System and methods for performing saliva-based diagnostic screenings
US-2024420847-A1 · Dec 19, 2024 · US
US9958458B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9958458-B2 |
| Application number | US-201113996951-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 27, 2011 |
| Priority date | Dec 27, 2010 |
| Publication date | May 1, 2018 |
| Grant date | May 1, 2018 |
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 disclosure provides methods for predicting a patient's response to biglycan therapy for diseases or conditions associated with an abnormal level or activity of biglycan; disorders associated with an unstable cytoplasmic membrane, for example, due to an unstable dystrophin associated protein complex (DAPC); disorders associated with abnormal synapses or neuromuscular junctions, including those resulting from an abnormal MuSK activation or acetylcholine receptor (AChR) aggregation. Examples of such diseases include muscular dystrophies, such as Duchenne's Muscular Dystrophy, Becker's Muscular Dystrophy, neuromuscular disorders and neurological disorders. This application also provides combination therapeutics, such as a biglycan therapeutic and a utrophin therapeutic.
Opening claim text (preview).
We claim: 1. A method of treating a muscular dystrophy in a patient in need thereof, the method comprising: (i) determining that a patient has a utrophin deficiency by measuring a level of membrane-associated utrophin at the sarcolemma in a sample of muscle cells from the patient and comparing with a reference value, wherein the utrophin deficiency is characterized by a decreased level of utrophin protein or activity; (ii) administering a first dose of a biglycan polypeptide to the patient, wherein the biglycan polypeptide comprises an amino acid sequence corresponding to amino acids 38-365 of SEQ ID NO: 11; and (iii) measuring the level of membrane-associated utrophin at the sarcolemma in a sample of muscle cells from the patient; and if the level of utrophin measured in (iii) is increased relative to the level of utrophin determined in (i), then (iv) administering a second dose of the biglycan polypeptide. 2. A method of treating a muscular dystrophy in a patient in need thereof, the method comprising: (i) determining that a patient has a utrophin deficiency by measuring the level of membrane-associated utrophin at the sarcolemma in a sample of muscle cells from the patient and comparing with a reference value, wherein the utrophin deficiency is characterized by a decreased level of utrophin protein or activity; (ii) administering a dose of a biglycan polypeptide to the patient to increase the level of utrophin at the sarcolemma in a patient in need thereof, wherein the biglycan polypeptide comprises an amino acid sequence corresponding to amino acids 38-365 of SEQ ID NO: 11; and (iii) measuring the level of membrane-associated utrophin at the sarcolemma in another sample of muscle cells from the patient. 3. A method of treating a muscular dystrophy in a patient in whom a utrophin deficiency characterized by a decreased level of utrophin protein or activity has been determined by measuring the level of membrane-associated utrophin at the sarcolemma in a sample of muscle cells from the patient and comparing with a reference value, comprising administering a dose of a biglycan polypeptide to the patient, wherein the biglycan polypeptide comprises an amino acid sequence corresponding to amino acids 38-365 of SEQ ID NO: 11, wherein the level of membrane-associated utrophin at the sarcolemma of muscle cells in the patient is increased after administration of the biglycan polypeptide.
Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title
Duchenne dystrophy · CPC title
Myotonic dystrophy · CPC title
Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems · CPC title
Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.