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Pediatric Antihypertensive Trial Failures: Analysis of Endpoints and Dose Range
Historically, drugs prescribed for children have not been studied in pediatric populations. Since 1997, however, a 6-month extension of marketing rights is granted if manufacturers conduct Food and Drug Administration (FDA)-defined pediatric trials. In nearly half the drugs studied, there were unexp...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2782749/ https://ncbi.nlm.nih.gov/pubmed/18332283 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/HYPERTENSIONAHA.107.108886 |
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