Treatment for obesity

US11497725B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11497725-B2
Application numberUS-202017028674-A
CountryUS
Kind codeB2
Filing dateSep 22, 2020
Priority dateJul 18, 2013
Publication dateNov 15, 2022
Grant dateNov 15, 2022

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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

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention relates to a method for treating or preventing obesity in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of certain carbamate compounds. The invention further relates to methods for reducing body weight and/or reducing food intake in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of certain carbamate compounds.

First claim

Opening claim text (preview).

We claim: 1. A method for reducing body weight or body weight gain in a human subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of Formula (I): or a pharmaceutically acceptable salt or ester thereof; wherein R is a member selected from the group consisting of alkyl of 1 to 8 carbon atoms, halogen, alkoxy of 1 to 3 carbon atoms, nitro, hydroxy, trifluoromethyl, and thioalkoxy of 1 to 3 carbon atoms; x is an integer of 0 to 3, with the proviso that R may be the same or different when x is 2 or 3; R 1 and R 2 are independently selected from the group consisting of hydrogen, alkyl of 1 to 8 carbon atoms, aryl, arylalkyl, cycloalkyl of 3 to 7 carbon atoms; or R 1 and R 2 can be joined to form a 5 to 7-membered heterocycle that is unsubstituted or substituted with one or more alkyl or aryl groups, wherein the heterocycle can comprise 1 to 2 nitrogen atoms and 0 to 1 oxygen atom, wherein the nitrogen atoms are not directly connected with each other or with the oxygen atom; said method comprises administering the compound of Formula (I) to the human subject in a dosing regimen comprising a daily dose of at least 200 mg/day, wherein the compound of Formula (I) or pharmaceutically acceptable salt thereof effects a decrease in body weight or body weight gain in the human subject by at least 0.6 kg from baseline at the 6th week of the dosing regimen. 2. The method of claim 1 , wherein x=0. 3. The method of claim 1 , wherein R 1 and R 2 are hydrogen and x=0. 4. The method of claim 1 , wherein the compound of Formula I is an enantiomer of Formula I substantially free of other enantiomers or an enantiomeric mixture wherein one enantiomer of Formula I predominates. 5. The method of claim 4 , wherein the enantiomer of Formula I predominates to the extent of about 98% or greater. 6. The method of claim 4 , wherein the enantiomer of Formula I is an enantiomer of Formula Ia: or a pharmaceutically acceptable salt or ester thereof. 7. The method of claim 6 , wherein the enantiomer of Formula Ia is the (R) or (D) enantiomer. 8. The method of claim 6 , wherein the enantiomer of Formula Ia is the (S) or (L) enantiomer. 9. The method of claim 6 , wherein the enantiomer of Formula Ia predominates to the extent of about 98% or greater. 10. The method of claim 4 , wherein the enantiomer of Formula I substantially free of other enantiomers is the compound of Formula Ib or an enantiomeric mixture wherein the compound of Formula Ib predominates: or a pharmaceutically acceptable salt or ester thereof. 11. The method of claim 10 , wherein the compound of Formula Ib predominates to the extent of about 98% or greater. 12. The method of claim 1 , wherein the compound of Formula I is administered orally. 13. The method of claim 1 , wherein the compound of Formula I is administered in the form of a capsule or tablet. 14. The method of claim 1 , wherein the compound of Formula I is administered in the form of a capsule at a dose of about 10 mg to about 1000 mg without any excipients.

Assignees

Inventors

Classifications

  • A61K31/27Primary

    of carbamic or thiocarbamic acids, meprobamate, carbachol, neostigmine · CPC title

  • Anorexiants; Antiobesity agents · CPC title

  • Mouth and digestive tract, i.e. intraoral and peroral administration · CPC title

  • Preparations in capsules, e.g. of gelatin, of chocolate {(A61K9/0004 takes precedence; bite capsules A61K9/0056)} · CPC title

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Frequently asked questions

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What does patent US11497725B2 cover?
The present invention relates to a method for treating or preventing obesity in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of certain carbamate compounds. The invention further relates to methods for reducing body weight and/or reducing food intake in a subject in need thereof, comprising administering to the subject a therapeutically e…
Who is the assignee on this patent?
Axsome Malta Ltd, Sk Biopharmaceuticals Co Ltd
What technology area does this patent fall under?
Primary CPC classification A61K31/27. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Nov 15 2022 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 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).