Who We Fund

Columbia University Medical Center

I am a pediatric oncologist and health outcomes researcher at Columbia University Irving Medical Center. My research aims to identify how social determinants of health drive care and outcomes in children, adolescents, and young adults (AYA) with leukemia and lymphoma. At Columbia, I am the institutional Principal Investigator for the Dana-Farber Cancer Institute ALL Consortium and I serve on the Children’s Oncology Group Hodgkin Lymphoma (HL) Steering Committee. In these roles I participate in the design and implementation of new clinical trials, and in the development of embedded health services studies. My recent work includes a series of large-scale analyses (using clinical trials and population data) evaluating outcomes by race/ethnicity and age in ALL and HL. Increasingly, I am working to identify barriers to clinical trial participation among diverse populations, and on leveraging the clinical trial infrastructure to collect prospective data on social determinants of health.

Program Name(s)

Career Development Program

Project Title

Leveraging cancer registries, clinical trials, and community partnerships to address disparities in pediatric, adolescent, and young adult lymphoma

University of Florida

Coming soon.

Program Name(s)

Equity in Access

Project Title

Enhancing Connection and Communication with Community-Based Oncology Practices to Improve Cancer Clinical Trial Recruitment: The ECCO Study

TAP Partner

Solu Therapeutics is a biotechnology company dedicated to developing next-generation therapeutics to eliminate disease-driving cells in cancer, immunology and other therapeutic areas. The company’s proprietary CyTAC (Cytotoxicity Targeting Chimera) and TicTAC (Therapeutic Index Control Targeting Chimera) platforms enable the development of innovative medicines that combine the target-binding capability of small molecules with the therapeutic power of biologics.

Program Name(s)

Therapy Acceleration Program

Project Title

A phase 1 study of STX-0712, a CCR2-CyTAC monocyte depletor, in patients with CMML

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

Icahn School of Medicine at Mount Sinai

Dr. Brody is Director of the Lymphoma Immunotherapy Program at Mount Sinai and a member of the Depart of Immunology. He has developed a robust clinical program and a translational Cancer Immunotherapy Lab which investigates basic and applied tumor immunology to develop novel therapies for lymphomas and CLL with results published in top-tier journals including Nature Medicine and Cancer Discovery.  Dr. Brody has pioneered a therapeutic vaccine approach—in situ vaccination—that induces anti-tumor immunity and regression of tumors throughout the body with clinical results published primarily for Follicular Lymphoma. Recently, his group discovered a novel approach ‘potentiating bystander killnig’ to improve immunotherapies by preventing a common escape mechanism that tumors use to evade CAR-T and bispecific antibody therapies.

Dr. Brody’s research receives funding from numerous grantors e.g. the NIH, Cancer Research Institute, Damon Runyon Foundation, and the Lymphoma Research Foundation.

Program Name(s)

Research Accelerator for Follicular Lymphoma

Project Title

Understanding and targeting rare Ag–(CD19/CD20–) Follicular Lymphoma cells to prevent post-immunotherapy antigen escape

Emory University

Dr. Ji is a health services researcher with extensive experience leveraging insurance payer data to study policy issues pertaining to U.S. healthcare systems, with an emphasis on Medicaid. Her research strives to understand the effect of Medicaid policies on healthcare access and outcomes for vulnerable youth and adults. She recently extended this experience to data on pediatric and adolescent/young adult (AYA) cancer survivorship. She co-leads (with Dr. Sharon Castellino) NCI 1R03CA259665-01 to investigate how the Affordable Care Act affects treatment timeliness and survival in AYAs with cancer. She leads a Medicaid initiative within the Childhood Cancer Survivor Study, where she oversees an ongoing linkage of administrative Medicaid data to a nationwide cohort of cancer survivors. She also leads a Junior Faculty Focused Award evaluating Medicaid coverage continuity for pediatric cancer survivors in a single institution.

Program Name(s)

Equity in Access

Project Title

Impact of Health Insurance on Mortality for Children and AYAs Newly Diagnosed with a Blood Cancer: A Population-Based Multistate Evaluation

TAP Partner

BioInvent International AB is a clinical-stage biotech company that discovers and develops novel and first-in-class immuno-modulatory antibodies for cancer therapy, with currently four drug candidates in five ongoing clinical programs in Phase 1/2 trials for the treatment of hematological cancer and solid tumors, respectively. The Company's validated, proprietary F.I.R.S.T™ technology platform identifies both targets and the antibodies that bind to them, generating many promising new drug candidates to fuel the Company's own clinical development pipeline and providing licensing and partnering opportunities.

Program Name(s)

Therapy Acceleration Program

Project Title

A phase 1/2 study of BI-1206, a monoclonal antibody to CD32b (FcyRIIB), in combination with rituximab and acalabrutinib in patients with indolent NHL that has relapsed or is refractory to rituximab

A phase 2 study of BI-1808, a monoclonal antibody to TNFR2, as a single agent and in combination with pembrolizumab in patients with solid tumors and CTCL

Winship Cancer Institute

Dr. Jean Koff is an Associate Professor in the Department of Hematology and Medical Oncology and Director of the Lymphoma Program’s Translational Research Team at Winship Cancer Institute of Emory University. Her clinical expertise in lymphoma is complemented by her research characterizing the immunologic and genetic factors that contribute to poor outcomes in lymphoma patient populations under-represented in most studies, such as African Americans and organ transplant recipients. She serves as an investigator on several team science projects involving multi-institutional cohorts of lymphoma patients with integrated analyses of clinical and molecular data, including the Lymphoma Epidemiology of Outcomes cohort study. Dr. Koff is the 2024 Chair of the Scientific Committee on Lymphoid Neoplasia for the American Society of Hematology. Her work has been funded by the Lymphoma Research Foundation, the American Association for Cancer Research, the American Cancer Society, and the NIH.

Program Name(s)

Specialized Center of Research Program

Project Title

Translating molecular profiles into treatment approaches to target disparities in lymphoma

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

Cincinnati Children’s Hospital Medical Center

I am an Assistant Professor at Cincinnati Children's Hospital Medical Center. My areas of research interest include drug development and signaling with focus on small GTPases. My research is both basic and translational.

My research efforts encompass several methodologies, including structural biology, biophysical and biochemical studies, cellular functional assays, and ultimately, identifying small molecule compounds that bind to and modulate GTPase signaling in in vivo pre-clinical models of cancer.

RAC GTPases are key regulators of cell growth. By reorganizing the actin cytoskeleton, RAC plays a key role in cancer cell metastasis. It is also involved in mechanisms of resistance to therapies. My lab's goal is to inhibit RAC in leukemia by understanding the molecular mechanisms driving its hyperactivity.

One of my lab’s groundbreaking discoveries is the identification of a small molecule inhibitor of VAV3, a RAC activator. Current research studies the efficacy of VAV3 inhibition in models of relapsed/recurrent leukemia.

Program Name(s)

Translational Research Program

Project Title

Overcoming RAS-driven Mechanisms of Resistance in Leukemia

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

Memorial Sloan Kettering Cancer Center

Dr. Maximilian Merz is a hematologist-oncologist and Associate Attending Physician at Memorial Sloan Kettering Cancer Center in New York specializing in multiple myeloma and focused on the optimization of CAR T therapies. Following his medical training in Heidelberg, Germany, and a research fellowship at Roswell Park Cancer Center in Buffalo, New York, he held a clinical leadership role as head of the Early Clinical Trial Unit in Leipzig, Germany. His translational research uses advanced bioinformatic analyses of longitudinal and spatially-resolved single-cell multi-omics to understand treatment response, resistance, and side effects. Dr. Merz has published as first and senior author in Nature Medicine, Nature Cancer, Cancer Cell, JCO, and Lancet Hematology, serves on the editorial board of Leukemia, and has received awards from ASH, ASCO, and EHA. His goal is to develop curative immunotherapies for multiple myeloma and to make long-term remission achievable for most patients by 2030.

Program Name(s)

Translational Research Program

Project Title

Deciphering the natural history of CAR T cells using single-cell resolution data