Combination of small molecule CD-47 inhibitors with other anti-cancer agents
The present invention relates to a composition of a CD47-SIRPα blocking agent and one or more anti-cancer agent(s), where the CD47-SIRPα blocking agents are represented by a compound of formula (I). The present invention also relates to a method of treating a cancer in a subject by administering a therapeutically effective amount of a CD47-SIRPα blocking agent represented by formula (I) in combination with one or more anti-cancer agent(s).
1. A combination comprising a CD47-SIRPα blocking agent and one or more anti-cancer agent(s), wherein the CD47-SIRPα blocking agent is represented by a compound of formula (I):
or a pharmaceutically acceptable salt thereof or an amide thereof or an ester thereof, or a stereoisomer thereof; wherein,
R a is hydrogen; and R 1 represents hydrogen, —(CH 2 ) 2 CONH 2 , —(CH 2 ) 2 COOH, —(CH 2 ) 3 NHC(═NH)NH 2 , —(CH 2 ) 4 NH 2 , —CH 2 CONH 2 , —CH 2 -aryl, or —CH 2 -heteroaryl; or R a and R 1 , together with the atoms to which they are attached form a pyrrolidine ring;
R 2 represents hydrogen, —(CH 2 ) 3 NHC(═NH)NH 2 , —(CH 2 ) 2 CONH 2 , —(CH 2 ) 2 COOH, —CH 2 -aryl, or —CH 2 -heteroaryl;
R b and R 3 , together with the atoms to which they are attached form a pyrrolidine ring.
2. The combination of claim 1 , wherein the anti-cancer agent is a chemotherapeutic agent or an immunomodulatory agent.
3. The combination of claim 2 , wherein the chemotherapeutic agent is a proteasome inhibitor (bortezomib, ixazomib and carfilzomib), Anthracyclines (Doxorubicin, Epirubicin, Daunorubicin, Idarubicin, Mitoxantrone), Oxaliplatin, Cyclophosphamide, Bleomycin, Vorinostat, Paclitaxel, 5-Fluorouracil, Cytarabine, BRAF inhibitory drugs (Dabrafenib, Vemurafenib), a PI3K inhibitor, Docetaxel, Mitomycin C, Sorafenib, or Tamoxifen, or a combination thereof.
4. The combination of claim 2 , wherein the chemotherapeutic agent is Abiraterone acetate, Afatinib, Aldesleukin, Alemtuzumab, Anastrozole, Axitinib, Belinostat, Bendamustine, Bicalutamide, Blinatumomab, Bosutinib, Brentuximab, Busulfan, Cabazitaxel, Capecitabine, Carboplatin, Carfilzomib, Carmustine, Ceritinib, Clofarabine, Crizotinib, Dacarbazine, Dactinomycin, Dasatinib, Degarelix, Denileukin, Denosumab, Enzalutamide, Eribulin, Erlotinib, Everolimus, Exemestane, Exemestane, Fludarabine, Fulvestrant, Gefitinib, Goserelin, Ibritumomab, Imatinib, Ipilimumab, Irinotecan, Ixabepilone, Lapatinib, Lenalidomide, Letrozole, Leucovorin, Leuprolide, Lomustine, Mechlorethamine, Megestrol, Nelarabine, Nilotinib, Nivolumab, Olaparib, Omacetaxine, Palbociclib, Pamidronate, Panitumumab, Panobinostat, Pazopanib, Pegaspargase, Pembrolizumab, Pemetrexed Disodium, Pertuzumab, Plerixafor, Pomalidomide, Ponatinib, Pralatrexate, Procarbazine, Radium 223, Ramucirumab, Regorafenib, rIFNa-2b, Romidepsin, Sunitinib, Temozolomide, Temsirolimus, Thiotepa, Tositumomab, Trametinib, Vinorelbine abarelix, aldesleukin, alitretinoin, allopurinol, altretamine, arsenic trioxide, asparaginase, azacitidine, bexarotene, baricitinib, bortezomib, busulfan intravenous, busulfan oral, calusterone, cetuximab, chlorambucil, cisplatin, cladribine, dalteparin sodium, decitabine, diftitox, disulfiram, dexrazoxane, dromostanolone propionate, eculizumab, estramustine, etoposide phosphate, etoposide, fentanyl citrate, filgrastim, floxuridine, gemcitabine, histrelin acetate, fosfamide, interferon alfa 2a, lapatinib ditosylate, levamisole, marizomib, meclorethamine, melphalan, mercaptopurine, methotrexate, methoxsalen, mitotane, nandrolone phenpropionate, nofetumomab, oprozomib, pegfilgrastim, pentostatin, pipobroman, plicamycin, procarbazine, quinacrine, rasburicase, ruxolitinib, rucaparib, streptozocin, teniposide, testolactone, thalidomide, thioguanine, topotecan, toremifene, tretinoin, uracil mustard, valrubicin, vinblastine, vincristine, niraparib, veliparib, talazoparib, zoledronate, Ibrutinib, Aflibercept, or Idelalisib.
5. The combination of claim 2 , wherein the immunomodulatory agent is a costimulatory molecule or a coinhibitory molecule comprising CTLA-4 (e.g., ipilimumab), 4-1BB (e.g., urelumab, and utomilumab), antibodies to PD-1 and PD-L1 (e.g., nivolumab, pembrolizumab, atezolizumab, Durvalumab and Camrelizumab), antibodies to cytokines (IL-10, TGF-.beta.), antibodies to TIM-3, antibodies to LAG3, antibodies to B7H3, antibodies to B7H4, or antibodies to B7H6, or a combination thereof.
6. The combination of claim 1 , wherein the anticancer agent is a therapeutic antibody targeting tumor antigens that stimulate activating Fc receptors (FcRs).
7. The combination of claim 6 , wherein the therapeutic antibody is selected from the group capable of triggering efficient phagocytosis comprising anti-CD20 (rituximab, tiuxetan, tositumomab), which combination finds particular use in the treatment of non-Hodgkin's B cell lymphomas and chronic lymphocytic leukemia (CLL); anti-CD22, (Epratuzumab) which combination finds particular use in the treatment of B cell leukemia and hairy cell leukemia; anti-CD52, (alemtuzumab) which combination finds particular use in the treatment of B cell and T cell leukemia, (chronic lymphocytic leukemia); anti-CD33 (gemtuzumab ozogomicin) which combination finds particular use in the treatment of myeloid leukemia (acute myelogenous leukemia); trastuzumab which combination finds particular use in the treatment of breast cancer; bevacizumab which combination finds particular use in the treatment of certain type of brain tumor, and certain types of cancers of kidney, lung, colon, rectum, cervix, ovary, or fallopian tube; cetuximab which combination finds particular use in the treatment of colon and head and neck cancer; panitumumab which combination finds particular use in the treatment of colorectal cancer; anti-CD38 (daratumumab) which combination finds particular use in the treatment of multiple myeloma; CD96, anti-CD44, anti-CD123 which combination finds particular use in the treatment of myelogenous leukemias; ofatumumab which combination finds particular use in the treatment of chronic lymphocytic leukemia; obinutuzumab which combination finds particular use in the treatment of follicular lymphoma; alemtuzumab which combination finds particular use in the treatment of B-cell chronic lymphocytic leukaemia; Ibritumomab tiuxetan which combination finds particular use in the treatment of B-cell non-Hodgkin lymphomas; dinutuximab which combination finds particular use in the treatment of neuroblastoma; and necitumumab which combination finds particular use in the treatment of lung cancer.
8. The combination of claim 1 , wherein R 1 represents hydrogen, —(CH 2 ) 2 CONH 2 , —(CH 2 ) 2 COOH, —(CH 2 ) 3 NHC(═NH)NH 2 , —(CH 2 ) 4 NH 2 , —CH 2 CONH 2 , —CH 2 -phenyl, or —CH 2 -imidazolyl.
9. The combination of claim 1 , wherein R 2 represents hydrogen, —(CH 2 ) 3 NHC(═NH)NH 2 , —(CH 2 ) 2 CONH 2 , —(CH 2 ) 2 COOH, —CH 2 -phenyl, or —CH 2 -imidazolyl.
10. The combination of claim 1 , wherein the CD47-SIRPα blocking agent is represented by a compound of formula (IA)
or a pharmaceutically acceptable salt or an amide or an ester, or a stereoisomer thereof; wherein, R 1 , R a and R 2 are as defined in claim 1 .
11. The combination of claim 10 , wherein R 1 represents hydrogen, —(CH 2 ) 2 CONH 2 , —(CH 2 ) 2 COOH, —(CH 2 ) 3 NHC(═NH)NH 2 , —(CH 2 ) 4 NH 2 , —CH 2 -phenyl, or —CH 2 -imidazolyl.
12. The combination of claim 10 , wherein R 2 represents hydrogen, —(CH 2 ) 3 NHC(═NH)NH 2 , —(CH 2 ) 2 CONH 2 , —(CH 2 ) 2 COOH, —CH 2 -phenyl, or —CH 2 -imidazolyl.
13. The combination of claim 1 , wherein the CD47-SIRPα blocking agent is represented by a compound of formula (IB)
or a pharmaceutically acceptable salt or an amide or an ester, or a stereoisomer thereof.
14. The combination of claim 13 , wherein R 1 represents hydrogen, —(CH 2 ) 2 CONH 2 , —(CH 2 ) 2 COOH, —(CH 2 ) 3 NHC(═NH)NH 2 , —(CH 2 ) 4 NH 2 , or —CH 2 -phenyl.
15. The combination of claim 13 , wherein R b and R 3 , together with the atoms to which they are attached form a pyrrolidine ring.
16. The combination of claim 1 , wherein the CD47-SIRPα blocking agent is selected from the group consisting of:
Compound
Structure
1
2
3
4
5
6
16
17
18
19
20
21
22
or a pharmaceutically acceptable salt or an amide or an ester, or a stereoisomer thereof.
17. A pharmaceutical composition comprising the combination of a CD47-SIRPα blocking agent and one or more anti-cancer agent(s) as claimed in claim 1 , and a pharmaceutically acceptable carrier.
18. A method for treating or delaying progression of diseases or disorders mediated by dysregulated CD47-SIRPα pathway in a subject, the method comprising administering to the subject in need thereof a therapeutically effective amount of an agent blocking CD47-SIRPα pathway in combination with a therapeutically effective amount of one or more anti-cancer agent(s), wherein the agent blocking CD47-SIRPα pathway is represented by compound of formula (I):
or a pharmaceutically acceptable salt or an amide or an ester, or a stereoisomer thereof; wherein,
R a is hydrogen; and R 1 represents hydrogen, —(CH 2 ) 2 CONH 2 , —(CH 2 ) 2 COOH, —(CH 2 ) 3 NHC(═NH)NH 2 , —(CH 2 ) 4 NH 2 , —CH 2 CONH 2 , —CH 2 -aryl, or —CH 2 -heteroaryl; or R a and R 1 , together with the atoms to which they are attached form a pyrrolidine ring;
R 2 represents hydrogen, —(CH 2 ) 3 NHC(═NH)NH 2 , —(CH 2 ) 2 CONH 2 , —(CH 2 ) 2 COOH, —CH 2 -aryl, or —CH 2 -heteroaryl;
R b and R 3 , together with the atoms to which they are attached form a pyrrolidine ring.
19. The method of claim 18 , wherein the subject presenting a dysregulated CD47-SIRPα pathway is a subject presenting with CD47+ disease cells.
20. The method of claim 18 , wherein the disease or disorder mediated by dysregulated CD47-SIRPα pathway is a cancer.
21. The method of claim 20 , wherein the cancer is selected from the group consisting of melanoma, renal cancer, prostate cancer, breast cancer, colon cancer and lung cancer, bone cancer, pancreatic cancer, skin cancer, cancer of the head or neck, cutaneous or intraocular malignant melanoma, uterine cancer, ovarian cancer, rectal cancer, cancer of the anal region, stomach cancer, testicular cancer, carcinoma of the fallopian tubes, carcinoma of the endometrium, carcinoma of the cervix, carcinoma of the vagina, carcinoma of the vulva, Hodgkin's Disease, non-Hodgkin's lymphoma, cancer of the esophagus, cancer of the small intestine, cancer of the endocrine system, cancer of the thyroid gland, cancer of the parathyroid gland, cancer of the adrenal gland, sarcoma of soft tissue, cancer of the urethra, cancer of the penis, chronic or acute leukemias including acute myeloid leukemia, acute lymphocytic leukemia, chronic myeloid leukemia, acute lymphoblastic leukemia, chronic lymphocytic leukemia, solid tumours of childhood, lymphocytic lymphoma, cancer of the bladder, cancer of the kidney or ureter, carcinoma of the renal pelvis, neoplasm of the central nervous system (CNS), non-small cell lung cancer (NSCLC), primary CNS lymphoma, tumour angiogenesis, spinal axis tumour, brain stem glioma, pituitary adenoma, Kaposi's sarcoma, epidermoid cancer, squamous cell cancer, T-cell lymphoma, B-cell lymphomas, myeloproliferative disorder/neoplasm (MPDS); myelodysplastic syndrome; giant cell myeloma, heavy-chain myeloma, light chain myeloma and Bence-Jones myeloma, environmentally induced cancers including those induced by asbestos (e.g., mesothelioma), and combinations of said cancers.