PEDIATRIC DRUG TRIALS IN CHINA

2015 ◽  
Vol 101 (1) ◽  
pp. e1.12-e1
Author(s):  
Guo-Xiang Hao ◽  
Xiao-Ling Wang ◽  
A-Dong Shen ◽  
Evelyne Jacqz-Aigrain ◽  
Wei Zhao

Background and objectiveThe introduction of the Pediatric Regulation by the European Union, together with the renewal of the Pediatric Rule by the US Food and Drug Administration on the requirements for pediatric labeling made it mandatory for sponsors to develop drugs for the pediatric population and promotes the pediatric drug trials in Europe and US. However, very little is known about the situation of pediatric drug trials in other countries, particularly in China, home to nearly 300 millions children. In order to support the global research in pediatric drug development and clarify the specific characteristics of pediatric drugs trials in China, we analyzed the drug trials registered in the Chinese Clincial Trial Registry database.MethodsThe pediatric drug trials registered in Chinese Clincial Trial Registry database between 2007 and 2014 were analyzed. The following information was extracted from the database by two authors: type of the trial, registered time, drug name, inclusion and exclusion criteria, population, number of patients, and sponsor.ResultsAmong all (4786) trials registered, 729 trials (15.2%) involved the pediatric population, and only 308 trials (6.4%) were pediatric drug trials. From 2007 to 2013 pediatric drug trials increased from 3 to 121. There were 66 pediatric drug trials including Chinese traditional medicine.ConclusionOur results demonstrated for the first time the situation of pediatric drug trials in China. Consistent with the initiatives of promoting pediatric drug development in Europe and US, the pediatric drug trial in China made a significant progress after 2012. The pediatric drug legislation is urgently needed in China.

2020 ◽  
Vol 25 (7) ◽  
pp. 565-573
Author(s):  
Gilbert J. Burckart ◽  
Clara Kim

This lecture was given by Dr. Burckart in association with presentation of the 2014 Sumner J. Yaffe Lifetime Achievement Award in Pediatric Pharmacology and Therapeutics, which is selected by the Pediatric Pharmacy Association. Multiple factors make conducting drug studies in the pediatric population difficult, resulting in a historic lack of information surrounding safe and efficacious drug dosing in children. The paradigm in pediatric drug development has shifted from normal science being that children are therapeutic orphans in the drug development system, to a model drift caused by pediatric legislation, to a model crisis caused by failed pediatric drug development trials, to finally a model revolution that includes pediatric patients routinely in drug development. Major regulatory actions and the accumulation of scientific evidence has created an environment where clinicians can expect properly labeled drug usage information for the pediatric population.


Author(s):  
Klaus Rose ◽  
Oishi Tanjinatus ◽  
Jane Grant‐Kels ◽  
Earl B. Ettienne ◽  
Pasquale Striano ◽  
...  

2006 ◽  
Vol 103 (1) ◽  
pp. 49-51 ◽  
Author(s):  
Lex W. Schultheis ◽  
Lisa L. Mathis ◽  
Rigoberto A. Roca ◽  
Arthur F. Simone ◽  
Sharon H. Hertz ◽  
...  

2015 ◽  
Vol 98 (3) ◽  
pp. 328-335 ◽  
Author(s):  
J Wang ◽  
D Avant ◽  
D Green ◽  
S Seo ◽  
J Fisher ◽  
...  

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