IP Library Granted Patent US 8,900,590
Granted Patent B2
US 8,900,590 · App. 13/208,754 · Granted Dec 2, 2014

Anti-hemagglutinin antibody compositions and methods of use thereof

Inventors: Ole Olsen (Everett, WA); Christina L. Boozer (Seattle, WA); Andres G. Grandea, III (Shoreline, WA)
Assignee: Theraclone Sciences, Inc.
A61K39/395C07K2317/33A61K45/06C07K2317/55C07K2317/21C07K2317/92G01N2333/11A61K47/4853A61K47/48384A61K39/42A61K2039/505C07K16/1018G01N2469/10G01N33/56983C07K2317/76
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Quick Facts
Patent No.
US 8,900,590
App. No.
13/208,754
Granted
Dec 2, 2014
Kind
B2
Abstract

The present invention provides novel human anti-Influenza antibodies and related compositions and methods. These antibodies are used in the prevention, inhibition, neutralization, diagnosis, and treatment of influenza infection.

Claims (12)

1. A composition comprising:

a) an isolated human monoclonal antibody, wherein said antibody comprises a VH CDR1 region comprising the amino acid sequence of DYSWN (SEQ ID NO: 34), a VH CDR2 region comprising the amino acid sequence of DTLHNGYTNYNPSLRG (SEQ ID NO: 35), a VH CDR3 region comprising the amino acid sequence of GSGGYGGFDYFGKLRTWDF (SEQ ID NO: 36), a VL CDR1 region comprising the amino acid sequence of RASQGIRNDLG (SEQ ID NO: 41), a VL CDR2 region comprising the amino acid sequence of GASSLQS (SEQ ID NO: 42), and a VL CDR3 region comprising the amino acid sequence of LQHNSYPYT (SEQ ID NO: 43), and

b) an isolated human monoclonal antibody, wherein said antibody comprises a VH CDR1 region comprising the amino acid sequence of NYGIS (SEQ ID NO: 174), a VH CDR2 region comprising the amino acid sequence of GIIPLFGAAKYAQKFQG (SEQ ID NO: 175), a VH CDR3 region comprising the amino acid sequence of APRVYEYYFDQ (SEQ ID NO: 176), a VL CDR1 region comprising the amino acid sequence of RASQSVSSSQLA (SEQ ID NO: 157), a VL CDR2 region comprising the amino acid sequence of GASTRAT (SEQ ID NO: 181), and a VL CDR3 region comprising the amino acid sequence of QQYSTSPPT (SEQ ID NO: 182), wherein at least one of the antibodies is directly conjugated to either a detectable label or therapeutic agent.

2. A composition comprising:

a) an isolated human monoclonal antibody comprising a heavy chain variable sequence comprising the amino acid sequence of SEQ ID NO: 33 and a light chain variable sequence comprising the amino acid sequence of SEQ ID NO: 40; and

b) an isolated human monoclonal antibody comprising a heavy chain variable sequence comprising the amino acid sequence of SEQ ID NO: 173 and a light chain variable sequence comprising the amino acid sequence of SEQ ID NO: 180,

wherein at least one of the antibodies is directly conjugated to either a detectable label or therapeutic agent.

3. A pharmaceutical composition comprising the composition of any one of claims 1 or 2 and a pharmaceutical carrier.

4. The pharmaceutical composition of claim 3 , further comprising an anti-viral drug, a viral entry inhibitor or a viral attachment inhibitor.

5. The pharmaceutical composition of claim 4 , wherein said anti-viral drug is a neuraminidase inhibitor, a HA inhibitor, a sialic acid inhibitor or an M2 ion channel inhibitor.

6. The pharmaceutical composition of claim 5 , wherein said neuraminidase inhibitor is zanamivir or oseltamivir phosphate.

7. A passive immunization composition comprising the composition of any one of claims 1 or 2 .

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Dec 29, 2015
From: MIDCAP FINANCIAL TRUST, AS AGENT FOR LENDERS
To: THERACLONE SCIENCES, INC.
Reel/Frame 037396/0957 →
SECURITY INTEREST Recorded Nov 19, 2015
From: THERACLONE SCIENCES, INC.
To: MIDCAP FINANCIAL TRUST
Reel/Frame 037146/0817 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 6, 2011
From: OLSEN, OLE; BOOZER, CHRISTINA L.; GRANDEA, ANDRES G., III
To: THERACLONE SCIENCES, INC.
Reel/Frame 026859/0088 →
Continuity (3)
Provisional Application 61373191 · Aug 12, 2010
Provisional Application 61386235 · Sep 24, 2010
Related Publication 20120039899A1 · Feb 16, 2012