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Conference Documentation: Therapeutic Antibodies

Published by: SMI Publishing, Ltd

Published: Jan. 30, 2006


Table of Contents


Day 1




8.30 Registration & Coffee




9.00 Chairman's Opening Remarks

Dr Søren Bregenholt, Director, Project Management, Symphogen A/S.




9.10 OVERVIEW OF THE THERAPEUTIC ANTIBODIES MARKET

The dynamic antibody industry


Market overview

Exploring the European therapeutic antibodies market

Improving the efficacy of mab therapeutics likely to benefit growth

Technology trends

The road ahead


Dr Mark Belsey, Analyst, Datamonitor.




9.50 ASSESSING AND GENERATING ANTIBODY IP

Learn how to protect antibodies through patenting and how to assess third party antibody patents


IP landscape for antibody phage display

Comparison of USPTO and EPO approaches to antibody claims

Strategies for protecting antibodies

Approaches for assessing third party antibody patents


Dr Diane Wilcock, Vice President, Intellectual Property, Cambridge Antibody Technology.




10.30 Morning Coffee




11.00 PRECLINICAL DEVELOPMENT

The development of antibodies


HuCAL ® Human Combatorial Antibody Library

Therapeutic antibodies in development

MOR antibody development

Collaborative development programmes


Dr Robert Friesen, Director, Preclinical Development, Morphosys A G.




11.40 SYNTHETIC THERAPEUTIC ANTIBODIES


Application of structure- based design to antibody development

High affinity antibodies dervied from synthetic repertoires

Structural and functional analysis of antigen recognition

Highly optimised synthetic libraries with limited amino acid diverisities

Implications for antibody engineering and therapeutic antibodies


Dr Frederic Fellouse, Research Scientist, Genentech.




12.20 Networking Lunch




1.50 ANTIBODY PHAGE DISPLAY

Novel therapeutic human antibody leads using phage display technology


Construction and use of Dyax novel phage and phagemid human antibody libraries

Novel antibody diversity combining careful synthetic design with natural human human donor diversity

Automated controlled phage display selcetion methods on purified protein targets, peptides and cells

High throughput screening methods to identify antibody leads

Case study: Tie-1 targeted inhibitor of tumour growth


Mr Rene Hoet, Senior Director, Discovery Research, Dyax.




2.30 ANTIBODY ENGINEERING

Assessment of antibody effector function in whole blood


Can antibody effector function be reliably measured in whole blood by flow cytometry?

Can models be established that predicts clinical observations?

Can this data be used to delineate mechanism of action?

Can such assays demonstrate on-target effects?


Dr John Ferbas, Principal Scientist, Amgen.




3.10 Afternoon Tea




3.40 PRACTICAL MEASURES FOR REDUCING IMMUNOGENICITY


Factors that influence immunogenicity of therapeutic proteins

Identification of T cell epitopes

Determining relative immunogenicity of proteins

Modification of T cell epitopes to reduce immunogencity


Dr Dave Estell, Vice President, Technology Research, Genencor International.




4.20 IMMUNOGENICITY AND REGULATORY STANDARDS

Identifying the route from CBER to CDER


Clinical development aspects

Identification and optimisation of immunogenic epitopes

Regulatory authorities - a long process to the final stage

The movement of antibody products from CBER to CDER


Dr Leon Hooftman, CMO, chroma therapeutics.




5.00 Chairman’s Closing Remarks and Close of Day One




Day 2




8.30 Registration & Coffee




9.00 Chairman's Opening Remarks

Dr Hans de Haard, Scientific Director, Ablynx.




9.10 DEVELOPMENT OF THERAPEUTIC ANTIBODIES TO GENOMIC DERIVED TARGETS

Dr Vivian Albert, Vice President, Development Sciences & Research, Human Genome Sciences.




9.50 NEW INNOVATIONS IN THE THERAPEUTIC ANTIBODIES MARKET

In vitro evolution of therapeutic antibodies using ribosome display


CAT-354 for treatment of severe asthma, an affinity-matured human anti-IL-13 antibody

Identification of mutation hot-spots and their synergistic contribution to antibody potency improvements

Exploring antibody-antigen interaction

optimisation of biophysical characteristics like stability or solubility

Application to other therapeutic proteins


Dr Patrick Dufner, Research Scientist, Cambridge Antibody Technology.




10.30 Morning Coffee




11.00 RITUXIMAB - CHANGING THE LANDSCAPE OF NHL/CLL TREATMENT

Non Hodgkin's Lymphoma and CLL


Brief review of NHL/CLL disease area and potential targets for antibody treatment

Treatment algorithms over the last 25 years in NHL/CLL

Structure and mode of action of Rituximab

Key data generated and published in the last few years

Impact of Rituximab on treatment guidelines and habits of NHL/CLL

Lessons we learnt so far to further improve antibody treatment in NHL/CLL


Elisabeth Wassner, Clinical Scientist, roche.




11.40 PATIENT SPECIFIC ANTIBODY THEREAPY FOR NON-HODGKINS LYMPHOMA

Alternative to phage display


Patient specific drug development

Rapid identification of recombinant antibodies using microarray displays

Rapid formulation of recombinant antibodies into therapeutic molecules

Functional cell-based screening of antibody libraries using microarray displays


Dr Dana Ault-Riche, CEO, Pointilliste.




12.20 Networking Lunch




1.50 INFECTIOUS DISEASES

Prophylaxis and treatment of infectious diseases with antibodies


Isolation of antibody specificities

Characterisation of antigens - epitopes and affinities

In vitro functional performance of teh antibodies

In vivo studies in small animals


Mr John de Kruif, Director, Antibody Research and Development, Crucell.




2.30 HOW CAMBRIDGE ANTIBODY TECHNOLOGY DELIVERS LEADS


Overview of selection therapies

Screening for function

IgG conversion


Dr Gerald Beste, Team Leader, Lead Discovery, Cambridge Antibody Technology.




3.10 Afternoon Tea




3.40 USING NANOBODIES AS NEW THERAPEUTIC ENTITIES

In vitro and in vivo efficacy data


The unique properties of Nanobodies and their potential as breakthrough therapeutics

Nanobodies against TNFa for the prevention of rheumatoid arthritis and inflammatory bowel disease

Anti Von Willebrand factor Nanobodies for prevention of arterial thrombosis

Nanobodies against CEA and EGFR for the treatment of cancer


Dr Hans de Haard, Scientific Director, Ablynx.




4.20 DEVELOPMENT OF RECOMBINANT HUMAN POLYCLONAL ANTIBODY THERAPEUTICS


Innovative technology for cloning cognate human antibodies

Expression of recombinant human polyclonal antibodies

Regulatory strategy for obtaining approval of recombinant polyclonal antibody pharmaceuticals

Development of Sym001; anti-RhD polyclonal antibodies for treatment of ITP and HDN


Dr Søren Bregenholt, Director, Project Management, Symphogen A/S.




5.00 Chairman’s Closing Remarks and Close of Conference

Abstract

SMi’s 6th Conference on ‘Therapeutic Antibodies’ will provide a forum for leading industry experts from major pharmaceutical companies to discuss and evaluate the latest challenges and problems facing the therapeutic antibodies market.

It is predicted that therapeutic antibodies will form one of the fastest growing segments of the pharmaceutical market, and is expected to be worth more than $86 billion dollars by the year 2025. The success of current marketed products has led to an explosion in antibody development, with hundreds of programmes currently in the pipeline.

This conference will discuss the latest developments and outline the most recent trends and innovations in the therapeutic antibodies market. Particular focus will be given to the latest regulatory standards and intellectual property, which affect developments in this market.

SMi’s Therapeutic Antibodies conference is a must attend event and will provide an excellent opportunity to network, enhance your company’s profile and keep you up-to-date on the latest issues in the market.

An unique opportunity to learn from leading industry experts, including:
  • Dr Rene Hoet, Director, Research & Technology, Dyax
  • Dr John de Kruif, Director, Antibody Research & Development, Crucell
  • Dr Dave Estell, Vice President, Technology, Genencor
  • Dr Robert Friesen, Director, Preclinical Development, MorphoSys
  • Dr Diane Wilcock, Vice President, Intellectual Property, Cambridge Antibody Technology
  • Dr Leon Hooftman, Chief Medical Officer, Chroma Therapeutics
  • Dr Hans de Haard, Scientific Director, Ablynx
  • Elisabeth Wassner, Clinical Scientist, F. Hoffmann-La Roche
  • Dr Frederic Fellouse, Senior Research Scientist, Genentech


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