IP Library › Granted Patent US 10,941,205
Granted Patent B2
US 10,941,205 · App. 15/941,655 · Granted Mar 9, 2021

Bispecific anti-human A-beta/human transferrin receptor antibodies and methods of use

Inventors: Harald Duerr (Starnberg, DE); Sebastian Fenn (Achmuehle/Eurasburg, DE); Ulrich Goepfert (Penzberg, DE); Sabine Imhof-Jung (Planegg, DE); Christian Klein (Bonstetten, CH); Laurent Lariviere (Munich, DE); Michael Molhoj (Munich, DE); Joerg Thomas Regula (Munich, DE); Petra Rueger (Penzberg, DE); Wolfgang Schaefer (Mannheim, DE)
Assignee: HOFFMANN-LA ROCHE INC.
C07K16/2881A61P25/28C07K16/18C07K16/468A61K2039/505C07K2317/31C07K2317/51C07K2317/515C07K2317/52C07K2317/522C07K2317/55C07K2317/56C07K2317/64
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Quick Facts
Patent No.
US 10,941,205
App. No.
15/941,655
Granted
Mar 9, 2021
Kind
B2
Abstract

Herein are provided bispecific anti-human A-beta/human transferrin receptor antibodies and methods of using the same.

Claims (19)

1. A bispecific antibody comprising

a) an antibody comprising two pairs each of an antibody light chain comprising the amino acids of SEQ ID NO: 1 and an antibody heavy chain comprising the amino acids of SEQ ID NO: 2, wherein the binding sites formed by each of the pairs of the heavy chain and the light chain specifically bind to a first antigen, and

b) an Fab fragment comprising the amino acid sequences of SEQ ID NO: 3 and SEQ ID NO: 4, wherein the Fab fragment is fused to the C-terminus of one of the heavy chains of the antibody, wherein the binding site of the Fab fragment specifically binds to a second antigen,

wherein the first antigen is human A-beta protein and the second antigen is human transferrin receptor.

2. A pharmaceutical formulation comprising the bispecific antibody according to claim 1 and a pharmaceutically acceptable carrier.

3. The bispecific antibody according to claim 1 for use as a medicament.

4. The bispecific antibody according to claim 1 for the treatment of Alzheimer's disease.

5. The bispecific antibody according to claim 1 , wherein the Fab fragment is fused to the C-terminus of the heavy chain by a peptidic linker; and

wherein (a) the heavy chain that is fused to the Fab fragment has as C-terminal heavy chain amino acid residues the tripeptide LSP wherein the proline thereof is directly fused to the first amino acid residue of the Fab fragment or of the peptidic linker via a peptide bond, and (b) the heavy chain that is not fused to the Fab fragment has as C-terminal heavy chain amino acid residues the tripeptide LSP, or SPG, or PGK.

6. The bispecific antibody according to claim 1 , wherein the Fab fragment is fused to the C-terminus of the heavy chain by a peptidic linker.

7. The bispecific antibody according to claim 1 , wherein

a) the heavy chain that is fused to the Fab fragment has as C-terminal heavy chain amino acid residues the tripeptide LSP wherein the proline thereof is directly fused to the first amino acid residue of the Fab fragment or of the peptidic linker via a peptide bond, and

b) the heavy chain that is not fused to the additional Fab fragments has as C-terminal heavy chain amino acid residues the tripeptide LSP, or SPG, or PGK.

8. The bispecific antibody according to claim 1 , wherein the antibody is monoclonal.

9. A method of treating an individual having Alzheimer's disease comprising administering to the individual an effective amount of the bispecific antibody according to any one of claims 1 , 6 , 7 , and 8 .

10. A method of inhibiting/slowing down the formation of plaques in the brain of an individual comprising administering to the individual an effective amount of the bispecific antibody according to any one of claims 1 , 6 , 7 , and 8 to inhibit/slow down the formation of plaques in the brain.

11. A medicament comprising the bispecific antibody according to any one of claims 1 , 6 , 7 , and 8 .

12. The medicament of claim 11 , wherein the medicament is effective for treatment of Alzheimer's disease.

13. The medicament of claim 11 , wherein the medicament is effective for inhibiting/slowing down the formation of plaques in the brain.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2025
From: DUERR, HARALD; FENN, SEBASTIAN; GOEPFERT, ULRICH; LARIVIERE, LAURENT; IMHOF-JUNG, SABINE; MOLHOJ, MICHAEL; REGULA, JOERG THOMAS; RUEGER, PETRA
To: ROCHE DIAGNOSTICS GMBH
Reel/Frame 070657/0391 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2025
From: KLEIN, CHRISTIAN
To: ROCHE GLYCART AG
Reel/Frame 070657/0401 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2025
From: SCHAEFER, WOLFGANG
To: ROCHE DIAGNOSTICS GMBH
Reel/Frame 070657/0405 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2025
From: ROCHE DIAGNOSTICS GMBH
To: F. HOFFMANN-LA ROCHE AG
Reel/Frame 070657/0420 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2025
From: F. HOFFMANN-LA ROCHE AG
To: HOFFMANN-LA ROCHE INC.
Reel/Frame 070657/0443 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2025
From: ROCHE GLYCART AG
To: F. HOFFMANN-LA ROCHE AG
Reel/Frame 070657/0448 →
Priority Claims (1)
EP 15188064 · Oct 2, 2015 · regional
Continuity (2)
Continuation PCTEP2016073411 · Sep 30, 2016
Related Publication 20180222992A1 · Aug 9, 2018
Cited By (6)
US 12,227,567 US 12,252,533 US 12,281,166 US 12,358,997 US 12,497,458 US 12,735,497