Who We Fund

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

Seattle Children's Hospital

Dr. Loh is a Professor of Pediatrics at the University of Washington and Seattle Children’s Hospital. She is the Division Head of Hematology, Oncology, Bone marrow transplant, and Cellular therapies and also directs the Ben Towne Center for Childhood Cancer and Blood Disorder Research. Over her 30-year career, Dr. Loh has studied primary patient samples in the laboratory to make seminal observations about leukemia pathogenesis that informs accurate molecular diagnoses, improves risk stratification, and identifies novel therapeutic approaches. These studies have been performed in juvenile myelomonocytic leukemia and acute lymphoblastic leukemia, leading to innovative clinical trials. Her strength as a collaborator and leader also allows her to capitalize on the expertise and strengths of individual scientists to create highly productive teams that produce cutting edge results, and this proposal will continue that trajectory with Dr. Price’s expertise.

Program Name(s)

Translational Research Program

Project Title

Affinity-Tuned T-Cell Engagers for Dual Targeting of B-Myeloid Mixed Phenotype Acute Leukemia

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

TAP Partner

Vittoria Biotherapeutics is developing novel CAR-T cell therapies that transcend the limitations of current cell therapies. Based on technology exclusively licensed from the University of Pennsylvania, Vittoria's proprietary Senza5 platform unlocks the antitumor potential of engineered T cells and utilizes a five-day manufacturing process to maximize stemness, durability, and target cell cytotoxicity. By acting on the fundamental biology of T cells, Senza5 can be used to improve the efficacy of engineered T cell therapies with pipeline applications in oncology and autoimmune diseases.

Program Name(s)

Therapy Acceleration Program

Project Title

A phase 1 study of VIPER-101, a CD5-edited dual population chimeric antigen receptor cell therapy, to enhance immunotherapy against T-cell non-Hodgkin lymphoma

Virginia Commonwealth University

Venkata Battula, Ph.D., serves as Assistant Director of Massey Comprehensive Cancer Center’s Cancer Research Training and Education Coordination (CRTEC) program and is a Professor in the Department of Internal Medicine at the VCU School of Medicine. He joined VCU Massey from The University of Texas MD Anderson Cancer Center, where he was an Associate Professor in the Departments of Leukemia and Breast Medical Oncology within the Division of Cancer Medicine. He earned his Ph.D. in Human Cell Biology from Justus Liebig University in Giessen, Germany, and brings extensive expertise in translational cancer research.

Dr. Battula’s research focuses on understanding how cancer cells develop resistance to chemotherapy, radiation, and targeted therapies; identifying novel drug resistance mechanisms; and developing new combination therapies. His work has been instrumental in identifying GD2 as a novel marker in patients with triple-negative breast cancer (TNBC), an aggressive subtype with limited treatment options. GD2, expressed on cancer stem cells, is associated with tumor growth and poor clinical outcomes. Building on these findings, Dr. Battula recently secured funding from the U.S. Department of Defense to initiate a clinical trial targeting GD2 in TNBC.

In his role within CRTEC, Dr. Battula is committed to expanding graduate-level training opportunities and advancing programs that prepare the next generation of cancer researchers.

Program Name(s)

Translational Research Program

Project Title

Arming NK Cells to Target B7-H3+ AML Cells

Mayo Clinic, Rochester

Grzegorz (Greg) Nowakowski, M.D., is a consultant and a Professor of Oncology and Medicine, Division of Hematology at Mayo Clinic in Rochester,Minnesota, where he also serves as the Aggressive B-cell Lymphoma Program Director, the Chairman of Education,and an Advanced Hematology Fellowship Program Director. Dr. Nowakowski received his MD from the Medical University of Warsaw, Poland. He completed his internal medicine residency at Yale University Medical School -Norwalk Hospital, Norwalk, Connecticut and his fellowship in Hematology and Medical Oncology at Mayo Clinic, Rochester, Minnesota. Dr Nowakowski joined the Mayo Clinic Lymphoma Group in 2006 as a Mayo Foundation Scholar.Heis an alumnus of the American Society of Hematology (ASH) Clinical Research Training Institute and American Society of Clinical Oncology (ASCO) Leadership Development Program. Dr. Nowakowski’s research focuses on the molecular classification and biology of lymphoproliferative disorders,new approaches to clinical trial design and novel therapies for lymphoma and hematological disorders. Heis an investigator in University of Iowa/Mayo Clinic Lymphoma Specialized Center of Research Excellence program, where he leads career enhancement program. Dr. Nowakowski has authored over 200 articles and numerous book chapters. Dr.Nowakowski serves as a principal investigator of multiple investigator-initiated and cooperative group clinical trials(ECOG, Alliance) and industry studies and serves and a member of ECOG Lymphoma Core Committee. Dr.Nowakowski also chairs the Lymphoma Committee and Hematological Malignancy Program in the Academic and Community Cancer Research United (ACCRU) network. He currently serves as a vice Chair of ASH Clinical Trial Innovation Subcommittee chair of ASCO Research Community Forum and ASCO Clinical Trial Access and Participation Taskforce. Dr. Nowakowski has served as Voting Member of the Oncology Drugs Advisory Committee (ODAC) to the Food and Drug Administration (FDA).

Program Name(s)

IMPACT

Project Title

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

University of Cambridge

George Vassiliou is Professor of Hematological Medicine, Director of the Blood Cancer United/Blood Cancer UK Specialist Center of Research (SCOR) in Myeloid Cancer Prevention and Co-lead of the Hematological Malignancies Virtual Institute at the University of Cambridge. He is also an Honorary Consultant Hematologist at Cambridge University Hospitals, where he founded and leads Europe’s first clonal hematopoiesis clinic. 

He studies the pre-clinical evolution, molecular pathogenesis and treatment of myeloid cancers. Highlights of his work include the co-discovery of the shared precursor of myeloid cancers, clonal hematopoiesis (CH), the description of its lifelong natural history and the first demonstration that individuals at risk of these cancers can be identified years in advance, opening the prospect of their prevention. He also developed the first genomic diagnostic tools for myeloid cancers, discovered mechanisms of how they develop and identified hundreds of potential treatment targets using the first genome-wide CRISPR genetic screen in any human cancer. His work has led to development of new treatments, including METTL3 inhibitors that are now in clinical trials against acute myeloid leukemia.

In recognition of his work, he was elected a Fellow of the Academy of Medical Sciences and awarded the European Haematology Association Research Excellence Award in 2026.

Program Name(s)

Specialized Center of Research Program

Project Title

Development of a clinical program for myeloid cancer prevention

The George Washington University

Dr. Vichare’s research investigates the impact of health policies on health equity. Her training as primary care physician and health services researcher, and professional experiences shape her research approaches. Her recent studies in collaboration with Dr. Luo and Ms. Erikson utilize Medicaid claims and generate foundational evidence on health workforce in Medicaid. She implements creative analytic approaches, including in her ongoing funded research projects that innovatively link physician race/ethnicity and Medicaid claims. The findings are critical to support policy improvements in health workforce diversity. Dr. Vichare has a solid understanding of Medicaid policies for cancer care. Her publications address salient issues relevant to the oncology specialty workforce, including a national study of radiation oncology workforce. Dr. Vichare developed an NQFendorsed quality measure to address variation in radiation therapy for bone metastasis. Her transdisciplinary research and resulting collaborations have produced notable publications (https://www.ncbi.nlm.nih.gov/myncbi/1t5tUQmM5aboAj/bibliography/public/). Dr. Vichare has a track record of successfully managing teams, budgets and creating realistic research plans and timelines. Her experience in cancer health policy, familiarity with oncology specialty workforce and research approaches grounded in contemporary health equity frameworks demonstrate her expertise and motivation necessary to lead the proposed project.

Program Name(s)

Equity in Access

Project Title

Addressing Inequities in Access to Care for Patients with Hematologic Malignancy: Understanding the Impact of Telehealth Policies in Medicaid

Columbia University Medical Center

I’m a Professor of Medicine and the Director of the Multiple Myeloma and Amyloidosis Program at Columbia University. I received my medical and doctorate degrees from Humboldt University. My postdoctoral training included residency and fellowship at Humboldt University and a research fellowship at the Dana-Farber Cancer Institute. Before joining the faculty at Columbia University, I was the Director of the Multiple Myeloma Program at the University of Pittsburgh Cancer Institute.

I’m an active translational researcher, serving as principal investigator for many clinical trials, including investigator-initiated studies for multiple myeloma and AL amyloidosis. My translational research focuses on the identification of novel targets for the treatment of multiple myeloma, myeloma bone disease, and amyloidosis. My research is funded by multiple RO1s and awards. As a frequent lecturer, I regularly present at annual meetings of the ASH and ASCO. I have also published over 100 original articles, editorials, chapters in such prestigious journals as JCO, JCI, Blood, and Cancer Research, etc

Program Name(s)

Translational Research Program

Project Title

Targeting the MMP-13/PD-1H signaling axis for multiple myeloma bone disease and immunosuppression

The University of Alabama at Birmingham

Dr. Goyal obtained his medical school diploma from Smt. N.H.L. Municipal Medical College in Ahmedabad, India, in 2011 and moved to the US to complete a residency in Internal Medicine from Creighton University Medical Center, Omaha, Nebraska in 2016. He pursued a fellowship in hematology-oncology from Mayo Clinic, Rochester, Minnesota from 2016-2019. He developed a unique focus in histiocytic neoplasms, including Erdheim-Chester disease, Langerhans cell histiocytosis, and Rosai-Dorfman disease. He conducted multiple studies describing the epidemiology, treatments, and outcomes of patients with histiocytosis and led to the establishment of first of its kind multidisciplinary Histiocytosis Working Group. He has led national and international guidelines on the diagnosis and management of these rare disease entities. He was subsequently recruited to join the Hematology-Oncology division at University of Alabama at Birmingham as an Assistant Professor in 2019 where he launched the Histiocytic Disorder Survivor Study to assess long-term outcomes among individuals with histiocytic neoplasms.

Program Name(s)

Special Grants

A Multi-Center, Multi-National Investigation of Survivorship and Patient-Reported Symptoms in Erdheim-Chester Disease

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

Albert Einstein College of Medicine

Dr. Keisuke Ito is an Associate Professor of Cell Biology and Medicine at the Albert Einstein College of Medicine, where he has also served as the Director of Scientific Resources at the Stem Cell Institute. After his postdoctoral training, first at Keio University, where he also completed his clinical training, and then at Harvard, he joined the Einstein faculty in 2012. Dr. Ito’s team has focused on advancing our understanding of the regulatory pathways controlling the equilibrium of stem cells. At the core of his work is the process of stem cell division, and the balance between self-renewal and differentiation, which directly impacts tissue homeostasis and the development of hematological malignancies. Dr. Ito is devoted to targeting mitophagy, a mitochondrial quality-control process, as a therapeutic strategy, and has cut a path along the leading edge of research into the role of Ten-eleven translocation in the pathogenesis of myelodysplastic syndrome.

Program Name(s)

Career Development Program

Targeting mitophagy of leukemia stem cells for therapy