Healthy Skepticism Library item: 11191
Warning: This library includes all items relevant to health product marketing that we are aware of regardless of quality. Often we do not agree with all or part of the contents.
 
Publication type: Journal Article
Ceci A, Felisi M, Baiardi P, Bonifazi F, Catapano M, Giaquinto C, Nicolosi A, Sturkenboom M, Neubert A, Wong I.
Medicines for children licensed by the European Medicines Agency (EMEA): the balance after 10 years.
Eur J Clin Pharmacol 2006 Nov; 62:(11):947-52
http://www.springerlink.com/content/p003t463tw551331/
Abstract:
OBJECTIVE: The 1995-2005 balance of EMEA activities in the field of paediatric medicines was evaluated, taking into account the number both of drugs authorised for children and paediatric studies supporting the Marketing Authorisation (MA).
METHODS: Data on drugs authorised by EMEA were extracted from EPARs (European Public Assessment Reports). Active substance, year of approval, anatomical, therapeutic and chemical (ATC) code, indication, orphan status, ages, and registrative clinical studies characteristics were assessed.
RESULTS: The percentage of authorised substances for paediatrics is 33.3%. This percentage decreased or increased when different subsets of medicines were considered [medicines for children under 2 years (23.4%), N-ATC code drugs (6%) and orphan drugs (46.4%)]. A total of 165 trials were included in the MA dossiers of 51 drugs at the time of approval, and additional 22 studies were added to the dossiers of 12 active substances submitted for paediatric variations. PK and Efficacy/Safety studies were performed for 32 (52%) active substances, while either one PK or one Efficacy/Safety study was carried out for 43 (69%) and 45 (73%) substances, respectively.
CONCLUSIONS: This report demonstrates that the total number of paediatric medicines approved by EMEA is stable over the 10-year period, while an increase in drugs to treat serious or orphan diseases has been observed. In addition, under the Centralised Procedure, a valuable number of paediatric trials have been submitted to support drug approval.
Keywords:
EMEA - Marketing authorisation - Paediatrics
Publication Types:
Comparative Study
Research Support, Non-U.S. Gov't
MeSH Terms:
Adolescent
Age Factors
Child
Child, Preschool
Databases, Factual
Drug Approval/legislation & jurisprudence*
Drug Utilization Review/trends*
Europe
Government Agencies*
Humans
Infant
Infant, Newborn
Licensure*
Orphan Drug Production/legislation & jurisprudence
Pediatrics
Pharmacoepidemiology/trends