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The book focuses on issues occurring at various stages of clinical research and development, including early-phase clinical development (such as bioavailability/bioequivalence), bench-to-bedside translational research, and late-phase clinical development. Numerous examples illustrate the impact of these issues on the evaluation of the safety and efficacy of the test treatment under investigation. The author also offers recommendations regarding possible resolutions of the problems.
Written by one of the preeminent experts in the field, this book provides a useful desk reference and state-of-the art examination of problematic issues in clinical trials for scientists in the pharmaceutical industry, medical/statistical reviewers in government regulatory agencies, and researchers and students in academia.
The book focuses on issues occurring at various stages of clinical research and development, including early-phase clinical development (such as bioavailability/bioequivalence), bench-to-bedside translational research, and late-phase clinical development. Numerous examples illustrate the impact of these issues on the evaluation of the safety and efficacy of the test treatment under investigation. The author also offers recommendations regarding possible resolutions of the problems.
Written by one of the preeminent experts in the field, this book provides a useful desk reference and state-of-the art examination of problematic issues in clinical trials for scientists in the pharmaceutical industry, medical/statistical reviewers in government regulatory agencies, and researchers and students in academia.
Shein-Chung Chow, Ph.D., is a professor in the Department of Biostatistics and Bioinformatics at Duke University School of Medicine. Dr. Chow is also an adjunct professor of clinical sciences at Duke-National University of Singapore Graduate Medical School and the editor-in-chief of the Journal of Biopharmaceutical Statistics. He has authored or co-authored more than 200 papers and 19 books, including the recently published Handbook of Adaptive Designs in Pharmaceutical and Clinical Development. He earned his Ph.D. in statistics from the University of Wisconsin-Madison.
Introduction. Good Statistical Practices. Bench-to-Bedside Translational Research. Bioavailability and Bioequivalence. Hypotheses for Clinical Evaluation and Significant Digits. Instability of Sample Size Calculation. Integrity of Randomization/Blinding. Clinical Strategy for Endpoint Selection. Protocol Amendments. Seamless Adaptive Trial Designs. Multiplicity in Clinical Trials. Independence of Data Monitoring Committee. Two-Way ANOVA versus One-Way ANOVA with Repeated Measures. Validation of QOL Instruments. Missing Data Imputation. Center Grouping. Non-Inferiority Margin. QT Studies with Recording Replicates. Multiregional Clinical Trials. Dose Escalation Trials. Enrichment Process in Target Clinical Trials. Clinical Trial Simulation. Traditional Chinese Medicine. The Assessment of Follow-On Biologic Products. Generalizability/Reproducibility Probability. Good Review Practices. Probability of Success. References. Index.
| Erscheinungsjahr: | 2020 |
|---|---|
| Genre: | Importe |
| Produktart: | Ratgeber |
| Rubrik: | Gesundheit |
| Thema: | Gesundheit |
| Medium: | Taschenbuch |
| ISBN-13: | 9780367576936 |
| ISBN-10: | 0367576937 |
| Sprache: | Englisch |
| Einband: | Kartoniert / Broschiert |
| Autor: | Chow, Shein-Chung |
| Hersteller: | Chapman and Hall/CRC |
| Verantwortliche Person für die EU: | Libri GmbH, Europaallee 1, D-36244 Bad Hersfeld, gpsr@libri.de |
| Maße: | 234 x 156 x 33 mm |
| Von/Mit: | Shein-Chung Chow |
| Erscheinungsdatum: | 30.06.2020 |
| Gewicht: | 0,916 kg |
Shein-Chung Chow, Ph.D., is a professor in the Department of Biostatistics and Bioinformatics at Duke University School of Medicine. Dr. Chow is also an adjunct professor of clinical sciences at Duke-National University of Singapore Graduate Medical School and the editor-in-chief of the Journal of Biopharmaceutical Statistics. He has authored or co-authored more than 200 papers and 19 books, including the recently published Handbook of Adaptive Designs in Pharmaceutical and Clinical Development. He earned his Ph.D. in statistics from the University of Wisconsin-Madison.
Introduction. Good Statistical Practices. Bench-to-Bedside Translational Research. Bioavailability and Bioequivalence. Hypotheses for Clinical Evaluation and Significant Digits. Instability of Sample Size Calculation. Integrity of Randomization/Blinding. Clinical Strategy for Endpoint Selection. Protocol Amendments. Seamless Adaptive Trial Designs. Multiplicity in Clinical Trials. Independence of Data Monitoring Committee. Two-Way ANOVA versus One-Way ANOVA with Repeated Measures. Validation of QOL Instruments. Missing Data Imputation. Center Grouping. Non-Inferiority Margin. QT Studies with Recording Replicates. Multiregional Clinical Trials. Dose Escalation Trials. Enrichment Process in Target Clinical Trials. Clinical Trial Simulation. Traditional Chinese Medicine. The Assessment of Follow-On Biologic Products. Generalizability/Reproducibility Probability. Good Review Practices. Probability of Success. References. Index.
| Erscheinungsjahr: | 2020 |
|---|---|
| Genre: | Importe |
| Produktart: | Ratgeber |
| Rubrik: | Gesundheit |
| Thema: | Gesundheit |
| Medium: | Taschenbuch |
| ISBN-13: | 9780367576936 |
| ISBN-10: | 0367576937 |
| Sprache: | Englisch |
| Einband: | Kartoniert / Broschiert |
| Autor: | Chow, Shein-Chung |
| Hersteller: | Chapman and Hall/CRC |
| Verantwortliche Person für die EU: | Libri GmbH, Europaallee 1, D-36244 Bad Hersfeld, gpsr@libri.de |
| Maße: | 234 x 156 x 33 mm |
| Von/Mit: | Shein-Chung Chow |
| Erscheinungsdatum: | 30.06.2020 |
| Gewicht: | 0,916 kg |
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