Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
  • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
  • A61K31/415—1,2-Diazoles
  • A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
  • A61K31/415—1,2-Diazoles
  • A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
  • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K39/00—Medicinal preparations containing antigens or antibodies
  • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
  • A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
  • A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
  • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
  • A61P35/02—Antineoplastic agents specific for leukemia
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
  • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
  • C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
  • C07K16/2887—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against CD20
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2317/00—Immunoglobulins specific features
  • C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
  • C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2317/00—Immunoglobulins specific features
  • C07K2317/40—Immunoglobulins specific features characterized by post-translational modification
  • C07K2317/41—Glycosylation, sialylation, or fucosylation
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2317/00—Immunoglobulins specific features
  • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
  • C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
  • C07K2317/732—Antibody-dependent cellular cytotoxicity [ADCC]

Definitions

• the present invention relates generally to the field of cancer therapy. More
• the present invention relates to methods and kits for inhibiting proliferation of a B-cell population and treating B-cell proliferative disorders, such as hematological cancers, by administering to a subject a combination of agents comprising: (i) at least one inhibitor of P13 kinase (P13K)-delta; (ii) at least one anti-CD20 antibody; and (iii) at least one inhibitor of Bruton's tyrosine kinase (BTK).
• P13K P13 kinase
• BTK Bruton's tyrosine kinase
• Targeted cancer therapies are drugs designed to interfere with specific molecules necessary for tumor growth and progression; they are broadly classified into monoclonal antibodies (mAbs) or small molecules.
• mAbs monoclonal antibodies
• Some examples of targeted therapies include monoclonal antibodies to CD20 (e.g., rituximab/Rituxan® for treating lymphomas), CD52 (e.g., alemtuzumab/Campath®), VEGF (e.g.,
• HER2 e.g., trastuzumab/Herceptin® for treating Her2+ breast and stomach cancers
• EGFR e.g., cetuximab/Erbitux® for treating colorectal cancer
• CTLA-4 e.g., ipilimumab/Y ervoy® for treating melanoma
• PD-1 e.g., MDX-1106, CT-011.
• Small molecule therapies target dysregulated pathways of cancer cells, e.g., RAS, RAF, P13K, MEK, JAK, STAT, and BTK.
• the combination treatment described herein is suitable for treating or delaying progression of B-cell proliferative disorders in a subject, such as hematological malignancies.
• kits for inhibiting proliferation of a B-cell population comprising (a) administering to the B-cell population a combination of agents, in therapeutically effective amounts, said combination of agents comprising: (i) at least one P13K-delta selective inhibitor; (ii) at least one anti-CD20 antibody; and (iii) at least one inhibitor of Bruton's tyrosine kinase (BTK); and (b) inhibiting proliferation of said B- cell population.
• a combination of agents comprising: (i) at least one P13K-delta selective inhibitor; (ii) at least one anti-CD20 antibody; and (iii) at least one inhibitor of Bruton's tyrosine kinase (BTK); and (b) inhibiting proliferation of said B- cell population.
• the P 13K-delta inhibitor is selected from the group
• TGR-1202 also known as umbralisib
• idelalisib idelalisib
• duvelisib ACP- 319
• INCB-50465 INCB-50465
• ME-401 ME-401
• At least one anti-CD20 antibody wherein at least one anti-CD20 antibody is ublituximab or an anti-CD20 antibody or antibody fragment that binds to the same epitope as ublituximab;
• BTK Bruton's tyrosine kinase
• the P13K-delta inhibitor of Formula A is (S)-2-(l-(4- ainino-3-(3-fluoro-4-isopropoxyphenyl)-lH-pyrazolo[3,4-d]pyrimidin-l-yl)ethyl)-6- fluoro-3-(3-fluorophenyl)-4H-chromen-4-one.
• the P13K-delta inhibitor of Formula A is (S)-2-(l-(4- ainino-3-(3-fluoro-4-isopropoxyphenyl)-lH-pyrazolo[3,4-d]pyrimidin-l-yl)ethyl)-6- fluoro-3-(3-fluorophenyl)-4H-chromen-4-one p-toluenesulfonic acid (PTSA) salt (also known as TGR-1202).
• PTSA p-toluenesulfonic acid
• the method of inhibiting proliferation of a B-cell population comprises promoting apoptosis of said B-cells.
• BCR B-cell receptor
• the P13K-delta inhibitor is administered daily at a dosage from: about 200 mg to about 1200 mg, about 400 mg to about 1000 mg, about 400 mg to about 800 mg, about 400 mg, about 500 mg, about 600 mg, about 700 mg, about 800 mg, about 900 mg, about 1000 mg, or about 1200 mg.
• TGR-1202 is administered at a dose of about 400 mg to about 1200 mg per day. In some embodiments, the TGR-1202 is administered at a dose of about 400 mg per day. In some embodiments, the TGR-1202 is administered at a dose of about 600 mg per day. In some embodiments, the TGR-1202 is administered at a dose of about 800 mg per day.
• the P13K-delta inhibitor is formulated for oral
• the P13K-delta inhibitor is TGR-1202 and it is formulated for oral administration. In some embodiments, TGR-1202 is administered in a fed-state.
• the anti-CD20 antibody is glycoengineered, exhibits a low fucose content in its Fc region, or is antibody-dependent cellular cytotoxicity (ADCC)- optimized.
• ADCC antibody-dependent cellular cytotoxicity
• the anti-CD20 antibody is ublituximab (also known as TG-
• the ublituximab comprises the VH CDR1, CDR2, and CDR3 region of sequences SEQ ID NOS: 1, 2, and 3, and the VL CDR1, CDR2, and CDR3 region of sequences SEQ ID NOS: 6, 7, and 8. In some embodiments, the ublituximab comprises the VH of SEQ ID NO: 4 and the VL of SEQ ID NO: 9.
• the ublituximab is administered at a dose from: about 450 mg to about 1200 mg, about 600 to about 1200 mg, about 600 to about 1000 mg, about 600 to about 900 mg, about 600 mg, about 700 mg, about 800 mg, or about 900 mg.
• Ublituximab may be administered about twice every week, about once every 1 to
• the ublituximab is administered at a dose of about 900 mg.
• the ublituximab is administered intravenously.
• the ublituximab is administered by intravenous infusion.
• the BTK inhibitor is selected from the group consisting of l-[(3R)-3-[4-Amino-3-(4-phenoxyphenyl)-lH-pyrazolo[3,4-d]pyrimidin-l-yl]piperidin-l- yl]prop-2-en-l-one (Imbruvica®, ibrutinib, or PCI-32765); l-(R)-3-[4-amino-3-(4- phenoxyphenyl)-lH-pyrazolo[3,4-d]pyrimidin-l-yl]piperidin-l-yl]-2,3,- dihy droxypropan- 1 -one (PCI-45227); 4- ⁇ 8-Amino-3-[(2S)- 1 -(2-butynoyl)-2- pyrrolidinyl]imidazo[l,5-a]pyrazin-l-yl ⁇ -N-
• the BTK inhibitor is l -[(3i?)-3-[4-Amino-3-(4- phenoxyphenyl)-lH-pyrazolo[3,4-(i]pyrimidin-l-yl]piperidin-l -yl]prop-2-en-l -one (ibrutinib).
• the BTK inhibitor is 4- ⁇ 8-Amino-3-[(25)-l-(2-butynoyl)-
• the ibrutinib is administered once daily at a dosage from: about 200 to about 800 mg, about 400 to about 600 mg, about 400 mg, about 420 mg, about 440 mg, about 480 mg, about 500 mg, about 520 mg, about 540 mg, about 560 mg, about 580 mg, or about 600 mg.
• the ibrutinib is administered once daily at a dosage of about 420 mg or about 560 mg per day. In some embodiments, the ibrutinib is administered once daily at a dosage of about 420 mg per day. In some embodiments, the ibrutinib is administered once daily at a dosage of about 560 mg per day.
• ibrutinib is administered orally.
• the B-cell population whose proliferation is to be inhibited is in a human subject.
• the human subject has a disease or disorder associated with excessive B-cell proliferation.
• the disease associated with excessive B-cell proliferation is cancer.
• a human subject has cancer.
• the cancer is a B-cell hematological malignancy.
• the B-cell hematological malignancy is lymphoma or leukemia.
• the B-cell hematological malignancy is selected from the group consisting of acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), acute monocytic leukemia (AMoL), chronic lymphocytic leukemia (CLL), high-risk CLL, small lymphocytic lymphoma (SLL), high-risk SLL, multiple myeloma (MM), non- Hodgkin's lymphoma (NHL), mantle cell lymphoma (MCL), follicular lymphoma (FL), Waldenstrom's macroglobulinemia (WM), diffuse large B-cell lymphoma (DLBCL), marginal zone lymphoma (MZL), Burkitt's lymphoma (BL), hairy cell leukemia (HCL), and Richter's transformation.
• ALL acute lymphocytic leukemia
• AML acute myeloid leukemia
• AML acute monocytic leukemia
• CLL chronic lymphocytic
• the B-cell hematological malignancy is selected from the group consisting of chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), non-Hodgkin's lymphoma (NHL), mantle cell lymphoma (MCL), follicular lymphoma (FL), diffuse large B-cell lymphoma (DLBCL), and marginal zone lymphoma (MZL).
• CLL chronic lymphocytic leukemia
• SLL small lymphocytic lymphoma
• NHL non-Hodgkin's lymphoma
• MCL mantle cell lymphoma
• FL diffuse large B-cell lymphoma
• MZL marginal zone lymphoma
• the hematological malignancy is selected from the group consisting of Burkitt's lymphoma, non-Burkitt high grade B cell lymphoma, primary mediastinal B-cell lymphoma (PMBL), immunoblastic large cell lymphoma, precursor B- lymphoblastic lymphoma, B cell prolymphocytic leukemia, lymphoplasmacytic lymphoma, plasma cell myeloma, plasmacytoma, mediastinal (thymic) large B cell lymphoma, intravascular large B cell lymphoma, primary effusion lymphoma, Hodgkin's lymphoma, or lymphomatoid granulomatosis.
• PMBL primary mediastinal B-cell lymphoma
• immunoblastic large cell lymphoma precursor B- lymphoblastic lymphoma
• B cell prolymphocytic leukemia lymphoplasmacytic lymphoma
• plasma cell myeloma plasmacytoma
• the cancer overexpresses CD20.
• the cancer is refractory to chemotherapy.
• the cancer is refractory to any agent described herein, i.e., an anti-CD20 antibody, a P13K delta selective inhibitor, or a BTK inhibitor, when said agent was administered individually (i.e., used as a monotherapy).
• the cancer is refractory to non-TGR-1202 P13K-delta inhibitors.
• the cancer is refractory to non-ublituximab anti-CD20 antibodies.
• the cancer is refractory to rituximab.
• the cancer is refractory to a BTK inhibitor.
• the cancer is refractory to ibrutinib.
• the cancer has relapsed.
• the human subject has one or more genetic mutations selected from the group consisting of 17p del, 1 lq del, p53, unmutated IgVH together with ZAP-70+ and/or CD38+, and trisomy 12.
• the agents (i, ii, and iii) of the methods described herein are administered separately.
• the agents (i, ii, and iii) of the methods described herein are administered sequentially, though a particular order (or sequence of administration) is not required. In some embodiments, the agents (i and iii) of the methods described herein are administered simultaneously or sequentially. [0043] In some embodiments, the combination of agents is sequentially administered in an induction, consolidation, and/or maintenance regimen.
• two of the agents i, ii, or iii are administered together in order to induce a partial anti-tumor response, followed by administration of the third agent to enhance the anti-tumor response.
• a complete anti-tumor response is observed following administration of all agents (e.g., i, ii, and iii, as disclosed herein) to said subject.
• a subject administered any of the methods described herein achieves a complete response with minimal residual disease (MRD).
• a subject administered any of the methods described herein achieves a partial reponse (PR) when all three agents are administered in combination.
• a subject administered any of the methods described herein achieves a partial response (PR) or a complete response (CR) that is durable for at least two months.
• At least one of the agents i, ii, or iii is administered in a maintenance therapy in order to keep the B-cell proliferative disorder from retuming after successful treatment.
• the agent is administered in maintenance therapy for an extended period of time, e.g., until unmanageable toxicity, or disease progression occurs.
• the maintenance therapy ends when disease progression occurs.
• the agents (i and iii) of the methods described herein are contained in the same pharmaceutical composition.
• the pharmaceutical composition is for oral administration.
• the methods described herein further comprises
• the at least one additional therapeutic agent is selected from the group consisting of mitotic inhibitors, alkylating agents, antimetabolites, anthracyclines, vinca alkaloids, plant alkaloids, nitrogen mustards, proteasome inhibitors, intercalating antibiotics, growth factor inhibitors, cell-cycle inhibitors, biological response modifiers, anti-hormones, angiogenesis inhibitors, anti- androgens, DNA interactive agents, purine analogues, topoisomerase I inhibitors, topoisomerase II inhibitors, tubulin interacting agents, hormonal agents, thymidilate synthase inhibitors, non-BTK and non-P13K-delta tyrosine kinase inhibitors, angiogenesis inhibitors, EGF inhibitors, VEGF inhibitors, CDK inhibitors, SRC inhibitors, c-Kit inhibitors, Herl/2 inhibitors, inhibitors of myc, anti-tumor antibodies, mono
• the at least one additional therapeutic agent is an anticancer agent selected from the group consisting of DNA interactive agents, such as cisplatin or doxorubicin; topoisomerase II inhibitors, such as etoposide; topoisomerase I inhibitors such as CPT-1 1 or topotecan; tubulin interacting agents, such as paclitaxel, docetaxel or the epothilones (for example ixabepilone), either naturally occurring or synthetic; hormonal agents, such as tamoxifen; thymidilate synthase inhibitors, such as 5- fluorouracil; and anti-metabolites, such as methotrexate; other tyrosine kinase inhibitors such as Iressa and OSI-774; angiogenesis inhibitors; EGF inhibitors; VEGF inhibitors; CDK inhibitors; SRC inhibitors; c-Kit inhibitors; Herl/2 inhibitors and monoclonal antibodies directed against growth factor receptors such as
• the at least one additional therapeutic agent is selected from the group consisting of a proteasome inhibitor, Bortezomib (Velcade®), Carfilzomib (PR-171), PR-047, disulfiram, lactacystin, PS-519, eponemycin, epoxomycin, aclacinomycin, CEP-1612, MG-132, CVT-63417, PS-341, vinyl sulfone tripeptide inhibitors, ritonavir, PI-083, (+/-)-7-methylomuralide, (-)-7-methylomuralide, lenalidomide, and combinations thereof.
• a proteasome inhibitor Bortezomib (Velcade®), Carfilzomib (PR-171), PR-047, disulfiram, lactacystin, PS-519, eponemycin, epoxomycin, aclacinomycin, CEP-1612, MG-132, CVT-63417
• the additional therapeutic agent is a combination of
• chemotherapies such as, e.g., "CHOP” (a combination including (i) cyclophosphamide such as Cytoxan, (ii) doxorubicin or other topoisomerase II inhibitors such as adriamycin, (iii) vincristine or other vincas such as Oncovin; and (iv) a steroid such as hydrocortisone or prednisolone); "R-CHOP” (a combination including rituxan, cyclophosphamide, doxorubicin, vincristine, and prednisone); "ICE” (a combination including ifosfamide, carboplatin, and etoposide); “R-ICE” (a combination including rituxan, ifosfamide, carboplatin, and etoposide); "R-ACVBP” (a combination of rituximab, doxorubicin, cyclophosphamide, vinde
• methods of inhibiting proliferation of a B-cell population comprising, (a) administering to the B-cell population a combination of agents, in therapeutically effective amounts, said combination of agents comprising: (i) TGR-1202; (ii) ublituximab; and (iii) ibrutinib; and (b) inhibiting proliferation of said B- cell population.
• the proliferation of the B-cell population is associated with a hematological malignancy.
• the hematological malignancy is selected from the group consisting of acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), multiple myeloma (MM), non-Hodgkin's lymphoma (NHL), mantle cell lymphoma (MCL), follicular lymphoma (FL), Waldenstrom's macroglobulinemia (WM), diffuse large B-cell lymphoma (DLBCL), marginal zone lymphoma (MZL), Burkitt's lymphoma, hairy cell leukemia (HCL), and Richter's transformation.
• ALL acute lymphocytic leukemia
• AML acute myeloid leukemia
• CLL chronic lymphocytic leukemia
• SLL small lymphocytic lymphoma
• kits comprising at least one P 13K-delta selective inhibitor, at least one anti-CD20 antibody, and at least one inhibitor of BTK; and (b) instruction for using a P13K-delta selective inhibitor in combination with an anti-CD20 antibody and an inhibitor of BTK.
• kits comprising at least one P13K-delta selective inhibitor of formula A, at least one anti-CD20 antibody, and at least one inhibitor of BTK.
• other agents that can be used to perform the methods described herein, and combinations thereof, are also included in the kit.
• the kit comprises (a) a P13K-delta selective inhibitor of formula A, as described herein, or a stereoisomer thereof, or a pharmaceutically acceptable salt, solvate, or prodrug thereof; an anti-CD20 antibody or fragment thereof that binds to the same epitope as ublituximab; and an inhibitor of BTK; and (b) instructions for using said P13K-delta selective inhibitor, in combination with
• ublituximab or an anti-CD20 antibody or fragment thereof that binds to the same epitope as ublituximab and an inhibitor of BTK.
• the inhibitor of BTK in the kit is ibrutinib. In some embodiments, the inhibitor of BTK in the kit is ibrutinib. In some
• the inhibitor of BTK in the kit is acalabrutinib.
• the P13K-delta selective inhibitor in the kit is (S)-2-(l-(4- ainino-3-(3-fluoro-4-isopropoxyphenyl)-lH-pyrazolo[3,4-d]pyrimidin-l-yl)ethyl)-6- fluoro-3-(3-fluorophenyl)-4H-chromen-4-one.
• the P13K-delta selective inhibitor in the kit is (S)-2-(l-(4-amino-3-(3-fluoro-4-isopropoxyphenyl)-lH- pyrazolo[3,4-d]pyrimidin-l-yl)ethyl)-6-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one p- toluenesulfonic acid (PTSA) salt (TGR-1202).
• the kit further comprises ublituximab or an anti-CD20 antibody or fragment thereof that binds to the same epitope as ublituximab.
• the kit further comprises one or more additional
• therapeutic agents that can be used to inhibit B-cell proliferation.
• Figure 2 is a bar graph depicting efficacy of the combination of TGR-1202 +
• Figure 3 is a bar graph depicting the number of days (duration) that patients with various histologies were on the study. Eighty one percent of patients were on study for more than six months. The median time on the study was 11.1 months (range 0.4-30.1+ months). "PD" indicates progressive disease.
• Figure 4 is a Table depicting efficacy of the combination of TGR-1202 +
• CD20 also known as B lymphocyte CD20 antigen, MS4A1, B
• lymphocyte surface antigen Bl, Bp35, and Leukocyte surface antigen Leu-16 refers to any native CD20, unless otherwise indicated.
• CD20 encompasses "full-length,” unprocessed CD20, as well as any form of CD20 that results from processing within the cell.
• the term also encompasses naturally occurring variants of CD20, e.g., splice variants, allelic variants, and isoforms.
• the CD20 polypeptides described herein can be isolated from a variety of sources, such as from human tissue types or from another source, or prepared by recombinant or synthetic methods.
• CD20 sequences include, but are not limited to, NCBI reference numbers NP_068769.2 and NP_690605.1.
• antibody means an immunoglobulin molecule that recognizes and specifically binds to a target, such as a protein, polypeptide, peptide, carbohydrate, polynucleotide, lipid, or combinations of the foregoing through at least one antigen recognition site within the variable region of the immunoglobulin molecule.
• antibody encompasses intact polyclonal antibodies, intact monoclonal antibodies, antibody fragments (such as Fab, Fab', F(ab')2, and Fv fragments), single chain Fv (scFv) mutants, multispecific antibodies such as bispecific antibodies generated from at least two intact antibodies, chimeric antibodies, humanized antibodies, human antibodies, fusion proteins comprising an antigen determination portion of an antibody, and any other modified immunoglobulin molecule comprising an antigen recognition site so long as the antibodies exhibit the desired biological activity.
• antibody fragments such as Fab, Fab', F(ab')2, and Fv fragments
• scFv single chain Fv mutants
• multispecific antibodies such as bispecific antibodies generated from at least two intact antibodies, chimeric antibodies, humanized antibodies, human antibodies, fusion proteins comprising an antigen determination portion of an antibody, and any other modified immunoglobulin molecule comprising an antigen recognition site so long as the antibodies exhibit the desired biological activity.
• An antibody can be of any of the five major classes of immunoglobulins: IgA, IgD, IgE, IgG, and IgM, or subclasses (isotypes) thereof (e.g., IgGl, IgG2, IgG3, IgG4, IgAl and IgA2), based on the identity of their heavy-chain constant domains referred to as alpha, delta, epsilon, gamma, and mu, respectively.
• the different classes of immunoglobulins have different and well known subunit structures and three-dimensional configurations.
• Antibodies can be naked or conjugated to other molecules such as toxins, radioisotopes, etc.
• a "blocking" antibody or an “antagonist” antibody is one which inhibits or
• blocking antibodies or antagonist antibodies substantially or completely inhibit the biological activity of the antigen.
• the biological activity is reduced by 10%, 20%, 30%, 50%, 70%, 80%, 90%, 95%, or even 100%.
• anti-CD20 antibody or "an antibody that binds to CD20” refers to an antibody that is capable of binding CD20 with sufficient affinity such that the antibody is useful as a diagnostic and/or therapeutic agent in targeting CD20.
• the extent of binding of an anti-CD20 antibody to an unrelated, non-CD20 protein is less than about 10% of the binding of the antibody to CD20 as measured, e.g., by a radioimmunoassay (RIA).
• RIA radioimmunoassay
• an antibody that binds to CD20 has a dissociation constant (Kd) of ⁇ 1 ⁇ , ⁇ 100 nM, ⁇ 10 nM, ⁇ 1 nM, or ⁇ 0.1 nM.
• antibody fragment refers to a portion of an intact antibody and refers to the antigenic determining variable regions of an intact antibody.
• antibody fragments include, but are not limited to, Fab, Fab', F(ab')2, and Fv fragments, linear antibodies, single chain antibodies, and multispecific antibodies formed from antibody fragments.
• a “monoclonal antibody” refers to a homogeneous antibody population involved in the highly specific recognition and binding of a single antigenic determinant, or epitope. This is in contrast to polyclonal antibodies that typically include different antibodies directed against different antigenic determinants.
• the term “monoclonal antibody” encompasses both intact and full-length monoclonal antibodies, as well as antibody fragments (such as Fab, Fab', F(ab')2, Fv), single chain (scFv) mutants, fusion proteins comprising an antibody portion, and any other modified immunoglobulin molecule comprising an antigen recognition site.
• “monoclonal antibody” refers to such antibodies made in any number of manners including but not limited to by hybridoma, phage selection, recombinant expression, and transgenic animals.
• humanized antibody refers to forms of non-human (e.g., murine) antibodies that are specific immunoglobulin chains, chimeric immunoglobulins, or fragments thereof that contain minimal non-human (e.g., murine) sequences.
• humanized antibodies are human immunoglobulins in which residues from the complementary determining region (CDR) are replaced by residues from the CDR of a non-human species (e.g., mouse, rat, rabbit, hamster) that have the desired specificity, affinity, and capability (Jones et al., Nature 327:522-525 (1986); Riechmann et al., Nature 332:323-327 (1988); Verhoeyen et al, Science 239: 1534-1536 (1988)).
• the Fv framework region (FR) residues of a human immunoglobulin are replaced with the corresponding residues in an antibody from a non-human species that has the desired specificity, affinity, and capability.
• the humanized antibody can be further modified by the substitution of additional residues either in the Fv framework region and/or within the replaced non-human residues to refine and optimize antibody specificity, affinity, and/or capability.
• the humanized antibody will comprise substantially all of at least one, and typically two or three, variable domains containing all or substantially all of the CDR regions that correspond to the non-human immunoglobulin whereas all or substantially all of the FR regions are those of a human immunoglobulin consensus sequence.
• the humanized antibody can also comprise at least a portion of an immunoglobulin constant region or domain (Fc), typically that of a human
• immunoglobulin examples of methods used to generate humanized antibodies are described in U. S. Patent Nos. 5,225,539 or 5,639,641.
• variable region of an antibody refers to the variable region of the antibody light chain or the variable region of the antibody heavy chain, either alone or in combination.
• the variable regions of the heavy and light chain each consist of four framework regions (FR) connected by three complementarity determining regions (CDRs), also known as hypervariable regions.
• the CDRs in each chain are held together in close proximity by the FRs and, with the CDRs from the other chain, contribute to the formation of the antigen-binding site of antibodies.
• There are at least two techniques for determining CDRs (1) an approach based on cross-species sequence variability (i.e., Kabat a/.
• the Kabat numbering system is generally used when referring to a residue in the variable domain (approximately residues 1 -107 of the light chain and residues 1 -1 13 of the heavy chain) (e.g., Kabat et al., Sequences of Immunological Interest. 5 th Ed. Public Health Service, National Institutes of Health, Bethesda, Md. (1991)).
• amino acid position numbering refers to the numbering system used for heavy chain variable domains or light chain variable domains of the compilation of antibodies in Kabat et al, Sequences of Proteins of Immunological Interest, 5 th Ed. Public Health Service, National Institutes of Health, Bethesda, Md. (1991). Using this numbering system, the actual linear amino acid sequence can contain fewer or additional amino acids corresponding to a shortening of, or insertion into, a FR or CDR of the variable domain.
• a heavy chain variable domain can include a single amino acid insert (residue 52a according to Kabat) after residue 52 of H2 and inserted residues (e.g., residues 82a, 82b, and 82c, etc. according to Kabat) after heavy chain FR residue 82.
• the Kabat numbering of residues can be determined for a given antibody by alignment at regions of homology of the sequence of the antibody with a "standard” Kabat numbered sequence. Chothia refers instead to the location of the structural loops (Chothia and Lesk, J. Mol. Biol. 79(5:901-917 (1987)).
• the end of the Chothia CDR-H1 loop when numbered using the Kabat numbering convention, varies between H32 and H34 depending on the length of the loop (this is because the Kabat numbering scheme places the insertions at H35A and H35B; if neither 35A nor 35B is present, the loop ends at 32; if only 35A is present, the loop ends at 33; if both 35A and 35B are present, the loop ends at 34).
• the AbM hypervariable regions represent a compromise between the Kabat CDRs and Chothia structural loops, and are used by Oxford Molecular's AbM antibody modeling software. Loop Kabul .A ⁇ Chothia
• human antibody means an antibody produced by a human or an
• human antibody having an amino acid sequence corresponding to an antibody produced by a human made using any technique known in the art.
• This definition of a human antibody includes intact or full-length antibodies, fragments thereof, and/or antibodies comprising at least one human heavy and/or light chain polypeptide such as, for example, an antibody comprising murine light chain and human heavy chain polypeptides.
• chimeric antibodies refers to antibodies wherein the amino acid
• sequence of the immunoglobulin molecule is derived from two or more species.
• variable region of both light and heavy chains corresponds to the variable region of antibodies derived from one species of mammals (e.g., mouse, rat, rabbit, etc.) with the desired specificity, affinity, and capability, while the constant regions are homologous to the sequences in antibodies derived from another (usually human) to avoid eliciting an immune response in that species.
• mammals e.g., mouse, rat, rabbit, etc.
• constant regions are homologous to the sequences in antibodies derived from another (usually human) to avoid eliciting an immune response in that species.
• epitopes or “antigenic determinant” are used interchangeably herein and refer to that portion of an antigen capable of being recognized and specifically bound by a particular antibody.
• the antigen is a polypeptide
• epitopes can be formed both from contiguous amino acids and noncontiguous amino acids juxtaposed by tertiary folding of a protein. Epitopes formed from contiguous amino acids are typically retained upon protein denaturing, whereas epitopes formed by tertiary folding are typically lost upon protein denaturing.
• An epitope typically includes at least 3, and more usually, at least 5 or 8-10 amino acids in a unique spatial conformation.
• Binding affinity generally refers to the strength of the sum total of noncovalent interactions between a single binding site of a molecule (e.g., an antibody) and its binding partner (e.g., an antigen). Unless indicated otherwise, as used herein, “binding affinity” refers to intrinsic binding affinity which reflects a 1 : 1 interaction between members of a binding pair (e.g., antibody and antigen).
• the affinity of a molecule X for its partner Y can generally be represented by the dissociation constant (Kd). Affinity can be measured by common methods known in the art, including those described herein.
• Low-affinity antibodies generally bind antigen slowly and tend to dissociate readily, whereas high- affinity antibodies generally bind antigen faster and tend to remain bound longer.
• a variety of methods of measuring binding affinity are known in the art, any of which can be used for purposes of the present invention. Specific illustrative embodiments are described herein.
• an antibody which has an affinity for an antigen of "0.6 nM or better” the antibody's affinity for the antigen is ⁇ 0.6 nM, i.e., 0.59 nM, 0.58 nM, 0.57 nM etc. or any value less than 0.6 nM.
• the phrase "substantially similar,” or “substantially the same,” as used herein, denotes a sufficiently high degree of similarity between two numeric values (generally one associated with an antibody of the invention and the other associated with a reference/comparator antibody) such that one of skill in the art would consider the difference between the two values to be of little or no biological and/or statistical significance within the context of the biological characteristics measured by said values (e.g., Kd values).
• the difference between said two values is less than about 50%, less than about 40%, less than about 30%, less than about 20%, or less than about 10% as a function of the value for the reference/comparator antibody.
• isolated is a polypeptide, antibody, polynucleotide, vector, cell, or composition which is in a form not found in nature. Isolated polypeptides, antibodies, polynucleotides, vectors, cells or compositions include those which have been purified to a degree that they are no longer in a form in which they are found in nature. In some embodiments, an antibody, polynucleotide, vector, cell, or composition which is isolated is substantially pure. [0083] As used herein, “substantially pure” refers to material which is at least 50% pure
• cancer and “cancerous” refer to or describe the physiological
• cancer e.g., carcinoma, lymphoma, blastoma, sarcoma, and leukemia.
• B-cell proliferative disorder As used herein, the term "B-cell proliferative disorder" or "B-cell
• lymphoproliferative disorder refers to a disease or disorder in a subject wherein a population of B-cells in the subject are produced in excessive quantities, such as seen in B-cell malignancies (B-cell cancers).
• B-cell cancer or "B-cell malignancy” refers to an uncontrolled or unregulated growth of B-cells in the blood, bone marrow, or lymph node.
• B-cell malignancy is a type of hematological malignancy that includes lymphomas, leukemias, and myelomas.
• the B-cell malignancy may be indolent or aggressive.
• Non-limiting examples of hematological malignancies that may be treated with the methods or kits of the invention include acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), multiple myeloma (MM), non-Hodgkin's lymphoma (NHL), mantle cell lymphoma (MCL), follicular lymphoma (FL), Waldenstrom's macroglobulinemia (WM), diffuse large B-cell lymphoma (DLBCL), marginal zone lymphoma (MZL), which includes extranodal MZL, nodal MZL, and splenic MZL, hairy cell leukemia (HCL), Burkitt's lymphoma (BL), and Richter's transformation.
• ALL acute lymphocytic leukemia
• AML acute myeloid leukemia
• CLL chronic lymphocytic leukemia
• the DLBCL is an activated B-cell DLBCL (ABC-DLBCL), a germinal center B-cell like DLBCL (GBC-DLBCL), a double hit DLBCL (DH-DLBCL), or a triple hit DLBCL (TH-DLBCL).
• ABS-DLBCL activated B-cell DLBCL
• GBC-DLBCL germinal center B-cell like DLBCL
• DH-DLBCL double hit DLBCL
• TH-DLBCL triple hit DLBCL
• high risk CLL means CLL characterized by at least one of the following genetic mutations: 17p del; l lq del; p53; unmutated IgVH together with ZAP-70+ and/or CD38+; and trisomy 12.
• Tuor and neoplasm refer to any mass of tissue that result from excessive cell growth or proliferation, either benign (noncancerous) or malignant (cancerous) including pre-cancerous lesions.
• cancer cell refers to the total population of cells derived from a tumor or a pre-cancerous lesion, including both non-tumorigenic cells, which comprise the bulk of the tumor cell population, and tumorigenic stem cells (cancer stem cells).
• tumorigenic stem cells cancer stem cells.
• tumorigenic stem cells cancer stem cells
• subject refers to any animal (e.g., a mammal), including, but not
• a cell “population” can refer to a single cell or to multiple cells.
• the cell or cells can be cells in culture (in vitro) or cells in an organism (in vivo).
• a cell population can be in a human subject or patient.
• a "B-cell population” refers to a single B-cell or multiple B-cells.
• B-cell also known as a "B lymphocyte” refers to a type of white blood cell (WBC) of the lymphocyte subtype.
• WBC white blood cell
• composition refers to a preparation which is in such form as to permit the biological activity of the active ingredient to be effective, and which contains no additional components which are unacceptably toxic to a subject to which the formulation would be administered.
• Such formulations can be sterile.
• an "effective amount” of an antibody or an agent as disclosed herein, is an
• an “effective amount” can be determined empirically and in a routine manner by those skilled in the art, in relation to the stated purpose.
• the term "therapeutically effective amount” refers to the amount of an agent (e.g., monoclonal antibody, small molecule, chemotherapeutic drug, etc . ), as disclosed herein, that is effective to "treat” a disease or disorder in a subject or mammal.
• the therapeutically effective amount of the agent or drug can reduce the number of cancer cells; reduce the tumor size; inhibit (i.e., slow to some extent and in a certain embodiment, stop) cancer cell infiltration into peripheral organs; inhibit (i.e., slow to some extent and in a certain embodiment, stop) tumor metastasis; inhibit, to some extent, tumor growth; and/or relieve to some extent one or more of the symptoms associated with the cancer. See the definition herein of "treating. " To the extent the drug can prevent growth and/or kill existing cancer cells, it can be cytostatic and/or cytotoxic. A
• prophylactically effective amount refers to an amount effective, at dosages and for periods of time necessary, to achieve the desired prophylactic result. Typically, but not necessarily, since a prophylactic dose is used in subjects prior to or at an earlier stage of disease, the prophylactically effective amount will be less than the therapeutically effective amount.
• Terms such as “treating,” “treatment,” “to treat,” “having a therapeutic effect,” alleviating,” “to alleviate,” or “slowing the progression of refer to both 1) therapeutic measures that cure, slow down, lessen symptoms of, and/or halt progression of a diagnosed pathologic condition or disorder, such as a hematological malignancy, and 2) prophylactic or preventative measures that prevent and/or slow the development of a targeted pathologic condition or disorder.
• those in need of treatment include those already with the disorder; those prone to have the disorder; and those in whom the disorder is to be prevented.
• a subject is successfully "treated” for cancer according to the methods of the present invention if the patient shows one or more of the following: reduction in cachexia, increase in survival time, elongation in time to tumor progression, reduction in tumor mass, reduction in tumor burden and/or a prolongation in time to tumor metastasis, time to tumor recurrence or progressive disease, tumor response, complete response (CR), partial response (PR), stable disease, progression free survival (PFS), overall survival (OS), each as measured by standards set by the National Cancer Institute and the U. S. Food and Drug Administration for the approval of new drugs. See, Johnson et al, J. Clin. Oncol. 27 : 1404-1411 (2003).
• the "therapeutic effect,” as defined above also encompasses a reduction in toxicity or adverse side effects, and/or an improvement in tolerability.
• a “combination" of an anti-CD20 antibody e.g., ublituximab
• a P 13K-delta selective inhibitor e.g., TGR-1202
• a BTK inhibitor e.g., ibrutinib
• a “combination of agents” refers to the administration of at least one of each of these three agents (could be more than one type of each agent) to the same population of B-cells or to the same subject simultaneously, sequentially, or both simultaneously and sequentially.
• administering constitutes administration of a combination of agents.
• a "combination of agents” can also include an anti- CD20 antibody (e.g., ublituximab), a P13K-delta selective inhibitor (e.g., TGR-1202), and a BTK inhibitor, and one or more additional therapeutic agents, as described herein.
• simultaneous administration of an anti-CD20 antibody or fragment thereof, a P13K-delta selective inhibitor, and a BTK inhibitor also constitutes administration of a combination of the anti-CD20 antibody or fragment thereof, P 13K-delta selective inhibitor, and a BTK inhibitor, regardless of whether the anti-CD20 antibody or fragment thereof, P13K-delta inhibitor, and the BTK inhibitor are administered together in a single pharmaceutical formulation or are administered simultaneously in separate
• compositions by either the same or different routes of administration.
• combination of agents is intended to include treatment regimens in which the agents are administered by the same or different route of administration or at the same or different time.
• induction refers to the first agent, or combination of agents, as disclosed herein, administered to treat a B-cell proliferative disorder. If the first agent or combination of agents does not result in a complete response or it causes severe side effects, other agents may be added or used instead (see “consolidation”). Induction is also called primary therapy, or primary treatment, and is administered with the goal of inducing some initial reduction in disease burden.
• induction therapy can include the use of an anti-CD20 inhibitor and a P 13K delta inhibitor.
• consolidation therapy refers to treatment that is given following induction therapy. Consolidation therapy is used to kill any malignant B- cells that may be left in the body following induction therapy. For example, if an anti- CD20 inhibitor and a P 13K delta inhibitor are used as induction therapy, consolidation therapy can include the use of a BTK inhibitor. Consolidation is also called
• maintenance therapy refers to treatment that is given to help keep the B-cell proliferative disorder from returning after successful treatment with the initial therapy.
• Maintenance therapy may include treatment with the same agents that were used in the consolidation phase, and the agents in this phase may be administered for an extended period of time.
• treatment does not show statistically significant improvement in response to that treatment when compared to no treatment or treatment with a placebo in a recognized animal model or human clinical trial, or which responds to an initial treatment, but grows as treatment continues.
• nucleotides of any length, and include DNA and RNA.
• the nucleotides can be deoxyribonucleotides, ribonucleotides, modified nucleotides or bases, and/or their analogs, or any substrate that can be incorporated into a polymer by DNA or RNA polymerase.
• a polynucleotide can comprise modified nucleotides, such as methylated nucleotides and their analogs. If present, modification to the nucleotide structure can be imparted before or after assembly of the polymer.
• the sequence of nucleotides can be interrupted by non-nucleotide components.
• polypeptide polypeptide
• peptide protein
• polymers of amino acids of any length can be linear or branched, it can comprise modified amino acids, and it can be interrupted by non-amino acids.
• the terms also encompass an amino acid polymer that has been modified naturally or by intervention; for example, disulfide bond formation, glycosylation, lipidation, acetylation, phosphorylation, or any other manipulation or modification, such as conjugation with a labeling component.
• polypeptides containing one or more analogs of an amino acid including, for example, unnatural amino acids, etc.
• polypeptides of this invention are based upon antibodies, in certain embodiments, the polypeptides can occur as single chains or associated chains.
• identity or percent “identity” in the context of two or more nucleic acids or polypeptides, refer to two or more sequences or subsequences that are the same or have a specified percentage of nucleotides or amino acid residues that are the same, when compared and aligned (introducing gaps, if necessary) for maximum
• sequence identity can be measured using sequence comparison software or algorithms or by visual inspection.
• Various algorithms and software are known in the art that can be used to obtain alignments of amino acid or nucleotide sequences.
• One such non-limiting example of a sequence alignment algorithm is the algorithm described in Karlin et al, Proc. Natl. Acad. Sci., 87:2264-2268 (1990), as modified in Karlin et al., Proc. Natl. Acad. Sci., 90:5873-5877 (1993), and incorporated into the NBLAST and XBLAST programs (Altschul et al, Nucleic Acids Res., 25:3389- 3402 (1991)).
• Gapped BLAST can be used as described in Altschul et al, Nucleic Acids Res., 25:3389-3402 (1997).
• BLAST-2, WU-BLAST-2 (Altschul et al, Methods in Enzymology, 26(5:460-480 (1996)), ALIGN, ALIGN-2 (Genentech, South San Francisco, California) or Megalign (DNASTAR) are additional publicly available software programs that can be used to align sequences.
• the percent identity between two nucleotide sequences is determined using the GAP program in GCG software (e.g., using a NWSgapdna.CMP matrix and a gap weight of 40, 50, 60, 70, or 90 and a length weight of 1, 2, 3, 4, 5, or 6).
• the GAP program in the GCG software package which incorporates the algorithm of Needleman and Wunsch (J. Mol. Biol. 45:444-453 (1970)), can be used to determine the percent identity between two amino acid sequences (e.g., using either a Blossum 62 matrix or a PAM250 matrix, and a gap weight of 16, 14, 12, 10, 8, 6, or 4 and a length weight of 1, 2, 3, 4, 5).
• the percent identity between nucleotide or amino acid sequences is determined using the algorithm of Myers and Miller (CABIOS, 4: 11-17 (1989)).
• the percent identity can be determined using the ALIGN program (version 2.0) and using a PAM120 with residue table, a gap length penalty of 12 and a gap penalty of 4.
• Appropriate parameters for maximal alignment by particular alignment software can be determined by one skilled in the art. In certain embodiments, the default parameters of the alignment software are used.
• the percentage identity "X" of a first amino acid sequence to a second sequence amino acid is calculated as 100 x (Y/Z), where Y is the number of amino acid residues scored as identical matches in the alignment of the first and second sequences (as aligned by visual inspection or a particular sequence alignment program) and Z is the total number of residues in the second sequence. If the length of a first sequence is longer than the second sequence, the percent identity of the first sequence to the second sequence will be longer than the percent identity of the second sequence to the first sequence.
• whether any particular polynucleotide has a certain percentage sequence identity can, in certain embodiments, be determined using the Bestfit program (Wisconsin Sequence Analysis Package, Version 8 for Unix, Genetics Computer Group, University Research Park, 575 Science Drive, Madison, WI 53711). Bestfit uses the local homology algorithm of Smith and Waterman, Advances in Applied Mathematics 2: 482 489 (1981), to find the best segment of homology between two sequences.
• the parameters are set such that the percentage of identity is calculated over the full length of the reference nucleotide sequence and that gaps in homology of up to 5% of the total number of nucleotides in the reference sequence are allowed.
• two nucleic acids or polypeptides of the invention are substantially identical, meaning they have at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, and in some embodiments at least 95%, 96%, 97%, 98%, 99% nucleotide or amino acid residue identity, when compared and aligned for maximum correspondence, as measured using a sequence comparison algorithm or by visual inspection.
• identity exists over a region of the sequences that is at least about 10, about 20, about 40-60 residues in length or any integral value therebetween, or over a longer region than 60-80 residues, at least about 90-100 residues, or the sequences are substantially identical over the full length of the sequences being compared, such as the coding region of a nucleotide sequence for example.
• the number or numerical range can vary from, for example, between 1% and 15% of the stated number or numerical range.
• the compound of the invention can contain one or more asymmetric centers
• stereoisomers is a general term for all isomers of
• chiral center refers to a carbon atom to which four different groups are attached.
• enantiomer and “enantiomeric” refer to a molecule that cannot be superimposed on its mirror image and hence is optically active wherein the enantiomer rotates the plane of polarized light in one direction and its mirror image compound rotates the plane of polarized light in the opposite direction.
• racemic refers to a mixture of equal parts of enantiomers and which mixture is optically inactive.
• resolution refers to the separation, concentration or depletion of one of the two enantiomeric forms of a molecule.
• Solvates typically do not significantly alter the physiological activity or toxicity of the compounds, and as such may function as pharmacological equivalents.
• solvate as used herein is a combination, physical association and/or solvation of a compound of the present disclosure with a solvent molecule, e.g. a disolvate, monosolvate or hemisolvate, where the ratio of solvent molecule to compound of the present disclosure is about 2: 1, about 1 : 1 or about 1 :2, respectively.
• This physical association involves varying degrees of ionic and covalent bonding, including hydrogen bonding.
• the solvate can be isolated, such as when one or more solvent molecules are incorporated into the crystal lattice of a crystalline solid.
• solvent encompasses both solution-phase and isolatable solvates.
• solvates of the invention can be present as solvated forms with a pharmaceutically acceptable solvent, such as water, methanol, ethanol, and the like, and it is intended that the disclosure includes both solvated and unsolvated forms of compounds of the invention.
• a pharmaceutically acceptable solvent such as water, methanol, ethanol, and the like
• One type of solvate is a hydrate.
• a "hydrate” relates to a particular subgroup of solvates where the solvent molecule is water.
• Solvates typically can function as pharmacological equivalents. Preparation of solvates is known in the art. See, e.g., Caira, M. et al, J. Pharmaceut. Sci. 93:601-611 (2004); van Tonder, E.C. et al. , AAPS Pharm. Sci. Tech.
• a typical, non-limiting, process of preparing a solvate would involve dissolving a compound of the invention in a desired solvent (organic, water, or a mixture thereof) at temperatures about 20°C to about 25°C, then cooling the solution at a rate sufficient to form crystals, and isolating the crystals by known methods, e.g. , filtration.
• a desired solvent organic, water, or a mixture thereof
• Analytical techniques such as infrared spectroscopy can be used to confirm the presence of the solvent in a crystal of the solvate.
• prodrug refers to a compound, which is an inactive precursor of a compound, converted into its active form in the body by normal metabolic processes. Prodrug design is discussed generally in Hardman, J.G. et al. (eds.), Goodman and Oilman's The Pharmacological Basis of Therapeutics, 9 th ed., pp. 11-16 (1996). A thorough discussion is provided in Higuchi et al, Prodrugs as Novel Delivery Systems, Vol. 14, ASCD Symposium Series, and in Roche (ed.), Bioreversible Carriers in Drug Design, American Pharmaceutical Association and Pergamon Press (1987).
• prodrugs can be converted into a pharmacologically active form through hydrolysis of, for example, an ester or amide linkage, thereby introducing or exposing a functional group on the resultant product.
• the prodrugs can be designed to react with an endogenous compound to form a water-soluble conjugate that further enhances the pharmacological properties of the compound, for example, increased circulatory half-life.
• prodrugs can be designed to undergo covalent modification on a functional group with, for example, glucuronic acid, sulfate, glutathione, amino acids, or acetate. The resulting conjugate can be inactivated and excreted in the urine, or rendered more potent than the parent compound.
• High molecular weight conjugates also can be excreted into the bile, subjected to enzymatic cleavage, and released back into the circulation, thereby effectively increasing the biological half-life of the originally administered compound.
• Prodrugs of the compounds of the invention are intended to be covered within the scope of this invention.
• the present invention also includes compounds which differ only in the presence of one or more isotopically enriched atoms, for example, replacement of hydrogen with deuterium or tritium, or the replacement of a carbon by 1 C- or 14 C-enriched carbon.
• the compounds of the present invention may also contain unnatural proportions of atomic isotopes at one or more of atoms that constitute such compounds.
• the compounds may be radiolabeled with radioactive isotopes, such as for example tritium ( H), iodine-125 ( 125 I) or carbon-14 ( 14 C). All isotopic variations of the compounds of the present invention, whether radioactive or not, are encompassed within the scope of the present invention.
• pharmaceutically acceptable addition salts include inorganic and organic acid addition salts and basic salts.
• the pharmaceutically acceptable salts include, but are not limited to, metal salts such as sodium salt, potassium salt, cesium salt and the like; alkaline earth metals such as calcium salt, magnesium salt and the like; organic amine salts such as triethylamine salt, pyridine salt, picoline salt, ethanolamine salt, triethanolamine salt, dicyclohexylamine salt, ⁇ , ⁇ '-dibenzylethylenediamine salt and the like; inorganic acid salts such as hydrochloride, hydrobromide, phosphate, sulphate and the like; organic acid salts such as citrate, lactate, tartrate, maleate, fumarate, mandelate, acetate,
• selective inhibitor as applied to a biologically active agent refers to the agent's ability to selectively reduce the target signaling activity as compared to off-target signaling activity, via direct or indirect interaction with the target.
• P 13K-delta selective inhibitor also known as P13K-5 inhibitor refers to a compound, which selectively inhibits the activity of the P13K-delta isoform more effectively than other isoforms of the P13K family ( ⁇ , ⁇ , and ⁇ ).
• the P 13K-delta selective inhibitor refers to a compound of Formula A, as described herein, which selectively inhibits the activity of the P13K-delta isoform more effectively than other isoforms of the P13K family ( ⁇ , ⁇ , and ⁇ ).
• a P13K-delta selective inhibitor of Formula A can be a compound that exhibits a 50% inhibitory concentration (IC5 0 ) with respect to the ⁇ type P13-kinase that is at least 20-fold, or lower, than the inhibitor's IC5 0 with respect to the rest of the other types P 13K isoforms (i. e. , a, ⁇ , and ⁇ ).
• BTK Bruton's tyrosine kinase
• ATK agammaglobulinemia tyrosine kinase
• BPK B-cell progenitor kinase
• BTK is a signal transduction protein that regulates normal B-cell development, differentiation and functioning, and has also been implicated in initiation, survival, and progression of mature B-cell lymphoproliferative disorders, such as B-cell malignancies. Akinleye, A. et al, J. Hematol. Oncol. 6.59 (2013). As used herein, BTK is from homo sapiens, as disclosed in U. S. Patent No. 6,326,469 (Gen Bank Acc. No. NP_000052).
• an "inhibitor of BTK” or “BTK inhibitor” refers to a small molecule that targets
• BTK BTK and either inhibits BTK tyrosine phosphorylation and/or B-cell activation and/or otherwise inhibits or diminishes or abolishes the biological activity of a BTK protein.
• An "irreversible BTK inhibitor” refers to a molecule that upon contact with BTK, causes the formation of a new covalent bond with an amino acid residue of BTK. Both reversible and irreversible inhibitors of BTK can be used in the methods and kits of the present invention.
• Embodiments of the invention include methods of producing a synergistic effect in the treatment of hematological cancer, wherein said effect is at least 5%, at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 100%, at least 200%, at least 500%, or at least 1000% greater than the corresponding additive effect.
• “Therapeutic synergy,” as used herein, means that the combined administration of agents, as described herein, (i.e., an anti-CD20 antibody and a P13K-delta selective inhibitor of Formula A and a BTK inhibitor) produces a therapeutic effect that is greater than the additive effects of the anti-CD20 antibody, the P13K-delta selective inhibitor, and the BTK inhibitor, when each is used alone and/or when two agents are combined.
• agents as described herein, (i.e., an anti-CD20 antibody and a P13K-delta selective inhibitor of Formula A and a BTK inhibitor) produces a therapeutic effect that is greater than the additive effects of the anti-CD20 antibody, the P13K-delta selective inhibitor, and the BTK inhibitor, when each is used alone and/or when two agents are combined.
• kits for inhibiting proliferation of a B-cell population comprising (a) administering to the B-cell population a combination of agents, in therapeutically effective amounts, said combination of agents comprising: (i) at least one P13K-delta selective inhibitor; (ii) at least one anti-CD20 antibody; and (iii) at least one inhibitor of Bruton's tyrosine kinase (BTK); and (b) inhibiting proliferation of said B- cell population.
• a combination of agents comprising: (i) at least one P13K-delta selective inhibitor; (ii) at least one anti-CD20 antibody; and (iii) at least one inhibitor of Bruton's tyrosine kinase (BTK); and (b) inhibiting proliferation of said B- cell population.
• At least one anti-CD20 antibody wherein at least one anti-CD20 antibody is ublituximab or an anti-CD20 antibody or antibody fragment that binds to the same epitope as ublituximab;
• BTK Bruton's tyrosine kinase
• this method is effective on subjects whose cancer has relapsed.
• the method of inhibiting proliferation of a B-cell population comprises promoting cell-cycle arrest.
• BCR B-cell receptor
• the B- cell proliferative disorder is a hematological malignancy.
• the hematological malignancy is selected from the group consisting of acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), multiple myeloma (MM), non-Hodgkin's lymphoma (NHL), mantle cell lymphoma (MCL), follicular lymphoma (FL), Waldenstrom's macroglobulinemia (WM), diffuse large B-cell lymphoma (DLBCL), marginal zone lymphoma (MZL), Burkitt's lymphoma (BL), hairy cell leukemia (HCL), and Richter's transformation.
• ALL acute lymphocytic leukemia
• AML acute myeloid leukemia
• CLL chronic lymphocytic leukemia
• SLL small lymphocytic lymphoma
• P13Ks The phosphoinositide 3-kinases (P13Ks) are a family of enzymes that regulate diverse biological functions in every cell type by generating phosphoinositide second- messenger molecules. P13Ks are involved in various cellular functions, including cell proliferation and survival, cell differentiation, intracellular trafficking, and immunity. As the activity of these phosphoinositide second messengers is determined by their phosphorylation state, the kinases and phosphatises that act to modify these lipids are central to the correct execution of intracellular signaling events.
• P13Ks phosphorylate lipids at the 3-hydroxyl residue of an inositol ring (Whitman et al., Nature 332:664 (1988)) to generate phosphorylated phospholipids (PIP3s), which act as second messengers recruiting kinases with lipid binding domains (including plekstrin homology (PH) regions), such as Akt and phosphoinositi de-dependent kinase- 1 (PDKl). Binding of Akt to membrane PIP3s causes the translocation of Akt to the plasma membrane, bringing Akt into contact with PDKl, which is responsible for activating Akt.
• PIP3s phosphorylated phospholipids
• the tumor- suppressor phosphatase PTEN (Phosphatase and Tensin homolog deleted on chromosome Ten) dephosphorylates PIP3 and therefore acts as a negative regulator of Akt activation.
• the P13Ks Akt and PDK1 are important in the regulation of many cellular processes including cell cycle regulation, proliferation, survival, apoptosis, and motility and are significant components of the molecular mechanisms of diseases such as cancer, diabetes, and immune inflammation (Vivanco et al., Nature Rev. Cancer 2:489 (2002); Phillips et al, Cancer 83:41 (1998)).
• the P13K family is comprised of four different classes: Classes I, II, III, and IV.
• Classes I- III are lipid kinases and Class IV are serine/threonine protein kinases.
• the members of the Class I family of P13Ks are dimers of a regulatory and a catalytic subunit.
• the Class I family consists of four isoforms, determined by the 110 kDa catalytic subunits ⁇ , ⁇ , ⁇ , and ⁇ . See Engelman, J.A., Nat Rev Genet 7:606-619 (2006); Carnero, A., Curr Cancer Drug Targets 8: 187-198 (2008); and Vanhaesebroeck, B., Trends Biochem Sci 30: 194-204 (2005).
• Class I can be subdivided into two subclasses: Class la, formed by the combination of pllO ⁇ , ⁇ , and ⁇ , and a regulatory subunit (p85, p55 or p50); and Class lb, formed by pi 10 ⁇ and plOl regulatory subunits.
• Class la formed by the combination of pllO ⁇ , ⁇ , and ⁇ , and a regulatory subunit (p85, p55 or p50); and Class lb, formed by pi 10 ⁇ and plOl regulatory subunits.
• the delta ( ⁇ ) isoform of P13K is highly expressed in cells of hematopoietic origin, and strongly upregulated, and often mutated, in various hematologic malignancies.
• P13K and related protein kinase pathways have been published by various groups, including, Liu et al , Nature Reviews Drug Discovery 8:627-644 (2009); Nathan et al, Mol. Cancer Ther. 8(1) (2009); and Marone et al. , Biochimica et Biophysica Acta 1784: 159-185 (2008).
• Two known inhibitors of P13K, LY294002 and Wortmannin are non-specific P13K inhibitors as they do not distinguish the four members of Class I P13K: ⁇ , ⁇ , ⁇ , and ⁇ .
• a number of P13K inhibitors have entered clinical trials for the treatment of cancers, and various types of cancers (including breast cancer, non-small cell lung cancer (NSCLC), and hematological cancers), are being considered as areas of therapeutic interest.
• NSCLC non-small cell lung cancer
• P13K-delta selective inhibitor is Idelalisib (trade name
• Zydelig® which was approved by the U.S. FDA in 2014 for the treatment of relapsed CLL (in combination with Rituxan®; see, Furman, R.R. et al., N. Eng. J. Med. 370:997- 1007 (2014)), relapsed follicular B-celi non-Hodgkin lymphoma (FL). and relapsed small lymphocytic lymphoma (SLL), another type of non-Hodgkin lymphoma.
• Zydelig® full prescribing information (Giiead Sciences), idelalisib has a unique and limiting toxicity profile including immune mediated colitis (grade 3 > 5%), pneumonitis (grade 3 > 4%), and transaminitis (grade 3 > 8%). Therefore the FDA's approval of Zydelig® comes with a boxed warning noting the possibility of fatal and serious toxicities including hepatic, severe diarrhea, colitis, pneumonitis and intestinal perforation. Id.
• duvelisib targets both P13K delta and gamma, at the dose under development (25 mg twice daily), it primarily inhibits just the delta isoform.
• Another P13K-delta selective inhibitor is ACP-319 (previously AMG-319). See, Lanasa, M.C. et ctl, Blood 122: Abstract 678 (2013).
• ACP-319 is currently in development by Acerta Pharma B. V
• ME-401 is a new oral P13K-delta selective inhibitor in development by MEI Pharma. See, Moreno, O.
• INCB-50465 is another P13K-delta selective inhibitor in development by Incyte Corporation that is in Phase I/II clinical trials for the treatment of B-cell malignancies. See, Forero-Torres, A. et al, "Preliminary safety, efficacy, and pharmacodynamics of a highly selective PI3K5 inhibitor, INCB050465, in patients with previously treated B-cell malignancies” (Abstract #CT056), presented at the AACR Annual Meeting, New Orleans (April 16-20, 2016).
• At least one P13K-delta selective inhibitor is used in the
• the P13K-delta selective inhibitor that is used in combination with the anti-CD20 antibodies and BTK inhibitors, described herein is a compound of formula A:
• the compound of Formula A is selected from one or more of,
• a P13K-delta inhibitor of formula A can be prepared using the general synthetic methods as disclosed in International Patent Appl. Publ. No. WO 201 1/055215 A2 and
• the P13K-delta inhibitor is administered to a subject daily at a dosage from: about 200 mg to about 1200 mg, about 400 mg to about 1000 mg, about
• the P 13K-delta inhibitor of Formula A is (S)-2-(l -(4- ainino-3-(3-fluoro-4-isopropoxyphenyl)-lH-pyrazolo[3,4-d]pyrimidin-l -yl)ethyl)-6- fluoro-3-(3-fluorophenyl)-4H-chromen-4-one.
• the P13K-delta inhibitor of Formula A is (S)-2-(l-(4- ainino-3-(3-fluoro-4-isopropoxyphenyl)-lH-pyrazolo[3,4-d]pyrimidin-l -yl)ethyl)-6- fluoro-3-(3-fluorophenyl)-4H-chromen-4-one p-toluenesulfonic acid (PTSA) salt (also known as (S)-2-(l -(4-amino-3-(3-fluoro-4-isopropoxyphenyl)-lH-pyrazolo [3, 4-d] pyrimidin-l-yl)-ethyl)-6-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one 4- methylbenzenesulfonate, TGR-1202, and umbralisib).
• PTSA p-toluenesulfonic acid
• TGR-1202 (or umbralisib) is a next generation P13K-delta inhibitor with a unique molecular structure and activity profile distinct from other P13K-delta inhibitors in development, including: (1) greater selectivity to the delta isoform of P13K; (2) a a prolonged half-life that enables once-daily dosing; and (3) a differentiated safety profile from other PI 3K-delta inhibitors, notably with respect to hepatic toxicity and colitis.
• TGR-1202 was evaluated in a single-agent Phase I dose-escalation study in
• TGR-1202 a novel once-daily PI3K5 inhibitor, in patients with relapsed or refractory hematologic malignancies
• J. Clinical Oncology (ASCO Annual Meeting Abstracts) 32 (15): 2513 (2014) The study reported that TGR-1202 was well-tolerated in patients with relapsed or refractory hematologic malignancies, with no reported hepatic toxicity and signs of clinical activity at doses > 800 mg each day. Id.
• the favorable safety profile of TGR-1202 compared to prior inhibitors has also been demonstrated in long- term follow up.
• the TGR-1202 is administered at a dose from about 400 mg to about 1200 mg per day. In some embodiments, the TGR-1202 is administered at a dose of about 400 mg per day. In some embodiments, the TGR-1202 is administered at a dose of about 600 mg per day. In some embodiments, the TGR-1202 is administered at a dose of about 800 mg per day.
• the P13K-delta inhibitor is formulated for oral
• the P13K-delta inhibitor is TGR-1202 and it is formulated for daily oral administration. In certain embodiments, TGR-1202 is administered in a fed-state.
• CD20 is a hydrophobic transmembrane phosphoprotein that is expressed
• CD20 is also strongly and homogeneously expressed in most mature B-cell malignancies, including, for example, most non-Hodgkin's B-cell lymphomas (NHL) and B-type Chronic Lymphocytic Leukemia's (B-CLL).
• NHL non-Hodgkin's B-cell lymphomas
• B-CLL B-type Chronic Lymphocytic Leukemia's
• the CD20 antigen is not expressed on haematopoietic stem cells or on plasmocytes.
• Anti-CD20 monoclonal antibodies have been, and continue to be, developed for the treatment of B-cell diseases.
• the chimeric anti-CD20 monoclonal antibody rituximab (Rituxan®) has become the standard therapy for many CD20-positive B-cell lymphomas and was the first mAb approved for any oncology indication. Demarest, SJ et al, mAbs 3:338-351 (2011). However, there are a substantial number of patients who are refractory to treatment with rituximab or who develop resistance in the course of prolonged treatment with rituximab (used as a single agent or even in combination with
• anti-CD20 antibodies and antigen-binding fragments thereof can be used in combination with a P13K-delta selective inhibitor and a BTK inhibitor to treat B-cell proliferative disorders, such as B-cell malignancies. More than one anti-CD20 antibody can be used in the methods and kits of the present invention.
• ublituximab ofatumumab (HuMax; Intracel), ocrelizumab, veltuzumab, GA101 (obinutuzumab), AME-133v (Applied Molecular Evolution), ocaratuzumab (Mentrik Biotech), PR0131921, tositumomab, ibritumomab-tiuxetan, hA20 (Immunomedics, Inc.), BLX-301 (Biolex Therapeutics), Reditux (Dr. Reddy's Laboratories), and PRO70769 (described in WO2004/056312).
• Rituximab is a genetically engineered chimeric murine/human monoclonal
• Rituximab is the antibody called "C2B8" in U.S. Patent No. 5,736,137.
• the amino acid sequence of rituximab antibody and exemplary methods for its production via recombinant expression in Chinese Hamster Ovary (CHO) cells are disclosed in U.S. Patent No. 5,736,137, which is herein incorporated by reference in its entirety.
• Rituximab is commercially available as
• Ofatumumab is an anti-CD20 IgGlK human monoclonal antibody. Studies
• Ublituximab also known as UTX, TG-1101, TGTX-1101, UtuxinTM, LFB-R603,
• TG20, EMAB603 is a chimeric monoclonal antibody targeting a unique epitope on the CD20 antigen and that has been glycoengineered for enhanced affinity for all variants of Fey RJIIa receptors, thereby demonstrating greater antibody-dependent cellular cytotoxicity ("ADCC") activity than rituximab and ofatumab.
• ADCC antibody-dependent cellular cytotoxicity
• Ublituximab is also described in U.S. Patent No. 9,234,045.
• Ublituximab was engineered for potent activity, exhibiting a unique primary amino acid sequence and allowing a low fucose content, designed to induce superior ADCC.
• Responses with single agent ublituximab were observed in rituximab refractory patients. Id.
• the anti-CD20 antibody used in the methods (and kits) described herein is ublituximab (also known as TG-1101) or an anti-CD20 antibody that binds to the same epitope as ublituximab.
• the anti-CD20 antibody is ublituximab.
• the ublituximab comprises the VH CDRl, CDR2, and CDR3 region of sequences SEQ ID NOS: 1, 2, and 3, and the VL CDRl, CDR2, and CDR3 region of sequences SEQ ID NOS: 6, 7, and 8.
• the ublituximab comprises the VH of SEQ ID NO: 4 and the VL of SEQ ID NO: 9.
• Ublituximab comprises the antibody sequences provided below:
• VH Variable heavy chain (VH) CDR1 : Gly Tyr Thr Phe Thr Ser Tyr Asn (SEQ ID NO: 1)
• VH Variable heavy chain (VH) CDR2: He Tyr Pro Gly Asn Gly Asp Thr (SEQ ID NO:2)
• VH Variable heavy chain (VH) CDR3: Ala Arg Tyr Asp Tyr Asn Tyr Ala Met Asp Tyr (SEQ ID NO:3)
• VH Variable heavy chain
• VP CDR1 Ser Ser Val Ser Tyr (SEQ ID NO:6)
• V Variable light chain (V ) CDR2: Ala Thr Ser (SEQ ID NO: 7)
• VL Variable light chain
• ublituximab is administered at a dose from: about 450 mg to about 1200 mg, about 600 to about 1200 mg, about 600 to about 1000 mg, about 600 to about 900 mg, about 600 mg, about 700 mg, about 800 mg, or about 900 mg. In certain embodiments, the ublituximab is administered at a dose of about 900 mg.
• Ublituximab may be administered about once every 1 to 9 weeks, about once every week, about twice every week, about once every 2 weeks, about once every 3 weeks, about once every 4 weeks, about once every 5 weeks, about once every 6 weeks, about once every 7 weeks, about once every 8 week, or about once every 9 weeks.
• dosage of ublituximab and/or frequency of administering ublituximab may change during the course of therapy (lowered or increased) depending upon the patient's clinical response, side effects, etc. . . .
• the ublituximab is administered intravenously, preferably by infusion.
• the anti-CD20 antibody or fragment thereof binds to the same epitope as ublituximab. In some embodiments, the anti-CD20 antibody or fragment thereof binds to a sequence comprising amino acids N153-S179 of CD20. In some embodiments, the anti-CD20 antibody or fragment thereof binds to a discontinuous epitope in amino acids N153-S179 of CD20.
• the anti-CD20 antibody or fragment thereof binds to CD20 with an affinity characterized by a dissociation constant KD of less than about 10 "7 M, less than about 10 "8 M or less than about 10 "9 M. In some embodiments, the anti-CD20 antibody or fragment thereof binds to CD20 with an affinity characterized by a dissociation constant KD of 10 "10 to 10 "9 M. In some embodiments the anti-CD20 antibody or fragment thereof binds to CD20 with an affinity characterized by a dissociation constant KD of 0.7 x 10 "9 M.
• the term “about” allows for the degree of variation inherent in the methods utilized for measuring antibody affinity. For example, depending on the level of precision of the instrumentation used, standard error based on the number of samples measured, and rounding error, the term “about 10-2 M" might include, for example, from 0.05 M to 0.005 M.
• the anti-CD20 antibody exhibits a high affinity to Fc- gammaRIII (CD 16).
• Fc- gammaRIII CD 16
• such antibodies are not displaced by IgG polyclonal antibodies, especially by IgG present in blood serum.
• the antibody binds to CD16 (e.g., expressed on a macrophage) with an affinity of at least 2xl0 6 M "1 , at least 2xl0 7 M _1 , 2xl0 8 M _1 or 2xl0 7 M _1 , e.g., as determined by Scatchard analysis or BIAcore technology (Label-free surface plasmon resonance based technology).
• the anti-CD20 antibody is glycoengineered.
• a "glycoengineered" anti-CD20 antibody means that the sugar molecules (N- glycan) in the Fc region of the antibody have been altered or engineered, either genetically, enzymatically, chemically, or selected for during the manufacturing process, in order to, e.g., increase the affinity of the antibody for Fc receptors on effector cells and/or to reduce its specific carbohydrate content in its Fc region.
• the anti-CD20 antibody exhibits a glycosylation partem characterized by low fucose content in its Fc region.
• a composition comprises anti-CD20 antibodies in which the antibodies comprise N- glycoside-linked sugar chains bound on the Fc-gamma glycosylation site (Asn 297, EU numbering), wherein among the N-glycoside-linked sugar chains of all the antibodies of the composition, the fucose content is less than 65%, less than 60%, less than 55%, less than 50%, less than 45%, or less than 40%. In some embodiments, among the N- glycoside-linked sugar chains of all the antibodies of the composition, the fucose content is 15 to 45% or 20 to 40%.
• the anti-CD20 antibody exhibits potent in vitro antibody- dependent cellular cytotoxicity (ADCC) and can be said to be "ADCC-optimized”.
• ADCC antibody-dependent cellular cytotoxicity
• the anti-CD20 antibody produces an ADCC plateau of at least about 10%, at least about 15%, at least about 20%, at least about 25%, or at least about 30% at a concentration of 50 ng/ml using natural killer (NK) cells from healthy donors.
• NK natural killer
• the anti-CD20 antibody produces an ADCC plateau at about 35% at a concentration of 50 ng/ml using NK cells from healthy donors.
• the anti-CD20 antibody can decrease NF-kappa-B activity.
• the anti-CD20 antibody can decrease SNAIL expression. In some embodiments, the anti-CD20 antibody can increase RKIP activity. In some embodiments, the anti-CD20 antibody can increase PTEN activity. In some embodiments, the anti- CD20 antibody can increase sensitization of a cell to TRAIL-apoptosis.
• the anti-CD20 antibody is Fc-gamma-RIIIA (CD 16)
• the anti- CD20 antibody is modified on Asn 297 (EU numbering) with N-glycosylations of the bi- antennary and/or oligomannoside type as described in U.S. Patent No. 7,931,895.
• the anti-CD20 antibody has high ADCC activity.
• Methods of producing antibodies with high ADCC activity are provided, for example, in U.S. Patent No. 7,713,524, which is herein incorporated by reference in its entirety.
• an isolated antibody or antigen-binding fragment, variant, or derivative thereof comprises, consists essentially of, or consists of an immunoglobulin heavy chain variable domain (VH domain), wherein at least one (i.e., one, two, or three) of the CDRs of the VH domain has an amino acid sequence that is at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or identical to the CDR1, CDR2, or CDR3 region of sequences SEQ ID NO: 1, 2, or 3, wherein an antibody or antigen-binding fragment thereof comprising the VH domain can specifically or preferentially bind to CD20.
• VH domain immunoglobulin heavy chain variable domain
• an isolated antibody or antigen-binding fragment, variant, or derivative thereof comprises, consists essentially of, or consists of an immunoglobulin heavy chain variable domain (VH domain), wherein at least one (i.e., one, two, or three) of the CDRs of the VH domain has an amino acid sequence identical, except for 1, 2, 3, 4, or 5 conservative amino acid substitutions, to the CDR1, CDR2 or CDR3 region of sequences SEQ ID NO: l, 2, or 3, wherein an antibody or antigen-binding fragment, variant, or derivative thereof comprising the VH domain can specifically or preferentially bind to CD20.
• VH domain immunoglobulin heavy chain variable domain
• an isolated antibody or antigen-binding fragment, variant, or derivative thereof comprises, consists essentially of, or consists of a VH domain that has an amino acid sequence that is at least 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to a VH amino acid sequence of SEQ ID NO:4, wherein an antibody or antigen-binding fragment, variant, or derivative thereof comprising the VH domain can specifically or preferentially bind to CD20.
• an isolated antibody or antigen-binding fragment, variant, or derivative thereof comprises, consists essentially of, or consists of a heavy chain that has an amino acid sequence that is at least 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to a heavy chain amino acid sequence comprising SEQ ID NOs: 4 and 5, wherein an antibody or antigen-binding fragment, variant, or derivative thereof comprising the heavy chain can specifically or preferentially bind to CD20.
• an isolated antibody or antigen-binding fragment, variant, or derivative thereof comprises, consists essentially of, or consists of an immunoglobulin light chain variable domain (VL domain), wherein at least one (i.e., one, two, or three) of the CDRs of the VL domain has an amino acid sequence that is at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or identical to the CDR1, CDR2, or CDR3 region of sequences SEQ ID NO:6, 7, or 8, wherein an antibody or antigen-binding fragment thereof comprising the VL domain can specifically or preferentially bind to CD20.
• VL domain immunoglobulin light chain variable domain
• an isolated antibody or antigen-binding fragment, variant, or derivative thereof comprises, consists essentially of, or consists of an immunoglobulin light chain variable domain (VL domain), wherein at least one (i.e., one, two, or three) of the CDRs of the VL domain has an amino acid sequence identical, except for 1, 2, 3, 4, or 5 conservative amino acid substitutions, to the CDR1, CDR2, or CDR3 region of SEQ ID NO:6, 7, or 8, wherein an antibody or antigen-binding fragment, variant, or derivative thereof comprising the VL domain can specifically or preferentially bind to CD20.
• VL domain immunoglobulin light chain variable domain
• an isolated antibody or antigen-binding fragment, variant, or derivative thereof comprises, consists essentially of, or consists of a VL domain that has an amino acid sequence that is at least 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to a VL amino acid sequence of SEQ ID NO:9, wherein an antibody or antigen-binding fragment, variant, or derivative thereof comprising the VL domain can specifically or preferentially bind to CD20.
• an isolated antibody or antigen-binding fragment, variant, or derivative thereof comprises, consists essentially of, or consists of a light chain that has an amino acid sequence that is at least 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to a light chain amino acid sequence comprising SEQ ID NOs: 9 and 10, wherein an antibody or antigen-binding fragment, variant, or derivative thereof comprising the light chain can specifically or preferentially bind to CD20.
• an isolated antibody or antigen-binding fragment, variant, or derivative thereof comprises, consists essentially of, or consists of an immunoglobulin heavy chain variable domain (VH domain) and an immunoglobulin light chain variable domain (VL domain), wherein at least one (i.e., one, two, or three) of the CDRs of the VH domain has an amino acid sequence that is at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or identical to the CDRl, CDR2, or CDR3 region of sequences SEQ ID NO: l, 2, or 3, wherein at least one (i.e., one, two, or three) of the CDRs of the VL domain has an amino acid sequence that is at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or identical to the CDRl, CDR2 or CDR3 region of sequences SEQ ID NO:6, 7, or 8, and wherein an antibody or antigen-binding
• an isolated antibody or antigen-binding fragment, variant, or derivative thereof comprises, consists essentially of, or consists of an immunoglobulin heavy chain variable domain (VH domain), and an immunoglobulin light chain variable domain (VL domain), wherein at least one (i.e., one, two, or three) of the CDRs of the VH domain has an amino acid sequence identical, except for 1, 2, 3, 4, or 5 conservative amino acid substitutions, to the CDRl, CDR2, or CDR3 region of sequences SEQ ID NO: 1, 2, or 3, wherein at least one (i.e., one, two, or three) of the CDRs of the VL domain has an amino acid sequence identical, except for 1, 2, 3, 4, or 5 conservative amino acid substitutions, to the CDRl, CDR2 or CDR3 region of SEQ ID NO:6, 7, or 8, and wherein an antibody or antigen-binding fragment, variant, or derivative thereof comprising the VH and VL can specifically or preferentially bind to CD20.
• VH domain immunoglobulin heavy chain
• the anti-CD20 antibody or antigen-binding fragment, variant, or derivative thereof comprises the VH CDRl, CDR2, and CDR3 region of sequences SEQ ID NO: l, 2, and 3, and the VL CDRl, CDR2, and CDR3 region of sequences SEQ ID NO:6, 7, and 8.
• an isolated antibody or antigen-binding fragment, variant, or derivative thereof comprises, consists essentially of, or consists of a VH domain and a VL domain, wherein the VH has an amino acid sequence that is at least 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to a VH amino acid sequence of SEQ ID NO:4, wherein the VL domain that has an amino acid sequence that is at least 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to a VL amino acid sequence of SEQ ID NO:9, and wherein an antibody or antigen-binding fragment, variant, or derivative thereof comprising the VH domain and VL domain can specifically or preferentially bind to CD20.
• an isolated antibody or antigen-binding fragment, variant, or derivative thereof comprises, consists essentially of, or consists of a heavy chain and a light chain, wherein the heavy chain has an amino acid sequence that is at least 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to a heavy chain amino acid sequence comprising SEQ ID NOs: 4 and 5, wherein the light chain has an amino acid sequence that is at least 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to a light chain amino acid sequence comprising SEQ ID NOs: 9 and 10, and wherein an antibody or antigen-binding fragment, variant, or derivative thereof comprising the heavy chain and light chain can specifically or preferentially bind to CD20.
• the anti-CD20 antibody is ublituximab.
• the anti-CD20 antibody is EMAB603 (see
• the anti-CD20 antibody is produced in the rat hybridoma
• YB2/0 cell line (cell YB2/3HL.P2.G11.16Ag.20, registered at the American Type Culture Collection under ATCC number CRL-1662).
• CD20 and retaining the desired activity depends on a number of factors.
• ionizable amino and carboxyl groups are present in the molecule, a particular polypeptide can be obtained as an acidic or basic salt, or in neutral form. All such preparations that retain their biological activity when placed in suitable environmental conditions are included in the definition of anti-CD20 antibodies as used herein.
• the primary amino acid sequence of the antibody can be augmented by derivatization using sugar moieties (glycosylation) or by other supplementary molecules such as lipids, phosphate, acetyl groups and the like. It can also be augmented by conjugation with saccharides. Certain aspects of such augmentation are accomplished through post-translational processing systems of the producing host; other such modifications can be introduced in vitro.
• modifications are included in the definition of an anti-CD20 antibody used herein so long as the desired properties of the anti-CD20 antibody are not destroyed. It is expected that such modifications can quantitatively or qualitatively affect the activity, either by enhancing or diminishing the activity of the polypeptide, in the various assays. Further, individual amino acid residues in the chain can be modified by oxidation, reduction, or other derivatization, and the polypeptide can be cleaved to obtain fragments that retain activity. Such alterations that do not destroy the desired properties (e.g., binding specificity for CD20) do not remove the polypeptide sequence from the definition of anti-CD20 antibodies of interest as used herein.
• desired properties e.g., binding specificity for CD20
• polypeptide variants are polypeptide variants.
• an anti-CD20 binding molecule e.g., an antibody or antigen-binding fragment, variant, or derivative thereof
• one of skill in the art can readily determine which modifications to the native protein's nucleotide or amino acid sequence will result in a variant that is suitable for use as a therapeutically active component of a pharmaceutical composition.
• mutations only in framework regions or only in CDR regions of an antibody molecule. Introduced mutations can be silent or neutral missense mutations, i.e., have no, or little, effect on an antibody's ability to bind antigen. These types of mutations can be useful to optimize codon usage, or improve a hybridoma's antibody production. Alternatively, non-neutral missense mutations can alter an antibody's ability to bind antigen. The location of most silent and neutral missense mutations is likely to be in the framework regions, while the location of most non-neutral missense mutations is likely to be in CDR, though this is not an absolute requirement. One of skill in the art would be able to design and test mutant molecules with desired properties such as no alteration in antigen-binding activity or alteration in binding activity (e.g., improvements in antigen-binding activity or change in antibody specificity).
• the encoded protein can routinely be expressed and the functional and/or biological activity of the encoded protein, (e.g., ability to immunospecifically bind at least one epitope of a CD20 polypeptide) can be determined using techniques described herein or by routinely modifying techniques known in the art.
• the anti-CD20 antibodies comprise at least one optimized complementarity-determining region (CDR).
• CDR complementarity-determining region
• Anti-CD20 activity can include, e.g., activity which modulates one or more of the following activities associated with CD20, e.g., the ability to induce apoptosis of B-cells, the ability to induce ADCC against B-cells (e.g., CLL cells), the ability to inhibit NF-kappaB activity, the ability to inhibit Snail expression, the ability to de-repress RKIP, the ability to de-repress PTEN, the ability to sensitize a tumor cell to TRAIL-apoptosis or any other activity associated with CD20.
• activities are described, for example, in Baritaki, S. et al., Int. J. Oncol.
• the modifications can involve replacement of amino acid residues within the CDR such that an anti-CD20 antibody retains specificity for the CD20 antigen and has improved binding affinity and/or improved anti-CD20 activity.
• the constant region domains has been deleted or otherwise altered so as to provide desired biochemical characteristics such as reduced effector functions, the ability to non-covalently dimerize, increased ability to localize at the site of a tumor, reduced serum half-life, or increased serum half-life when compared with a whole, unaltered antibody of approximately the same immunogenicity.
• certain antibodies are domain deleted antibodies which comprise a polypeptide chain similar to an immunoglobulin heavy chain, but which lack at least a portion of one or more heavy chain domains.
• one entire domain of the constant region of the modified antibody will be deleted, for example, all or part of the CH2 domain will be deleted.
• the Fc In certain anti-CD20 antibodies or antigen-binding fragments thereof, the Fc
• modifications of the constant region can be used to modify disulfide linkages or oligosaccharide moieties that allow for enhanced localization due to increased antigen specificity or antibody flexibility.
• the resulting physiological profile, bioavailability and other biochemical effects of the modifications can easily be measured and quantified using well know immunological techniques without undue
• an anti-CD20 antibody or antigen-binding fragment thereof will not elicit a deleterious immune response in the animal to be treated, e.g., in a human.
• anti-CD20 antibodies or antigen-binding fragments thereof can be modified to reduce their immunogenicity using art-recognized techniques.
• antibodies can be humanized, primatized, deimmunized, or chimeric antibodies can be made. These types of antibodies are derived from a non-human antibody, typically a murine or primate antibody, that retains or substantially retains the antigen-binding properties of the parent antibody, but which is less immunogenic in humans.
• CDRs complementarity determining regions
• Modified forms of antibodies or antigen-binding fragments thereof can be made from whole precursor or parent antibodies using techniques known in the art.
• Anti-CD20 antibodies or antigen-binding fragments thereof can be made or
• antibody molecules or fragments thereof are "recombinantly produced,” i.e., are produced using recombinant DNA technology.
• Anti-CD20 antibodies or fragments thereof can be generated by any suitable method known in the art including generation of polyclonal antibodies or preparation of monoclonal antibodies, e.g., through hybridoma or phage display.
• a variety of host-expression vector systems can be utilized to express antibody molecules.
• the host cell can be co-transfected with two expression vectors, the first vector encoding a heavy chain derived polypeptide and the second vector encoding a light chain derived polypeptide.
• the two vectors can contain identical selectable markers which enable equal expression of heavy and light chain polypeptides.
• a single vector can be used which encodes both heavy and light chain polypeptides. In such situations, the light chain is advantageously placed before the heavy chain to avoid an excess of toxic free heavy chain (Proudfoot, Nature 322:52 (1986); Kohler, Proc. Natl. Acad. Sci. USA 77:2197 (1980)).
• the host cell can also be transfected with a single vector encoding a heavy chain derived polypeptide and a light chain derived polypeptide.
• the coding sequences for the heavy and light chains can comprise cDNA or genomic DNA.
• the expression vector or vectors can be transferred to a host cell by conventional techniques and the transfected cells are then cultured by conventional techniques to produce an antibody.
• host cells containing a polynucleotide encoding an antibody, or a heavy or light chain thereof, operably linked to a heterologous promoter are provided.
• vectors encoding both the heavy and light chains can be co-expressed in the host cell for expression of the entire immunoglobulin molecule.
• Host-expression systems represent vehicles by which the coding sequences of interest can be produced and subsequently purified, but also represent cells which can, when transformed or transfected with the appropriate nucleotide coding sequences, express a CD20 antibody in situ.
• These include but are not limited to microorganisms such as bacteria (e.g. , E. coli, B. subtilis) transformed with recombinant bacteriophage DNA, plasmid DNA or cosmid DNA expression vectors containing antibody coding sequences; yeast (e.g., Saccharomyces, Pichia) transformed with recombinant yeast expression vectors containing antibody coding sequences; insect cell systems infected with recombinant virus expression vectors (e.g.
• baculovirus containing antibody coding sequences
• plant cell systems infected with recombinant virus expression vectors (e.g. , cauliflower mosaic virus, CaMV; tobacco mosaic virus, TMV) or transformed with recombinant plasmid expression vectors (e.g.
• Ti plasmid containing antibody coding sequences
• mammalian cell systems e.g., COS, CHO, BLK, 293, 3T3 cells harboring recombinant expression constructs containing promoters derived from the genome of mammalian cells (e.g., metallothionein promoter) or from mammalian viruses (e.g., the adenovirus late promoter; the vaccinia virus 7.5K promoter).
• Bacterial cells such as Escherichia coli, or eukaryotic cells, e.g., for the expression of whole recombinant antibody molecules, are used for the expression of a recombinant antibody molecule.
• mammalian cells such as Chinese hamster ovary cells (CHO)
• CHO Chinese hamster ovary cells
• a vector such as the major intermediate early gene promoter element from human cytomegalovirus
• the anti-CD20 antibody is produced in a host cell that is not a CHO cell.
• an antibody Once an antibody has been recombinantly expressed, it can be purified by any method known in the art for purification of an immunoglobulin molecule, for example, by chromatography (e.g., ion exchange, affinity, particularly by affinity for the specific antigen after Protein A, and sizing column chromatography), centrifugation, differential solubility, or by any other standard technique for the purification of proteins.
• chromatography e.g., ion exchange, affinity, particularly by affinity for the specific antigen after Protein A, and sizing column chromatography
• centrifugation e.g., centrifugation, differential solubility, or by any other standard technique for the purification of proteins.
• the anti-CD20 antibody is produced by a rat hybridoma cell line. In some embodiments, the anti-CD20 antibody is produced in YB2/0 (ATCC CRL-1662)
• the anti-CD20 antibody is ublituximab and it is
• the ublituximab is administered at a dose of about 900 mg about once every 1 to 9 weeks.
• BTK is a member of the Tec family of non-receptor tyrosine kinases and is a key signaling enzyme expressed in all hematopoietic cells types except T lymphocytes and natural killer (NK) cells.
• BTK is a key component of the B-cell signaling pathway linking cell surface B-cell receptor (BCR) stimulation to downstream intracellular responses.
• BCR cell surface B-cell receptor
• BTK regulates B-cell development, activation, signaling, and survival (Kurosaki, T., Curr Op lmm 72:276-281 (2000); Schaeffer, E M. and Schwartzberg, P.L., Curr Op lmm 12: 282-288 (2000)).
• BTK plays a role in a number of other hematopoetic cell signaling pathways, e.g., Toll like receptor (TLR) and cytokine receptor-mediated TNF- alpha production in macrophages, IgE receptor (FcepsilonRI) signaling in mast cells, inhibition of Fas/APO-1 apoptotic signaling in B-lineage lymphoid cells, and collagen- stimulated platelet aggregation.
• TLR Toll like receptor
• FcepsilonRI IgE receptor
• BTK functions as an important regulator of cell proliferation and cell survival in various B-cell malignancies.
• the BTK inhibitor is selected from the group consisting of l -[(3R)-3-[4-Amino-3-(4-phenoxyphenyl)-lH-pyrazolo[3,4-d]pyrimidin-l-yl]piperidin-l - yl]prop-2-en-l-one (Imbruvica®, ibrutinib, or PCI-32765); l-(R)-3-[4-amino-3-(4- phenoxyphenyl)-lH-pyrazolo[3,4-d]pyrirnidin-l-yl]piperidin-l -yl]-2,3,- dihy droxypropan- 1 -one (PCI-45227); 4- ⁇ 8-Amino-3-[(2S)- 1 -(2-butynoyl)-2- pyrrolidinyl]imidazo[l,5-a]pyrazin-l-
• the BTK inhibitor is 4- ⁇ 8-Amino-3-[(2S)-l-(2-butynoyl)-
• the BTK inhibitor is l-[(37?)-3-[4-Amino-3-(4- phenoxyphenyl)-lH-pyrazolo[3,4-(i]pyrimidin-l-yl]piperidin-l-yl]prop-2-en-l-one (ibrutinib). See, Imbruvica® full prescribing information (Pharmacyclics LLC and Janssen Biotech, Inc.). Also, see Honigsberg, L A. et al, PNAS 707: 13075-13080 (2010) and U.S. Patent Nos. 7,514,444, 8,697,711, 8,703,780, 8,088,309, and 8,088,781.
• the ibrutinib is administered once daily at a dosage from: about 200 to about 800 mg, about 400 to about 600 mg, about 400 mg, about 420 mg, about 440 mg, about 480 mg, about 500 mg, about 520 mg, about 540 mg, about 560 mg, about 580 mg, or about 600 mg.
• the ibrutinib is administered once daily at a dosage of about 420 mg or about 560 mg per day. In some embodiments, the ibrutinib is administered once daily at a dosage of about 420 mg per day. In some embodiments, the ibrutinib is administered once daily at a dosage of about 560 mg per day.
• the B-cell population whose proliferation is to inhibited is in a human subject.
• the human subject has a disease or disorder associated with excessive B-cell proliferation.
• the disease associated with excessive B-cell proliferation is cancer.
• a human subject has cancer.
• the cancer is a hematological malignancy.
• the hematological malignancy is lymphoma, leukemia, or myeloma.
• the hematological malignancy is selected from the group consisting of acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), multiple myeloma (MM), non-Hodgkin's lymphoma (NHL), mantle cell lymphoma (MCL), follicular lymphoma (FL), Waldenstrom's macroglobulinemia (WM), diffuse large B-cell lymphoma (DLBCL), marginal zone lymphoma (MZL), including extranodal and nodal MZL, hairy cell leukemia (HCL), Burkitt's lymphoma (BL), and Richter's transformation.
• ALL acute lymphocytic leukemia
• AML acute myeloid leukemia
• CLL chronic lymphocytic leukemia
• SLL small lymphocytic lymphoma
• MM multiple myelo
• the hematological malignancy is selected from the group consisting of chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), non-Hodgkin's lymphoma (NHL), mantle cell lymphoma (MCL), follicular lymphoma (FL), diffuse large B-cell lymphoma (DLBCL), and marginal zone lymphoma (MZL).
• CLL chronic lymphocytic leukemia
• SLL small lymphocytic lymphoma
• NHL non-Hodgkin's lymphoma
• MCL mantle cell lymphoma
• FL diffuse large B-cell lymphoma
• MZL marginal zone lymphoma
• the cancer overexpresses CD20.
• the cancer is refractory to chemotherapy.
• the cancer is refractory to non-TGR-1202 P13K-delta inhibitors.
• the cancer is refractory to non-ublituximab anti-CD20 antibodies.
• the cancer is refractory to any agent described herein, i.e., an anti-CD20 antibody, a P13K delta selective inhibitor, or a BTK inhibitor, when said agent was administered individually to a subject (i.e, used as a monotherapy).
• agent described herein i.e., an anti-CD20 antibody, a P13K delta selective inhibitor, or a BTK inhibitor
• the cancer is refractory to a BTK inhibitor.
• the cancer is refractory to ibrutinib.
• the cancer is refractory to rituximab.
• the cancer has relapsed.
• the human subject has one or more genetic mutations selected from the group consisting of 17p del, 1 lq del, p53, unmutated IgVH together with ZAP-70+ and/or CD38+, and trisomy 12.
• the agents i.e., i, ii, and iii, as described herein
• the agents (i.e., i, ii, and iii) to be used in combination in the methods described herein are administered to a subject sequentially, although, as noted below, the particular order of administration is not an issue.
• the agents (i.e., i and iii) which will be used in combination with the anti-CD20 antibody (i.e., ii) in the methods described herein, are administered to the subject simultaneously or sequentially.
• the agents (i.e., i and iii) are contained in the same pharmaceutical composition.
• the agents (i.e., i and iii) are formulated for oral administration.
• the combination of agents is sequentially administered in induction, consolidation, and/or maintenance regimens.
• two of the agents i, ii, or iii are administered together in order to induce a partial anti-tumor response, followed by administration of the third agent to enhance the anti-tumor response.
• a complete anti-tumor response is observed following administration of all agents (e.g., i, ii, and iii, as disclosed herein) to said subject.
• a subject administered any of the methods described herein achieves a complete response with minimal residual disease (MRD).
• a subject administered any of the methods described herein achieves a partial reponse (PR) when all three agents are administered in combination.
• a subject administered any of the methods described herein achieves a partial response (PR) or a complete response (CR) that is durable for at least two months.
• At least one of the agents, i, ii, and/or iii is administered in a maintenance therapy in order to keep the B-cell proliferative disorder from returning after successful treatment.
• the agent is administered in maintenance therapy for an extended period of time, e.g., until unmanageable toxicity, or disease progression occurs.
• the maintenance therapy ends when disease progression occurs.
• UTX infusion continues being administered every three months until disease progression.
• TGR- 1202 single agent therapy is administered daily until disease progression.
• ibrutinib single agent therapy is administered daily until disease progression.
• TGR-1202 and ibrutinib therapies are administered daily until disease progression.
• the methods described herein further comprises
• the at least one additional therapeutic agent is selected from the group consisting of mitotic inhibitors, alkylating agents, antimetabolites, anthracyclines, vinca alkaloids, plant alkaloids, nitrogen mustards, proteasome inhibitors, intercalating antibiotics, growth factor inhibitors, cell-cycle inhibitors, biological response modifiers, anti-hormones, angiogenesis inhibitors, anti- androgens, DNA interactive agents, purine analogues, topoisomerase I inhibitors, topoisomerase II inhibitors, tubulin interacting agents, hormonal agents, thymidilate synthase inhibitors, non-BTK and non-P13K-delta tyrosine kinase inhibitors, angiogenesis inhibitors, EGF inhibitors, VEGF inhibitors, CDK inhibitors, SRC inhibitors, c-Kit inhibitors, Herl/2 inhibitors, inhibitors of myc, anti-tumor antibodies, mono
• the at least one additional therapeutic agent is an anticancer agent selected from the group consisting of DNA interactive agents, such as cisplatin or doxorubicin; topoisomerase II inhibitors, such as etoposide; topoisomerase I inhibitors such as CPT-1 1 or topotecan; tubulin interacting agents, such as paclitaxel, docetaxel or the epothilones (for example ixabepilone), either naturally occurring or synthetic; hormonal agents, such as tamoxifen; thymidilate synthase inhibitors, such as 5- fluorouracil; and anti-metabolites, such as methotrexate; other tyrosine kinase inhibitors such as Iressa and OSI-774; angiogenesis inhibitors; EGF inhibitors; VEGF inhibitors; CDK inhibitors; SRC inhibitors; c-Kit inhibitors; Herl/2 inhibitors and monoclonal antibodies directed against growth factor receptors such as
• the at least one additional therapeutic agent is selected from the group consisting of a proteasome inhibitor, Bortezomib (Velcade ® ), Carfilzomib (PR-171), PR-047, disulfiram, lactacystin, PS-519, eponemycin, epoxomycin, aclacinomycin, CEP-1612, MG-132, CVT-63417, PS-341, vinyl sulfone tripeptide inhibitors, ritonavir, PI-083, (+/-)-7-methylomuralide, (-)-7-methylomuralide, lenalidomide, and combinations thereof.
• a proteasome inhibitor Bortezomib (Velcade ® ), Carfilzomib (PR-171), PR-047, disulfiram, lactacystin, PS-519, eponemycin, epoxomycin, aclacinomycin, CEP-1612, MG-132, CV
• the at least one additional therapeutic agent is a combination of chemotherapies, known to treat hematological malignancies, such as, e.g., "CHOP" (a combination including (i) cyclophosphamide such as Cytoxan, (ii) doxorubicin or other topoisomerase II inhibitors such as adriamycin, (iii) vincristine or other vincas such as Oncovin; and (iv) a steroid such as hydrocortisone or prednisolone); "R-CHOP” (a combination including rituxan, cyclophosphamide, doxorubicin, vincristine, and prednisone); "ICE” (a combination including ifosfamide, carboplatin, and etoposide); “R- ICE” (a combination including rituxan, ifosfamide, carboplatin, and etoposide); "R-
• any oncolytic agent that is routinely used in a cancer therapy context finds use in the therapeutic methods of the present disclosure.
• the U.S. Food and Drug Administration maintains a formulary of oncolytic agents approved for use in the United States. International counterpart agencies to the FDA maintain similar formularies.
• the "product labels" required on all U.S. approved chemotherapeutics describe approved indications, dosing information, toxicity data, and the like, for the exemplary agents.
• the combination of agents comprising a P13K-delta inhibitor, an anti-CD20 antibody, and a BTK inhibitor can be administered in any order or at any interval as determined by those skilled in the art.
• a P13K-delta inhibitor of formula A, ublituximab or an anti-CD20 antibody that binds to the same epitope as ublituximab, and a BTK inhibitor can be administered sequentially (in any order), simultaneously, or via any combination of sequential and simultaneous administrations.
• Any combination of a P13K-delta inhibitor of formula A, ublituximab or an anti-CD20 antibody that binds to the same epitope as ublituximab, and a BTK inhibitor can be administered in the same pharmaceutical compositions or in separate
• a P 13K-delta inhibitor of formula A and a BTK inhibitor can be administered in the same pharmaceutical composition.
• Administration of the combination of agents can be performed according to any number of desired intervals of minutes (e.g. , 0-60 minutes), hours (e.g. , 0-24 hours), days (e.g. , 0-7 days), and/or weeks (e.g. , 0-52 weeks), as can be decided and determined by one of skill in the art.
• the dosing can also vary over time, for example, starting with a once weekly dose for a period of time (e.g. , for 1, 2, 3, 4, 5, or 6 weeks) followed by dosing once every two weeks, once every three weeks, once every four weeks, once every five weeks, or once every six weeks.
• the P13K-delta selective inhibitor, the anti-CD20 antibody, and the BTK inhibitor that are to be used in combination in the methods of the invention can be formulated into pharmaceutical compositions for administration to mammals, including humans.
• the pharmaceutical compositions comprise pharmaceutically acceptable carriers, including, e.g., ion exchangers, alumina, aluminum stearate, lecithin, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium carboxymethylcellulose, polyacrylates, waxes, polyethylene-polyoxypropylene-block polymers, polyethylene glycol and wool fat
• agents to be used in combination in accordance with the methods of the invention can be administered by any suitable method, e.g., orally, parenterally, intraventricularly, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir.
• suitable method e.g., orally, parenterally, intraventricularly, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir.
• the mode of administration for each agent does not have to be the same.
• the P13K-delta inhibitor (e.g., TGR-1202) is
• the BTK inhibitor e.g., Ibrutinib
• the BTK inhibitor is administered orally.
• parenteral includes subcutaneous, intravenous,
• parenteral formulations can be a single bolus dose, an infusion, or a loading bolus dose followed with a maintenance dose. These compositions can be administered at specific fixed or variable intervals, e.g., once a day, or on an "as needed" basis.
• the anti-CD20 antibody ublituximab is administered intravenously (IV), preferably by infusion.
• compositions can be orally administered in an acceptable dosage form including, e.g., capsules, tablets, aqueous suspensions, or solutions. Certain pharmaceutical compositions also can be administered by nasal aerosol or inhalation. Such compositions can be prepared as solutions in saline, employing benzyl alcohol or other suitable preservatives, absorption promoters to enhance bioavailability, and/or other conventional solubilizing or dispersing agents.
• a specific dosage and treatment regimen for any particular patient will depend upon a variety of factors, including the particular therapeutic agents used, the patient's age, body weight, general health, sex, and diet, and the time of administration, rate of excretion, drug combination, and the severity of the disease being treated. In some cases, dosages may need to be modified based on scan or biopsy results. Judgment of such factors by medical caregivers is within the ordinary skill in the art. Dosage will also depend on the individual patient to be treated, the route of administration, the type of formulation, the characteristics of the compound used, tumor burden, and the desired effect. The amount used can be determined by pharmacological and pharmacokinetic principles well known in the art.
• the anti-CD20 antibody is ublituximab and it is
• the ublituximab is administered at a dose from: about 450 mg to about 1200 mg, about 600 to about 1200 mg, about 600 to about 1000 mg, about 600 to about 900 mg, about 600 mg, about 700 mg, about 800 mg, or about 900 mg.
• the ublituximab is administered at a dose of about 900 mg.
• Ublituximab may be administered about twice every week, about once every 1 to
• ublituximab is administered on day 1, 8, and 15 of cycle 1 and cycle 2 and day 1 on cycles 4, 6, 9, and 12, wherein each cycle is 28 days.
• a P13K-delta selective inhibitor of formula A is
• a dosage from: about 200 mg to about 1200 mg, about 400 mg to about 1000 mg, about 400 mg to about 800 mg, about 400 mg, about 500 mg, about 600 mg, about 700 mg, about 800 mg, about 900 mg, about 1000 mg, or about 1200 mg.
• the P 13K-delta selective inhibitor of formula A is (S)-2-(l-
• TGR-1202 (4-ainino-3-(3-fluoro-4-isopropoxyphenyl)-lH-pyrazolo[3,4-d]pyrimidin-l -yl)ethyl)-6- fluoro-3-(3-fluorophenyl)-4H-chromen-4-one PTSA salt (TGR-1202) and it is administered at a dose from about 400 mg to about 1200 mg per day. In some embodiments, the TGR-1202 is administered at a dose of about 400 mg per day. In some embodiments, the TGR-1202 is administered at a dose of about 600 mg per day. In some embodiments, the TGR-1202 is administered at a dose of about 800 mg per day.
• the BTK inhibitor is l -[(3i?)-3-[4-Amino-3-(4- phenoxyphenyl)-lH-pyrazolo[3,4-(i]pyrimidin-l-yl]piperidin-l -yl]prop-2-en-l -one (ibrutinib).
• the ibrutinib is administered once daily at a dosage from: about 200 to about 800 mg, about 400 to about 600 mg, about 400 mg, about 420 mg, about 440 mg, about 480 mg, about 500 mg, about 520 mg, about 540 mg, about 560 mg, about 580 mg, or about 600 mg.
• the ibrutinib is administered at a dose of about 420 mg per day or about 560 mg per day. In some embodiments, the ibrutinib is administered at a dose of about 420 mg per day. In some embodiments, the ibrutinib is administered at a dose of about 560 mg per day.
• the dosages of other non- ibrutinab BTK inhibitors that can be used in the methods of the invention can be routinely determined by those skilled in the art based on the scientific/medical literature.
• Supplementary active compounds can also be incorporated into the methods and kits of the present invention.
• an anti-CD20 antibody, a P13K-delta selective inhibitor, and a BTK inhibitor can be coformulated with and/or coadministered with one or more additional therapeutic agents.
• the methods and kits could be coformulated with anti-cancer agents such as DNA interactive agents, such as cisplatin or doxorubicin; topoisomerase II inhibitors, such as etoposide; topoisomerase I inhibitors such as CPT-11 or topotecan; tubulin interacting agents, such as paclitaxel, docetaxel or the epothilones (for example ixabepilone), either naturally occurring or synthetic; hormonal agents, such as tamoxifen; thymidilate synthase inhibitors, such as 5- fluorouracil; and anti-metabolites, such as methotrexate; other tyrosine kinase inhibitors such as Iressa and OSI-774; angiogenesis inhibitors; EGF inhibitors; VEGF inhibitors; CDK inhibitors; SRC inhibitors; c-Kit inhibitors; Herl/2 inhibitors and monoclonal antibodies directed against growth factor receptors such as erbitux (EGF)
• DNA interactive agents
• the additional active agent can also be a proteasome inhibitor, Bortezomib (V el cade ® ), Carfilzomib (PR-171), PR-047, disulfiram, lactacystin, PS-519, eponemycin, epoxomycin, aclacinomycin, CEP-1612, MG-132, CVT-63417, PS-341, vinyl sulfone tripeptide inhibitors, ritonavir, PI-083, (+/-)-7- methylomuralide, (-)-7-methylomuralide, lenalidomide (Revlimid®), or a combination thereof.
• a proteasome inhibitor Bortezomib (V el cade ® ), Carfilzomib (PR-171), PR-047, disulfiram, lactacystin, PS-519, eponemycin, epoxomycin, aclacinomycin, CEP-1612,
• kits comprising (a) at least one P13K-delta selective inhibitor, at least one anti-CD20 antibody, and at least one inhibitor of BTK; and (b) instruction for using a P13K-delta selective inhibitor in combination with an anti- CD20 antibody and an inhibitor of BTK.
• a kit comprising at least one P13K-delta selective inhibitor of formula A, at least one anti-CD20 antibody that is ublituximab or an antibody that binds to the same epitope as ublituximab, and at least one inhibitor of BTK.
• kits can include, for example, other compounds and/or compositions to treat B-cell malignancies known to those skilled in the art, a device(s) for administering the compounds and/or compositions, and written instructions in a form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals or biological products.
• a kit comprises (a) a P13K-delta selective inhibitor of formula A (e.g., TGR-1202), or a stereoisomer thereof, or a pharmaceutically acceptable salt, solvate, or prodrug thereof; ublituximab or an anti-CD20 antibody or fragment thereof that binds to the same epitope as ublituximab; and an inhibitor of BTK, and (b) instructions for using said P13K-delta selective inhibitor in combination with ublituximab or an anti-CD20 antibody or fragment thereof that binds to the same epitope as ublituximab and an inhibitor of BTK.
• formula A e.g., TGR-1202
• the inhibitor of BTK in the kit is ibrutinib. In some embodiments, the inhibitor of BTK in the kit is ibrutinib. In some
• the inhibitor of BTK in the kit is acalabrutimib.
• the P 13K-delta selective inhibitor in the kit is (S)-2-(l -(4- ainino-3-(3-fluoro-4-isopropoxyphenyl)-lH-pyrazolo[3,4-d]pyrimidin-l -yl)ethyl)-6- fluoro-3-(3-fluorophenyl)-4H-chromen-4-one.
• the P13K-delta selective inhibitor in the kit is (S)-2-(l-(4- ainino-3-(3-fluoro-4-isopropoxyphenyl)-lH-pyrazolo[3,4-d]pyrimidin-l -yl)ethyl)-6- fluoro-3-(3-fluorophenyl)-4H-chromen-4-one PTSA salt (TGR-1202, also known as umbralisib).
• the kit further comprises ublituximab or an anti-CD20 antibody or fragment thereof that binds to the same epitope as ublituximab.
• the kit further comprises ublituximab.
• kits comprising (a) a P13K-delta selective inhibitor of formula A, an anti-CD20 antibody, a BTK inhibitor, or a combination thereof; and (b) an additional anti-cancer agent.
• the kit comprises TGR-1202, ublituximab, and ibrutinib or another inhibitor of BTK (as described herein), and a chemotherapeutic agent selected from the group consisting of DNA interactive agents, such as cisplatin or doxorubicin; topoisomerase II inhibitors, such as etoposide;
• topoisomerase I inhibitors such as CPT-11 or topotecan
• tubulin interacting agents such as paclitaxel, docetaxel or the epothilones (for example ixabepilone), either naturally occurring or synthetic
• hormonal agents such as tamoxifen; thymidilate synthase inhibitors, such as 5-fluorouracil
• anti-metabolites such as methotrexate
• other tyrosine kinase inhibitors such as Iressa and OSI-774
• angiogenesis inhibitors EGF inhibitors; VEGF inhibitors; CDK inhibitors; SRC inhibitors; c-Kit inhibitors
• Herl/2 inhibitors and monoclonal antibodies directed against growth factor receptors such as erbitux (EGF) and herceptin (Her2); and other protein kinase modulators.
• EGF erbitux
• Her2 herceptin
• Combinations of a P13K-delta selective inhibitor of Formula A, ubltuximab or an anti-CD20 antibody that binds the same epitope as ublituximab, and a BTK inhibitor can be used in methods of treating B-cell proliferative diseases (such as B-cell malignancies) in a subject.
• a P13K-delta selective inhibitor of Formula A can be used in the manufacture of a medicament for the treatment of a B-cell proliferative disorder, wherein the P13K-delta selective inhibitor of Formula A is to be administered in combination (e.g., sequentially or simultaneously) with an anti-CD20 antibody that is ublituximab or an antibody that binds to the same epitope as ublituximab, and a BTK inhibitor.
• an anti-CD20 antibody can be used in the manufacture of a medicament for the treatment of a B-cell proliferative disorder, wherein the anti-CD20 antibody is to be administered in combination (e.g., sequentially or simultaneously) with a P13K-delta selective inhibitor of Formula A and a BTK inhibitor.
• the anti-CD20 antibody is to be administered in combination (e.g., sequentially or simultaneously) with a P13K-delta selective inhibitor of Formula A and a BTK inhibitor.
• the anti-CD20 antibody is ublituximab.
• the P13K- delta selective inhibitor is TGR-1202.
• the anti-CD20 antibody is ublituximab and the P13K-delta selective inhibitor is TGR-1202.
• the invention further provides a method of inhibiting P13K-delta isoform and/or
• CD20, and/or BTK in a subject by administering to the subject an effective amount of the agents of the present invention in combination.
• the invention further provides a method of treating, preventing, and/or inhibiting a P13K-delta-mediated disease, disorder or condition and/or a CD20-mediated disease, disorder, or condition (such as cancer or other proliferative disease or disorder) and/or a BTK-mediated disease, disorder, or condition in a patient by administering to the a patient an effective amount of the agents of the present invention in combination.
• the invention further provides a method of treating a P13K-delta isoform- and/or
• CD20- or BTK-associated disease, disorder or condition in a patient by administering to the patient an effective amount of the agents of the present invention in combination.
• the amount of the agents administered in combination is sufficient to treat a P13K-delta isoform- and/or CD20- and/or BTK-associated disease, disorder, or condition by selective inhibition of P13K-delta and/or CD20 and/or BTK.
• the invention further provides a method of treating a B-cell proliferative disease by administering to a patient in need of such treatment an effective amount of at least one P13K delta selective inhibitor, at least one anti-CD20 antibody, and at least one BTK inhibitor.
• the anti-CD20 antibody is ublituximab.
• the P13K-delta selective inhibitor is TGR-1202.
• the BTK inhibitor is ibrutinib.
• the anti-CD20 antibody is ublituximab and the P13K-delta selective inhibitor is TGR-1202.
• the anti-CD20 antibody is ublituximab
• the P13K-delta selective inhibitor is TGR-1202
• the BTK inhibtor is ibrutinib.
• the invention further provides a method of treating a B-cell proliferative disease by administering to a patient in need of such treatment an effective amount of at least one P13K delta selective inhibitor of formula A, at least one anti-CD20 antibody that is ublituximab or an antibody that binds to the same epitope as ublituximab, and at least one BTK inhibitor of the present invention.
• the amounts of the agents administered in combination are sufficient to treat the B-cell proliferative disease by selective inhibition of P13K-delta, and/or inhibition of CD20, and/or inhibition of BTK.
• the B-cell proliferative disorder is a B- cell malignancy (e.g., lymphoma, leukemia, or myeloma).
• the anti- CD20 antibody is ublituximab.
• the P13K-delta selective inhibitor is TGR-1202.
• the BTK inhibitor is ibrutinib.
• the anti-CD20 antibody is ublituximab and the P13K-delta selective inhibitor is TGR-1202.
• the anti-CD20 antibody is ublituximab
• the P13K-delta selective inhibitor is TGR-1202
• the BTK inhibtor is ibrutinib.
• the invention further provides a method for treating a B-cell proliferative disease by administering to a patient in need of such treatment an effective amount of a combination of the agents of the present invention, in further combination
• the amount of the P13K-delta selective inhibitor of Formula A administered is sufficient to treat (or facilitate treatment of) the B-cell proliferative disease by selective inhibition of P 13K-delta.
• the combinations of the agents of the present invention are particularly useful in the treatment of a variety of hematological cancers, such as, but not limited to, e.g., acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), multiple myeloma (MM), non- Hodgkin's lymphoma (NHL), mantle cell lymphoma (MCL), follicular lymphoma (FL), Waldenstrom's macroglobulinemia (WM), diffuse large B-cell lymphoma (DLBCL), marginal zone lymphoma (MZL), hairy cell leukemia (HCL), Burkitt's lymphoma (BL), and Richter's transformation.
• ALL acute lymphocytic leukemia
• AML acute myeloid leukemia
• CLL chronic lymphocytic leukemia
• SLL small lymphocytic lympho
• leukemias would find use in the combination of agents of the invention, such as, e.g., B- cell prolymphocytic leukemia, lymphoplasmacytic lymphoma, plasma cell
• myeloma/plasmacytoma myeloma/plasmacytoma, Hodgkin's lymphoma, and Burkitt's lymphoma/Burkitt's cell leukemia.
• Non-Hodgkin's Lymphoma is aggressive NHL or indolent NHL.
• aggressive NHL include B-cell neoplasms, diffuse large B- cell lymphoma (DLBCL), T/NK cell neoplasms, anaplastic large cell lymphoma, peripheral T-cell lymphomas, precursor B-lymphoblastic leukemia/lymphoma, precursor T-lymphoblastic leukemia/lymphoma, Burkitt's lymphoma, adult T-cell lymphoma/leukemia (HTLV1+), primary CNS lymphoma, mantle cell lymphoma (MCL), polymorphic post-transplantation lymphoproliferative disorder (PTLD), AIDS-related lymphoma, true histiocytic lymphoma, and blastic NK-cell lymphoma.
• B-cell neoplasms diffuse large B- cell lymphoma (DLBCL), T/NK cell neoplasms, anaplastic
• indolent NHL include follicular lymphoma, small lymphocytic lymphoma, marginal zone lymphoma (such as extranodal marginal zone lymphoma (also called mucosa associated lymphoid tissue—MALT lymphoma), nodal marginal zone B-cell lymphoma (monocytoid B-cell lymphoma), splenic marginal zone lymphoma), and lymphoplasmacytic lymphoma (Waldenstrom's macroglobulinemia).
• a subject has aggressive NHL or indolent NHL.
• a patient has a condition selected from the group consisting of mantle cell lymphoma (MCL), diffuse large B cell lymphoma (DLBCL), follicular lymphoma (FL), acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), multiple myeloma (MM), and marginal zone lymphoma.
• MCL mantle cell lymphoma
• DLBCL diffuse large B cell lymphoma
• FL follicular lymphoma
• ALL acute lymphocytic leukemia
• AML acute myeloid leukemia
• CLL chronic lymphocytic leukemia
• SLL small lymphocytic lymphoma
• MM multiple myeloma
• agents of the present invention as modulators of apoptosis are useful in the treatment, prevention, and inhibition of cancer (including, but not limited to, the types of B-cell malignancies mentioned above).
• Chemoprevention involves inhibiting the development of invasive cancer by blocking the initiating mutagenic event, blocking the progression of pre-malignant cells that have already suffered an insult, or inhibiting tumor relapse.
• the compounds are also useful in inhibiting tumor angiogenesis and metastasis.
• One embodiment of the invention is a method of inhibiting tumor angiogenesis or metastasis in a patient by administering an effective amount of one or more compounds of the present invention.
• one or more additional therapeutic agents can be administered with the combination of agents of the present invention.
• the combination of agents of the present invention are useful in combining (administered together or sequentially) with known anti-cancer treatments such as radiation therapy or with one or more cytostatic, cytotoxic or anticancer agents, such as, for example, DNA interactive agents, such as cisplatin or doxorubicin; topoisomerase II inhibitors, such as etoposide; topoisomerase I inhibitors such as CPT-11 or topotecan; tubulin interacting agents, such as paclitaxel, docetaxel or the epothilones (for example ixabepilone), either naturally occurring or synthetic; hormonal agents, such as tamoxifen; thymidilate synthase inhibitors, such as 5-fluorouracil; and anti-metabolites, such as methotrexate; other tyrosine kinase inhibitors such
• the additional active agent can also be a proteasome inhibitor, Bortezomib (Velcade ® ), Carfilzomib (PR-171), PR-047, disulfiram, lactacystin, PS-519, eponemycin, epoxomycin, aclacinomycin, CEP- 1612, MG-132, CVT-63417, PS-341, vinyl sulfone tripeptide inhibitors, ritonavir, PI-083, (+/-)-7-methylomuralide, (-)-7-methylomuralide, lenalidomide (Revlimid®), or a combination thereof.
• a proteasome inhibitor Bortezomib (Velcade ® ), Carfilzomib (PR-171), PR-047, disulfiram, lactacystin, PS-519, eponemycin, epoxomycin, aclacinomycin, CEP- 1612, MG-
• steroidal anti-inflammatory drugs e.g, prednisone or prednisolone
• NSAIDs non-steroidal anti -inflammatory drugs
• ImSAIDs immune selective anti-inflammatory derivatives
• a patient has a relapsed or refractory condition (i.e., B-cell cancer).
• the subject is refractory to chemotherapy treatment, or in relapse after treatment with chemotherapy.
• the subject is refractory to a non-TGR-1202 P13K-delta inhibitor.
• the subject is refractory to an agent (i, ii, or iii) described herein, where the agent was administered individually (i.e., as a monotherapy).
• the cancer is resistant to treatment with rituximab. In some embodiments, the cancer shows a reduced response to treatment with rituximab. In some embodiments, the subject has previously been treated with rituximab.
• the methods comprise reducing the level of NF- kappa-B activity, reducing SNAIL expression, increasing RKIP activity, increasing PTEN activity, increasing tumor sensitivity to TRAIL-apoptosis, reducing the level of P13K- delta activity or a combination thereof in a subject.
• the described triplet combination depletes B-cells from human whole blood to a greater extent than either the P 13K-delta inhibitor of formula A, the anti-CD20 antibody ublituximab, or the BTK inhibitor alone depletes B-cells from human whole blood.
• the combination of the P13K-delta inhibitor of formula A, the anti-CD20 antibody ublituximab, and the BTK inhibitor depletes B-cells from human whole blood to a greater extent than the sum of the depletion by the P13K-delta inhibitor of formula A, the depletion by the anti-CD20 antibody ublituximab, and the depletion by the BTK inhibitor.
• the antibody, and the BTK inhibitor are used in a method of treating a disease or disorder associated with excessive B-cell proliferation, wherein the method comprises
• a P13K-delta inhibitor of formula A, the anti-CD20 antibody ublituximab, and the BTK inhibitor are used in a method of treating a disease or disorder associated with excessive B-cell activity, wherein the method comprises administration of a P 13K-delta inhibitor of formula A, the anti-CD20 antibody, and the BTK inhibitor to a subject in need thereof.
• a P13K-delta inhibitor of formula A, the anti-CD20 antibody, and the BTK inhibitor are used in a method of treating a disease or disorder associated with excessive number of B-cells, wherein the method comprises administration of a P 13K- delta inhibitor of formula A, the anti-CD20 antibody, and the BTK inhibitor to a subject in need thereof.
• the anti-CD20 antibody is ublituximab.
• the P13K-delta selective inhibitor is TGR-1202.
• the BTK inhibitor is ibrutinib.
• the anti-CD20 antibody is ublituximab and the P13K-delta selective inhibitor is TGR-1202.
• the anti- CD20 antibody is ublituximab
• the P13K-delta selective inhibitor is TGR-1202
• the BTK inhibtor is ibrutinib.
• the agents of the present disclosure are administered to a subject (e.g. , a human subject)
• the agents can be administered as a composition that comprises a pharmaceutically acceptable carrier or excipient, by any appropriate route, such as intradermal, intramuscular, intraperitoneal, parenteral, intravenous, subcutaneous, intranasal, epidural, oral, sublingual, buccal, intracerebral, intravaginal, transdermal, transmucosal, rectal, by inhalation, or topical. Delivery can be either local or systemic.
• compositions can take the form of solutions, suspensions, emulsions, tablets, pills, pellets, powders, multi-particulates, capsules, capsules containing liquids, capsules containing powders, capsules containing multi-particulates, lozenges, sustained- release formulations, suppositories, transmucosal films, sub-lingual tablets or tabs, aerosols, sprays, or any other form suitable for use.
• the composition is in the form of a tablet.
• the composition is in the form of a capsule.
• suitable pharmaceutical excipients are described in
• the agents of the present disclosure are formulated for oral administration in the form of tablets, capsules, gelcaps, caplets, lozenges, aqueous or oily solutions, suspensions, granules, powders, emulsions, syrups, or elixirs, for example.
• the tablets can be compressed, enteric-coated, sugar-coated, film-coated, multiply compressed or multiply layered.
• the agents of the present disclosure are formulated into a pharmaceutical composition for intravenous administration.
• such compositions comprise sterile isotonic aqueous buffer.
• the compositions can also include a solubilizing agent.
• the ingredients are supplied either separately or mixed together in unit dosage form, for example, as a dry lyophilized powder or water free concentrate in a hermetically sealed container such as an ampule or sachette indicating the quantity of active agent.
• the compositions can be dispensed, for example, with an infusion bottle containing sterile pharmaceutical grade water or saline.
• an ampule of sterile water for injection or saline can be provided so that the ingredients can be mixed prior to administration. Examples
• Example 1 Triple Combination of a P13K-delta Inhibitor of Formula A (TGR-1202), an
• Ublituximab is a novel glycoengineered type 1 chimeric IgGl mAb targeting a unique epitope on the CD20 antigen that is not targeted by rituximab or ofatumumab. See, Miller, J. et al, Blood 120: Abstract No. 2756 (2012); Deng, C. el. al., J. Clin. Oncol 3/ : Abstract No. 8575 (2013); O'Connor, O.A. et al., J. Clin. Oncol. 32:5s (2014), (suppl; Abstract No. 8524).
• Ublituximab was glycoengineered for potent activity, exhibiting a unique primary amino acid sequence and a low fucose content, which was designed to induce superior antibody-dependent cell-mediated cytotoxicity ("ADCC"). Responses with single agent ublituximab have been observed in rituximab refractory patients. Id.
• Umbralisib (also known as TGR-1202) is a next generation, highly specific, once daily, orally available, P13K-delta inhibitor, active in patients with a wide variety of relapsed or refractory (rel/ref) hematologic malignancies. See, O' Connor, O.A. et al., Blood 126: Abstract No. 4154 (201 5): Burris, H. et al, J Clin Oncol 33 (2015) (suppl; abstract 7069); Burns, H. et ⁇ ; .. .1 Clin Oncol 32:5s, (2014) (suppl; abstract 2513); Burris, H. et al. Blood 124: Abstract No. 1984 (2014).
• TGR-1202 has a unique molecular structure that provides it with an advantageous safety profile, notably with respect to hepatic toxicity and colitis. Id. The favorable safety profile of TGR-1202 compared to prior inhibitors has been demonstrated, including in long-term follow up. Burris, H. et al. "Long-term follow-up of the PI3 delta inhibitor TGR-1202 demonstrates a
• the orally-administered BTK inhibitor ibrutinib is currently FDA-approved and marketed under the name Imbruvica® for the treatment of a variety of B-cell neoplasms, such as mantle cell lymphoma, CLL, and Waldenstrom's macroglobulinemia (a form of non-Hodgkin's lymphoma (NHL)). See, Imbruvica® full prescribing information (Pharmacyclics LLC and Janssen Biotech, Inc.). Also, see Honigsberg, L.A. et al, PNAS 707: 13075-13080 (2010) and U.S. Patent Nos. 7,514,444, 8,697,711, 8,703,780, 8,088,309, and 8,088,781.
• FL follicular lymphoma
• CLL chronic lymphocytic leukemia
• SLL small lymphocytic lymphoma
• DLBCL diffuse large B-cell lymphoma
• MZL marginal zone lymphoma
• MCL mantle cell lymphoma
• the median patient age was 65 years (range 32-85).
• the 29 male and 9 female patients had received a median of 3 prior treatment regimens (range 0-6).
• the number of patients with 3 or more prior therapies was 21 (55%).
• TGR-1202 dose escalation starting with micronized doses of 400 mg (cohort 1), followed by 600 mg (cohort 2), and 800 mg (cohort 3).
• TGR-1202 was administered once a day in combination with ibrutinib, which was administered once a day at 420 mg (for CLL patients) and 560 mg (for NHL patients). Both TGR-1202 and ibrutinib were administered once daily beginning on day 1 of cycle 1. See, FIG. 1.
• Ublituximab (UTX), however, was not administered daily. UTX was administered to patients by intravenous infusion at a dose of 900 mg on days 1, 8, and 15 of cycle 1 and day 1 of cycles 2, 3, 4, 5, 6, 9, and 12. Each cycle was 28 days. Scans were performed at week 8 and every 12 weeks thereafter to assess efficacy. After month 12, all patients continued on both TGR-1202 and ibrutinib daily therapy. See, FIG. 1.
• TGR-1202 and ibrutinib was well-tolerated in the 38 patients at dose levels of TGR-1202 up through 800 mg, the highest dose level tested to date in the study.
• DLT dose limiting toxicity
• FIG. 2 is a bar graph depicting efficacy as reflected in the best percent change from baseline in disease burden in all patients who had received at least one post baseline scan to assess disease/tumor burden.
• FIG. 4 presents efficacy results in terms of the level of clinical response (i.e., CR, PR, ORR, SD, and PD).
• MZL marginal zone lymphoma
• follicular lymphoma FL
• 80% (4 of 5) achieved an objective response including 2 with prior autologous stem cell transplantation (ASCT), 1 refractory to prior ibrutinib, and 1 with 5 prior lines of rituximab-based therapy.
• ASCT autologous stem cell transplantation
• MCL mantle cell lymphoma
• 100% of patients (4 of 4) achieved an objective response with 2 patients achieving a complete response (CR), as determined by radiography with bone marrow confirmation pending, and 2 patients achieving a partial response (PR). See, FIGS. 2 and 4.
• One MCL patient remains on study now for close to 800 days. (FIG. 3).
• DLBCL B-Cell Lymphoma
• the DLBCL patients had a median of four prior therapies, and 4 out of the 6 patients with DLBCL were of the non-germinal center B-cell-like (GCB) subtype. See, FIG. 4.
• GCB non-germinal center B-cell-like
• Duration of study 81% of patients were on the study for more than 6 months.
• the median time on the study was 11.1 months (range 0.4 - 30.1+ months). (See FIG. 3).
• One CLL patient and one FL patient has been on the study for over 900 days.
• P13K-delta inhibitor and a BTK inhibitor used to treat B-cell malignancies.
• the combination of UTX + TGR-1202 + ibrutinib was well-tolerated with clinical activity observed across heavily pre-treated and high-risk B-cell malignancies.

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