IP Library Granted Patent US 10,695,341
Granted Patent B2
US 10,695,341 · App. 15/527,998 · Granted Jun 30, 2020

Compositions and methods for treating endometriosis

Inventors: Meera Nanjundan (Tampa, FL); Kyle A. Bauckman (St. Louis, MO); Idhaliz Flores (Ponce, PR)
Assignees: University of South Florida; Ponce Health Sciences University
A61K31/4706A61K31/4709A61K31/7105A61P15/00C12N15/113G01N33/689C12N2310/14C12N2320/31C12N2320/32C12N2320/35G01N2333/46G01N2800/364
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Quick Facts
Patent No.
US 10,695,341
App. No.
15/527,998
Granted
Jun 30, 2020
Kind
B2
Abstract

Provided herein are methods of treating and/or preventing endometriosis or symptom thereof, assays for diagnosing/prognosing endometriosis, compositions and formulations for treating and/or preventing endometriosis or symptom thereof, and populations of endometiotic cells, including life-extended populations of cells.

Claims (13)

1. A method of treating endometriosis in a subject in need thereof comprising:

administering an autophagic inhibitor to the subject in an amount effective to treat endometriosis in the subject.

2. The method of claim 1 , wherein the autophagic inhibitor is selected from the group consisting of chloriquine, Lys05, hydroxychloriquine, pharmaceutically acceptable salts thereof, ATG5 siRNA, ATG7 siRNA, or combinations thereof.

3. The method of claim 1 , wherein the autophagic inhibitor is hydroxychloriquine.

4. The method of claim 1 , wherein the effective amount ranges from about 1 mg/kg to about 200 mg/kg.

5. The method of claim 1 , wherein the effective amount is administered in a dosage form formulated for oral, vaginal, intravenous, transdermal, subcutaneous, intraperitoneal, or intramuscular administration.

6. A method comprising:

contacting an endometriotic lesion cell with an autophagic inhibitor in an amount effective to treating the edometriotic lesion.

7. The method of claim 6 , wherein contacting an endometriotic lesion cell with an effective amount of an autophagic inhibitor prevents recurrance of an endometriotic lesion cell.

8. The method of claim 6 , wherein the autophagic inhibitor is selected from the group consisting of chloriquine, Lys05, hydroxychloriquine, pharmaceutically acceptable salts thereof, ATG5 siRNA, ATG7 siRNA, or combinations thereof.

9. The method of claim 6 , wherein the autophagic inhibitor is hydroxychloriquine.

10. The method of claim 6 , wherein the effective amount ranges from about 1 mg/kg to about 200 mg/kg.

11. The method of claim 6 , wherein the endometriotic lesion cell has greater expression as compared to a control cell of at least one autophagic marker selected from the group consisting of ATG7, ATG5, and hVps34.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 5, 2020
From: NANJUNDAN, MEERA; BAUCKMAN, KYLE A.
To: UNIVERSITY OF SOUTH FLORIDA
Reel/Frame 052568/0349 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 5, 2020
From: FLORES, IDHALIZ
To: PONCE HEALTH SCIENCES UNIVERSITY
Reel/Frame 052568/0418 →
CONFIRMATORY LICENSE Recorded Jun 20, 2017
From: UNIVERSITY OF SOUTH FLORIDA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 042903/0136 →
Continuity (2)
Provisional Application 62081464 · Nov 18, 2014
Related Publication 20190388413A1 · Dec 26, 2019