US2007037765A1PendingUtilityA1
Formulations comprising antisense nucleotides to connexins
Est. expiryJan 27, 2019(expired)· nominal 20-yr term from priority
A61P 43/00A61P 29/00A61P 25/00C07H 21/04A61P 17/16C12N 2310/11C12N 2320/32C12N 15/111A61K 38/00A61P 17/02A61K 31/711A61P 17/12C12N 15/1138A61P 17/00
60
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Claims
Abstract
A therapeutic and/or cosmetic formulation comprising at least one anti-sense polynucleotide to a connexin protein together with a pharmaceutically acceptable carrier or vehicle is useful in site specific down regulation of connexin protein expression, particularly in reduction of neuronal cells death, wound healing, reduction of inflammation, decrease of scar formation and skin rejuvenation and thickening.
Claims
exact text as granted — not AI-modified1 - 36 . (canceled)
37 . A pharmaceutical composition comprising a connexin 43 antisense polynucleotide and a pharmaceutically acceptable carrier in an amount effective for reducing connexin expression.
38 . A pharmaceutical composition according to claim 37 which is formulated for topical administration.
39 . A pharmaceutical compound according to claim 38 wherein which comprises said composition comprises an amount of antisense polynucleotide sufficient for treatment of a wound.
40 . A pharmaceutical composition according to claim 37 formulated with a connexin antisense polynucleotide in an amount sufficient to downregulate the expression of a connexin protein in a mammal.
41 . A pharmaceutical composition according to claim 37 formulated with a connexin antisense polynucleotide in an amount sufficient to decrease cell death in a tissue of a mammal.
42 . A pharmaceutical composition according to claim 37 formulated with a connexin antisense polynucleotide in an amount sufficient to decrease inflammation in a tissue of a mammal.
43 . A pharmaceutical composition according to claim 37 formulated with a connexin antisense polynucleotide in an amount sufficient for treatment of a wound in a tissue of a mammal.
44 . A pharmaceutical composition according to claim 37 wherein said connexin antisense polynucleotide is targeted to a connexin selected from connexin 43, connexin 26, connexin 31.1, connexin 32 or connexin 36.
45 . A pharmaceutical composition according to claim 37 wherein said antisense polynucleotide is targeted to connexin 43.
46 . A pharmaceutical composition of claim 37 wherein said polynucleotide is a oligonucleotide.
47 . A pharmaceutical composition of claim 37 wherein said polynucleotide is a unmodified phosphodiester oligonucleotide.
48 . A pharmaceutical composition of claim 37 wherein said connexin antisense polynucleotide is about 12 to about 40 nucleotides in length.
49 . A pharmaceutical composition of claim 48 wherein said connexin antisense polynucleotide is about 30 nucleotides in length.
50 . A pharmaceutical composition of claim 49 wherein said connexin antisense polynucleotide comprises SEQ ID NO: 1.
51 . A pharmaceutical composition of claim 49 wherein said connexin antisense polynucleotide comprises SEQ ID NO: 2.
52 . A pharmaceutical composition of claim 49 wherein said connexin antisense polynucleotide comprises SEQ ID NO: 3.
53 . A pharmaceutical composition of claim 37 formulated as a cream, ointment, gel, emulsion, or paint.
54 . A pharmaceutical composition of claim 53 formulated as a gel.
55 . A pharmaceutical composition of claim 54 formulated as a gel for topical administration.
56 . A pharmaceutical composition of claim 37 wherein the polynucleotide is formulated for parenteral, intramuscular, intracerebral, intravenous, subcutaneous or transdermal administration.Join the waitlist — get patent alerts
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