Concentration-QT (C-QT) modeling has been conducted for multiple compounds at various stages of development in different therapeutic areas. Data from available single and multiple ascending-dose (SAD/MAD) studies were pooled to construct population C-QT models, with post hoc predictions of concentration from a pharmacokinetic model.
Author(s): Shashank Rohatagi, Timothy Carrothers, Jonathan Wagg, Tatiana Khariton
Year: 2009 年 11 月 1 日
