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A modern in vivo pharmacokinetic paradigm: combining snapshot, rapid and full PK approaches to optimize and expedite early drug discovery.
Li, Chun; Liu, Bo; Chang, Jonathan; Groessl, Todd; Zimmerman, Matthew; He, You-Qun; Isbell, John; Tuntland, Tove.
Afiliación
  • Li C; Department of Metabolism and Pharmacokinetics, Genomics Institute of the Novartis Research Foundation, Novartis Institute of Biomedical Research, San Diego, CA, USA.
Drug Discov Today ; 18(1-2): 71-8, 2013 Jan.
Article en En | MEDLINE | ID: mdl-22982770
ABSTRACT
Successful drug discovery relies on the selection of drug candidates with good in vivo pharmacokinetic (PK) properties as well as appropriate preclinical efficacy and safety profiles. In vivo PK profiling is often a bottleneck in the discovery process. In this review, we focus on the tiered in vivo PK approaches implemented at the Genomics Institute of the Novartis Research Foundation (GNF), which includes snapshot PK, rapid PK and full PK studies. These in vivo PK approaches are well integrated within discovery research, allow tremendous flexibility and are highly efficient in supporting the diverse needs and increasing demand for in vivo profiling. The tiered in vivo PK studies expedite compound profiling and help guide the selection of more desirable compounds into efficacy models and for progression into development.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Farmacocinética / Diseño de Fármacos / Modelos Biológicos Límite: Animals / Humans Idioma: En Revista: Drug Discov Today Asunto de la revista: FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Año: 2013 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Farmacocinética / Diseño de Fármacos / Modelos Biológicos Límite: Animals / Humans Idioma: En Revista: Drug Discov Today Asunto de la revista: FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Año: 2013 Tipo del documento: Article País de afiliación: Estados Unidos