US2017314042A1PendingUtilityA1

Genetically modified msc and therapeutic methods

Assignee: UNIV CALIFORNIAPriority: Aug 31, 2012Filed: Nov 14, 2016Published: Nov 2, 2017
Est. expiryAug 31, 2032(~6.1 yrs left)· nominal 20-yr term from priority
A61K 48/005C12N 2740/15043C12N 15/86
61
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Claims

Abstract

This disclosure relates to vectors, isolated cells, compositions, and methods for the treatment of critical limb ischemia and associated disorders. One aspect of the disclosure relates to a vector comprising a nucleic acid encoding a 165A isoform VEGF protein and a promoter that regulates expression of the nucleic acid encoding the VEGF.

Claims

exact text as granted — not AI-modified
1 . A method for treating peripheral artery disease and/or critical limb ischemia in a patient in need thereof comprising administering to the patient an effective amount of an isolated marrow stromal cell comprising a lentiviral vector, wherein the vector comprises:
 (a) a nucleic acid encoding a 165A isoform VEGF protein or an equivalent thereof, and   (b) a promoter that regulates expression of the nucleic acid encoding the 165A isoform VEGF or an equivalent thereof.

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