Testing Medications in Children
- 31 October 2002
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 347 (18), 1462-1470
- https://doi.org/10.1056/nejmhpr021646
Abstract
To stimulate more evaluation of the safety and efficacy of medications in children, two federal regulations were established. The pediatric exclusivity provision gives an additional six months of patent protection to companies that voluntarily test a medication in children, whereas the pediatric rule requires pediatric studies if a drug is important for children.Keywords
This publication has 17 references indexed in Scilit:
- Ethicists Fault Review of Children's StudyScience, 2002
- Off label prescribing to children in primary care in Germany: retrospective cohort studyBMJ, 2002
- Unlicensed and off label drug use by children in the community: cross sectional studyBMJ, 2002
- Unlicensed and off label prescription of drugs to children: population based cohort studyBMJ, 2002
- Improving Protection for Research SubjectsNew England Journal of Medicine, 2002
- Unapproved and Off-Label Use of Drugs in a Children's HospitalNew England Journal of Medicine, 2000
- The Ethics of Clinical Trials: A Child's ViewPublished by Cambridge University Press (CUP) ,2000
- Representation of African-Americans, Hispanics, and Whites in National Cancer Institute Cancer Treatment TrialsJNCI Journal of the National Cancer Institute, 1996
- PATHOLOGIC EFFECTS OF ELIXIR OF SULFANILAMIDE (DIETHYLENE GLYCOL) POISONINGJAMA, 1938
- ELIXIR OF SULFANILAMIDEMASSENGILLJAMA, 1937