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Titlebook: Applications of Pharmacokinetic Principles in Drug Development; Rajesh Krishna Textbook 2004 Kluwer Academic/Plenum Publishers, New York 2

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发表于 2025-3-21 18:49:52 | 显示全部楼层 |阅读模式
期刊全称Applications of Pharmacokinetic Principles in Drug Development
影响因子2023Rajesh Krishna
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图书封面Titlebook: Applications of Pharmacokinetic Principles in Drug Development;  Rajesh Krishna Textbook 2004 Kluwer Academic/Plenum Publishers, New York 2
影响因子This volume is an important advancement in the application ofpharmacokinetic (PK) and pharmacodynamic (PO) principles to . drug development. The series of topics presented deal with the application of these tools to everyday decisions that a pharmaceutical scientist encounters. The ability to integrate these topics using PK and PO methods has optimized drug development pathways in the clinic. New technologies in the areas of in vitro assays that are more predictive of human absorption and metabolism and advancement in bioanalytical assays are leading the way to minimize drug failures in later, more expensive clinical development programs. of Pharmacokinetics and pharmacodynamics have become an important component understanding the drug action on the body and is becoming increasingly important in drug labeling due to it‘s potential for predicting drug behavior in populations that may be difficult to study in adequate numbers during drug development. The ability to correlate drug exposure to effect and model it during the drug development value chain provides valuable insight into optimizing the next steps to derive maximum information from each study. These principles and modeling t
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Sekundärprophylaxe in der Gefäßchirurgie assure in vivo bioavailability / bioequivalence (BA/BE). Assessing the risk / benefit criteria and global regulatory requirements that may include human studies for formulation or chemistry changes is a key component when determining the ultimate benefit of contemplated product changes.
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Textbook 2004s of topics presented deal with the application of these tools to everyday decisions that a pharmaceutical scientist encounters. The ability to integrate these topics using PK and PO methods has optimized drug development pathways in the clinic. New technologies in the areas of in vitro assays that
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K. J. Husfeldt,R. Raschke,M. Mühee to market is only 10-20% (Prentis et al., 1988; Kennedy, 1997). While many factors contribute to a high failure rate, it is somewhat surprising that poor pharmacokinetic properties, such as poor oral bioavailability, account for almost half of the failures in clinical development.
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H. Schumacher,N. Diehm,J. R. Allenberges and the width of the therapeutic window between effective and toxic blood concentrations, specific subpopulations might require a dose regimen which diverges from the population average regimen. Unmasking and exploring these special populations during clinical development is one of the focuses of clinical pharmacology.
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