Nonclinical Development of Biologics, Vaccines and Specialty Biologics, Second Edition, is a complete reference devoted to the nonclinical safety assessment of novel biopharmaceuticals, vaccines, cell and gene therapies, and oncology therapeutics. Updated and revised, the new edition compares and contrasts these types of biologics with one another and with small molecule drugs, while incorporating the most current and essential international regulatory guidelines. This book discusses the different types of biologics, as well as early characterization strategies, principles of study design, nonclinical pharmacokinetics and pharmacodynamics, nonclinical assays, and regulatory guidelines. A coedited book with chapters authored by leading experts in the field, this comprehensive reference provides critical insights to all researchers involved in early through late-stage biologics.
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Preface
Section I: Development of Biopharmaceuticals
1. Overview of Biopharmaceuticals and Comparison with Small-molecule Drug Development
2. Nonclinical Development of Monovalent and Polyvalent Biopharmaceuticals
3. Regulatory Guidelines and their Application in the Nonclinical Evaluation of Biological Medicines
4. Early De-risking Strategy for Novel Biotherapeutics
5. Pharmacokinetics, Pharmacodynamics, and Bioanalytics
Section II: Vaccines
6. Introduction to Vaccines and Adjuvants
7. Global Regulatory Guidelines for Vaccines
8. Special Considerations for the Nonclinical Safety Assessment of Vaccines
Section III: Specialty Biologics and Indications
9. Gene Therapy
10. Cell Therapy
11. Biological Therapies for Cancer
12. Considerations in the Development of Pluripotent Stem Cell-based Therapies
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Valuable reference providing an up-to-date perspective on the process of nonclinical safety assessments and comprehensive reviews on biopharmaceuticals
Provides in-depth coverage of the process of nonclinical safety assessment and comprehensive reviews of each type of biopharmaceutical
Discusses the most pertinent international regulatory guidelines
Covers early derisking strategies and designs of safety assessment programs for novel biopharmaceuticals and vaccines
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Produktdetaljer
ISBN
9780443133442
Publisert
2024-11-18
Utgave
2. utgave
Utgiver
Vendor
Academic Press Inc
Vekt
1160 gr
Høyde
235 mm
Bredde
191 mm
Aldersnivå
P, 06
Språk
Product language
Engelsk
Format
Product format
Innbundet
Antall sider
482