IP Library Granted Patent US 11,401,334
Granted Patent B2
US 11,401,334 · App. 16/646,836 · Granted Aug 2, 2022

Combination treatment for cancer with anti-BCMA binding protein and proteosome inhibitor

Inventors: Sanjay Khandekar (Collegeville, PA); Patrick Mayes (Devon, PA); Joanna Opalinska (Collegeville, PA)
Assignee: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
C07K16/2878A61K31/573A61K31/69A61K39/3955A61K39/39558A61K47/6817A61P35/00C07K16/2896C07K16/30C07K19/00A61K2039/505A61K2039/545C07K2317/56C07K2317/76C07K2317/92C07K2319/55
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Quick Facts
Patent No.
US 11,401,334
App. No.
16/646,836
Granted
Aug 2, 2022
Kind
B2
Abstract

Disclosed herein is a method of treating cancer, such as multiple myeloma, involving the combination of an anti-BCMA antigen binding protein (e.g., an anti-BCMA antibody) and a proteasome inhibitor (e.g. bortezomib). The combinations can also include an anti-inflammatory compound (e.g. dexamethasone).

Claims (20)

1. A method of treating relapsed/refractory multiple myeloma in a subject that has been treated with at least one prior cancer treatment comprising administering:

1.9 mg/kg, 2.5 mg/kg, or 3.4 mg/kg of an anti-B-cell maturation antigen (BCMA) antibody-drug conjugate on day 1 of a 21-day cycle; wherein the anti-BCMA antibody drug conjugate comprises an antibody comprising the heavy chain amino acid sequence set forth in SEQ ID NO:9 and the light chain amino acid sequence set forth in SEQ ID NO:10, and wherein the antibody is conjugated to monomethyl auristatin F (MMAF);

1.3 mg/m 2 of bortezomib on days 1, 4, 8, and 11 of a 21-day cycle; and

20 mg of dexamethasone on days 1, 2, 4, 5, 8, 9, 11, and 12 of a 21-day cycle.

2. A method of treating relapsed/refractory multiple myeloma in a subject that has been treated with at least one prior cancer treatment comprising administering:

1.9 mg/kg, 2.5 mg/kg, or 3.4 mg/kg of an anti-B-cell maturation antigen (BCMA) antibody-drug conjugate on day 1 of a 21-day cycle; wherein the anti-BCMA antibody drug conjugate comprises an antibody comprising the heavy chain amino acid sequence set forth in SEQ ID NO:9 and the light chain amino acid sequence set forth in SEQ ID NO:10, and wherein the antibody is conjugated to monomethyl auristatin F (MMAF);

1.3 mg/m 2 of bortezomib on days 1, 4, 8, and 11 of a 21-day cycle; and

40 mg of dexamethasone on days 1, 2, 4, 5, 8, 9, 11, and 12 of a 21-day cycle.

3. A method of treating relapsed/refractory multiple myeloma in a subject that has been treated with at least one prior cancer treatment comprising administering:

1.9 mg/kg, 2.5 mg/kg, or 3.4 mg/kg of an anti-B-cell maturation antigen (BCMA) antibody-drug conjugate on day 1 of a 28-day cycle; wherein the anti-BCMA antibody drug conjugate comprises an antibody comprising the heavy chain amino acid sequence set forth in SEQ ID NO:9 and the light chain amino acid sequence set forth in SEQ ID NO:10, and wherein the antibody is conjugated to monomethyl auristatin F (MMAF);

one of 15 mg/m 2 , 20 mg/m 2 , 27 mg/m 2 , 36 mg/m 2 , 45 mg/m 2 , or 56 mg/m 2 of carfilzomib on days 1, 2, 8, 9, 15, and 16 of a 28-day cycle; and

one of 20 mg or 40 mg of dexamethasone on days 1, 2, 8, 9, 15, 16, 22, and 23 of a 28-day cycle.

4. A method of treating relapsed/refractory multiple myeloma in a subject that has been treated with at least one prior cancer treatment comprising administering:

1.9 mg/kg, 2.5 mg/kg, or 3.4 mg/kg of an anti-B-cell maturation antigen (BCMA) antibody-drug conjugate on day 1 of a 28-day cycle; wherein the anti-BCMA antibody drug conjugate comprises an antibody comprising the heavy chain amino acid sequence set forth in SEQ ID NO:9 and the light chain amino acid sequence set forth in SEQ ID NO:10, and wherein the antibody is conjugated to monomethyl auristatin F (MMAF);

one of 15 mg/m 2 , 20 mg/m 2 , 27 mg/m 2 , 36 mg/m 2 , 45 mg/m 2 , or 56 mg/m 2 of carfilzomib on days 1, 2, 15, and 16 of a 28-day cycle; and

one of 20 mg or 40 mg of dexamethasone on days 1, 2, 8, 9, 15, 16, 22, and 23 of a 28-day cycle.

5. A method of treating relapsed/refractory multiple myeloma in a subject that has been treated with at least one prior cancer treatment comprising administering:

1.9 mg/kg, 2.5 mg/kg, or 3.4 mg/kg of an anti-B-cell maturation antigen (BCMA) antibody-drug conjugate on day 1 of a 28-day cycle; wherein the anti-BCMA antibody drug conjugate comprises an antibody comprising the heavy chain amino acid sequence set forth in SEQ ID NO:9 and the light chain amino acid sequence set forth in SEQ ID NO:10, and wherein the antibody is conjugated to monomethyl auristatin F (MMAF);

one of 2.3 mg, 3 mg, or 4 mg of ixazomib on days 1, 8, and 15 of a 28-day cycle; and

one of 20 mg or 40 mg of dexamethasone on days 1, 8, 15, and 22 of a 28-day cycle.

Assignments (2)
CHANGE OF ADDRESS Recorded Oct 8, 2025
From: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
To: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
Reel/Frame 073032/0390 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 16, 2021
From: KHANDEKAR, SANJAY; MAYES, PATRICK; OPALINSKA, JOANNA
To: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
Reel/Frame 057188/0675 →
Continuity (2)
Provisional Application 62558575 · Sep 14, 2017
Related Publication 20200270354A1 · Aug 27, 2020