Biological Drug Products: Development and Strategies

Overview

This book overviews the fundamental aspects, challenges, and development strategies for biological drug entities. It is divided into 5 parts, covering general aspects in the development of biologics (Part 1) and challenges and strategies in the development of specific types of biologics (Parts 2-5). In the overview section, contributing authors discuss the development process, safety and clinical assessments, manufacturing, and regulatory and intellectual property issues. Following this opening, the major classes...

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Overview

This book overviews the fundamental aspects, challenges, and development strategies for biological drug entities. It is divided into 5 parts, covering general aspects in the development of biologics (Part 1) and challenges and strategies in the development of specific types of biologics (Parts 2-5). In the overview section, contributing authors discuss the development process, safety and clinical assessments, manufacturing, and regulatory and intellectual property issues. Following this opening, the major classes of biologics are discussed: proteins and peptides, vaccines, oligonucleotides, and gene and regenerative medicines. A concluding section details administration and delivery routes and systems. The book incorporates both lessons learned and future directions to make for a valuable resource and reference for pharmaceutical scientists involved in the dynamic field of biologics.

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Editorial Reviews

From the Publisher
“Thus, it will be a valuable resource for both novice and expert alike.” (ChemMedChem, 1 October 2014)
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Product Details

  • ISBN-13: 9781118148891
  • Publisher: Wiley
  • Publication date: 10/21/2013
  • Edition number: 1
  • Pages: 744
  • Sales rank: 1,205,114
  • Product dimensions: 6.10 (w) x 9.40 (h) x 1.70 (d)

Meet the Author

WEI WANG, PhD, is a Research Fellow for Pfizer BioTherapeutics Pharmaceutical Sciences. In addition, Dr. Wang is Adjunct Professor in the School of Pharmacy and Health Sciences at the University of the Pacific.

MANMOHAN SINGH, PhD, is Head of Technical Development at Novartis Vaccines and Diagnostics. Dr. Singh has authored over 120 peer-reviewed manuscripts, reviews, and book chapters in the area of vaccine formulations and adjuvant research. He is also an Adjunct Professor at the Eshelman School of Pharmacy at University of North Carolina, Chapel Hill.

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Table of Contents

Dedication

Preface

Part 1. General Aspects 1

Chapter 1. An Overview of Discovery and Development Process For Biologics 3
Heather H. Shih, Paula Miller and Douglas C. Harnish

Chapter 2. Nonclinical Safety Assessment of Biologics, Including Vaccines 31
Liangbiao George Hu, David W. Clarke

Chapter 3 Clinical Assessment of Biologics Agents 57
Lesley Ann Saketkoo, Shikha Mittoo and Luis R. Espinoza

Chapter 4. Key Regulatory Guidelines for Development of Biologics In The U.S. And Europe 75
Richard Kingham, Gabriela Klasa and Krista Hessler Carver

Chapter 5. Landscape and Consideration of Intellectual Property for Development Of Biosimilars 111
Srikumaran Melethil

Chapter 6. Scientific Aspects of Sterility Assurance, Sterility, Asepsis, and Sterilization 133
James E. Akers and James P. Agalloco

Part 2. Proteins/Peptides 163

Chapter 7. Cell Cell Culture Processes in Monoclonal Antibody Production 165
Feng Li, Amy (Yijuan) Shen and Ashraf Amanullah

Chapter 8. Protein/Peptide Purification and Virus Reduction 203
Beckley K. Nfor, Esteban Freydell and Marcel Ottens

Chapter 9. Chemical and Genetic Modification 233
M Farys, C Ginn, G Badescu, K Peciak, E Pawlisz, H Khalili and S Brocchini

Chapter 10. Analytical Characterization of Proteins/Peptides 285
Yajun Jennifer Wang and Brian Hosken

Chapter 11. Protein/Peptide Formulation Development 323
Satoshi Ohtake and Wei Wang

Chapter 12. Regulatory Strategies and Lessons in the Development Of Biosimilars 367
Umang S. Shah

Part 3. Vaccines 409

Chapter 13. Vaccine Development – History, Current Status and Future Trends 411
Leo Van Der Pol and Jean-Pierre Amorij

Chapter 14. Role and Application of Adjuvants and Delivery Systems in Vaccines 437
Rajesh K. Gupta

Chapter 15. Methods for Characterizing Proteins in Aluminum Adjuvant Formulations 469
Martinus A.H. Capelle, Emilie Poirier and Tudor Arvinte

Part 4. Novel Biologics 487

Chapter 16. The State Of The Art and Future of Gene Medicines 489
Frank Jacobs, Stephanie C. Gordts and Bart De Geest

Chapter 17. Nucleic Acid Vaccines 531
Rachel Buglione-Corbett, John Suschak, Shixia Wang and Shan Lu

Chapter 18. Multifunctional Polymeric Nano-Systems for Rna Interference Therapy 569
Arun Iyer, Shanthi Ganesh, Qiong L. Zhou and Mansoor Amiji

Chapter 19. Advent and Maturation of Regenerative Medicine 601
Abner M. Mhashilkar and Anthony Atala

Part 5. Product Administration/Delivery 629

Chapter 20. Conventional and Novel Container Closure/Delivery Systems 631
Joseph Wong and Mahesh V. Chaubal

Chapter 21. Controlled-Release Systems for Biologics 655
Mayura Oak, Rhishikesh Mandke, Buddhadev Layek, Gitanjali Sharma and Jagdish Singh

Chapter 22. Routes of Delivery for Biological Drug Products 677
Darrell J. Irvine, Xingfang Su and Brandon Kwong

INDEX 725

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