US2022096627A1PendingUtilityA1
Compositions and methods for treating viral infections through stimulated innate immunity in combination with antiviral compounds
Est. expirySep 19, 2034(~8.1 yrs left)· nominal 20-yr term from priority
A61K 38/05Y02A50/30A61K 9/0078A61K 31/215A61K 38/07A61K 38/08A61K 31/7056A61K 38/06A61K 31/24A61K 2039/55561A61K 39/39A61K 45/06A61P 31/12
66
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Claims
Abstract
Embodiments are directed to compositions and methods for treating viral infections.
Claims
exact text as granted — not AI-modified1 . A composition comprising: (a) lipopeptide, (b) immune stimulatory oligodeoxy nucleotide, and (c) antiviral pharmaceutical.
2 . The composition of claim 1 , wherein the lipopeptide is PAM 2 CSK 4 .
3 . The composition of claim 1 , wherein the immune stimulatory oligodeoxynucleotide is a type C oligodeoxynucleotide (ODN).
4 . The composition of claim 3 , wherein the immune stimulatory oligodeoxynucleotide is ODN2395 or ODNM362 or ODN10101.
5 . The composition of claim 1 , wherein the antiviral pharmaceutical is oseltamivir or ribavirin.
6 . The composition of claim 1 , wherein the composition is formulated for administration to the lungs.
7 . A method of treating, inhibiting, or attenuating a viral infection comprising administering an effective amount of the composition of claim 1 to an individual that has or is at risk of viral infection.
8 . The method of claim 7 , wherein the subject has been exposed to a virus.
9 . The method of claim 7 , wherein the virus is a Adenoviridae, Coronaviridae, Filoviridae, Flaviviridae, Hepadnaviridae, Herpesviridae, Orthomyxoviridae, Paramyxovirinae, Pneumovirinae, Picomaviridae, Poxyiridae, Retroviridae, or Togaviridae.
10 . The method of claim 7 , wherein the virus is Parainfluenza, Influenza, H5N1, Marburg, Ebola, Severe acute respiratory syndrome coronavirus (SARS-COV), Middle eastern respiratory syndrome coronavirus (MERS-COV), yellow fever virus, human respiratory syncytial, Hantavirus, or Vaccinia virus.
11 . The method of claim 7 , wherein the composition is administered by nebulization.
12 . The method of claim 7 , wherein the lipopeptide, immune stimulatory oligonucleotide and anti-viral drug are administered in an amount of from about 0.1 mg/kg to about 100 mg/kg of the individual's body weight.
13 . A method of treating, inhibiting, or attenuating a viral infection comprising administering an effective amount of the composition comprising an aerosolized (a) lipopeptide and (b) immune stimulatory oligodeoxy nucleotide in combination with a composition comprising an anti-viral pharmaceutical to an individual that has or is at risk of viral infection.
14 . The method of claim 13 , wherein the lipopeptide is PAM 2 CSK 4 and wherein the immune stimulatory oligodeoxynucleotide is ODN2395 or ODNM362 or ODN10101.
15 . The method of claim 13 , wherein the immune stimulatory oligodeoxynucleotide is a type C oligodeoxynucleotide (ODN).
16 . (canceled)
17 . The method of claim 13 , wherein the antiviral pharmaceutical is oseltamivir or ribavirin.
18 - 19 . (canceled)
20 . The composition of claim 1 , wherein the composition is formulated for nebulization.
21 . A nebulizer comprising (a) lipopeptide, (b) immune stimulatory oligodeoxy nucleotide, and (c) anti-viral pharmaceutical.
22 - 25 . (canceled)
26 . The composition of claim 1 , wherein the composition comprises 16 μM lipopeptide and 4 μM immune stimulatory oligodeoxy nucleotide.
27 . The composition of claim 1 , wherein the molar ratio of lipopeptide to immune stimulatory oligodexy nucleotide is 4:1.Join the waitlist — get patent alerts
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