Who We Fund

TAP Partner

Faron is a clinical stage biopharmaceutical company focused on building the future of immunotherapy by harnessing the power of the immune system to tackle cancer and inflammation. The precision immunotherapy in clinical development has the potential to provide permanent immune stimulation for difficult-to-treat cancers through targeting myeloid function.

Program Name(s)

Therapy Acceleration Program

Project Title

A phase 2 study of Bexmarilimab, an anti-Clever1 monoclonal antibody, in combination with azacitidine in patients with high-risk MDS

University of California at Davis

In 1997, I began as an academic physician at UC Davis. I developed a productive, independent laboratory-based research program, and as the Director of Hematologic Malignancies Program created one of the most productive clinical trials programs at the UC Davis Comprehensive Cancer Center. I currently am the deLeuze Endowed Professor for the non-toxic cure for lymphoma, Director of Bone Marrow and Stem Cell Transplantation and the interim Division Chief of Malignant Hematology Cellular Therapy and Transplantation.

My research has focused on immune-mediated therapeutics to reduce toxicity and enhance efficacy, including development of antibody drug conjugates, antibody-targeted liposomes, development of alternative natural products, and bi- and tri-specific antibodies. 

This work resulted in some 38 publications, 3 VA Merit and 12 intramural awards, and 3 patents (1 pending), which has facilitated ongoing funding of my lab and established me as an expert in targeted immuno-therapeutics.

Program Name(s)

Translational Research Program

Project Title

Gene-edited CD19 CAR-T cells with superior proliferation, persistence and serial-killing activity

Centre Hospitalier Universitaire Vaudois

Caroline Arber obtained her Doctor of Medicine from the University of Basel, Switzerland, and specialized in Internal Medicine and Hematology, with a focus on hematologic malignancies and stem cell transplant. To dive into the T cell engineering field, she moved to the Center for Cell and Gene Therapy, Baylor College of Medicine, USA, where she was a research fellow (2010-2014) and an Assistant Professor (2014-2017). Since 2017 she is an Associate Professor, Research Group leader and Attending Physician at the Lausanne University Hospital, University of Lausanne and Ludwig Institute for Cancer Research Lausanne, Switzerland. She leads a translational research group investigating novel T cell engineering strategies for hematologic malignancies. She also studies the impact of the bone marrow immune microenvironment on outcomes of CAR T cell therapies in myeloma. She has published several last author papers in journals such as Blood, JITC, Cancer Immunology Research, Science Advances.

Program Name(s)

Translational Research Program

Project Title

Designed biosensor to enhance CAR T cell therapy for multiple myeloma

Dana-Farber Cancer Institute

Dr. Lane’s laboratory and translational research focuses on the biology of high-risk blood cancers, including acute myeloid leukemia (AML), myelodysplastic syndrome (MDS), and blastic plasmacytoid dendritic cell neoplasm (BPDCN). His goal is to identify new therapeutic targets and to understand treatment resistance. He is an associate professor of medicine at Harvard Medical School, a physician in the Leukemia Program, and a lab investigator in the Division of Hematologic Neoplasia in the Department of Medical Oncology at the Dana-Farber Cancer Institute. He is director of the BPDCN Center at Dana-Farber. He is also an associate member of the Broad Institute of Harvard and MIT. Dr. Lane received a bachelor’s degree in biomedical engineering from Vanderbilt University, and MD and PhD degrees from Washington University. He completed a residency in internal medicine at Brigham and Women’s Hospital and fellowships in hematology and medical oncology at the Dana-Farber Cancer Institute.

Program Name(s)

Career Development Program

Project Title

Blastic plasmacytoid dendritic cell neoplasm (BPDCN): understanding disease biology to improve therapy

Imperial College, University of London

After completing a PhD in Immunology at Trinity College Dublin, I moved to Imperial College London to study how persistent infection with a virus causes Leukemia, Lymphoma and other diseases. The virus in question is Human T cell leukemia virus type-1 (HTLV-1), which infects the very cells which defend us against viruses: T cells. Around 5% of virus-carriers develop aggressive blood cancer (Adult T cell leukemia/lymphoma, ATL), in which one infected T cell becomes malignant. ATL is very difficult to treat, and people with the most aggressive forms survive for less than a year. I made the game-changing discovery that ATL-like T cells circulate in the blood of carriers who go on to develop ATL years before they show symptoms of ATL. I am now developing new diagnostics which can detect ATL early, and together with clinicians at the U.K. National Centre for Human Retrovirology and the Memorial Sloan Kettering Cancer Centre, will test whether a recently licenced drug can eliminate ATL-like T cells in high-risk carriers.

Program Name(s)

Translational Research Program

Project Title

Detection and treatment of Adult T cell leukemia/lymphoma in the premalignant stage.

Mayo Clinic

Dr. Thomas Witzig received the B.S. degree in biology at Illinois State University and the M.D. degree at University of Illinois College of Medicine. He completed an internal medicine residency at the University of Iowa followed by a clinical fellowship in hematology/oncology at Mayo Clinic.  He completed a year of laboratory research in multiple myeloma and lymphoma under the direction of Drs. Philip Greipp and Robert A. Kyle.  Dr. Witzig has been on the staff at Mayo Clinic since 1986. 

 Dr. Witzig’s clinical and research interests focus on blood cancers, especially non-Hodgkin and Hodgkin lymphoma. His current focus is on agents that interfere with the DNA damage repair pathways and understanding the role of maladaptive inflammation in lymphoproliferative diseases. He has been a leader in the development of radioimmunotherapy, mTOR inhibitors, and immunomodulatory drugs such as lenalidomide.  His group was the first to report the effectiveness rituximab for the autoimmune diseases that are IgG4 mediated and involve organs such as the orbit and pancreas. His research has been funded by the National Cancer Institute and the Predolin Foundation, among other organizations.  During COVID-19 his lab discovered one of the mechanisms that the COVID-19 virus uses to cause severe disease. This is now being investigated in patients with Long COVID-19. Dr. Witzig has been honored with several awards during his career, including the Department of Medicine Outstanding Investigator, the Henry S. Plummer Distinguished Physician, and most recently the Barbara Woodward Lips Professor 1.

He has served as a teacher and mentor and has given numerous international, national and regional presentations, in addition to invited presentations.  Dr. Witzig has co-authored more than 500 articles, books, book chapters, letters, and more than 600 abstracts.

Program Name(s)

IMPACT

Project Title

REACH: Recruitment Expansion through community Access to Clinical trials in Hematologic malignancies

TAP Partner

Rgenta Therapeutics is developing a pipeline of oral, small-molecule RNA-targeting medicines with an initial focus on oncology and neurological disorders. Rgenta has a proprietary platform to mine the massive genomics data to identify targetable RNA processing events and to design small-molecule glues to modulate the interactions among the spliceosome, regulatory proteins, and RNAs. 

Rgenta is working closely with TAP to further develop RNA-targeting molecules by supporting preclinical studies with the goal of moving towards clinical development in hematological malignancies. 

Program Name(s)

Therapy Acceleration Program

Project Title

Supporting development of RNA-targeting molecules for blood cancers

St. Jude Children's Research Hospital

Dr. Trent Hall is currently a Postdoctoral Research Associate in the laboratory of Dr. John Crispino at St. Jude Children’s Research Hospital in Memphis, TN. Dr. Hall received his doctorate from the University of Tennessee Health Science Center in 2020 studying hematopoietic stem cell development in Dr. Shannon McKinney-Freeman’s laboratory. Dr. Hall’s current research interests include predisposition to myeloid malignancies and hematopoietic development.

Program Name(s)

Career Development Program

Project Title

Identifying novel regulators of leukemic progression in GATA2-deficiency syndrome

Washington University in St. Louis

Stefan Tarnawsky, M.D.; Ph.D. is a Hematology/Oncology fellow and junior physician scientist at the Washington University School of Medicine in Saint Louis, MO. His research focus is understanding the origin of myeloid blood cancers. His graduate work at Indiana University with Dr. Merv Yoder and Dr. Rebecca Chan focused on the prenatal origin of childhood blood cancers. This work led to a F30 award from the NHLBI and three first-author research publications, including one in the Journal of Clinical Investigations. Currently, under the mentorship of Dr. Matt Walter, M.D., Stefan studies how splicing factor gene mutations dysregulate blood cell growth. He thereby aims to identify novel therapies for the ~50% of myelodysplastic syndrome patients and ~20% of acute myeloid leukemia patients that have these mutations. His career goal is to continue this research focus as an independent investigator studying and treating blood cancer patients at an academic medical center.

Program Name(s)

Career Development Program

Project Title

The Role of TP53 in Mutant U2AF1 Myelodysplastic Syndromes

MD Anderson Cancer Center

Dr. Carter, a Professor in the Section of Molecular Hematology and Therapy, Department of Leukemia has 20+ years of experience in molecular biology, biochemistry, and leukemia research. Her research focuses on understanding the mechanisms of drug resistance and targeting anti-apoptotic proteins and cell survival signaling pathways in myeloid leukemia. She is developing mechanism-based combinational strategies in therapy-resistant AML to overcome drug resistance and eradicate myeloid leukemia cells and leukemia stem/progenitor cells. She has published extensively in the field and several clinical trials have been developed based on her pre-clinical studies. Her recent works demonstrated the effectiveness and mechanisms of action of combined inhibition of antiapoptotic proteins Bcl-2 and Mcl-1 using BH3 mimetics (Blood Cancer Journal, 2023) and targeting HSP90 epichaperomes (Blood, 2023) in TP53 mutant AML.

Program Name(s)

Translational Research Program

Project Title

Targeting TP53-Y220C mutant AML

Washington University in St. Louis

Dr. Tyler Parsons completed his PhD research at Oakland University and the Beaumont Research Institute in the lab of Dr. Gerard Madlambayan where he published on the role of blood stem cells in tumor response to radiation therapy. During the final year of his PhD, he was diagnosed with a myeloproliferative neoplasm (MPN) which directed his career focus and passion to furthering the understanding of MPNs and their transformation potential to leukemia. To this end, he joined the lab of Dr. Grant Challen at Washington University School of Medicine (St. Louis) where he is investigating clonal evolution in MPNs and the mutational trajectory leading to secondary leukemia. The aim of his post-doctoral fellowship is to describe the clonal architecture of MPN disease progression to leukemia which could lead to early detection and improved disease surveillance. He is passionate about improving outcomes for patients by advancing our understanding of both the biology and disease evolution of MPNs.

Program Name(s)

Career Development Program

Project Title

Mechanisms of Clonal Evolution in the Transformation of MPN to sAML

Rutgers University

A PharmD by training, I then obtained my PhD guided by Dr. Manuel Serrano at the CNIO studying Sirt1 role in metabolism and cancer, which led to 4 first-author and 1 corresponding papers, plus 11 co authorships. Next, I joined the Ferrando Lab at Columbia University where I published two seminal papers identifying a NOTCH1-driven Myc enhancer critical for T-cell development and leukemia, and dissecting the role of cancer metabolism in the resistance to anti-NOTCH1 therapy. I started my independent career at Rutgers in July 2017. In these 4 years, I have established a highly successful and productive laboratory, as reflected by the multiple funding sources obtained (including R01, ACS or AACR grants, among others), as well as by the publication of 3 corresponding author studies: a Blood Cancer Discovery paper identifying an enhancer of PTEN in leukemia; a Leukemia paper describing the antileukemic effects of SHMT inhibition; and a Blood paper describing the therapeutic effects of mitochondrial uncoupling in T-ALL.

Program Name(s)

Career Development Program

Project Title

Therapeutic exploitation of novel mouse models and metabolic interventions in leukemia