IP Library Granted Patent US 10,183,070
Granted Patent B2
US 10,183,070 · App. 15/883,334 · Granted Jan 22, 2019

Patent

Inventors: Kathrin Ute Jansen (New York, NY); Annaliesa Sybil Anderson (Upper Saddle River, NJ); Judith Absalon (New York, NY); Jose Miguel Aste-Amezaga (Harleysville, PA); Johannes Frederik Beeslaar (Farnham, GB); David Cooper (Monroe, NY); John Erwin Farley (Chapel Hill, NC); Leah Diane Fletcher (Geneseo, NY); Shannon Lea Harris (Nanuet, NY); Thomas Richard Jones (New City, NY); Isis Kanevsky (New York, NY); Lakshmi Khandke (Nanuet, NY); Paul Liberator (Holmdel, NJ); John Lance Perez (Doylestown, PA); Lynn Marie Phelan (Lake Hiawatha, NJ); Gary Warren Zlotnick (San Antonio, TX)
Assignee: Pfizer Inc.
A61K39/095A61K31/7028A61K47/10A61K47/183A61K47/26A61K47/646A61K47/6415A61P31/00C07K14/22C07K16/1217
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Quick Facts
Patent No.
US 10,183,070
App. No.
15/883,334
Granted
Jan 22, 2019
Kind
B2
Abstract

In one aspect, the invention relates to a composition including a factor H binding protein (fHBP) and a Neisseria meningitidis non-serogroup B capsular polysaccharide. The invention further relates to uses of a composition that includes fHBP, such as, for example, uses to elicit an immune response against N. meningitidis serogroup B strains and non-serogroup B strains. The compositions and methods described herein are directed to administration in humans, including adults, adolescents, toddlers, and infants.

Claims (16)

1. An immunogenic composition comprising: a) a liquid composition comprising (i) a first lipidated polypeptide comprising the amino acid sequence set forth in SEQ ID NO: 1; and (ii) a second lipidated polypeptide comprising the amino acid sequence set forth in SEQ ID NO: 2 and aluminum; and

b) a lyophilized composition comprising

i) a Neisseria meningitidis serogroup A (MenA) capsular saccharide conjugated to an adipic acid dihydrazide (ADH) linker by 1-cyano-4-dimethylamino pyridinium tetrafluoroborate, wherein the linker is conjugated to tetanus toxoid (TT) by carbodiimide chemistry (MenAAH-TT conjugate);

ii) a Neisseria meningitidis serogroup C (MenC) capsular saccharide conjugated to an ADH linker by 1-cyano-4-dimethylamino pyridinium tetrafluoroborate, wherein the linker is conjugated to tetanus toxoid (TT) by carbodiimide chemistry (MenCAH-TT conjugate);

iii) a Neisseria meningitidis serogroup W135 (MenW) capsular saccharide directly conjugated to tetanus toxoid (TT) by 1-cyano-4-dimethylamino pyridinium tetrafluoroborate, in the absence of a linker (MenW-TT conjugate); and

iv) a Neisseria meningitidis serogroup Y (MenY) capsular saccharide directly conjugated to tetanus toxoid (TT) by 1-cyano-4-dimethylamino pyridinium tetrafluoroborate, in the absence of a linker (MenY-TT conjugate) wherein the lyophilized composition is reconstituted with the liquid composition.

2. The immunogenic composition according to claim 1 , wherein the aluminum comprises aluminum phosphate.

3. The immunogenic composition according to claim 1 , further comprising polysorbate-80.

4. The immunogenic composition according to claim 1 , wherein the lyophilized composition does not contain aluminum.

5. The immunogenic composition according to claim 1 , wherein the first polypeptide and the second polypeptide are bound to the aluminum.

6. The immunogenic composition according to claim 1 , wherein the composition further comprises Tris-HCl; sodium chloride; sucrose; histidine; polysorbate 80; and aluminum phosphate.

7. The immunogenic composition according to claim 1 , wherein the concentration of polypeptides bound to the aluminum in the immunogenic composition is decreased by at most 10% after 24 hours, as compared to the concentration of polypeptides bound to the aluminum in the liquid composition prior to reconstituting the lyophilized composition.

8. The immunogenic composition according to claim 1 , wherein the concentration of MenA AH -TT conjugate in the immunogenic composition is decreased by at most 10% after 24 hours, as compared to the concentration of the MenA AH -TT conjugate in the lyophilized composition.

9. The immunogenic composition according to claim 1 , wherein the concentration of MenC AH -TT conjugate in the immunogenic composition is decreased by at most 10% after 24 hours, as compared to the concentration of the MenC AH -TT conjugate in the lyophilized composition.

10. The immunogenic composition according to claim 1 , wherein the concentration of MenW-TT conjugate in the immunogenic composition is decreased by at most 10% after 24 hours, as compared to the concentration of the MenW-TT conjugate in the lyophilized composition.

11. The immunogenic composition according to claim 1 , wherein the concentration of MenY-TT conjugate in the immunogenic composition is decreased by at most 10% after 24 hours, as compared to the concentration of the MenY-TT conjugate in the lyophilized composition.

Assignments (1)
ASSIGNEE ADDRESS CORRECTION Recorded Mar 20, 2023
From: PFIZER INC.
To: PFIZER INC.
Reel/Frame 063119/0087 →
Continuity (5)
Provisional Application 62613945 · Jan 5, 2018
Provisional Application 62503295 · May 8, 2017
Provisional Application 62452963 · Jan 31, 2017
Provisional Application 62623233 · Jan 29, 2018
Related Publication 20180214532A1 · Aug 2, 2018
Cited By (2)
US 12,383,611 US 12,497,432