US20110071176A1 - Pharmaceutical composition comprising omega-3 fatty acid and hydroxy-derivative of a statin and methods of using same - Google Patents

Pharmaceutical composition comprising omega-3 fatty acid and hydroxy-derivative of a statin and methods of using same Download PDF

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US20110071176A1
US20110071176A1 US12/888,994 US88899410A US2011071176A1 US 20110071176 A1 US20110071176 A1 US 20110071176A1 US 88899410 A US88899410 A US 88899410A US 2011071176 A1 US2011071176 A1 US 2011071176A1
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hydroxy
atorvastatin
derivative
statin
pharmaceutical composition
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Jonathan Rowe
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Amarin Pharmaceuticals Ireland Ltd
Amarin Pharma Inc
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Amarin Pharma Inc
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Assigned to BIOPHARMA SECURED DEBT FUND II HOLDINGS CAYMAN LP reassignment BIOPHARMA SECURED DEBT FUND II HOLDINGS CAYMAN LP SECURITY AGREEMENT Assignors: AMARIN PHARMACEUTICALS IRELAND LIMITED
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Priority to US14/729,615 priority patent/US10493058B2/en
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Priority to US16/653,001 priority patent/US11007173B2/en
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
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    • A61K31/33—Heterocyclic compounds
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    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
    • A61K31/202—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids having three or more double bonds, e.g. linolenic
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    • A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/12—Carboxylic acids; Salts or anhydrides thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4841—Filling excipients; Inactive ingredients
    • A61K9/4858—Organic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A—HUMAN NECESSITIES
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    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Definitions

  • Cardiovascular disease is one of the leading causes of death in the United States and most European countries. It is estimated that over 70 million people in the United States alone suffer from a cardiovascular disease or disorder including but not limited to high blood pressure, coronary heart disease, dislipidemia, congestive heart failure and stroke. A need exists for improved treatments for cardiovascular-related diseases and disorders.
  • a pharmaceutical composition comprising a statin or derivative of a statin, for example a hydroxy-derivative of a statin, or a pharmaceutically acceptable salt thereof and an omega-3 fatty acid and is provided.
  • a statin or derivative of a statin for example a hydroxy-derivative of a statin, or a pharmaceutically acceptable salt thereof and an omega-3 fatty acid and is provided.
  • hydroxy-derivative of a statin herein refers to a parent statin compound (i.e. known class of HMG-CoA reductase inhibitors) having at least one hydroxy substituent group.
  • a hydroxyl group is attached to a phenyl ring of the parent statin.
  • a pharmaceutical composition comprising a hydroxy-derivative of a statin or a pharmaceutically acceptable salt thereof and an oil comprising an omega-3 fatty acid.
  • the oil comprises at least 95% by weight eicosapentaenoic acid or derivative thereof, for example ethyl eicosapentaenoate.
  • the hydroxy-derivative of a statin is selected from a hydroxy-derivative of atorvastatin, mevastatin, pitavastatin, pravastatin, rosuvastatin, fluvastatin, simvastatin, lovastatin, cerivastatin and pharmaceutically acceptable salts thereof.
  • the hydroxy-derivative of a statin is selected from ortho or para hydroxy-atorvastatin, p-hydroxy atorvastatin calcium, p-hydroxy atorvastatin disodium, o-hydroxy atorvastatin calcium, o-hydroxy atorvastatin lactone, o-hydroxy atorvastatin-d5 calcium, o-hydroxy atorvastatin-d5 disodium, o-hydroxy atorvastatin-d5 lactone, 2-hydroxy atorvastatin bisodium, p-hydroxy atorvastatin lactone, p-hydroxy atorvastatin-d5 calcium, p-hydroxy atorvastatin-d5 lactone, and 4-hydroxy atorvastatin bisodium.
  • the oil comprises one or more of: (a) about 0.2% to about 0.5% by weight ethyl octadecatetraenoate, (b) about 0.05% to about 0.20% by weight ethyl nonaecapentaenoate, (c) about 0.2% to about 3% by weight ethyl arachidonate, (d) about 0.3% to about 0.5% by weight ethyl eicosatetraenoate, (e) about 0.8% to about 0.25% by weight ethyl heneicosapentaenoate, (f) about 0.02% to about 0.1% by weight ethyl 17E-icosapentaenoate, (g) about 0.02% to about 0.1% by weight ethyl 5-icosapentanoate, (h) about 0.01% to about 0.15% by weight ethyl 5E,8E-icosapentaenoate, (i) about 0.01% to about 0.01% to about
  • the invention provides a method of treating a cardiovascular-related disease in a subject in need thereof comprising administering a composition as described herein to the subject.
  • the cardiovascular-related disease is artherosclerosis.
  • FIG. 1 shows effects of EPA, DHA and EPA/DHA, in combination with atorvastatin, atorvastatin o-hydroxy metabolite, simvastatin or rosuvastatin, on membrane lipid peroxidation.
  • FIG. 2 shows effects of EPA in combination with atorvastatin, atorvastatin o-hydroxy metabolite, simvastatin or rosuvastatin, on membrane lipid peroxidation.
  • FIG. 3 shows effects of DHA in combination with atorvastatin, atorvastatin o-hydroxy metabolite, simvastatin or rosuvastatin, on membrane lipid peroxidation.
  • FIG. 4 shows effects of EPA/DHA in combination with atorvastatin, atorvastatin o-hydroxy metabolite, simvastatin or rosuvastatin, on membrane lipid peroxidation.
  • FIG. 5 shows effects of atorvastatin, atorvastatin o-hydroxy metabolite, simvastatin or rosuvastatin, in combination with EPA, DHA or EPA/DHA on membrane lipid peroxidation.
  • FIG. 6 shows effects of atorvastatin, in combination with EPA, DHA or EPA/DHA, on membrane lipid peroxidation.
  • FIG. 7 shows effects of atorvastatin o-hydroxy metabolite in combination with EPA, DHA or EPA/DHA, on membrane lipid peroxidation.
  • FIG. 8 shows effects of simvastatin, in combination with EPA, DHA or EPA/DHA, on membrane lipid peroxidation.
  • FIG. 9 shows effects of rosuvastatin in combination with EPA, DHA or EPA/DHA, on membrane lipid peroxidation.
  • the invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising a statin or hydroxy-derivative of a statin or pharmaceutically acceptable salt thereof and an oil comprising an omega-3 fatty acid.
  • the hydroxy-derivative of a statin comprises hydroxy-atorvastatin of the following structure:
  • hydroxy-derivative of a statin comprises hydroxy-fluvastatin of the following structure:
  • the hydroxy-derivative of a statin comprises hydroxy-lovastatin, for example of the following structure:
  • hydroxy-derivative of a statin comprises hydroxy-simvastatin, for example of the following structure:
  • hydroxy-derivative of a statin comprises hydroxy-cerivastatin, for example of the following structure:
  • hydroxy-derivative of a statin comprises hydroxy-pitavastatin, for example of the following structure:
  • the hydroxy-derivative of a statin is selected from ortho or para hydroxy-atorvastatin and salts thereof, for example p-hydroxy atorvastatin calcium, p-hydroxy atorvastatin disodium, o-hydroxy atorvastatin calcium, o-hydroxy atorvastatin lactone, o-hydroxy atorvastatin-d5 calcium, o-hydroxy atorvastatin-d5 disodium, o-hydroxy atorvastatin-d5 lactone, 2-hydroxy atorvastatin bisodium, p-hydroxy atorvastatin lactone, p-hydroxy atorvastatin-d5 calcium, p-hydroxy atorvastatin-d5 lactone, and 4-hydroxy atorvastatin bisodium.
  • the statin comprises atorvastatin, simvastatin or rosuvastatin.
  • a composition of the invention comprises a statin, hydroxy-derivative of a statin or a pharmaceutically acceptable salt thereof in an amount of about 0.01 mg to about 500 mg, about 0.1 mg to about 250 mg, or about 1 mg to about 100 mg, for example about 1 mg, about 5 mg, about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 60 mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, or about 500 mg.
  • compositions of the invention comprise and oil.
  • the oil comprises a fatty acid, for example an omega-3 fatty acid.
  • the omega-3 fatty acid comprises eicosapentaenoic acid or a pharmaceutically acceptable ester, derivative, conjugate or salt thereof, or mixtures of any of the foregoing, collectively referred to herein as “EPA.”
  • EPA pharmaceutically acceptable
  • the oil comprises at least about 95% by weight EPA.
  • the EPA comprises all-cis eicosa-5,8,11,14,17-pentaenoic acid.
  • the EPA comprises an eicosapentaenoic acid ester.
  • the EPA comprises a C 1 -C 5 alkyl ester of eicosapentaenoic acid.
  • the EPA comprises eicosapentaenoic acid ethyl ester, eicosapentaenoic acid methyl ester, eicosapentaenoic acid propyl ester, or eicosapentaenoic acid butyl ester.
  • the EPA comprises all-cis eicosa-5,8,11,14,17-pentaenoic acid ethyl ester.
  • the EPA is in the form of ethyl-EPA, lithium EPA, mono-, di- or triglyceride EPA or any other ester or pharmaceutically acceptable salt of EPA, or the free acid form of EPA.
  • the EPA may also be in the form of a 2-substituted derivative or other derivative which slows down its rate of oxidation but does not otherwise change its biological action to any substantial degree.
  • the oil comprises docosahexaenoic acid (DHA) or a derivative thereof, for example ethyl-DHA. In another embodiment, the oil comprises at least about 95% by weight DHA or derivative thereof, for example E-DHA.
  • DHA docosahexaenoic acid
  • E-DHA E-DHA
  • the oil contains not more than about 10%, not more than about 9%, not more than about 8%, not more than about 7%, not more than about 6%, not more than about 5%, not more than about 4%, not more than about 3%, not more than about 2%, not more than about 1%, or not more than about 0.5%, by weight, DHA or derivative thereof such as ethyl-DHA, if any.
  • a composition of the invention contains substantially no docosahexaenoic acid or derivative thereof.
  • a composition useful in the present invention contains no docosahexaenoic acid or derivative thereof.
  • the oil comprises ethyl eicosapentaenoate and ethyl docosahexaenoic acid in a mole ratio of about 1:1 to about 1.5:1, about 1.1:1 to about 1.4:1, for example about 1.3:1.
  • the oil contains less than 10%, less than 9%, less than 8%, less than 7%, less than 6%, less than 5%, less than 4%, less than 3%, less than 2%, less than 1%, less than 0.5% or less than 0.25%, by weight, of any fatty acid other than EPA.
  • fatty acid other than EPA include linolenic acid (LA), arachidonic acid (AA), docosahexaenoic acid (DHA), alpha-linolenic acid (ALA), stearadonic acid (STA), eicosatrienoic acid (ETA) and/or docosapentaenoic acid (DPA).
  • an oil useful in a composition of the invention contains about 0.1% to about 4%, about 0.5% to about 3%, or about 1% to about 2%, by weight, of total fatty acids other than ethyl-EPA and/or ethyl-DHA.
  • an oil useful in compositions of the invention has one or more of the following features: (a) eicosapentaenoic acid ethyl ester represents at least about 96%, at least about 97%, or at least about 98%, by weight, of all fatty acids present; (b) the oil contains not more than about 4%, not more than about 3%, or not more than about 2%, by weight, of total fatty acids other than eicosapentaenoic acid ethyl ester; (c) the oil contains not more than about 0.6%, not more than about 0.5%, or not more than about 0.4% of any individual fatty acid other than eicosapentaenoic acid ethyl ester; (d) the oil has a refractive index (20° C.) of about 1 to about 2, about 1.2 to about 1.8 or about 1.4 to about 1.5; (e) the composition has a specific gravity (20° C.) of about 0.8 to about 1.0, about 0.85 to about 0.
  • the oil comprises at least about 95% by weight ethyl eicosapentaenoate (EPA-E), about 0.2% to about 0.3% by weight ethyl octadecatetraenoate (ODTA-E), about 0.05% to about 0.20% by weight ethyl nonaecapentaenoate (NDPA-E), about 0.2% to about 0.4% by weight ethyl arachidonate (AA-E), about 0.3% to about 0.5% by weight ethyl eicosatetraenoate (ETA-E), and about 0.05% to about 0.15% ethyl heneicosapentaenoate (HPA-E).
  • EPA-E ethyl eicosapentaenoate
  • ODTA-E ethyl octadecatetraenoate
  • NDPA-E nonaecapentaenoate
  • AA-E ethyl arachidonate
  • the oil comprises at least about 96% by weight ethyl eicosapentaenoate, about 0.22% to about 0.28% by weight ethyl octadecatetraenoate, about 0.075% to about 0.15% by weight ethyl nonaecapentaenoate, about 0.25% to about 0.35% by weight ethyl arachidonate, about 0.3% to about 0.4% by weight ethyl eicosatetraenoate (ETA-E), and about 0.075% to about 0.15% ethyl heneicosapentaenoate (HPA-E).
  • ETA-E ethyl eicosapentaenoate
  • HPA-E ethyl heneicosapentaenoate
  • the oil comprises one or more of: (a) about 0.2% to about 0.5% by weight ethyl octadecatetraenoate, (b) about 0.05% to about 0.20% by weight ethyl nonaecapentaenoate, (c) about 0.2% to about 3% by weight ethyl arachidonate, (d) about 0.3% to about 0.5% by weight ethyl eicosatetraenoate, (e) about 0.8% to about 0.25% by weight ethyl heneicosapentaenoate, (f) about 0.02% to about 0.1% by weight ethyl 17E-icosapentaenoate, (g) about 0.02% to about 0.1% by weight ethyl 5-icosapentanoate, (h) about 0.01% to about 0.15% by weight ethyl 5E,8E-icosapentaenoate, (i) about 0.01% to about 0.01% to about
  • the oil comprises any one or more, any two or more, any three or more, any four or more, any five or more, any six or more, any seven or more, any eight or more, any nine or more, any ten or more, any eleven or more, any twelve or more, any thirteen or more, any fourteen or more or all fifteen of: (a)-(o) immediately above.
  • the oil comprises at least about 95% ethyl eicosapentaeoate, by weight, and about 0.2% to about 3.5% ethyl arachidonate, by weight.
  • EPA is present in a composition of the invention in an amount of about 50 mg to about 5000 mg, about 75 mg to about 2500 mg, or about 100 mg to about 1000 mg, for example about 75 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 625 mg, about 650 mg, about 675 mg, about 700 mg, about 725 mg, about 750 mg, about 775 mg, about 800 mg, about 825 mg, about 850 mg, about 875 mg, about 900 mg, about 925 mg, about 950 mg, about 975 mg, about 1000 mg, about 1025 mg, about 1050 mg, about 1075 mg, about 1100 mg, about 1025 mg, about 1050 mg, or about 100
  • a composition of the invention is present in a capsule, for example a capsule comprising gelatin. In still another embodiment, at least about 100 mg to about 2 g of such a composition is present in each capsule.
  • the invention provides a method for treatment and/or prevention of a cardiovascular-related disease comprising administering a composition or compositions as disclosed herein to a subject in need thereof.
  • the invention provides a method for treatment and/or prevention of cardiovascular-related diseases comprising co-administering to a subject in need thereof a first pharmaceutical composition comprising a hydroxy-derivative of a statin and a second pharmaceutical composition comprising an oil as set forth herein.
  • co-administering” and “co-administration” herein includes administering two or more compositions as part of a coordinated dosing regime whether the compositions are administered sequentially, substantially simultaneously or individually.
  • cardiovascular-related disease refers to any disease or disorder of the heart or blood vessels (i.e. arteries and veins) or any symptom thereof.
  • cardiovascular-related diseases include hypertriglyceridemia, hypercholesterolemia, mixed dyslipidemia, coronary heart disease, vascular disease, stroke, atherosclerosis, arrhythmia, hypertension, myocardial infarction, and other cardiovascular events.
  • treatment in relation a given disease or disorder, includes, but is not limited to, inhibiting the disease or disorder, for example, arresting the development of the disease or disorder; relieving the disease or disorder, for example, causing regression of the disease or disorder; or relieving a condition caused by or resulting from the disease or disorder, for example, relieving, preventing or treating symptoms of the disease or disorder.
  • prevention in relation to a given disease or disorder means: preventing the onset of disease development if none had occurred, preventing the disease or disorder from occurring in a subject that may be predisposed to the disorder or disease but has not yet been diagnosed as having the disorder or disease, and/or preventing further disease/disorder development if already present.
  • the present invention provides a method of blood lipid therapy comprising administering to a subject or subject group in need thereof a pharmaceutical composition or compositions as described herein.
  • the subject or subject group has hypertriglyceridemia, hypercholesterolemia, mixed dyslipidemia and/or very high triglycerides.
  • the subject or subject group being treated has a baseline triglyceride level (or mean or median baseline triglyceride level in the case of a subject group), fed or fasting, of about 200 mg/dl to about 500 mg/d1.
  • the subject or subject group has a baseline LDL-C level (or mean or median baseline LDL-C level), despite statin therapy, of about 40 mg/dl to about 100 mg/d1.
  • the subject or subject group being treated in accordance with methods of the invention has a body mass index (BMI or mean BMI) of not more than about 45 kg/m 2 .
  • the subject or subject group being treated in accordance with methods of the invention exhibits a fasting baseline absolute plasma level of free total fatty acid (or mean thereof) not greater than about 300 nmol/ml, not greater than about 250 nmol/ml, not greater than about 200 nmol/ml, not greater than about 150 nmol/ml, not greater than about 100 nmol/ml, or not greater than about 50 nmol/ml.
  • the subject or subject group being treated in accordance with methods of the invention exhibits a fasting baseline absolute plasma level of free EPA (or mean thereof in the case of a subject group) not greater than about 0.70 nmol/ml, not greater than about 0.65 nmol/ml, not greater than about 0.60 nmol/ml, not greater than about 0.55 nmol/ml, not greater than about 0.50 nmol/ml, not greater than about 0.45 nmol/ml, or not greater than about 0.40 nmol/ml.
  • the subject or subject group being treated in accordance with methods of the invention exhibits a baseline fasting plasma level (or mean thereof) of free EPA, expressed as a percentage of total free fatty acid, of not more than about 3%, not more than about 2.5%, not more than about 2%, not more than about 1.5%, not more than about 1%, not more than about 0.75%, not more than about 0.5%, not more than about 0.25%, not more than about 0.2% or not more than about 0.15%.
  • free plasma EPA and/or total fatty acid levels are determined prior to initiating therapy.
  • the subject or subject group being treated in accordance with methods of the invention exhibits a fasting baseline absolute plasma level of free EPA (or mean thereof) not greater than about 1 nmol/ml, not greater than about 0.75 nmol/ml, not greater than about 0.50 nmol/ml, not greater than about 0.4 nmol/ml, not greater than about 0.35 nmol/ml, or not greater than about 0.30 nmol/ml.
  • the subject or subject group being treated in accordance with methods of the invention exhibits a fasting baseline plasma, serum or red blood cell membrane EPA level not greater than about 150 ⁇ g/ml, not greater than about 125 ⁇ g/ml, not greater than about 100 ⁇ g/ml, not greater than about 95 ⁇ g/ml, not greater than about 75 ⁇ g/ml, not greater than about 60 ⁇ g/ml, not greater than about 50 ⁇ g/ml, not greater than about 40 ⁇ g/ml, not greater than about 30 ⁇ g/ml, or not greater than about 25 ⁇ g/ml.
  • methods of the present invention comprise a step of measuring the subject's (or subject group's mean) baseline lipid profile prior to initiating therapy.
  • methods of the invention comprise the step of identifying a subject or subject group having one or more of the following: baseline non-HDL-C value (or mean value) of about 200 mg/dl to about 400 mg/dl, for example at least about 210 mg/dl, at least about 220 mg/dl, at least about 230 mg/dl, at least about 240 mg/dl, at least about 250 mg/dl, at least about 260 mg/dl, at least about 270 mg/dl, at least about 280 mg/dl, at least about 290 mg/dl, or at least about 300 mg/dl; baseline total cholesterol value (or mean value) of about 250 mg/dl to about 400 mg/dl, for example at least about 260 mg/dl, at least about 270 mg/dl, at least about 280 mg/dl or at least about 290
  • the subject or subject group upon treatment in accordance with the present invention, for example over a period of about 1 to about 200 weeks, about 1 to about 100 weeks, about 1 to about 80 weeks, about 1 to about 50 weeks, about 1 to about 40 weeks, about 1 to about 20 weeks, about 1 to about 15 weeks, about 1 to about 12 weeks, about 1 to about 10 weeks, about 1 to about 5 weeks, about 1 to about 2 weeks or about 1 week, the subject or subject group exhibits one or more of the following outcomes:
  • y a reduction or increase in one or more of serum phospholipid and/or red blood cell content of docosahexaenoic acid (DHA), docosapentaenoic acid (DPA), arachidonic acid (AA), palmitic acid (PA), staeridonic acid (SA) or oleic acid (OA) compared to baseline or placebo control.
  • DHA docosahexaenoic acid
  • DPA docosapentaenoic acid
  • AA arachidonic acid
  • PA palmitic acid
  • SA staeridonic acid
  • OA oleic acid
  • methods of the present invention comprise measuring baseline levels of one or more markers set forth in (a)-(y) above prior to dosing the subject or subject group.
  • the methods comprise administering a composition as disclosed herein to the subject after baseline levels of one or more markers set forth in (a)-(y) are determined, and subsequently taking an additional measurement of said one or more markers.
  • the subject or subject group upon treatment with a composition of the present invention, for example over a period of about 1 to about 200 weeks, about 1 to about 100 weeks, about 1 to about 80 weeks, about 1 to about 50 weeks, about 1 to about 40 weeks, about 1 to about 20 weeks, about 1 to about 15 weeks, about 1 to about 12 weeks, about 1 to about 10 weeks, about 1 to about 5 weeks, about 1 to about 2 weeks or about 1 week, the subject or subject group exhibits any 2 or more of, any 3 or more of, any 4 or more of, any 5 or more of, any 6 or more of, any 7 or more of, any 8 or more of, any 9 or more of, any 10 or more of, any 11 or more of, any 12 or more of, any 13 or more of, any 14 or more of, any 15 or more of, any 16 or more of, any 17 or more of, any 18 or more of, any 19 or more of, any 20 or more of, any 21 or more of, any 22 or more of, any 23 or more, any 24 or more, or all 25 of outcomes (a
  • the subject or subject group upon treatment with a composition of the present invention, exhibits one or more of the following outcomes:
  • a reduction in triglyceride level of at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55% or at least about 75% (actual % change or mean % change) as compared to baseline or placebo control;
  • a reduction in lipoprotein(a) levels of at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, or at least about 100% (actual % change or mean % change) compared to baseline or placebo control;
  • FPG fasting plasma glucose
  • HbA 1c hemoglobin A 1c
  • a reduction in homeostasis model index insulin resistance of at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, or at least about 100% (actual % change or mean % change) compared to baseline or placebo control;
  • hsCRP high sensitivity C-reactive protein
  • (x) a reduction or increase in one or more of serum phospholipid and/or red blood cell DHA, DPA, AA, PA and/or OA of at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55% or at least about 75% (actual % change or mean % change) compared to baseline or placebo control; and/or
  • methods of the present invention comprise measuring baseline levels of one or more markers set forth in (a)-(y) prior to dosing the subject or subject group. In another embodiment, the methods comprise administering a composition as disclosed herein to the subject after baseline levels of one or more markers set forth in (a)-(y) are determined, and subsequently taking a second measurement of the one or more markers as measured at baseline for comparison thereto.
  • the subject or subject group upon treatment with a composition of the present invention, for example over a period of about 1 to about 200 weeks, about 1 to about 100 weeks, about 1 to about 80 weeks, about 1 to about 50 weeks, about 1 to about 40 weeks, about 1 to about 20 weeks, about 1 to about 15 weeks, about 1 to about 12 weeks, about 1 to about 10 weeks, about 1 to about 5 weeks, about 1 to about 2 weeks or about 1 week, the subject or subject group exhibits any 2 or more of, any 3 or more of, any 4 or more of, any 5 or more of, any 6 or more of, any 7 or more of, any 8 or more of, any 9 or more of, any 10 or more of, any 11 or more of, any 12 or more of, any 13 or more of, any 14 or more of, any 15 or more of, any 16 or more of, any 17 or more of, any 18 or more of, any 19 or more of, any 20 or more of, any 21 or more of, any 22 or more of, any 23 or more of, any 24 or more of, or all 25 or more
  • Parameters (a)-(y) can be measured in accordance with any clinically acceptable methodology.
  • triglycerides, total cholesterol, HDL-C and fasting blood sugar can be sample from serum and analyzed using standard photometry techniques.
  • VLDL-TG, LDL-C and VLDL-C can be calculated or determined using serum lipoprotein fractionation by preparative ultracentrifugation and subsequent quantitative analysis by refractometry or by analytic ultracentrifugal methodology.
  • Apo A1, Apo B and hsCRP can be determined from serum using standard nephelometry techniques.
  • Lipoprotein (a) can be determined from serum using standard turbidimetric immunoassay techniques.
  • LDL particle number and particle size can be determined using nuclear magnetic resonance (NMR) spectrometry.
  • Remnants lipoproteins and LDL-phospholipase A2 can be determined from EDTA plasma or serum and serum, respectively, using enzymatic immunoseparation techniques.
  • Oxidized LDL, intercellular adhesion molecule-1 and interleukin-2 levels can be determined from serum using standard enzyme immunoassay techniques. These techniques are described in detail in standard textbooks, for example Tietz Fundamentals of Clinical Chemistry, 6 th Ed. (Burtis, Ashwood and Borter Eds.), WB Saunders Company.
  • a subject or subjects fast for up to 12 hours prior to blood sample collection, for example about 10 hours.
  • the present invention provides a method of treating or preventing primary hypercholesterolemia and/or mixed dyslipidemia (Fredrickson Types IIa and IIb) in a subject in need thereof, comprising administering to the subject one or more compositions as disclosed herein.
  • the present invention provides a method of reducing triglyceride levels in a subject or subjects when treatment with a statin or niacin extended-release monotherapy is considered inadequate (Frederickson type IV hyperlipidemia).
  • the present invention provides a method of treating or preventing risk of recurrent nonfatal myocardial infarction in a subject with a history of myocardial infarction, comprising administering to the subject one or more compositions as disclosed herein.
  • the present invention provides a method of treating, slowing progression of or promoting regression of atherosclerotic disease in a subject in need thereof, comprising administering to a subject in need thereof one or more compositions as disclosed herein.
  • the present invention provides a method of inhibiting oxidation of lipopoproteins in a subject in need thereof, comprising administering to a subject in need thereof one or more compositions as disclosed herein.
  • the present invention provides a method of scavenging free radicals in a subject in need thereof, comprising administering to a subject in need thereof one or more compositions as disclosed herein.
  • the present invention provides a method of inhibiting metal ion chelation of lipoproteins in a subject in need thereof, comprising administering to a subject in need thereof one or more compositions as disclosed herein.
  • the present invention provides a method of treating or preventing very high serum triglyceride levels (e.g. Types IV and V hyperlipidemia) in a subject in need thereof, comprising administering to the subject one or more compositions as disclosed herein.
  • very high serum triglyceride levels e.g. Types IV and V hyperlipidemia
  • a composition of the invention is administered to a subject in an amount sufficient to provide a daily dose of ethyl-eicosapentaenoate of about 1 mg to about 10,000 mg, 25 about 5000 mg, about 50 to about 3000 mg, about 75 mg to about 2500 mg, or about 100 mg to about 1000 mg, for example about 75 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 625 mg, about 650 mg, about 675 mg, about 700 mg, about 725 mg, about 750 mg, about 775 mg, about 800 mg, about 825 mg, about 850 mg, about 875 mg, about 900 mg, about 925 mg, about 950 mg, about
  • a composition of the invention is administered to a subject in an amount sufficient to provide a daily dose of hydroxy-derivative of a statin of about 0.01 mg to about 500 mg, about 0.1 mg to about 250 mg, or about 1 mg to about 100 mg, for example about 1 mg about 5 mg, about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 60 mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, or about 500 mg.
  • any of the methods disclosed herein are used in treatment of a subject or subjects that consume a traditional Western diet.
  • the methods of the invention include a step of identifying a subject as a Western diet consumer or prudent diet consumer and then treating the subject if the subject is deemed a Western diet consumer.
  • the term “Western diet” herein refers generally to a typical diet consisting of, by percentage of total calories, about 45% to about 50% carbohydrate, about 35% to about 40% fat, and about 10% to about 15% protein.
  • a Western diet may alternately or additionally be characterized by relatively high intakes of red and processed meats, sweets, refined grains, and desserts, for example more than 50%, more than 60% or more or 70% of total calories come from these sources.
  • any of the methods disclosed herein are used in treatment of a subject or subjects that consume less than (actual or average) about 150 g, less than about 125 g, less than about 100 g, less than about 75 g, less than about 50 g, less than about 45 g, less than about 40 g, less than about 35 g, less than about 30 g, less than about 25 g, less than about 20 g or less than about 15 g of fish per day.
  • any of the methods disclosed herein are used in treatment of a subject or subjects that consume less than (actual or average) about 10 g, less than about 9 g, less than about 8 g, less than about 7 g, less than about 6 g, less than about 5 g, less than about 4 g, less than about 3 g, less than about 2 g per day of omega-3 fatty acids from dietary sources.
  • any of the methods disclosed herein are used in treatment of a subject or subjects that consume less than (actual or average) about 2.5 g, less than about 2 g, less than about 1.5 g, less than about 1 g, less than about 0.5 g, less than about 0.25 g, or less than about 0.2 g per day of EPA and DHA or derivative of either from dietary sources.
  • a composition as described herein is administered to a subject once or twice per day.
  • 1, 2, 3 or 4 capsules, each containing about 500 mg to about 1 g of a composition as described herein, are administered to a subject daily.
  • 1 or 2 capsules, each containing about 1 g of a composition as described herein, are administered to the subject in the morning, for example between about 5 am and about 11 am, and 1 or 2 capsules, each containing about 1 g of a composition as described herein, are administered to the subject in the evening, for example between about 5 pm and about 11 pm.
  • compositions useful in accordance with methods of the invention are orally deliverable.
  • oral administration include any form of delivery of a therapeutic agent or a composition thereof to a subject wherein the agent or composition is placed in the mouth of the subject, whether or not the agent or composition is swallowed.
  • oral administration includes buccal and sublingual as well as esophageal administration.
  • the composition is present in a capsule, for example a soft gelatin capsule.
  • a composition for use in accordance with the invention can be formulated as one or more dosage units.
  • dose unit and “dosage unit” herein refer to a portion of a pharmaceutical composition that contains an amount of a therapeutic agent suitable for a single administration to provide a therapeutic effect.
  • dosage units may be administered one to a plurality (i.e. 1 to about 10, 1 to 8, 1 to 6, 1 to 4 or 1 to 2) of times per day, or as many times as needed to elicit a therapeutic response.
  • the invention provides use of any composition described herein for treating moderate to severe hypertriglyceridemia in a subject in need thereof, comprising: providing a subject having a fasting baseline triglyceride level of about 500 mg/dl to about 1500 mg/dl and administering to the subject a pharmaceutical composition as described herein.
  • the composition comprises about 1 g to about 4 g of eicosapentaenoic acid ethyl ester, wherein the composition contains substantially no docosahexaenoic acid.
  • statins e.g. atorvastatin, rosuvastatin, simvastatin and hydroxy-atorvastatin
  • statin derivative e.g. atorvastatin, rosuvastatin, simvastatin and hydroxy-atorvastatin
  • EPA and DHA were tested individually at a fixed concentration of 10.0 ⁇ M or in combination at 5.65 ⁇ M and 4.35 ⁇ M (EPA and DHA, respectively), which is a mole ratio of 1.3:1.
  • LOOH lipid peroxide
  • C/P cholesterol-to-phospholipid
  • Levels of lipid hydroperoxides were also measured for EPA, DPH and EPA/DPH in cholesterol-enriched membrane prepared in the absence and presence of a statin.
  • 1,2-Dilinoleoyl-3-sn-phosphatidylcholine was obtained from Avanti Polar Lipids (Alabaster, Ala.) and stored in chloroform (25 mg/ml) at ⁇ 80° C. until use. Cholesterol obtained and stored in chloroform (10 mg/ml) at ⁇ 20° C.
  • CHOD-iodide color reagent was prepared according to a procedure modified from El-Saadani et al. (El-Saadani M, Esterbauer H, El-Sayed M, Goher M, Nassar A Y, Jurgens G.
  • statin was prepared in ethanol just prior to experimental use and added together with component lipids containing fixed amounts of EPA, DPH or EPA/DPH at equimolar levels.
  • the compounds and lipids were added in combination during membrane sample preparation to ensure full incorporation into the lipid bilayers.
  • Membrane samples consisting of DLPC ⁇ cholesterol, with cholesterol-to-phospholipid (C/P) mole ratios ranging from 0.5 to 1.5, were prepared as follows. Component lipids (in chloroform) were transferred to 13 ⁇ 100 mm test tubes and shell-dried under a steady stream of nitrogen gas while vortex mixing. The lipid was co-dried with EPA, DPH or EPA/DPH prepared in the absence or presence of a statin at equimolar levels.
  • C/P cholesterol-to-phospholipid
  • lipid membrane samples were subjected to time-dependent autoxidation by incubating at 37° C. in an uncovered, shaking water bath. Small aliquots of each sample were removed at 24 h intervals and combined with 1.0 ml of active CHOD-iodide color reagent. To ensure spectrophotometric readings within the optimum absorbance range, sample volumes taken for measurement of lipid peroxide formation were adjusted for length of peroxidation and range between 100 and 10 ⁇ l. Test samples were immediately covered with foil and incubated at room temperature for >4 h in the absence of light. Absorbances were measured against a CHOD blank at 365 nm using a Beckman DU-640 spectrophotometer.
  • the CHOD colorimetric assay is based on the oxidation of iodide (I) by lipid hydroperoxides (LOOH) and proceeds according to the following reaction scheme:
  • the quantity of triiodide anion (I 3 ⁇ ) liberated in this reaction is directly proportional to the amount of lipid hydroperoxides present in the membrane sample.
  • the molar absorptivity value ( ⁇ ) of I 3 ⁇ is 2.46 ⁇ 10 4 M ⁇ 1 cm ⁇ 1 at 365 nm.
  • EPA, DHA and EPA/DHA plus hydroxy-atorvastatin exhibited significantly lower lipid hydroperoxide formation compared to control.
  • EPA plus hydroxy-atorvastatin exhibited significantly lower lipid hydroperoxide formation compared to EPA+ atorvastatin, EPA+ simvastatin or EPA+ rosuvastatin.
  • DHA plus hydroxy-atorvastatin exhibited significantly lower lipid hydroperoxide formation compared to DHA+ atorvastatin, DHA+ simvastatin or DHA+ rosuvastatin.
  • EPA/DHA plus hydroxy-atorvastatin exhibited significantly lower lipid hydroperoxide formation than EPA/DHA plus atorvastatin.
  • EPA, DHA and EPA/DHA plus hydroxy-atorvastatin or rosuvastatin exhibited significantly lower lipid hydroperoxide formation compared to control.

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