Abstract
The Kind-Philipp foundation invited a group of international experts from academia, industry, and regulatory institutions to discuss aspects of new drug development in pediatric oncology. The current design, conduct and infrastructure of clinical trials in Europe and the United States, recent regulatory changes of drug development, and the impact of the likely availability of more targeted anti-cancer agents on drug development for pediatric cancers were discussed. This included a review of risk factors, surrogate markers, novel targets, and new anti-cancer agents for pediatric cancers. A special effort was made to define the requirements of well performed clinical trials, including target evaluation, trial design, use of pharmacokinetic (PK) studies, surrogate markers, ethical, and statistical aspects. The greater need for collaboration beyond the National level was recognized.
Original language | English (US) |
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Pages (from-to) | 236-239 |
Number of pages | 4 |
Journal | Klinische Padiatrie |
Volume | 214 |
Issue number | 4 |
DOIs | |
State | Published - Jul 1 2002 |
Keywords
- Cancer
- Childhood
- Clinical trial
- Targeted therapy
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health