Method for treating neurotrauma

US10071072B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10071072-B2
Application numberUS-201715417943-A
CountryUS
Kind codeB2
Filing dateJan 27, 2017
Priority dateMar 14, 2011
Publication dateSep 11, 2018
Grant dateSep 11, 2018

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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.

The invention relates to a composition comprising: i) one or more of uridine and cytidine, or salts, phosphates, acyl derivatives or esters thereof; ii) a lipid fraction comprising at least one of docosahexaenoic acid (22:6; DHA), eicosapentaenoic acid (20:5; EPA) and docosapentaenoic acid (22:5; DPA), or esters thereof, in which the lipid fraction comprises less than 2 weight % of α-linolenic acid (ALA), calculated on the weight of all fatty acids; iii) choline, or salts or esters thereof; for use in the prevention or treatment of neurotrauma, traumatic brain injury, cerebral palsy and spinal cord injury.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for treating neurotrauma, traumatic brain injury, or cerebral palsy in a subject in need thereof, the method comprising administering to the subject a composition comprising: (i) one or more of uridine, cytidine, or salts or esters thereof; (ii) a lipid fraction comprising at least one of docosahexaenoic acid (22:6; DHA), eicosapentaenoic acid (20:5; EPA) and docosapentaenoic acid (22:5; DPA), and less than 2 weight % of α-linolenic acid (ALA), calculated on the weight of all fatty acids; (iii) choline, or salts or esters thereof; and (iv) at least one B complex vitamin selected from the group consisting of vitamin B6, vitamin B12 and vitamin B9. 2. The method according to claim 1 for treating traumatic brain injury or neurotrauma, said composition comprising (i) one or more of uridine, cytidine, or phosphates thereof. 3. The method according to claim 1 , wherein the lipid fraction comprises medium chain fatty acids, wherein the sum of medium chain fatty acids C6:0+C7:0+C8:0 over the sum of C9:0 and C10:0 is less than 2:1. 4. The method according to claim 1 , wherein the lipid fraction comprises fatty acids of less than 14 carbon atoms in an amount of less than 2 weight %, based on total fatty acids. 5. The method according to claim 1 , wherein the composition further comprises cysteine and taurine in an amount of less than 25 mg of their sum per 100 ml of the composition. 6. The method according to claim 1 , wherein the composition further comprises linoleic acid (LA) in an amount of less than 15 g/100 g fatty acids. 7. The method according to claim 6 , wherein the B complex vitamin is selected from the group consisting of vitamin B6, B9 and B12. 8. The method according to claim 1 , wherein the lipid fraction comprises 9 to 300 mg/100 kJ DHA+EPA+DPA. 9. The method according to claim 1 , wherein the lipid fraction comprises 9 to 300 mg/100 kJ DHA+EPA. 10. The method according to claim 1 , wherein the composition comprises 1.5 to 130 mg/100 kJ of one or more of uridine, cytidine, or salts, phosphates or esters thereof, calculated as uridine and cytidine. 11. The method according to claim 1 , wherein the composition comprises 1 to 300 mg/100 kJ of choline, or salts or esters thereof, calculated as choline. 12. The method according to claim 1 , wherein the composition further comprises one or more selected from the group consisting of vitamin C or vitamin E and selenium. 13. The method according to claim 1 , wherein the composition further comprises at least one phospholipid. 14. The method according to claim 1 , wherein the composition is a nutritional product. 15. The method according to claim 12 , wherein the composition comprises, per 100 ml of liquid: 100-500 mg EPA, 1000-1500 mg DHA, 80-600 mg phospholipids, 200-600 mg choline, 400-800 mg uridine monophosphate (UMP), 20-60 mg alpha-TE (vitamin E), 60-100 mg vitamin C, 40-80 μg selenium, 1-5 μg vitamin B12, 0.5-2 mg vitamin B6, and 200-600 μg folic acid. 16. The method according to claim 1 , said composition comprising vitamin B6, B9 and B12. 17. A method for treating neurotrauma, traumatic brain injury, or cerebral palsy in a subject in need thereof, the method comprising administering to the subject a kit of parts comprising: i) one or more of uridine, cytidine, or salts or esters thereof; ii) a lipid fraction comprising at least one of docosahexaenoic acid (22:6; DHA), eicosapentaenoic acid (20:5; EPA) and docosapentaenoic acid (22:5; DPA), and less than 2 weight % of α-linolenic acid (ALA), calculated on the weight of all fatty acids; iii) choline, or salts or esters thereof; and iv) at least one B complex vitamin selected from the group consisting of vitamin B6, vitamin B12 and vitamin B9. 18. The method according to claim 17 , said kit comprising (i) one or more of uridine, cytidine, or phosphates thereof. 19. The method according to claim 17 , said kit comprising vitamin B6, B9 and B12. 20. The method according to claim 17 , for treating traumatic brain injury or neurotrauma, said kit comprising (i) one or more of uridine, cytidine, or phosphates thereof. 21. The method according to claim 20 , for treating traumatic brain injury. 22. The method according to claim 2 , for treating traumatic brain injury. 23. The method according to claim 2 , wherein the composition is a liquid composition with between 0.8 and 1.4 kcal per ml.

Assignees

Inventors

Classifications

  • Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

  • for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia · CPC title

  • for treating abnormal movements, e.g. chorea, dyskinesia · CPC title

  • Drugs for disorders of the nervous system · CPC title

  • Nutrients, e.g. vitamins, minerals · CPC title

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What does patent US10071072B2 cover?
The invention relates to a composition comprising: i) one or more of uridine and cytidine, or salts, phosphates, acyl derivatives or esters thereof; ii) a lipid fraction comprising at least one of docosahexaenoic acid (22:6; DHA), eicosapentaenoic acid (20:5; EPA) and docosapentaenoic acid (22:5; DPA), or esters thereof, in which the lipid fraction comprises less than 2 weight % of …
Who is the assignee on this patent?
Nutricia Nv
What technology area does this patent fall under?
Primary CPC classification A23D7/003. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Sep 11 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). 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).