Nutritional composition useful in the treatment of IBD patients

US10137108B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10137108-B2
Application numberUS-201615544088-A
CountryUS
Kind codeB2
Filing dateJan 22, 2016
Priority dateJan 23, 2015
Publication dateNov 27, 2018
Grant dateNov 27, 2018

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

Compositions and methods are provided that are useful in the treatment of inflammatory bowel disease (IBD) patients. The Compositions and methods are suitable in the prevention or postponement of a relapse in inflammatory bowel disease patients.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for achieving a result selected from the group consisting of treatment of inflammatory bowel disease (IBD), prolonging remission of IBD, and maintaining or improving the mucosa health status of a patient having IBD or in remission from IBD, the method comprising: administering a composition comprising (a) free form amino acids comprising 9.0-11.0 g threonine in free form/100 g of the composition, 7.0-10.0 g serine in free form/100 g of the composition, and 7.0-9.0 g proline in free form/100 g of the composition; (b) carbohydrates and proteins comprising whey TGF-Beta; and (c) at least one essential fatty acid to the patient, the carbohydrates are 10-50 energy percent of the composition, total proteins comprising the free form amino acids and the proteins comprising the whey TGF-Beta are 30-60 energy percent of the composition, and fats comprising the at least one essential fatty acid are 10-40 energy percent of the composition, the patient has initiated therapy comprising at least one of infliximab or adalimumab at least 12 weeks prior to initiating the administering of the composition to the patient. 2. The method of claim 1 , wherein the composition is administered to the patient for at least 10 weeks. 3. The method of claim 1 , wherein the administration of the composition is efficacious with respect to medical indications from IBD for a time point selected from any time point between 10 and 60 weeks. 4. The method of claim 1 , wherein the IBD is selected from the group consisting of Crohn's Disease and ulcerative colitis. 5. The method of claim 1 , wherein the composition is administered in combination with a medicament effective against IBD. 6. The method of claim 1 comprising reconstituting the composition from a dry powder formulation into water. 7. The method of claim 1 , wherein the composition comprises 0.1-1.0 g alpha-linolenic acid/100 g, 1.0-8.0 g linolenic acid/100 g, 0.01 g-0.2 g eicosapentaenoic acid/100 g, and 0.005-0.200 g docosahexaenoic acid/100 g. 8. The method of claim 5 , wherein the medicament comprises 5-aminosalicylic acid (5-ASA). 9. The method of claim 1 , wherein the composition is orally administered to the patient between meals for at least 24 weeks in an amount that contains 400 to 1000 kcal per daily dose. 10. The method of claim 1 , wherein the proteins of the composition consist of whey, casein, the threonine in free form, the serine in free form, the proline in free form, and the whey TGF-Beta. 11. The method of claim 1 , wherein the threonine in free form, the serine in free form, and the proline in free form are the only free form amino acids in the composition. 12. The method of claim 1 , wherein the carbohydrates are 20-40 energy percent of the composition, the total proteins are 35-55 energy percent of the composition, and the fats are 15-35 energy percent of the composition. 13. The method of claim 1 , wherein the carbohydrates are 25-35 energy percent of the composition, the total proteins are 40-50 energy percent of the composition, and the fats are 18-25 energy percent of the composition. 14. The method of claim 1 , wherein the patient is in remission from IBD.

Assignees

Inventors

Classifications

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

  • Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] · CPC title

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

  • Dairy proteins · CPC title

  • A61K31/401Primary

    Proline; Derivatives thereof, e.g. captopril · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US10137108B2 cover?
Compositions and methods are provided that are useful in the treatment of inflammatory bowel disease (IBD) patients. The Compositions and methods are suitable in the prevention or postponement of a relapse in inflammatory bowel disease patients.
Who is the assignee on this patent?
Nestec Sa
What technology area does this patent fall under?
Primary CPC classification A61K31/401. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Nov 27 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).