IP Library Granted Patent US 10,034,849
Granted Patent B2
US 10,034,849 · App. 15/600,124 · Granted Jul 31, 2018

Omega-3 compositions, dosage forms, and methods of use

Inventors: Olav Sandnes (Mount Bethel, PA); Bruce A. Miller (Mount Bethel, PA); Jorn Dyerberg (Charlottenlund, DK); Steen Stender (Copenhagen N, DK)
Assignee: MARINE INGREDIENTS, LLC
A61K31/202A61K35/60A61K35/618
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Quick Facts
Patent No.
US 10,034,849
App. No.
15/600,124
Granted
Jul 31, 2018
Kind
B2
Abstract

Omega-3 compositions, dosage forms, and methods of use are disclosed herein. The omega-3 compositions and dosage forms disclosed herein may comprise DHA and EPA at a ratio of about 5:2. The omega-3 compositions and dosage forms disclosed herein may comprise re-esterified triglycerides. Methods of treatment using the compositions and dosage forms are also disclosed.

Claims (23)

1. A method of reducing the resting heart rate of a

subject, the method comprising:

administering a therapeutically-effective amount of a processed marine oil composition comprising fatty acid esters, wherein the fatty acid esters comprise esters of omega-3 polyunsaturated fatty acids (PUFAs), including re-esterified esters of 4Z,7Z, 10Z,13Z,16Z,19Z-docosahexaenoic acid (DHA) and re-esterified esters of 5Z,8Z,11Z, 14Z,17Z-eicosapentaenoic acid (EPA), wherein a ratio of re-esterified esters of DHA to re-esterified esters of EPA is about 2.5:1 to about 4:1, wherein at least about 50% of the fatty acid esters are re-esterified triglycerides (rTGs).

2. The method of claim 1 , wherein a dose of DHA is at least about 1800 mg/day.

3. The method of claim 2 , wherein the dose of DHA is about 1800 mg/day to about 2400 mg/day.

4. The method of claim 2 , wherein a dose of EPA is about 700 mg/day to about 1000 mg/day.

5. The method of claim 2 , wherein the dose of DHA is about 900 mg to about 1200 mg, twice a day, and the dose of EPA is about 350 mg to about 500 mg, twice a day.

6. The method of claim 1 , wherein about 55% to about 70% of the fatty acid esters are re-esterified triglycerides (rTGs).

7. The method of claim 1 , wherein about 25% to about 45% of the fatty acid esters are re-esterified diglycerides (rDGs).

8. The method of claim 1 , wherein about 0 wt % to about 5 wt % of the fatty acid-esters are re-esterified monoglycerides (rMGs).

9. The method of claim 1 , wherein about 5 wt % or less of the fatty acid esters are in the form of ethyl esters.

10. The method of claim 1 , wherein at least about 60 wt % of the fatty acid esters are esters of PUFAs.

11. The method of claim 1 , wherein at least about 15 wt % of the marine oil is derived from cephalopod oil.

12. A method of increasing high-density lipoprotein cholesterol (HDL-c) in a subject, the method comprising:

administering a therapeutically-effective amount of a processed marine oil composition comprising fatty acid esters, wherein the fatty acid esters comprise esters of omega-3 polyunsaturated fatty acids (PUFAs), including at least about 450 mg of re-esterified esters of 4Z,7Z,10Z,13Z,16Z,19Z-docosahexaenoic acid (DHA) and at least about 150 mg of re-esterified esters of 5Z,8Z,11Z,14Z,17Z-eicosapentaenoic acid (EPA), wherein at least about 50% of the fatty acid esters are re-esterified triglycerides (rTGs).

13. The method of claim 12 , wherein the ratio of re-esterified esters of DHA to EPA is about 5:2.

14. The method of claim 12 , wherein at least about 55% of the fatty acid esters are re-esterified triglycerides (rTGs).

15. The method of claim 12 , wherein about 0 wt % to about 35 wt % of the fatty acid esters are esters of mono-unsaturated fatty acids.

16. The method of claim 12 , wherein about 0 wt % to about 5 wt % of the fatty acid esters are esters of saturated fatty acids.

17. The method of claim 12 , wherein at least about 50 wt % of the fatty acid esters are either re-esterified esters of DHA or re-esterified esters of EPA.

18. The method of claim 12 , wherein at least about 80% of the PUFAs are DHA and EPA.

19. A method of reducing triglycerides in a subject's blood, the method comprising:

administering a therapeutically-effective amount of a processed marine oil composition comprising fatty acid esters, wherein the fatty acid esters comprise esters of omega-3 polyunsaturated fatty acids (PUFAs), including re-esterified esters of 4Z,7Z,10Z,13Z,16Z,19Z-docosahexaenoic acid (DHA) and re-esterified esters of 5Z,8Z,11Z, 14Z,17Z-eicosapentaenoic acid (EPA), wherein a ratio of re-esterified esters of DHA to re-esterified esters of EPA is about 2.5:1 to about 4:1, wherein at least about 50% of the fatty acid esters are re-esterified triglycerides (rTGs).

Assignments (5)
RELEASE OF SECURITY INTEREST IN PATENT AND TRADEMARKS Recorded Jan 10, 2025
From: GLAS TRUST CORPORATION LIMITED, AS SECURITY AGENT
To: INNOVA SOFTGEL LLC; MARINE INGREDIENTS, LLC
Reel/Frame 069870/0896 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2021
From: GENTOFTE HOSPITAL
To: MARINE INGREDIENTS, LLC
Reel/Frame 058465/0914 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2021
From: STENDER, STEEN
To: GENTOFTE HOSPITAL
Reel/Frame 058465/0943 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2021
From: SANDNES, OLAV E.; MILLER, BRUCE A., JR.; DYNBERG, JORN, MD
To: MARINE INGREDIENTS, LLC
Reel/Frame 058465/0965 →
SECURITY INTEREST Recorded Sep 9, 2019
From: INNOVA SOFTGEL LLC; MARINE INGREDIENTS LLC
To: GLAS TRUST CORPORATION LIMITED
Reel/Frame 050316/0495 →
Continuity (5)
Division 15146680 · May 4, 2016
Continuation PCTUS2015034372 · Jun 5, 2015
Provisional Application 62019289 · Jun 30, 2014
Provisional Application 62009145 · Jun 6, 2014
Related Publication 20170252313A1 · Sep 7, 2017