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Phase I dose-escalation study of the thioxanthone SR271425 administered intravenously once every 3 weeks in patients with advanced malignancies

This study was performed to determine the dose limiting toxicity (DLT), the recommended phase II dose and the pharmacokinetic profile for SR271425, given over 1 h every 3 weeks. The initial starting dose of SR271425 was 17 mg/m(2). Patient selection was based on common phase I criteria as well as ad...

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Autores principales: Goncalves, Priscila H., High, Francine, Juniewicz, Paul, Shackleton, Gareth, Li, Jing, Boerner, Scott, LoRusso, Patricia M.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2008
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3771109/
https://ncbi.nlm.nih.gov/pubmed/18449472
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10637-008-9135-2
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