Study title: Multiple dose, open-label, multicentric study for the conversion of immediate release Oxycodone (OxyIR) dose to controlled release Oxycodone (OxyContin) in order to assess the pharmacokinetics and characterize the efficacy and safety in pediatric patients from 6 to 16 years old. (USA & EU)
Type of medicine: Medicines containing chemical active substances | |||||
Therapeutic area: Anesthesia and Analgesia | |||||
Brands: Please see report, Please see report, Please see report | |||||
MAH holders: Please see report | |||||
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Active substance: OXYCODONE | |||||
ATC code: N02AA05 | |||||
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Scope of study: Clinical | |||||
Population of study subjects: | Preterm newborn Infants | Newborn infants (1 to 27 days) | Infants and toddlers (28 days to 24 months) | Children (2 to 11 years) | Adolescents (12 to 18 years) |
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