IP Library Granted Patent US 11,045,428
Granted Patent B2
US 11,045,428 · App. 16/289,424 · Granted Jun 29, 2021

Decreased adhesivity receptor-targeted nanoparticles for Fn14-positive tumors

Inventors: Anthony J. Kim (Clarksville, MD); Graeme F. Woodworth (Baltimore, MD); Jeffrey A. Winkles (Frederick, MD); Aniket Wadajkar (Germantown, MD)
Assignee: University Of Maryland, Baltimore
A61K9/51A61K9/5031A61K31/337A61K47/60A61K47/6855A61K47/6921A61P35/00C07K16/2875A61K2039/505C07K2317/55C07K2317/56C07K2317/92
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Quick Facts
Patent No.
US 11,045,428
App. No.
16/289,424
Granted
Jun 29, 2021
Kind
B2
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.

Claims (16)

1. A drug delivery nanoparticle, comprising:

a) a nanoparticle having a hydrodynamic diameter of about 100 nm;

b) a coating of polyethylene glycol with a surface density of about 14.1 polyethylene glycol molecules per 100 nm 2 ;

c) an anti-Fn14 antibody that specifically binds to the cell surface of a breast cancer cell or metastatic breast cancer cell with a surface density of about 0.02 antibody molecules per 100 nm 2 ; and

d) a therapeutic agent,

wherein the nanoparticle penetrates extracellular matrix,

wherein the nanoparticle has minimal non-specific binding to extracellular matrix, and

wherein the nanoparticle treats breast cancer and metastatic breast cancer.

2. The drug delivery nanoparticle of claim 1 , wherein the anti-Fn14 antibody is selected from the group consisting of ITEM4, ITEM4-SH, ITEM4 scFv, and ITEM4 Fab.

3. A pharmaceutical composition, comprising a pharmaceutically acceptable vehicle and the drug delivery nanoparticle of claim 1 .

4. A method of treating breast cancer, comprising administering to a subject in need a therapeutically effective amount of the drug delivery nanoparticle of claim 1 .

5. A method of treating breast cancer, comprising administering to a subject in need a therapeutically effective amount of the pharmaceutical composition of claim 3 .

6. The method of claim 4 , wherein the breast cancer is metastatic breast cancer.

7. The method of claim 5 , wherein the breast cancer is metastatic breast cancer.

8. The drug delivery nanoparticle of claim 1 , wherein the breast cancer is triple-negative breast cancer.

9. The method of claim 4 , wherein the breast cancer is triple-negative breast cancer.

Assignments (2)
CONFIRMATORY LICENSE Recorded Nov 7, 2022
From: UNIVERSITY OF MARYLAND BALTIMORE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 061885/0198 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 20, 2019
From: KIM, ANTHONY J.; WOODWORTH, GRAEME F.; WINKLES, JEFFREY A.; WADAJKAR, ANIKET
To: UNIVERSITY OF MARYLAND, BALTIMORE
Reel/Frame 048646/0175 →
Continuity (3)
Continuation In Part 15528555
Provisional Application 62083011 · Nov 21, 2014
Related Publication 20190328677A1 · Oct 31, 2019