Who We Fund

Albert Einstein College of Medicine

Program Name(s)

Career Development Program

Project Title

Glycotyping as a novel approach to study leukemia stem cell heterogeneity and function

Princess Margaret Cancer Centre, University Health Network

Tak W. Mak is an international leader in cancer and immunology research. He is best known for his cloning of the human T cell receptor in 1984, which led to the CAR-T therapies now approved for leukemias/lymphomas. His lab also generated numerous genetically modified mouse strains to identify key factors in immune disorders and cancers. His group’s demonstration that CTLA4 negatively regulates T cell activation paved the way for checkpoint inhibitor immunotherapy. Most recently, his team showed that T and B cells produce acetylcholine in a manner influencing tumorigenesis and autoimmunity. On the biotech front, Dr. Mak co-founded Agios Pharmaceuticals, which produced two IDH inhibitors that are now FDA-approved for treatment of AML. The Mak team has also developed two novel agents targeting aneuploid cancer cells. These agents have shown promise in phase 2 clinical trials. Dr. Mak has published >950 papers, holds 20 patents, and has received over 35 national and international awards.

Program Name(s)

Specialized Center of Research Program

Project Title

The Immune Niche in the Development of Hematological Malignancies and Implications for Novel Therapy

Columbia University Medical Center

Jennifer Amengual, MD is an Associate Professor of Medicine at Columbia University in the Division of Hematology and Oncology. As a physician-scientist, her research goals are to directly translate observations and concepts developed in the laboratory to rational targeted therapies for patients with lymphoma. Dr. Amengual has led many investigator-initiated trials based on data generated in her laboratory through the NCI Cooperative Group Networks, SWOG and ETCTN. Columbia University is a tertiary care center that performs a high number of organ transplants and has an enrichment of PTLD patients. This has generated great interest in how to improve screening and treatment for these patients. Dr. Amengual has spearheaded a PTLD working group that encompasses transplant, infectious disease, lymphoma and cellular therapy specialists from both the adult and pediatric groups. This has led to the development of several studies providing the foundation for the proposed clinical trial.

Program Name(s)

Academic Clinical Trials Program (ACT)

Project Title

Defining ctDNA monitoring and immune modulation in a novel, risk stratified clinical trial for PTLD

Atrium Health Foundation

I am a physician scientist, specializing in lymphoma therapy. My area of research is focused on the development of new therapeutic approaches in lymphoma by engineering special nanoparticle-based drug-delivery platforms. My team has pioneered a novel high-precision drug delivery system using “click chemistry”, which is composed of high-affinity binding chemical couples. By using this novel technique, we have shown an 8-fold increase in tumor uptake of small molecule drugs compared to the conventional drug delivery, with no discernable toxicity in lymphoma models. My second major area of research involves cell signaling pathways, and their impact on lymphoma cell survival. If this novel targeted therapy platform proves successful, pretargeted nanoparticle approach can be utilized to enhance the potency and precision of small molecule drugs for treatment of relapsed mantle cell lymphoma and transformed follicular lymphoma, which are associated with chemoresistance and poor prognosis.

Program Name(s)

Translational Research Program

Project Title

Next-Generation Targeted Therapy in Mantle Cell Lymphoma and Transformed Follicular Lymphoma

Vanderbilt University Medical Center

Dr. Dusetzina is an associate professor in the Department of Health Policy and an Ingram associate professor of cancer research at Vanderbilt University School of Medicine. She received her PhD in Pharmaceutical Science from the University of North Carolina at Chapel Hill and post-doctoral training at the Department of Health Care Policy at Harvard. She is a health services researcher focusing on the intersection between health policy, epidemiology, and economics related to prescription drugs. Dr. Dusetzina’s work has contributed to the evidence base for the role of drug costs on patient access to care and policy changes that might improve patient access and reduce spending on high-priced drugs, including those used to treat cancer. She has been recognized for her work at a national level, including being an invited participant for two working group meetings on “Patient Access to Affordable Cancer Drugs,” hosted by the President’s Cancer Panel, and being selected to co-author a National Academies of Sciences, Engineering and Medicine report on the same topic. Dr. Dusetzina was recently appointed to the Medicare Payment Advisory Commission and is engaged in national policy related to access to care for Medicare beneficiaries. Dr. Dusetzina will co-direct the project with Dr. Nicholas, who has considerable experience using the Health and Retirement Study to assess economic effects of health.

Program Name(s)

Equity in Access

Project Title

Making the Right Choice: Medicare Plan Selection and Access to Cancer Care

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

Dimericon is a private biotech company focused on exploring crosslinked helix dimers (Dimericons) as therapeutics and templates for small molecule development. Dimericon’s technology targets hard-to-drug intracellular protein-protein interactions using rationally designed mimetics of helix dimers. The Seed round of financing will support preclinical studies to further develop the current cFLIP inhibitor lead compound, DMRX1004, to be an IND ready clinical candidate in hematological malignancies.

Program Name(s)

Therapy Acceleration Program

Project Title

Supporting development of dimericons (crosslinked helix dimers) for blood cancers

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

Columbia University Medical Center

Dr. Teresa Palomero is a molecular and cellular biologist. She is a Professor at Columbia University in the Institute for Cancer Genetics. Her laboratory focuses on the identification of molecular alterations responsible for the development of Peripheral T-cell lymphomas, a heterogeneous group of very aggressive lymphoid malignances. Dr. Palomero has been a pioneer in the genomic analysis of Peripheral T-cell lymphoma cases and in the development of mouse models for better understanding the evolution of the disease and test novel therapeutic agents. Her extensive work on hematologic malignancies has led to the identification of key genomic alterations in leukemia and lymphoma including some currently used for molecular diagnosis.

Dr. Palomero scientific work has been published in top tier scientific journals including Nature Genetics, Nature Medicine and Cancer Cell, among others.

Program Name(s)

Discovery

Project Title

Targeting Microenvironment Determinants in Peripheral T-cell Lymphoma

Fred Hutchinson Cancer Center

I am an Associate Professor of Medicine (Hematology, Oncology, and Transplantation) at Fred Hutch with clinical trial and computational expertise. I have a broad background with a Master of Science in Clinical Investigation combined with computational sciences training, including a PhD in evolutionary models of aging and a KL2 career development award focused on microbiome bioinformatics. I leverage my clinical and computational expertise to make cancer treatment safer by improving supportive care. I characterize microbiota disruptions in patients with cancer, investigate their clinical significance, and test microbiota restorative therapeutics to improve clinical outcomes. Recently, I led the largest clinical trial of FMT in allogeneic stem cell transplant recipients to date. We used findings from this trial to design the proposed randomized placebo-controlled phase 2 trial of third-party FMT to prevent aGVHD after transplantation.

Program Name(s)

Academic Clinical Trials Program (ACT)

Project Title

Fecal microbiota transplantation to prevent acute GVHD after allogeneic stem cell transplantation

University of California, San Francisco

Dr. Elliot Stieglitz is a physician-scientist at the University of California, San Francisco whose research focuses on children diagnosed with juvenile myelomonocytic leukemia (JMML). He recently chaired a study, ADVL1512, a phase II clinical trial that tested the safety of trametinib in children with relapsed JMML. This trial met its primary objective and closed to accrual at the end of 2022. Dr. Stieglitz’s main laboratory focus is on developing novel therapies for JMML including CAR-T cells. He has generated patient-derived xenograft (PDX) models of JMML that will serve as the pre-clinical model in which to test CAR-T cells on this grant. These PDXs were generated in collaboration with Dr. Eric Padron, a key opinion leader in CMML and a collaborator on this grant. Dr. Stieglitz has also collaborated extensively with Dr. Tasian, an international leader in CAR-T therapy who is a Co-PI on this grant. This multi-disciplinary team will work together to advance CLL-1 CAR-T cells and trametinib into the clinic for CMML and JMML patients.

Program Name(s)

CMML Initiative

Project Title

CLL-1 CAR-T cells and trametinib for the treatment of Ras-mutated CMML and JMML

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