Method for treating pervasive development disorders

US9624526B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9624526-B2
Application numberUS-201113313708-A
CountryUS
Kind codeB2
Filing dateDec 7, 2011
Priority dateDec 17, 1999
Publication dateApr 18, 2017
Grant dateApr 18, 2017

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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.

A method of utilizing the chymotrypsin level of an individual as a measure of the success of neuropeptides, and peptides or digestive enzyme administration to such individuals, and in particular, as a prognosticative of potential neuropeptides, peptides, and digestive enzyme administration for persons having ADD, ADHD, Autism and other PDD related disorders. A method for determining the efficacy of neuropeptides, peptides, or digestive enzymes for the treatment of an individual diagnosed with a pervasive developmental disorder (PDD) comprises obtaining a sample of feces from an individual, determining a quantitative level of chymotrypsin present in the sample, and correlating the quantitative level of chymotrypsin determined to be present in the sample with the PDD to determine the efficacy of treating the individual with neuropeptides, peptides, or digestive enzyme administration.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for treating an individual having an autistic disorder, the method comprising measuring a level of fecal chymotrypsin in a sample from the individual and administering to the individual three or more doses per day of an effective amount of digestive enzymes if the individual has a subnormal level of fecal chymotrypsin to promote changes in autistic behavior by ameliorating a symptom of the autistic disorder, wherein the digestive enzymes comprise a protease, an amylase and a lipase. 2. The method of claim 1 , wherein the symptom comprises an impairment in making eye contact with another individual. 3. The method of claim 1 , wherein the symptom comprises a lack of social interaction. 4. The method of claim 1 , wherein the symptom comprises a delay in, or lack of, spoken language. 5. The method of claim 1 , wherein the symptom comprises a repetitive pattern of behavior such as arm flapping. 6. The method of claim 1 , wherein the symptom comprises hyperactivity. 7. The method of claim 1 , wherein the symptom comprises a lack of a formed bowel movement. 8. The method of claim 1 , wherein the symptom comprises a lack of toilet training. 9. The method of claim 1 , wherein the method comprises administering digestive enzymes comprising approximately 4,000 to approximately 60,000 United States Pharmacopeia (U.S.P.) Units/tablet on a daily basis. 10. The method of claim 1 , wherein the digestive enzymes further comprise a cellulase, a sucrase, or a maltase, either singularly or in any combination thereof. 11. The method of claim 1 , wherein the method comprises administering an amount of digestive enzymes on a daily basis, wherein said amount is determined according to the age of the individual. 12. The method of claim 1 , wherein the digestive enzymes comprise pancreatic enzymes. 13. The method of claim 1 , wherein the protease comprises trypsin or chymotrypsin. 14. The method of claim 1 , wherein the level of fecal chymotrypsin is measured by an enzymatic spectrophotometry method. 15. The method of claim 1 , wherein administration of the digestive enzymes improves protein digestion.

Assignees

Inventors

Classifications

  • Drugs for disorders of the nervous system · CPC title

  • C12Q1/37Primary

    involving peptidase or proteinase · CPC title

  • for pancreatic disorders, e.g. pancreatic enzymes · CPC title

  • Monitoring or testing the effects of treatment, e.g. of medication · CPC title

  • Trypsin (3.4.21.4) · CPC title

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What does patent US9624526B2 cover?
A method of utilizing the chymotrypsin level of an individual as a measure of the success of neuropeptides, and peptides or digestive enzyme administration to such individuals, and in particular, as a prognosticative of potential neuropeptides, peptides, and digestive enzyme administration for persons having ADD, ADHD, Autism and other PDD related disorders. A method for determining the efficac…
Who is the assignee on this patent?
Fallon Joan M, Curemark Llc
What technology area does this patent fall under?
Primary CPC classification C12Q1/37. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 18 2017 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 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).