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Expanding Patient Access to Investigational New Drugs: Overview of Intermediate and Widespread Treatment Investigational New Drugs, and Emergency Authorization in Public Health Emergencies

Individual patients with life-threatening or severely debilitating diseases can petition the U.S. Food and Drug Administration (FDA) through their physicians to have expanded access (EA) to drugs that are in clinical trials but have not reached full FDA approval (the “single-patient” investigational...

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Détails bibliographiques
Publié dans:JACC Basic Transl Sci
Auteur principal: Van Norman, Gail A.
Format: Artigo
Langue:Inglês
Publié: Elsevier 2018
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6058931/
https://ncbi.nlm.nih.gov/pubmed/30062226
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jacbts.2018.02.001
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