NANOVALENT PHARMACEUTICALS INC — Department of Health and Human Services STTR Phase I: 102

Description

DESCRIPTION provided by applicant This Phase I STTR project seeks to demonstrate proof of principle that novel targetable nanoparticles can delivery therapeutic substances to human tumor cells and reduce tumor burden in metastatic cancer The concept for these nanoparticles is based on the polymerized liposome nanoparticle PLN that displays functional antibodies that target tumor cell surface markers The therapeutic cargos are encapsulated cytotoxic drugs that comprise the front line treatment for Ewing sarcoma Upon recognition by the tumor cell the nanoparticle binds gets taken into the cell endocytosed and the nanoparticle cargo is released ultimately allowing availability of the drug to kill the cancer cel This project fits well within the mission of the NCI to develop new nanotechnology based therapeutics Treatment resistant metastases are the ultimate cause of death in most cancer patients Systemic therapy for metastases is generally ineffective A reliable low toxic highly effective therapy is urgently needed to treat both relapse patients and treatment resistant metastases The specific aims of this proposal are therefore to carry out efficient encapsulation of cancer drugs inside targeted PLNs and demonstrate efficacy in killing cancer cells in a xenograft mouse model of metastatic human Ewing sarcoma NanoValentandapos s goal at the conclusion of the STTR Phase II is to assemble the necessary data for an IND submission to the FDA for approval of this novel therapy initially for use in relapsed Ewing sarcoma patients PUBLIC HEALTH RELEVANCE Toxicity of drugs used to treat cancer is the major limiting factor in effective chemotherapy The collateral damage to bone marrow GI tract liver heart and other normal tissues limits the amount of chemotherapeutic agent a patient can receive This project seeks to develop a method to encapsulate cancer drugs inside tiny particles and deliver these loaded particles directly and efficiently to cancer cells This will widen the window of treatment by getting more drug to the tumor preventing drug uptake by normal tissue thereby reducing toxic side effects and saving patientsandapos lives