Who We Fund

Cleveland Clinic

Paolo Caimi is a physician and clinical investigator at the Cleveland Clinic, where he is also the Associate Bone Marrow Transplant Director for Cellular Therapy. Dr. Caimi completed his medical training at the Pontificia Universidad Catolica de Chile in Santiago, Chile. He finished residency at Johns Hopkins University / Sinai Hospital Residency Program in Internal Medicine followed by a hematology and oncology fellowship at Case Western Reserve University. His clinical focus is on the care of patients with lymphoid malignancies and his research is centered around early phase trials, with an emphasis on phase I trials of cellular therapy.

Program Name(s)

Academic Clinical Trials Program (ACT)

Project Title

BAFF-ligand CAR T-cells and pre-apheresis B-cell lymphodepletion for relapsed/refractory CLL

The Children's Hospital of Philadelphia

Sarah K Tasian, MD PhD is a pediatric oncologist and physician-scientist at the Children’s Hospital of Philadelphia (CHOP) and an Associate Professor of Pediatrics at the University of Pennsylvania School of Medicine who is interested in development of molecularly-targeted therapeutics and immunotherapies for children with high-risk leukemias. She specialises in the clinical care of children with leukemia and lymphoma, is an internationally-recognized expert in pediatric ALL and AML biology and novel therapeutics, and serves as Chief of the Hematologic Malignancies Program at CHOP, where she holds the Joshua Kahan Endowed Chair in Pediatric Leukemia Research. Her federally-funded translational laboratory research program focuses upon preclinical and early-phase clinical testing of small molecule inhibitors and chimeric antigen receptor (CAR) T cell immunotherapies in high-risk genetic subsets of childhood ALL, AML, and JMML. As an experienced clinical trialist, Dr Tasian also has several leadership roles in the Children’s Oncology Group ALL and Myeloid Diseases executive committees and is the clinical trials leader of the international Blood Cancer United PedAL consortium, working collaboratively with colleagues across the world to advance precision medicine therapeutics for children with relapsed/refractory leukemias.

Program Name(s)

Career Development Program

Project Title

Precision Medicine Inhibitor and Immunotherapy Approaches for High-Risk Childhood Leukemias

St. Jude Children's Research Hospital

I am a pediatric oncologist, who is interested in using the patient’s immune system to fight cancer. I grew up in Germany and moved to the US in 1992 after obtaining my medical degree. After completing my training in pediatric and oncology, I became faculty at the Cancer Center of Texas Children’s Hospital and the Center for Cell and Gene Therapy at Baylor College of Medicine. In the laboratory I focused on developing immune cell therapies for cancer patients, which I translated with my research team into the clinic. In addition, I managed pediatric cancer patients, who underwent bone marrow transplantation, and participated in numerous clinical studies. In 2017 I became Chair of the Department of Bone Marrow Transplantation and Cellular Therapy at St. Jude Children’s Research Hospital. The department focuses on evaluating novel transplant and cell therapy approaches using genetic engineering approaches to augment the ability of the immune system to fight cancer.

Program Name(s)

Translational Research Program

Project Title

CD70-directed CAR T-cell therapy for the treatment of relapsed/refractory pediatric AML

Fred Hutchinson Cancer Center

Dr Dhodapkar is a physician-scientist with expertise in clinical/translational research in cancer immunology/dendritic cell (DC) biology and in immunobiology of myeloma (MM) and related diseases. Following training in immunology in the lab of Nobel Laureate (Late) Ralph Steinman, Dhodapkar lab has been focused on studies of immunobiology of myeloma and cancer immunology. His clinical practice has been focused on patients with myeloma for past 20+ years. He carried the earliest studies of adoptive human DC transfer and in vivo targeting of human DCs. His laboratory has made several seminal contributions to MM biology and cancer immunology. In terms of clinical research in MM, he has led several clinical studies, including the first clinical studies that led to the discovery of anti-myeloma effects of thalidomide (UArk98-003), first US national cooperative group studies in precursor gammopathies(S0120), AL amyloidosis(S9826) and co-led the first phase III studies (E3A06) showing successful prevention of clinical MM. He has served on several panels for clinical guidelines, including as lead for SITC clinical immunotherapy guidelines panel for myeloma. He has co-led the cancer immunology programs at Yale and Emory for the past decade. His work has been cited >34K times with h-index 87. Relevant to the current proposal, he/his group has played a major role in clinical development of T-cell engagers as well as IMiDs in MM, developed the first genetically-humanized model for myeloma and provided new insights into spatial immunology.

Program Name(s)

Academic Clinical Trials Program (ACT)

Project Title

Pilot trial of microbial targeting to prevent myeloma

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

Medical College of Wisconsin

Siegfried Janz, MD, DSc, Professor and William G. Schuett, Jr., Multiple Myeloma Endowed Chair directs translational myeloma research at the Division of Hematology, Oncology & Bone Marrow Transplantation, Department of Medicine, Medical College of Wisconsin Milwaukee. After obtaining his medical degree and board certification in Clinical Immunology from Leipzig University Medical School, Germany, he received advanced training in genetic and biological pathways of myeloma development at the National Cancer Institute, NIH, Bethesda, Maryland. In 2018 he relocated his laboratory to Milwaukee, where he works in close association with his clinical colleagues to enhance our understanding of the natural history of myeloma and improve myeloma treatment and outcomes. His ongoing efforts concentrate on the design and testing of novel immunotherapies that rely on patient-derived T lymphocytes to seek out and kill myeloma.

Program Name(s)

Translational Research Program

Project Title

Improving outcomes of multiple myeloma using TGF-beta resistant BCMA-targeted CAR T cells

Icahn School of Medicine at Mount Sinai

My name is Ivan Odak and I am a postdoctoral researcher in the Brody lab. I am an accomplished researcher with 20 authored papers, 9 of which as first or last author. I obtained my PhD summa cum laude from Hannover Biomedical Research School in Germany, where I also worked as a postdoc in the lab of Reinhold Förster. Though challenging, I find science primarily enjoyable, and I like using my skills to tackle important questions in the field of immuno-therapy. The colleagues see me as tireless force in the workplace and I often use my positive attitude and energy to motivate others. My ultimate goal is to establish my own lab dedicated to research and discovery of cancer immunotherapies.

Program Name(s)

Career Development Program

Project Title

Prevention of antigen escape by modulation of off-target tumor killing in T cells

Perelman School of Medicine at the University of Pennsylvania

Dr. Liling Wan is an Assistant Professor at the University of Pennsylvania. She received a B.S. in Biological Sciences and Biotechnology from Tsinghua University and a Ph.D. in Molecular Biology from Princeton University. She conducted postdoctoral research at Rockefeller University where she studied chromatin regulators in cancer. The Wan lab studies basic gene regulatory mechanisms and how these mechanisms are dysregulated in cancer, with the goal of harnessing these insights for therapeutics. Her research has revealed how chromatin “reader” proteins impact gene regulation in cancer such as acute myeloid leukemia and led to early drug development efforts targeting these mechanisms. Dr. Wan has been recognized for her innovative and impactful research through numerous awards including AACR NextGen Star, NIH Pathway to Independence Award, the NIH Director’s New Innovator Award, and was recently named a Pew-Stewart Scholar, V Foundation Scholar, and ASH Scholar.

Program Name(s)

Career Development Program

Project Title

Epigenetic Mechanisms in Acute Myeloid Leukemia

Memorial Sloan Kettering Cancer Center

I am the Edward P. Evans Chair in MDS at Memorial Sloan Kettering Cancer Center (MSK) where I also serve as Chair of the Molecular Pharmacology Program. My clinical areas of expertise are in myeloid malignancies, chronic lymphocytic leukemia, and rare forms of leukemias (hairy cell leukemia, CMML, BPDCN, and histiocytoses). 

Over the last ten years, my laboratory has been focused on understanding alterations in the process of RNA splicing in cancer. Motivated by the discovery of high frequency mutations in the splicing machinery in leukemias and MDS, my lab’s work has led to the development of several therapeutic approaches for these genetic subtypes of cancer. I have received the Seldin-Smith Award for Pioneering Research from the American Society of Clinical Investigation, the Dameshek Prize from the American Society of Hematology, and the Pershing Square Sohn Prize for Young Investigators in Cancer Research.

Program Name(s)

Discovery

Project Title

TCR T cells for the treatment of SRSF2 mutant myeloid neoplasms

Dana-Farber Cancer Institute

I graduated from Columbia College of Physicians & Surgeons, where I stayed for Internal Medicine residency training/chief residency before moving to Boston for fellowship training in hematology/oncology at Dana-Farber/Mass General Cancer Center. I stayed on as faculty in the lymphoma program at Dana-Farber and am now an Assistant Professor of Medicine at Harvard Medical School.  My research interests are in the clinical and translational study of immunotherapies for lymphoma, with a particular interest in cellular immunotherapies. I also serve as the Medical Director of the Immune Effector Cell Therapy program at Dana-Farber, which houses our commercial and research cell therapy programs across the Institute.  I am the principal investigator of industry-sponsored and investigator-initiated clinical trials involving cellular therapies for lymphoma, and lead retrospective and translational studies to identify mechanisms of response and resistance to these therapies.

Program Name(s)

Career Development Program

Project Title

CAR T-cell therapy in central nervous system (CNS) lymphoma: a study in safety and efficacy and a model in which to study mechanisms of neurotoxicity

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

Emory University

I am a cancer biologist and Associate Professor in the Department of Hematology and Medical Oncology at the Winship Cancer Institute, Emory University School of Medicine. I am a recipient of the Lexie Clayton Impact Award from The Leukemia & Lymphoma Society. My research focus includes understanding how metabolic states regulate specific cancer hallmarks such as the evasion of cell death; proliferation and growth; and invasion and metastasis to identify targetable metabolic vulnerabilities. We have an interest in investigating how mitochondrial metabolism impacts multiple myeloma therapy efficacy and more recently are examining how the bone marrow niche is regulated by neural signaling. My research lab comprised of talented scientist trainees, who in collaboration with the Winship team of multiple myeloma physicians and scientists are endeavoring to ask provocative and innovative questions for curing multiple myeloma.

Program Name(s)

Translational Research Program

Project Title

Deciphering the metabolic basis for t(11;14) multiple myeloma venetoclax sensitivity

Investigating anti-neoplastic effects of beta blockers in multiple myeloma