Method of Ameliorating Clotting Pathologies and Related Materials and Methods

US2017333389A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2017333389-A1
Application numberUS-201715653863-A
CountryUS
Kind codeA1
Filing dateJul 19, 2017
Priority dateJul 19, 2012
Publication dateNov 23, 2017
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Methods for reducing blood clotting in a subject are provided, including methods to reduce the risk of and/or treat blot clotting pathologies. Also provided are compositions useful to reduce the risk or treat blood clotting pathologies.

First claim

Opening claim text (preview).

What is claimed is: 1 . A method of reducing blood clotting in a stroke survivor subject in need thereof, comprising: administering a pharmaceutically-effective formulation of a tocotrienol-containing composition, and, administering pharmaceutically-effective formulation of clopigrel, and optionally, administering pharmaceutically-effective formulation of aspirin, sufficient to reduce risk of a further stroke in the subject. 2 . The method of claim 1 , wherein the tocotrienol-containing composition comprises: d-alpha-tocotrienol, d-gamma-tocotrienol, and d-delta-tocotrienol. 3 . The method of claim 1 , wherein the tocotrienol-containing composition comprises: d-alpha-tocotrienol, d-gamma-tocotrienol, d-delta-tocotrienol, and d-alpha-tocopherol. 4 . The method of claim 1 , wherein the tocotrienol-containing composition comprises: d-alpha-tocotrienol 61.52 mg, d-gamma-tocotrienol 112.80 mg, d-delta-tocotrienol 25.68 mg, d-alpha-tocopherol 91.60 IU, plant squalene 51.28 mg, phytosterol complex 20.48 mg, and phytocarotenoid complex 360.00 ug. 5 . A method of claim 1 , which comprises administering up to 400 mg of the tocotrienol-containing composition for at least 30 days, and a pharmaceutically-effective dose of the tocotrienol-containing composition weekly thereafter. 6 . The method of claim 1 , wherein the formulation comprises a dose of the tocotrienol-containing composition selected from the group consisting of: approximately 200 mg to approximately 1000 mg in one weekly dose; approximately 300 mg to approximately 1000 mg in one weekly dose; approximately 400 mg to approximately 500 mg in one weekly dose. 7 . The method of claim 1 , wherein the tocotrienol-containing composition is an orally-delivered supplement. 8 . A method of reducing blood clotting in a subject in need thereof, comprising administering a pharmaceutically-effective formulation of at least one isoform of a tocotrienol and reducing blood clotting in a subject. 9 . The method of claim 8 , wherein the formulation comprises a dose of tocotrienol selected from the group consisting of: approximately 10 mg to approximately 1000 mg per day; approximately 50 mg to approximately 500 mg per day; approximately 100 mg to approximately 500 mg per day; approximately 200 mg to approximately 500 mg per day; approximately 300 mg to approximately 500 mg per day; up to approximately 400 mg per day. 10 . The method of claim 8 , wherein the formulation comprises a dose of tocotrienol selected from the group consisting of: approximately 200 mg to approximately 1000 mg in one weekly dose; approximately 300 mg to approximately 1000 mg in one weekly dose; approximately 400 mg to approximately 500 mg in one weekly dose. 11 . The method of claim 8 , wherein the formulation is administered as a dose regimen selected from the group consisting of: approximately every other day; approximately every third day; approximately every fourth day; approximately every fifth day; approximately every sixth day; approximately every seventh day; approximately every other week; approximately once a month; approximately twice a month; approximately three times a month; approximately four times a month; approximately five times a month; approximately six times a month; approximately seven times a month; and approximately eight times a month. 12 . The method of claim 8 , wherein the formulation is an orally-delivered supplement. 13 . The method of claim 12 , wherein the oral supplement is delivered by one or more of: a capsule, a tablet pill, a colloid, a piece of chewing gum, a gel, a drink, a food additive, a thin film dissolving strip, an emulsified food spread, an emulsion, a syrup, a meat food, a dairy food, and an egg. 14 . The method of claim 8 , wherein the subject is selected from a population at elevated risk for a blood clotting pathology selected from the group consisting of: transient ischemic attack (TIA); stroke; embolism; and cardiac arrest. 15 . The method of claim 8 , wherein the subject is selected from the group consisting of: wherein the subject is selected from: a person who has suffered a previous blood clotting pathology; a person who has suffered a stroke; a person who has suffered a cardiac event; a person who has suffered from transient ischemic attack; a person who has suffered an embolism; a person who has suffered a thrombosis; a person with a genetic predisposition for pathologic blood clotting; a person with biomarkers for pathologic blood clotting; and a person who takes anticoagulants. 16 . A method of reducing risk of a second stroke in a stroke patient in need thereof, comprising administering a pharmaceutically-effective formulation of at least one isoform of a tocotrienol and reducing risk of a second stroke in a stroke patient in need thereof. 17 . A method of claim 16 , which further comprises administering to the patient a pharmaceutically-effective amount of clopidogrel. 18 . A method of claim 16 , which comprises administering up to 400 mg of at least one tocotrienol for at least 30 days, and a pharmaceutically-effective dose of at least one tocotrienol weekly thereafter.

Assignees

Inventors

Classifications

  • Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors · CPC title

  • for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis · CPC title

  • A23L15/00Primary

    Egg products; Preparation or treatment thereof · CPC title

  • by carboxylic acids, e.g. acetylsalicylic acid · CPC title

  • for carnivorous animals, e.g. cats or dogs · CPC title

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What does patent US2017333389A1 cover?
Methods for reducing blood clotting in a subject are provided, including methods to reduce the risk of and/or treat blot clotting pathologies. Also provided are compositions useful to reduce the risk or treat blood clotting pathologies.
Who is the assignee on this patent?
Univ Ohio State
What technology area does this patent fall under?
Primary CPC classification A23L15/00. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Nov 23 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).