Welcome to hubXchange’s Philadelphia Antibody Therapeutics Xchange 2024, bringing together executives from pharma and biotech to address and find solutions to the key issues faced in developing antibody therapeutics, through a series of roundtable discussions.
Discussion topics will cover Target Selection, Lead Identification & Optimization, Formats & Scaffolds, Bi/Multi-Specifics and Emerging Technologies.
Take advantage of this unique highly interactive meeting format designed for maximum engagement and collaboration with your peers.
Please note this is an In-Person meeting.
VENUE DETAILS:
Doubletree by Hilton Philadelphia Airport,
4509 Island Avenue,
Philadelphia, PA, 19153, US
SNAPSHOTS OF DISCUSSION TOPICS
- Different criteria for target selection depending on the type of biologic modality
- Difficult targets: how to screen and prioritize candidates
- Next generation antibodies addressing the road blocks for first generations
- Challenges of using single domain antibodies as new modalities of multifunctional biologics
- Novel technology to improve antibody access into solid tumors by using targeted enzymes
- Bispecific Antibodies for T-cell Redirection
- Novel delivery modes for biologics – beyond parenteral administration and beyond classical protein administration
- Emerging antibody based immune targets and technologies
Full Xchange Agenda
Target Selection
Opening Address & Keynote Presentation by Nona Biosciences
Integrated Services of ADC Discovery and Development
- Fully human antibody discovery using Harbour Mice
- ADC Discovery including both well-known and novel linker payload and various conjugation methods.
- In vitro and in vivo evaluation of ADC including binding, affinity, internalization, cytotoxicity, plasma stability, PK, efficacy, and toxicology studies, etc
Joe holds a BS from Fudan University and a PhD from University of Delaware, followed by postdoctoral trainings at Lankenau Medical Research Center and Zeneca Pharmaceuticals. Prior to joining Harbour BioMed, he was in small biotechs (Pharmacopeia and Ligand Pharmaceuticals) and large MNC (BMS). Joe has 25 years of combined experience in drug discovery of both small molecules and biologics in therapeutic areas of immuno-oncology, immunology, and genetic diseases.
Spotlight Presentation by WuXi Biologics
Innovative Platforms for Rapid and Cost-Effective HTP Antibody & Protein Production
As the field of biologics development advances, the demand for efficient, high-throughput (HTP) antibody and protein production grows. This talk showcases innovative HTP antibody and protein production platforms: Ultra 96+, 777, Quick ‘n’ Clean, Mini Protein Line and T Cell Mate, all powered by our ultra-high titer transient CHO system. These platforms are designed for rapid, cost-effective HTP production across various drug targets, from mAb to bsAb to new modalities like mini proteins and soluble TCRs. Each platform addresses specific challenges at different stages of drug discovery, expediting your drug development process.
Julia Su is an accomplished scientist and industry expert with a Ph.D. from Louisianan State University and post-doctoral training at the University of Washington. With over a decade of research experience in mRNA vaccines, gene cell therapy, and immunotherapy, Dr. Su possesses a robust technical background and a fervent passion for scientific discovery. Within WuXi Biologics’ Protein Sciences Department, she is renowned for her proficiency in protein and antibody production, adept at translating scientific innovations into practical solutions.
Paul Royle is the technical sales manager for Bio-Rad’s Custom Antibody Service (HuCAL®) and has been with Bio-Rad’s antibody division for over 10 years. Prior to this he worked in an immunology diagnostics company for almost 7 years. Paul holds a degree and PhD from the University of Nottingham (UK), and has post-doctoral research experience from the University of Warwick (UK).
Lead Identification & Optimization
Opening Address & Keynote Presentation by Nona Biosciences
Integrated Services of ADC Discovery and Development
- Fully human antibody discovery using Harbour Mice
- ADC Discovery including both well-known and novel linker payload and various conjugation methods.
- In vitro and in vivo evaluation of ADC including binding, affinity, internalization, cytotoxicity, plasma stability, PK, efficacy, and toxicology studies, etc
Joe holds a BS from Fudan University and a PhD from University of Delaware, followed by postdoctoral trainings at Lankenau Medical Research Center and Zeneca Pharmaceuticals. Prior to joining Harbour BioMed, he was in small biotechs (Pharmacopeia and Ligand Pharmaceuticals) and large MNC (BMS). Joe has 25 years of combined experience in drug discovery of both small molecules and biologics in therapeutic areas of immuno-oncology, immunology, and genetic diseases.
Difficult targets: how to screen and prioritize candidates
- Ab. diversity generation
- How to select the best screening based on target biology
- How critical is developability as a screening factor
Stewart is currently leading Incyte’s in vivo antibody discovery group, where he oversees the design and implementation of immunization campaigns, B cell selection strategies, as well as primary screening assays that serve to assess the therapeutic potential of early antibody candidates. Stewart joined Incyte in September 2022, with a background in B cell biology and antibody gene sequencing. Prior to joining Incyte, Stewart was an Instructor in the Department of Microbiology at the University of Alabama, Birmingham, where his research focused on clonal evolution of B lymphocyte responses to bacterial cell wall carbohydrates and the characterization of tissue-specific B cell repertoires in human tissue. He holds a PhD in Immunology from the University of Alabama at Birmingham, and a BS in Molecular Biology from the University of Central Florida.
Poster Presentation by Immunoprecise Antibodies
Diversity, de-risking, down-selection: The value of amplified lead antibody selection
Shuji Sato holds a PhD from Tufts University in Massachusetts and completed his postdoctoral training at the New England Primate Research Center, Harvard Medical School. Prior to joining IPA, he previously worked other biotech & pharma companies, including Cell Signaling Technology and Pfizer, and most recently, he held the position of Associate Director, Antibody Discovery with Dragonfly Therapeutics.
Spotlight Presentation by WuXi Biologics
Innovative Platforms for Rapid and Cost-Effective HTP Antibody & Protein Production
As the field of biologics development advances, the demand for efficient, high-throughput (HTP) antibody and protein production grows. This talk showcases innovative HTP antibody and protein production platforms: Ultra 96+, 777, Quick ‘n’ Clean, Mini Protein Line and T Cell Mate, all powered by our ultra-high titer transient CHO system. These platforms are designed for rapid, cost-effective HTP production across various drug targets, from mAb to bsAb to new modalities like mini proteins and soluble TCRs. Each platform addresses specific challenges at different stages of drug discovery, expediting your drug development process.
Julia Su is an accomplished scientist and industry expert with a Ph.D. from Louisianan State University and post-doctoral training at the University of Washington. With over a decade of research experience in mRNA vaccines, gene cell therapy, and immunotherapy, Dr. Su possesses a robust technical background and a fervent passion for scientific discovery. Within WuXi Biologics’ Protein Sciences Department, she is renowned for her proficiency in protein and antibody production, adept at translating scientific innovations into practical solutions.
Selection of antigen targets for antibody drug conjugates
- Compared to a conventional herapeutic antibody, what are the most important factors to be considered to an antibody for use in an ADC?
- How do you see non-IgG formats (for example: scFv, VHH, Fab) contributing to ADCs in the future?
- Antibody Drug Conjugates are diversifying with new linkers and new payloads. In what ways do these opportunities change the antigens that can be targeted?
- Most ADCs are for treatment of cancer. What non-cancer indications do you see in the future?
Seah, CEO of Medicovestor, Inc., boasts 25+ years of leadership in academia and biotech. His roles include Product Development Consultant for major players like Bausch Health and Genzyme, and Pediatric Lead at Sanofi. Additionally, he serves as Independent Director for Emmaus Medicals, Inc., and Advisor for Genie Therapeutics, Inc. As a former oncologist, Seah offers not just scientific and industry expertise but also clinical insights. Graduating with distinction from Aberdeen University, he pursued MD and PhD training in the UK, contributing significantly to antibody engineering. He holds 11 patents, published 180+ manuscripts, and secured over $18M in research grants, notably from the National Cancer Institute. He is an Adjunct Professor at SUNY Upstate Medical University and the Section Editor of Journal of Translational Medicine.
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Formats & Scaffolds
Opening Address & Keynote Presentation by Nona Biosciences
Integrated Services of ADC Discovery and Development
- Fully human antibody discovery using Harbour Mice
- ADC Discovery including both well-known and novel linker payload and various conjugation methods.
- In vitro and in vivo evaluation of ADC including binding, affinity, internalization, cytotoxicity, plasma stability, PK, efficacy, and toxicology studies, etc
Joe holds a BS from Fudan University and a PhD from University of Delaware, followed by postdoctoral trainings at Lankenau Medical Research Center and Zeneca Pharmaceuticals. Prior to joining Harbour BioMed, he was in small biotechs (Pharmacopeia and Ligand Pharmaceuticals) and large MNC (BMS). Joe has 25 years of combined experience in drug discovery of both small molecules and biologics in therapeutic areas of immuno-oncology, immunology, and genetic diseases.
- How to design a bi/multi-specific?
- How to deal with the making and testing the numbers of bi/multi-specific variants?
- How much in vitro assessment should be performed before heading into an in vivo animal study?
- How important is off disease testing and how early in the pipeline should it be applied?
- Are there any trustworthy correlation between in vitro and in vivo assays?
Mark has over 30 years of pre-clinical R&D experience at SmithKline Beecham/GSK, Centocor/Janssen of J&J, and Tavotek Biotherapeutics. He implemented 5 phage display based platforms that have indirectly and directly generated biological candidates into IND stage and lately into the market. He was a key contributor to the initial engineering of the anti-IL5 antibody (Nucala) and a lead contributor to the generation of an anti-GPRC5d bi-specific antibody (Talvey). Currently, Mark leads the TavoSelect platform at Tavotek Biotherapeutics that generates sdAbs called VHOs. Tavotek is currently focused on solid tumors and unmet hematological cancers, whereas their latest asset in Phase 1 clinical trial, is a multi-specific biologic called TAVO412.
Spotlight Presentation by WuXi Biologics
Innovative Platforms for Rapid and Cost-Effective HTP Antibody & Protein Production
As the field of biologics development advances, the demand for efficient, high-throughput (HTP) antibody and protein production grows. This talk showcases innovative HTP antibody and protein production platforms: Ultra 96+, 777, Quick ‘n’ Clean, Mini Protein Line and T Cell Mate, all powered by our ultra-high titer transient CHO system. These platforms are designed for rapid, cost-effective HTP production across various drug targets, from mAb to bsAb to new modalities like mini proteins and soluble TCRs. Each platform addresses specific challenges at different stages of drug discovery, expediting your drug development process.
Julia Su is an accomplished scientist and industry expert with a Ph.D. from Louisianan State University and post-doctoral training at the University of Washington. With over a decade of research experience in mRNA vaccines, gene cell therapy, and immunotherapy, Dr. Su possesses a robust technical background and a fervent passion for scientific discovery. Within WuXi Biologics’ Protein Sciences Department, she is renowned for her proficiency in protein and antibody production, adept at translating scientific innovations into practical solutions.
Bi/Multi-Specifics
Opening Address & Keynote Presentation by Nona Biosciences
Integrated Services of ADC Discovery and Development
- Fully human antibody discovery using Harbour Mice
- ADC Discovery including both well-known and novel linker payload and various conjugation methods.
- In vitro and in vivo evaluation of ADC including binding, affinity, internalization, cytotoxicity, plasma stability, PK, efficacy, and toxicology studies, etc
Joe holds a BS from Fudan University and a PhD from University of Delaware, followed by postdoctoral trainings at Lankenau Medical Research Center and Zeneca Pharmaceuticals. Prior to joining Harbour BioMed, he was in small biotechs (Pharmacopeia and Ligand Pharmaceuticals) and large MNC (BMS). Joe has 25 years of combined experience in drug discovery of both small molecules and biologics in therapeutic areas of immuno-oncology, immunology, and genetic diseases.
Novel technology to improve antibody access into solid tumors by using targeted enzymes
- Understand relevant disease biology;
- Design molecule to meet the challenge of the disease environment;
- Create molecule for differentiation
Mark is the Chief Scientific Officer at Tavotek Biotherapeutics. He has nearly 35 years of experience in new drug discovery for AbbVie/Abbott Laboratories and Janssen. Prior to joining Tavotek, Dr. Chiu was the Head of the Process Analytical Sciences at Biotherapeutics Development and Head of Antibody Engineering in the Biologics Research Department at Janssen, the pharmaceutical branch of Johnson & Johnson (JNJ). His leadership resulted in more than 15 New Molecular Entities with 6 projects transitioning from Phase 1 to Phase 3 trials with 4 approved drugs. Dr. Chiu received his A.B. in Biophysics from University of California at Berkeley; Ph.D. degree from the University of Illinois at Urbana-Champaign, and then completed postdoctoral training at the Laboratory of Physical Chemistry at the Federal Institute of Technology at Zurich, Switzerland and the Department of Microbiology at the University of Basel Biocentre.
Spotlight Presentation by WuXi Biologics
Innovative Platforms for Rapid and Cost-Effective HTP Antibody & Protein Production
As the field of biologics development advances, the demand for efficient, high-throughput (HTP) antibody and protein production grows. This talk showcases innovative HTP antibody and protein production platforms: Ultra 96+, 777, Quick ‘n’ Clean, Mini Protein Line and T Cell Mate, all powered by our ultra-high titer transient CHO system. These platforms are designed for rapid, cost-effective HTP production across various drug targets, from mAb to bsAb to new modalities like mini proteins and soluble TCRs. Each platform addresses specific challenges at different stages of drug discovery, expediting your drug development process.
Julia Su is an accomplished scientist and industry expert with a Ph.D. from Louisianan State University and post-doctoral training at the University of Washington. With over a decade of research experience in mRNA vaccines, gene cell therapy, and immunotherapy, Dr. Su possesses a robust technical background and a fervent passion for scientific discovery. Within WuXi Biologics’ Protein Sciences Department, she is renowned for her proficiency in protein and antibody production, adept at translating scientific innovations into practical solutions.
Poster Presentation by Evitria
In silico optimization of polishing for bispecific antibodies using ion-exchange chromatography via bispecific format-based panel screening
Optimization of ion-exchange chromatography for polishing of bispecific antibodies (BsABs) is a significant challenge. A time-consuming step for salt-gradient elution is pH-optimization. To polish BsABs with > 95% final purity a computational tool was created in-house that can be used to model physicochemical behaviour of BsABs and co-expressed byproducts. The script only requires the primary sequence of the individual chains as input to help choose optimal pH for elution. This purification optimization is supported by an in-house developed paneled screening approach which enables bispecific format exploration and maximizes heterodimer yields.
Dylan Brethour is a Senior Account Manager at evitria AG, a company whose mission is to provide the highest quality, research-grade antibody and protein reagents to support antibody therapeutic developers. Dylan joined evitria in June 2023 with a background in supporting biotechnology and pharmaceutical companies through antibody sequencing and characterization services, and more widely supporting research teams as a life sciences reagent provider. Dylan holds a Master of Science in Laboratory Medicine and Pathobiology from the University of Toronto and a Bachelor of Science with Joint Honours in Biomedical Sciences and Psychology from the University of Waterloo.
Bispecific antibodies for T-cell redirection
- Improving the selectivity of T-cell-engaging bispecific antibodies
- Managing the cytokine release syndrome
- Using inhibitory checkpoint-blocking antibodies to improve the clinical outcomes of individuals receiving CD3+ bispecific T-cell redirection therapies
Elisabeth is currently heading the Antibody Engineering team at the Tri-Institutional Therapeutic Discovery Institute (Tri-I TDI) in New York, bridging partnerships in academia and industry to develop antibody-based therapies. In this role, she oversees the generation and optimization of biologics drug candidates, leads therapeutic antibody discovery programs, and coaches a functional team of scientists and managers. Prior to joining TDI, Elisabeth was a Research Assistant professor at the Albert Einstein College of Medicine. Her work guided the development of antiviral antibodies. Elisabeth is passionate about identifying and implementing strategies to drive innovation and to improve drug development processes. She thrives to motivate people to push against barriers and to inspire upcoming generations to leave a positive impact on the world.
Emerging Technologies
Opening Address & Keynote Presentation by Nona Biosciences
Integrated Services of ADC Discovery and Development
- Fully human antibody discovery using Harbour Mice
- ADC Discovery including both well-known and novel linker payload and various conjugation methods.
- In vitro and in vivo evaluation of ADC including binding, affinity, internalization, cytotoxicity, plasma stability, PK, efficacy, and toxicology studies, etc
Joe holds a BS from Fudan University and a PhD from University of Delaware, followed by postdoctoral trainings at Lankenau Medical Research Center and Zeneca Pharmaceuticals. Prior to joining Harbour BioMed, he was in small biotechs (Pharmacopeia and Ligand Pharmaceuticals) and large MNC (BMS). Joe has 25 years of combined experience in drug discovery of both small molecules and biologics in therapeutic areas of immuno-oncology, immunology, and genetic diseases.
Novel delivery modes for biologics – beyond parenteral administration and beyond classical protein administration
- Improving PK.
- Old chain requirements.
- Burden of medical devices for administration
Dr. Rachel Liberatore is the President and Chief Scientific Officer at RenBio, a biotechnology company in New York developing a platform technology for the DNA-based delivery of monoclonal antibodies and therapeutic proteins. Previously, as a postdoctoral fellow at the Aaron Diamond AIDS Research Center, she used genetic techniques to understand how intrinsic cellular defenses restrict the spreading of retroviruses, including HIV-1. She also studied the elicitation of antiviral antibodies directed at viral envelope proteins. Dr. Liberatore received her bachelor’s degree in Molecular Biology from Princeton University and her Ph.D. in Cellular, Molecular, and Biomedical Studies from Columbia University.
Poster Presentation by Rapid Novor
Antibody discovery dead ends and new approaches: The Power of polyclonal sequencing
Antibody discovery remains one of the most challenging aspects in antibody therapeutic development. Novel proteomics-based approaches to antibody discovery offers a promising strategy to overcome roadblocks often associated with other discovery technologies. With REpAb polyclonal sequencing, antibody discovery with mass spectrometry enables the exploration of the natural immune repertoire with unparalleled antibody diversity and creates a pathway for the discovery of novel antibodies.
Anthony works with leading researchers in antibody discovery and diagnostic development to understand their needs and ensure that REpAb® polyclonal antibody sequencing technology complements existing approaches and/or provides a complete end-to-end solution. Anthony is dedicated to solving challenging technical problems in the biomedical field while enriching the lives of humans around the world.
Spotlight Presentation by WuXi Biologics
Innovative Platforms for Rapid and Cost-Effective HTP Antibody & Protein Production
As the field of biologics development advances, the demand for efficient, high-throughput (HTP) antibody and protein production grows. This talk showcases innovative HTP antibody and protein production platforms: Ultra 96+, 777, Quick ‘n’ Clean, Mini Protein Line and T Cell Mate, all powered by our ultra-high titer transient CHO system. These platforms are designed for rapid, cost-effective HTP production across various drug targets, from mAb to bsAb to new modalities like mini proteins and soluble TCRs. Each platform addresses specific challenges at different stages of drug discovery, expediting your drug development process.
Julia Su is an accomplished scientist and industry expert with a Ph.D. from Louisianan State University and post-doctoral training at the University of Washington. With over a decade of research experience in mRNA vaccines, gene cell therapy, and immunotherapy, Dr. Su possesses a robust technical background and a fervent passion for scientific discovery. Within WuXi Biologics’ Protein Sciences Department, she is renowned for her proficiency in protein and antibody production, adept at translating scientific innovations into practical solutions.
Emerging antibody based immune targets and technologies
- How can we overcome of preclinical models for clinical translation of novel bio-therapeutics?
- How can we better predict clinical safety and immunogenicity of complex bio-therapeutics?
- What are the key criteria for selection and prioritization of novel candidates for clinical development to optimize quality over quantity of clinical pipeline?
- What are the new technologies that can accelerate early clinical development and PoC for novel antibody based cancer therapeutics?
Translational and early clinical development scientist with >15 years of industry immuno-oncology development. Scientific and development background in immunology, hematology, oncology, cellular and antibody-based therapy (native mAb, bi-specifics, CAR, immune-targeted therapeutic payload constructs). Expertise in clinical biomarker development, PK/PD, proof of mechanism, biomarker based oncology endpoints. Broad knowledge of current and emerging clinical IO therapy landscape across solid and hematologic malignancy. Currently leading Precision medicine strategy team in a large biopharmaceutical organization.