Journal Article10.1542/PEDS.2010-3381
Globalized pediatric research.
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TL;DR: Only 11% of the trials reviewed by Pasquali et al were conducted solely outside the United States, a far smaller proportion than the “approximately one-third” in the study of adult trials by large US pharmaceutical firms reported by Glickman et al.
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Abstract: Pasquali et al1 have provided important data regarding pediatric studies conducted under pediatric exclusivity provisions of US laws that have been highly successful in incentivizing the generation of much needed information regarding pediatric usage of drugs.2 However, the authors raised many theoretical concerns about global pediatric trials while providing few data to support such concerns. Our own experience questions whether an examination of all of the data should be undertaken before reaching the broad conclusions presented in the article. Only 11% of the trials reviewed by Pasquali et al were conducted solely outside the United States, a far smaller proportion than the “approximately one-third” in the study of adult trials by large US pharmaceutical firms reported by Glickman et al,3 notwithstanding the assertion by Pasquali et al that their findings were similar to those of Glickman et al. Although data regarding indication were not presented for this 11%, Pasquali et al noted that several overseas trials in their study were performed …
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Citations
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Safe and Effective Medicines for Children: Pediatric Studies Conducted Under the Best Pharmaceuticals for Children Act and the Pediatric Research Equity Act
Marilyn J. Field,Thomas F. Boat +1 more
- 03 Apr 2013
TL;DR: A committee appointed by the IOM reviewed and assessed a representative sample of labeling changes and other FDA actions related to requested or required studies for the period from July 1, 1998, through December 31, 2010.
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Pediatric clinical trials in Latin America and Guyana: present views of local practitioners and ways to embrace the future.
Sara Arenas-Lopez,Carlos Fajardo,Adolf Valls i Soler,Jorge Raúl García-Corzo,Ma Victoria Lima-Rogel,Graciela Calle,Roberio Leite,Edgard Lobos,Querida Hume-Wright,Stuart MacLeod +9 more
TL;DR: There is some momentum toward the development of a Latin American network for the facilitation and supervision of pediatric clinical research in the North, Central, and South American regions.
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References
International Conference On Harmonisation Of Technical Requirements For Registration Of Pharmaceuticals For Human Use
John Abraham
- 01 Jan 2010
TL;DR: The official goal of the ICH is to harmonize inconsistent technical regulatory standards across different regions and countries in order to avoid costly, wasteful, and duplicative testing in pharmaceutical development.
Ethical and scientific implications of the globalization of clinical research
Seth W. Glickman,John G. McHutchison,Eric D. Peterson,Charles B. Cairns,Charles B. Cairns,Robert A. Harrington,Robert M. Califf,Kevin A. Schulman +7 more
TL;DR: The authors discuss the implications of the globalization of clinical research and make recommendations about how to address the challenges that have emerged.
Globalization of Pediatric Research: Analysis of Clinical Trials Completed for Pediatric Exclusivity
TL;DR: The majority of published pediatric trials conducted under the Pediatric Exclusivity Provision included sites outside the United States, and more than one-third of trials enrolled patients in developing/transition countries.
Economic Return of Clinical Trials Performed Under the Pediatric Exclusivity Program
Jennifer S. Li,Eric L. Eisenstein,Henry G. Grabowski,Elizabeth D. Reid,Barry Mangum,Kevin A. Schulman,John V. Goldsmith,M. Dianne Murphy,Robert M. Califf,Daniel K. Benjamin +9 more
TL;DR: The economic return for pediatric exclusivity is variable and as an incentive to complete much-needed clinical trials in children, Pediatrics Exclusivity can generate lucrative returns or produce more modest returns on investment.