US20120129853A1 - Methods of treatment using selective bcl-2 inhibitors - Google Patents

Methods of treatment using selective bcl-2 inhibitors Download PDF

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US20120129853A1
US20120129853A1 US13/301,898 US201113301898A US2012129853A1 US 20120129853 A1 US20120129853 A1 US 20120129853A1 US 201113301898 A US201113301898 A US 201113301898A US 2012129853 A1 US2012129853 A1 US 2012129853A1
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methyl
piperazin
chlorophenyl
sulfonyl
benzamide
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Steven Elmore
Andrew Souers
Li Chun Wang
Tariq Ghayur
Stuart J. Perper
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AbbVie Inc
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Abbott Laboratories
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Priority to US13/301,898 priority Critical patent/US20120129853A1/en
Assigned to ABBOTT LABORATORIES reassignment ABBOTT LABORATORIES ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SOUERS, ANDREW, GHAYUR, TARIQ, PERPER, STUART J., WANG, LI CHUN, ELMORE, STEVEN
Publication of US20120129853A1 publication Critical patent/US20120129853A1/en
Assigned to ABBVIE INC. reassignment ABBVIE INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ABBOTT LABORATORIES
Priority to US14/535,070 priority patent/US9345702B2/en
Priority to US15/136,582 priority patent/US9872861B2/en
Priority to US15/838,605 priority patent/US20180369250A1/en
Priority to US16/415,515 priority patent/US20200222413A1/en
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    • 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
    • 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
    • A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Definitions

  • This invention pertains to methods of treating systemic lupus erythematosus, lupus nephritis or Sjogren's Syndrome with compounds that selectively inhibit the activity of Bcl-2 anti-apoptotic proteins.
  • the current invention is directed to treatment with compounds that selectively inhibit the activity of Bcl-2 proteins, with a lesser affinity for inhibiting the activity of other Bcl-2 family proteins, including Bcl- x L .
  • Anti-apoptotic Bcl-2 proteins are associated with a number of diseases. There is therefore an existing need in the therapeutic arts for compounds that inhibit the activity of anti-apoptotic Bcl-2 proteins.
  • the Bcl-2 family of proteins are the key regulators of mitochondria-dependent apoptosis in nucleated cells and consists of both anti-apoptotic (Bcl-x L , Bcl-2, Bcl-w, Al, Mcl-1) and pro-apoptotic (Bak, Bax, Bid, Bim, Bad, Bik, Bmf, Noxa, Puma) members
  • Bcl-2 protein is associated with many physiologic functions, including the inhibition of apoptosis in the body, in some cases resulting in proliferation of cells affected by the Bcl-2 inhibition. As such, inhibition of Bcl-2 protein may reduce cell proliferation, leading to improved outcomes related to the treatment and prevention of cancer.
  • Bcl-2 proteins in bladder cancer brain cancer, breast cancer, bone marrow cancer, cervical cancer, chronic lymphocytic leukemia, colorectal cancer, esophageal cancer, hepatocellular cancer, lymphoblastic leukemia, follicular lymphoma, lymphoid malignancies of T-cell or B-cell origin, melanoma, myelogenous leukemia, myeloma, oral cancer, ovarian cancer, non-small cell lung cancer, prostate cancer, small cell lung cancer, spleen cancer, and the like is described in commonly-owned PCT US 2004/36770, published as WO 2005/049593, and PCT US 2004/37911, published as WO 2005/024636.
  • One embodiment of the current invention pertains to a method for treating systemic lupus erythematosus (SLE) or lupus nephritis by administering a therapeutically effective amount of a compound that selectively inhibits Bcl-2 proteins.
  • SLE systemic lupus erythematosus
  • lupus nephritis by administering a therapeutically effective amount of a compound that selectively inhibits Bcl-2 proteins.
  • the selective Bcl-2 inhibitors generally have the following Formula (I):
  • a 1 is N or CH
  • B 1 is OR 1 or NHR 1 ;
  • Y 1 is CN, NO 2 , CF 3 , F or Cl;
  • R 1 is (CH 2 ) n R 2 ;
  • R 2 is cycloalkyl or heterocyclyl; wherein the heterocyclyl and cycloalkyl are optionally substituted with one or more independently selected R 4 , OR 4 , OH, CN, or F;
  • R 3 is heteroaryl; wherein the heteroaryl is optionally substituted with one or more independently selected NH 2 , Cl, or F;
  • R 4 is alkyl, cycloalkyl, heterocyclyl, or spiroheterocyclyl; wherein the alkyl is optionally substituted with one or more F;
  • R 5 is deuterium
  • each R 6 is independently selected from CH 3 , spirocyclopropyl and OH;
  • n 0, 1, 2, 3, 4, 5, or 6;
  • n 0 or 1
  • p 0, 1, or 2.
  • the method of treating SLE or lupus nephritis may also comprise administering a pharmaceutically acceptable salt of a selective Bcl-2 inhibitor.
  • a selective Bcl-2 inhibitor has a binding affinity (K i ) of less than about 1 nanomolar for Bcl-2.
  • a selective Bcl-2 inhibitor has a binding affinity (K i ) of less than about 100 picomolar for Bcl-2.
  • a selective Bcl-2 inhibitor may also have a binding affinity (K i ) for Bcl-2 that is approximately 500 times less than the binding affinity for Bcl-x L .
  • the selective Bcl-2 inhibitor may include N-( ⁇ 5-chloro-6-[(4-fluorotetrahydro-2H-pyran-4-yl)methoxy]pyridin-3-yl ⁇ sulfonyl)-4-(4- ⁇ [2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl ⁇ piperazin-1-yl)-2-[(6-fluoro-1H-indazol-4-yl)oxy]benzamide; 4-(4- ⁇ [2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl ⁇ piperazin-1-yl)-N- ⁇ [4-( ⁇ [(2S)-4-cyclopropylmorpholin-2-yl]methyl ⁇ amino)-3-nitrophenyl]sulfonyl ⁇ -2-(1H-pyrrolo[2,3-b]pyridin-5-yloxy)benz
  • Another embodiment of the current invention pertains to a method for treating Sjogren's Syndrome by administering a therapeutically effective amount of a compound that selectively inhibits Bcl-2 proteins.
  • the selective Bcl-2 inhibitors generally have the following Formula (I):
  • a 1 is N or CH
  • B 1 is OR 1 or NHR 1 ;
  • Y 1 is CN, NO 2 , CF 3 , F or Cl;
  • R 1 is (CH 2 ) n R 2 ;
  • R 2 is cycloalkyl or heterocyclyl; wherein the heterocyclyl and cycloalkyl are optionally substituted with one or more independently selected R 4 , OR 4 , OH, CN, or F;
  • R 3 is heteroaryl; wherein the heteroaryl is optionally substituted with one or more independently selected NH 2 , Cl, or F;
  • R 4 is alkyl, cycloalkyl, heterocyclyl, or spiroheterocyclyl; wherein the alkyl is optionally substituted with one or more F;
  • R 5 is deuterium
  • each R 6 is independently selected from CH 3 , spirocyclopropyl and OH;
  • n 0, 1, 2, 3, 4, 5, or 6;
  • n 0 or 1
  • p 0, 1, or 2.
  • the method of treating Sjogren's Syndrome may also comprise administering a pharmaceutically acceptable salt of a selective Bcl-2 inhibitor.
  • a selective Bcl-2 inhibitor has a Bcl-2 binding affinity (K i ) of less than about 1 nanomolar.
  • a selective Bcl-2 inhibitor has a Bcl-2 binding affinity (K i ) of less than about 100 picomolar.
  • the selective Bcl-2 inhibitor may also have a binding affinity (K i ) for Bcl-2 that is approximately 500 times less than the binding affinity (K i ) for Bcl-x L .
  • the selective Bcl-2 inhibitor may include N-( ⁇ 5-chloro-6-[(4-fluorotetrahydro-2H-pyran-4-yl)methoxy]pyridin-3-yl ⁇ sulfonyl)-4-(4- ⁇ [2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl ⁇ piperazin-1-yl)-2-[(6-fluoro-1H-indazol-4-yl)oxy]benzamide; 4-(4- ⁇ [2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl ⁇ piperazin-1-yl)-N- ⁇ [4-( ⁇ [(2S)-4-cyclopropylmorpholin-2-yl]methyl ⁇ amino)-3-nitrophenyl]sulfonyl ⁇ -2-(1H-pyrrolo[2,3-b]pyridin-5-yloxy)
  • FIG. 1 illustrates the (A) effect of treatment with a non-selective Bcl-2 inhibitor (Compound 2) on both lymphocyte (left) and platelet (right) counts, as well as the (B) effect of treatment with a selective Bcl-2 inhibitor (Compound 1) on both lymphocyte numbers (left) and platelet counts (right) in peripheral blood of (NZB ⁇ NZW)F i mice.
  • Compound 1 a selective Bcl-2 inhibitor
  • C C
  • D D
  • E E
  • F F
  • G H
  • I further illustrate the effects of Compounds 1, 17, 5, 7, 8, 9, and 12, respectively, on the lymphocyte numbers (left) and platelet counts (right) in peripheral blood of C57BL/6 mice.
  • FIG. 2 illustrates the effect of treatment with a selective Bcl-2 inhibitor (Compound 3) in mice on lymphocytes and platelets. Specifically, FIG. 2 illustrates the effects of treating mice NZBWF1 with Compound 3 at doses of 30 mg/kg and 100 mg/kg, compared to treatment with phosal vehicle control, and also illustrates the exposure of Compound 3, as measured 24 hours after the last dose.
  • Compound 3 a selective Bcl-2 inhibitor
  • FIG. 3 illustrates the reduction in T cells and B cells in mice treated with various doses of a selective Bcl-2 inhibitor (Compound 3), as compared to treatment with phosal vehicle. Specifically, FIG. 3 illustrates the reduction in CD4+ T cells, CD8+ T Cells, and CD19+ B cells in mice treated with doses of Compound 3 including 30 mg/kg, 100 mg/kg, and 300 mg/kg.
  • Compound 3 a selective Bcl-2 inhibitor
  • FIG. 4 illustrates the efficacy of treatment with a selective Bcl-2 inhibitor (Compound 1) in a spontaneous (NZB ⁇ NZW)F 1 murine model of lupus as assessed by (A) incidence of severe proteinuria (PU ⁇ 300 mg/dL) and (B) Kaplan-Meier cumulative survival.
  • FIG.4 further illustrates the efficacy of treatment with a selective Bcl-2 inhibitor (Compound 17) in a spontaneous (NZB ⁇ NZW)F 1 murine model of lupus as assessed by (C) incidence of severe proteinuria (PU ⁇ 300 mg/dL) and (D) Kaplan-Meier cumulative survival.
  • Asterisks represent a statistical significance of P ⁇ 0.05.
  • FIG. 5 illustrates the effect of treatment with a selective Bcl-2 inhibitor (Compound 1), as well as treatment with mycophenolate mofetil (MMF), on inhibition of anti-ds DNA titer production in a spontaneous SLE model for Compound 1 at 30 mg/kg and 100 mg/kg, and MMF at 100 mg/kg compared to vehicle controls.
  • Asterisks represent statistical significance of P ⁇ 0.05.
  • FIG. 6 illustrates the representative images demonstrating a reduction of infiltrates in renal tissue in spontaneous lupus nephritis mice, after dosing with a selective Bcl-2 inhibitor (Compound 1), as evidenced by histological assessment. Magnification 200 ⁇ .
  • FIG. 7 illustrates changes in histology scores for renal tissue treated with one of three treatment regimens: treatment with the vehicle, treatment with Compound 1 at a dose of 30 mg/kg and 100 mg/kg, and treatment with MMF at a dose of 100 mg/kg, as they related to histological signs of glomerulonephritis, tubular changes, and perivascular infiltrates.
  • FIG. 7 illustrates a statistically significant improvement in glomerulonephritis, tubular changes, and perivascular infiltrates in the mice receiving treatment with 30 mg/kg and 100 mg/kg Compound 1.
  • FIG. 8 illustrates immunoglobulin G (IgG), B cell, and T cell deposition in renal tissue for spontaneous lupus nephritis mice dosed with phosal vehicle, Compound 1 at doses of 30 mg/kg and 100 mg/kg, and MMF at a dose of 100 mg/kg. Specifically, mice treated with Compound 1 showed decreased deposition of IgG, B cells, and T cells, as compared to phosal vehicle.
  • IgG immunoglobulin G
  • B cell B cell
  • Compound 1 at doses of 30 mg/kg and 100 mg/kg
  • MMF at a dose of 100 mg/kg.
  • mice treated with Compound 1 showed decreased deposition of IgG, B cells, and T cells, as compared to phosal vehicle.
  • FIG. 9 illustrates the efficacy of treatment with a selective Bcl-2 inhibitor (Compound 1), MMF and BAFFR3-Ig in an IFN ⁇ -induced SLE model as assessed by (A) incidence of severe proteinuria (PU>300 mg/dL) and (B) Kaplan-Meier cumulative survival. Asterisks represent a statistical significance of P ⁇ 0.05.
  • FIG. 10 illustrates anti-ds DNA production in IFNa- induced (NZBxNZW)F1 mice treated with a selective Bcl-2 inhibitor (Compound 1), at doses ranging from 3-30 mg/kg, compared to vehicle control, as evidenced by Immunoglobulin G (IgG) levels.
  • Compound 1 a selective Bcl-2 inhibitor
  • FIG. 11 illustrates representative images demonstrating the reduction of periductular infiltrates in the submandibular salivary gland of spontaneous murine model mice treated with a selective Bcl-2 inhibitor (Compound 1), with a magnification 200 ⁇ .
  • Compound 1 a selective Bcl-2 inhibitor
  • FIG. 12 illustrates the histology scores for submandibular salivary gland tissue treated with one of three treatment regimens: treatment with a phosal vehicle, treatment with a selective Bcl-2 inhibitor (Compound 1) at a dose of 10 mg/kg; and treatment with Compound 1 at a dose of 30 mg/kg and 100 mg/kg.
  • Treatment with a phosal vehicle treatment with a selective Bcl-2 inhibitor (Compound 1) at a dose of 10 mg/kg
  • Compound 1 at a dose of 30 mg/kg and 100 mg/kg.
  • the methods of the current invention are directed to treating various disease states by administering to a patient in need thereof a therapeutically effective amount of a selective Bcl-2 inhibitor.
  • Bcl-2 expression may play a role in the development and disease state progression associated with a number of autoimmune disorders.
  • the inhibition of Bcl-2 protein may also have a positive impact on the treatment of autoimmune diseases including systemic lupus erythematosus (SLE), lupus nephritis and Sjogren's Syndrome.
  • treat refers to a method of alleviating or abrogating a disease and/or its attendant symptoms.
  • prevent refers to a method of preventing the onset of a disease and/or its attendant symptoms or barring a subject from acquiring a disease.
  • prevent also include delaying the onset of a disease and/or its attendant symptoms and reducing a subject's risk of acquiring a disease.
  • terapéuticaally effective amount refers to that amount of the compound being administered sufficient to prevent development of or alleviate to some extent one or more of the symptoms of the condition or disorder being treated.
  • modulate refers to the ability of a compound to increase or decrease the function, or activity, of a Bc-2 protein.”
  • composition as used herein is intended to encompass a product comprising the specified ingredients in the specified amounts, as well as any product which results, directly or indirectly, from combination of the specified ingredients in the specified amounts.
  • pharmaceutically acceptable it is meant the carrier, diluent or excipient must be compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.
  • the “subject” is defined herein to include animals such as mammals, including, but not limited to, primates (e.g., humans), cows, sheep, goats, horses, dogs, cats, rabbits, rats, mice and the like. In suitable embodiments, the subject is a human.
  • the disease states that may be treated with the methods of the current invention include those that result from autoimmune and inflammatory process, specifically systemic lupus erythematosus (SLE), lupus nephritis, Sjogren's Syndrome and combinations thereof.
  • SLE is a chronic systemic autoimmune disease (or autoimmune connective tissue disease) that can affect any part of the body. As occurs in other autoimmune diseases, the immune system attacks the body's cells and tissue, resulting in inflammation and tissue damage. SLE most commonly affects the heart, joints, skin, lungs, blood vessels, liver, kidneys, and nervous system. Accordingly, disease states in which the SLE has affected the kidneys may be termed lupus nephritis.
  • Sjogren's Syndrome also known as “Mikulicz disease” and “Sicca syndrome,” is a systemic autoimmune disease in which immune cells attack and destroy the exocrine glands that produce tears and saliva.
  • Sjogren's Syndrome typically suffer from a decreased ability to adequately produce saliva and tears, resulting in excessive dry mouth and dry eyes.
  • the methods of the current invention are directed to the treatment of SLE and lupus nephritis. In another embodiment, the methods of the invention are directed to the treatment of Sjogren's Syndrome.
  • the methods of the current invention comprise treatment with a selective Bcl-2 inhibitor.
  • Ki is used as an objective measurement for comparative binding affinity.
  • a compound that has a higher binding affinity for the target substrate compared to a second substrate will display a Ki value for the target substrate that is lower than the second substrate. This is due to the fact that the compound has a higher affinity for the target substrate, and a lesser concentration of the compound is required to bind to and elicit an effect on the target substrate, as compared to the second substrate.
  • selective Bcl-2 inhibitors have a higher affinity for Bcl-2 proteins compared to Bcl-xL proteins, meaning that a lesser concentration of the selective Bcl-2 inhibitor is required to elicit an effect on the Bcl-2 inhibitor, as compared to the concentration required to elicit an effect on the Bcl-xL proteins.
  • the language stating that a compound has a competitive binding affinity (K i ) for Bcl-2 that is less than the binding affinity (K i ) for Bcl-x L should be construed to mean that the compound has a more selective affinity for Bcl-2 than Bcl-x L , as evidenced by a K i value for Bcl-2 that is less than the K i value for Bcl-x L .
  • phase “selective Bcl-2 inhibitor” refers to compounds that have a binding affinity (K i ) of (a) less than about 500 nanomolar, less than about 400 nanomolar, less than about 300 nanomolar, less than about 200 nanomolar, less than about 100 nanomolar, less than about 50 nanomolar, less than about 25 nanomolar, less than about 10 nanomolar, less than about 5 nanomolar, less than about 1 nanomolar, less than about 900 picomolar, less than about 800 picomolar, less than about 700 picomolar, less than about 600 picomolar, less than about 500 picomolar, less than about 400 picomolar, less than about 300 picomolar, less than about 200 picomolar, less than about 100 picomolar, and less than about 50 picomolar to Bcl-2; and (b) a competitive binding affinity (K i ) for Bcl-2 that is at least about 500, at least about 1000, at least about 2000, at least about 2500, at least about 3000, at least about
  • the selective Bcl-2 inhibitor compounds that can be used in the methods of the present invention are those compounds having a binding affinity (K i ) of less than about 100 picomolar for Bcl-2 and a binding affinity (K i ) for Bcl-2 that is approximately 500 times less than the binding affinity for Bcl-x L , a binding affinity (K i ) of less than about 100 picomolar for Bcl-2 and a binding affinity (K i ) for Bcl-2 that is approximately 1000 times less than the binding affinity for Bcl-x L , a binding affinity (K i ) of less than about 100 picomolar for Bcl-2 and a binding affinity (K i ) for Bcl-2 that is approximately 2000 times less than the binding affinity for Bcl-x L , a binding affinity (K i ) of less than about 100 picomolar for Bcl-2 and a binding affinity (K i ) for Bcl-2 that is approximately 2500 times less than the binding
  • Selective Bcl-2 inhibitor compounds that can be used in the methods of the current invention may generally be considered any compound having the following Formula (I):
  • a 1 is N or CH
  • B 1 is OR 1 or NHR 1 ;
  • Y 1 is CN, NO 2 , CF 3 , F or Cl;
  • R 1 is (CH 2 ) n R 2 ;
  • R 2 is cycloalkyl or heterocyclyl; wherein the heterocyclyl and cycloalkyl are optionally substituted with one or more independently selected R 4 , OR 4 , OH, CN, or F;
  • R 3 is heteroaryl; wherein the heteroaryl is optionally substituted with one or more independently selected NH 2 , Cl, or F;
  • R 4 is alkyl, cycloalkyl, heterocyclyl, or spiroheterocyclyl; wherein the alkyl is optionally substituted with one or more F;
  • R 5 is deuterium
  • each R 6 is independently selected from CH 3 , spirocyclopropyl and OH;
  • n 0, 1, 2, 3, 4, 5, or 6;
  • n 0 or 1
  • p 0, 1, or 2.
  • variable moieties herein are represented by identifiers (capital letters with numerical and/or alphabetical superscripts) and may be specifically embodied.
  • variable moiety herein may be the same or different as another specific embodiment having the same identifier.
  • alkenyl as used herein, means a straight or branched hydrocarbon chain containing from 2 to 10 carbons and containing at least one carbon-carbon double bond.
  • C x -C y alkyl means a straight or branched hydrocarbon chain containing at least one carbon-carbon double bond containing x to y carbon atoms.
  • C 2 -C 4 alkenyl means an alkenyl group containing 2-4 carbon atoms.
  • alkenyl include, but are not limited to buta-2,3-dienyl, ethenyl, 2-propenyl, 2-methyl-2-propenyl, 3-butenyl, 4-pentenyl, 5-hexenyl, 2-heptenyl, 2-methyl-1-heptenyl, and 3-decenyl.
  • alkenylene means a divalent group derived from a straight or branched chain hydrocarbon of 2 to 4 carbon atoms and contains at least one carbon-carbon double bond.
  • C x -C y alkylene means a divalent group derived from a straight or branched hydrocarbon chain containing at least one carbon-carbon double bond and containing x to y carbon atoms.
  • Representative examples of alkenylene include, but are not limited to, —CH ⁇ CH— and —CH 2 CH ⁇ CH—.
  • alkyl as used herein, means a straight or branched, saturated hydrocarbon chain containing from 1 to 10 carbon atoms.
  • C x -C y alkyl means a straight or branched chain, saturated hydrocarbon containing x to y carbon atoms.
  • C 2 -C 10 alkyl means a straight or branched chain, saturated hydrocarbon containing 2 to 10 carbon atoms.
  • alkyl examples include, but are not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, n-hexyl, 3-methylhexyl, 2,2-dimethylpentyl, 2,3-dimethylpentyl, n-heptyl, n-octyl, n-nonyl, and n-decyl.
  • alkylene means a divalent group derived from a straight or branched, saturated hydrocarbon chain of 1 to 10 carbon atoms, for example, of 1 to 4 carbon atoms.
  • C x -C y alkylene means a divalent group derived from a straight or branched chain, saturated hydrocarbon containing x to y carbon atoms.
  • C 2 -C 6 alkylene means a straight or branched chain, saturated hydrocarbon containing 2 to 6 carbon atoms.
  • alkylene examples include, but are not limited to, —CH 2 —, —CH 2 CH 2 —, —CH 2 CH 2 CH 2 —, —CH 2 CH 2 CH 2 CH 2 —, and —CH 2 CH(CH 3 )CH 2 —.
  • alkynyl as used herein, means a straight or branched chain hydrocarbon group containing from 2 to 10 carbon atoms and containing at least one carbon-carbon triple bond.
  • C x -C y alkynyl means a straight or branched chain hydrocarbon group containing from x to y carbon atoms.
  • Representative examples of alkynyl include, but are not limited, to acetylenyl, 1-propynyl, 2-propynyl, 3-butynyl, 2-pentynyl, and 1-butynyl.
  • alkynylene means a divalent radical derived from a straight or branched chain hydrocarbon group containing from 2 to 10 carbon atoms and containing at least one carbon-carbon triple bond.
  • aryl (alone or in combination with another term(s)) means an aromatic carbocyclyl containing from 6 to 14 carbon ring atoms.
  • An aryl may be monocyclic or polycyclic (i.e., may contain more than one ring). In the case of polycyclic aromatic rings, only one ring the polycyclic system is required to be unsaturated while the remaining ring(s) may be saturated, partially saturated or unsaturated.
  • aryls include phenyl, naphthalenyl, indenyl, indanyl, and tetrahydronapthyl.
  • carbocyclyl (alone or in combination with another term(s)) means a saturated cyclic (i.e., “cycloalkyl”), partially saturated cyclic (i.e., “cycloalkenyl”), or completely unsaturated (i.e., “aryl”) hydrocarbyl substituent containing from 3 to 14 carbon ring atoms (“ring atoms” are the atoms bound together to form the ring or rings of a cyclic substituent).
  • a carbocyclyl may be a single-ring (monocyclic) or polycyclic ring structure.
  • a carbocyclyl may be a single ring structure, which typically contains from 3 to 8 ring atoms, more typically from 3 to 6 ring atoms, and even more typically 5 to 6 ring atoms.
  • Examples of such single-ring carbocyclyls include cyclopropyl (cyclopropanyl), cyclobutyl (cyclobutanyl), cyclopentyl (cyclopentanyl), cyclopentenyl, cyclopentadienyl, cyclohexyl (cyclohexanyl), cyclohexenyl, cyclohexadienyl, and phenyl.
  • a carbocyclyl may alternatively be polycyclic (i.e., may contain more than one ring).
  • polycyclic carbocyclyls include bridged, fused, and spirocyclic carbocyclyls.
  • a spirocyclic carbocyclyl one atom is common to two different rings.
  • An example of a spirocyclic carbocyclyl substituent is spirocyclopropyl.
  • a spirocyclic carbocyclyl one atom is common to two different rings.
  • An example of a spirocyclic carbocyclyl is spiropentanyl.
  • the rings share at least two common non-adjacent atoms.
  • bridged carbocyclyls examples include bicyclo[2.2.1]heptanyl, bicyclo[2.2.1]hept-2-enyl, and adamantanyl.
  • two or more rings may be fused together, such that two rings share one common bond.
  • two- or three-fused ring carbocyclyls include naphthalenyl, tetrahydronaphthalenyl (tetralinyl), indenyl, indanyl (dihydroindenyl), anthracenyl, phenanthrenyl, and decalinyl.
  • cyclic moiety means benzene, phenyl, phenylene, cycloalkane, cycloalkyl, cycloalkylene, cycloalkene, cycloalkenyl, cycloalkenylene, cycloalkyne, cycloalkynyl, cycloalkynylene, heteroarene, heteroaryl, heterocycloalkane, heterocycloalkyl, heterocycloalkene, heterocycloalkenyl and spiroalkyl.
  • cycloalkylene or “cycloalkyl” or “cycloalkane” as used herein, means a monocyclic or bridged hydrocarbon ring system.
  • the monocyclic cycloalkyl is a carbocyclic ring system containing three to eight carbon atoms, zero heteroatoms and zero double bonds. Examples of monocyclic ring systems include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl.
  • the monocyclic ring may contain one or two alkylene bridges, each consisting of one, two, or three carbon atoms, each linking two non-adjacent carbon atoms of the ring system.
  • Non-limiting examples of such bridged cycloalkyl ring systems include bicyclo[3.1.1]heptane, bicyclo[2.2.1]heptane, bicyclo[2.2.2]octane, bicyclo[3.2.2]nonane, bicyclo[3.3.1]nonane, bicyclo[4.2.1]nonane, tricyclo[3.3.1.0 3,7 ]nonane (octahydro-2,5-methanopentalene or noradamantane), and tricyclo[3.3.1.1 3,7 ]decane (adamantane).
  • the monocyclic and bridged cycloalkyl can be attached to the parent molecular moiety through any substitutable atom contained within the ring system.
  • cycloalkenylene or “cycloalkenyl” or “cycloalkene” as used herein, means a monocyclic or a bridged hydrocarbon ring system.
  • the monocyclic cycloalkenyl has four-, five-, six-, seven- or eight carbon atoms and zero heteroatoms.
  • the four-membered ring systems have one double bond, the five-or six-membered ring systems have one or two double bonds, and the seven- or eight-membered ring systems have one, two, or three double bonds.
  • monocyclic cycloalkenyl groups include, but are not limited to, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, and cyclooctenyl.
  • the monocyclic cycloalkenyl ring may contain one or two alkylene bridges, each consisting of one, two, or three carbon atoms, each linking two non-adjacent carbon atoms of the ring system.
  • Representative examples of the bicyclic cycloalkenyl groups include, but are not limited to, 4,5,6,7-tetrahydro-3aH-indene, octahydronaphthalenyl, and 1,6-dihydro-pentalene.
  • the monocyclic and bicyclic cycloalkenyl can be attached to the parent molecular moiety through any substitutable atom contained within the ring systems.
  • cycloalkyne or “cycloalkynyl,” or “cycloalkynylene,” as used herein, means a monocyclic or a bridged hydrocarbon ring system.
  • the monocyclic cycloalkynyl has eight or more carbon atoms, zero heteroatoms, and one or more triple bonds.
  • the monocyclic cycloalkynyl ring may contain one or two alkylene bridges, each consisting of one, two, or three carbon atoms, each linking two non-adjacent carbon atoms of the ring system.
  • the monocyclic and bridged cycloalkynyl can be attached to the parent molecular moiety through any substitutable atom contained within the ring systems.
  • heteroaryl or “heteroarylene,” as used herein, means a five-membered or six-membered aromatic ring having at least one carbon atom and one or more than one independently selected nitrogen, oxygen or sulfur atom.
  • the heteroarenes of this invention are connected through any adjacent atoms in the ring, provided that proper valences are maintained.
  • heteroaryl (alone or in combination with another term(s)) means an aromatic heterocyclyl containing from 5 to 14 ring atoms.
  • a heteroaryl may be a single ring or 2 or 3 fused rings.
  • heteroaryl substituents include 6-membered ring substituents such as pyridyl, pyrazyl, pyrimidinyl, pyridazinyl, and 1,3,5-, 1,2,4- or 1,2,3-triazinyl; 5-membered ring substituents such as imidazyl, furanyl, thiophenyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, 1,2,3-, 1,2,4-, 1,2,5-, or 1,3,4-oxadiazolyl and isothiazolyl; 6/5-membered fused ring sub stituents such as benzothiofuranyl, benzisoxazolyl, benzoxazolyl, imidazolyl, indolyl, benzoimidazolyl, pyrrolo[2,3-b]pyridinyl, purinyl, and anthranilyl; and 6/6-membered
  • heterocyclyl (alone or in combination with another term(s)) means a saturated (i.e., “heterocycloalkyl”), partially saturated (i.e., “heterocycloalkenyl”), or completely unsaturated (i.e., “heteroaryl”) ring structure containing a total of 3 to 14 ring atoms. At least one of the ring atoms is a heteroatom (i.e., oxygen, nitrogen, or sulfur), with the remaining ring atoms being independently selected from the group consisting of carbon, oxygen, nitrogen, and sulfur.
  • a heterocyclyl may be a single-ring (monocyclic) or polycyclic ring structure.
  • a heterocyclyl may be a single ring, which typically contains from 3 to 7 ring atoms, more typically from 3 to 6 ring atoms, and even more typically 5 to 6 ring atoms.
  • single-ring heterocyclyls include furanyl, dihydrofuranyl, tetrahydrofuranyl, tetrahydropyranyl, thiophenyl (thiofuranyl), dihydrothiophenyl, tetrahydrothiophenyl, pyrrolyl, pyrrolinyl, pyrrolidinyl, imidazolyl, imidazolinyl, imidazolidinyl, pyrazolyl, pyrazolinyl, pyrazolidinyl, triazolyl, tetrazolyl, oxazolyl, oxazolidinyl, isoxazolidinyl, isoxazolidinyl, isoxazolyl, thiazolyl, iso
  • a heterocyclyl may alternatively be polycyclic (i.e., may contain more than one ring).
  • polycyclic heterocyclyls include bridged, fused, and spirocyclic heterocyclyls.
  • a spirocyclic heterocyclyl one atom is common to two different rings.
  • examples of spirocyclic heterocyclyls include 2-oxaspiro[3.5]nonanyl.
  • polycyclic heterocyclyls include bridged, fused, and spirocyclic heterocyclyls.
  • one atom is common to two different rings.
  • examples of spirocyclic heterocyclyl include 2-oxaspiro[3.5]nonanyl.
  • a bridged heterocyclyl the rings share at least two common non-adjacent atoms.
  • two or more rings may be fused together, such that two rings share one common bond.
  • fused ring heterocyclyls containing two or three rings include indolizinyl, pyranopyrrolyl, 4H-quinolizinyl, purinyl, naphthyridinyl, pyrrolo[2,3-b]pyridinyl, pyridopyridinyl (including pyrido[3,4-b]-pyridinyl, pyrido[3,2-b]-pyridinyl, or pyrido[4,3-b]-pyridinyl), and pteridinyl.
  • fused-ring heterocyclyls include benzo-fused heterocyclyls, such as indolyl, indazoyl, isoindolyl (isobenzazolyl, pseudoisoindolyl), indoleninyl (pseudoindolyl), isoindazolyl (benzpyrazolyl), benzoimidazolyl, benzazinyl (including quinolinyl (1-benzazinyl) or isoquinolinyl (2-benzazinyl)), phthalazinyl, quinoxalinyl, quinazolinyl, benzodiazinyl (including cinnolinyl (1,2-benzodiazinyl) or quinazolinyl (1,3-benzodiazinyl)), benzopyranyl (including chromanyl or isochromanyl), benzoxazinyl (including 1,3,2-benzoxazinyl, 1,4,2-benzoxazinyl
  • heterocycloalkyl (alone or in combination with another term(s)) means a saturated heterocyclyl.
  • heterocycloalkene or “heterocycloalkenyl,” or “heterocycloalkenylene,” as used herein, means monocyclic or bridged three-, four-, five-, six-, seven-, or eight-membered ring containing at least one heteroatom independently selected from the group consisting of O, N, and S and one or more double bonds.
  • the monocyclic and bridged heterocycloalkene are connected to the parent molecular moiety through any substitutable carbon atom or any substitutable nitrogen atom contained within the rings.
  • the nitrogen and sulfur heteroatoms in the heterocycle rings may optionally be oxidized and the nitrogen atoms may optionally be quarternized.
  • heterocycloalkene groups include, but are not limited to, tetrahydrooxocinyl, 1,4,5,6-tetrahydropyridazinyl, 1,2,3,6-tetrahydropyridinyl, dihydropyranyl, imidazolinyl, isothiazolinyl, oxadiazolinyl, isoxazolinyl, oxazolinyl, pyranyl, pyrazolinyl, pyrrolinyl, thiadiazolinyl, thiazolinyl, and thiopyranyl.
  • phenylene means a divalent radical formed by removal of a hydrogen atom from phenyl.
  • spiroalkyl means alkylene, both ends of which are attached to the same carbon atom and is exemplified by C 2 -spiroalkyl, C 3 -spiroalkyl, C 4 -spiroalkyl, C 5 -spiroalkyl, C 6 -spiroalkyl, C 7 -spiroalkyl, C 8 -spiroalkyl, C 9 -spiroalkyl and the like.
  • spiroheteroalkyl means spiroalkyl having one or two CH 2 moieties replaced with independently selected O, C(O), CNOH, CNOCH 3 , S, S(O), SO 2 or NH and one or two CH moieties unreplaced or replaced with N.
  • spiroheteroalkenyl means spiroalkenyl having one or two CH 2 moieties replaced with independently selected O, C(O), CNOH, CNOCH 3 , S, S(O), SO 2 or NH and one or two CH moieties unreplaced or replaced with N and also means spiroalkenyl having one or two CH 2 moieties unreplaced or replaced with independently selected O, C(O), CNOH, CNOCH 3 , S, S(O), SO 2 or NH and one or two CH moieties replaced with N.
  • spirocyclo means two substituents on the same carbon atom, that, together with the carbon atom to which they are attached, form a cycloalkane, heterocycloalkane, cycloalkene, or heterocycloalkene ring.
  • C 2 -O 5 -spiroalkyl means C 2 -spiroalkyl, C 3 -spiroalkyl, C 4 -spiroalkyl, and C 5 -spiroalkyl.
  • C 2 -spiroalkyl means eth-1,2-ylene, both ends of which replace hydrogen atoms of the same CH 2 moiety.
  • C 3 -spiroalkyl means prop-1,3-ylene, both ends of which replace hydrogen atoms of the same CH 2 moiety.
  • C 4 -spiroalkyl means but-1,4-ylene, both ends of which replace hydrogen atoms of the same CH 2 moiety.
  • C 5 -spiroalkyl means pent-1,5-ylene, both ends of which replace hydrogen atoms of the same CH 2 moiety.
  • C 6 -spiroalkyl means hex-1,6-ylene, both ends of which replace hydrogen atoms of the same CH 2 moiety.
  • NH protecting group means trichloroethoxycarbonyl, tribromoethoxycarbonyl, benzyloxycarbonyl, para-nitrobenzylcarbonyl, ortho-bromobenzyloxycarbonyl, chloroacetyl, dichloroacetyl, trichloroacetyl, trifluoroacetyl, phenylacetyl, formyl, acetyl, benzoyl, tert-amyloxycarbonyl, tert-butoxycarbonyl, para-methoxybenzyloxycarbonyl, 3,4-dimethoxybenzyl-oxycarbonyl, 4-(phenylazo)benzyloxycarbonyl, 2-furfuryl-oxycarbonyl, diphenylmethoxycarbonyl, 1,1-dimethylpropoxy-carbonyl, isopropoxycarbonyl, phthaloyl, succinyl, alanyl, leucyl,
  • C(O)OH protecting group means methyl, ethyl, n-propyl, isopropyl, 1,1-dimethylpropyl, n-butyl, tert-butyl, phenyl, naphthyl, benzyl, diphenylmethyl, triphenylmethyl, para-nitrobenzyl, para-methoxybenzyl, bis(para-methoxyphenyl)methyl, acetylmethyl, benzoylmethyl, para-nitrobenzoylmethyl, para-bromobenzoylmethyl, para-methanesulfonylbenzoylmethyl, 2-tetrahydropyranyl 2-tetrahydrofuranyl, 2,2,2-trichloro-ethyl, 2-(trimethylsilyl)ethyl, acetoxymethyl, propionyloxymethyl, pivaloyloxymethyl, phthalimidomethyl, succinimidomethyl, cyclopropyl
  • OH or SH protecting group means benzyloxycarbonyl, 4-nitrobenzyloxycarbonyl, 4-bromobenzyloxycarbonyl, 4-methoxybenzyloxycarbonyl, 3,4-dimethoxybenzyloxycarbonyl, methoxycarbonyl, ethoxycarbonyl, tert-butoxycarbonyl, 1,1-dimethylpropoxycarbonyl, isopropoxycarbonyl, isobutyloxycarbonyl, diphenylmethoxycarbonyl, 2,2,2-trichloroethoxycarbonyl, 2,2,2-tribromoethoxycarbonyl, 2-(trimethylsilyl)ethoxycarbonyl, 2-(phenylsulfonyl)ethoxycarbonyl, 2-(triphenylphosphonio)ethoxycarbonyl, 2-furfuryloxycarbonyl, 1-adamantyloxycarbonyl, vinyloxycarbonyl, allyloxycarbonyl, S
  • a non-hydrogen radical is in the place of hydrogen radical on a carbon or nitrogen of the substituent.
  • a substituted alkyl substituent is an alkyl substituent in which at least one non-hydrogen radical is in the place of a hydrogen radical on the alkyl substituent.
  • monofluoroalkyl is alkyl substituted with a fluoro radical
  • difluoroalkyl is alkyl substituted with two fluoro radicals. It should be recognized that if there are more than one substitution on a substituent, each non-hydrogen radical may be identical or different (unless otherwise stated).
  • substituent may be either (1) not substituted or (2) substituted. If a substituent is described as being optionally substituted with up to a particular number of non-hydrogen radicals, that substituent may be either (1) not substituted; or (2) substituted by up to that particular number of non-hydrogen radicals or by up to the maximum number of substitutable positions on the substituent, whichever is less. Thus, for example, if a substituent is described as a heteroaryl optionally substituted with up to 3 non-hydrogen radicals, then any heteroaryl with less than 3 substitutable positions would be optionally substituted by up to only as many non-hydrogen radicals as the heteroaryl has substitutable positions.
  • tetrazolyl (which has only one substitutable position) would be optionally substituted with up to one non-hydrogen radical.
  • an amino nitrogen is described as being optionally substituted with up to 2 non-hydrogen radicals, then a primary amino nitrogen will be optionally substituted with up to 2 non-hydrogen radicals, whereas a secondary amino nitrogen will be optionally substituted with up to only 1 non-hydrogen radical.
  • the selective Bcl-2 inhibitor compounds of the current invention encompass all possible combinations of the substituents for the genus compound of Formula (I). Suitable examples of compounds that fall within the scope of the current invention include, but are not limited to, N-( ⁇ 5-chloro-6-[(4-fluorotetrahydro-2H-pyran-4-yl)methoxy]pyridin-3-yl ⁇ sulfonyl)-4-(4- ⁇ [2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl ⁇ piperazin-1-yl)-2-[(6-fluoro-1H-indazol-4-yl)oxy]benzamide; 4-(4- ⁇ [2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl ⁇ piperazin-1-yl)-N- ⁇ [4-(
  • the selective Bcl-2 inhibitor compounds used in the methods of the current invention may also include a pharmaceutically acceptable salt form of a compound having Formula (I).
  • pharmaceutically acceptable salt(s) means those salts of the selective Bcl-2 inhibitors of the invention that are safe and effective for administration to a patient and that do not adversely affect the therapeutic qualities of the compound.
  • Pharmaceutically acceptable salts include salts of acidic or basic groups present in compounds of the invention.
  • Pharmaceutically acceptable acid addition salts include, but are not limited to, hydrochloride, hydrobromide, hydroiodide, nitrate, sulfate, bisulfate, phosphate, acid phosphate, isonicotinate, acetate, lactate, salicylate, citrate, tartrate, pantothenate, bitartrate, ascorbate, succinate, maleate, gentisinate, fumarate, gluconate, glucaronate, saccharate, formate, benzoate, glutamate, methanesulfonate, ethanesulfonate, benzensulfonate, p-toluenesulfonate and pamoate (i.e., 1,1′-methylene-bis-(2-hydroxy-3-naphthoate)) salts.
  • Suitable base salts include, but are not limited to, aluminum, calcium, lithium, magnesium, potassium, sodium, zinc, and diethanolamine salts.
  • Suitable base salts include, but are not limited to, aluminum, calcium, lithium, magnesium, potassium, sodium, zinc, and diethanolamine salts.
  • the compounds used in the methods of the current invention may also comprise geometric isomers.
  • Compounds of this invention may contain carbon-carbon double bonds or carbon-nitrogen double bonds in the E or Z configuration, wherein the term “E” represents higher order substituents on opposite sides of the carbon-carbon or carbon-nitrogen double bond and the term “Z” represents higher order substituents on the same side of the carbon-carbon or carbon-nitrogen double bond as determined by the Cahn-Ingold-Prelog Priority Rules.
  • the compounds of this invention may also exist as a mixture of “E” and “Z” isomers. Substituents around a cycloalkyl or heterocycloalkyl are designated as being of cis or trans configuration.
  • the invention contemplates the various isomers and mixtures thereof resulting from the disposal of substituents around an adamantane ring system.
  • Two substituents around a single ring within an adamantane ring system are designated as being of Z or E relative configuration.
  • the selective Bcl-2 inhibitor compounds may also contain asymmetrically substituted carbon atoms in the R or S configuration, in which the terms “R” and “S” are as defined by the IUPAC 1974 Recommendations for Section E, Fundamental Stereochemistry, Pure Appl. Chem. (1976) 45, 13-10.
  • Compounds having asymmetrically substituted carbon atoms with equal amounts of R and S configurations are racemic at those carbon atoms. Atoms with an excess of one configuration over the other are assigned the configuration present in the higher amount, such an excess of about 85%-90%, an excess of about 95%-99%, or an excess greater than about 99%. Accordingly, this invention includes racemic mixtures, relative and absolute stereoisomers, and mixtures of relative and absolute stereoisomers.
  • the selective Bcl-2 inhibitor compounds used in the methods of the current invention containing NH, C(O)OH, OH or SH moieties may have attached thereto prodrug-forming moieties.
  • the prodrug-forming moieties are removed by metabolic processes and release the compounds having the freed hydroxyl, amino or carboxylic acid in vivo.
  • Prodrugs are useful for adjusting such pharmacokinetic properties of the compounds as solubility and/or hydrophobicity, absorption in the gastrointestinal tract, bioavailability, tissue penetration, and rate of clearance.
  • the compounds used in the various embodiments can also exist in isotope-labeled or isotope-enriched form containing one or more atoms having an atomic mass or mass number different from the atomic mass or mass number most abundantly found in nature.
  • Isotopes can be radioactive or non-radioactive isotopes.
  • Isotopes of atoms such as hydrogen, carbon, phosphorous, sulfur, fluorine, chlorine, and iodine include, but are not limited to, 2 H, 3 H, 13 C, 14 C 15 N, 18 O, 32 P, 35 S, 18 F, 36 Cl, and 125 I.
  • Compounds that contain other isotopes of these and/or other atoms are within the scope of this invention.
  • the isotope-labeled compounds contain deuterium ( 2 H), tritium ( 3 H) or 14 C isotopes.
  • Isotope-labeled compounds of this invention can be prepared by the general methods well known to persons having ordinary skill in the art. Such isotope-labeled compounds can be conveniently prepared by carrying out the procedures disclosed in the Examples disclosed herein and Schemes by substituting a readily available isotope-labeled reagent for a non-labeled reagent.
  • compounds may be treated with isotope-labeled reagents to exchange a normal atom with its isotope, for example, hydrogen for deuterium can be exchanged by the action of a deuteric acid such as D 2 SO 4 /D 2 O.
  • a deuteric acid such as D 2 SO 4 /D 2 O.
  • the isotope-labeled compounds of the invention may be used as standards to determine the effectiveness of Bcl-2 inhibitors in binding assays.
  • Isotope containing compounds have been used in pharmaceutical research to investigate the in vivo metabolic fate of the compounds by evaluation of the mechanism of action and metabolic pathway of the nonisotope-labeled parent compound (Blake et al. J. Pharm. Sci. 64, 3, 367-391 (1975)).
  • Such metabolic studies are important in the design of safe, effective therapeutic drugs, either because the in vivo active compound administered to the patient or because the metabolites produced from the parent compound prove to be toxic or carcinogenic (Foster et al., Advances in Drug Research Vol. 14, pp.
  • non-radio active isotope containing drugs such as deuterated drugs called “heavy drugs,” can be used for the treatment of diseases and conditions related to Bcl-2 activity.
  • Increasing the amount of an isotope present in a compound above its natural abundance is called enrichment.
  • Examples of the amount of enrichment include from about 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 16, 21, 25, 29, 33, 37, 42, 46, 50, 54, 58, 63, 67, 71, 75, 79, 84, 88, 92, 96, to about 100 mol %.
  • Stable isotope labeling of a drug can alter its physico-chemical properties such as pKa and lipid solubility. These effects and alterations can affect the pharmacodynamic response of the drug molecule if the isotopic substitution affects a region involved in a ligand-receptor interaction. While some of the physical properties of a stable isotope-labeled molecule are different from those of the unlabeled one, the chemical and biological properties are the same, with one important exception: because of the increased mass of the heavy isotope, any bond involving the heavy isotope and another atom will be stronger than the same bond between the light isotope and that atom. Accordingly, the incorporation of an isotope at a site of metabolism or enzymatic transformation will slow said reactions potentially altering the pharmacokinetic profile or efficacy relative to the non-isotopic compound.
  • the current methods may also incorporate a prodrug form of the selective Bcl-2 inhibitor compound.
  • Prodrugs are derivatives of an active drug designed to ameliorate some identified, undesirable physical or biological property.
  • the physical properties are usually solubility (too much or not enough lipid or aqueous solubility) or stability related, while problematic biological properties include too rapid metabolism or poor bioavailability which itself may be related to a physicochemical property.
  • Prodrugs are usually prepared by: a) formation of ester, hemi esters, carbonate esters, nitrate esters, amides, hydroxamic acids, carbamates, imines, Mannich bases, phosphates, phosphate esters, and enamines of the active drug, b) functionalizing the drug with azo, glycoside, peptide, and ether functional groups, c) use of aminals, hemi-aminals, polymers, salts, complexes, phosphoramides, acetals, hemiacetals, and ketal forms of the drug.
  • the methods of the current invention may involve administration of the compounds having Formula (I) by, for example, at least one mode selected from parenteral, subcutaneous, intramuscular, intravenous, intrarticular, intrabronchial, intraabdominal, intracapsular, intracartilaginous, intracavitary, intracelial, intracerebellar, intracerebroventricular, intracolic, intracervical, intragastric, intrahepatic, intramyocardial, intraosteal, intrapelvic, intrapericardiac, intraperitoneal, intrapleural, intraprostatic, intrapulmonary, intrarectal, intrarenal, intraretinal, intraspinal, intrasynovial, intrathoracic, intrauterine, intravesical, bolus, vaginal, rectal, buccal, sublingual, intranasal, and transdermal.
  • parenteral subcutaneous, intramuscular, intravenous, intrarticular, intrabronchial, intraabdominal, intracapsular, intracartilaginous,
  • the “therapeutically effective amount” of the current invention refers to that amount of the compound being administered sufficient to prevent development of or alleviate to some extent one or more of the symptoms of the condition or disorder being treated.
  • Therapeutically effective amounts of compounds having Formula (I) depend on the recipient of the treatment, the disorder being treated and the severity thereof, the composition containing the compound, the time of administration, the route of administration, the duration of treatment, the compound potency, its rate of clearance and whether or not another drug is co-administered.
  • the methods of the current invention involve administering a dose of the selective Bcl-2 inhibitor ranging from about 0.001 mg/kg to about 1000 mg/kg.
  • the methods involve administering a dose of selective Bcl-2 inhibitor ranging from about 0.01 mg/kg to about 500 mg/kg. In a further embodiment, the methods involve administering a dose of selective Bcl-2 inhibitor ranging from about 0.1 mg/kg to about 300 mg/kg.
  • the methods of the current invention may have illustrated improved efficacy in treating disease states such as SLE, lupus nephritis, and Sjogren's Syndrome compared to methods currently known within the art due to the fact that the compounds disclosed herein may selectively inhibit the Bcl-2 protein.
  • the Bcl-2 family of proteins is a group of proteins that have regulatory effects on many developmental and homeostasis functions, such as apoptosis (programmed cell death).
  • the Bcl-2 family includes other proteins include Bcl-x L and Bcl-w.
  • inhibition of the Bcl-x L protein has been shown to have an adverse impact on platelet counts, in some cases resulting in thrombocytopenia.
  • the selective Bcl-2 inhibitor compounds having Formula (I) have shown a higher binding affinity (as evidenced by lower K, values) for Bcl-2 compared to other Bcl-2 family proteins, such as Bcl-x L and Bcl-w.
  • the methods of the current invention provide the advantages of inhibition of the Bcl-2 protein, with a decreased risk of the adverse effects associated with Bcl-x L and Bcl-w inhibition.
  • the binding affinity for the various proteins is measured as a value of K i which represents the amount of the compound required to inhibit a physiologic process or compound (such as a protein) by 50%.
  • the selective Bcl-2 compounds used in the methods of the current invention generally have a binding affinity (K i ) of less than about 1 micromolar, less than about 500 nanomolar, less than about 400 nanomolar, less than about 300 nanomolar, less than about 200 nanomolar, less than about 100 nanomolar, less than about 50 nanomolar, less than about 25 nanomolar, less than about 10 nanomolar, less than about 5 nanomolar, less than about 1 nanomolar, less than about 900 picomolar, less than about 800 picomolar, less than about 700 picomolar, less than about 600 picomolar, less than about 500 picomolar, less than about 400 picomolar, less than about 300 picomolar, less than about 200 picomolar, and less than about 100 picomolar to Bcl-2.
  • K i binding affinity
  • the selective Bcl-2 inhibitors used in the methods of the current invention selectively bind to and elicit a response on Bcl-2 proteins at much lower concentrations than those required to bind to and elicit a response on Bcl-x L .
  • the selective Bcl-2 inhibitor when the selective Bcl-2 inhibitor is administered to the patient, the inhibitor is more prone to inhibit Bcl-2, rather than Bcl-x L .
  • the selective inhibitors used in the methods of the current invention tend to have a competitive binding affinity (K i ) for Bcl-2 that is at least about 500, at least about 1000, at least about 2000, at least about 2500, at least about 3000, at least about 3500, and at least about 4000 times less than the binding affinity for Bcl-x L .
  • K i competitive binding affinity
  • the methods of the invention include administering compounds having Formula (I) with or without an excipient.
  • Excipients include, for example, encapsulating materials or additives such as absorption accelerators, antioxidants, binders, buffers, coating agents, coloring agents, diluents, disintegrating agents, emulsifiers, extenders, fillers, flavoring agents, humectants, lubricants, perfumes, preservatives, propellants, releasing agents, sterilizing agents, sweeteners, solubilizers, wetting agents and mixtures thereof.
  • encapsulating materials or additives such as absorption accelerators, antioxidants, binders, buffers, coating agents, coloring agents, diluents, disintegrating agents, emulsifiers, extenders, fillers, flavoring agents, humectants, lubricants, perfumes, preservatives, propellants, releasing agents, sterilizing agents, sweeteners, solubilizers, wetting agents and mixtures thereof.
  • Excipients for preparation of compositions comprising a compound having Formula (I) to be administered orally in solid dosage form include, for example, agar, alginic acid, aluminum hydroxide, benzyl alcohol, benzyl benzoate, 1,3-butylene glycol, carbomers, castor oil, cellulose, cellulose acetate, cocoa butter, corn starch, corn oil, cottonseed oil, cross-povidone, diglycerides, ethanol, ethyl cellulose, ethyl laureate, ethyl oleate, fatty acid esters, gelatin, germ oil, glucose, glycerol, groundnut oil, hydroxypropylmethyl cellulose, isopropanol, isotonic saline, lactose, magnesium hydroxide, magnesium stearate, malt, mannitol, monoglycerides, olive oil, peanut oil, potassium phosphate salts, potato starch, povidone, propylene glycol, Ring
  • Excipients for preparation of compositions comprising a compound of this invention having Formula (I) to be administered ophthalmically or orally in liquid dosage forms include, for example, 1,3-butylene glycol, castor oil, corn oil, cottonseed oil, ethanol, fatty acid esters of sorbitan, germ oil, groundnut oil, glycerol, isopropanol, olive oil, polyethylene glycols, propylene glycol, sesame oil, water and mixtures thereof.
  • Excipients for preparation of compositions comprising a compound of this invention having Formula (I) to be administered osmotically include, for example, chlorofluorohydrocarbons, ethanol, water and mixtures thereof.
  • Excipients for preparation of compositions comprising a compound of this invention having Formula (I) to be administered parenterally include, for example, 1,3-butanediol, castor oil, corn oil, cottonseed oil, dextrose, germ oil, groundnut oil, liposomes, oleic acid, olive oil, peanut oil, Ringer's solution, safflower oil, sesame oil, soybean oil, U.S.P. or isotonic sodium chloride solution, water and mixtures thereof.
  • Excipients for preparation of compositions comprising a compound of this invention having Formula (I) to be administered rectally or vaginally include, for example, cocoa butter, polyethylene glycol, wax and mixtures thereof.
  • the methods of the current invention encompass methods of administering the selective Bcl-2 inhibitor alone or in combination with other therapeutic products.
  • Many proteins have been implicated in general autoimmune and inflammatory responses. Accordingly, it may be possible to combine the selective Bcl-2 inhibitors with compounds capable of altering the function of other proteins implicated in general autoimmune and inflammatory responses.
  • proteins associated with autoimmune and inflammatory response include C5, CCL1 (1-309), CCL11 (eotaxin), CCL13 (mcp-4), CCL15 (MIP-1d), CCL16 (HCC-4), CCL17 (TARC), CCL18 (PARC), CCL19, CCL2 (mcp-1), CCL20 (MIP-3a), CCL21 (MIP-2), CCL23 (MPIF-1), CCL24 (MPIF-2/eotaxin-2), CCL25 (TECK), CCL26, CCL3 (MIP-1a), CCL4 (MIP-1b), CCL5 (RANTES), CCL7 (mcp-3), CCL8 (mcp-2), CXCL1, CXCL10 (IP-10), CXCL11 (I-TAC/IP-9), CXCL12 (SDF1), CXCL13, CXCL14, CXCL2, CXCL3, CXCL5 (ENA-78 / LIX), CXCL6 (GCP-2), CXCL9
  • the invention can be used alone or in combination with an additional agent, e.g., a therapeutic agent, the additional agent being selected by the skilled artisan for its intended purpose.
  • the additional agent can be a therapeutic agent, recognized in the art as being useful to treat the disease or condition being treated by the present invention.
  • the additional agent also can be an agent that imparts a beneficial attribute to the therapeutic composition e.g., an agent that affects the viscosity of the composition.
  • combinations which are to be included within this invention are those combinations comprising treatment with the selective Bcl-2 inhibitors described herein and one or more additional therapeutic agents.
  • Combinations to treat autoimmune and inflammatory diseases are non-steroidal anti-inflammatory drug(s) also referred to as NSAIDS which include drugs like ibuprofen.
  • NSAIDS non-steroidal anti-inflammatory drug(s) also referred to as NSAIDS which include drugs like ibuprofen.
  • Other combinations are corticosteroids including prednisolone; the well known side-effects of steroid use can be reduced or even eliminated by tapering the steroid dose required when treating patients in combination with this invention.
  • Non-limiting examples of therapeutic agents for lupus with this invention can be combined include the following: cytokine suppressive anti-inflammatory drug(s) (CSAIDs); antibodies to or antagonists of other human cytokines or growth factors, for example, TNF, LT, IL-1, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-12, IL-13, IL-15, IL-16, IL-17A, IL-17F, IL-18, IL-21, IL-22, IL-23, IL-25, IL-33, interferons (for example, alpha, beta, gamma etc), Tweak, BAFF/BLyS, April, chemokines.
  • CSAIDs cytokine suppressive anti-inflammatory drug(s)
  • the invention can be combined with antibodies to cell surface molecules such as CD2, CD3, CD4, CD8, CD16, CD19, CD20, CD22, CD25, CD28, CD30, CD32, CD40, CD45, CD47, CD52, CD54, CD64, CD69, CD72, CD79, CD80 (B7.1), CD86 (B7.2), CD90, CD100, CD200, CTLA, ICOS-1, B7RP, BR3, TACI, BCMA, or their ligands including CD154 (gp39 or CD40L).
  • cell surface molecules such as CD2, CD3, CD4, CD8, CD16, CD19, CD20, CD22, CD25, CD28, CD30, CD32, CD40, CD45, CD47, CD52, CD54, CD64, CD69, CD72, CD79, CD80 (B7.1), CD86 (B7.2), CD90, CD100, CD200, CTLA, ICOS-1, B7RP, BR3, TACI, BCMA, or their ligands including CD154 (gp
  • the invention may also be combined with agents, such as mycophenolate mofetil (MMF), cytoxan, Bortezomib, methotrexate, 6-MP, azathioprine sulphasalazine, mesalazine, olsalazine chloroquinine/hydroxychloroquine, penicillamine, aurothiomalate (intramuscular and oral), azathioprine, cochicine, corticosteroids (oral, inhaled and local injection), selective glucocorticoid receptor modulators (SGRMs), O beta-2 adrenoreceptor agonists (salbutamol, terbutaline, salmeterol), xanthines (theophylline, aminophylline), cromoglycate, nedocromil, ketotifen, ipratropium and oxitropium, cyclosporin, FK506, rapamycin, mycophenolate mofetil, leflu
  • Examples of therapeutic agents for SLE (Lupus) and lupus nephritis, in which the invention can be combined include the following: NSAIDs, for example, diclofenac, naproxen, ibuprofen, piroxicam, indomethacin; COX2 inhibitors, for example, Celecoxib, rofecoxib, valdecoxib; anti-malarials, for example, hydroxychloroquine; Steroids, for example, prednisone, prednisolone, budenoside, dexamethasone; Cytotoxics, for example, azathioprine, cyclophosphamide, mycophenolate mofetil, methotrexate; inhibitors of PDE4 or purine synthesis inhibitor, for example Cellcept.
  • NSAIDs for example, diclofenac, naproxen, ibuprofen, piroxicam, indomethacin
  • COX2 inhibitors for
  • binding proteins incorporated into the methods of the invention may also be combined with agents such as sulfasalazine, 5-aminosalicylic acid, olsalazine, Imuran and agents which interfere with synthesis, production or action of proinflammatory cytokines such as IL-1, for example, caspase inhibitors like IL-1 ⁇ converting enzyme inhibitors and IL-lra.
  • the invention may also be used with T cell signaling inhibitors, for example, tyrosine kinase inhibitors; or molecules that target T cell activation molecules, for example, CTLA-4-IgG or anti-B7 family antibodies, anti-PD-1 family antibodies.
  • the invention can be combined with IL-11 or anti-cytokine antibodies, for example, fonotolizumab (anti-IFNg antibody), anti-interferon alpha, or anti-receptor receptor antibodies, for example, anti-IL-6 receptor antibody and antibodies to B-cell surface molecules.
  • IL-11 or anti-cytokine antibodies for example, fonotolizumab (anti-IFNg antibody), anti-interferon alpha, or anti-receptor receptor antibodies, for example, anti-IL-6 receptor antibody and antibodies to B-cell surface molecules.
  • the invention may also be used with inhibitors of HMGB1, HDGF.
  • the invention may also be used with inhibitors of toll receptors 1, 2, 3, 4, 7, and 9.
  • the invention may also be used with inhibitors of dendritic cell makers BDCA-1, 2 and 3.
  • the invention may also be used with agents which promote regulatory T cell function.
  • the invention may also be used with LW 394 (abetimus), agents that inhibit complement, for example, anti-C5, anti-C5a, deplete or inactivate B-cells, for example, Rituximab (anti-CD20 antibody), lymphostat-B (anti-BlyS antibody), anti-CD22, TNF antagonists, for example, anti-TNF antibodies, Adalimumab (PCT Publication No.
  • WO 97/29131 HUMIRA
  • CA2 REMICADE
  • CDP 571 TNFR-Ig constructs, (p75TNFRIgG (ENBREL) and p55TNFRIgG (LENERCEPT)) and inhibitors of other bcl-2 family members such as Bcl-x L , Mcl-1, A-1 etc.
  • therapeutic agents used to treat Sjogren's Syndrome include, but are not limited to artificial tears, cyclosporine, cevimeline, pilocarpine, NSAIDs, corticosteroids, immunosuppressants, disease-modifying anti-rheumatic drugs (DMARDs) such as methotrexate, and hydroxychloroquine.
  • DMARDs disease-modifying anti-rheumatic drugs
  • the binding protein used in the methods of the invention has an on rate constant (K on ) to the one or more targets selected from the group consisting of: at least about 10 2 M ⁇ 1 s ⁇ 1 ; at least about 10 3 M ⁇ 1 s ⁇ 1 ; at least about 10 4 M ⁇ 1 s ⁇ 1 ; at least about 10 5 M ⁇ 1 s ⁇ 1 ; and at least about 10 6 M ⁇ 1 s ⁇ 1 , as measured by surface plasmon resonance.
  • K on on rate constant
  • the binding protein of the invention has an on rate constant (K on ) to one or more targets between 10 2 M ⁇ 1 s ⁇ 1 and 10 3 M ⁇ 1 s ⁇ 1 ; between 10 3 M ⁇ 1 s ⁇ 1 and 10 4 M ⁇ 1 s ⁇ 1 ; between 10 4 M ⁇ 1 s ⁇ 1 and 10 5 M ⁇ 1 s ⁇ 1 ; or between 10 5 M ⁇ 1 s ⁇ 1 and 10 6 M ⁇ 1 s ⁇ 1 , as measured by surface plasmon resonance.
  • K on on rate constant
  • the binding protein has an off rate constant (K off ) for one or more targets selected from the group consisting of: at most about 10 ⁇ 3 s ⁇ 1 ; at most about 10 ⁇ 4 s ⁇ 1 ; at most about 10 ⁇ 5 s ⁇ 1 ; and at most about 10 ⁇ 6 s ⁇ 1 , as measured by surface plasmon resonance.
  • K off off rate constant
  • the binding protein of the invention has an off rate constant (K off ) to one or more targets of 10 ⁇ 3 s ⁇ 1 to 10 4 s ⁇ 1 ; of 10 ⁇ 4 s ⁇ 1 to10 ⁇ 5 s ⁇ 1 ; or of 10 ⁇ 5 s ⁇ 1 to 10 ⁇ 6 s ⁇ 1 , as measured by surface plasmon resonance.
  • K off off rate constant
  • the binding protein has a dissociation constant (K D ) to one or more targets selected from the group consisting of: at most about 10 ⁇ 7 M; at most about 10 ⁇ 8 M; at most about 10 ⁇ 9 M; at most about 10 ⁇ 10 M; at most about 10 ⁇ 11 M; at most about 10 ⁇ 12 M; and at most 10 ⁇ 13 M.
  • K D dissociation constant
  • the binding protein of the invention has a dissociation constant (K D ) to its targets of 10 ⁇ 7 M to 10 ⁇ 8 M; of 10 ⁇ 8 M to 10 ⁇ 9 M; of 10 ⁇ 9 M to 10 ⁇ 10 M; of 10 ⁇ 10 to 10 ⁇ 11 M; of 10 ⁇ 11 M to 10 ⁇ 12 M; or of 10 ⁇ 12 to M 10 ⁇ 13 M.
  • K D dissociation constant
  • the binding protein is a conjugate comprising a binding protein and an agent selected from the group consisting of an immunoadhesion molecule, an imaging agent, a therapeutic agent, and a cytotoxic agent.
  • imaging agents include a radiolabel, an enzyme, a fluorescent label, a luminescent label, a bioluminescent label, a magnetic label, and biotin.
  • radiolabels include 3H, 14C, 35S, 90Y, 99Tc, 111In, 125I, 131I, 177Lu, 166Ho, and 153Sm.
  • the therapeutic or cytotoxic agent is selected from the group consisting of an anti-metabolite, an alkylating agent, an antibiotic, a growth factor, a cytokine, an anti-angiogenic agent, an anti-mitotic agent, an anthracycline, toxin, and an apoptotic agent.
  • the binding protein is a crystallized binding protein, for example, a carrier-free pharmaceutical controlled release crystal.
  • the crystallized binding protein has a greater half life in vivo than the soluble counterpart of the binding protein.
  • the crystallized binding protein retains biological activity.
  • the binding protein described herein is glycosylated.
  • the glycosylation is a human glycosylation pattern.
  • a further embodiment provides a vector comprising the isolated nucleic acid disclosed herein wherein the vector is selected from the group consisting of pcDNA; pTT (Durocher et al., Nucleic Acids Research 2002, Vol 30, No.2); pTT3 (pTT with additional multiple cloning site; pEFBOS (Mizushima, S. and Nagata, S., (1990) Nucleic Acids Research Vol 18, No. 17); pBV; pJV; pcDNA3.1 TOPO, pEF6 TOPO and pBJ.
  • the vector is a vector disclosed in U.S. Patent Application Ser. No. 61/021,282.
  • a host cell is transformed with the vector disclosed herein.
  • the host cell is a prokaryotic cell.
  • the host cell is E.Coli.
  • the host cell is a eukaryotic cell.
  • the eukaryotic cell is selected from the group consisting of a protist cell, an animal cell, an avian cell, a plant cell and a fungal cell.
  • the host cell is a mammalian cell including, but not limited to, CHO, COS; NSO, SP2, PER.C6 or a fungal cell such as Saccharomyces cerevisiae; or an insect cell such as Sf9.
  • Another aspect of the invention provides a method of producing a binding protein disclosed herein comprising culturing any one of the host cells also disclosed herein in a culture medium under conditions sufficient to produce the binding protein.
  • 50%-75% of the binding protein produced by this method is a dual specific tetravalent binding protein.
  • 75%-90% of the binding protein produced by this method is a dual specific tetravalent binding protein.
  • 90%-95% of the binding protein produced is a dual specific tetravalent binding protein.
  • compositions for the release of a binding protein wherein the composition comprises a formulation that in turn comprises a crystallized binding protein, as disclosed herein, and an ingredient, and at least one polymeric carrier.
  • the polymeric carrier is a polymer selected from one or more of the group consisting of: poly (acrylic acid), poly (cyanoacrylates), poly (amino acids), poly (anhydrides), poly (depsipeptide), poly (esters), poly (lactic acid), poly (lactic-co-glycolic acid) or PLGA, poly (b-hydroxybutryate), poly (caprolactone), poly (dioxanone); poly (ethylene glycol), poly ((hydroxypropyl) methacrylamide, poly [(organo)phosphazene], poly (ortho esters), poly (vinyl alcohol), poly (vinylpyrrolidone), maleic anhydride- alkyl vinyl ether copolymers, pluronic polyols, albumin, alginate, cellulose and
  • the ingredient is selected from the group consisting of albumin, sucrose, trehalose, lactitol, gelatin, hydroxypropyl- ⁇ - cyclodextrin, methoxypolyethylene glycol and polyethylene glycol.
  • Another embodiment provides a method for treating a mammal comprising the step of administering to the mammal an effective amount of the composition disclosed herein.
  • the invention also provides a pharmaceutical composition comprising a binding protein, as disclosed herein and a pharmaceutically acceptable carrier.
  • the pharmaceutical composition comprises at least one additional therapeutic agent for treating a disorder.
  • the additional agent is selected from the group consisting of: a therapeutic agent, an imaging agent, a cytotoxic agent, an angiogenesis inhibitor (including but not limited to an anti-VEGF antibody or a VEGF-trap), a kinase inhibitor (including but not limited to a KDR and a TIE-2 inhibitor), a co-stimulation molecule blocker (including but not limited to anti-B7.1, anti-B7.2, CTLA4-Ig, anti-CD20), an adhesion molecule blocker (including but not limited to an anti-LFA-1 antibody, an anti-E/L selectin antibody, a small molecule inhibitor), an anti-cytokine antibody or functional fragment thereof (including but not limited to an anti-IL-18, an anti-TNF, and an anti-IL-6/cytokine receptor antibody), methotrex
  • the invention provides a method of treating a patient suffering from a disorder comprising the step of administering any one of the binding proteins disclosed herein before, concurrent, or after the administration of a second agent, as discussed herein.
  • the second agent is selected from the group consisting of budenoside, epidermal growth factor, corticosteroids, cyclosporin, sulfasalazine, aminosalicylates, 6-mercaptopurine, azathioprine, metronidazole, lipoxygenase inhibitors, mesalamine, olsalazine, balsalazide, antioxidants, thromboxane inhibitors, IL-1 receptor antagonists, anti-IL-1 ⁇ mAbs, anti-IL-6 or IL-6 receptor mAbs, growth factors, elastase inhibitors, pyridinyl-imidazole compounds, antibodies or agonists of TNF, LT, IL-1, IL-2, IL-6,
  • the anti-idiotype antibody includes any protein or peptide containing molecule that comprises at least a portion of an immunoglobulin molecule such as, but not limited to, at least one complementarily determining region (CDR) of a heavy or light chain or a ligand binding portion thereof, a heavy chain or light chain variable region, a heavy chain or light chain constant region, a framework region, or any portion thereof, that can be incorporated into a binding protein of the present invention.
  • CDR complementarily determining region
  • a binding protein of the invention can be used alone or in combination to treat such diseases. It should be understood that the binding proteins can be used alone or in combination with an additional agent, e.g., a therapeutic agent, the additional agent being selected by the skilled artisan for its intended purpose.
  • the additional agent can be a therapeutic agent art-recognized as being useful to treat the disease or condition being treated by the antibody of the present invention.
  • the additional agent also can be an agent that imparts a beneficial attribute to the therapeutic composition e.g., an agent which affects the viscosity of the composition.
  • the combinations which are to be included within this invention are those combinations useful for their intended purpose.
  • the agents set forth below are illustrative for purposes and not intended to be limited.
  • the combinations, which are part of this invention can be the antibodies of the present invention and at least one additional agent selected from the lists below.
  • the combination can also include more than one additional agent, e.g., two or three additional agents if the combination is such that the formed composition can perform its intended function.
  • Combinations to treat autoimmune and inflammatory diseases are non-steroidal anti- inflammatory drug(s) also referred to as NSAIDS which include drugs like ibuprofen.
  • NSAIDS non-steroidal anti- inflammatory drug(s) also referred to as NSAIDS which include drugs like ibuprofen.
  • Other combinations are corticosteroids including prednisolone; the well known side-effects of steroid use can be reduced or even eliminated by tapering the steroid dose required when treating patients in combination with the DVD Igs of this invention.
  • Non-limiting examples of therapeutic agents for rheumatoid arthritis with which an antibody, or antibody portion, of the invention can be combined include the following: cytokine suppressive anti-inflammatory drug(s) (CSAIDs); antibodies to or antagonists of other human cytokines or growth factors, for example, TNF, LT, IL-1, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-15, IL-16, IL-18, IL-21, IL-23, interferons, EMAP-II, GM-CSF, FGF, and PDGF.
  • CSAIDs cytokine suppressive anti-inflammatory drug
  • binding proteins incorporated into the methods of the invention, or antigen binding portions thereof, can be combined with antibodies to cell surface molecules such as CD2, CD3, CD4, CD8, CD25, CD28, CD30, CD40, CD45, CD69, CD80 (B7.1), CD86 (B7.2), CD90, CTLA or their ligands including CD154 (gp39 or CD40L).
  • cell surface molecules such as CD2, CD3, CD4, CD8, CD25, CD28, CD30, CD40, CD45, CD69, CD80 (B7.1), CD86 (B7.2), CD90, CTLA or their ligands including CD154 (gp39 or CD40L).
  • Combinations of therapeutic agents may interfere at different points in the autoimmune and subsequent inflammatory cascade; examples include TNF antagonists like chimeric, humanized or human TNF antibodies, Adalimumab, (WO 97/29131), CA2 (RemicadeTM), CDP 571, and soluble p55 or p75 TNF receptors, derivatives, thereof, (p75TNFR1gG (EnbrelTM) or p55TNFR1gG (Lenercept), and also TNF ⁇ converting enzyme (TACE) inhibitors; similarly IL-1 inhibitors (Interleukin-1-converting enzyme inhibitors, IL-1RA etc.) may be effective for the same reason. Other combinations include Interleukin 11.
  • TNF antagonists like chimeric, humanized or human TNF antibodies, Adalimumab, (WO 97/29131), CA2 (RemicadeTM), CDP 571, and soluble p55 or p75 TNF receptors, derivatives, thereof, (p75TNFR1gG (EnbrelTM
  • Yet another combination includes key players of the autoimmune response which may act parallel to, dependent on or in concert with IL-12 function; especially are IL-18 antagonists including IL-18 antibodies or soluble IL-18 receptors, or IL-18 binding proteins. It has been shown that IL-12 and IL-18 have overlapping but distinct functions and a combination of antagonists to both may be most effective. Yet another combination are non-depleting anti-CD4 inhibitors. Yet other combinations include antagonists of the co-stimulatory pathway CD80 (B7.1) or CD86 (B7.2) including antibodies, soluble receptors or antagonistic ligands.
  • binding proteins incorporated into the methods of the invention may also be combined with agents, such as methotrexate, 6-MP, azathioprine sulphasalazine, mesalazine, olsalazine chloroquinine/hydroxychloroquine, pencillamine, aurothiomalate (intramuscular and oral), azathioprine, cochicine, corticosteroids (oral, inhaled and local injection), beta-2 adrenoreceptor agonists (salbutamol, terbutaline, salmeteral), xanthines (theophylline, aminophylline), cromoglycate, nedocromil, ketotifen, ipratropium and oxitropium, cyclosporin, FK506, rapamycin, mycophenolate mofetil, leflunomide, NSAIDs, for example, ibuprofen, corticosteroids such as prednisolone, phosphodieste
  • NSAIDS for example, diclofenac, naproxen, ibuprofen, piroxicam, indomethacin
  • COX2 inhibitors for example, Celecoxib, rofecoxib, valdecoxib
  • anti-malarials for example, hydroxychloroquine
  • Steroids for example, prednisone, prednisolone, budenoside, dexamethasone
  • Cytotoxics for example, azathioprine, cyclophosphamide, mycophenolate mofetil, methotrexate
  • inhibitors of PDE4 or purine synthesis inhibitor for example Cellcept.
  • binding proteins incorporated into the methods of the invention may also be combined with agents such as sulfasalazine, 5-aminosalicylic acid, olsalazine, Imuran and agents which interfere with synthesis, production or action of proinflammatory cytokines such as IL-1, for example, caspase inhibitors like IL-1 ⁇ converting enzyme inhibitors and IL-1ra.
  • binding proteins incorporated into the methods of the invention may also be used with T cell signaling inhibitors, for example, tyrosine kinase inhibitors; or molecules that target T cell activation molecules, for example, CTLA-4-IgG or anti-B7 family antibodies, anti-PD-1 family antibodies.
  • binding proteins incorporated into the methods of the invention can be combined with IL-11 or anti-cytokine antibodies, for example, fonotolizumab (anti-IFNg antibody), or anti-receptor receptor antibodies, for example, anti-IL-6 receptor antibody and antibodies to B-cell surface molecules.
  • Antibodies of the invention or antigen binding portion thereof may also be used with LJP 394 (abetimus), agents that deplete or inactivate B-cells, for example, Rituximab (anti-CD20 antibody), lymphostat-B (anti-BlyS antibody), TNF antagonists, for example, anti-TNF antibodies, Adalimumab (PCT Publication No.
  • WO 97/29131 HUMIRA
  • CA2 REMICADE
  • CDP 571 TNFR-Ig constructs, (p75TNFRIgG (ENBREL) and p55TNFRIgG (LENERCEPT)) and bcl-2 inhibitors, because bcl-2 overexpression in transgenic mice has been demonstrated to cause a lupus like phenotype (see Marquina, Regina et al., Journal of Immunology (2004), 172(11), 7177-7185), therefore inhibition is expected to have therapeutic effects.
  • compositions of the invention may include a “therapeutically effective amount” or a “prophylactically effective amount” of a binding protein of the invention.
  • a “therapeutically effective amount” refers to an amount effective, at dosages and for periods of time necessary, to achieve the desired therapeutic result.
  • a therapeutically effective amount of the binding protein may be determined by a person skilled in the art and may vary according to factors such as the disease state, age, sex, and weight of the individual, and the ability of the binding protein to elicit a desired response in the individual.
  • a therapeutically effective amount is also one in which any toxic or detrimental effects of the antibody, or antibody portion, are outweighed by the therapeutically beneficial effects.
  • prophylactically effective amount refers to an amount effective, at dosages and for periods of time necessary, to achieve the desired prophylactic result. Typically, 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.
  • Dosage regimens may be adjusted to provide the optimum desired response (e.g., a therapeutic or prophylactic response). For example, a single bolus may be administered, several divided doses may be administered over time or the dose may be proportionally reduced or increased as indicated by the exigencies of the therapeutic situation. It is especially advantageous to formulate parenteral compositions in dosage unit form for ease of administration and uniformity of dosage.
  • Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the mammalian subjects to be treated; each unit containing a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier.
  • An exemplary, non-limiting range for a therapeutically or prophylactically effective amount of a binding protein of the invention is 0.1-20 mg/kg, for example, 1-10 mg/kg. It is to be noted that dosage values may vary with the type and severity of the condition to be alleviated. It is to be further understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions, and that dosage ranges set forth herein are exemplary only and are not intended to limit the scope or practice of the claimed composition.
  • additional compounds show selective binding affinity for Bcl-2 over Bcl-xL and other Bcl-2 family proteins. Additional compounds also inhibit Bcl-2 dependent cell lines than Bcl-xL dependent cell lines.
  • Cellular inhibition and killing by Compound 1 displays the hallmarks of apoptotic cell death, including rapid cytochrome c release, caspase-3 and -7 activation, and membrane phosphatidylserine (PS) externalization.
  • Compound 1 cell killing is caspase-dependent and can be ablated by the pan caspase inhibitor z-VAD-fmk. Cell killing is completely inhibited when Bax and Bak, the essential downstream effectors, are genetically ablated.
  • mice were treated four days with Compound 1 (1-100 mg/kg, orally every day) and cell numbers were measured with a Cell Dyn hematology analyzer.
  • Compound 1 resulted in a dose dependent decrease in lymphocytes while maintaining normal platelet counts compared to control.
  • Compound 2 also resulted in a decrease in lymphocytes, but caused a significant decrease in platelet counts.
  • Vehicle 1 1.38 83 1.32 83 3 2.3 63 1.34 79 4 2.62 57 1.72 73 5 0.98 84 1.02 84 6 1.91 69 0.98 85 7 0.89 85 0.95 85 8 0.92 85 1.02 84 9 0.75 88 0.88 86 10 2.25 65 2.48 71 11 1.76 73 1.71 80 12 1.44 78 2.21 74 13 2.32 64 2.61 70 14 3.02 54 2.33 73 15 1.85 72 1.65 81 16 1.77 73 1.99 77 17 1.84 77 1.30 83
  • FIGS. 2 and 3 The results of this experiment are illustrated in FIGS. 2 and 3 .
  • Compound 3 resulted in a dose dependent decrease in lymphocytes while maintaining normal platelet counts compared to a phosal vehicle control.
  • the 30 mg/kg and 100 mg/kg doses of Compound 3 resulted in lymphocyte reductions of 47% and 66%, respectively, without significantly affecting platelet counts.
  • FIG. 2 Compound 3 resulted in a dose dependent decrease in lymphocytes while maintaining normal platelet counts compared to a phosal vehicle control.
  • the 30 mg/kg and 100 mg/kg doses of Compound 3 resulted in lymphocyte reductions of 47% and 66%, respectively, without significantly affecting platelet counts.
  • FIG. 1 the 30 mg/kg and 100 mg/kg doses of Compound 3 resulted in lymphocyte reductions of 47% and 66%, respectively, without significantly affecting platelet counts.
  • Compound 3 illustrates a statistically significant decrease in CD4+ T cells, CD8+ T cells, and CD19+ B cells, for doses of Compound 3 comprising 100 mg/kg and 300 mg/kg.
  • these pharmacodynamic studies illustrate the ability of Compound 3, a selective Bcl-2 inhibitor to effectively reduce lymphocytes, without the adverse effects associated with non-selective Bcl-2 inhibitors.
  • Renal histopathological changes include severe glomerulonephritis, mesangial and peripheral proliferative changes, capillary membrane thickening, tubular atrophy, and infiltration of lymphocytes and monocytes/macrophages as in the majority of human SLE patients. These changes result in disruption of kidney function as evidenced by severe proteinuria (PU) greater than 300 mg/dL as measured by albumin sticks, followed by mortality as measured by survival.
  • PU severe proteinuria
  • Two of the clinical benchmarks for lupus nephritis, MMF and cyclophosphamide have been shown to decrease autoantibody titer, improve renal pathology, delay onset of severe proteinuria and prolong survival in these animals. (See Gelfand, M. C. and A. D.
  • NZB ⁇ NZWF1 females were purchased from The Jackson Laboratory (Bar Harbor, Me., USA) and maintained in a conventional animal housing facility throughout the experiment.
  • Proteinuria (PU) and survival were monitored weekly, followed by biweekly measurement of lymphocyte and platelet counts, and anti-ds DNA production.
  • PK parameters were also measured throughout the study.
  • Severe PU was defined by two consecutive weekly measurements of PU 300 mg/dl using Albustix test strips (VWR). When mice became moribund, they were sacrificed according to Institutional Animal Care and Use Committee protocols. PU and survival data were presented as Kaplan-Meyer survival curves using Graphpad Prism software and group differences were considered significant at the level of p ⁇ 0.05. Histologic scores were analyzed using ANOVA analysis. Anti-ds DNA were analyzed using one-way ANOVA analysis and Tukey post-test.
  • treatment with Compound 1 resulted in the delayed onset of severe PU in a dose-dependent fashion, reaching significance at 10, 30 and 100 mg/kg,
  • treatment with Compound 1 at 3, 10, 30, and 100 mg/kg significantly prolonged survival as illustrated in FIG. 4B and Table 3A.
  • These data also correlated with a dose-dependent and sustained reduction of lymphocytes in peripheral blood, with 30 and 100 mg/kg dosing of Compound 1 both resulting in 70% lymphopenia.
  • Efficacy on both disease endpoints at the 30 mg/kg dose of Compound 1 was comparable to MMF treatment at 100 mg/kg.
  • the exposure in this model at the 30 mg/kg dosing was 40 l ug.h/mL. Similar efficacy results were also obtained for Compound 17 as illustrated in FIG. 4 C, D and Table 3B.
  • Compound 1 triggers apoptosis of lymphocytes that are responsible for production of antibodies, which play a role in the progression of systemic lupus erythematosus, as well as Sjogren's Syndrome.
  • treatment with Compound 1 would decrease anti-ds DNA titer.
  • anti-dsDNA antibody levels were measured by ELISA and assigned arbitrary activity unit concentrations per ml relative to a standard plasma pool derived from proteinuric 9-10 month old NZB/W mice.
  • ELISA assay was performed by coating plates with poly-L-lysine followed by calf-thymus DNA.
  • Diluted mouse plasma was incubated and developed using anti-IgG HRP conjugated antibodies and the mean OD from duplicate wells was compared to a titrated standard curve of pooled high tittered anti-dsDNA plasma.
  • the undiluted standard plasma pool was arbitrarily assigned a value of 1000 anti-dsDNA Units/ml.
  • a linear regression analysis was then used to calculate the relative units of a given sample multiplied by the given dilution factor.
  • the results of this experiment are illustrated in FIG. 5 .
  • the IgG anti-ds DNA levels increased from an average of ⁇ 100 unit/mL at baseline (25 week) to an average of ⁇ 600 unit/mL by week 32, with a further increase to ⁇ 1800 unit/mL by week 40.
  • the apparent increase in anti-ds DNA titer occurred with a concomitant increase in disease severity and incidence as measured by PU and survival.
  • treatment with Compound 1 at 30 and 100 mg/kg significantly inhibited the increase in anti-ds DNA titer compared to vehicle control, comparable to the effect observed with MMF.
  • FIGS. 6 and 7 illustrate the results of the histological assessment
  • FIG. 8 illustrates the effect of selective Bcl-2 inhibitor treatment on IgG deposition, B cells, and T cells in the kidneys.
  • FIG. 6 phosal vehicle dosed spontaneous lupus nephritis mice typically had extensive renal infiltrates, as evidenced by tubular casts, dilated tubules, glomeruloclerosis, and cell infiltrates. Renal tissue infiltrates in spontaneous lupus nephritis mice dosed with 30 or 100 mg/kg of Compound 1 were small, discrete and less frequent.
  • FIG. 7 includes a bar graph illustrating the difference in histology scores for renal tissue that was not treated, tissue treated with Compound 1 at doses of 30 mg/kg and 100 mg/kg, and tissue treated with MMF at a dose of 100 mg/kg. As noted in FIG.
  • the tissue treated with Compound 1 at doses of 30 mg/kg and 100 mg/kg showed a statistically significant improvement (decrease in severity) in histology scores, as they pertained to glomerulonephritis, tubular changes, and perivascular infiltrates.
  • FIG. 8 illustrates a decrease in IgG deposition in renal tissue treated with Compound 1 at a dose of 30 mg/kg, as well as decreases in B cell and T cell numbers in renal tissue treated with Compound 1 at a dose of 100 mg/kg.
  • the selective Bcl-2 inhibitor, Compound 1 illustrated an amelioration in the deposition of IgG, infiltration and expansion of B cells, and T cells in renal tissue, and also resulted in a statistically significant improvement in histological scores, as compared to treatment with phosal vehicle.
  • BAFFR3-Ig a surrogate for Belimumab
  • IFN ⁇ -induced (NZB ⁇ NZW)F 1 model BAFFR3-Ig specifically blocks binding of BAFF/BLyS to its cognate receptor BAFFR3, resulting in systemic reduction in B cell numbers in lymphoid organs (See Kayagaki, N., et al., BAFF/BLyS receptor 3 binds the B cell survival factor BAFF ligand through a discrete surface loop and promotes processing of NF-kappaB2. Immunity, 2002. 17(4): p. 515-24). Treatment was initiated in a late-prophylactic mode (7 days after IFNa adenovirus).
  • mice (NZB ⁇ NZW)F1 mice (The Jackson Laboratory), 13-15 wk old, were injected with a single intravenous dose of IFN- ⁇ adenovirus (Abbott) at a concentration of 5 ⁇ 10 9 viral particles/mouse.
  • Treatment groups consisted of administration of Compound 1 in doses ranging from 1-100mg/kg/day, given orally; mycophenolate mofetil (MMF) at a dose of 100 mg/kg/day, given orally; and BAFFR3-Ig (BAFF/BLyS blocker) at a dose of 15 mg/kg, 3 ⁇ /week, by intraperitoneal injection. All treatment groups were administered treatment 7 days after adenovirus injection.
  • MMF mycophenolate mofetil
  • BAFFR3-Ig BAFF/BLyS blocker
  • mice were monitored weekly for proteinuria (PU) using Albustix test strips (VWR). Severe PU was defined by consecutive weekly measurements of PU ⁇ 300 mg/dl. When mice became moribund, they were sacrificed according to Institutional Animal Care and Use Committee protocols.
  • PU proteinuria
  • Anti-dsDNA antibody levels were measured by ELISA and assigned arbitrary activity unit concentrations per ml relative to a standard plasma pool derived from proteinuric 9-10 month old NZB/W mice.
  • ELISA assay was performed by coating plates with poly-L-lysine followed by calf-thymus DNA. Diluted mouse plasma was incubated and developed using anti-IgG HRP conjugated antibodies and the mean OD from duplicate wells was compared to a titrated standard curve of pooled high tittered anti-dsDNA plasma.
  • the undiluted standard plasma pool was arbitrarily assigned a value of 1000 anti-dsDNA Units/ml.
  • a linear regression analysis was then used to calculate the relative units of a given sample multiplied by the given dilution factor. The results of this experiment are illustrated in FIG. 10 .
  • Sjogren's Syndrome is a chronic disease state that affects the moisture-producing glands of the body, including the salivary glands of the mouth.
  • penetration of the selective Bcl-2 inhibitors into the salivary glands of patients with Sjogren's Syndrome could provide an effective treatment to decrease lymphocytes associated with Sjogren's Syndrome, without the dose-limiting thrombocytopenia associated with non-selective Bcl-2 inhibition.
  • a histologic assessment of the penetration of selective Bcl-2 inhibitors into the salivary glands of spontaneous murine model for lupus was performed to test this theory.
  • sublingual and submandibular salivary glands were fixed in 10% neutral-buffered formalin and paraffin embedded.
  • Five ⁇ m sections were H&E stained and semiquantitatively scored (0-4) by an experienced pathologist for inflammatory cell infiltrates.
  • Salivary gland infiltrate scoring categories (1) 3 or fewer small periductular foci, (2) 3 or more medium sized foci, (3) several extensive foci, and (4) coalescing to diffuse infiltrates.
  • the histologic assessment of the submandibular tissue sections is illustrated in FIG. 11 .
  • FIG. 11 phosal vehicle dosed spontaneous lupus nephritis mice typically had extensive to coalescing periductular infiltrates. Salivary gland infiltrates in spontaneous lupus nephritis mice dosed with 30 or 100 mg/kg of Compound 1 were small, discrete and less frequent.
  • FIG. 12 includes a bar graph illustrating the difference in histology scores for submandibular tissue that was not treated, tissue treated with Compound 1 at a dose of 10 mg/kg, and tissue treated with Compound 1 at doses of 30 mg/kg and 100 mg/kg. As noted in FIG.
  • the tissue treated with Compound 1 at doses of 30 mg/kg and 100 mg/kg illustrated histology scores showed a statistically significant improvement in histology scores, as evidenced by the fact that the histology scores for 30 mg/kg and 100 mg/kg treatment were less severe.
  • Sjogren's Syndrome is an inflammatory disease that affects the moisture- producing glands of the body, including the salivary gland. Histologic assessment of salivary glands in spontaneous murine models was performed to determine if treatment with a selective Bcl-2 inhibitor could decrease the inflammatory processes in the salivary gland, and ultimately provide a treatment option for Sjogren's Syndrome. The histological assessment showed that doses of 30 mg/kg and 100 mg/kg of Compound 1 resulted in decreased inflammation in the salivary glands, as evidenced by an improvement in the histology score from 3-4 in mice that were not treated to a score of 1-2 in mice that were treated. Thus, it was determined that selective Bcl-2 inhibitors may provide an effective treatment for patients with Sjogren's Syndrome.

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