IP Library › Granted Patent US 12,178,803
Granted Patent B2
US 12,178,803 · App. 17/272,413 · Granted Dec 31, 2024

CD47 blockade with PARP inhibition for disease treatment

Inventors: Lisa Danae Schultz Johnson (Etobicoke, CA); Lei Cui (Newton, MA)
Assignee: Pfizer Inc.
A61K31/4184A61K31/166A61K31/454A61K31/5025A61K41/0038A61P35/00C07K14/70503
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Quick Facts
Patent No.
US 12,178,803
App. No.
17/272,413
Granted
Dec 31, 2024
Kind
B2
Abstract

CD47+ disease cells such as cancer cells are treated using a combination of CD47 blocking agent and poly-(ADP-ribose) polymerase (PARP) inhibitor. The CD47 blocking agent can be SIRPαFc and the PARP inhibitor niraparib. The anti-cancer effect of niraparib is enhanced in the presence of SIRPαFc. Specific combinations include SIRPαFc forms that comprise an Fc that is either IgG1 or preferably IgG4 isotype. These combinations are useful particularly to treat solid tumours and blood cancers including lymphomas, leukemias and myelomas.

Claims (13)

1. A method for treating a subject presenting with CD47+ disease cells, comprising administering to the subject a PARP inhibitor and a CD47 blocking agent in combination with radiation therapy, wherein the CD47 blocking agent is a CD47-binding SIRPα polypeptide and wherein the CD47-binding SIRPα polypeptide is an Fc fusion protein comprising a CD47-binding region of soluble human SIRPα.

2. The method according to claim 1 , wherein the PARP inhibitor is an inhibitor of PARP-1.

3. The method according to claim 1 , wherein the PARP inhibitor is talazoparib, veliparib, niraparib, olaparib, rucaparib, or iniparib.

4. The method according to claim 1 , wherein the Fc fusion protein comprises SEQ ID NO: 8.

5. The method according to claim 1 , wherein the Fc fusion protein comprises SEQ ID NO: 9.

6. The method according to claim 1 , wherein the Fc fusion protein comprises soluble SIRPα having one or more activity-enhancing amino acid substitutions selected from L 4 V/I, V 6 I/L, A 21 V, V 27 |/L, I 31 T/S/F, E 47 V/L, K 53 R, E 54 Q, H 56 P/R, S 66 T/G, K 68 R, V 92 I, F 94 V/L, V 63 I, and F 103 V.

7. The method according to claim 1 , wherein the radiation therapy is external beam radiation therapy.

8. The method according to claim 1 , wherein the CD47+ disease cells are CD47+ cancer cells.

9. The method according to claim 8 , wherein the CD47+ cancer cells are blood cancers or solid tumours.

10. The method according to claim 8 , wherein the cancer cells are cells of a cancer type selected from acute lymphocytic leukemia (ALL); acute myeloid leukemia (AML); chronic lymphocytic leukemia (CLL); chronic myelogenous leukemia (CML); myeloproliferative disorder/neoplasm (MPDS); and myelodysplastic syndrome.

11. The method according to claim 8 wherein the cancer is a lymphoma selected from a non-Hodgkin's lymphoma, both indolent and aggressive non-Hodgkin's lymphoma, T cell lymphoma, CD20+ lymphoma, Burkitt's lymphoma, and small cell follicular lymphoma, and large cell follicular lymphoma.

12. The method according to claim 8 , wherein the cancer is a myeloma selected from multiple myeloma (MM), giant cell myeloma, heavy-chain myeloma, and light chain or Bence-Jones myeloma.

13. The method according to claim 8 , wherein the cancer is melanoma, ovarian cancer, CTCL, mycosis fungoides, breast cancer, or glioblastoma.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 21, 2023
From: PF ARGENTUM IP HOLDINGS LLC
To: PFIZER INC.
Reel/Frame 063042/0098 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2022
From: TRILLIUM THERAPEUTICS ULC
To: PF ARGENTUM IP HOLDINGS LLC
Reel/Frame 060221/0327 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 1, 2021
From: CUI, LEI; JOHNSON, LISA DANAE SCHULTZ
To: TRILLIUM THERAPEUTICS INC.
Reel/Frame 055442/0367 →
Continuity (2)
Provisional Application 62726497 · Sep 4, 2018
Related Publication 20210315864A1 · Oct 14, 2021