US2007231330A1PendingUtilityA1
Method for the improvement of neuronal regeneration
Assignee: NEURAXO BIOPHARMACEUTICALS GMBPriority: May 14, 1997Filed: Mar 16, 2007Published: Oct 4, 2007
Est. expiryMay 14, 2017(expired)· nominal 20-yr term from priority
A61K 31/192A61K 31/164A61K 31/194A61K 31/16A61K 31/198A61K 31/444A61K 31/4015A61K 31/4402A61K 31/366A61K 31/44A61K 31/275A61K 31/401A61K 31/00A61K 38/00A61K 31/122C07K 16/18
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Claims
Abstract
A method for the improvement of neuronal regeneration by prevention or inhibition of basal membrane formation induced by a lesion of neuronal tissue.
Claims
exact text as granted — not AI-modified1 - 17 . (canceled)
18 . A method of enhancing regeneration of injuries caused by a lesion of neuronal tissue comprising local administration of an inhibitor of basal membrane formation to enhance axonal regeneration by specific inhibition of basal membrane formation induced.
19 . The method according to claim 18 , wherein the inhibitor is selected from the group consisting of antibodies against collagen IV; Fe-chelating agents; inhibitors of amino acids hydroxylases, such as prolyl-4-hydroxylase, lysine-hydroxylase; 2-oxoglutarate competitiors; antisense oligo nucleotides or oligo nucleotide analogs; siRNAs; aptamers.
20 . The method of claim 19 , wherein the inhibitor is selected from the group consisting of pyridine derivatives, such as 5-arylcarbonylamino- or 5-arylcarbamoyl-derivatives, 2-carboxylate, 2,5, dicarboxylate, their ethyl esters or ethyl amides, or dimethoxylamides; 3,4′-bipyridine, such as 5 amino-6-(1H)-one, 1,6-dihydro-2-methyl-6-oxo-5-carbonitril; 2,2′-dipyridine, such as 5,5′-dicarboxylic acid or its pharmaceutically acceptable salts, 4,4′-dicarboxylic acid ethyl ester or ethyl amide; 3,4′-dihydroxybenzoate, such as the diethyl ester; proline and its structural and functional analoges; β-aminopropionitrile; desferrioxamine; desferasirox; anthracyclines; 2,7,8-trihydroxy anthraquinones, fibrostatin-C; coumalic acid or its pharmaceutically acceptable salts; 5-oxaproline, β-lactam antibiotics.
21 . The method of claim 18 , wherein the inhibitor is administered in combination with a substance that stimulates neuronal growth.
22 . The method of claim 19 , wherein the inhibitor is administered in combination with a substance that stimulates neuronal growth.
23 . The method of claim 20 , wherein the inhibitor is administered in combination with a substance that stimulates neuronal growth.
24 . The method of claim 18 , wherein the inhibitor is administered in an amount in an amount of 1 ng/kg to 1 mg/kg body weight.
25 . The method of claim 19 , wherein the inhibitor is administered in an amount of 1 ng/kg to 1 mg/kg body weight.
26 . The method of claim 20 , wherein the inhibitor is administered in an amount of 1 ng/kg to 1 mg/kg body weight.
27 . The method of claim 21 , wherein the inhibitor is administered in an amount of 1 ng/kg to 1 mg/kg body weight.
28 . The method of claim 22 , wherein the inhibitor is administered in an amount of 1 ng/kg to 1 mg/kg body weight.
29 . The method of claim 23 , wherein the inhibitor is administered to an amount of 1 ng/kg to 1 mg/kg body weight.Join the waitlist — get patent alerts
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