IP Library Granted Patent US 11,027,021
Granted Patent B2
US 11,027,021 · App. 16/085,460 · Granted Jun 8, 2021

Combinations of PBD-based antibody drug conjugates with Bcl-2 inhibitors

Inventors: William Arthur (Bainbridge Island, WA); Robert Thurman (Kenmore, WA); Travis Biechele (Seattle, WA); Rory Rohm (Monroe, WA)
Assignee: Seagen Inc.
A61K47/6867A61K39/39558A61K47/6803A61K47/6849A61P35/02C07K16/2803C07K16/2875C07K16/2884C07K16/32C07K2317/24
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Quick Facts
Patent No.
US 11,027,021
App. No.
16/085,460
Granted
Jun 8, 2021
Kind
B2
Abstract

This invention relates to treatment of cancer using antibody drug conjugates that comprise PBD molecules in combination with Bcl-2 inhibitors.

Claims (13)

1. A method of treating cancer in a subject in need of such treatment, the method comprising administering an antibody drug conjugate (ADC) and a Bcl-2 inhibitor, wherein the ADC comprises an antibody conjugated to a PBD cytotoxic agent, wherein the Bcl-2 inhibitor is selected from the group consisting of ABT-199 and ABT-263, and wherein the antibody is selected from the group consisting of:

a) an anti-CD33 antibody comprising the light chain variable region of SEQ ID NO: 1 and the heavy chain variable region of SEQ ID NO: 2; and

b) and anti-CD19 antibody comprising the light chain variable region of SEQ ID NO: 10 and the heavy chain variable region of SEQ ID NO: 11.

2. The method of claim 1 , wherein the PBD cytotoxic agent has the formula

3. The method of claim 1 , wherein the Bcl-2 inhibitor is ABT-199.

4. The method of claim 1 , wherein the Bcl-2 inhibitor is ABT-263.

5. The method of claim 2 , wherein the antibody is an anti-CD33 antibody comprising the light chain variable region of SEQ ID NO: 1 and the heavy chain variable region of SEQ ID NO: 2.

6. The method of claim 5 , wherein the antibody is h2H12.

7. The method of claim 6 , wherein the Bcl-2 inhibitor is ABT-199.

8. The method of claim 1 , wherein the antibody is an anti-CD33 antibody comprising the light chain variable region of SEQ ID NO: 1 and the heavy chain variable region of SEQ ID NO: 2.

9. The method of claim 8 , wherein the cancer is acute myeloid leukemia or myelodysplastic syndrome.

10. The method of claim 1 , wherein the antibody is an anti-CD19 antibody comprising the light chain variable region of SEQ ID NO: 10 and the heavy chain variable region of SEQ ID NO: 11.

11. The method of claim 10 , wherein the cancer is selected from the group consisting of non-hodgkins lymphoma, diffuse large B-cell lymphoma, acute lymphocytic leukemia, and chronic lymphocytic lymphoma.

Assignments (1)
CHANGE OF NAME Recorded Oct 19, 2020
From: SEATTLE GENETICS, INC.
To: SEAGEN INC.
Reel/Frame 054122/0812 →
Continuity (4)
Provisional Application 62308778 · Mar 15, 2016
Provisional Application 62356814 · Jun 30, 2016
Provisional Application 62428770 · Dec 1, 2016
Related Publication 20190076549A1 · Mar 14, 2019