The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jun. 29, 2021

Filed:

Feb. 28, 2019
Applicant:

University of Maryland, Baltimore, Baltimore, MD (US);

Inventors:

Anthony J. Kim, Clarksville, MD (US);

Graeme F. Woodworth, Baltimore, MD (US);

Jeffrey A. Winkles, Frederick, MD (US);

Aniket Wadajkar, Germantown, MD (US);

Assignee:

University Of Maryland, Baltimore, Baltimore, MD (US);

Attorneys:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61K 9/51 (2006.01); A61K 9/50 (2006.01); C07K 16/28 (2006.01); A61K 47/69 (2017.01); A61P 35/00 (2006.01); A61K 47/68 (2017.01); A61K 47/60 (2017.01); A61K 31/337 (2006.01); A61K 39/00 (2006.01);
U.S. Cl.
CPC ...
A61K 9/51 (2013.01); A61K 9/5031 (2013.01); A61K 31/337 (2013.01); A61K 47/60 (2017.08); A61K 47/6855 (2017.08); A61K 47/6921 (2017.08); A61P 35/00 (2018.01); C07K 16/2875 (2013.01); A61K 2039/505 (2013.01); C07K 2317/55 (2013.01); C07K 2317/56 (2013.01); C07K 2317/92 (2013.01);
Abstract

Metastatic triple negative breast cancer (TNBC) still carries a dismal prognosis with the current treatment paradigms. The effectiveness of drug treatment for many solid tumors such as TNBC is limited by tumor heterogeneity, lack of tumor specificity, off-target toxicities, and transient therapeutic action(s). Strategies that provide tumor-specific, sustained concentrations of drugs to the tumors and tumor receptor-specific binding, while reducing off-target effects are needed to ensure sufficient tumor cell uptake within the primary and metastatic tumor microenvironment. The decreased non-specific adhesivity, receptor-targeted nanoparticle formulations ('DART' nanoparticles) of the invention were assessed for clinical potential in directing biological agents to the cell surface receptor Fn14, which is expressed in many solid cancer types, including TNBC primary tumors and metastatic lesions. They are contemplated for use against solid tumors, particularly brain tumors such as glioblastoma and breast cancer, including metastatic breast cancer.


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