IP Library Granted Patent US 9,963,513
Granted Patent B2
US 9,963,513 · App. 14/764,967 · Granted May 8, 2018

Method for the selection of antibodies against BCMA

Inventors: Minh Diem Vu (Wollerau, CH); Klaus Strein (Weinheim, DE); Ekkehard Moessner (Kreuzlingen, CH); Ralf Hosse (Cham, CH); Oliver Ast (Bassersdorf, CH); Anne Freimoser-Grundschober (Zürich, CH); Marina Bacac (Zürich, CH); Tanja Fauti (Zürich, CH); Christian Klein (Bonstetten, CH); Pablo Umana (Wollerau, CH); Samuel Moser (Rotkreuz, CH)
Assignee: ENGMAB SÀRL
C07K16/2878A61K39/395C07K16/2809C07K16/3061G01N33/6863A61K2039/505C07K16/28C07K16/2863C07K2317/31C07K2317/56C07K2317/565C07K2317/66C07K2317/71C07K2317/732C07K2317/76C07K2317/92G01N2333/7151G01N2500/04
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Quick Facts
Patent No.
US 9,963,513
App. No.
14/764,967
Granted
May 8, 2018
Kind
B2
Abstract

An antibody specifically binding to human BCMA, characterized in that the binding of said antibody is not reduced by APRIL and not reduced by BAFF, said antibody does not alter APRIL-dependent NF-κB activation, BAFF-dependent NF-κB activation, and does not alter NF-κB activation without BAFF and APRIL is useful as a therapeutic agent.

Claims (6)

1. A method of treating multiple myeloma (MM) comprising administering a bispecific antibody specifically binding to human B cell maturation factor (BCMA) and CD3 to a subject in need thereof, wherein

c) said bispecific antibody comprises variable heavy and light chains of anti-CD3ϵ antibody SP34; and, wherein said bispecific antibody comprises variable heavy and light chains of an antibody specifically binding to BCMA wherein variable domain VH comprises the amino acid sequence of SEQ ID NO:59 and variable domain VL comprises the amino acid sequence of SEQ ID NO:89.

2. A method according to claim 1 wherein the bispecific antibody binds BCMA extracellular domain with a dissociation constant (Kd) of 10 −8 M or less.

3. A method according to claim 1 wherein the bispecific antibody binds specifically to cynomolgus BCMA.

4. A method according to claim 1 wherein the bispecific antibody comprises an Fc portion and is administered subcutaneously once or twice a week in the dose range of 1 to 100 mg/m 2 /week.

5. A method according to claim 1 wherein the bispecific antibody comprises an Fc portion and is administered subcutaneously once or twice a week in the dose range of 0.25 to 25 mg/m 2 /week.

Assignments (7)
NUNC PRO TUNC ASSIGNMENT Recorded Apr 17, 2023
From: ENGMAB SÀRL
To: ENGMAB BETA HOLDINGS LLC
Reel/Frame 063353/0350 →
NUNC PRO TUNC ASSIGNMENT Recorded Apr 17, 2023
From: ENGMAB BETA HOLDINGS LLC
To: BRISTOL-MYERS SQUIBB COMPANY
Reel/Frame 063353/0610 →
CHANGE OF NAME Recorded Oct 3, 2017
From: ENGMAB AG
To: ENGMAB SÀRL
Reel/Frame 043765/0474 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2016
From: MOESSNER, EKKEHARD; HOSSE, RALF; AST, OLIVER; FREIMOSER-GRUNDSCHOBER, ANNE; BACAC, MARINA; FAUTI, TANJA; KLEIN, CHRISTIAN; UMANA, PABLO; MOSER, SAMUEL
To: ROCHE GLYCART AG
Reel/Frame 037935/0156 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2016
From: F. HOFFMANN-LA ROCHE AG
To: ENGMAB AG
Reel/Frame 037935/0212 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2016
From: VU, MINH DIEM; STREIN, KLAUS
To: ENGMAB AG
Reel/Frame 037935/0251 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2016
From: ROCHE GLYCART AG
To: F. HOFFMANN-LA ROCHE AG
Reel/Frame 037935/0970 →
Priority Claims (2)
EP 13000570 · Feb 5, 2013 · regional
EP 13000571 · Feb 5, 2013 · regional
Continuity (1)
Related Publication 20150368351A1 · Dec 24, 2015