Literature DB >> 22453190

Clinical pharmacology and orphan drugs: an informational inventory 2006-2010.

E D Bashaw1, L Fang.   

Abstract

Clinical pharmacology can have an important impact on the development of orphan drugs, i.e., therapeutic agents for rare diseases. This topic was explored at a US Food and Drug Administration (FDA) Advisory Committee meeting in March 2011.1 At that meeting, preliminary data were presented regarding the breakdown of the clinical pharmacology content in the approvals for orphan drugs in 2006–2010.These data, along with follow-up observations, are presented here, focusing on the in vivo study content and the relevant populations.

Mesh:

Year:  2012        PMID: 22453190     DOI: 10.1038/clpt.2012.23

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  4 in total

1.  Orphan drugs, orphan diseases. The first decade of orphan drug legislation in the EU.

Authors:  Roberta Joppi; Vittorio Bertele'; Silvio Garattini
Journal:  Eur J Clin Pharmacol       Date:  2012-10-23       Impact factor: 2.953

Review 2.  The evidence framework for precision cancer medicine.

Authors:  Jeffrey A Moscow; Tito Fojo; Richard L Schilsky
Journal:  Nat Rev Clin Oncol       Date:  2017-12-19       Impact factor: 66.675

3.  Drugs for rare disorders.

Authors:  Serge Cremers; Jeffrey K Aronson
Journal:  Br J Clin Pharmacol       Date:  2017-06-27       Impact factor: 4.335

4.  Dose-finding studies in drug development for rare genetic diseases.

Authors:  Lingshan Wang; Jie Wang; Ji Feng; Mary Doi; Salvatore Pepe; Michael Pacanowski; Robert N Schuck
Journal:  Orphanet J Rare Dis       Date:  2022-04-05       Impact factor: 4.123

  4 in total

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