Composition combination containing enriched hill shaddock oil
US-2024325485-A1 · Oct 3, 2024 · US
US11197840B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11197840-B2 |
| Application number | US-201615780913-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 2, 2016 |
| Priority date | Dec 4, 2015 |
| Publication date | Dec 14, 2021 |
| Grant date | Dec 14, 2021 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention relates generally to methods for the treatment and/or prophylaxis of mental illness involving administration of 10-HDA. More particularly, methods are taught herein for the treatment and/or prophylaxis of obsessive compulsive disorder, anxiety disorder or a condition characterised by one or more symptoms of a obsessive compulsive disorder or an anxiety disorder.
Opening claim text (preview).
What is claimed is: 1. A method for the treatment of a repetitive behavioral pattern in a subject having obsessive compulsive disorder, comprising administering to a mammal in need thereof an effective amount of 10-hydroxy-2-decenoic acid or a pharmaceutically acceptable salt thereof. 2. The method of claim 1 , comprising administering an effective amount of trans 10-hydroxy-2-decenoic acid or a pharmaceutically acceptable salt thereof. 3. The method of claim 1 , comprising administering an effective amount of cis 10-hydroxy-2-decenoic acid or a pharmaceutically acceptable salt thereof. 4. The method of claim 1 , comprising administering an effective amount of a racemic mixture of trans and cis 10-hydroxy-2-decenoic acid or a pharmaceutically acceptable salts thereof. 5. The method of claim 1 , wherein the 10-hydroxy-2-decenoic acid or a pharmaceutically acceptable salt thereof is administered as a composition. 6. The method of claim 5 , wherein the composition comprises royal jelly, an extract of royal jelly, or a composition derived from royal jelly. 7. The method of claim 1 , wherein the effective amount of 10-hydroxy-2-decenoic acid or a pharmaceutically acceptable salt thereof is in the range of 0.01 to 6000 mg/day, 0.1 to 5000 mg/day, 1 to 4000 mg/day, 10 to 3000 mg/day, 100 to 2000 mg/day, or 500 to 1500 mg/day. 8. The method of claim 1 , wherein the effective amount of 10-hydroxy-2-decenoic acid or a pharmaceutically acceptable salt thereof is selected from the group consisting of 0.5 mg/day, 1 mg/day, 5 mg/day, 10 mg/day, 50 mg/day, 100 mg/day, 250 mg/day, 500 mg/day, 750 mg/day, 1000 mg/day, 1500 mg/day and 2000 mg/day. 9. The method of claim 1 , wherein the mammal is a human.
having one or two double bonds, e.g. oleic, linoleic acids · CPC title
Drugs for disorders of the nervous system · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.