The clinical outcomes of three pivotal clinical trials with paliperidone ER, an atypical antipsychotic were prospectively predicted with a model using a limited amount of paliperidone ER pharmacokinetic data, human in vivo D2-receptor occupancy data and the generally accepted D2-receptor derived therapeutic window hypothesis. The latter was further substantiated using historical risperidone safety data. Model predictions guided the selection of the dose range for clinical trials, particularly with regards to the extremes of the dose range studied. © American Association of Pharmaceutical Scientists 2011.
CITATION STYLE
de Ridder, F., & Vermeulen, A. (2011). Balancing efficacy and safety in the clinical development of an atypical antipsychotic, paliperidone extended-release. AAPS Advances in the Pharmaceutical Sciences Series, 2011(1), 345–361. https://doi.org/10.1007/978-1-4419-7415-0_16
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