Lavoisier S.A.S.
14 rue de Provigny
94236 Cachan cedex
FRANCE

Heures d'ouverture 08h30-12h30/13h30-17h30
Tél.: +33 (0)1 47 40 67 00
Fax: +33 (0)1 47 40 67 02


Url canonique : www.lavoisier.fr/livre/autre/monoclonal-antibodies/shire/descriptif_3570923
Url courte ou permalien : www.lavoisier.fr/livre/notice.asp?ouvrage=3570923

0 article 

 Frais de port 0,01€*

Exclusivité web : à partir de 35 euros d’achat, frais de port à 1 centime pour les expéditions vers la France métropolitaine, la Suisse et l’UE avec Colissimo ou GLS

Monoclonal Antibodies Meeting the Challenges in Manufacturing, Formulation, Delivery and Stability of Final Drug Product

Langue : Anglais

Auteur :

Couverture de l’ouvrage Monoclonal Antibodies

Monoclonal antibodies (MAbs) are currently the major class of protein bio therapeutic being developed by biotechnology and pharmaceutical companies. Monoclonal Antibodiesdiscusses the challenges and issues revolving around development of a monoclonal antibody produced by recombinant DNA technology into a therapeutic agent.This book covers downstream processing which includes design of processes to manufacture the formulation, formulation design, fill and finish into closure systems and routes of administration. The characterization of the final drug product is covered where the use of biophysical methods combined with genetic engineering is used to understand the solution properties of the formulation. The latter has become very important since many indications such as arthritis and asthma require the development of formulations for subcutaneous delivery (SC). The development of formulations for IV delivery is also important and comes with a different set of challenges. The challenges and strategies that can overcome these limitations are discussed in this book, starting with an introduction to these issues, followed by chapters detailing strategies to deal with them. Subsequent chapters explore the processing and storage of mAbs, development of delivery device technologies and conclude with a chapter on the future of mAbs in therapeutic remedies.

  • Introduction: Pharmaceutical Development
  • Chapter 1: Current status of monoclonal antibodies in development
  • Chapter 2:Stability of mAbs
  • Routes of degradation encountered during processing and storage
  • Overview of analytical tools used to characterize and monitor stability
  • Methods to evaluate in vivo stability
  • Chapter 3: Challenges in intravenous (IV) administration
  • Chapter 4: Challenges in subcutaneous (SC) administration
  • Chapter 5:Strategies to deal with these challenges
  • IV strategies
  • SC strategies
  • Chapter 6:Development of delivery device technology to deal with the challenges of highly viscous mAb formulations at high concentration
  • Chapter 7:The molecular basis of high viscosity of mAbs at high concentration
  • Chapter 8:Conclusions
  • The future of mAbs as Therapeutics
Steven J. Shire is currently consulting and serving as an adjunct faculty member of the USC School of Pharmacy and University of Connecticut School of Pharmaceutical Sciences. He was at Genentech for 32 years where the majority of his career was in the pharmaceutical development department. He retired in June 2013 as Staff Scientist in the Late Stage Pharmaceutical Development Department. He has been responsible for directing research and development of formulations for a variety of recombinant human proteins including Pulmozyme® and Xolair®. Dr. Shire has served as the chair of the American Association of Pharmaceutical Scientists (AAPS) Biotechnology Section, and was elected as a Fellow of AAPS in 1998 and member at large to the AAPS Executive Council in 2001. He has published over 80 reviews and papers dealing with various aspects of formulation and pharmaceutical development of therapeutic proteins.
  • Discusses the challenges to develop MAbs for intravenous (IV) and subcutaneous delivery (SC)
  • Presents strategies to meet the challenges in development of MAbs for SC and IV administration
  • Discusses the use of biophysical analytical tools coupled with MAb engineering to understand what governs MAb properties at high concentration