IP Library Granted Patent US 10,189,906
Granted Patent B2
US 10,189,906 · App. 14/440,165 · Granted Jan 29, 2019

Antibody that binds CD269 (BCMA) suitable for use in the treatment of plasma cell diseases such as multiple myeloma and autoimmune diseases

Inventors: Martin Lipp (Glienicke, DE); Felix Oden (Berlin, DE); Uta Höpken (Berlin, DE); Gerd Müller (Berlin, DE); Oliver Daumke (Berlin, DE); Stephen Marino (Berlin, DE); Daniel Olal (Berlin, DE)
Assignee: MAX-DELRÜCK-CENTRUM FÜR MOLEKULARE MEDIZIN
C07K16/2878A61K47/6867C07K16/3061A61K2039/505C07K2317/24C07K2317/34C07K2317/41C07K2317/55C07K2317/565C07K2317/73C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 10,189,906
App. No.
14/440,165
Granted
Jan 29, 2019
Kind
B2
Abstract

The invention relates to antibodies or antibody fragments that bind CD269 (BCMA), thereby disrupting the interaction between CD269 and its native ligands (BAFF and APRIL), and their use in the treatment of plasma cell-mediated diseases such as multiple myeloma and autoimmune diseases.

Claims (13)

1. A method for the treatment of a medical disorder in a human subject, wherein the medical disorder is associated with the presence of pathogenic B cells expressing B cell maturation antigen (BCMA), the method comprising administering to the human subject an isolated monoclonal antibody or an antigen binding fragment thereof that binds CD269 (BCMA), wherein said antibody or antigen binding fragment thereof comprises:

(i) a VH domain, wherein said VH domain comprises CDR H1 comprising SEQ ID No. 1 (RYWMS) or SEQ ID No. 15 (DYWMS), CDR H2 comprising SEQ ID No. 2 (EINPDSSTINYAPSLKD) or SEQ ID No. 16 (EINPDSSTINYAPSLKG) and CDR H3 comprising SEQ ID No. 3 (SLYYDYGDAMDYW), and

(ii) a VL domain, wherein said VL domain comprises CDR L1 comprises SEQ ID No. 4 (KASQSVDSNVA), CDR L2 comprises SEQ ID No. 5 (SASLRFS) or SEQ ID No. 17 (SDDLRFS) and CDR L3 comprises SEQ ID No. 6 (QQYNNYPLTFG),

wherein the medical disorder associated with the presence of pathogenic B cells is a cancer of plasma cells or a cancer of B lymphocytes.

2. The method of claim 1 , wherein the cancer of plasma cells is multiple myeloma, plasmacytoma, Waldenström macroglobulinemia or plasma cell leukemia, or the cancer of B lymphocytes is Hodgkin's disease.

3. The method of claim 1 , wherein the VL and VH domains are fused to the human Ig kappa and IgG1 constant domains, respectively.

4. The method of claim 1 , wherein the isolated monoclonal antibody or antigen binding fragment thereof comprises a VH domain comprising SEQ ID No. 7 and a VL domain comprising SEQ ID No. 8.

5. The method of claim 1 , wherein the isolated monoclonal antibody or antigen binding fragment thereof is a chimeric, humanized, partially humanized, bi-specific or a single chain antibody, or combination thereof.

6. The method of claim 1 , wherein the isolated monoclonal antibody or antigen binding fragment thereof comprises:

(i) a VH domain comprising a sequence of one of SEQ ID No. 18 to 25, and

(ii) a VL domain comprising a sequence of one of SEQ ID No. 26 to 56.

7. The method of claim 1 , wherein the isolated monoclonal antibody or antigen binding fragment thereof is glycosylated.

8. The method of claim 7 , wherein the isolated monoclonal antibody or antigen binding fragment thereof comprises an N-linked oligosaccharide chain at Asn297 of the heavy chain.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2018
From: LIPP, MARTIN; ODEN, FELIX; HOPKEN, UTA; MULLER, GERD; DAUMKE, OLIVER; MARINO, STEPHEN; OLAL, DANIEL
To: MAX-DELBRÜCK-CENTRUM FÜR MOLEKULARE MEDIZIN
Reel/Frame 046760/0638 →
Priority Claims (3)
EP 12190970 · Nov 1, 2012 · regional
EP 13156091 · Feb 21, 2013 · regional
EP 13180548 · Aug 15, 2013 · regional
Continuity (1)
Related Publication 20150284467A1 · Oct 8, 2015
Cited By (2)
US 12,258,412 US 12,576,131