Who We Fund

Cincinnati Children's Hospital

Dr. Bailee Kain is from Geneseo, IL and received her B.S. in Biochemistry from University of Missouri in 2016. She completed her doctoral thesis work at Baylor College of Medicine in Dr. Katherine King's laboratory, where she studied how antigenically diverse pathogens reprogram hematopoietic stem cells to induce innate immune cross-protection. In November 2022, Bailee joined Dr. Lee Grimes lab at Cincinnati Children's Hospital Medical Center (CCHMC) as a postdoctoral research fellow. In the Grimes lab, she has focused on determining the oncogenic potential of novel variants found in African Ancestry AML patients, including PHIP. Through nominating PHIP as a functional oncogene, she hopes to combat cancer health disparities by making AML screening, risk stratification, and therapeutic strategies more inclusive. Following her training, Bailee's goal to is to develop an independent research program focused on understanding the disease mechanism of ancestry specific variants found in AML.

Program Name(s)

Career Development Program

Project Title

Functionalizing novel PHIP variants in ancestry-specific acute myeloid leukemia

Brigham and Women’s Hospital

Christopher Hergott, M.D., Ph.D. is a postdoctoral fellow at the Dana-Farber Cancer Institute (DFCI) and Associate Pathologist in hematopathology at Brigham and Women's Hospital (BWH) in Boston. He obtained his undergraduate degree in Biochemistry from the University of Rochester and his medical and graduate degrees from the University of Pennsylvania. He completed residency (and chief residency) in Clinical Pathology and a clinical fellowship in Hematopathology at BWH before beginning his postdoctoral research training in the laboratory of Dr. Benjamin Ebert at DFCI. Christopher's research interests lie at the intersection of inflammation and hematopoiesis, with a particular focus on clonal hematopoiesis and its progression to myeloid malignancies. In his free time, Christopher enjoys playing guitar, reading, and travelling.

Program Name(s)

Career Development Program

Project Title

Defining the role of IL-17A in propelling clonal cytopenia of undetermined significance

Dana-Farber Cancer Institute

Eric Smith, MD PhD is Director of Translational Research for Immune Effector Cell Therapies at Dana-Farber Cancer Institute (DFCI) where his primary responsibility is as PI of a gene and cell engineering pre-clinical laboratory. He is an Assistant Professor at Harvard Medical School (Immunology PhD Faculty); Associate Member at the Broad Institute of Harvard and MIT; a Member at the Parker Institute for Cancer Immunotherapy; and the founding faculty director of the IMmunotherapy Platform for Antibody and CAR Therapeutics Development and Translation (IMPACT2) Center at DFCI. He received his MD/PhD and internal medicine training at the Mount Sinai School of Medicine and medical oncology and post-doctoral training at Memorial Sloan Kettering Cancer Center and stayed on as faculty in the Cellular Engineering Center and Myeloma/Cellular Therapy services. He was recruited to DFCI in 2020 to advance the home-grown adoptive cellular therapy pipeline there. The Smith Lab for Genetic and Cellular Engineering focuses on pre-clinical efforts to advance the field and developing therapies for both hematologic and solid tumors for the benefit of patients. More than a dozen clinical trials have been initiated stemming from his team’s lab work. The most developed of which is a first-in-class CAR targeting GPRC5D, a target he described as important for the immunotherapy of myeloma; he and his colleagues reported the phase I study in NEJM, and a phase II multi-center registration study is now ongoing.

Program Name(s)

Discovery

Project Title

Interrogating T-cell apoptotic priming to improve CAR-T persistence in treatment of lymphoid malignancies

Oregon Health & Science University

Dr. Maxson is an assistant professor in the Knight Cancer Institute, where she investigates the cellular and molecular changes that cause myeloid leukemias. She pursued her undergraduate studies at Scripps College and then completed her Ph.D. in Cell Biology in the area of protein trafficking and processing. As a postdoctoral fellow in the laboratories of Drs. Jeff Tyner and Brian Druker, she integrated genomic and functional screening data to identify novel therapeutic targets in leukemia. Notably, Dr. Maxson identified mutations in CSF3R in the vast majority of patients with chronic neutrophilic leukemia. She discovered that these mutations confer sensitivity to JAK inhibitors, which resulted in a clinical trial for these patients. The Maxson laboratory works to understand how genomic changes manifest at the cellular level to promote cancer formation and progression. Her long-term goal is to use this understanding to develop lifesaving treatments for patients with leukemia.

Program Name(s)

Career Development Program

Project Title

Targeting the interplay between signaling and transcriptional dysfunction in myeloid leukemias

Garvan Institute of Medical Research

Peter trained at the University of Wales College of Medicine and Cambridge and Oxford Universities in the UK. In 2003 he joined Sheffield University and became joint Director of the Mellanby Center for Bone Research and Head of Department of Human Metabolism. In 2011 Peter joined the Garvan Institute of Medical Research in Sydney where he is Director of the Cancer Plasticity and Dormancy program. Peter is an international leader in understanding myeloma bone disease. He discovered key molecular pathways that cause myeloma bone disease. This research contributed to development of bone targeted therapies, including anti-RANKL and zoledronic acid, that are now in routine clinical use globally. Peter’s current research is investigating molecular pathways, including the Wnt pathway and sclerostin, that target osteoblasts, restore lost bone, increase bone strength and stop fractures. He is also investigating the role of bone cells in controlling myeloma cell dormancy and disease relapse.

Program Name(s)

Translational Research Program

Project Title

Targeting the Osteogenic Lineage as a Therapeutic Strategy in Multiple Myeloma

Dana-Farber Cancer Institute

Program Name(s)

Career Development Program

Project Title

Mechanisms of oncogenic transcription in NPM1-mutant myeloid leukemia

Beckman Research Institute of the City of Hope

Stephen J. Forman, MD, is a hematologist-oncologist, international expert in leukemia, lymphoma, and bone marrow transplant (BMT), and pioneer in immunotherapy. Dr. Forman has spent his 45-year career at City of Hope (COH), leading the Department of Hematology for 38 years and directing the Hematology Malignancies Research Institute since 2015. Under his leadership, COH developed one of the world’s largest and most successful BMT centers, which has led to dramatic increase in survival rates for blood cancers. He also directs the T cell Therapeutics Research Laboratories, the goal of which is to develop new ways to use the immune system to fight cancer. In this role, he leads a team of scientists in developing chimeric antigen receptor (CAR)-engineered T cells for treatment of a variety of cancers, including leukemia. Based on this research, Dr. Forman has led the advancement of multiple laboratory discoveries to the clinic, including CD19-directed CAR T cells for adults with leukemia.

Program Name(s)

Academic Clinical Trials Program (ACT)

Project Title

CD19-CAR T cells as Consolidation for Older Adults with Acute Lymphoblastic Leukemia in Remission

Dana-Farber Cancer Institute

Dr. Chen is a Clinical Investigator and Attending Physician in the Adult Leukemia Program at Dana-Farber Cancer Institute. He attended Stanford University School of Medicine and completed Internal Medicine residency at Massachusetts General Hospital and Medical Oncology fellowship at Dana-Farber Cancer Institute. His research interest is in the development of novel therapies for advanced myeloid neoplasms such as acute leukemias and myelodysplastic syndromes, with particular focuses on cell therapies and epigenetic approaches. 

Program Name(s)

Translational Research Program

Project Title

Memory-like natural killer cells and venetoclax to eradicate measurable residual disease in AML

TAP Partner

Dren Bio is a clinical-stage biopharmaceutical company focused on developing therapeutic antibodies for the treatment of cancer, autoimmune and other serious diseases. Dren Bio’s pipeline encompasses two distinct programs, the first focusing on the engineering of antibodies with enhanced antibody-dependent cellular cytotoxicity (“ADCC”) capabilities and the second revolving around its proprietary Targeted Myeloid Engager and Phagocytosis Platform.

Program Name(s)

Therapy Acceleration Program

Project Title

A phase 1/2 study of DR-01, an anti-CD94 monoclonal antibody, in patients with large granular lymphocytic leukemia or cytotoxic lymphomas

A phase 1 study of DR-0201, a bispecific myeloid engager, in patients with B-NHL

Maine Medical Center

Dr. Michaela Reagan is a Faculty Scientist II at the MaineHealth Institute for Research and an Associate Professor at Tufts University School of Medicine. She received her B.S. in general Engineering from Harvey Mudd College (2006) and Ph.D. from Tufts University in Biomedical Engineering in the field of breast cancer bone metastasis (2011). She then performed her post-doctoral research at the Dana-Farber Cancer Institute in the laboratory of Dr. Irene Ghobrial (2011-2015). Dr. Reagan is a member of the Finance Committee of the American Society of Bone and Mineral Research (ASBMR) and is the past chair of the ASBMR’s Women’s Committee. Since 2015, she has led innovative, transdisciplinary, basic and translational research in the Reagan Laboratory at MaineHealth with the goal of identifying cancer vulnerabilities that can lead to new treatments or cures for multiple myeloma (MM) patients. Her unique research is focused on the interactions between obesity, adipocytes and myeloma cells.

Program Name(s)

Career Development Program

Project Title

Multiple Myeloma Support from the Microenvironment: Bone Marrow Adipocytes and the Fatty Acid Binding Proteins

Houston Methodist Research Institute

I am a translational tumor immunologist. I have 30 years of experience as a well-funded and published researcher and am one of the leading investigators in the fields of tumor immunology in myeloma and other cancers. My laboratory has been working on: (1) characterizing myeloma- and tumor-specific T cells and their subsets and examining their functions, (2) identifying novel myeloma-associated antigens and better methods for immunotherapy, (3) investigating the cross-talk between the tumor microenvironment (TME) and immune system, (4) conducting clinical trials to evaluate the efficacy of immunizing patients with idiotype or dendritic cell-based vaccines, and (5) exploring immunotherapies using myeloma antigens such as DKK1. Our recent research focuses on: (a) developing novel therapeutic mAbs and CAR-T cells for cancers, (b) identifying T-cell subsets that have potent antitumor effects after adoptive transfer, and (c) identifying TME components that induce tumor drug resistance.

Program Name(s)

Translational Research Program

Project Title

Developing Novel CAR-T Cell Therapy For Hematologic Malignancies

Medical College of Wisconsin

Nirav Shah, MD, MSHP is currently an Associate Professor of Medicine at the Medical College of Wisconsin, Division of Hematology and Oncology, specializing in lymphoma, stem cell transplant, and CAR-T therapy. He graduated with honors and Alpha Omega Alpha honor society membership from University of Illinois at Chicago College of Medicine in 2008. He then completed his Internal Medicine residency at the Harvard affiliated Massachusetts General Hospital in 2011. Following residency, he went to the University of Pennsylvania where he completed Hematology/Oncology fellowship and received a Master of Science in Health Policy research in 2015. His current focus is the development of dual targeted anti-CD20, anti-CD19 CAR-T cells (CAR20.19) for B-cell malignancies. Results of a Phase 1 trial with CAR20.19 T-cells were published in Nature Medicine in Oct. 2020. Data from that study directed development of three new CAR20.19 clinical trials led by Dr. Shah all actively enrolling patients.

Program Name(s)

Career Development Program

Project Title

Improving Bispecific CD20/CD19 CAR T-cell Therapy to Overcome Resistance Mechanisms in B-cell Malignancies