IP Library Granted Patent US 11,680,087
Granted Patent B2
US 11,680,087 · App. 17/126,712 · Granted Jun 20, 2023

Patent

Inventors: Annaliesa Sybil Anderson (Upper Saddle River, NJ); Rasappa Gounder Arumugham (Lansdale, PA); John Erwin Farley (Chapel Hill, NC); Leah Diane Fletcher (Geneseo, NY); Shannon Lea Harris (Nanuet, NY); Kathrin Ute Jansen (New York, NY); Thomas Richard Jones (New City, NY); Lakshmi Khandke (Nanuet, NY); Bounthon Loun (North Reading, MA); John Lance Perez (Doylestown, PA); Gary Warren Zlotnick (San Antonio, TX)
Assignee: Pfizer Inc.
C07K14/22A61K39/0016A61K39/095A61K39/12A61K39/13A61K39/295A61K39/39C12N7/00A61K2039/5252A61K2039/545A61K2039/55505A61K2039/55511A61K2039/70C12N2710/20034C12N2770/32634Y02A50/30
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Quick Facts
Patent No.
US 11,680,087
App. No.
17/126,712
Granted
Jun 20, 2023
Kind
B2
Abstract

In one aspect, the invention relates to a composition including a first polypeptide having the sequence set forth in SEQ ID NO: 1 and a second polypeptide having the sequence set forth in SEQ ID NO: 2. In one embodiment, the composition includes about 120 μg/ml of a first polypeptide including the amino acid sequence set forth in SEQ ID NO: 1, 120 μg/ml of a second polypeptide including the amino acid sequence set forth in SEQ ID NO: 2, about 2.8 molar ratio polysorbate-80 to the first polypeptide, about 2.8 molar ratio polysorbate-80 to the second polypeptide, about 0.5 mg/ml aluminum, about 10 mM histidine, and about 150 mM sodium chloride. In one embodiment, a dose of the composition is about 0.5 ml in total volume. In one embodiment, two-doses of the composition induce a bactericidal titer against diverse heterologous subfamily A and subfamily B strains in a human.

Claims (3)

1. A method of inducing a bactericidal immune response in a human against a Neisseria meningitidis serogroup B subfamily A strain and against a Neisseria meningitidis serogroup B subfamily B strain, comprising administering to the human an effective amount of a composition comprising polypeptide antigens from N. meningitidis serogroup B, wherein said antigens consist of: a) a first lipidated polypeptide comprising the amino acid sequence set forth in SEQ ID NO: 1, and b) a second lipidated polypeptide comprising the amino acid sequence set forth in SEQ ID NO: 2; wherein the method further comprises administering to the human an immunogenic composition against human papillomavirus (HPV), wherein the HPV antigens in said immunogenic composition consist of recombinant L1 protein antigens of HPV types 6, 11, 16, and 18.

2. The method according to claim 1 , wherein the immunogenic composition against human papillomavirus is administered to the human within 24 hours of administering said composition against Neisseria meningitidis.

3. The method according to claim 1 , further comprising inducing an immune response against any one of human papillomavirus types 6, 11, 16, 18, or any combination thereof.

Assignments (1)
ASSIGNEE ADDRESS CORRECTION Recorded Mar 20, 2023
From: PFIZER INC.
To: PFIZER INC.
Reel/Frame 063119/0087 →
Continuity (6)
Continuation 15728610 · Oct 10, 2017
Division 14470922 · Aug 27, 2014
Provisional Application 61989432 · May 6, 2014
Provisional Application 61926717 · Jan 13, 2014
Provisional Application 61875068 · Sep 8, 2013
Related Publication 20210101943A1 · Apr 8, 2021