US2017314042A1PendingUtilityA1
Genetically modified msc and therapeutic methods
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-modified1 . 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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