IP Library Granted Patent US 10,925,888
Granted Patent B2
US 10,925,888 · App. 16/290,122 · Granted Feb 23, 2021

Administration of nicotinamide mononucleotide in the treatment of disease

Inventors: Shin-ichiro Imai (Saint Louis, MO); Rajendra Apte (Clayton, MO)
Assignee: Washington University
A61K31/706A61K9/0014A61K9/0048A61K9/0053A61K31/455A61K31/7064
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Quick Facts
Patent No.
US 10,925,888
App. No.
16/290,122
Granted
Feb 23, 2021
Kind
B2
Abstract

Disclosed are methods and compositions related to methods of treating, ameliorating, mitigating, slowing, arresting, preventing or reversing various diseases and conditions, including age-related obesity, age-related increases in blood lipid levels, age-related decreases in insulin sensitivity, age-related decreases in memory function, and age-related changes in eye function such as macular degeneration. The methods comprise administering nicotinamide mononucleotide (NMN) to a subject. In some embodiments, the administration can be oral administration. Also disclosed are pharmaceutical compositions comprising NMN.

Claims (21)

1. A method of treating dry eye in a subject, comprising: administering to a subject in need of treatment a pharmaceutically effective amount of nicotinamide mononucleotide (NMN).

2. A method in accordance with claim 1 , wherein the dry eye is age-associated dry eye.

3. A method in accordance with claim 1 , wherein the NMN is administered orally in a pharmaceutically acceptable formulation selected from the group consisting of a pill, a tablet, a caplet, a capsule, a chewable tablet, a quick dissolve tablet, a powder, a granule, an effervescent tablet, a hard gelatin capsule, a soft gelatin capsule, a non-aqueous liquid, an aqueous liquid, a suspension, a solution, an emulsion, a syrup, a sterilized aqueous suspension, a sterilized aqueous solution, a non-aqueous suspension, a non-aqueous solution, and a lyophilized formulation.

4. A method in accordance with claim 1 , wherein the NMN is administered parenterally in a pharmaceutically acceptable formulation selected from the group consisting of a non-aqueous liquid, an aqueous liquid, a suspension, a solution, an emulsion, a syrup, a sterilized aqueous suspension, a sterilized aqueous solution, a non-aqueous suspension, a non-aqueous solution, a lyophilized formulation.

5. A method in accordance with claim 1 , wherein the NMN is administered intravenously.

6. A method in accordance with claim 1 , wherein the NMN is administered enterically.

7. A method in accordance with claim 1 , wherein the NMN is administered parenterally.

8. A method in accordance with claim 1 , wherein the NMN is administered is topically.

9. A method in accordance with claim 8 , wherein the topical administration is administering an eye drop.

10. A method in accordance with claim 1 , wherein the NMN is administered intraocularly.

11. A method in accordance with claim 1 , wherein the subject is a mammal.

12. A method in accordance with claim 1 , wherein the subject is a human.

13. A method of increasing tear production in a subject, comprising: administering to a subject in need of treatment a pharmaceutically effective amount of nicotinamide mononucleotide (NMN).

14. A method in accordance with claim 13 , wherein the NMN is administered orally in a pharmaceutically acceptable formulation selected from the group consisting of a pill, a tablet, a caplet, a capsule, a chewable tablet, a quick dissolve tablet, a powder, a granule, an effervescent tablet, a hard gelatin capsule, a soft gelatin capsule, a non-aqueous liquid, an aqueous liquid, a suspension, a solution, an emulsion, a syrup, a sterilized aqueous suspension, a sterilized aqueous solution, a non-aqueous suspension, a non-aqueous solution, and a lyophilized formulation.

15. A method in accordance with claim 13 , wherein the NMN is administered parenterally in a pharmaceutically acceptable formulation selected from the group consisting of a nonaqueous liquid, an aqueous liquid, a suspension, a solution, an emulsion, a syrup, a sterilized aqueous suspension, a sterilized aqueous solution, a non-aqueous suspension, a non-aqueous solution, a lyophilized formulation.

16. A method in accordance with claim 13 , wherein the subject is a mammal.

17. A method in accordance with claim 13 , wherein the subject is a human.

18. A method in accordance with claim 13 , wherein the NMN is administered is topically.

19. A method in accordance with claim 18 , wherein the topical administration is administering an eye drop.

20. A method in accordance with claim 13 , wherein the NMN is administered intraocularly.

21. A method of suppressing an age-associated accumulation of intraretinal deposits in a subject, comprising: administering to a subject in need of treatment a pharmaceutically effective amount of nicotinamide mononucleotide (NMN).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 21, 2019
From: IMAI, SHIN-ICHIRO; APTE, RAJENDRA
To: WASHINGTON UNIVERSITY
Reel/Frame 049240/0478 →
Continuity (6)
Continuation 15783845 · Oct 13, 2017
Continuation 14855293 · Sep 15, 2015
Continuation PCTUS2014030920 · Mar 17, 2014
Provisional Application 61947387 · Mar 3, 2014
Provisional Application 61801188 · Mar 15, 2013
Related Publication 20190224223A1 · Jul 25, 2019