IP Library Patent Application 17905930
Patent Application
App. No. 17/905,930

COMPOSITIONS AND METHODS FOR EYE HEALTH COMPRISING VERY LONG CHAIN FATTY ACIDS

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
17/905,930
Abstract

The present disclosure describes compositions comprising at least one very long chain fatty acid chosen from C 26+ acids (5n-3), prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing. The compositions are useful in methods for treating conditions associated with a loss of visual acuity including, for example, age-related macular degeneration.

Claims (50)

1 . A composition for visual health comprising at least one very long chain fatty acid chosen from C 26+ acids (5n-3), prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing.

2 . The composition of claim 1 , wherein the composition comprises 1 mg to 1000 mg of the at least one very long chain fatty acid chosen from C 26+ acids (5n-3) or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of at least one very long chain fatty acid chosen from C 26+ acids (5n-3).

3 . The composition of claim 1 , wherein the composition comprises 10 mg to 500 mg of the at least one very long chain fatty acid chosen from C 26+ acids (5n-3) or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of at least one very long chain fatty acid chosen from C 26+ acids (5n-3).

4 . The composition of claim 1 , wherein the composition comprises 25 mg to 100 mg of the at least one very long chain fatty acid chosen from C 26+ acids (5n-3) or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of at least one very long chain fatty acid chosen from C 26+ acids (5n-3).

5 . The composition of claim 1 , wherein the composition comprises 40 mg of at least one very long chain fatty acid chosen from C 26+ acids (5n-3) or an equivalent amount of prodrugs, pharmaceutically acceptable salts, and/or pharmaceutically acceptable salts of prodrugs of C 26+ acid (5n-3) groups.

6 . The composition of claim 1 , wherein the C 26+ acids (5n-3) is a C 26 acid (5n-3), C 28 acid (5n-3), C 30 acid (5n-3), C 32 acid (5n-3), and/or C 34 acid (5n-3).

7 . The composition of claim 1 , wherein the composition further comprises at least one additional component chosen from:

at least one very long chain fatty acid chosen from C 26+ acids (6n-3), prodrugs thereof, pharmaceutically acceptable salts thereof, and pharmaceutically acceptable salt of a prodrug of at least one very long chain fatty acid chosen from C 26+ acids (6n-3).

docosahexanoic acid, prodrugs thereof, and/or pharmaceutically acceptable salts of any of the foregoing;

eicosapentanoic acid, prodrugs thereof, and/or pharmaceutically acceptable salts of any of the foregoing;

vitamin C, prodrugs thereof, and/or pharmaceutically acceptable salts of any of the foregoing;

vitamin E, prodrugs thereof, and/or pharmaceutically acceptable salts of any of the foregoing;

zinc, prodrugs thereof, and/or pharmaceutically acceptable salts of any of the foregoing;

copper, prodrugs thereof, and/or pharmaceutically acceptable salts of any of the foregoing;

lutein, prodrugs thereof, and/or pharmaceutically acceptable salts of any of the foregoing; and

zeaxanthin, prodrugs thereof, and/or pharmaceutically acceptable salts of any of the foregoing.

8 . The composition of claim 1 , wherein the composition further comprises 20 mg to 350 mg of docosahexanoic acid or an equivalent amount of a prodrug, a pharmaceutically acceptable salt, and/or a pharmaceutically acceptable salt of a prodrug of docosahexanoic acid.

9 . The composition of claim 1 , wherein the composition further comprises 20 mg to 650 mg of eicosapentanoic acid or an equivalent amount of a prodrug, a pharmaceutically acceptable salt, and/or a pharmaceutically acceptable salt of a prodrug of eicosapentanoic acid.

10 . The composition of claim 1 , wherein the composition further comprises 350 mg to 800 mg of vitamin C or an equivalent amount of a prodrug, a pharmaceutically acceptable salt, and/or a pharmaceutically acceptable salt of a prodrug of vitamin C.

11 . The composition of claim 1 , wherein the composition further comprises 50 mg to 550 mg of vitamin E or an equivalent amount of a prodrug, a pharmaceutically acceptable salt, and/or a pharmaceutically acceptable salt of a prodrug of vitamin E.

12 . The composition of claim 1 , wherein the composition further comprises 20 mg to 90 mg of zinc or an equivalent amount of a prodrug, a pharmaceutically acceptable form, and/or a pharmaceutically acceptable salt of a prodrug of zinc.

13 . The composition of claim 1 , wherein the composition further comprises 1.5 mg to 2.5 mg of copper or an equivalent amount of a prodrug, a pharmaceutically acceptable form, and/or a pharmaceutically acceptable salt of a prodrug of copper.

14 . The composition of claim 1 , wherein the composition further comprises 5 mg to 50 mg of lutein or an equivalent amount of a prodrug, a pharmaceutically acceptable salt, and/or a pharmaceutically acceptable salt of a prodrug of lutein.

15 . The composition of claim 1 , wherein the composition comprises 1 mg to 20 mg of zeaxanthin or an equivalent amount of a prodrug, a pharmaceutically acceptable salt, and/or a pharmaceutically acceptable salt of a prodrug of zeaxanthin.

16 . The composition of claim 1 , wherein the composition comprises: optionally 1 mg to 200 mg at least one C 26+ acid (6n-3) or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of at least one C 26+ acid (6n-3); 40 mg at least one C 26+ acid (5n-3) or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of at least one C 26+ acid (5n-3); 200 mg docosahexanoic acid or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of docosahexanoic acid; and 40 mg eicosapentanoic acid or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of eicosapentanoic acid.

17 . The composition of claim 1 , wherein the composition comprises: optionally 1 mg to 200 mg C 26+ acid (6n-3) or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of C 26+ acid (6n-3); 40 mg at least one C 26-34 acid (5n-3) or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of at least one C 26-34 acid (5n-3); 200 mg docosahexanoic acid or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of docosahexanoic acid; and 40 mg eicosapentanoic acid or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of eicosapentanoic acid.

18 . The composition of claim 1 , wherein the composition comprises: 500.0 mg vitamin C or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of vitamin C; 180.0 mg vitamin E or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of vitamin E; 80.0 mg zinc or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of zinc; 2.0 mg copper or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of zinc; up to 200.0 mg at least one C 26+ acid (6n-3) or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of at least one C 26+ acid (6n-3); 200.0 mg docosahexanoic acid or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of docosahexanoic acid; 40.0 mg at least one C 26+ acid (5n-3); and 40.0 mg eicosapentanoic acid or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of eicosapentanoic acid.

19 . The composition of claim 1 , wherein the composition comprises: 500.0 mg vitamin C or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of vitamin C; 180.0 mg vitamin E or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of vitamin E; 80.0 mg zinc or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of zinc; 2.0 mg copper or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of copper; up to 200.0 mg C 26+ acid (6n-3) or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of C 26+ acid (6n-3); 200 mg docosahexanoic acid or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of docosahexanoic acid; 40.0 mg at least one C 26-34 acid (5n-3) or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of C 26-34 acid (5n-3); and 40.0 mg eicosapentanoic acid or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of eicosapentanoic acid.

20 . The composition of claim 18 , further comprising 10.0 mg lutein or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of lutein and 2.0 mg zeaxanthin or an equivalent amount of a prodrug, pharmaceutically acceptable salt, and/or pharmaceutically acceptable salt of a prodrug of zeaxanthin.

21 . The composition of claim 1 , further comprising at least one additional active ingredient.

22 . The composition of claim 21 , wherein the at least one additional active ingredient is chosen from

Vitamin C, prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing;

Vitamin E, prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing;

zinc, prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing;

copper, prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing;

Vitamin B1, prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing;

Vitamin B2, prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing;

Vitamin B3, prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing;

Vitamin B5, prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing;

Vitamin B6, prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing;

Vitamin B7, prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing;

Vitamin B9, prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing;

Vitamin B12, prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing;

lutein, prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing; and

zeaxanthin, prodrugs thereof, and pharmaceutically acceptable salts of any of the foregoing.

23 . The composition of claim 1 , wherein the composition is in the form of one or more tablets, capsules, soft gels, liquid, or powder.

24 . The composition of claim 1 , wherein the composition is a daily dosage.

25 . A method of delaying the progression and/or onset macular degeneration, the method comprising administering to a subject in need thereof a composition according to claim 1 .

26 . A method for treating and/or preventing at least one disease, disorder, and/or condition associated with a loss of visual acuity, the method comprising administering to a subject a composition according to claim 1 .

27 . The method of claim 25 , wherein the composition is administered daily to the subject in one, two, three, or four daily doses.

Assignments (7)
ASSIGNMENT OF SECURITY INTEREST IN PATENTS PREVIOUSLY RECORDED AT REEL/FRAME (067501/0955) Recorded Aug 14, 2025
From: CITIBANK, N.A., AS RESIGNING AGENT
To: JPMORGAN CHASE BANK, N.A., AS SUCCESSOR AGENT
Reel/Frame 072460/0665 →
PATENT SECURITY AGREEMENT Recorded Jul 1, 2025
From: BAUSCH & LOMB INCORPORATED; ALDEN OPTICAL LABORATORIES, INC.; BAUSCH + LOMB IRELAND LIMITED
To: CITIBANK, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 071773/0871 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 23, 2024
From: BAUSCH + LOMB IRELAND LIMITED
To: CITIBANK, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 067527/0251 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 22, 2024
From: BAUSCH + LOMB IRELAND LIMITED
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 067501/0955 →
CONFIRMATORY PATENTS ASSIGNMENT Recorded May 20, 2024
From: BAUSCH HEALTH IRELAND LIMITED
To: BAUSCH + LOMB IRELAND LIMITED
Reel/Frame 067471/0378 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 11, 2022
From: BAUSCH HEALTH US, LLC
To: BAUSCH HEALTH IRELAND LIMITED
Reel/Frame 061382/0519 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 11, 2022
From: STEIN, DANIEL J.; DIVITO, MELINDA; HOSTEN, LESTER
To: BAUSCH HEALTH US, LLC
Reel/Frame 061382/0442 →