Project Grant F30CA295068

Award Date 1/2/25
Completion Date 8/25/28
Dollars Obligated $87K
Federal Grant Program
93.398
Assistance Type
Project Grant
Place of Performance
Minnesota, USA
Similar Awards
This Project Grant award from the National Science Foundation's (NSF) Technology, Innovation, and Partnerships program (CFDA 47.084) provides $275,000 to Targeting Systems to develop a novel intramuscular gene delivery platform capable of sustained expression and endogenous secretion of bispecific natural killer cell engager (BIKE) therapeutics to treat solid tumors like hepatocellular carcinoma. The platform aims to deliver BIKEs in a less invasive manner than current immunotherapies,...
This federal Project Grant award of $882,000, provided by the National Institute of Biomedical Imaging and Bioengineering (NIBIB) under the Discovery and Applied Research for Technological Innovations to Improve Human Health program (CFDA 93.286), aims to engineer hybrid extracellular vesicles (HEVs) derived from natural killer (NK) cells and combine them with liposomes containing anticancer drugs and imaging dyes. The key objectives are to: 1) engineer the NK cell-derived extracellular vesicles...
The National Institute of Allergy and Infectious Diseases (NIAID) awarded a $235,500 Project Grant under the Allergy and Infectious Diseases Research program (CFDA 93.855) to Rutgers, The State University of New Jersey. The project aims to develop a novel trispecific killer cell engager (TRIKE) that can efficiently activate natural killer (NK) cells to effectively eliminate pathogenic immune cells in patients with systemic lupus erythematosus (SLE). The research will rigorously evaluate the...
This National Science Foundation (NSF) Technology, Innovation, and Partnerships (CFDA 47.084) Project Grant award of $273,388 to Histone Therapeutics, a woman-owned small business, aims to epigenetically modify natural killer (NK) cells to enhance their ability to detect and kill cancer cells. The goal is to develop a broad-spectrum NK cell therapy that can be used in combination with current cancer treatments to improve effectiveness without increasing side effects. The project will assess...
This $1,477,396 Project Grant award from the National Cancer Institute's Cancer Treatment Research program (CFDA 93.395) supports research to develop a novel approach to enhance the efficacy and durability of CD19-targeted chimeric antigen receptor (CAR) T-cell therapy for B-cell non-Hodgkin's lymphoma (B-NHL). The key products and services to be delivered under this 5-year award include: Conducting two pilot clinical trials to evaluate the safety and feasibility of administering CMV-specific...
This $249,645 Project Grant awarded by the National Cancer Institute (CFDA 93.395 - Cancer Treatment Research) to The Children's Hospital Corporation (doing business as Boston Children's Hospital) will support research to develop a novel precision medicine strategy for cancer immunotherapy. The key objectives are to use advanced gene editing techniques to generate tumor-specific B cells that can be adoptively transferred to trigger both humoral and cellular anti-tumor immunity. The research will...
This Project Grant award from the National Cancer Institute (CFDA 93.395 - Cancer Treatment Research) to the Sloan-Kettering Institute for Cancer Research provides $402,600.00 to develop novel chimeric antigen receptor (CAR) T-cell therapies targeting the U5 small nuclear ribonucleoprotein (U5 snRNP) complex for the treatment of acute myeloid leukemia (AML). The key products and services to be delivered under this 5-year award include: Testing the efficacy and safety of CAR T-cells targeting the...
This federal Project Grant award in the amount of $513,859 from the National Cancer Institute (CFDA 93.395 - Cancer Treatment Research) aims to develop a novel cell-based immunotherapy platform using hematopoietic stem cells (HSCs) engineered with chimeric antigen receptor (CAR) technology. The overarching goal is to generate continuously renewing CAR-expressing natural killer (NK) cells that can provide long-term, effective anti-tumor immunity. The research focuses on leveraging naturally...
This Project Grant award from the National Institute of Allergy and Infectious Diseases (NIAID), under the Allergy and Infectious Diseases Research program (CFDA 93.855), provides $299,921 to Ubiquitx Inc., a New York-based biotechnology company, to develop and evaluate a novel therapeutic platform called Chimeric Ligands for Induced Proximity (CLIPS). The CLIPS platform leverages advances in protein engineering, artificial intelligence, and mRNA therapeutics to upregulate the presentation of...
This Project Grant award from the National Cancer Institute's (NCI) Cancer Research Manpower (CFDA 93.398) program provides $154,642 to the Sloan-Kettering Institute for Cancer Research to elucidate the evolving immunopeptidome of metastatic colorectal cancer. The key objectives are to systematically identify conserved cancer-specific peptide targets derived from fetal WNT-pathway genes in patient-derived organoids, validate the biological role of the NKD1 target in cancer progression, and...

ENGINEERING IMMUNE ENGAGERS - PROJECT SUMMARY/ABSTRACT NATURAL KILLER (NK) CELL ENGAGERS ARE A PROMISING ANTICANCER THERAPY THAT POTENTLY LEVERAGES THE IMMUNE SYSTEM WHILE PROVIDING AN EXCEPTIONAL SAFETY PROFILE. TRISPECIFIC KILLER CELL ENGAGERS (TRIKES) ARE NK CELL ENGAGERS THAT MEDIATE NK CELL KILLING OF TUMOR CELLS THROUGH MULTISPECIFIC BINDING. TRIKES CONTAIN A TUMOR BINDING DOMAIN, AN IL-15 CYTOKINE, AND A CD16 ENGAGER. THE IL-15 AND CD16 ENGAGER STIMULATE ROBUST NK CELL ACTIVATION AND TUMOR CELL KILLING WHILE THE TUMOR BINDING DOMAIN TARGETS THE THERAPY TO THE TUMOR MICROENVIRONMENT. EXPANSION OF THE TRIKE PLATFORM TO TARGET NEW TUMOR-ASSOCIATED ANTIGENS REQUIRES INTEGRATION OF NOVEL TRIKE TUMOR BINDING DOMAINS. THIS PROCESS IS BOTTLENECKED BY DIFFICULTIES PRESERVING TRIKE FUNCTIONALITY AND DEVELOPABILITY (I.E. SUFFICIENT STABILITY, AGGREGATION, AND RECOMBINANT YIELD FOR THERAPEUTIC USE) UPON THE ADDITION OF A NEW TUMOR BINDING DOMAIN. THIS PROJECT WILL TRANSFORM THE TRIKE DISCOVERY PROCESS BY INTERROGATING THE IMPACT OF SPECIFIC TUMOR BINDING DOMAIN PROPERTIES ON THE RESULTANT TRIKE'S FUNCTIONALITY AND DEVELOPABILITY, INCLUDING USE OF INNOVATIVE HYPERSTABLE MINIPROTEINS. SPECIFICALLY, AIM 1 WILL INVESTIGATE THE IMPACT OF TUMOR BINDER SCAFFOLD ARCHITECTURE BY COMPARING THE PERFORMANCE OF SEVERAL DIFFERENT SCAFFOLDS WITHIN TRIKES, INCLUDING ANTIBODY FRAGMENTS AND HMINIPROTEINS. AIM 2 WILL INVESTIGATE THE IMPACT OF PREEMPTIVELY OPTIMIZING TUMOR BINDER STABILITY AND RECOMBINANT YIELD BEFORE INSERTION INTO TRIKES. THIS WILL BE ACCOMPLISHED BY SYSTEMATICALLY VARYING TUMOR BINDER STABILITY AND RECOMBINANT YIELD AND QUANTIFYING THE IMPACT ON TRIKE FUNCTIONALITY AND DEVELOPABILITY. THESE INVESTIGATIONS WILL INVOLVE THE PRODUCTION AND CHARACTERIZATION OF EXPERIMENTAL TUMOR BINDING DOMAINS AND TRIKES TARGETING B7-H3, AN ESTABLISHED TUMOR-ASSOCIATED ANTIGEN. THE PRIMARY GOAL OF THIS WORK IS TO INFORM THE DESIGN OF TRIKE TUMOR TARGETING DOMAINS, THEREBY STREAMLINING THE EXPANSION OF THE PLATFORM TO NEW THERAPEUTIC TARGETS. FURTHERMORE, THIS PROJECT WILL ADVANCE THE DEVELOPMENT OF TRIKES AS A THERAPEUTIC OPTION FOR B7-H3 POSITIVE CANCERS.

Posted 7/2/24, 12:00 AM