IP Library Patent Application 15754807
Patent Application
App. No. 15/754,807

NOROVIRUS VACCINE

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Patent No.
US None
App. No.
15/754,807
Abstract

A dry powder norovirus vaccine is provided, which comprises at least two norovirus antigens representing different genogroups. The vaccine may be produced by formulation with a mixture of different antigens or combination of monovalent powders with each containing one antigen. The formulated vaccine is suitable for mucosal administration and soluble in aqueous solutions for parenteral administration. A method of immunization is also provided, which comprises at least one administration of the vaccine via mucosal and/or parental route. The immunization may have multiple administrations of the vaccine, i.e., one or more immunizations via a mucosal route followed by one or more immunizations via a parenteral route or vice versa, to maximize both mucosal and systemic immune responses and protection against norovirus infections.

Claims (30)

1 - 47 . (canceled)

48 . A multivalent norovirus dry powder vaccine composition comprising:

a first norovirus virus-like particle (VLP) antigen of GI genotype;

a second norovirus VLP antigen of GII genotype; and

an anionic polysaccharide.

49 . The composition of claim 48 , wherein the multivalent norovirus dry powder vaccine composition is suitable for both parenteral and mucosal routes of administration.

50 . The composition of claim 48 , wherein the amount of norovirus VLP antigen of GI genotype is about 10 μg to 50 μg per 20 mg dry powder vaccine composition.

51 . The composition of claim 48 , wherein the amount of norovirus VLP antigen of GII genotype is about 10 μg to 50 μg per 20 mg dry powder composition.

52 . The composition of claim 48 , wherein the anionic polysaccharide is in the amount of about 0.25% of the composition.

53 . The composition of claim 48 , wherein the mean microparticle diameter of the dry powder vaccine composition is 24 μm to 37 μm.

54 . The composition of claim 48 , wherein the anionic polysaccharide is sodium polygalacturonate.

55 . The composition of claim 48 , wherein the amount of norovirus VLP antigen of GI genotype and the amount of norovirus VLP antigen of GII genotype are in a proportion in the range of 1:1 to 3:1.

56 . A method of immunizing a mammalian subject against a norovirus infection with a multivalent norovirus dry powder vaccine composition comprising a norovirus VLP antigen of GI genotype, a norovirus VLP antigen of GII genotype, and an ionic polysaccharide, the method comprising:

administering to the subject at least one dose of the vaccine composition, thereby initiating an immune response against a norovirus antigen sufficient to confer active immunity against a norovirus infection in the subject.

57 . The method of claim 56 , wherein the vaccine composition is administered by mucosal route and/or parental route.

58 . The method of claim 56 , further comprising reconstituting the vaccine composition in aqueous solution, wherein the vaccine composition is administered by a parenteral route.

59 . The method of claim 56 , wherein at least 20 mg of the vaccine composition is administered by the mucosal route.

60 . The method of claim 56 , wherein at least 5 μg of the norovirus VLP antigen of GI genotype and at least 5 μg of norovirus VLP antigen of GII genotype is administered in each dose.

61 . The method of claim 57 , wherein the total dose per subject administered by mucosal route and/or parental route is at least 50 μg of norovirus VLP antigen of GI genotype and at least 50 μg of norovirus VLP antigen of GII genotype.

62 . A method for producing a multivalent dry powder norovirus vaccine composition suitable for both parenteral and mucosal routes of administration comprising:

a. obtaining a first solution comprising a norovirus virus-like particle (VLP) antigen of GI genotype;

b. introducing to the first solution, an anionic polysaccharide;

c. drying the first solution with the anionic polysaccharide to a substantially non-aqueous state, thereby producing a first dry powder formulation;

d. obtaining a second solution comprising a norovirus VLP antigen of GII genotype;

e. introducing to the second solution an anionic polysaccharide;

f. drying the second solution with the anionic polysaccharide to a substantially non-aqueous state, thereby producing a second dry powder formulation;

g. combining the first and second dry powder formulations to form a multivalent dry powder norovirus vaccine formulation.

63 . The method of claim 62 , wherein the drying is by lyophilization.

64 . The method of claim 62 , wherein the drying is by spray drying.

65 . The method of claim 62 , wherein the norovirus VLP of GI genotype and norovirus VLP of GII genotype are obtained by expressing the recombinant virus-like particles in an expression system selected from the group consisting of: prokaryote cells, eukaryote cells, E. coli cells, S. cerevisiae cells, insect cells, mammalian cells, HEK293 cells, CHO cells, tobacco mosaic virus, and baculovirus.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Aug 20, 2020
From: MIDCAP FINANCIAL TRUST, AS AGENT
To: OLOGY BIOSERVICES, INC.; NANO ADM, LLC
Reel/Frame 053561/0070 →
SECURITY INTEREST SUPPLEMENT Recorded Jun 12, 2020
From: OLOGY BIOSERVICES, INC.; MAMO ADM, LLC
To: MIDCAP FINANCIAL TRUST, AS AGENT
Reel/Frame 052927/0061 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 21, 2018
From: COBB, RON; SPRINGER, MICHAEL; NI, YAWEI
To: OLOGY BIOSERVICES, INC.
Reel/Frame 046641/0249 →