Treatment with Statin and Omega-3 Fatty Acids and a Combination Product Thereof

1 . A pharmaceutical composition in unit dose form, comprising an essentially homogeneous solution comprising a statin essentially dissolved in solvent system comprising natural or synthetic omega-3 fatty acids or pharmaceutically acceptable esters, derivatives, conjugates, precursors or salts thereof, or mixtures thereof, wherein less than 10% of the statin is undissolved in the solvent system.

2 . The pharmaceutical composition of claim 1 , wherein the statin and the omega-3 fatty acids are the only active agents in the pharmaceutical composition.

3 . The pharmaceutical composition of claim 1 , wherein the solvent system further comprises at least one solubilizer in an amount of 50% or less w/w based on the total weight of the solvent system.

4 . The pharmaceutical composition of claim 3 , wherein the at least one solubilizer comprises a hydrophilic solvent.

5 . The pharmaceutical composition of claim 4 , wherein the hydrophilic solvent is present in an amount of 20% or less w/w based on the total weight of the solvent system.

6 . The pharmaceutical composition of claim 3 , wherein the at least one solubilizer comprises a surfactant.

7 . The pharmaceutical composition of claim 6 , wherein the surfactant is present in an amount of 20% or less w/w based on the total weight of the solvent system.

8 . The pharmaceutical composition of claim 3 , wherein the at least one solubilizer comprises a hydrophilic solvent and a surfactant.

9 . The pharmaceutical composition of claim 8 , wherein the hydrophilic solvent and the surfactant are present together in an amount of 20% or less w/w based on the total weight of the solvent system.

10 . The pharmaceutical composition of claim 1 , wherein no more than 10% of the dissolved statin precipitates out of the solution when the pharmaceutical composition is stored at room temperature and 60% relative humidity for a period of at least one month.

11 . The pharmaceutical composition of claim 1 , wherein the statin is simvastatin.

12 . A pharmaceutical composition in unit dose form, comprising a statin and natural or synthetic omega-3 fatty acids or pharmaceutically acceptable esters, derivatives, conjugates, precursors or salts thereof, or mixtures thereof, wherein at least 90% of the initial amount of the statin in the composition at an initial measurement time (t 0 ) is maintained after one month storage at room temperature and 60% relative humidity.

13 . A method of treating a subject having one or more conditions selected from the group consisting of hypertriglyceridemia, hypercholesteremia, coronary heart disease (CHD), heart failure, cardiac arrhythmias, ischemic dementia, hypertension, coagulation related disorders, nephropathy, retinopathy, cognitive disorders, autoimmune diseases, inflammatory diseases, metabolic syndrome, vascular disease, atherosclerotic disease and related conditions, comprising administering to the subject a pharmaceutical composition as claimed in claim 1 .

14 . The method of claim 13 , wherein prior to the first administration to the subject of the pharmaceutical composition, the subject has triglyceride levels of about 200 to about 499 mg/dl.

15 . The method of claim 13 , wherein prior to the first administration to the subject of the pharmaceutical composition, the subject has triglyceride levels of greater than 499 mg/dl.

16 . The method of claim 13 , wherein prior to the first administration to the subject of the pharmaceutical composition, the subject has triglyceride levels of about 150 to about 199 mg/dl.

17 . A method for the treatment and/or prevention and/or reduction of cardiac events and/or cardiovascular events and/or vascular events and/or symptoms in a subject, comprising administering to the subject a pharmaceutical composition as claimed in claim 1 .

18 . The method of claim 17 , wherein prior to the first administration to the subject of the pharmaceutical composition, the subject has triglyceride levels of about 200 to about 499 mg/dl.

19 . The method of claim 17 , wherein prior to the first administration to the subject of the pharmaceutical composition, the subject has triglyceride levels of greater than 499 mg/dl.

20 . The method of claim 17 , wherein prior to the first administration to the subject of the pharmaceutical composition, the subject has triglyceride levels of about 150 to about 199 mg/dl.