Integration of Pharmacokinetics, Pharmacodynamics, and Toxicokinetics in Rational Drug Development
Published on 30. May 2013
Book
Paperback/Softback
XVI, 270 pages
978-1-4757-1522-4 (ISBN)
Description
Proceedings of a conference sponsored by the American Association of Pharmaceutical Scientists, the U.S. Food and Drug Administration, and the American Society for Clinical Pharmacology and Therapeutics, held in Arlington, Virginia, April 24-26, 1991
More details
Edition
Softcover reprint of the original 1st ed. 1993
Language
English
Place of publication
New York
United States
Target group
Professional and scholarly
Research
Illustrations
5 s/w Abbildungen
XVI, 270 p. 5 illus.
Dimensions
Height: 244 mm
Width: 170 mm
Thickness: 16 mm
Weight
502 gr
ISBN-13
978-1-4757-1522-4 (9781475715224)
DOI
10.1007/978-1-4757-1520-0
Schweitzer Classification
Other editions
Additional editions
A. Yacobi | J.P. Skelly | Vinod P. Shah
Integration of Pharmacokinetics, Pharmacodynamics, and Toxicokinetics in Rational Drug Development
E-Book
11/2013
Springer
€117.69
Available for download
Avraham Yacobi | etc.
Integration of Pharmacokinetics, Pharmacodynamics and Toxicokinetics in Rational Drug Development
Proceedings of a Conference Sponsored by the American Association of Pharmaceutical Scientists, the U.S. Food and Drug Administration and the American Society for Clinical Pharmacology and Therapeutics, Held in Arlington, Virginia, April 24-26, 1991
Book
04/1993
Kluwer Academic / Plenum Publishers
€109.28
Article exhausted; check different version
Content
Rationale for the Effective Use of Pharmacokinetics and Pharmacodynamics in Early Drug Development.- The Case for Preclinical Pharmacodynamics.- Utility of Kinetic, Dynamic, and Metabolic Data in Nonclinical Pharmacology/Toxicology Studies.- Preclinical Pharmacokinetic & Pharmacodynamic Studies.- Pharmacokinetics and Drug Metabolism in Animal Studies (ADME, Protein Binding, Mass Balance, Animal Models).- Nonclinical Considerations: Disposition of Drugs.- Use of Acute Toxicity Data in the Design and Interpretation of Subchronic and Chronic Toxicity Studies.- Use of Pharmacokinetics and Pharmacodynamics in Preclinical Studies to Guide Dosage Escalation Schemes in Phase I Studies of Anticancer Drugs.- Use of Toxicokinetic Principles in Drug Development: Bridging Preclinical and Clinical Studies.- Methodology for Preclinical Pharmacodynamic Studies.- Preclinical Pharmacodynamics of Central Nervous System Active Agents.- Preclinical Pharmacodynamics of Antihypertensives.- Preclinical Pharmacodynamics of Anxiolytics: Effects of Chronic Benzodiazepine Administration.- Guidelines for Development of a New Diuretic Agent.- Preclinical Pharmacodynamics of Anti-Inflammatory Drugs.- Preclinical & Clinical Pharmacokinetics.- The Role of Pharmacokinetics in the Drug Development Process.- Implementation of an Effective Pharmacokinetics Research Program in Industry.- Pharmacoepidemiology, Population Pharmacokinetics and New Drug Development.- Assessment of Pharmacokinetic Drug Interactions in Clinical Drug Development.- Clinical Pharmacodynamics.- Pharmacokinetic/Pharmacodynamic Models and Methods.- Pharmacokinetic and Pharmacodynamic Modeling Applied to Anesthetic Drugs.- Pharmacodynamic/Pharmacokinetic Relationships for Rapidly Acting Drugs (NSAIDS) in Rheumatoid Arthritis: Problems and Preliminary Solutions.- The Value of Plasma-Warfarin Measurement.- Clinical Pharmacodynamics of Cardiovascular Agents: Focus on Sudden Cardiac Death.- The Benzodiazepines: Kinetic-Dynamic Relationships.- Application of Pharmacodynamics & Pharmacokinetics in the Drug Development Process.- The Integration of Pharmacodynamics and Pharmacokinetics in Rational Drug Development.- Concentration-Controlled Trials: Basic Concepts, Design, and Implementation.- Summary Report.- Opportunities for Integration of Pharmacokinetics, Pharmacodynamics and Toxicokinetics in Rational Drug Development.