US2023338503A1PendingUtilityA1
Parenteral norovirus vaccine formulations
Est. expiryJul 11, 2031(~5 yrs left)· nominal 20-yr term from priority
A61K 39/12A61K 39/125A61K 39/39A61K 2039/55505A61P 31/12A61P 31/14A61K 2039/5258A61K 2039/545A61K 2039/55572A61K 2039/70C12N 2770/16034A61P 37/04
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Claims
Abstract
The present invention relates to single dose parenteral vaccine compositions comprising mixtures of monovalent Norovirus virus-like particles. Methods of conferring protective immunity against Norovirus infections in a human subject by administering such compositions are also disclosed.
Claims
exact text as granted — not AI-modified1 . A buffered composition comprising a first monovalent VLP derived from a first Norovirus genogroup and a second monovalent VLP derived from a second Norovirus genogroup wherein said buffer is L-histidine, and wherein the composition is formulated as a liquid.
2 . The buffered composition of claim 1 , wherein said L-histidine is present at a concentration of between about 15 mM to about 50 mM.
3 . The buffered composition of claim 2 , wherein said L-histidine is present at a concentration of between about 20 mM to about 25 mM.
4 . The buffered composition of claim 1 , wherein the pH of the composition is between about 6.0 to about 7.0.
5 . The buffered composition of claim 4 , wherein the pH of the composition is between about 6.2 to about 6.8.
6 . The buffered composition of claim 1 , further comprising a pharmaceutically acceptable salt.
7 . The buffered composition of claim 6 , wherein the salt is selected from the group consisting of sodium chloride, potassium chloride, sodium sulfate, ammonium sulfate and sodium citrate.
8 . The buffered composition of claim 7 , wherein said salt is sodium chloride.
9 . The buffered composition of claim 8 , wherein the concentration of sodium chloride is between about 10 mM and about 200 mM.
10 . The buffered composition of claim 9 , wherein the concentration of sodium chloride is between about 100 mM and about 150 mM.
11 . The buffered composition of claim 1 , wherein said first Norovirus genogroup is genogroup I.
12 . The buffered composition of claim 1 , wherein one of the Norovirus genogroups is genogroup II.
13 . The buffered composition of claim 11 , wherein the second Norovirus genogroup is genogroup II.
14 . The buffered composition of claim 13 , wherein the first monovalent VLP is derived from Norovirus genotype GI.1 and the second monovalent VLP is derived from Norovirus genotype GII.4.
15 . The buffered composition of claim 13 , wherein said second monovalent VLP contains capsid proteins derived from a consensus sequence of genogroup II noroviruses.
16 . The buffered composition of claim 1 , further comprising at least one adjuvant.
17 . The buffered composition of claim 16 , wherein said adjuvant is selected from the group consisting of monophosphoryl lipid A (MPL) and alum.
18 . The buffered composition of claim 1 , further comprising MPL and alum.
19 . A method of inducing an immune response in a subject, comprising administering to the subject the buffered composition of claim 1 .
20 . A vaccine formulation comprising the composition of claim 1 .
21 . A method of inducing an immune response in a subject, comprising administering to the subject the vaccine formulation of claim 20 .Join the waitlist — get patent alerts
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