IP Library Granted Patent US 9,481,725
Granted Patent B2
US 9,481,725 · App. 14/212,189 · Granted Nov 1, 2016

Antibodies to HGF and compositions containing

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Quick Facts
Patent No.
US 9,481,725
App. No.
14/212,189
Granted
Nov 1, 2016
Kind
B2
Abstract

The present invention is directed to antibodies and fragments thereof having binding specificity for HGF. Another embodiment of this invention relates to the antibodies described herein, and binding fragments thereof, comprising the sequences of the V H , V L and CDR polypeptides described herein, and the polynucleotides encoding them. The invention also contemplates conjugates of anti-HGF antibodies and binding fragments thereof conjugated to one or more functional or detectable moieties. The invention also contemplates methods of making said anti-HGF antibodies and binding fragments thereof. Embodiments of the invention also pertain to the use of anti-HGF antibodies, and binding fragments thereof, for the diagnosis, assessment and treatment of diseases and disorders associated with HGF.

Claims (28)

1. An anti-human hepatocyte growth factor (anti-human HGF) antibody or antibody fragment comprising

a variable heavy chain comprising the CDR1 sequence of SEQ ID NO: 44, the CDR2 sequence of SEQ ID NO: 46, and the CDR3 sequence of SEQ ID NO: 48; and a variable light chain comprising the CDR1 sequence of SEQ ID NO: 64, the CDR2 sequence of SEQ ID NO: 66, and the CDR3 sequence of SEQ ID NO: 68.

2. The anti-human HGF antibody or antibody fragment of claim 1 comprising:

(i) a chimeric, humanized, or human antibody or antibody fragment;

(ii) an scFv fragment, Fab fragment, Fab′ fragment, F(ab′)2 fragment or a monovalent antibody fragment;

(iii) an antibody or antibody fragment that substantially or entirely lacks N-glycosylation and/or O-glycosylation;

(iv) an antibody or antibody fragment which comprises a human constant domain;

(v) an antibody which contains human IgG1, IgG2, IgG3, or IgG4 antibody constant regions;

(vi) an antibody or antibody fragment which comprises an Fc region that has been modified to alter at least one of effector function, half-life, proteolysis, or glycosylation;

(vii) an antibody which contains an Fc region which contains one or more mutations that alters or eliminates N- and/or O-glycosylation;

(viii) an antibody or antibody fragment which is directly or indirectly attached to a detectable label or therapeutic agent;

(ix) an antibody or antibody fragment which when administered to a human subject inhibits or neutralizes at least one biological effect elicited by HGF;

(x) an antibody or antibody fragment which binds to HGF with a K D that is less than about 100 nM; or

(xi) an antibody or antibody fragment which is attached to one or more detectable moieties selected from a fluorescent dye, enzyme, substrate, bioluminescent material, radioactive material, chemiluminescent moiety, or mixtures thereof.

3. The anti-human HGF antibody or antibody fragment of claim 1 comprising a variable heavy chain and a variable light chain that are each at least 90% identical to the variable heavy and light chains of SEQ ID NO: 42 and SEQ ID NO: 62, respectively.

4. The antibody or antibody fragments of claim 3 comprising human IgG1, IgG2, IgG3 or IgG4 constant regions.

5. The antibody or antibody fragment of claim 3 , comprising the heavy chain of SEQ ID NO: 41 and the light chain of SEQ ID NO: 61.

6. The anti-human HGF antibody or antibody fragment of claim 1 comprising a variable heavy chain and a variable light chain that are each at least 95% identical to the variable heavy and light chains of SEQ ID NO: 42 and SEQ ID NO: 62, respectively.

7. The antibody or antibody fragment of claim 1 comprising

a variable heavy chain and a variable light chain that are each at least 96% identical to the variable heavy and light chains of SEQ ID NO: 42 and SEQ ID NO: 62, respectively.

8. The antibody or antibody fragment of claim 1 ,

a variable heavy chain and a variable light chain that are each at least 97% identical to the variable heavy and light chains of SEQ ID NO: 42 and SEQ ID NO: 62, respectively.

9. The antibody or antibody fragment of claim 1 ,

a variable heavy chain and a variable light chain that are each at least 98% identical to the variable heavy and light chains of SEQ ID NO: 42 and SEQ ID NO: 62, respectively.

10. The antibody or antibody fragment of claim 1 comprising

a variable heavy chain and a variable light chain that are each at least 99% identical to the variable heavy and light chains of SEQ ID NO: 42 and SEQ ID NO: 62, respectively.

11. The antibody or antibody fragment of claim 1 comprising

the variable heavy chain and the variable light chain of SEQ ID NO: 42 and SEQ ID NO: 62, respectively.

Assignments (3)
CHANGE OF NAME Recorded Jun 23, 2020
From: ALDER BIOPHARMACEUTICALS, INC.
To: LUNDBECK SEATTLE BIOPHARMACEUTICALS, INC.
Reel/Frame 053020/0143 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 23, 2020
From: LUNDBECK SEATTLE BIOPHARMACEUTICALS, INC
To: H. LUNDBECK A/S
Reel/Frame 053020/0205 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 20, 2014
From: DUTZAR, BENJAMIN H.; ANDERSON, KATIE; KOVACEVICH, BRIAN R.; FELDHAUS, ANDREW L.; LATHAM, JOHN A.; GARCIA-MARTINEZ, LEON F.
To: ALDER BIOPHARMACEUTICALS, INC.
Reel/Frame 033979/0001 →