Literature DB >> 23938865

Unintended consequences of regulatory initiatives in childhood cancer drug development.

Peter C Adamson1.   

Abstract

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Year:  2013        PMID: 23938865     DOI: 10.1001/jamapediatrics.2013.2488

Source DB:  PubMed          Journal:  JAMA Pediatr        ISSN: 2168-6203            Impact factor:   16.193


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  7 in total

1.  Completion Rate and Reporting of Mandatory Pediatric Postmarketing Studies Under the US Pediatric Research Equity Act.

Authors:  Thomas J Hwang; Liat Orenstein; Aaron S Kesselheim; Florence T Bourgeois
Journal:  JAMA Pediatr       Date:  2019-01-01       Impact factor: 16.193

Review 2.  Improving the outcome for children with cancer: Development of targeted new agents.

Authors:  Peter C Adamson
Journal:  CA Cancer J Clin       Date:  2015-03-09       Impact factor: 508.702

3.  New regulatory paradigms for innovative drugs to treat pediatric diseases.

Authors:  Thomas J Hwang; Florence T Bourgeois
Journal:  JAMA Pediatr       Date:  2014-10       Impact factor: 16.193

Review 4.  Drug discovery in paediatric oncology: roadblocks to progress.

Authors:  Peter C Adamson; Peter J Houghton; Giorgio Perilongo; Kathy Pritchard-Jones
Journal:  Nat Rev Clin Oncol       Date:  2014-09-16       Impact factor: 66.675

Review 5.  A New Ethical Challenge for Institutional Review Boards (IRBs)/Ethics Committees (ECs) in the Assessment of Pediatric Clinical Trials.

Authors:  Klaus Rose; Hans Kummer
Journal:  Children (Basel)       Date:  2015-05-28

6.  Use of Modeling and Simulation in the Design and Conduct of Pediatric Clinical Trials and the Optimization of Individualized Dosing Regimens.

Authors:  C Stockmann; J S Barrett; J K Roberts; Cmt Sherwin
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2015-11-13

Review 7.  The contributions of the European Medicines Agency and its pediatric committee to the fight against childhood leukemia.

Authors:  Klaus Rose; Philip D Walson
Journal:  Risk Manag Healthc Policy       Date:  2015-11-05
  7 in total

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