns; however, developing drugs to treat the wide spectrum of human diseases and disorders is a moral imperative. How do we best navigate the balance between protecting the individual vs. the greater good? Global government regulatory bodies are accountable for ensuring that medical experiments on human subjects are appropriately justified and subject to close oversight. In this article, we focus on two major global health authorities, the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA), and the path to legally treating humans with new investigational products.


Assuntos
Ensaios Clínicos como Assunto/legislação & jurisprudência , Aplicação de Novas Drogas em Teste/legislação & jurisprudência , Controle Social Formal , Europa (Continente) , Experimentação Humana/ética , Humanos , Estados Unidos , United States Food and Drug Administration
3.
Trends Genet ; 18(1): 29-34, 2002 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-11750698

RESUMO

Odorant receptor genes comprise the largest known family of G-protein-coupled receptors in vertebrates. These receptor genes are tightly clustered in the genomes of every vertebrate organism investigated, including zebrafish, mice and humans, and they appear to have expanded and duplicated throughout evolution. In a mechanism that has yet to be elucidated, each olfactory neuron expresses a single receptor gene. This highly restricted expression pattern underlies the ability to distinguish between a wide variety of odorants. Here, we address the evolutionary expansion of odorant receptor genes and the role genomic organization of these genes might have in their tightly regulated expression.


Assuntos
Receptores Odorantes/genética , Alelos , Animais , Evolução Biológica , Regulação da Expressão Gênica , Genoma , Humanos , Camundongos , Modelos Genéticos , Família Multigênica , Neurônios Receptores Olfatórios/metabolismo , Peixe-Zebra/genética
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