Providing more than just a comprehensive history, critical vocabulary, insightful compilation of motivations, and clear explanation of the state-of-the-art of modern clinical trial simulation, this book supplies a rigorous framework for employing simulation as an experiment, according to a predefined simulation plan, that reflects good simulation practices. The book discusses how to clinical trial designs according to their probability for success, techniques to define distributions of virtual subjects' characteristics, methods to determine the sensitivity of the trial design, and the population relationship between dosing schedules and patient response.
Simulation For Designing Clinical Trial
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Inside This Book
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First Sentence:
The decision processes of designing clinical trials have followed a largely ad hoc manner, driven by empiricism and embracing concepts such as "what was done previously" and "it has always been done this way." Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
clinical trial simulation, parameter estimation efficiency, trial simulator, certain response rate, interoccasion variability, virtual trial, simulated clinical trial, pain severity score, population pharmacokinetic studies, healthy volunteer data, posterior predictive check, population pharmacokinetic study, population pharmacokinetic parameters, bootstrap data sets, dose options, population pharmacokinetic model, patient vectors, central arterial pressure, proposed study design, simulation plan, population clearance, simulation team, protocol deviations, population parameter estimates, virtual patients Key Phrases - Capitalized Phrases (CAPs): (learn more)
Clin Pharmacol Ther, New York, Pharmacokinet Biopharm, Pharmacokin Biopharm, Clin Pharmacokinet, Pharm Res, Monte Carlo, San Francisco, Annu Rev Pharmacol Toxicol, Pharsight Corporation, Georgetown University, Pharm Sci, University of California, Acad Sci, Academic Press, Population Approach Group, Desk Reference, European Cooperation, John Wiley, Microsoft Excel, Mountain View, World War, Drug Inf, New Jersey, Normalised Sensitivity New!
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Front Cover | Table of Contents | First Pages | Index | Surprise Me!
The decision processes of designing clinical trials have followed a largely ad hoc manner, driven by empiricism and embracing concepts such as "what was done previously" and "it has always been done this way." Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
clinical trial simulation, parameter estimation efficiency, trial simulator, certain response rate, interoccasion variability, virtual trial, simulated clinical trial, pain severity score, population pharmacokinetic studies, healthy volunteer data, posterior predictive check, population pharmacokinetic study, population pharmacokinetic parameters, bootstrap data sets, dose options, population pharmacokinetic model, patient vectors, central arterial pressure, proposed study design, simulation plan, population clearance, simulation team, protocol deviations, population parameter estimates, virtual patients Key Phrases - Capitalized Phrases (CAPs): (learn more)
Clin Pharmacol Ther, New York, Pharmacokinet Biopharm, Pharmacokin Biopharm, Clin Pharmacokinet, Pharm Res, Monte Carlo, San Francisco, Annu Rev Pharmacol Toxicol, Pharsight Corporation, Georgetown University, Pharm Sci, University of California, Acad Sci, Academic Press, Population Approach Group, Desk Reference, European Cooperation, John Wiley, Microsoft Excel, Mountain View, World War, Drug Inf, New Jersey, Normalised Sensitivity New!
Books on Related Topics | Concordance | Text Stats Browse Sample Pages:
Front Cover | Table of Contents | First Pages | Index | Surprise Me!
Citations (learn more)
This book cites 100
books:
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1
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- Modern Pharmaceutics by Gilbert S. Banker on 4 pages
- Bayesian Data Analysis, Second Edition (Chapman & Hall/CRC Texts in Statistical Science) by Andrew Gelman on page 16, page 150, and page 390
- Drug Stability: Principles and Practices (Drugs and the Pharmaceutical Sciences) by Jens T. Carstensen in Front Matter (1), Front Matter (2), and Front Matter (3)
- Pharmaceutical Process Validation: An International Third Edition (Drugs and the Pharmaceutical Sciences) by Robert A. Nash in Front Matter (1), Front Matter (2), and Front Matter (3)
- Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms (Drugs and the Pharmaceutical Sciences) by James McGinity in Front Matter (1), and Front Matter (2)
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