Skip to main content
Book cover

Biosimilars

A New Generation of Biologics

  • Book
  • © 2013

Overview

  • Analysis of the complete legal and regulatory framework

  • Approach of the context of copies of biology and biotechnology drugs

  • Details the registration conditions

  • Analysis of these drugs’ marketing (drug safety, prices and distribution channels, substitution and interchangeability…)

  • Investments’ costs and returns on investments are also pointed out

  • A section is focused on the US approach

  • Includes supplementary material: sn.pub/extras

This is a preview of subscription content, log in via an institution to check access.

Access this book

eBook USD 99.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book USD 129.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book USD 129.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Other ways to access

Licence this eBook for your library

Institutional subscriptions

Table of contents (7 chapters)

Keywords

About this book

Biologics have revolutionised the treatment of many severe conditions, delivering exceptional clinical results but also producing exceptionally high prices. As patents expire, copies and price competition are expected throughout the world. However, due to the intrinsic heterogeneity and molecular complexity of biologic medicinal products, their copies cannot simply be authorized under the “generic rule” valid for small chemical entities.

 

In response, a dedicated regulation was issued in the European Union. It is based on the concept of “biological medicinal products similar to a biological reference product”, or “biosimilars”. This book analyses the context of biotechnological production and addresses the European legal framework for biosimilar market approval. It highlights post-market authorisation issues, such as Risk Management Plans and substitution of products, and outlines some other issues, such as cost management and international nomenclature.

 

This book is primarily intended for hospital-based physicians and pharmacists. It will also be a valuable resource for all actors from all countries who want to better understand the emergence of these new medicinal products within the European context.

Editors and Affiliations

  • Hôpital Saint Antoine, Paris, France

    Jean-Louis Prugnaud

  • , Dept Sc pharmaceutiques et biologiques, Université Paris Descartes, Paris, France

    Jean-Hugues Trouvin

About the editors

Jean-Louis Prugnaud is a pharmacist, former head of pharmacy department at Saint-Antoine Hospital, Paris, France. He is Member of the French Commission of drugs’ distribution authorization, President of the Commission of gene and cellular therapy and President of the pharmaceutical working group on biological and biothechnological drugs. Jean-Hugues Trouvin works at AFSSAPS (French health products safety agency) and at the pharmaceutical and biological sciences department at the Paris Descartes University in Paris, France. Preface: Christian K. Schneider is Chairman, CHMP of the Similar Biological (Biosimilar) Medicinal Products Working Party (BMWP), member of the European Medicines Agency( London, United Kingdom) and works at the Paul-Ehrlich-Institut, Federal Agency for Sera and Vaccines (Langen, Germany) and at the Centre for Experimental and Clinical Infection Research (Hannover, Germany).

Bibliographic Information

  • Book Title: Biosimilars

  • Book Subtitle: A New Generation of Biologics

  • Editors: Jean-Louis Prugnaud, Jean-Hugues Trouvin

  • DOI: https://doi.org/10.1007/978-2-8178-0336-4

  • Publisher: Springer Paris

  • eBook Packages: Medicine, Medicine (R0)

  • Copyright Information: Springer-Verlag France 2013

  • Hardcover ISBN: 978-2-8178-0335-7Published: 21 November 2012

  • Softcover ISBN: 978-2-8178-0514-6Published: 14 December 2014

  • eBook ISBN: 978-2-8178-0336-4Published: 27 November 2012

  • Edition Number: 1

  • Number of Pages: XVIII, 90

  • Additional Information: Original French edition published by Springer-Verlag, Paris, 2011

  • Topics: Oncology, Nephrology, Pharmacy, Pharmaceutical Sciences/Technology, Immunology

Publish with us