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Industry's No 1 Immunogenicity Event: Discover the latest technologies, regulations and trends shaping the detection, management and prediction of immunogenicity before and during clinical trials

Unpublished case studies on risk assessment, assay development, acid dissociation assays, biosimilars, IgE, PK/PD, cut points, neutralising antibody assays

  • Benefit from 10 brand new, data-driven case studies to optimise your immunogenicity testing strategies – only available at this conference
  • Hear exclusive, unpublished data on Merck's ground-breaking strategy for automating the acid dissociation step - could you be doing the same?
  • Be the first to hear about Biogen Idec’s brand new assay platform and how it being implemented across the company’s pipeline of products
  • Genentech’s Group Leader, Eric Wakshall, makes his only conference trip over to Europe during 2011 to reveal the company’s risk-assessment strategy for immunogenicity programmes – how does yours compare?
  • Is our prior knowledge of immunogenicity assays flawed?  read more

Join industry's leading companies, regulators and academics

Join industry's leading companies, regulators and academics

Dr Michael Tovey Director of Research Institute Andre Lwoff

Dr Robert M. Umek Director of External Scientific Affairs Meso Scale Discovery

Robin Thorpe Head, Biotherapeutics NIBSC

Professor Roy Jefferis Division of Immunity and
Infection
University of Birmingham, UK

Dr Matthew Baker CSO Antitope

Dr Joel Richard Senior Director, Head of Drug Product Development Ipsen, France

Dr Arno Kromminga CEO, Immunology IPM BIOTECH

 

Full list of speakers:

  • Dr Eric Wakshall, Group Leader, Senior Scientist, Genentech, USA
  • Dr Michael Tovey, Director, Laboratory of Viral Oncology, Institute Andre Lwoff, France
  • Dr Dong Geng, Director, Regeneron, USA
  • Dr Daniel Kramer, Corporate Expert Immunogenicity, Merck Serono, Germany
  • Dr Theo Rispins, Sanquin, The Netherlands
  • Dr Stephen Ulrich, Senior Scientist II, Clinical Immunology, Human Genome Sciences, USA
  • Dr Robin Thorpe, Head of Biotherapeutics Group, NIBSC, UK
  • Dr Lakshmi Amaravadi, Director, Clinical Science & Technology, BiogenIdec, USA
  • Dr Stefan Kostense, Associate Director Clinical Assays, GLP Facility Manager, Crucell Holland BV, The Netherlands
  • Dr Nadja S Prang-Richard, BioChallenges Consulting SARL, France
  • Dr Matthew Baker, Chief Scientific Officer, R&D , Antitope, UK
  • Professor Roy Jefferis, Professor Emeritus: Molecular Immunology, School of Immunity & Infection, University of Birmingham, UK
  • Dr Joel Richard, Senior Director, Head of Drug Product Development, Pharmaceutical Development, Ipsen, France
  • Dr Julia Schleypen, Head of Protein Bioanalytics Development, Roche Diagnostics, Germany
  • Dr Helen Loughrey, Director, Immunology and Formulation Development, Theratechnologies, Canada
  • Dr Lorella Di Donato, VP Analytical Operations, CIRION Biopharma Research Inc, Canada 
  • Dr Robert Umek, Director, Research and Critical Reagents, MSD
  • Dr Jorgen Dahlstrom, Scientific Director, Phadia, Sweden
  • Dr Houston Gilbert, Biostatistian, Non Clinical Biostatistics, Genentech, USA


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Testimonials 2010

"This is one of the best conferences I've attended. Combining open discussions on scientific, clinical and industrial issues"
Senior Manager, Teva Pharmaceuticals

"Congratulations on organising one of the best recent meetings on immunogenicity"
Dr Michael Tovey, Director, Institute Andre Lwoff, Speaker 2010

Brand new sessions on novel assay, new testing platforms and risk assessment

Key sessions covered at the conference:

Day 1:

  • Getting your immunogenicity programme off to the best start possible
  • Is our understanding of immunogenicity assays flawed?
  • New homogenous detection technology for detecting ADAs
  • Novel methods for detecting adas
  • Developing IgE specific assays
  • Regulatory update on immunogenicity for biosimilars and mabs

Day 2:

  • Developing a universal platform technology for immunogenicity testing
  • Using pk/pd anlysis to assess impact of HAHA
  • Moving into pre-clinical development
  • Directing immune deviation towards “self-cure”
  • A clinician’s insight into immunogenicity – what does it all mean for the patient?
  • Reducing the risk of immunogenicity
  • The impact of Formulation on immunogenicity

 

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Companeis who have attended in last 2 years

Abbott GmbH & Co KG Ablynx AlgoNomics NV AstraZeneca Astrazeneca R&D Axicorp GmbH Baxter Baxter Innovations GmbH Bayer Schering Pharma AG Biocon Ltd
Biogen Idec International GmbH BiogeneriX AG BioInvent International BioMonitor A/S Bionor Immuno AS BioReliance Corporation Biotest AG Bos Consultancy CEVEC Pharmaceuticals GmbH Charles River Laboratories
Chugai Pharmaceutical Co Ltd Cirion Clinical Trial Services Inc Covance Laboratories Ltd Crucell CSL Behring GmbH DAIT NIAID NIH Eurofins Medinet F. Hoffmann-La Roche Ltd Ferring Pharmaceuticals AS Flamel Technologies
ForteBio Inc Fresenius Biotech GmbH Gedeon Richter Plc GlaxoSmithKline GSK Biologicals S.A H Lundbeck AS Helix BioPharma Corporation Hofmann la Roche Huntingdon Life Sciences Icon Development Solutions
Inno Biologics SDN BHD Institute of Molecular Genetics Academy of Science Instituto Grifols S A LFB Biotechnologies Lundbeck MDS Pharma Services MedImmune Merck KGaA Merck Serono SpA MicroCoat Biotechnologie GmbH
Micromet AG Molecular Partners AG MorphoSys AG NDA Regulatory Service Notox BV Novartis Novo Nordisk A/S Nycomed GmbH Phadia AB Pharmanet
Pharming Technologies BV PRA International Proteomika SL Quotient Bioresearch Regeneron Pharmaceuticals Inc Research Toxicology Center SpA Roche Diagnostics GmbH Sanofi Aventis R&D Schering Plough Solvay Pharmaceuticals GmbH
Symphogen AS Synexel Research International Teva Pharmaceutical Industries Ltd Texcell Theratechnologies Inc ThromboGenics NV TNO Quality of Life University Autonoma de Barcelona

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