Abstract
There is a well-known knowledge gap regarding the efficacy and safety of
medicines in children of all ages and children are often treated with
medicines off-label. Children are thus deprived of treatment based on the
same quality of information that guides treatment in adults. The knowledge
gap regarding efficacy and safety of medicines in children has been
acknowledged by authorities and is reflected in legislation both in North
America and in the European Union. Recent reports on the effects of
legislation indicates that paediatric clinical trials remain a
challenge.
Paediatric clinical trials are needed in the entire developmental age
spectrum and are especially needed in certain therapy areas. Paediatric
clinical trials have special features compared with trials in adults, and
these need to be taken into account. These special features include
scientific issues related to small samples and heterogeneity, the
consent/assent procedure, the need for age-appropriate study information,
specific outcomes and safety issues related to development and maturation.
Competence in paediatric clinical trials is required in both designing,
planning, co-ordinating and organising paediatric clinical trials, as well
as research infrastructure and networks to increase power and disseminate
information and expert advice. Strengthening of paediatric clinical research
is essential to facilitate generating the data that will let children enjoy
new medical advances in a similar manner as adults.
Subject
Pediatrics, Perinatology and Child Health
Cited by
29 articles.
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