The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Aug. 29, 2017

Filed:

Feb. 29, 2016
Applicant:

Regents of the University of Minnesota, Minneapolis, MN (US);

Inventors:

Michael T. Bowser, Inver Grove Heights, MN (US);

Gianluigi Veglia, Minneapolis, MN (US);

Meng Jing, Minneapolis, MN (US);

Raffaello Verardi, Minneapolis, MN (US);

Joseph M. Metzger, St. Paul, MN (US);

Brian Raymond Thompson, Hugo, MN (US);

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K 31/70 (2006.01); C07H 21/02 (2006.01); C07H 21/04 (2006.01); C12N 15/115 (2010.01); C12N 15/113 (2010.01); G01N 33/53 (2006.01); C12N 5/00 (2006.01);
U.S. Cl.
CPC ...
C12N 15/115 (2013.01); C12N 15/113 (2013.01); G01N 33/5308 (2013.01); C12N 2310/16 (2013.01); C12N 2310/18 (2013.01); C12N 2320/30 (2013.01); G01N 2500/02 (2013.01);
Abstract

This disclosure describes, in one aspect, a composition that generally includes an xNA molecule comprising at least six nucleotides, in an amount effective to improve at least one indicator of myocyte function and a pharmaceutically acceptable carrier. In another aspect, this disclosure describes a method of treating cardiac disease. Generally, the method includes administering to a subject a composition that includes an xNA molecule having at least six nucleotides, in an amount effective to improve at least one indicator of myocyte function, and a pharmaceutically acceptable carrier. In another aspect, this disclosure describes a method for evaluating the efficacy of treatment of cardiac disease. Generally, the method includes administering to a subject a composition that includes a first xNA molecule comprising a predetermined length in an amount effective to increase myocyte relaxation, then selecting a predetermined length of a second xNA molecule for at least one subsequent treatment. If treatment with the first xNA results in more myocyte relaxation than is desired, then the predetermined length of the second xNA molecule is shorter than the predetermined length of the first xNA. If, on the other hand, treatment with the first xNA results in less myocyte relaxation than is desired then the predetermined length of the second xNA molecule is longer than the predetermined length of the first xNA.


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