Therapeutic and diagnostic methods involving biglycan and utrophin

US9958458B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9958458-B2
Application numberUS-201113996951-A
CountryUS
Kind codeB2
Filing dateDec 27, 2011
Priority dateDec 27, 2010
Publication dateMay 1, 2018
Grant dateMay 1, 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.

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.

First claim

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.

Assignees

Inventors

Classifications

  • 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

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 US9958458B2 cover?
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, inclu…
Who is the assignee on this patent?
Amenta Alison R, Yilmaz Atilgan, Mckechnie Beth A, and 2 more
What technology area does this patent fall under?
Primary CPC classification G01N33/6893. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue May 01 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).