In Vivo Engineering of Immune Cells (IVEIC) for Cancer Immunotherapy (Speaker Bios)
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Adrian Bot, M.D., Ph.D.
Capstan therapeutics
CSO
Adrian Bot, M.D., Ph.D. is the founding Chief Scientific Officer and Executive Vice President of Research and Development at Capstan Therapeutics, a company developing next generation precision medicines with focus on in vivo CAR engineering. Dr. Bot has 26 years of experience in biopharmaceutical industry with focus on discovery and development of targeted therapies in general, and immunotherapies in particular. Previously, he held leadership roles at Kite Pharma and Kite, a Gilead Company, including Chief Scientific Officer and Vice President of Translational Medicine and Discovery Research, respectively. At Kite, he contributed to the development of first-in-class CAR T cell therapy products for cancer. Dr. Bot also served in various senior R&D leadership positions at MannKind Corp and Alliance Pharmaceutical Corp, La Jolla, California. He obtained his M.D. in Romania in 1993, his Ph.D. in Biomedical Sciences at Mount Sinai School of Medicine in New York in 1998 and subsequently, he was a Guest Scientist at the Scripps Research Institute in La Jolla, California.
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Yevgeny Brudno, Ph.D.
University of North Carolina and North Carolina State University
Implantable Sponges for Same-Day Bedside CAR T Cell Therapys
Yevgeny (Yev) Brudno received dual B.A. degrees in Chemistry and Biophysics from the University of Pennsylvania and his PhD in Chemistry from Harvard University, working with David Liu to develop directed evolution technologies. From there, Yev worked as a postdoctoral fellow at the Wyss Institute at Harvard with Prof. David Mooney, developing controlled release drug delivery technologies for cancer and regenerative medicine. Yev’s research interests span bioconjugate chemistry, materials science, and cellular immunotherapy. Mostly recently, his lab develops materials to transform CAR T cell therapy to increase potency and patient access through bedside and in vivo approaches. Our lab’s research is rooted in the belief that advances in biomaterials and the basic molecular sciences can generate meaningful change in how therapies are designed, produced, and administered.
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Ryan Crisman, Ph.D.
ryan.crisman@umoja-biopharma.com
Umoja Biopharma
Co-founder and CTO
Ryan Crisman is the co-founder and Chief Technical Officer at Umoja Biopharma. Before starting Umoja in 2019, Ryan served as the Executive Director for the Gates Biomanufacturing Facility, where he was responsible for building out and staffing this protein and cell therapy CDMO. He was instrumental in growing the facility’s cGMP capabilities and delivering many first in human therapeutic products to patients. While at Juno Therapeutics, Ryan led the JCAR017 CMC program and was the Head of Late Stage Process Development. He has also held scientific leadership positions at Zymogenetics and CMC Biologics.
Ryan holds a Ph.D. in Chemical Engineering from the University of Colorado, Boulder, and a bachelor’s degree in Chemical Engineering from Washington State University. -
James Dahlman, Ph.D.
Emory Medical School / Georgia Tech
Associate Professor
James Dahlman is the McCamish Early Career Professor in the Department of Biomedical Engineering at Georgia Tech and Emory School of Medicine. His lab works at the interface of chemical engineering, genomics, and gene editing by applying big data approaches to nanomedicine. The lab is known for developing DNA barcoded nanoparticles to measure how hundreds of nanoparticles deliver mRNA and siRNA in multiple cell types from a single animal in vivo. The lab uses these approaches to deliver RNA outside the liver.
James was a co-founder and Board Chairman of Guide Therapeutics, which was acquired by Beam Therapeutics. His trainees have become investors, started companies, and work in some of the most cutting-edge organizations in RNA therapeutics. James received his Ph.D. in 2015 from the Harvard-MIT HST Program, where he studied with Robert Langer, and as a post-doc, studied CRISPR-Cas9 with Feng Zhang. -
Justin Eyquem, Ph.D
University of California, San Francisco
In vivo site-specific engineering to reprogram T cells
Justin Eyquem, PhD, is the Director of the Center for Immune Cell Engineering and an Assistant Professor of Medicine in the Division of Hematology and Oncology at UC San Francisco (UCSF). He is also an Investigator at the Gladstone-UCSF Institute for Genomic Immunology.
He holds Master’s degrees in bioengineering and genetics from the Paris School of Agronomy (AgroParisTech) and the University Paris VII. He earned his PhD in immunology and molecular biology from University Paris VII (in collaboration with Cellectis) and trained as a postdoctoral fellow in the laboratory of Michel Sadelain at Memorial Sloan-Kettering Cancer Center. In 2019, he joined UCSF as a Parker Fellow and became an Assistant Professor in 2021. He is a member of the Parker Institute for Cancer Immunotherapy, the Helen Diller Family Comprehensive Cancer Center, and UCSF ImmunoX.
Dr. Eyquem’s research focuses on optimizing genetically modified immune T cells, known as CAR-T cells, to fight cancers and other diseases. He has pioneered methods to edit the genome of human CAR-T cells and developed techniques to reprogram their functions both outside the body (ex vivo) and inside the body (in vivo). Additionally, he leads a preclinical team dedicated at designing the most effective therapies for a UCSF clinical pipeline. Finally, he participated in multiple collaborations to facilitate the manufacturing of CAR-T cells for clinical use, including a UCSF clinical trial in Myeloma set to begin by the end of 2024.
His work has earned him several awards, including the 2019 Parker Fellow Award, the 2023 ASGCT Outstanding New Investigator Award, and the 2024 Pew-Stewart Award. The technologies he developed have been licensed to multiple biotech and pharma companies, resulting in multiple ongoing clinical trials. Additionally, he co-founded cell and gene therapy companies, which focus on developing drugs for cancer, autoimmune disorders, and genetic diseases. -
Daria Fedyukina, Ph.D.
ARPA-H
Program Manager
Dr. Daria Fedyukina is a Program Manager at the Health Science Futures office of ARPA-H. Before joining ARPA-H, Daria founded BioHeights, a consulting company that provided portfolio, R&D, and commercial strategy services to gene and cell therapy companies, as well as licensing partner scouting and technology commercialization services to academic institutions. Prior to that, she worked in the commercial and portfolio planning group of REGENXBIO, where she was responsible for portfolio expansion and for assessing the technical and commercial potential of gene therapies. Before REGENXBIO, she was a management consultant at global consulting firm L.E.K. Consulting in Boston, MA and London UK. Daria earned a doctorate in chemistry from the University of Wisconsin-Madison, where her research spanned organic synthesis, protein folding, and nuclear magnetic resonance imaging of protein structure. Before graduate studies, Daria worked as a research scientist at LG Chemical in Daejeon, South Korea.
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Charles Gersbach, PhD
Duke University
John W. Strohbehn Distinguished Professor of Biomedical Engineering
Dr. Charles A. Gersbach is the John W. Strohbehn Distinguished Professor of Biomedical Engineering at Duke University and the Director of the Duke Center for Advanced Genomic Technologies. His research interests are in genome and epigenome editing, gene therapy, regenerative medicine, biomolecular and cellular engineering, synthetic biology, and genomics. His work has led to new approaches to study genome structure and function, program cell biology, and treat genetic disease. Dr. Gersbach’s work has been recognized through awards including the NIH Director’s New Innovator Award, the NSF CAREER Award, the Outstanding New Investigator Award from the American Society of Gene and Cell Therapy, and induction as a Fellow of the American Institute for Medical and Biological Engineering and member of the National Academy of Inventors. He is also the co-founder of three biotechnology companies and an advisor to several others.
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Daniel Getts, MBA PhD
Myeloid Therapeutics
CEO
Dr. Getts is the CEO and co-founder of Myeloid Therapeutics, a clinical-stage immunology company based in Cambridge. Myeloid is renowned as the first company in the world to deliver in vivo CAR therapy to humans. Dr. Getts is also the founder of Aurora Biosynthetics, a Myeloid subsidiary focused on GMP DNA & RNA manufacturing, based in Sydney, Australia.
Prior to founding Myeloid, Dr. Getts was the Vice President of Research at TCR2 Therapeutics (NASDAQ: TCRR), where he was a member of the leadership team that successfully secured a Series B financing round of $120 million and an IPO of approximately $80 million. His primary responsibilities included leading the company’s target discovery, preclinical, and translational research programs.
Before his tenure at TCR2, Dr. Getts was the primary inventor, founder, and Chief Scientific Officer of Cour Pharmaceuticals Development Company. Cour is a nanotechnology platform company dedicated to addressing autoimmunity and inflammation. During his time there, Dr. Getts was instrumental in negotiating several pharmaceutical collaborations and licenses, including a significant partnership with Takeda.
Earlier in his career, Dr. Getts served as the Director of Research & Development at Tolera Therapeutics. In this role, he was the lead immunologist responsible for advancing the company’s monoclonal antibody program from discovery to Phase 3.
Dr. Getts has received numerous honors and awards and holds over 100 patents and patent applications. Since 2010, he has played a direct or indirect role in bringing nine novel RNA, cell, and immune products from discovery to the clinic. He is widely published, with over 50 peer-reviewed publications in prestigious journals, including Nature Biotechnology, Science Translational Medicine, and Nature Communications.
Dr. Getts completed his postdoctoral training at Northwestern University in Stephen Miller’s laboratory. He holds a PhD in Medicine from the University of Sydney and an MBA from Western Michigan University. -
Saar Gill, M.D., Ph.D.
Saar.Gill2@pennmedicine.upenn.edu
University of Pennsylvania
Associate Professor of Medicine
Dr. Gill obtained his medical degree and Ph.D in immunology from the University of Melbourne, and trained in hematology at St Vincent’s Hospital, the Royal Melbourne Hospital and the Peter MacCallum Cancer Centre. In 2008 he moved to the United States, first to pursue a post-doctoral fellowship in cellular therapy at Stanford University, and then in 2011 to the University of Pennsylvania where he is now an associate professor of medicine. Dr Gill is also the Scientific Director of Penn’s Center for Cell Therapy and Transplantation, and a co-director of the Parker Institute for Cancer Immunotherapy at the University of Pennsylvania.
Dr. Gill’s clinical practice is in leukaemia and bone marrow transplantation. He has led clinical trials of chimeric antigen receptor (CAR) T cells for chronic and acute leukemias. Dr. Gill’s research laboratory focuses on the interface between adoptive cellular therapy and genetic engineering, with a strong translational focus. Dr. Gill has authored over 100 peer-reviewed papers and is listed as an inventor on over 60 patents. He has spun out two biotechnology companies that currently employ over 100 people in Philadelphia. Dr. Gill’s past trainees hold independent academic appointments at the University of Melbourne, the Israel Institute of Technology, Mayo Clinic, Washington University, and at the University of Pennsylvania School of Medicine. -
Michael Klichinsky, Pharm.D., Ph.D.
michael.klichinsky@carismatx.com
Carisma Therapeutics
Chief Scientific Officer
Michael invented and developed chimeric antigen receptor macrophage and monocyte (CAR-M) therapy, and is the Scientific Co-Founder and Chief Scientific Officer of Carisma Therapeutics in Philadelphia, PA. In his role as Chief Scientific Officer, he oversees the research & discovery efforts of the company utilizing ex vivo and in vivo cell therapies for oncology, autoimmunity, and fibrosis. His work led to the first CAR-M and CAR-Monocyte clinical trials which are currently underway for patients with advanced solid tumors. Michael previously earned a PhD in Pharmacology from the University of Pennsylvania and a PharmD degree from the Philadelphia College of Pharmacy.
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Gabriel Kwong, Ph.D.
Department of Biomedical Engineering Georgia Tech and Emory School of Medicine
Associate Professor
Dr. Kwong is an Associate Professor in the Wallace H. Coulter Department of Biomedical Engineering at Georgia Tech and Emory University. He earned his B.S. from UC Berkeley and his Ph.D. from Caltech both in Bioengineering. His research program is centered at the interface of bioengineering, immunology and medicine. His group pioneers cell therapies and biosensors to address frontier challenges in cancer, transplantation medicine, and infectious diseases. Among his distinctions, Dr. Kwong is a recipient of the NIH Director's New Innovator and Pioneer Awards, and currently leads the $49.5 million Cancer and Organ Degradome Atlas (CODA) project, a multi-institutional research enterprise supported by ARPA-H to revolutionize multi-cancer early detection. Dr. Kwong co-founded two biotechnology companies and holds over 35 issued or pending patents.
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Peter W. Marks, M.D., Ph.D.
United States Food and Drug Administration
Director, Center for Biologics Evaluation and Research
Peter Marks received his graduate degree in cell and molecular biology and his medical degree at New York University and completed Internal Medicine residency and Hematology/Medical Oncology training at Brigham and Women’s Hospital in Boston. He has worked in academic settings teaching and caring for patients and in industry on drug development and is an author or co-author of over 125 publications. He joined the FDA in 2012 as Deputy Center Director for CBER and became Center Director in 2016 and is a Fellow of the American College of Physicians and a member of the National Academy of Medicine.
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Matthias Stephan, M.D., Ph.D.
Fred Hutchinson Cancer Center
In vivo macrophage reprogramming: Localized BiTE secretion for retargeting T cells to tumor
Dr. Stephan is Professor in the Translational Science and Therapeutics Division at Fred Hutchinson Cancer Center in Seattle. After attending medical school in Germany, he trained in CAR T-cell therapy with Dr. Michel Sadelain at MSKCC, and bioengineering at MIT. In 2017 his group first published a mRNA nanoparticle-based method to program antigen-recognizing capabilities into lymphocytes circulating in vivo. Based on this research, he co-founded Tidal Therapeutics in 2019, which was acquired by Sanofi in April 2021. His team also developed biomaterial implants for in situ programming of CAR T-cells. This platform was recently licensed by Jupiter Bioventures for further development with the goal to reduce the time and cost of CAR T therapies by creating synthetic lymph nodes that are made outside the patient and then implanted using a minimally invasive procedure.
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Fyodor Urnov, Ph.D.
University of California, Berkeley
Professor of Molecular and Cell Biology
Fyodor Urnov is a Professor of Molecular and Cell Biology at the University of California, Berkeley, and Director of Technology & Translation at the Innovative Genomics Institute (IGI). A pioneer in the field of therapeutic genome editing, Fyodor’s research focuses on advancing genome editing technology and pushing the boundaries of how it can be applied to solve real-world problems.
Fyodor trained as an undergraduate in Biology at Moscow State University, and then studied the interplay between chromatin and transcription factors for his Ph.D. at Brown University (with Susan Gerbi) and as a postdoctoral fellow at the NIH (with Alan Wolffe).
In his work at Sangamo Therapeutics (2000–16), Fyodor and colleagues demonstrated the first use of zinc-finger nucleases to edit DNA in human cell and coined the term “genome editing.” Fyodor then led collaborative teams to establish at-scale applications of genome editing for human somatic cell genetics and model animal and crop reverse genetics. Fyodor was a key member of the team that developed the first-in- human application of genome editing (2009), and then led a cross-functional team from basic discovery to IND of first-in-human clinical trials for the hemoglobinopathies beta-thalassemia and sickle cell disease (trials currently ongoing in partnership with UCSF Benioff Children’s Hospital and UCLA Broad Stem Cell Research Center).
At the IGI, Fyodor works in collaborative teams to develop first-in-human applications of experimental CRISPR-based therapeutics for sickle cell disease (with Mark Walters, UCSF), genetic disorders of the immune system (with Alexander Marson, UCSF/IGI), radiation injury (with Jonathan Weissman, MIT/Whitehead Institute), cystic fibrosis (with Ross Wilson, IGI), and neurological disorders (with Weill Neurohub and Roche/Genentech). -
Thomas George Whitehead,
Emily Whitehead Foundation
Founder
Tom Whitehead is a keynote speaker, author, and journeyman lineman for Penelec, a FirstEnergy Company. He is also the proud father of Emily, and co-founder of the Emily Whitehead Foundation, which raises funds and awareness for pediatric cancer immunotherapy research. Tom and his wife Kari founded the Emily Whitehead Foundation in honor of their daughter Emily who was diagnosed at age five with an aggressive form of leukemia that failed to respond to chemotherapy. As a last hope, Emily was enrolled in a clinical trial and became the first pediatric patient in the world to receive CAR T-cell therapy. The therapy worked and Emily is now 11 years cancer free and considered cured.
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Wilson W Wong, Ph.D.
Boston University
Associate Professor
Dr. Wilson Wong is an Associate Professor of Biomedical Engineering at Boston University. He is also a founding member of the Biological Design Center. He received his B.S. and Ph.D. in Chemical Engineering from UC Berkeley and UCLA, respectively. He obtained his postdoctoral training from UCSF. Dr. Wong's lab combines engineering, biological network design, molecular biology, and immunology to develop genetic tools for basic biomedical research and cell and gene therapy. A specific goal is to design robust and reliable methods to perform complex cellular computations in a spatiotemporally controlled manner, which will have significant implications in engineering complex tissues and designing cellular therapy with improved safety and specificity. Dr. Wong's research has been recognized by the NIH Director's New Innovator Award, NSF CAREER Award, ACS Synthetic Biology Young Investigator Award, and the College of Engineering Early Career Excellence in Research Award.
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Wen Xue, Ph.D.
UMass Chan Medical School
Associated Professor
Dr. Wen Xue is an associate professor with tenure at the RNA Therapeutics Institute at the University of Massachusetts Medical School. He did Ph.D. training with Dr. Scott Lowe at the Cold Spring Harbor labs and Stony Brook University (2005-2009) and postdoctoral training under the mentorship of Dr. Tyler Jacks at MIT (2009-2014). His research focuses on cancer genetics using mouse models and study of genetic diseases using CRISPR genome editing. His lab has pioneered a series in vivo application of novel CRISPR-based techniques to correct or study genetic diseases in mouse models. He has received awards including the NIH Director’s New Innovator Award and Scientific Merit Award of the Lung Cancer Research Foundation. He is on the editorial board of Hepatology, Human Gene Therapy, and FASEB.