US2021069225A1PendingUtilityA1
Liponucleotide-based therapy for ards
Assignee: OHIO STATE INNOVATION FOUNDATIONPriority: Jun 27, 2016Filed: Nov 19, 2020Published: Mar 11, 2021
Est. expiryJun 27, 2036(~9.9 yrs left)· nominal 20-yr term from priority
Inventors:Ian Davis
A61K 31/7068A61K 47/18A61K 47/24A61P 11/00A61K 47/26C07H 19/20A61K 47/50A61K 47/549
55
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Claims
Abstract
Compositions and method are therefore disclosed for treating ARDS. In particular, disclosed a composition that contains one, two, or more cytidine diphosphate (CDP)-conjugated precursors selected from the group consisting of CDP-choline, CDP-ethanolamine, and CDP-diacylglycerol (CDP-DAG) in a pharmaceutically acceptable carrier for use in treating ARDS.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for preventing an acute respiratory distress syndrome (ARDS) in a subject, comprising administering to a subject at risk for ARDS an effective amount of a composition comprising one or more cytidine diphosphate (CDP)-conjugated precursors selected from the group consisting of CDP-choline, CDP-ethanolamine, CDP-diacylglycerol (CDP-DAG), and combinations thereof, wherein CDP-conjugated precursors are the only active ingredient and/or wherein the composition does not comprise a nucleotide.
2 . The method of claim 1 , wherein the composition comprises two or more cytidine diphosphate (CDP)-conjugated precursors selected from the group consisting of CDP-choline, CDP-ethanolamine, and CDP-diacylglycerol (CDP-DAG), in a pharmaceutically acceptable carrier.
3 . The method of claim 1 , wherein the composition comprises CDP-choline.
4 . The method of claim 1 , wherein the composition comprises CDP-choline, CDP-DAG, and CDP-ethanolamine.
5 . The method of claim 1 , wherein the composition consists essentially of CDP-choline and CDP-DAG in a pharmaceutically acceptable carrier.
6 . The method of claim 1 , wherein the composition is administered intravenously, orally, or by inhalation.
7 . The method of claim 1 , wherein the composition is in a powder or tablet form.
8 . The method of claim 1 , wherein the subject has a direct lung insult capable of causing ARDS.
9 . The method of claim 8 , wherein the direct lung insult is selected from the group consisting of a viral, bacterial, or fungal infection; toxic gas inhalation; a lung cancer; chemotherapy; acid aspiration; and chest trauma.
10 . The method of claim 9 , wherein the infection comprises influenza.
11 . The method of claim 1 , further comprising treating the subject with surfactant therapy.
12 . The method of claim 1 , wherein the composition is administered to the subject prior to infection with one or more influenza virus strains.
13 . The method of claim 1 , wherein the composition is administered after the subject has been infected with one or more influenza virus strains but before said subject has developed ARDS.Join the waitlist — get patent alerts
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