IP Library Granted Patent US 12,029,745
Granted Patent B2
US 12,029,745 · App. 17/549,584 · Granted Jul 9, 2024

Effects of LGM2605 on a primate model of asthma

Inventors: Melpo Christofidou-Solomidou (Eagleville, PA); Angela Haczku (Davis, CA)
Assignees: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA; THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
A61K31/7032A61K9/0053A61P11/06A61P39/00
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Quick Facts
Patent No.
US 12,029,745
App. No.
17/549,584
Granted
Jul 9, 2024
Kind
B2
Abstract

The invention provides compositions and methods for treating asthma in a subject in need thereof comprising administering chemically synthesized secoisolaricirecinol diglucoside (SDG), and in particular, a racemic mixture of the SDG (LGM2605), stereoisomers thereof, metabolites thereof, and analogs thereof. Also provided are methods for treating or preventing ozone-induced damage in a subject in need thereof.

Claims (17)

1. A method for treating asthma in a human subject in need thereof, the method comprising: administering to the subject a therapeutically effective amount of chemically synthesized secoisolaricirecinol diglucoside (SDG).

2. The method of claim 1 , wherein the chemically synthesized SDG comprises a racemic mixture of the SDG.

3. The method of claim 1 , wherein administration of the chemically synthesized SDG alleviates or eliminates respiratory airway hyperactivity in the subject.

4. The method of claim 3 , wherein the respiratory airway is an upper respiratory airway, a lower respiratory airway or a combination thereof.

5. The method of claim 1 , wherein administration of the chemically synthesized SDG alleviates or eliminates bronchoalveolar lavage (BAL) inflammation in the subject, and wherein alleviation or elimination of the BAL inflammation comprises reducing BAL neutrophilia and eosinophilia.

6. The method of claim 1 , wherein the chemically synthesized SDG inhibits surfactant protein-D (SP-D) de-oligomerization.

7. The method of claim 1 , wherein the chemically synthesized SDG is administered in a dietary composition.

8. The method of claim 1 , wherein the chemically synthesized SDG is administered orally.

9. A method for treating ozone-induced damage in a human subject who has been or will be exposed to a dose of ozone, the method comprising: orally administering to the subject a therapeutically effective amount of chemically synthesized SDG.

10. The method of claim 9 , wherein the chemically synthesized SDG comprises a racemic mixture of the SDG.

11. The method of claim 9 , wherein administration of the chemically synthesized SDG alleviates or eliminates airway hyperactivity in the subject.

12. The method of claim 9 , wherein the ozone-induced damage is airway hyperactivity, airway inflammation, oxidative stress of a airway or a combination thereof.

13. The method of claim 12 , wherein the airway is an upper airway, a lower airway or a combination thereof.

14. The method of claim 9 , wherein the chemically synthesized SDG inhibits surfactant protein-D (SP-D) de-oligomerization.

15. The method of claim 9 , wherein the chemically synthesized SDG is administered in a dietary composition.

16. The method of claim 9 , wherein the chemically synthesized SDG is in a concentration about 1 nanomolar (nM) to about 1 molar (M).

17. The method of claim 16 , wherein the SDG concentration is about 25 μM to about 250 μM.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2022
From: CHRISTOFIDOU-SOLOMIDOU, MELPO
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 059411/0750 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2022
From: HACZKU, ANGELA
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 059411/0817 →
Continuity (5)
Continuation 16153494 · Oct 5, 2018
Continuation In Part 15315349
Provisional Application 62101293 · Jan 8, 2015
Provisional Application 62005330 · May 30, 2014
Related Publication 20240173342A1 · May 30, 2024