IP Library Granted Patent US 8,455,472
Granted Patent B2
US 8,455,472 · App. 12/815,569 · Granted Jun 4, 2013

Compositions and methods for lowering triglycerides without raising LDL-C levels in a subject on concomitant statin therapy

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Quick Facts
Patent No.
US 8,455,472
App. No.
12/815,569
Granted
Jun 4, 2013
Kind
B2
Abstract

In various embodiments, the present invention provides compositions and methods for treating and/or preventing cardiovascular-related diseases in subject in need thereof.

Claims (19)

1. A method of lowering triglycerides in a subject on stable statin therapy having baseline fasting triglycerides of about 200 mg/dl to about 500 mg/dl, the method comprising administering to the subject about 4 capsules per day, each capsule comprising about 900 mg to about 1 g of ethyl eicosapentaenoate and not more than about 3% docosahexaenoic acid or its esters, by weight of all fatty acids present, for a period of at least about 12 weeks.

2. The method of claim 1 wherein the subject has a baseline LDL-C level of about 40 mg/dl to about 115 mg/dl.

3. The method of claim 2 wherein the step of administering said 4 capsules to the subject daily for the period effects a reduction in serum LDL-C.

4. The method of claim 3 wherein the step of administering said 4 capsules to the subject daily for the period effects at least a 5% reduction in fasting triglycerides and a reduction in LDL-C in the subject.

5. The method of claim 3 wherein the step of administering said 4 capsules daily for the period effects at least a 5% reduction in LDL-C in the subject.

6. The method of claim 3 wherein the step of administering said 4 capsules to the subject daily for the period effects at least a 10% reduction in triglycerides in the subject.

7. The method of claim 3 wherein the step of administering said 4 capsules to the subject daily for the period effects at least a 15% reduction in triglycerides in the subject.

8. The method of claim 7 wherein the step of administering said 4 capsules to the subject daily for the period effects a reduction in Apolipoprotein B, total cholesterol, and lipoprotein associated phospholipase A2 in the subject.

9. The method of claim 1 wherein each capsule comprises at least about 95% ethyl eicosapentaenoate by weight of all fatty acids.

10. The method of claim 9 wherein each capsule comprises about 0.22% to about 0.4% ethyl octadecatetraenoate by weight of all fatty acids, about 0.075% to about 0.2% by weight ethyl nonaecapentaenoate by weight of all fatty acids, about 0.25% to about 0.40% ethyl arachidonate by weight of all fatty acids, about 0.3% to about 0.4% ethyl eicosatetraenoate by weight of all fatty acids, and about 0.075% to about 0.25% ethyl heneicosapentaenoate by weight of all fatty acids.

11. The method of claim 1 wherein the capsules have a shell.

12. The method of claim 11 wherein the shell comprises gelatin.

13. The method of claim 1 wherein the statin is selected from the group consisting of atorvastatin, rosuvastatin and simvastatin.

14. The method of claim 1 wherein the subject has a baseline body mass index not greater than 45 kg/m 2 .

15. The method of claim 1 comprising administering said 4 capsules to the subject daily for the period of 12 weeks to effect at least a 15% reduction in triglycerides and a reduction in LDL-C levels compared to a placebo controlled subject.

16. The method of claim 15 comprising administering said 4 capsules to the subject daily for the period to effect at least a 5% reduction in LDL-C compared to a placebo controlled subject.

17. The method of claim 16 comprising administering said 4 capsules to the subject daily for the period to effect at least a 5% reduction in apolipoprotein B compared to a placebo controlled subject.

18. The method of claim 13 wherein the statin comprises rosuvastatin.

19. The method of claim 18 comprising administering said 4 capsules to the subject daily for the period to effect at least a 15% reduction in triglycerides and at least a 5% reduction in LDL-C compared to a subject on the stable statin therapy for said period who has not received said 4 capsules each comprising a fill material comprising about 900 mg to about 1 g of ethyl eicosapentaenoate and not more than about 3% docosahexaenoic acid or its esters, by weight of all fatty acids present.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Nov 19, 2020
From: CPPIB CREDIT EUROPE S.À R.L.
To: AMARIN PHARMACEUTICALS IRELAND LIMITED
Reel/Frame 054484/0552 →
SECURITY INTEREST Recorded Dec 21, 2017
From: AMARIN PHARMACEUTICALS IRELAND LIMITED
To: CPPIB CREDIT EUROPE S.À R.L.
Reel/Frame 044938/0257 →
PATENT SECURITY ASSIGNMENT AND ASSUMPTION AGREEMENT Recorded Dec 20, 2017
From: BIOPHARMA SECURED DEBT FUND II HOLDINGS CAYMAN LP
To: CPPIB CREDIT EUROPE S.À R.L.
Reel/Frame 044956/0395 →
SECURITY AGREEMENT Recorded Dec 19, 2012
From: AMARIN PHARMACEUTICALS IRELAND LIMITED
To: BIOPHARMA SECURED DEBT FUND II HOLDINGS CAYMAN LP
Reel/Frame 029499/0087 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 31, 2012
From: AMARIN PHARMA INC.
To: AMARIN PHARMACEUTICALS IRELAND LIMITED
Reel/Frame 028295/0491 →