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Cancer Biologics: Delivery and Targeting plus Novel Modes of Action

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Thursday, February 4

 

ENGINEERING FOR DELIVERY

8:25 AM Chairperson's Remarks

Tugrul Kararli, Ph.D., President & Founder, Pharmacircle

8:30 Tumor Targeting Theory-Kinetic & Diffusive Processes that Determine Antibody Macro & Microdistribution

K. Dane Wittrup, Ph.D., C.P. Dubbs Professor, Chemical Engineering & Biological Engineering, Associate Director, Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology

A diverse array of tumor targeting agents ranging in size from peptides to nanoparticles is currently under development for applications in cancer imaging and therapy. However, it remains largely unclear how size differences among these molecules influence their targeting properties. Here we develop a simple, mechanistic model that can be used to understand and predict the complex interplay between molecular size, affinity, and tumor uptake.

9:00 Nanoparticle Agents for Tumor Targeting and Penetration

Shuming Nie, Ph.D., Wallace H. Coulter Distinguished Faculty Chair in Biomedical Engineering, Director of Emory-Georgia Tech Cancer Nanotechnology Center, Professor of BME. Chemistry, Materials Science and Engineering, and Hematology and Oncology, Emory University and Georgia Institute of Technology

Nanoparticles have functional and structural properties not available from discrete molecules or bulk materials. When conjugated with monoclonal antibodies, peptides or small molecules, nanoparticles can be used to target malignant tumors with high specificity and affinity. We developed a new class of biocompatible and nontoxic nanoparticles for in vivo tumor targeting and detection based on self-assembled nanostructures and pegylated colloidal gold. 

9:30 Delivery of Antibodies - Market Analysis & Overview

Tugrul Kararli, Ph.D., President & Founder, Pharmacircle

10:00 Sponsored Presentation (Sponsorship Opportunity Available)

10:30 Poster Competition Refreshment Break & Raffles in the Exhibit Hall

 

DELIVERY OF ANTIBODIES

11:30 Engineered Antibodies for Molecular Imaging of Cancer

Anna M. Wu, Ph.D., Professor, David Geffen School of Medicine at UCLA

Cancer-targeting antibodies have been optimized for in vivo imaging by conversion into fragments such as diabodies, minibodies, and scFv-Fc. Recombinant fragments recognizing a variety of cell-surface markers have been labeled with positron-emitting radionuclides (I-124, Cu-64, F-18) for positron-emission tomography (PET) detection of tumors in preclinical models. ImmunoPET represents a broad platform for conducting "immunohistochemistry in vivo" to address biological questions in living organisms, including target expression, target coverage, and response to therapy.

12:00 Advanced Polymer Conjugate Technology for Optimization of Cancer Therapeutics

Christine Loehrlein, Ph.D., A.D., New Products and Technology Strategy Research, Nektar Therapeutics

Conjugation of a therapeutic agent to polyethylene glycol and other polymers is a general strategy that can be used to optimize pharmacological parameters of that drug, with the ability to affect both its efficacy and side effect profile.   Nektar's Advanced Polymer Conjugate Technology platform can be used to enable a wide range of molecules, including proteins, peptides, small molecule oral and parenteral drugs, and antibody fragments.  Nektar is currently using this approach to develop advanced oncolytics with sustained exposure to tumor cells, and exploring opportunities to extend this technology to other cancer therapeutics.

12:30 Luncheon Presentation (Sponsorship Opportunity Available) or Lunch on Your Own

1:45 Ice Cream Refreshment Break in the Exhibit Hall

 

PLENARY KEYNOTE SESSION

2:15 Plenary Keynote Introduction

2:25 Chips, Clones and Living Beyond 100

Paul J.H. Schoemaker, Ph.D., M.B.A., Chairman and Chief Executive Officer, Decision Strategies International, Inc.; Research Director, Mack Center for Technological Innovation, The Wharton School; Adjunct Professor of Marketing, The Wharton School Adjunct Professor, Wharton School of Business

As information technologies and life sciences continue to converge, new business opportunities and challenges will arise for the field of diagnostics and beyond. This keynote reviews the deeper forces shaping the future of the biosciences, from social and economic to technological and political, including the stresses they will introduce for existing business models and healthcare. Not only will bioconvergence introduce new products, services and competitors, it may create entirely new industries on a scale larger than the computer revolution has to date. Several broad scenarios will be painted for the state of the biosciences in 2025 and the forces that might take us there, summarizing a multi-year strategy study conducted and supervised by the speaker at the Wharton school. 

3:05 Refreshment Break in the Exhibit Hall

 

NOVEL MODES OF ACTION
FOR CANCER BIOTHERAPEUTICS

BI- AND TRI-SPECIFIC ANTIBODIES 

3:45 Chairperson's Remarks

Stefan Dbel, Ph.D., Director, Biotechnology, Technische Universitt Braunschweig, Germany

3:50 Mode of BiTE Antibody Action in Cancer Therapy

Patrick Baeuerle, Ph.D., CSO and Senior Vice President, Research & Development, Micromet AG

BiTE (bispecific T cell engager) antibody blinatumumab targets CD19 on B cell malignancies and has provided clinical proof of concept in phases 1 and 2. We will discuss the mode of BiTE antibody action in inducing highly efficient cancer cells lysis, and provide background on how BiTE antibodies are produced, are administered in the clinic, and have been pre-clinically developed.

4:20 Catumaxomab (Removab), the First EC-approved Trifunctional Bispecific Antibody: The Road from Pre-clinical Development to Approval and Beyond

Diane Seimetz, Ph.D., M.D.R.A., CSO and Executive Vice President, Fresenius Biotech GmbH

Catumaxomab, a targeted therapy for intraperitoneal treatment of malignant ascites, targets the epithelial cell-adhesion molecule (EpCAM) and CD3 evoking T-cell cytotoxicity on EpCAM-expressing tumor cells. The Fc-region of catumaxomab provides a third functional binding site, which binds and activates Fcγ-receptor-positive accessory cells. The development rationale, pre-clinical and clinical data, approval process and preparations for further clinical development will be presented.

4:50 Bispecific EGFR-IGF1R Program

Eric Furfine, Ph.D., Senior Vice President, Research and Pre-clinical Development, Adnexus Therapeutics, a Bristol-Myers Squibb R&D Company

Adnectins offer several potential advantages compared to traditional targeted biologics, including speed of discovery, efficient manufacturing, and the ability to create multi-functional targeted products. We are currently advancing products combining two Adnectins to enable modulation of two distinct targets. We will present methods to engineer and optimize multi-specific Adnectins, and pre-clinical data on a bispecific Adnectin to EGFR and IGF1R.

5:20 Multi-specific Antibody by Design

Changshou Gao, Ph.D., Principal Scientist, Antibody Discovery and Protein Engineering, MedImmune LLC  

We'll discuss efforts to engineer and optimize multispecific antibody formats to address the challenges pertaining to bispecific and multispecific molecules, and provide data of our multispecific constructs with excellent expression level, great biophysical stability, good in vitro and in vivo activities, and potential manufacturing feasibility. Our multispecific constructs retain similar in vivo half-life and effector functions to their parental antibodies.

5:50 Close of Day

 

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