Overview

Since 1972, which marks the invention of recombinant engineering, more than 500 therapeutic proteins have been approved for clinical use. Today, biological drugs constitute almost 70% of all new drugs and have a biological origin. The first edition of this book dealt with biosimilars, and this edition (i.e., the second edition) focuses on new drugs, yet limits to therapeutic proteins. Newer technologies for drug development represent the updated topics in the book and include repur-posing, AI- driven identification of newer designs, novel expression systems, manufacturing using these systems, rapidly changing regulatory pathways, and legal hurdles. This edition discusses how to identify, develop, manufacture, and take multibillion dollar products to market within the shortest possible time. Features: Complete and thorough coverage of the regulatory and technological challenges of developing generic therapeutic proteins Comprehensive, discovery to market, newer technologies, regulatory planning and IP hurdles are included that are not found elsewhere Expanded volume that must be in the hands of every company interested in biological drugs, including the mRNA-based biopharmaceutical companies fast appearing on the market Discusses how to identify, develop, manufacture, and take multibillion dollar products to market in the shortest possible time Renowned author and entrepreneur in the field of drug discovery and production

Full Product Details

Author:   Sarfaraz Niazi (PharmSci Inc., USA)
Publisher:   Taylor & Francis Ltd
Imprint:   CRC Press
Edition:   2nd edition
Weight:   2.030kg
ISBN:  

9781032489605

ISBN 10:   103248960
Pages:   388
Publication Date:   15 April 2024
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   Not yet available  
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Table of Contents

Chapter 1 Biosimilar Biopharmaceuticals Chapter 2 Regulatory Requirements Chapter 3 Development Master Plan Chapter 4 Trends in Recombinant Proteins Manufacturing Chapter 5 Analytical Assessment Chapter 6 Clinical Pharmacology Assessment Chapter 7 Clinical Immunogenicity Assessment Chapter 8 Clinical Efficacy Assessment Chapter 9 Recombinant Manufacturing System Chapter 10 Upstream Processing Chapter 11 Downstream Process Chapter 12 Formulation of Biopharmaceuticals Chapter 13 Quality and Compliance Systems Chapter 14 Intellectual Property Issues for Scientists Chapter 15 Advances in Biomanufacturing

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Author Information

Sarfaraz K Niazi, Ph.D., is an Adjunct Professor at the University of Illinois. He has authored 60+ major books, 100+ research papers, and 100+ patents, mainly in bioprocessing. He has hands-on experience establishing biopharmaceutical projects, from concept to market, including setting up the first biosimilar company in the US and leading to several FDA approvals. He serves as an advisor to several regulatory agencies, including the FDA.

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