IP Library Granted Patent US 9,505,826
Granted Patent B2
US 9,505,826 · App. 13/996,733 · Granted Nov 29, 2016

Modified antibody with improved half-life

Inventors: David Wilson (Fremont, CA); Tetsuya Taura (Palo Alto, CA)
Assignee: Teva Pharmaceuticals Australia Pty Ltd
C07K16/00C07K16/2803C07K2317/52C07K2317/90
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Quick Facts
Patent No.
US 9,505,826
App. No.
13/996,733
Granted
Nov 29, 2016
Kind
B2
Abstract

The present invention relates to antibodies, immunoglobulin constructs or immunoglobulin IgG4 fusion proteins whose in vivo half-lives are increased by the combination of (i) a modified IgG4 Fc region or FcRn binding domain thereof and (ii) a modified IgG4 hinge region sequence.

Claims (9)

1. A modified antibody, immunoglobulin construct, or immunoglobulin IgG4 fusion protein that specifically binds to Interleukin 5 (IL-5), comprising the complementarity determining regions (CDRs) of the heavy chain variable domain amino acid sequence of SEQ ID NO: 7, and the CDRs of the light chain variable domain amino acid sequence of SEQ ID NO: 8,

a human IgG4 Fc region comprising the amino acid substitutions M252Y, S254T and T256E numbered according to the EU index as in Kabat, and

a human IgG4 core hinge region comprising the amino acid substitution S228P according to the EU index as in Kabat;

wherein the combination of the amino acid substitutions S228P, M252Y, S254T and T256E results in a synergistic increase in the circulating half-life of the modified antibody, immunoglobulin construct, or immunoglobulin IgG4 fusion protein in vivo as compared to the circulating half-life in vivo of the antibody, immunoglobulin construct, or immunoglobulin IgG4 fusion protein which has been modified to comprise the amino acid substitutions S228P or M252Y, S254T and T256E.

2. The modified antibody, immunoglobulin construct, or immunoglobulin IgG4 fusion protein according to claim 1 , wherein the modified antibody, immunoglobulin construct, or immunoglobulin IgG4 fusion protein comprises the heavy chain constant domain amino acid sequence of SEQ ID NO:6, the heavy chain variable domain amino acid sequence of SEQ ID NO:7, and a light chain comprising the amino acid sequence of SEQ ID NO: 8.

3. The isolated antibody, immunoglobulin construct, or immunoglobulin IgG4 fusion protein according to claim 1 , wherein the modified antibody, immunoglobulin construct, or immunoglobulin IgG4 fusion protein comprises a light chain comprising the amino acid sequence of SEQ ID NO:8.

4. The modified antibody, immunoglobulin construct, or immunoglobulin IgG4 fusion protein according to claim 1 , wherein the modified antibody, immunoglobulin construct, or immunoglobulin IgG4 fusion protein is recombinantly-fused or chemically-conjugated to a moiety.

5. The modified antibody, immunoglobulin construct, or immunoglobulin IgG4 fusion protein according to claim 4 , wherein the moiety is selected from the group consisting of a therapeutic agent, a cytotoxin, a radioisotope, an immunomodulatory agent, an anti-angiogenic agent, an anti-neovascularization and/or vascularization agent, a toxin, an anti-proliferative agent, a pro-apoptotic agent, a chemotherapeutic agent, and a therapeutic nucleic acid.

6. A composition, comprising the modified antibody, immunoglobulin construct or immunoglobulin IgG4 fusion protein according to claim 1 and a pharmaceutically acceptable excipient or carrier.

Assignments (2)
CHANGE OF NAME Recorded Nov 20, 2013
From: CEPHALON AUSTRALIA PTY. LTD.
To: TEVA PHARMACEUTICALS AUSTRALIA PTY LTD
Reel/Frame 031636/0319 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 12, 2013
From: WILSON, DAVID; TAURA, TETSUYA
To: CEPHALON AUSTRALIA PTY LTD.
Reel/Frame 030987/0001 →
Continuity (2)
Provisional Application 61425858 · Dec 22, 2010
Related Publication 20130281677A1 · Oct 24, 2013