WO2006034797A1 - Thermodynamically stable form of bay 43-9006 tosylate - Google Patents

Thermodynamically stable form of bay 43-9006 tosylate Download PDF

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Publication number
WO2006034797A1
WO2006034797A1 PCT/EP2005/010119 EP2005010119W WO2006034797A1 WO 2006034797 A1 WO2006034797 A1 WO 2006034797A1 EP 2005010119 W EP2005010119 W EP 2005010119W WO 2006034797 A1 WO2006034797 A1 WO 2006034797A1
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WO
WIPO (PCT)
Prior art keywords
compound
polymorph
formula
treatment
pharmaceutical composition
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PCT/EP2005/010119
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French (fr)
Inventor
Alfons Grunenberg
Jana Lenz
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Bayer Healthcare Ag
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Priority to AU2005289100A priority Critical patent/AU2005289100B2/en
Priority to US11/664,363 priority patent/US8877933B2/en
Priority to CA2581843A priority patent/CA2581843C/en
Priority to NZ553804A priority patent/NZ553804A/en
Priority to EP05797740A priority patent/EP1797038B1/en
Priority to SI200531571T priority patent/SI1797038T1/en
Priority to DK05797740.7T priority patent/DK1797038T3/en
Priority to JP2007533905A priority patent/JP5215666B2/en
Priority to KR1020107011544A priority patent/KR101239489B1/en
Priority to PL05797740T priority patent/PL1797038T3/en
Priority to CN2005800407750A priority patent/CN101065360B/en
Priority to ES05797740T priority patent/ES2387812T3/en
Priority to BRPI0515946-6A priority patent/BRPI0515946A/en
Priority to KR1020127030937A priority patent/KR101381454B1/en
Application filed by Bayer Healthcare Ag filed Critical Bayer Healthcare Ag
Publication of WO2006034797A1 publication Critical patent/WO2006034797A1/en
Priority to IL181734A priority patent/IL181734A/en
Priority to NO20071508A priority patent/NO344272B1/en
Priority to HK08104454.3A priority patent/HK1114605A1/en
Priority to HRP20120662TT priority patent/HRP20120662T1/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81—Amides; Imides
    • 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
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system

Definitions

  • the present invention relates to a novel form, thermodynamically stable at room temperature, of the tosylate salt of 4- ⁇ 4-[( ⁇ [4-chloro-3-(trifluoromethyl)phenyl]amino ⁇ carbonyl)amino]phenoxy ⁇ - N-methylpyridine-2-carboxamide, to processes for its preparation, to pharmaceutical compositions comprising it and to its use in the control of disorders.
  • WO 03/068228 relates, inter alia, to the use of the compound of the formula (I) for the treatment of disorders in which angiogenesis plays an important role, for example in tumor growth.
  • WO 03/047579 relates to arylureas in combination with cytotoxic or cytostatic compounds for the treatment of cancer.
  • the compounds and their salts, disclosed in WO 00/42012, for example tosylates, are described there as inhibitors of the enzyme Raf kinase and may be used for the treatment of disorders, for example cancer.
  • the compound of the formula (D) is prepared in the manner described in WO 00/42012.
  • the compound of the formula (I) is prepared according to a general standard method for the preparation of tosylate salts, as described in example 1 of the working examples. Li this method, the compound of the formula (T) is obtained in one crystal polymorph which is referred to hereinbelow as polymorph ⁇ .
  • Polymorph ⁇ has a transition point of 194°C and a characteristic X-ray diffractogram, IR spectrum, Raman spectrum, FIR spectrum and NIR spectrum (Tab. 1-6, Fig. 1-6). It has been found that polymorph II is metastable.
  • inventive polymorph I of the compound of the formula (I) is thermodynamically stable at room temperature and is storage-stable even after processing via suspensions and is therefore particularly suitable for use in pharmaceutical formulations, for example suspensions or creams, but also in other preparations which are prepared via suspended active ingredient, for example in aqueous granulation or wet grinding.
  • the present invention provides the compound of the formula (T) in the polymorph I.
  • the inventive use of the compound of the formula (I) in the stable polymorph I ensures that an undesired conversion to another polymorph and an associated change in the properties of the compound of the formula (I), for example solubility or bioavailabilty, are prevented. This increases the safety and quality of preparations comprising the compound of the formula (I) and the risk to the patient is reduced.
  • the compound of the formula (I) in the polymorph I melts under decomposition at 223-231 0 C and is thus clearly differentiable from polymorph II (conversion point 194 0 C) and polymorph III (melting point 187-19O 0 C).
  • the ethanol solvate of the compound of the formula (I) and the methanol solvate of the compound of the formula (I) have losses of mass in thermogravimetric analysis (TGA) of 6.7% and 4.8% respectively (Fig- 1).
  • a pharmaceutical formulation comprises the compound of the formula (T) mainly in the polymorph I and no significant fractions of another form, for example of another polymorph or of a solvate of the compound of the formula (T).
  • the pharmaceutical composition preferably contains more than 90 percent by weight, more preferably more than 95 percent by weight, of the compound of the formula (T) in the polymorph I related to the total amount of the compound of the formula (T) present in the composition.
  • the present invention further provides the use of the compound of the formula (T) in the polymorph I for the treatment of disorders.
  • the present invention further provides the use of the compound of the formula (I) in the polymorph I for the preparation of a pharmaceutical composition for the treatment of disorders.
  • Preference is given to using it for the treatment of disorders which feature abnormal angiogenesis or hyperpermeability processes, bone marrow diseases, for example leukemia, or treatment of carcinoma, for example carcinoma of the lung, of the pancreas, of the thyroid gland, of the kidney or of the intestine, or for the treatment of carcinogenic cell growth.
  • the compound of the formula (I) in the polymorph I of the present invention can be used to treat, modulate and/or prevent any disease or condition mediated by one or more cellular signal transduction pathways involving raf, VEGFR, PDGFR, p38, and/or flt-3 kinases.
  • mediated indicates, e.g., that the signaling molecule is part of the pathway which is aberrant or disturbed in the disease and/or condition.
  • module it is meant that the functional activity of the pathway (or a component of it) is changed in comparison to its normal activity in the absence of the compound. This effect includes any quality or degree of modulation, including, increasing, agonizing, augmenting, enhancing, facilitating, stimulating, decreasing, blocking, inhibiting, reducing, diminishing, antagonizing, etc. - A -
  • kinase activity it is meant a catalytic activity in which a phosphate from adenosine triphosphate (ATP) is transferred to an amino acid residue (e.g., serine, threonine, or tyrosine) in a protein substrate.
  • a compound can modulate kinase activity, e.g., inhibiting it by directly competing with ATP for the ATP-binding pocket of the kinase, by producing a conformational change in the enzyme's structure that affects its activity (e.g., by disrupting the biologically-active three- dimensional structure), etc.
  • Kinase activity can be determined routinely using conventional assay methods.
  • Kinase assays typically comprise the kinase enzyme, substrates, buffers, and components of a detection system.
  • a disease or condition "mediated" by raf, VEGFR, PDGFR, p38, and/or fit-3 indicates that one of these receptors is a part of a signal transduction pathway that is involved in any aspect of the disease phenotype (e.g., where a defect in the receptor itself is involved in "causing” the disease; where stimulation of the receptor by its ligand induces cell motility, migration, and/or proliferation that produces a disease phenotype; where receptor stimulation or phosphorylation results in restenosis; any functional activity of raf, VEGFR, PDGFR, p38, and/or flt-3 that, when inappropriately expressed, results in a disease symptom and/or phenotype).
  • treating is used conventionally, e.g., the management or care of a subject for the purpose of combating, alleviating, reducing, relieving, improving the condition of, etc., of a disease or disorder.
  • Raf associated diseases include, e.g., cell-proliferation disorders, cancer, tumors, etc.;
  • VEGFR-2 associated diseases include, e.g., cancer, tumor growth, inflammatory disease, rheumatoid arthritis, retinopathy, psoriasis, glomerulonephritis, asthma, chronic bronchitis, atherosclerosis, transplant rejection, conditions involving angiogenesis, etc.;
  • VEGFR-3 associated diseases include, e.g., cancer, corneal disease, inflamed cornea, corneal transplantation, lymphatic hyperplasia, conditions involving lymphangiogenesis, etc.;
  • PDGFR-beta associated diseases include, e.g., diseases or conditions characterized by cell proliferation, cell matrix production, cell movement, and/or extracellular matrix production.
  • diseases or conditions include, e.g., tumors, malignancies, cancer, metastasis, chronic myeloid leukemia, inflammation, renal disease, diabetic nephropathy, mesangial proliferative glomerulonephritis, fibrotic conditions, atherosclerosis, restenosis, hypertension-related arteriosclerosis, venous bypass graft arteriosclerosis, scleroderma, interstitial pulmonary diseases, synovial disorders, arthritis, leukemias, lymphomas, etc;
  • Flt-3 associated diseases include, e.g., immune-related disorders, blood cell disorders, conditions involving hematopoietic cell development (e.g., T-cells, B-cells, dendritic cells, cancer, anemia, HTV, acquired immune deficiency syndrome, etc.
  • immune-related disorders e.g., blood cell disorders, conditions involving hematopoietic cell development (e.g., T-cells, B-cells, dendritic cells, cancer, anemia, HTV, acquired immune deficiency syndrome, etc.
  • p38 associated diseases include inflammatory disorders, immunomodulatory disorders, and other disorders that have been linked to abnormal cytokine production, especially TNF-alpha, or abnormal MMP activity. These disorders include, but are not limited to, rheumatoid arthritis, COPD, osteoporosis, Crohn's disease and psoriasis.
  • Methods of the present invention include modulating tumor cell proliferation, including inhibiting cell proliferation.
  • the latter indicates that the growth and/or differentiation of tumor cells is reduced, decreased, diminished, slowed, etc.
  • proliferation includes any process which relates to cell growth and division, and includes differentiation and apoptosis.
  • raf kinases play a key role in the activation of the cytoplasmic signaling cascade involved in cell proliferation, differentiation, and apoptosis. For example, studies have found that inhibiting c-raf by anti-sense oligonucleotides can block cell proliferation. Any amount of inhibition is considered therapeutic.
  • Methods of the present invention also include treating mammalian hyper-proliferative disorders.
  • Hyper-proliferative disorders include but are not limited to solid tumors, such as cancers of the breast, respiratory tract, brain, reproductive organs, digestive tract, urinary tract, eye, liver, skin, head and neck, thyroid, parathyroid and their distant metastases. Those disorders also include lymphomas, sarcomas, and leukemias.
  • Any tumor or cancer can be treated, including, but not limited to, cancers having one or more mutations in raf, ras, VEFGR, PDGFR, p38, and/or flt-3, as well as any upstream or downstream member of the signaling pathways of which they are a part.
  • a cancer can be treated with a compound of the present invention irrespective of the mechanism which is responsible for it.
  • cancers of any organ can be treated, including cancers of, but are not limited to, e.g., colon, pancreas, breast, prostate, bone, liver, kidney, lung, testes, skin, pancreas, stomach, colorectal cancer, renal cell carcinoma, hepatocellular carcinoma, melanoma, etc.
  • breast cancer include, but are not limited to, invasive ductal carcinoma, invasive lobular carcinoma, ductal carcinoma in situ, and lobular carcinoma in situ.
  • cancers of the respiratory tract include, but are not limited to, small-cell and non- small-cell lung carcinoma, as well as bronchial adenoma and pleuropulmonary blastoma.
  • brain cancers include, but are not limited to, brain stem and hypophtalmic glioma, cerebellar and cerebral astrocytoma, medulloblastoma, ependymoma, as well as neuroectodermal and pineal tumor.
  • Tumors of the male reproductive organs include, but are not limited to, prostate and testicular cancer.
  • Tumors of the female reproductive organs include, but are not limited to, endometrial, cervical, ovarian, vaginal, and vulvar cancer, as well as sarcoma of the uterus.
  • Tumors of the digestive tract include, but are not limited to, anal, colon, colorectal, esophageal, gallbladder, gastric, pancreatic, rectal, small-intestine, and salivary gland cancers.
  • Tumors of the urinary tract include, but are not limited to, bladder, penile, kidney, renal pelvis, ureter, and urethral cancers.
  • Eye cancers include, but are not limited to, intraocular melanoma and retinoblastoma.
  • liver cancers include, but are not limited to, hepatocellular carcinoma (liver cell carcinomas with or without fibrolamellar variant), cholangiocarcinoma (intrahepatic bile duct carcinoma), and mixed hepatocellular cholangiocarcinoma.
  • Skin cancers include, but are not limited to, squamous cell carcinoma, Kaposi's sarcoma, malignant melanoma, Merkel cell skin cancer, and non-melanoma skin cancer.
  • Head-and-neck cancers include, but are not limited to, laryngeal, hypopharyngeal, nasopharyngeal, and/or oropharyngeal cancers, and lip and oral cavity cancer.
  • Lymphomas include, but are not limited to, AIDS-related lymphoma, non-Hodgkin's lymphoma, cutaneous T-cell lymphoma, Hodgkin's disease, and lymphoma of the central nervous system.
  • Sarcomas include, but are not limited to, sarcoma of the soft tissue, osteosarcoma, malignant fibrous histiocytoma, lymphosarcoma, and rhabdomyosarcoma.
  • Leukemias include, but are not limited to, acute or chronic, acute myeloid leukemia, acute lymphoblastic leukemia, acute Lymphocytic Leukemia, chronic lymphocytic leukemia, chronic myelogenous leukemia, hairy cell leukemia, undifferentiated AML, promyelocyte leukemia, myelomonocytic leukemia, monocytic, leukemia, or erythroleukemia, megakaryoblastic leukemia, etc.
  • compounds of the present invention can also cause tumor regression, e.g., a decrease in the size of a tumor, or in the extent of cancer in the body.
  • the present invention also relates to methods of modulating angiogenesis and/or lymphangiogenesis in a system comprising cells, comprising administering to the system an effective amount of a compound described herein.
  • a system comprising cells can be an in vivo system, such as a tumor in a patient, isolated organs, tissues, or cells, in vitro assays systems (CAM, BCE, etc), animal models (e.g., in vivo, subcutaneous, cancer models), hosts in need of treatment (e.g., hosts suffering from diseases having angiogenic and/or lymphangiogenic component, such as cancer), etc.
  • angiogenesis e.g., abnormal angiogenesis
  • pathological conditions are associated with the growth of extraneous blood vessels. These include, e.g., diabetic retinopathy, neovascular glaucoma, psoriasis, retrolental fibroplasias, angiofibroma, inflammation, etc.
  • the increased blood supply associated with cancerous and neoplastic tissue encourages growth, leading to rapid tumor enlargement and metastasis.
  • the growth of new blood and lymph vessels in a tumor provides an escape route for renegade cells, encouraging metastasis and the consequence spread of the cancer.
  • Methods of the present invention also relate to treating and/or preventing disorders or conditions associated with, or resulting from, vascular hyperpermeability.
  • VEGF increases endothelial cell permeability.
  • any condition which results in the release of VEGF can be associated with vascular hyperpermeability and its accompanying deleterious effects.
  • the present invention provides for the treatment or prevention of any condition or disorder associated with, or resulting from, vascular hyperpermeability, regardless of the mechanism of action.
  • Edema formation is a life-threatening complication of various diseases of the central nervous system, including head injury, tumors, stroke, hypoxia, and high altitude sickness.
  • the underlying cause of edema is vascular hyperpermeability.
  • Compounds of the present invention can be utilized to treat and/or prevent vascular hyperpermeability, thereby treating and/or preventing edema, and the deleterious effects associated with it.
  • hyperpermeability conditions include, but are not limited to, tissue edema (e.g., lung, kidney, brain, etc.), vasogenic brain edema, chronic inflammation, wound healing, ischemia, tumors, atherosclerosis, peripheral vascular disease, ascites, effusions, exudates, nephrotic edema, primary glomerular disease, peripheral artery disease, diabetic retinopathy, diabetic retinal disease, obstruction of respiratory airways during asthma and other pulmonary disorders, circulatory collapse in sepsis, acute lung injury, acute respiratory distress syndrome, etc.
  • tissue edema e.g., lung, kidney, brain, etc.
  • vasogenic brain edema chronic inflammation, wound healing, ischemia, tumors, atherosclerosis
  • peripheral vascular disease ascites, effusions, exudates, nephrotic edema, primary glomerular disease, peripheral artery disease, diabetic retinopathy, diabetic retinal disease, obstruction of respiratory airways during asthma and other
  • Assays for vascular permeability can be done routinely, e.g., Heiss et al., J. Clin. Invest., 98:1400- 1408, 1996; Fischer et al., Am. J. Physiol., 276(4 Pt l):C812-20, 1999; Fischer et al., Am. J. Physiol. Cell. Physiol., 279:C935-C944, 2000.
  • the compound of the formula (J) in the polymorph I of this invention also has a broad therapeutic activity to treat or prevent the progression of a broad array of diseases, such as inflammatory conditions, coronary restenosis, tumor-associated angiogenesis, atherosclerosis, autoimmune diseases, inflammation, certain kidney diseases associated with proliferation of glomerular or mesangial cells, and ocular diseases associated with retinal vessel proliferation, psoriasis, hepatic cirrhosis, diabetes, atherosclerosis, restenosis, vascular graft restenosis, in-stent stenosis, angiogenesis, ocurlar diseases, pulmonary fibrosis, obliterative bronchiolitis, glomerular nephritis, rheumatoid arthritis.
  • diseases such as inflammatory conditions, coronary restenosis, tumor-associated angiogenesis, atherosclerosis, autoimmune diseases, inflammation, certain kidney diseases associated with proliferation of glomerular or mesangial cells, and ocular diseases associated with retina
  • the present invention also provides for treating, preventing, modulating, etc., one or more of the following conditions in humans and/or other mammals: retinopathy, including diabetic retinopathy, ischemic retinal-vein occlusion, retinopathy of prematurity and age related macular degeneration; rheumatoid arthritis, psoriasis, or bullous disorder associated with subepidermal blister formation, including bullous pemphigoid, erythema multiforme, or dermatitis herpetiformis, rheumatic fever, bone resorption, postmenopausal osteoperosis, sepsis, gram negative sepsis, septic shock, endotoxic shock, toxic shock syndrome, systemic inflammatory response syndrome, inflammatory bowel disease (Crohn's disease and ulcerative colitis), Jarisch-Herxheimer reaction, asthma, adult respiratory distress syndrome, acute pulmonary fibrotic disease, pulmonary sarcoidosis, allergic respiratory disease, silicos
  • HTV human immunodeficiency virus
  • papilloma blastoglioma, Kaposi's sarcoma, melanoma
  • lung cancer ovarian cancer
  • prostate cancer squamous cell carcinoma, astrocytoma, head cancer, neck cancer, bladder cancer, breast cancer, colorectal cancer, thyroid cancer, pancreatic cancer, gastric cancer, hepatocellular carcinoma, leukemia, lymphoma, Hodgkin's disease, Burkitt's disease, arthritis, rheumatoid arthritis, diabetic retinopathy, angiogenesis, restenosis, in-stent restenosis, vascular graft restenosis, pulmonary fibros
  • the present invention further provides a method for the prevention or treatment of diseases, especially of the aforementioned diseases, using an effective amount of the compound of the formula (I) in the polymorph I.
  • the compound of the formula (I) in the polymorph I of this invention can be administered as the sole pharmaceutical agent or in combination with one or more other pharmaceutical agents where the combination causes no unacceptable adverse effects. This may be of particular relevance for the treatment of hyper-proliferative diseases such as cancer, hi this instance, the compound of this invention can be combined with known cytotoxic agents, signal transduction inhibitors, with other anti-cancer agents, or with antiemetics, as well as with admixtures and combinations thereof..
  • the compound of the formula (T) in the polymorph I of the present invention can be combined with cytotoxic anti-cancer agents.
  • cytotoxic anti-cancer agents can be found in the 1 lth Edition of the Merck Index (1996). These agents include, by no way of limitation, asparaginase, bleomycin, carboplatin, carmustine, chlorambucil, cisplatin, colaspase, cyclophosphamide, cytarabine, dacarbazine, dactinomycin, daunorubicin, doxorubicin (adriamycine), epirubicin, etoposide, 5-fluorouracil, hexamethylmelamine, hydroxyurea, ifosfamide, irinotecan, leucovorin, lomustine, mechlorethamine, 6-mercaptopurine, mesna, methotrexate, mitomycin C, mitoxantrone, predni
  • cytotoxic drugs suitable for use with the compounds of the invention include, but are not limited to, those compounds acknowledged to be used in the treatment of neoplastic diseases in Goodman and Gilman's The Pharmacological Basis of Therapeutics (Ninth Edition, 1996, McGraw- Hill).
  • agents include, by no way of limitation, aminoglutethimide, L-asparaginase, azathioprine, 5-azacytidine cladribine, busulfan, diethylstilbestrol, 2 ⁇ 2'-difluorodeoxycytidine, docetaxel, erythrohydroxynonyladenine, ethinyl estradiol, 5-fluorodeoxyuridine, 5-fluoro- deoxyuridine monophosphate, fludarabine phosphate, fluoxymesterone, flutamide, hydroxyprogesterone caproate, idarubicin, interferon, medroxyprogesterone acetate, megestrol acetate, melphalan, mitotane, paclitaxel, pentostatin, N-phosphonoacetyl-L-aspartate (PALA), plicamycin, semustine, teniposide, testosterone propionate, thiotepa, trimethylmelamine
  • the compound of the formula (T) in the polymorph I of the present invention can be combined with antiemetics.
  • Antiemetics suitable for use with the compounds of the invention include, but are not limited to, antihistamines, Hi receptor blockers, 5-HT 3 antagonists, neuroleptics, anticholinergics, dopamine antagonists, serotonin antagonists, glucocorticoids or cannabinoids. These agents include, by no way of limitation, meclozin, dimenhydrinate, phenothiazin derivatives (e.g. thiethylperazin, triflupromazin), benzamide or benzimidazolon derivatives (e.g.
  • metoclopramid bromoprid, domperidon
  • butyrophenones scopalamin
  • pyridoxine chlorphenoxamin
  • granisetron ondansetron
  • tropisetron tropisetron
  • dexamethason Preference is given to the antiemetics: granisetron, ondansetron, tropisetron, or dexamethason.
  • Combination mean for the purposes of the invention not only a dosage form which contains all the components (so-called fixed combinations), and combination packs containing the components separate from one another, but also components which are administered simultaneously or sequentially, as long as they are employed for the prophylaxis or treatment of the same disease.
  • the active ingredients of the combination according to the invention can be converted in a known manner into the usual formulations, which may be liquid or solid formulations. Examples are tablets, coated tablets, pills, capsules, granules, aerosols, syrups, emulsions, suspensions, solutions.
  • the combination according to the invention is well tolerated and in some cases is effective even in low dosages, a wide range of formulation variants is possible.
  • one possibility is to formulate the individual active ingredients of the combination according to the invention separately. In this case, it is not absolutely necessary for the individual active ingredients to be taken at the same time; on the contrary, sequential intake may be advantageous to achieve optimal effects.
  • the active ingredients are present in the primary packaging in each case in separate containers which may be, for example, tubes, bottles or blister packs.
  • Such separate packaging of the components in the joint primary packaging is also referred to as a kit.
  • compositions which are suitable and preferred for the combination according to the invention are also fixed combinations.
  • "Fixed combination” is intended here to mean pharmaceutical forms in which the components are present together in a fixed ratio of amounts.
  • Such fixed combinations may be, for example, in the form of oral solutions, but they are preferably solid oral pharmaceutical preparations, e.g. capsules or tablets.
  • This invention also relates to pharmaceutical compositions containing the compound of the formula (1) in the polymorph I of the present invention and methods of administering to a patient in need thereof a pharmaceutical composition of this invention.
  • a patient for the purpose of this invention, is a mammal, including a human, in need of treatment for the particular condition or disease.
  • compositions of the present invention are comprised of a pharmaceutically acceptable carrier and a pharmaceutically effective amount of the compound of the formula (I) in the polymorph I of the present invention.
  • a pharmaceutically acceptable carrier is any carrier which is relatively non-toxic and innocuous to a patient at concentrations consistent with effective activity of the active ingredient so that any side effects ascribable to the carrier do not vitiate the beneficial effects of the active ingredient.
  • a pharmaceutically effective amount of compound is that amount which produces a result or exerts an influence on the particular condition being treated.
  • the compound of the formula (I) in the polymorph I may be administered in a suitable manner, for example by the oral, parenteral, pulmonary, nasal, sublingual, lingual, buccal, rectal, dermal, transdermal, conjunctival or otic route, or as an implant or stent.
  • inventive compounds may be administered in suitable administration forms.
  • suitable administration forms are those which function according to the prior art and deliver the compound of the formula (1) in the polymorph I in a rapid and/or modified manner, for example tablets (noncoated or coated tablets, for example with coatings which are resistant to gastric juice or have retarded dissolution or are insoluble and which control the release of the inventive compound), tablets which disintegrate rapidly in the oral cavity or films/wafers, films/lyophilizates, capsules (for example hard or soft gelatin capsules), sugar-coated tablets, granules, pellets, powders, suspensions or aerosols.
  • tablets noncoated or coated tablets, for example with coatings which are resistant to gastric juice or have retarded dissolution or are insoluble and which control the release of the inventive compound
  • tablets which disintegrate rapidly in the oral cavity or films/wafers films/lyophilizates
  • capsules for example hard or soft gelatin capsules
  • sugar-coated tablets granules, pellets, powders, suspensions or aerosols.
  • Parenteral administration can take place with avoidance of an absorption step (for example in an intravenous, intraarterial, intracardiac, intraspinal or intralumbar manner) or with inclusion of an absorption (for example in an intramuscular, subcutaneous, intracutaneous, percutaneous or intraperitoneal manner).
  • Administration forms suitable for parenteral application include injection and infusion preparations in the form of suspensions, lyophilizates or sterile powders.
  • Suitable for the other administration routes are, for example, medicinal forms for inhalation (including powder inhalers, nebulizers), tablets for lingual, sublingual or buccal administration, films/wafers or capsules, suppositories, preparations for the ear or eye, vaginal capsules, aqueous suspensions (lotions, shaking mixtures), lipophilic suspensions, ointments, creams, transdermal therapeutic systems (for example patches), pastes, dusting powders, implants or stents.
  • medicinal forms for inhalation including powder inhalers, nebulizers
  • tablets for lingual, sublingual or buccal administration films/wafers or capsules, suppositories, preparations for the ear or eye, vaginal capsules, aqueous suspensions (lotions, shaking mixtures), lipophilic suspensions, ointments, creams, transdermal therapeutic systems (for example patches), pastes, dusting powders, implants or stents.
  • the inventive compound may be converted to the application forms listed. This may take place in a known manner by mixing with inert, nontoxic, pharmaceutically suitable excipients.
  • excipients include carriers (for example, microcrystalline cellulose, lactose, mannitol), solvents (for example, liquid polyethylene glycols), emulsifiers and dispersants or wetting agents (for example, sodium dodecylsulfate, polyoxysorbitan oleate), binders (for example, polyvinylpyrrolidone), synthetic and natural polymers (for example, albumin), stabilizers (for example, antioxidants such as ascorbic acid), dyes (for example, inorganic pigments such as iron oxides) and substances for masking flavors and/or odors.
  • carriers for example, microcrystalline cellulose, lactose, mannitol
  • solvents for example, liquid polyethylene glycols
  • emulsifiers and dispersants or wetting agents for example, sodium dodecyls
  • the present invention further provides medicaments which comprise at least the compound of the formula (I) in the polymorph I, typically together with one or more inert, nontoxic, pharmaceutically suitable excipients, for example binders, fillers, etc, and to the use thereof for the aforementioned purposes.
  • medicaments which comprise at least the compound of the formula (I) in the polymorph I, typically together with one or more inert, nontoxic, pharmaceutically suitable excipients, for example binders, fillers, etc, and to the use thereof for the aforementioned purposes.
  • the effective dosage of the compounds of this invention can readily be determined for treatment of each desired indication.
  • the amount of the active ingredient to be administered in the treatment of one of these conditions can vary widely according to such considerations as the particular compound and dosage unit employed, the mode of administration, the period of treatment, the age and sex of the patient treated, and the nature and extent of the condition treated.
  • the total amount of the active ingredient to be administered can range from about 0.001 mg/kg to about 200 mg/kg, and preferably from about 0.1 mg/kg to about 50 mg/kg body weight per day.
  • a unit dosage may preferably contain from about 5 mg to about 4000 mg of active ingredient, and can be administered one or more times per day.
  • the daily dosage for oral administration will preferably be from 0.1 to 50 mg/kg of total body weight.
  • the daily dosage for administration by injection, including intravenous, intramuscular, subcutaneous and parenteral injections, and use of infusion techniques will preferably be from 0.1 to 10 mg/kg of total body weight.
  • the daily rectal dosage regimen will preferably be from 0.1 to 50 mg/kg of total body weight.
  • the daily vaginal dosage regimen will preferably be from 0.1 to 50 mg/kg of total body weight.
  • the daily topical dosage regimen will preferably be from 0.1 to 10 mg/kg administered between one to four times daily.
  • the transdermal concentration will preferably be that required to maintain a daily dose of from 0.1 to 10 mg/kg.
  • the daily inhalation dosage regimen will preferably be from 0.1 to 10 mg/kg of total body weight. Other dosages and amounts can be selected routinely.
  • the invention further provides a process for preparing the compound of the formula (T) in the polymorph I, by effecting the compound of the formula (I) in the polymorph DL, obtained as described in example 1, in an inert solvent at a temperature of, for example, from 5O 0 C up to the reflux temperature of the solvent, preferably from 60 to 80 0 C, in the absence of crystals of a solvate of the compound of the formula (T), for example in the absence of crystals of the methanol solvate or the ethanol solvate of the compound of formula (T), for up to one day.
  • the mixture is cooled to from -30 0 C to room temperature, preferably from -25 0 C to 10 0 C, and the crystals are isolated and dried.
  • the compound of the formula (T) is thus obtained in the polymorph I.
  • the invention likewise provides a process for preparing the compound of the formula (T) in the polymorph I, by effecting the compound of the formula (I) in the polymorph ⁇ , obtained as described in example 1, in an inert solvent at a temperature of, for example, from 10 0 C up to the reflux temperature of the solvent, preferably at room temperature, for up to one day. Subsequently, the mixture is seeded with crystals of the compound of the formula (I) in the polymorph I and stirred or shaken, for example at room temperature, for from 1 hour to 14 days, preferably from 2 hours to 7 days. The crystals are isolated and dried. The compound of the formula (T) is thus obtained in the polymorph I.
  • the invention likewise provides a process for preparing the compound of the formula (I) in the polymorph I, by effecting the compound of the formula (T) in the polymorph ⁇ , obtained as described in example 1, in an inert solvent until the desired degree of conversion is attained, preferably until quantitative conversion to the polymorph I. If appropriate, crystals of the compound of the formula (T) in the polymorph I are added. The resulting crystals are isolated and, to remove solvent present, dried to constant weight at room temperature or at elevated temperature, for example from 40 to 80 0 C. The compound of the formula (T) is thus obtained in the polymorph I.
  • Effecting the compound of the formula (I) in the polymorph II in an inert solvent means, that for example the compound of the formula (I) in the polymorph ⁇ is dissolved completely (solution) or only in part (suspension).
  • the mixture can be, for example stirred or shaken.
  • Suitable inert solvents are lower alcohols, for example methanol, ethanol, n-propanol, isopropanol, n- butanol, sec-butanol, isobutanol, or ketones such as acetone, or alkanes such as n-pentane, cyclopentane, n-hexane, cyclohexane, or tetrahydrofuran, or acetonitrile, or toluene, or ethyl acetate, or mixtures of the solvents mentioned, or mixtures of the solvents mentioned with water.
  • lower alcohols for example methanol, ethanol, n-propanol, isopropanol, n- butanol, sec-butanol, isobutanol, or ketones such as acetone, or alkanes such as n-pentane, cyclopentane, n-hexane, cyclohe
  • Isopropanol, ethylacetate or a mixture thereof are used most preferably as inert solvents.
  • the crystals are cooled to from -3O 0 C to room temperature, preferably from -25 to 10 0 C, isolated and dried.
  • the compound of the formula (T) is thus obtained in the polymorph I.
  • the mixture is subsequently seeded with crystals of the compound of the formula (I) in the polymorph I and stirred or shaken, for example at room temperature, for from 1 hour to 14 days, preferably from 2 hours to 7 days.
  • the crystals are isolated and dried.
  • the compound of the formula (I) is thus obtained in the polymorph I.
  • Most preferably isopropanol, ethylacetate or a mixture thereof is used as solvent.
  • the compound of the formula (T) is thus obtained in the polymorph I. Most preferably isopropanol, ethylacetate or a mixture thereof is used as solvent.
  • the compound of the formula (T) may likewise be prepared in the polymorph I by heating the compound of the formula (T) in the polymorph ⁇ to from 195 to 222°C, preferably from 195 to 215°C, for example at a heating rate of from 10 0 C to 3O 0 C per minute, preferably from 15°C to 25°C per minute, and subsequently cooling to from 10 0 C to 30 0 C, preferably to room temperature, for example at a cooling rate of from 1°C to 4 0 C per minute, preferably from I 0 C to 3 0 C per minute.
  • the compound of the formula (I) in the polymorph IH can be prepared by effecting the compound of the formula (I) in the polymorph II in an inert solvent, for example methanol. Filtration is effected after from 1 day to 1 week, and the product is dried and heat-treated at from 145 to 16O 0 C for from 15 minutes to 1 hour. The compound of the formula (T) is thus obtained in the polymorph IH.
  • an inert solvent for example methanol.
  • the methanol solvate of the compound of the formula (T) can be prepared by effecting the compound of the formula (T) in the polymorph II in methanol. After 1 week, filtration is effected, and the product is dried and stored under a methanol atmosphere for from 5 hours to 1 week. The methanol solvate of the compound of the formula (I) is thus obtained with a methanol content of 4.8% by weight.
  • the ethanol solvate of the compound of the formula (I) can be prepared by effecting the compound of the formula (T) in the polymorph ⁇ in ethanol. After 1 week, filtration is effected and the product is dried. The ethanol solvate of the compound of the formula (I) is thus obtained with an ethanol factor of 6.7 percent by weight.
  • the processes are generally carried out at atmospheric pressure. However, it is also possible to work at elevated pressure or at reduced pressure (for example in a range of from 0.5 to 5 bar).
  • thermograms were obtained using a DSC 7 or Pyris-1 differential scanning calorimeter and TGA 7 thermogravimetric analyzer from Perkin-Elmer.
  • the X-ray diffractograms were registered in a Stoe transmission diffractometer.
  • the IR, FIR, NER and Raman spectra were recorded using IFS 66v (IR, FIR), IFS 28/N (NIR) and RFS 100 (Raman) Fourier spectrometers from Bruker.
  • Example 1 4-(4-[(([4-Chloro-3-(trifluoromethv ⁇ phenvnaminokarbonyl)aniino1phenoxyl-iV- methyIpyridine-2-carboxamide tosylate in the polymorph II
  • Example 4 Preparation of the methanol solvate of 4-(4-f( ⁇ f4-chloro-3-(trifluoro- methyDphenyllaminolcarbonv ⁇ aminolphenoxyl- ⁇ -methylpyridine-Z-carboxamide tosylate
  • Example 5 Preparation of the ethanol solvate of 4-f4-f((f4-chloro-3-(triflnoro- methyl)phenyllamino ⁇ earbonyl)aminoIphenoxy)- ⁇ -inethylpyridine-2-earboxamide tosylate

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Abstract

The present invention relates to a novel form, thermodynamically stable at room temperature, of the tosylate salt of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)amino]phenoxy}-N-methylpyridine-2-carboxamide, to processes for its preparation, to medicaments comprising it and to its use in the control of disorders.

Description

Thermodynamically stable form of a tosylate salt
The present invention relates to a novel form, thermodynamically stable at room temperature, of the tosylate salt of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)amino]phenoxy}- N-methylpyridine-2-carboxamide, to processes for its preparation, to pharmaceutical compositions comprising it and to its use in the control of disorders.
The tosylate salt of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)amino]phenoxy}-N- methylpyridine-2-carboxamide is mentioned in WO 03/068228 and WO 03/047579 and corresponds to the compound of the formula (I):
Figure imgf000002_0001
WO 03/068228 relates, inter alia, to the use of the compound of the formula (I) for the treatment of disorders in which angiogenesis plays an important role, for example in tumor growth. WO 03/047579 relates to arylureas in combination with cytotoxic or cytostatic compounds for the treatment of cancer.
The compound 4- {4-[( { [4-chloro-3-(trifluoromethy l)phenyl] amino } carbony l)amino]phenoxy } -N- methylpyridine-2-carboxamide is described in WO 00/42012 and corresponds to the compound of the formula (II):
Figure imgf000002_0002
The compounds and their salts, disclosed in WO 00/42012, for example tosylates, are described there as inhibitors of the enzyme Raf kinase and may be used for the treatment of disorders, for example cancer. The compound of the formula (D) is prepared in the manner described in WO 00/42012. The compound of the formula (I) is prepared according to a general standard method for the preparation of tosylate salts, as described in example 1 of the working examples. Li this method, the compound of the formula (T) is obtained in one crystal polymorph which is referred to hereinbelow as polymorph π. Polymorph π has a transition point of 194°C and a characteristic X-ray diffractogram, IR spectrum, Raman spectrum, FIR spectrum and NIR spectrum (Tab. 1-6, Fig. 1-6). It has been found that polymorph II is metastable.
Surprisingly, two further polymorphs and two solvates of the compound of the formula (I) have been found. The compound of the formula (T) in the polymorph I melts under decomposition at 223-2310C, the compound of the formula (T) in the polymorph EI melts at 187-1900C. The monomethanol solvate of the compound of the formula (I) contains 4.8% methanol and the monoethanol solvate of the compound of the formula (T) 6.7% ethanol. The inventive polymorph I of the compound of the formula (I) is thermodynamically stable at room temperature and is storage-stable even after processing via suspensions and is therefore particularly suitable for use in pharmaceutical formulations, for example suspensions or creams, but also in other preparations which are prepared via suspended active ingredient, for example in aqueous granulation or wet grinding.
The present invention provides the compound of the formula (T) in the polymorph I. The inventive use of the compound of the formula (I) in the stable polymorph I ensures that an undesired conversion to another polymorph and an associated change in the properties of the compound of the formula (I), for example solubility or bioavailabilty, are prevented. This increases the safety and quality of preparations comprising the compound of the formula (I) and the risk to the patient is reduced.
Polymorph I of the compound of the formula (I), in comparison to polymorph π, polymorph IH, the ethanol and methanol solvate, has a clearly differentiable X-ray diffractogram, NIR spectrum, FIR spectrum and Raman spectrum (Fig. 2-6). The compound of the formula (I) in the polymorph I melts under decomposition at 223-2310C and is thus clearly differentiable from polymorph II (conversion point 1940C) and polymorph III (melting point 187-19O0C). Unlike those solvent-free forms, the ethanol solvate of the compound of the formula (I) and the methanol solvate of the compound of the formula (I) have losses of mass in thermogravimetric analysis (TGA) of 6.7% and 4.8% respectively (Fig- 1).
The inventive compound of the formula (I) in the polymorph I is used in high purity in pharma¬ ceutical formulations. For reasons of stability, a pharmaceutical formulation comprises the compound of the formula (T) mainly in the polymorph I and no significant fractions of another form, for example of another polymorph or of a solvate of the compound of the formula (T). The pharmaceutical composition preferably contains more than 90 percent by weight, more preferably more than 95 percent by weight, of the compound of the formula (T) in the polymorph I related to the total amount of the compound of the formula (T) present in the composition.
Method for treatment:
The present invention further provides the use of the compound of the formula (T) in the polymorph I for the treatment of disorders. Preference is given to using it for the treatment of disorders which feature abnormal angiogenesis or hyperpermeability processes, bone marrow diseases, for example leukemia, or treatment of carcinoma, for example carcinoma of the lung, of the pancreas, of the thyroid gland, of the kidney or of the intestine, or for the treatment of carcinogenic cell growth.
The present invention further provides the use of the compound of the formula (I) in the polymorph I for the preparation of a pharmaceutical composition for the treatment of disorders. Preference is given to using it for the treatment of disorders which feature abnormal angiogenesis or hyperpermeability processes, bone marrow diseases, for example leukemia, or treatment of carcinoma, for example carcinoma of the lung, of the pancreas, of the thyroid gland, of the kidney or of the intestine, or for the treatment of carcinogenic cell growth.
The compound of the formula (I) in the polymorph I of the present invention can be used to treat, modulate and/or prevent any disease or condition mediated by one or more cellular signal transduction pathways involving raf, VEGFR, PDGFR, p38, and/or flt-3 kinases.
The term "mediated" indicates, e.g., that the signaling molecule is part of the pathway which is aberrant or disturbed in the disease and/or condition.
While not wishing to be bound by any theory or mechanism of action, it has been found that compounds of the present invention possess the ability to modulate raf, VEGFR, PDGFR, p38, and/or flt-3 kinase activity. The methods of the present invention, however, are not limited to any particular mechanism or how the compounds achieve their therapeutic effect.
By the term "modulate," it is meant that the functional activity of the pathway (or a component of it) is changed in comparison to its normal activity in the absence of the compound. This effect includes any quality or degree of modulation, including, increasing, agonizing, augmenting, enhancing, facilitating, stimulating, decreasing, blocking, inhibiting, reducing, diminishing, antagonizing, etc. - A -
By the phrase "kinase activity," it is meant a catalytic activity in which a phosphate from adenosine triphosphate (ATP) is transferred to an amino acid residue (e.g., serine, threonine, or tyrosine) in a protein substrate. A compound can modulate kinase activity, e.g., inhibiting it by directly competing with ATP for the ATP-binding pocket of the kinase, by producing a conformational change in the enzyme's structure that affects its activity (e.g., by disrupting the biologically-active three- dimensional structure), etc. Kinase activity can be determined routinely using conventional assay methods. Kinase assays typically comprise the kinase enzyme, substrates, buffers, and components of a detection system.
A disease or condition "mediated" by raf, VEGFR, PDGFR, p38, and/or fit-3 indicates that one of these receptors is a part of a signal transduction pathway that is involved in any aspect of the disease phenotype (e.g., where a defect in the receptor itself is involved in "causing" the disease; where stimulation of the receptor by its ligand induces cell motility, migration, and/or proliferation that produces a disease phenotype; where receptor stimulation or phosphorylation results in restenosis; any functional activity of raf, VEGFR, PDGFR, p38, and/or flt-3 that, when inappropriately expressed, results in a disease symptom and/or phenotype).
The term "treating" is used conventionally, e.g., the management or care of a subject for the purpose of combating, alleviating, reducing, relieving, improving the condition of, etc., of a disease or disorder.
Diseases and conditions that can be treated include any of those mentioned above and below, as well as:
Raf associated diseases include, e.g., cell-proliferation disorders, cancer, tumors, etc.;
VEGFR-2 associated diseases include, e.g., cancer, tumor growth, inflammatory disease, rheumatoid arthritis, retinopathy, psoriasis, glomerulonephritis, asthma, chronic bronchitis, atherosclerosis, transplant rejection, conditions involving angiogenesis, etc.;
VEGFR-3 associated diseases include, e.g., cancer, corneal disease, inflamed cornea, corneal transplantation, lymphatic hyperplasia, conditions involving lymphangiogenesis, etc.;
PDGFR-beta associated diseases include, e.g., diseases or conditions characterized by cell proliferation, cell matrix production, cell movement, and/or extracellular matrix production. Specific examples, include, e.g., tumors, malignancies, cancer, metastasis, chronic myeloid leukemia, inflammation, renal disease, diabetic nephropathy, mesangial proliferative glomerulonephritis, fibrotic conditions, atherosclerosis, restenosis, hypertension-related arteriosclerosis, venous bypass graft arteriosclerosis, scleroderma, interstitial pulmonary diseases, synovial disorders, arthritis, leukemias, lymphomas, etc;
Flt-3 associated diseases include, e.g., immune-related disorders, blood cell disorders, conditions involving hematopoietic cell development (e.g., T-cells, B-cells, dendritic cells, cancer, anemia, HTV, acquired immune deficiency syndrome, etc.
p38 associated diseases include inflammatory disorders, immunomodulatory disorders, and other disorders that have been linked to abnormal cytokine production, especially TNF-alpha, or abnormal MMP activity. These disorders include, but are not limited to, rheumatoid arthritis, COPD, osteoporosis, Crohn's disease and psoriasis.
Methods of the present invention include modulating tumor cell proliferation, including inhibiting cell proliferation. The latter indicates that the growth and/or differentiation of tumor cells is reduced, decreased, diminished, slowed, etc. The term "proliferation" includes any process which relates to cell growth and division, and includes differentiation and apoptosis. As discussed above, raf kinases play a key role in the activation of the cytoplasmic signaling cascade involved in cell proliferation, differentiation, and apoptosis. For example, studies have found that inhibiting c-raf by anti-sense oligonucleotides can block cell proliferation. Any amount of inhibition is considered therapeutic.
Methods of the present invention also include treating mammalian hyper-proliferative disorders. Hyper-proliferative disorders include but are not limited to solid tumors, such as cancers of the breast, respiratory tract, brain, reproductive organs, digestive tract, urinary tract, eye, liver, skin, head and neck, thyroid, parathyroid and their distant metastases. Those disorders also include lymphomas, sarcomas, and leukemias.
Any tumor or cancer can be treated, including, but not limited to, cancers having one or more mutations in raf, ras, VEFGR, PDGFR, p38, and/or flt-3, as well as any upstream or downstream member of the signaling pathways of which they are a part. As discussed earlier, a cancer can be treated with a compound of the present invention irrespective of the mechanism which is responsible for it.
Cancers of any organ can be treated, including cancers of, but are not limited to, e.g., colon, pancreas, breast, prostate, bone, liver, kidney, lung, testes, skin, pancreas, stomach, colorectal cancer, renal cell carcinoma, hepatocellular carcinoma, melanoma, etc. Examples of breast cancer include, but are not limited to, invasive ductal carcinoma, invasive lobular carcinoma, ductal carcinoma in situ, and lobular carcinoma in situ.
Examples of cancers of the respiratory tract include, but are not limited to, small-cell and non- small-cell lung carcinoma, as well as bronchial adenoma and pleuropulmonary blastoma.
Examples of brain cancers include, but are not limited to, brain stem and hypophtalmic glioma, cerebellar and cerebral astrocytoma, medulloblastoma, ependymoma, as well as neuroectodermal and pineal tumor.
Tumors of the male reproductive organs include, but are not limited to, prostate and testicular cancer. Tumors of the female reproductive organs include, but are not limited to, endometrial, cervical, ovarian, vaginal, and vulvar cancer, as well as sarcoma of the uterus.
Tumors of the digestive tract include, but are not limited to, anal, colon, colorectal, esophageal, gallbladder, gastric, pancreatic, rectal, small-intestine, and salivary gland cancers.
Tumors of the urinary tract include, but are not limited to, bladder, penile, kidney, renal pelvis, ureter, and urethral cancers.
Eye cancers include, but are not limited to, intraocular melanoma and retinoblastoma.
Examples of liver cancers include, but are not limited to, hepatocellular carcinoma (liver cell carcinomas with or without fibrolamellar variant), cholangiocarcinoma (intrahepatic bile duct carcinoma), and mixed hepatocellular cholangiocarcinoma.
Skin cancers include, but are not limited to, squamous cell carcinoma, Kaposi's sarcoma, malignant melanoma, Merkel cell skin cancer, and non-melanoma skin cancer.
Head-and-neck cancers include, but are not limited to, laryngeal, hypopharyngeal, nasopharyngeal, and/or oropharyngeal cancers, and lip and oral cavity cancer.
Lymphomas include, but are not limited to, AIDS-related lymphoma, non-Hodgkin's lymphoma, cutaneous T-cell lymphoma, Hodgkin's disease, and lymphoma of the central nervous system.
Sarcomas include, but are not limited to, sarcoma of the soft tissue, osteosarcoma, malignant fibrous histiocytoma, lymphosarcoma, and rhabdomyosarcoma.
Leukemias include, but are not limited to, acute or chronic, acute myeloid leukemia, acute lymphoblastic leukemia, acute Lymphocytic Leukemia, chronic lymphocytic leukemia, chronic myelogenous leukemia, hairy cell leukemia, undifferentiated AML, promyelocyte leukemia, myelomonocytic leukemia, monocytic, leukemia, or erythroleukemia, megakaryoblastic leukemia, etc.
In addition to inhibiting the proliferation of tumor cells, compounds of the present invention can also cause tumor regression, e.g., a decrease in the size of a tumor, or in the extent of cancer in the body.
The present invention also relates to methods of modulating angiogenesis and/or lymphangiogenesis in a system comprising cells, comprising administering to the system an effective amount of a compound described herein. A system comprising cells can be an in vivo system, such as a tumor in a patient, isolated organs, tissues, or cells, in vitro assays systems (CAM, BCE, etc), animal models (e.g., in vivo, subcutaneous, cancer models), hosts in need of treatment (e.g., hosts suffering from diseases having angiogenic and/or lymphangiogenic component, such as cancer), etc.
Inappropriate and ectopic expression of angiogenesis (e.g., abnormal angiogenesis) can be deleterious to an organism. A number of pathological conditions are associated with the growth of extraneous blood vessels. These include, e.g., diabetic retinopathy, neovascular glaucoma, psoriasis, retrolental fibroplasias, angiofibroma, inflammation, etc. In addition, the increased blood supply associated with cancerous and neoplastic tissue, encourages growth, leading to rapid tumor enlargement and metastasis. Moreover, the growth of new blood and lymph vessels in a tumor provides an escape route for renegade cells, encouraging metastasis and the consequence spread of the cancer.
Methods of the present invention also relate to treating and/or preventing disorders or conditions associated with, or resulting from, vascular hyperpermeability.
For example, VEGF increases endothelial cell permeability. As a consequence, any condition which results in the release of VEGF, especially in higher than normal amounts, can be associated with vascular hyperpermeability and its accompanying deleterious effects. The present invention, however, provides for the treatment or prevention of any condition or disorder associated with, or resulting from, vascular hyperpermeability, regardless of the mechanism of action.
Edema formation is a life-threatening complication of various diseases of the central nervous system, including head injury, tumors, stroke, hypoxia, and high altitude sickness. The underlying cause of edema is vascular hyperpermeability. Compounds of the present invention can be utilized to treat and/or prevent vascular hyperpermeability, thereby treating and/or preventing edema, and the deleterious effects associated with it. Other hyperpermeability conditions (or conditions that produce vascular hypermeability), include, but are not limited to, tissue edema (e.g., lung, kidney, brain, etc.), vasogenic brain edema, chronic inflammation, wound healing, ischemia, tumors, atherosclerosis, peripheral vascular disease, ascites, effusions, exudates, nephrotic edema, primary glomerular disease, peripheral artery disease, diabetic retinopathy, diabetic retinal disease, obstruction of respiratory airways during asthma and other pulmonary disorders, circulatory collapse in sepsis, acute lung injury, acute respiratory distress syndrome, etc.
Assays for vascular permeability can be done routinely, e.g., Heiss et al., J. Clin. Invest., 98:1400- 1408, 1996; Fischer et al., Am. J. Physiol., 276(4 Pt l):C812-20, 1999; Fischer et al., Am. J. Physiol. Cell. Physiol., 279:C935-C944, 2000.
The compound of the formula (J) in the polymorph I of this invention also has a broad therapeutic activity to treat or prevent the progression of a broad array of diseases, such as inflammatory conditions, coronary restenosis, tumor-associated angiogenesis, atherosclerosis, autoimmune diseases, inflammation, certain kidney diseases associated with proliferation of glomerular or mesangial cells, and ocular diseases associated with retinal vessel proliferation, psoriasis, hepatic cirrhosis, diabetes, atherosclerosis, restenosis, vascular graft restenosis, in-stent stenosis, angiogenesis, ocurlar diseases, pulmonary fibrosis, obliterative bronchiolitis, glomerular nephritis, rheumatoid arthritis.
The present invention also provides for treating, preventing, modulating, etc., one or more of the following conditions in humans and/or other mammals: retinopathy, including diabetic retinopathy, ischemic retinal-vein occlusion, retinopathy of prematurity and age related macular degeneration; rheumatoid arthritis, psoriasis, or bullous disorder associated with subepidermal blister formation, including bullous pemphigoid, erythema multiforme, or dermatitis herpetiformis, rheumatic fever, bone resorption, postmenopausal osteoperosis, sepsis, gram negative sepsis, septic shock, endotoxic shock, toxic shock syndrome, systemic inflammatory response syndrome, inflammatory bowel disease (Crohn's disease and ulcerative colitis), Jarisch-Herxheimer reaction, asthma, adult respiratory distress syndrome, acute pulmonary fibrotic disease, pulmonary sarcoidosis, allergic respiratory disease, silicosis, coal worker's pneumoconiosis, alveolar injury, hepatic failure, liver disease during acute inflammation, severe alcoholic hepatitis, malaria (Plasmodium falciparum malaria and cerebral malaria), non-insulin-dependent diabetes mellitus (NIDDM), congestive heart failure, damage following heart disease, atherosclerosis, Alzheimer's disease, acute encephalitis, brain injury, multiple sclerosis (demyelation and oligodendrocyte loss in multiple sclerosis), advanced cancer, lymphoid malignancy, pancreatitis, impaired wound healing in infection, inflammation and cancer, myelodysplastic syndromes, systemic lupus erythematosus, biliary cirrhosis, bowel necrosis, radiation injury/ toxicity following administration of monoclonal antibodies, host-versus-graft reaction (ischemia reperfusion injury and allograft rejections of kidney, liver, heart, and skin), lung allograft rejection (obliterative bronchitis), or complications due to total hip replacement, ad an infectious disease selected from tuberculosis, Helicobacter pylori infection during peptic ulcer disease, Chaga's disease resulting from Trypanosoma cruzi infection, effects of Shiga-like toxin resulting from E. coli infection, effects of enterotoxin A resulting from Staphylococcus infection, meningococcal infection, and infections from Borrelia burgdorferi, Treponema pallidum, cytomegalovirus, influenza virus, Theiler's encephalomyelitis virus, and the human immunodeficiency virus (HTV), papilloma, blastoglioma, Kaposi's sarcoma, melanoma, lung cancer, ovarian cancer, prostate cancer, squamous cell carcinoma, astrocytoma, head cancer, neck cancer, bladder cancer, breast cancer, colorectal cancer, thyroid cancer, pancreatic cancer, gastric cancer, hepatocellular carcinoma, leukemia, lymphoma, Hodgkin's disease, Burkitt's disease, arthritis, rheumatoid arthritis, diabetic retinopathy, angiogenesis, restenosis, in-stent restenosis, vascular graft restenosis, pulmonary fibrosis, hepatic cirrhosis, atherosclerosis, glomerulonephritis, diabetic nephropathy, thrombic micoangiopathy syndromes, transplant rejection, psoriasis, diabetes, wound healing, inflammation, and neurodegenerative diseases, hyperimmune disorders, hemangioma, myocardial angiogenesis, coronary and cerebral collateral vascularization, ischemia, corneal disease, rabeosis, neovascular glaucoma, macular degeneration retinopathy of prematurity, wound healing, ulcer Helicobacter related diseases, fractures, endometriosis, a diabetic condition, cat scratch fever, thyroid hyperplasia, asthma or edema following burns, trauma, chronic lung disease, stroke, polyps, cysts, synovitis, chronic and allergic inflammation, ovarian hyperstimulation syndrome, pulmonary and cerebral edema, keloid, fibrosis, cirrhosis, carpal tunnel syndrome, adult respiratory distress syndrome, ascites, an ocular condition, a cardiovascular condition, Crow-Fukase (POEMS) disease, Crohn's disease, glomerulonephritis, osteoarthritis, multiple sclerosis, graft rejection, Lyme disease, sepsis, yon Hippel Lindau disease, pemphigoid, Paget's disease, polycystic kidney disease, sarcoidosis, throiditis, hyperviscosity syndrome, Osler-Weber-Rendu disease, chronic occlusive pulmonary disease, radiation, hypoxia, preeclampsia, menometrorrhagia, endometriosis, infection by Herpes simplex, ischemic retinopathy, corneal angiogenesis, Herpes Zoster, human immunodeficiency virus, parapoxvirus, protozoa, toxoplasmosis, and tumor-associated effusions and edema.
The present invention further provides a method for the prevention or treatment of diseases, especially of the aforementioned diseases, using an effective amount of the compound of the formula (I) in the polymorph I. Combination with other pharmaceutical agents:
The compound of the formula (I) in the polymorph I of this invention can be administered as the sole pharmaceutical agent or in combination with one or more other pharmaceutical agents where the combination causes no unacceptable adverse effects. This may be of particular relevance for the treatment of hyper-proliferative diseases such as cancer, hi this instance, the compound of this invention can be combined with known cytotoxic agents, signal transduction inhibitors, with other anti-cancer agents, or with antiemetics, as well as with admixtures and combinations thereof..
hi one embodiment, the compound of the formula (T) in the polymorph I of the present invention can be combined with cytotoxic anti-cancer agents. Examples of such agents can be found in the 1 lth Edition of the Merck Index (1996). These agents include, by no way of limitation, asparaginase, bleomycin, carboplatin, carmustine, chlorambucil, cisplatin, colaspase, cyclophosphamide, cytarabine, dacarbazine, dactinomycin, daunorubicin, doxorubicin (adriamycine), epirubicin, etoposide, 5-fluorouracil, hexamethylmelamine, hydroxyurea, ifosfamide, irinotecan, leucovorin, lomustine, mechlorethamine, 6-mercaptopurine, mesna, methotrexate, mitomycin C, mitoxantrone, prednisolone, prednisone, procarbazine, raloxifen, streptozocin, tamoxifen, thioguanine, topotecan, vinblastine, vincristine, and vindesine.
Other cytotoxic drugs suitable for use with the compounds of the invention include, but are not limited to, those compounds acknowledged to be used in the treatment of neoplastic diseases in Goodman and Gilman's The Pharmacological Basis of Therapeutics (Ninth Edition, 1996, McGraw- Hill). These agents include, by no way of limitation, aminoglutethimide, L-asparaginase, azathioprine, 5-azacytidine cladribine, busulfan, diethylstilbestrol, 2\ 2'-difluorodeoxycytidine, docetaxel, erythrohydroxynonyladenine, ethinyl estradiol, 5-fluorodeoxyuridine, 5-fluoro- deoxyuridine monophosphate, fludarabine phosphate, fluoxymesterone, flutamide, hydroxyprogesterone caproate, idarubicin, interferon, medroxyprogesterone acetate, megestrol acetate, melphalan, mitotane, paclitaxel, pentostatin, N-phosphonoacetyl-L-aspartate (PALA), plicamycin, semustine, teniposide, testosterone propionate, thiotepa, trimethylmelamine, uridine, and vinorelbine.
In another embodiment, the compound of the formula (T) in the polymorph I of the present invention can be combined with antiemetics. Antiemetics suitable for use with the compounds of the invention include, but are not limited to, antihistamines, Hi receptor blockers, 5-HT3 antagonists, neuroleptics, anticholinergics, dopamine antagonists, serotonin antagonists, glucocorticoids or cannabinoids. These agents include, by no way of limitation, meclozin, dimenhydrinate, phenothiazin derivatives (e.g. thiethylperazin, triflupromazin), benzamide or benzimidazolon derivatives (e.g. metoclopramid, bromoprid, domperidon), butyrophenones, scopalamin, pyridoxine, chlorphenoxamin, granisetron, ondansetron, tropisetron, and dexamethason. Preference is given to the antiemetics: granisetron, ondansetron, tropisetron, or dexamethason.
"Combination" mean for the purposes of the invention not only a dosage form which contains all the components (so-called fixed combinations), and combination packs containing the components separate from one another, but also components which are administered simultaneously or sequentially, as long as they are employed for the prophylaxis or treatment of the same disease.
The active ingredients of the combination according to the invention can be converted in a known manner into the usual formulations, which may be liquid or solid formulations. Examples are tablets, coated tablets, pills, capsules, granules, aerosols, syrups, emulsions, suspensions, solutions.
Since the combination according to the invention is well tolerated and in some cases is effective even in low dosages, a wide range of formulation variants is possible. Thus, one possibility is to formulate the individual active ingredients of the combination according to the invention separately. In this case, it is not absolutely necessary for the individual active ingredients to be taken at the same time; on the contrary, sequential intake may be advantageous to achieve optimal effects. It is appropriate with such separate administration to combine the formulations of the individual active ingredients, for example tablets or capsules, simultaneously together in a suitable primary packaging. The active ingredients are present in the primary packaging in each case in separate containers which may be, for example, tubes, bottles or blister packs. Such separate packaging of the components in the joint primary packaging is also referred to as a kit.
Further formulation variants which are suitable and preferred for the combination according to the invention are also fixed combinations. "Fixed combination" is intended here to mean pharmaceutical forms in which the components are present together in a fixed ratio of amounts. Such fixed combinations may be, for example, in the form of oral solutions, but they are preferably solid oral pharmaceutical preparations, e.g. capsules or tablets.
Pharmaceutical compositions:
This invention also relates to pharmaceutical compositions containing the compound of the formula (1) in the polymorph I of the present invention and methods of administering to a patient in need thereof a pharmaceutical composition of this invention.
A patient, for the purpose of this invention, is a mammal, including a human, in need of treatment for the particular condition or disease.
The pharmaceutical compositions of the present invention are comprised of a pharmaceutically acceptable carrier and a pharmaceutically effective amount of the compound of the formula (I) in the polymorph I of the present invention.
A pharmaceutically acceptable carrier is any carrier which is relatively non-toxic and innocuous to a patient at concentrations consistent with effective activity of the active ingredient so that any side effects ascribable to the carrier do not vitiate the beneficial effects of the active ingredient.
A pharmaceutically effective amount of compound is that amount which produces a result or exerts an influence on the particular condition being treated.
The compound of the formula (I) in the polymorph I may be administered in a suitable manner, for example by the oral, parenteral, pulmonary, nasal, sublingual, lingual, buccal, rectal, dermal, transdermal, conjunctival or otic route, or as an implant or stent.
For these application routes, the inventive compounds may be administered in suitable administration forms.
For oral administration, suitable administration forms are those which function according to the prior art and deliver the compound of the formula (1) in the polymorph I in a rapid and/or modified manner, for example tablets (noncoated or coated tablets, for example with coatings which are resistant to gastric juice or have retarded dissolution or are insoluble and which control the release of the inventive compound), tablets which disintegrate rapidly in the oral cavity or films/wafers, films/lyophilizates, capsules (for example hard or soft gelatin capsules), sugar-coated tablets, granules, pellets, powders, suspensions or aerosols.
Parenteral administration can take place with avoidance of an absorption step (for example in an intravenous, intraarterial, intracardiac, intraspinal or intralumbar manner) or with inclusion of an absorption (for example in an intramuscular, subcutaneous, intracutaneous, percutaneous or intraperitoneal manner). Administration forms suitable for parenteral application include injection and infusion preparations in the form of suspensions, lyophilizates or sterile powders.
Suitable for the other administration routes are, for example, medicinal forms for inhalation (including powder inhalers, nebulizers), tablets for lingual, sublingual or buccal administration, films/wafers or capsules, suppositories, preparations for the ear or eye, vaginal capsules, aqueous suspensions (lotions, shaking mixtures), lipophilic suspensions, ointments, creams, transdermal therapeutic systems (for example patches), pastes, dusting powders, implants or stents.
The inventive compound may be converted to the application forms listed. This may take place in a known manner by mixing with inert, nontoxic, pharmaceutically suitable excipients. These excipients include carriers (for example, microcrystalline cellulose, lactose, mannitol), solvents (for example, liquid polyethylene glycols), emulsifiers and dispersants or wetting agents (for example, sodium dodecylsulfate, polyoxysorbitan oleate), binders (for example, polyvinylpyrrolidone), synthetic and natural polymers (for example, albumin), stabilizers (for example, antioxidants such as ascorbic acid), dyes (for example, inorganic pigments such as iron oxides) and substances for masking flavors and/or odors.
The present invention further provides medicaments which comprise at least the compound of the formula (I) in the polymorph I, typically together with one or more inert, nontoxic, pharmaceutically suitable excipients, for example binders, fillers, etc, and to the use thereof for the aforementioned purposes.
Dosage of the pharmaceutical compositions of the present invention:
Based upon standard laboratory techniques known to evaluate compounds useful for the treatment of any of the aforementioned disorders, by standard toxicity tests and by standard pharmacological assays for the determination of treatment of the conditions identified above in mammals, and by comparison of these results with the results of known medicaments that are used to treat these conditions, the effective dosage of the compounds of this invention can readily be determined for treatment of each desired indication. The amount of the active ingredient to be administered in the treatment of one of these conditions can vary widely according to such considerations as the particular compound and dosage unit employed, the mode of administration, the period of treatment, the age and sex of the patient treated, and the nature and extent of the condition treated.
The total amount of the active ingredient to be administered can range from about 0.001 mg/kg to about 200 mg/kg, and preferably from about 0.1 mg/kg to about 50 mg/kg body weight per day. A unit dosage may preferably contain from about 5 mg to about 4000 mg of active ingredient, and can be administered one or more times per day. The daily dosage for oral administration will preferably be from 0.1 to 50 mg/kg of total body weight. The daily dosage for administration by injection, including intravenous, intramuscular, subcutaneous and parenteral injections, and use of infusion techniques will preferably be from 0.1 to 10 mg/kg of total body weight. The daily rectal dosage regimen will preferably be from 0.1 to 50 mg/kg of total body weight. The daily vaginal dosage regimen will preferably be from 0.1 to 50 mg/kg of total body weight. The daily topical dosage regimen will preferably be from 0.1 to 10 mg/kg administered between one to four times daily. The transdermal concentration will preferably be that required to maintain a daily dose of from 0.1 to 10 mg/kg. The daily inhalation dosage regimen will preferably be from 0.1 to 10 mg/kg of total body weight. Other dosages and amounts can be selected routinely.
Nevertheless, it may in some cases be advantageous to deviate from the amounts specified, depending on body weight, administration route, individual behavior toward the active ingredient, type of preparation and time or interval over which the administration is effected. For instance, less than the aforementioned minimum amounts may be sufficient in some cases, while the upper limit specified has to be exceeded in other cases. In the case of administration of relatively large amounts, it may be advisable to divide these into several individual doses over the day.
Process for preparing:
The invention further provides a process for preparing the compound of the formula (T) in the polymorph I, by effecting the compound of the formula (I) in the polymorph DL, obtained as described in example 1, in an inert solvent at a temperature of, for example, from 5O0C up to the reflux temperature of the solvent, preferably from 60 to 800C, in the absence of crystals of a solvate of the compound of the formula (T), for example in the absence of crystals of the methanol solvate or the ethanol solvate of the compound of formula (T), for up to one day. The mixture is cooled to from -300C to room temperature, preferably from -250C to 100C, and the crystals are isolated and dried. The compound of the formula (T) is thus obtained in the polymorph I.
The invention likewise provides a process for preparing the compound of the formula (T) in the polymorph I, by effecting the compound of the formula (I) in the polymorph π, obtained as described in example 1, in an inert solvent at a temperature of, for example, from 100C up to the reflux temperature of the solvent, preferably at room temperature, for up to one day. Subsequently, the mixture is seeded with crystals of the compound of the formula (I) in the polymorph I and stirred or shaken, for example at room temperature, for from 1 hour to 14 days, preferably from 2 hours to 7 days. The crystals are isolated and dried. The compound of the formula (T) is thus obtained in the polymorph I.
The invention likewise provides a process for preparing the compound of the formula (I) in the polymorph I, by effecting the compound of the formula (T) in the polymorph π, obtained as described in example 1, in an inert solvent until the desired degree of conversion is attained, preferably until quantitative conversion to the polymorph I. If appropriate, crystals of the compound of the formula (T) in the polymorph I are added. The resulting crystals are isolated and, to remove solvent present, dried to constant weight at room temperature or at elevated temperature, for example from 40 to 800C. The compound of the formula (T) is thus obtained in the polymorph I.
Effecting the compound of the formula (I) in the polymorph II in an inert solvent means, that for example the compound of the formula (I) in the polymorph π is dissolved completely (solution) or only in part (suspension). The mixture can be, for example stirred or shaken.
Suitable inert solvents are lower alcohols, for example methanol, ethanol, n-propanol, isopropanol, n- butanol, sec-butanol, isobutanol, or ketones such as acetone, or alkanes such as n-pentane, cyclopentane, n-hexane, cyclohexane, or tetrahydrofuran, or acetonitrile, or toluene, or ethyl acetate, or mixtures of the solvents mentioned, or mixtures of the solvents mentioned with water. Preference is given to methanol, ethanol, n-propanol, isopropanol, acetone, tetrahydrofuran, acetonitrile, toluene, ethyl acetate, mixtures of the solvents mentioned or mixtures of the solvents mentioned with water. Isopropanol, ethylacetate or a mixture thereof are used most preferably as inert solvents.
Preference is given to preparing the compound of the formula (T) in the polymorph I by effecting the compound of the formula (I) in the polymorph π, obtained as described in example 1, in methanol, ethanol, a mixture of both solvents or a mixture of both solvents with water, preferably a 1:1 mixture with water, and shaking or stirring at a temperature of from 500C up to the reflux temperature of the solvent, preferably at from 60 to 800C, in the absence of crystals of a solvate of the compound of the formula (T), for example in the absence of crystals of the methanol solvate or the ethanol solvate of the compound of formula (T), for up to one day. The crystals are cooled to from -3O0C to room temperature, preferably from -25 to 100C, isolated and dried. The compound of the formula (T) is thus obtained in the polymorph I. Most preferably isopropanol, ethylacetate or a mixture thereof is used as solvent.
Preference is likewise given to preparing the compound of the formula (T) in the polymorph I by effecting the compound of the formula (T) in the polymorph II, obtained as described in example 1 , in methanol, ethanol, a mixture of both solvents or a mixture of both solvents with water, and shaking or stirring at a temperature of from 1O0C up to the reflux temperature of the solvent, preferably at room temperature, for up to 1 day. The mixture is subsequently seeded with crystals of the compound of the formula (I) in the polymorph I and stirred or shaken, for example at room temperature, for from 1 hour to 14 days, preferably from 2 hours to 7 days. The crystals are isolated and dried. The compound of the formula (I) is thus obtained in the polymorph I. Most preferably isopropanol, ethylacetate or a mixture thereof is used as solvent.
Preference is likewise given to preparing the compound of the formula (I) in the polymorph I by effecting the compound of the formula (I) in the polymorph π, obtained as described in example 1, in an inert solvent apart from methanol and/or ethanol, preferably isopropanol, acetone, tetrahydrofuran, acetonitrile, ethyl acetate, toluene, or a mixture thereof and stirring or shaking at a temperature of from 1O0C up to the reflux temperature of the solvent, preferably at from room temperature to 9O0C, for up to 2 weeks, preferably from 1 day up to one week. If appropriate, the mixture is cooled to room temperature and the crystals are isolated and dried. The compound of the formula (T) is thus obtained in the polymorph I. Most preferably isopropanol, ethylacetate or a mixture thereof is used as solvent.
The compound of the formula (T) may likewise be prepared in the polymorph I by heating the compound of the formula (T) in the polymorph π to from 195 to 222°C, preferably from 195 to 215°C, for example at a heating rate of from 100C to 3O0C per minute, preferably from 15°C to 25°C per minute, and subsequently cooling to from 100C to 300C, preferably to room temperature, for example at a cooling rate of from 1°C to 40C per minute, preferably from I0C to 30C per minute. The compound of the formula (I) in the polymorph IH can be prepared by effecting the compound of the formula (I) in the polymorph II in an inert solvent, for example methanol. Filtration is effected after from 1 day to 1 week, and the product is dried and heat-treated at from 145 to 16O0C for from 15 minutes to 1 hour. The compound of the formula (T) is thus obtained in the polymorph IH.
The methanol solvate of the compound of the formula (T) can be prepared by effecting the compound of the formula (T) in the polymorph II in methanol. After 1 week, filtration is effected, and the product is dried and stored under a methanol atmosphere for from 5 hours to 1 week. The methanol solvate of the compound of the formula (I) is thus obtained with a methanol content of 4.8% by weight.
The ethanol solvate of the compound of the formula (I) can be prepared by effecting the compound of the formula (T) in the polymorph π in ethanol. After 1 week, filtration is effected and the product is dried. The ethanol solvate of the compound of the formula (I) is thus obtained with an ethanol factor of 6.7 percent by weight.
The processes are generally carried out at atmospheric pressure. However, it is also possible to work at elevated pressure or at reduced pressure (for example in a range of from 0.5 to 5 bar).
The weight data in the tests and examples which follow are, unless stated otherwise, percentages by weight; parts are parts by weight. Solvent ratios, dilution ratios and concentration data of liquid/liquid solutions are based on each case on the volume.
Working examples
The thermograms were obtained using a DSC 7 or Pyris-1 differential scanning calorimeter and TGA 7 thermogravimetric analyzer from Perkin-Elmer. The X-ray diffractograms were registered in a Stoe transmission diffractometer. The IR, FIR, NER and Raman spectra were recorded using IFS 66v (IR, FIR), IFS 28/N (NIR) and RFS 100 (Raman) Fourier spectrometers from Bruker.
Example 1 : 4-(4-[(([4-Chloro-3-(trifluoromethvπphenvnaminokarbonyl)aniino1phenoxyl-iV- methyIpyridine-2-carboxamide tosylate in the polymorph II
903 g of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)amino]phenoxy}-N-methyl- pyridine-2-carboxamide, prepared as described in WO 00/42012, are initially charged in 2700 ml of ethanol. 451.7 g of p-toluenesulfonic acid monohydrate are dissolved in 1340 g of ethanol and added dropwise at room temperature. The suspension is stirred at room temperature for 1 hour, then filtered off with suction, and the residue is washed three times with 830 ml each time of ethanol. The drying is effected at 5O0C under reduced pressure with supply of air. 1129.6 g of the title compound in the polymorph II are obtained.
Example 2: Preparation of 4-{4-f(ff4-chIoro-3-(triflαoromethyI)phenyl]amino}carbonvI)- aminoiphenoxyl-iV-methylpyridine-2-carboxamide tosylate in the polymorph I
Example 2.1
5 mg of the tosylate salt of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)amino]- phenoxy}-N-methylpyridine-2-carboxamide in the polymorph II are heated to 2000C at a heating rate of 20°C/min and subsequently cooled to room temperature at a cooling rate of 2°C/min. The sample is tested thermoanalytically (DSC) and corresponds to the title compound in the polymorph I.
Example 2.2
75 mg of the tosylate salt of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)- amino]phenoxy}-N-methylpyridine-2-carboxamide in polymorph II are dissolved in 10 ml of ethanol/water (1:1) at approximately 800C and filtered. The mixture is divided into two samples and sample A is crystallized in a refrigerator at +8°C and sample B in a freezer at -200C. After vaporization of the solvent mixtures, the two crystals of sample A and B are tested thermoanalytically (DSC). Both samples correspond to the title compound in the polymorph I. Example 2.3
In each case 400 mg of the tosylate salt of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]- amino}carbonyl)amino]phenoxy}-N-methylpyridine-2-carboxamide in the polymorph π are sus¬ pended in a) 8 ml of methanol and b) in 8 ml of ethanol and each stirred at room temperature for 2 hours. The suspensions are each seeded with 2 mg of the title compound in the polymorph I and subsequently stirred at room temperature for 1 week. After filtration, the solid residues of the two samples are dried at room temperature. The residues are each tested thermoanalytically (DSC) and correspond to the title compound in the polymorph I.
Example 2.4
200 mg of the tosylate salt of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)- amino]phenoxy}-N-methylpyridine-2-carboxamide in the polymorph II are suspended in 5 ml of ethanol/water (1:1 v/v) and stirred at room temperature for 2 hours. The suspension is seeded with 2 mg of the title compound in the polymorph I and subsequently stirred at room temperature for 1 week. After filtration, the solid residue is dried at room temperature. The residue is tested thermoanalytically (DSC) and corresponds to the title compound in the polymorph I.
Example 2.5
In each case 50 mg of the tosylate salt of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}- carbonyl)amino]phenoxy}-N-methylpyridine-2-carboxarnide in the polymorph II are admixed with in each case 2 ml of a) isopropanol, b) acetone, c) tetrahydrofuran, d) actetonitrile, e) ethyl acetate and f) toluene, and in each case stirred at room temperature for 6 days. In the case of c) tetrahydrofuran and f) toluene another 1 ml of the particular solvent is added. The suspensions are each filtered and the particular residues are dried at room temperature. The residues are each tested by X-ray diffractometry and correspond to the title compound in the polymorph I.
Example 2.6
200 mg of the tosylate salt of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)- amino]phenoxy}-N-methylpyridine-2-carboxamide in the polymorph II are suspended in 4 ml of toluene and the suspension is stirred at 800C for one week. After cooling to room temperature, the residue is filtered, dried at room temperature and tested by X-ray diffractometry. The title compound is obtained in the polymorph I. Example 3: Preparation of 4-(4-f(([4-chIoro-3-(trifluoromethyl)phenylføinino}carbonvD- amino]phenoxy)-iV-methylpyridine-2-carboxamide tosylate in the polymorph HI
3.5 g of the tosylate salt of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)- amino]phenoxy}-N-methylpyridine-2-carboxamide in the polymorph II are suspended in 15 ml of methanol and stirred at room temperature. After one week, the suspension is filtered and the residue dried at room temperature. Subsequently, the product is heat-treated at 1500C for 30 min. The residue is analyzed by X-ray diffractometry and corresponds to the title compound in the polymorph HI.
Example 4: Preparation of the methanol solvate of 4-(4-f({f4-chloro-3-(trifluoro- methyDphenyllaminolcarbonvπaminolphenoxyl-Ν-methylpyridine-Z-carboxamide tosylate
3.5 g of the tosylate salt of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)amino]- phenoxy}-N-methylpyridine-2-carboxamide in the polymorph π are suspended in 15 ml of methanol and stirred at room temperature. After one week, the suspension is filtered and the residue is dried at room temperature. Subsequently, the product is stored in a desiccator with a methanol atmosphere for one day. The residue is analyzed by X-ray diffractometry and corresponds to the methanol solvate of the title compound with a methanol content of 4.8 percent by weight.
Example 5: Preparation of the ethanol solvate of 4-f4-f((f4-chloro-3-(triflnoro- methyl)phenyllamino}earbonyl)aminoIphenoxy)-Ν-inethylpyridine-2-earboxamide tosylate
3 g of the tosylate salt of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)amino]- phenoxy}-N-methylpyridine-2-carboxamide in the polymorph II are suspended in 15 ml of ethanol and stirred at room temperature. After one week, the suspension is filtered and the residue is dried at room temperature. The residue is analyzed by X-ray diffractometry and corresponds to the ethanol solvate of the title compound with an ethanol content of 6.7 percent by weight. Tab. 1 : Differential Scanning Calorimetry and Thermogravimetrv
Figure imgf000022_0001
* — = melting under decomposition
** = Conversion point
Tab. 2: X-ray difrractometry
Figure imgf000022_0002
Figure imgf000023_0001
Figure imgf000024_0001
Figure imgf000025_0001
Tab. 3: IR spectroscopy
Figure imgf000026_0001
Figure imgf000027_0001
Figure imgf000028_0001
Tab. 4: Raman spectroscopy
Figure imgf000029_0001
Figure imgf000030_0001
Figure imgf000031_0001
Figure imgf000032_0001
Tab. 5: FIR spectroscopy
Figure imgf000033_0001
Figure imgf000034_0001
Tab. 6: NIR spectroscopy
Figure imgf000035_0001
Figure imgf000036_0001

Claims

What is claimed is:
1. A compound of the formula (T)
Figure imgf000037_0001
in the polymorph I.
A preparation of the compound of the formula (I) in the polymorph I, which comprises effecting the compound of the formula (T) in the polymorph II in an inert solvent until quantitative conversion to the polymorph I.
The preparation of the compound of the formula (T) in the polymorph I of claim 2, wherein the compound of the formula (T) in the polymorph II is effected in an inert solvent and seeded with crystals of the compound of the formula (I) in the polymorph I.
The preparation of the compound of the formula (I) in the polymorph I, wherein the compound of the formula (I) in the polymorph π is heated to from 195 to 222°C at a heating rate of from 10 to 30°C per minute and subsequently cooled to from 10 to 3O0C at a cooling rate of from 1 to 4°C per minute.
A compound of the formula (I) in the polymorph I for the treatment of disorders which feature abnormal angiogenesis or hyperpermeability processes, bone marrow diseases, carcinoma or carcinogenic cell growth.
A compound of the formula (T) in the polymorph I as claimed in claim 5 for the treatment of leukemia or for the treatment of carcinoma of the lung, of the pancreas, of the thyroid gland, of the kidney or of the intestine.
The use of the compound of the formula (I) in the polymorph I for the preparation of a pharmaceutical composition for the treatment of disorders which feature abnormal angiogenesis or hyperpermeability processes, bone marrow diseases, carcinoma or carcinogenic cell growth.
8. The use of the compound of the formula (I) in the polymorph I for the preparation of a pharmaceutical composition as claimed in claim 7 for the treatment of leukemia or for the treatment of carcinoma of the lung, of the pancreas, of the thyroid gland, of the kidney or of the intestine.
9. A pharmaceutical composition comprising the compound of the formula (T) mainly in the polymorph I and no significant fractions of another form of the compound of the formula (I)-
10. The pharmaceutical composition as claimed in claim 9 containing more than 90 percent by weight of the compound of the formula (I) in the polymorph I related to the total amount of the compound of the formula (T) present in the composition.
11. The pharmaceutical composition as claimed in one of claims 9 or 10 for the treatment of disorders.
12. The pharmaceutical composition as claimed in one of claims 9 to 11 for the treatment of disorders which feature abnormal angiogenesis or hyperpermeability processes, bone marrow diseases, carcinoma or carcinogenic cell growth.
13. The pharmaceutical composition as claimed in one of claims 9 to 12 for the treatment of leukemia or for the treatment of carcinoma of the lung, of the pancreas, of the thyroid gland, of the kidney or of the intestine.
14. The pharmaceutical composition as claimed in one of claims 9 to 13, comprising one or more inert, nontoxic, pharmaceutically suitable excipients.
15. A method for treating disorders which feature abnormal angiogenesis or hyper¬ permeability processes, bone marrow diseases, carcinoma or carcinogenic cell growth, using an effective amount of the compound of the formula (T) in the polymorph I or of a pharmaceutical composition as defined in one of claims 9 to 14.
16. The method as claimed in claim 15 for the treatment of leukemia or for the treatment of carcinoma of the lung, of the pancreas, of the thyroid gland, of the kidney or of the intestine.
17. A compound of the formula (T) in the polymorph I, obtainable by dissolving or suspending the compound of the formula (T) in the polymorph II in an inert solvent and stirring or shaking it until quantitative conversion to the polymorph I.
18. A compound of the formula (T) as claimed in claim 17, obtainable by dissolving or suspending the compound of the formula (T) in the polymorph II in an inert solvent and seeding it with crystals of the compound of the formula (T) in the polymorph I.
19. A combination comprising the compound of the formula (I) in the polymorph I and one or more other pharmaceutical agents.
20. The combination as claimed in claim 19 wherein the one or more other pharmaceutical agents are cytotoxic agents, signal transduction inhibitors, anti-cancer agents, or antiemetics.
21. The pharmaceutical composition as claimed in one of the claims 9 to 14 comprising one or more other pharmaceutical agents.
22. The pharmaceutical composition as claimed in claim 21 wherein the one or more other pharmaceutical agents are cytotoxic agents, signal transduction inhibitors, anti-cancer agents, or antiemetics.
PCT/EP2005/010119 2004-09-29 2005-09-20 Thermodynamically stable form of bay 43-9006 tosylate WO2006034797A1 (en)

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KR1020107011544A KR101239489B1 (en) 2004-09-29 2005-09-20 Thermodynamically stable form of bay 43-9006 tosylate
KR1020127030937A KR101381454B1 (en) 2004-09-29 2005-09-20 Thermodynamically stable form of bay 43-9006 tosylate
CA2581843A CA2581843C (en) 2004-09-29 2005-09-20 Thermodynamically stable form of bay 43-9006 tosylate
NZ553804A NZ553804A (en) 2004-09-29 2005-09-20 Thermodynamically stable form of bay 43-9006 tosylate
EP05797740A EP1797038B1 (en) 2004-09-29 2005-09-20 Thermodynamically stable form of bay 43-9006 tosylate
SI200531571T SI1797038T1 (en) 2004-09-29 2005-09-20 Thermodynamically stable form of bay 43-9006 tosylate
DK05797740.7T DK1797038T3 (en) 2004-09-29 2005-09-20 Thermodynamically stable form of bay 43-9006 tosylate
CN2005800407750A CN101065360B (en) 2004-09-29 2005-09-20 Thermodynamically stable form of BAY 43-9006 tosylate
PL05797740T PL1797038T3 (en) 2004-09-29 2005-09-20 Thermodynamically stable form of bay 43-9006 tosylate
AU2005289100A AU2005289100B2 (en) 2004-09-29 2005-09-20 Thermodynamically stable form of bay 43-9006 tosylate
JP2007533905A JP5215666B2 (en) 2004-09-29 2005-09-20 Thermodynamically stable form of BAY 43-9006 tosylate
ES05797740T ES2387812T3 (en) 2004-09-29 2005-09-20 Thermodynamically stable form of BAY 43-9006 tosylate
BRPI0515946-6A BRPI0515946A (en) 2004-09-29 2005-09-20 tosylate salt, its preparation and use, as well as pharmaceutical composition comprising the same
US11/664,363 US8877933B2 (en) 2004-09-29 2005-09-20 Thermodynamically stable form of a tosylate salt
IL181734A IL181734A (en) 2004-09-29 2007-03-06 Polymorph i of sorafenib tosylate, pharmaceutical compositions comprising it and its use in the manufacture of medicaments
NO20071508A NO344272B1 (en) 2004-09-29 2007-03-22 Thermodynamically stable form of BAY 43-9006 tosylate
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007053574A2 (en) 2005-10-31 2007-05-10 Bayer Pharmaceuticals Corporation Combinations comprising sorafenib and interferon for the treatment of cancer
WO2009092070A1 (en) * 2008-01-17 2009-07-23 Sicor Inc. Polymorph form iii of sorafenib tosylate, sorafenib tosylate methanol solvate and sorafenib tosylate ethanol solvate, and processes for preparation thereof
WO2009106825A1 (en) * 2008-02-27 2009-09-03 Cipla Limited Polymorphs of sorafenib and salts thereof
WO2010079498A2 (en) * 2009-01-12 2010-07-15 Hetero Research Foundation Novel polymorph of sorafenib tosylate
US7838541B2 (en) 2002-02-11 2010-11-23 Bayer Healthcare, Llc Aryl ureas with angiogenesis inhibiting activity
WO2010142678A2 (en) * 2009-06-12 2010-12-16 Ratiopharm Gmbh Polymorphs of 4-[4-[[4-chloro-3-(trifluoromethyl)phenyl]carbamoylamino]phenoxy]-n-methyl-pyridine-2-carboxamide
US7897623B2 (en) 1999-01-13 2011-03-01 Bayer Healthcare Llc ω-carboxyl aryl substituted diphenyl ureas as p38 kinase inhibitors
WO2011036647A1 (en) 2009-09-24 2011-03-31 Ranbaxy Laboratories Limited Process for the preparation of sorafenib tosylate
WO2011036648A1 (en) 2009-09-24 2011-03-31 Ranbaxy Laboratories Limited Polymorphs of sorafenib acid addition salts
WO2011058522A1 (en) 2009-11-12 2011-05-19 Ranbaxy Laboratories Limited Sorafenib ethylsulfonate salt, process for preparation and use
WO2011076711A2 (en) 2009-12-23 2011-06-30 Ratiopharm Gmbh Polymorphs of 4-[4-[[4-chloro-3-(trifluoromethyl)phenyl]carbamoylamino]phenoxy]-n-methylpyridine-2-carboxamide
WO2011092663A2 (en) 2010-01-29 2011-08-04 Ranbaxy Laboratories Limited 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl]ureido}phenoxy)-n2-methylpyridine-2-carboxamide dimethyl sulphoxide solvate
US8076488B2 (en) 2003-02-28 2011-12-13 Bayer Healthcare Llc Bicyclic urea derivatives useful in the treatment of cancer and other disorders
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US20120101261A1 (en) * 2009-04-15 2012-04-26 Fondazione Irccs Istituto Nazionale Dei Tumori Use of multi-kinase inhibitors in the treatment of vascular hyperpermeability
WO2012071425A1 (en) 2010-11-22 2012-05-31 Teva Pharmaceutical Industries Ltd. Solid state forms of sorafenib besylate, and processes for preparations thereof
WO2013000909A1 (en) 2011-06-28 2013-01-03 Bayer Intellectual Property Gmbh Topical ophthalmological pharmaceutical composition containing sorafenib
EP2559431A1 (en) 2011-08-17 2013-02-20 Ratiopharm GmbH Pharmaceutical composition comprising 4-[4-[[4-chloro-3-(trifluoromethyl)phenyl]carbamoylamino]phenoxy]-N-methyl-pyridine-2-carboxamide
WO2013110644A1 (en) 2012-01-23 2013-08-01 Sandoz Ag Pharmaceutical composition containing crystalline sorafenib tosylate
WO2013175483A1 (en) * 2012-05-23 2013-11-28 Shilpa Medicare Limited Process for preparing crystalline sorafenib tosylate
WO2013175506A2 (en) 2012-05-21 2013-11-28 Hetero Research Foundation Process for sorafenib tosylate polymorph iii
US8796250B2 (en) 2003-05-20 2014-08-05 Bayer Healthcare Llc Diaryl ureas for diseases mediated by PDGFR
WO2014118807A1 (en) * 2013-02-04 2014-08-07 Intas Pharmaceuticals Limited A novel process for the preparation of sorafenib tosylate form iii
WO2014138905A1 (en) * 2013-03-14 2014-09-18 Apotex Technologies Inc. Forms of sorafenib tosylate and processes for the preparation thereof
US8877933B2 (en) 2004-09-29 2014-11-04 Bayer Intellectual Property Gmbh Thermodynamically stable form of a tosylate salt
RU2568638C1 (en) * 2015-02-26 2015-11-20 Индивидуальный предприниматель Михайлов Олег Ростиславович CRYSTALLINE β-MODIFICATION OF 4-[4-({[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]CARBAMOYL}AMINO)PHENOXY]-N-METHYL-PYRIDINE-2-CARBOXAMIDE OF p-TOLUENE SULPHONATE, METHOD FOR PRODUCTION THEREOF AND PHARMACEUTICAL COMPOSITION BASED THEREON
US9381177B2 (en) 2010-10-01 2016-07-05 Bayer Intellectual Property Gmbh Substituted N-(2-arylamino)aryl sulfonamide-containing combinations
EP3109236A1 (en) * 2015-06-23 2016-12-28 F.I.S.- Fabbrica Italiana Sintetici S.p.A. Scalable process for the preparation of sorafenib tosylate ethanol solvate and sorafenib tosylate form iii
US9737488B2 (en) 2005-03-07 2017-08-22 Bayer Healthcare Llc Pharmaceutical composition for the treatment of cancer
WO2018211336A2 (en) 2018-09-07 2018-11-22 Alvogen Malta Operations (Row) Ltd Solid dosage form containing sorafenib tosylate
US10653684B2 (en) 2002-02-11 2020-05-19 Bayer Healthcare Llc Aryl ureas with angiogenisis inhibiting activity

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2297490T3 (en) 2003-07-23 2008-05-01 Bayer Pharmaceuticals Corporation OMEGA-CARBOXIARILDIFENILUREA FLUORO REPLACED FOR THE TREATMENT AND PREVENTION OF DISEASES AND AFFECTIONS.
AR062927A1 (en) * 2006-10-11 2008-12-17 Bayer Healthcare Ag 4- [4- ([[4- CHLORINE-3- (TRIFLUOROMETILE) PHENYL) CARBAMOIL] AMINO] -3- FLUOROPHENOXY) -N- METHYLPIRIDIN-2-MONOHIDRATED CARBOXAMIDE
JP2010509382A (en) * 2006-11-14 2010-03-25 バイエル・シェーリング・ファルマ・アクチェンゲゼルシャフト Polymorph II of 4- [4-({[4-Chloro-3- (trifluoromethyl) phenyl] carbamoyl} amino) -3-fluorophenoxy] -N-methylpyridine-2-carboxamide II
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US11179322B2 (en) 2018-07-10 2021-11-23 Novocure Gmbh Methods and compositions for treating tumors with TTFields and sorafenib
US20210403495A1 (en) 2018-11-01 2021-12-30 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
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US20220354951A1 (en) 2019-08-02 2022-11-10 Onehealthcompany, Inc. Treatment of Canine Cancers
CN117088809A (en) * 2022-05-12 2023-11-21 浙江工业大学 Sorafenib-malonic acid eutectic crystal and preparation method thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003068228A1 (en) * 2002-02-11 2003-08-21 Bayer Pharmaceuticals Corporation Aryl ureas with angiogenesis inhibiting activity

Family Cites Families (52)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5629425A (en) 1994-09-19 1997-05-13 Eli Lilly And Company Haloalkyl hemisolvates of 6-hydroxy-2-(4-hydroxyphenyl)-3-[4-piperidinoethoxy)-benzoyl]benzo[b]thiophene
CO4410191A1 (en) 1994-09-19 1997-01-09 Lilly Co Eli SYNTHESIS OF 3- [4- (2-AMINOETOXI) BENZOIL] -2-ARYL-6- HYDROXYBENZO [b] THIOPHENES
AU1153097A (en) 1996-06-07 1998-01-05 Eisai Co. Ltd. Stable polymorphs of donepezil (1-benzyl-4-{(5,6-dimethoxy-1-indanon)-2-yl}methylpiperidine ) hydrochloride and process for production
BR9711541A (en) 1996-09-23 1999-08-24 Lilly Co Eli Olanzapine dihydrate
US6344476B1 (en) 1997-05-23 2002-02-05 Bayer Corporation Inhibition of p38 kinase activity by aryl ureas
US6187799B1 (en) 1997-05-23 2001-02-13 Onyx Pharmaceuticals Inhibition of raf kinase activity using aryl ureas
US7329670B1 (en) 1997-12-22 2008-02-12 Bayer Pharmaceuticals Corporation Inhibition of RAF kinase using aryl and heteroaryl substituted heterocyclic ureas
US7517880B2 (en) 1997-12-22 2009-04-14 Bayer Pharmaceuticals Corporation Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas
CA2359244C (en) 1999-01-13 2013-10-08 Bayer Corporation .omega.-carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors
US7928239B2 (en) 1999-01-13 2011-04-19 Bayer Healthcare Llc Inhibition of RAF kinase using quinolyl, isoquinolyl or pyridyl ureas
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
EP1140840B1 (en) 1999-01-13 2006-03-22 Bayer Pharmaceuticals Corp. -g(v)-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
ME00275B (en) 1999-01-13 2011-02-10 Bayer Corp ?-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US7235576B1 (en) 2001-01-12 2007-06-26 Bayer Pharmaceuticals Corporation Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US7371763B2 (en) 2001-04-20 2008-05-13 Bayer Pharmaceuticals Corporation Inhibition of raf kinase using quinolyl, isoquinolyl or pyridyl ureas
ES2275931T5 (en) 2001-12-03 2018-10-23 Bayer Healthcare Llc Aryl urea compounds in combination with other cytostatic or cytotoxic agents for the treatment of human cancers
GB0129876D0 (en) 2001-12-13 2002-02-06 Smithkline Beecham Plc Novel pharmaceutical
US20030207872A1 (en) 2002-01-11 2003-11-06 Bayer Corporation Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
WO2003068229A1 (en) 2002-02-11 2003-08-21 Bayer Pharmaceuticals Corporation Pyridine, quinoline, and isoquinoline n-oxides as kinase inhibitors
WO2003068746A1 (en) 2002-02-11 2003-08-21 Bayer Pharmaceuticals Corporation Aryl ureas as kinase inhibitors
GB0203412D0 (en) 2002-02-13 2002-04-03 Pharmagene Lab Ltd 5-HT 2B receptor antagonists
KR20040089456A (en) 2002-03-29 2004-10-21 소니 가부시끼 가이샤 Optical disk identifying device, optical disk identifying method, optical disk recorder, and optical disk reproducing device
CN1290893C (en) 2002-05-03 2006-12-20 詹森药业有限公司 Polymeric microemulsions
US7351534B2 (en) * 2003-01-27 2008-04-01 Oregon Health & Sciences University Gene mutation associated with age-related macular degeneration
UY28213A1 (en) 2003-02-28 2004-09-30 Bayer Pharmaceuticals Corp NEW CYANOPIRIDINE DERIVATIVES USEFUL IN THE TREATMENT OF CANCER AND OTHER DISORDERS.
US7378233B2 (en) * 2003-04-12 2008-05-27 The Johns Hopkins University BRAF mutation T1796A in thyroid cancers
PT1626714E (en) 2003-05-20 2007-08-24 Bayer Pharmaceuticals Corp Diaryl ureas for diseases mediated by pdgfr
ES2297490T3 (en) 2003-07-23 2008-05-01 Bayer Pharmaceuticals Corporation OMEGA-CARBOXIARILDIFENILUREA FLUORO REPLACED FOR THE TREATMENT AND PREVENTION OF DISEASES AND AFFECTIONS.
ATE517885T1 (en) 2004-04-30 2011-08-15 Bayer Healthcare Llc SUBSTITUTED PYRAZOLYL UREA DERIVATIVES FOR THE TREATMENT OF CANCER
WO2006026501A1 (en) 2004-08-27 2006-03-09 Bayer Pharmaceuticals Corporation New pharmaceutical compositions for the treatment of cancer
MY191349A (en) 2004-08-27 2022-06-17 Bayer Pharmaceuticals Corp New pharmaceutical compositions for the treatment of hyper-proliferative disorders
BRPI0515946A (en) 2004-09-29 2008-08-12 Bayer Healthcare Ag tosylate salt, its preparation and use, as well as pharmaceutical composition comprising the same
WO2006034796A1 (en) 2004-09-29 2006-04-06 Bayer Healthcare Ag Process for the preparation of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)amino]phenoxy}-n-methylpyridine-2-carboxamide
US7271763B2 (en) * 2005-03-03 2007-09-18 The United States Of America As Represented By The Secretary Of The Army Hybrid-phased communication array
JP5304241B2 (en) 2005-03-07 2013-10-02 バイエル・ヘルスケア・エルエルシー Pharmaceutical composition comprising omega-carboxyaryl substituted diphenylurea for the treatment of cancer
US8329408B2 (en) 2005-10-31 2012-12-11 Bayer Healthcare Llc Methods for prognosis and monitoring cancer therapy
CA2627873A1 (en) 2005-10-31 2007-05-10 Scott Wilhelm Treatment of cancer with sorafenib
KR20080067000A (en) 2005-11-10 2008-07-17 바이엘 헬스케어 아게 Diaryl urea for treating pulmonary hypertension
WO2007059154A2 (en) 2005-11-14 2007-05-24 Bayer Healthcare Llc Treatment of cancers with acquired resistance to kit inhibitors
AR062927A1 (en) 2006-10-11 2008-12-17 Bayer Healthcare Ag 4- [4- ([[4- CHLORINE-3- (TRIFLUOROMETILE) PHENYL) CARBAMOIL] AMINO] -3- FLUOROPHENOXY) -N- METHYLPIRIDIN-2-MONOHIDRATED CARBOXAMIDE
WO2008055629A1 (en) 2006-11-09 2008-05-15 Bayer Schering Pharma Aktiengesellschaft Polymorph iii of 4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]-n-methylpyridine-2-carboxamide
JP2010509382A (en) 2006-11-14 2010-03-25 バイエル・シェーリング・ファルマ・アクチェンゲゼルシャフト Polymorph II of 4- [4-({[4-Chloro-3- (trifluoromethyl) phenyl] carbamoyl} amino) -3-fluorophenoxy] -N-methylpyridine-2-carboxamide II
JP2010514691A (en) 2006-12-20 2010-05-06 バイエル ヘルスケア リミティド ライアビリティ カンパニー 4- {4-[({3-tert-butyl-1- [3- (hydroxymethyl) phenyl] -1H-pyrazol-5-yl} carbamoyl) amino] -3-fluorophenoxy} -N-methylpyridine- 2-carboxamide and its prodrugs and salts for the treatment of cancer
US20100173954A1 (en) 2007-01-19 2010-07-08 Bayer Healthcare Llc Treatment of cancers having resistance to chemotherapeutic agents
US8680124B2 (en) 2007-01-19 2014-03-25 Bayer Healthcare Llc Treatment of cancers with acquired resistance to kit inhibitors
US8217061B2 (en) 2008-01-17 2012-07-10 Sicor Inc. Polymorphs of sorafenib tosylate and sorafenib hemi-tosylate, and processes for preparation thereof
WO2010048304A2 (en) 2008-10-21 2010-04-29 Bayer Healthcare Llc Identification of signature genes associated with hepatocellular carcinoma
AR081060A1 (en) 2010-04-15 2012-06-06 Bayer Schering Pharma Ag PROCEDURE TO PREPARE 4- {4 - [({[4-CHLORINE-3- (TRIFLUOROMETIL) PHENYL] AMINO} CARBONYL) AMINO] -3-FLUOROPHENOXY} -N-METHYLPIRIDIN-2-CARBOXAMIDE
US20130183268A1 (en) 2010-07-19 2013-07-18 Bayer Healthcare Llc Drug combinations with fluoro-substituted omega-carboxyaryl diphenyl urea for the treatment and prevention of diseases and conditions
MX2013003695A (en) 2010-10-01 2013-05-20 Bayer Ip Gmbh Substituted n-(2-arylamino)aryl sulfonamide-containing combinations.
WO2013000909A1 (en) 2011-06-28 2013-01-03 Bayer Intellectual Property Gmbh Topical ophthalmological pharmaceutical composition containing sorafenib
PE20141031A1 (en) 2011-06-28 2014-08-21 Bayer Healthcare Llc TOPICAL OPHTHALMOLOGICAL PHARMACEUTICAL COMPOSITION CONTAINING REGORAFENIB

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003068228A1 (en) * 2002-02-11 2003-08-21 Bayer Pharmaceuticals Corporation Aryl ureas with angiogenesis inhibiting activity

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
HOTTE S J ET AL: "BAY 43-9006: EARLY CLINICAL DATA IN PATIENTS WITH ADVANCED SOLID MALIGNANCIES", CURRENT PHARMACEUTICAL DESIGN, BENTHAM SCIENCE PUBLISHERS, SCHIPHOL, NL, vol. 8, no. 25, 2002, pages 2249 - 2253, XP001145745, ISSN: 1381-6128 *

Cited By (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8841330B2 (en) 1999-01-13 2014-09-23 Bayer Healthcare Llc Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US7897623B2 (en) 1999-01-13 2011-03-01 Bayer Healthcare Llc ω-carboxyl aryl substituted diphenyl ureas as p38 kinase inhibitors
US10653684B2 (en) 2002-02-11 2020-05-19 Bayer Healthcare Llc Aryl ureas with angiogenisis inhibiting activity
US8242147B2 (en) 2002-02-11 2012-08-14 Bayer Healthcare Llc Aryl ureas with angiogenisis inhibiting activity
US7838541B2 (en) 2002-02-11 2010-11-23 Bayer Healthcare, Llc Aryl ureas with angiogenesis inhibiting activity
US8076488B2 (en) 2003-02-28 2011-12-13 Bayer Healthcare Llc Bicyclic urea derivatives useful in the treatment of cancer and other disorders
US8796250B2 (en) 2003-05-20 2014-08-05 Bayer Healthcare Llc Diaryl ureas for diseases mediated by PDGFR
US8877933B2 (en) 2004-09-29 2014-11-04 Bayer Intellectual Property Gmbh Thermodynamically stable form of a tosylate salt
US9737488B2 (en) 2005-03-07 2017-08-22 Bayer Healthcare Llc Pharmaceutical composition for the treatment of cancer
EP2289515A3 (en) * 2005-10-31 2012-04-11 Bayer HealthCare LLC Combinations comprising a diaryl urea and an interferon
WO2007053574A2 (en) 2005-10-31 2007-05-10 Bayer Pharmaceuticals Corporation Combinations comprising sorafenib and interferon for the treatment of cancer
WO2007053574A3 (en) * 2005-10-31 2008-03-13 Bayer Pharmaceuticals Corp Combinations comprising sorafenib and interferon for the treatment of cancer
US8217061B2 (en) 2008-01-17 2012-07-10 Sicor Inc. Polymorphs of sorafenib tosylate and sorafenib hemi-tosylate, and processes for preparation thereof
WO2009092070A1 (en) * 2008-01-17 2009-07-23 Sicor Inc. Polymorph form iii of sorafenib tosylate, sorafenib tosylate methanol solvate and sorafenib tosylate ethanol solvate, and processes for preparation thereof
WO2009106825A1 (en) * 2008-02-27 2009-09-03 Cipla Limited Polymorphs of sorafenib and salts thereof
WO2010079498A3 (en) * 2009-01-12 2011-11-17 Hetero Research Foundation Novel polymorph of sorafenib tosylate
WO2010079498A2 (en) * 2009-01-12 2010-07-15 Hetero Research Foundation Novel polymorph of sorafenib tosylate
US20120101261A1 (en) * 2009-04-15 2012-04-26 Fondazione Irccs Istituto Nazionale Dei Tumori Use of multi-kinase inhibitors in the treatment of vascular hyperpermeability
WO2010142678A2 (en) * 2009-06-12 2010-12-16 Ratiopharm Gmbh Polymorphs of 4-[4-[[4-chloro-3-(trifluoromethyl)phenyl]carbamoylamino]phenoxy]-n-methyl-pyridine-2-carboxamide
WO2010142678A3 (en) * 2009-06-12 2011-03-24 Ratiopharm Gmbh Polymorphs of 4-[4-[[4-chloro-3-(trifluoromethyl)phenyl]carbamoylamino]phenoxy]-n-methyl-pyridine-2-carboxamide
WO2011036647A1 (en) 2009-09-24 2011-03-31 Ranbaxy Laboratories Limited Process for the preparation of sorafenib tosylate
WO2011036648A1 (en) 2009-09-24 2011-03-31 Ranbaxy Laboratories Limited Polymorphs of sorafenib acid addition salts
US8609854B2 (en) 2009-09-24 2013-12-17 Ranbaxy Laboratories Limited Process for the preparation of sorafenib tosylate
US8604208B2 (en) 2009-09-24 2013-12-10 Ranbaxy Laboratories Limited Polymorphs of sorafenib acid addition salts
US8552197B2 (en) 2009-11-12 2013-10-08 Ranbaxy Laboratories Limited Sorafenib ethylsulfonate salt, process for preparation and use
WO2011058522A1 (en) 2009-11-12 2011-05-19 Ranbaxy Laboratories Limited Sorafenib ethylsulfonate salt, process for preparation and use
WO2011076711A2 (en) 2009-12-23 2011-06-30 Ratiopharm Gmbh Polymorphs of 4-[4-[[4-chloro-3-(trifluoromethyl)phenyl]carbamoylamino]phenoxy]-n-methylpyridine-2-carboxamide
WO2011076711A3 (en) * 2009-12-23 2011-09-09 Ratiopharm Gmbh Polymorphs of salts of 4- [4- [ [4-chloro-3- (trifluoromethyl) phenyl] carbamoylamino] phenoxy] -n-methylpyridine - 2 - carboxamide
WO2011092663A2 (en) 2010-01-29 2011-08-04 Ranbaxy Laboratories Limited 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl]ureido}phenoxy)-n2-methylpyridine-2-carboxamide dimethyl sulphoxide solvate
US8618305B2 (en) 2010-01-29 2013-12-31 Ranbaxy Laboratories Limited Sorafenib dimethyl sulphoxide solvate
US9381177B2 (en) 2010-10-01 2016-07-05 Bayer Intellectual Property Gmbh Substituted N-(2-arylamino)aryl sulfonamide-containing combinations
WO2012071425A1 (en) 2010-11-22 2012-05-31 Teva Pharmaceutical Industries Ltd. Solid state forms of sorafenib besylate, and processes for preparations thereof
WO2013000909A1 (en) 2011-06-28 2013-01-03 Bayer Intellectual Property Gmbh Topical ophthalmological pharmaceutical composition containing sorafenib
WO2013023970A1 (en) 2011-08-17 2013-02-21 Ratiopharm Gmbh Pharmaceutical composition comprising 4-[4[[4-chloro-3-(trifluoromethyl)phenyl]carbamoylamino]phenoxy]-n-methylpyridine-2-carboxamide
EP2559431A1 (en) 2011-08-17 2013-02-20 Ratiopharm GmbH Pharmaceutical composition comprising 4-[4-[[4-chloro-3-(trifluoromethyl)phenyl]carbamoylamino]phenoxy]-N-methyl-pyridine-2-carboxamide
EP2806860A1 (en) 2012-01-23 2014-12-03 Sandoz AG Pharmaceutical composition containing crystalline sorafenib tosylate
US9227938B2 (en) 2012-01-23 2016-01-05 Sandoz Ag Pharmaceutical composition containing crystalline sorafenib tosylate
WO2013110644A1 (en) 2012-01-23 2013-08-01 Sandoz Ag Pharmaceutical composition containing crystalline sorafenib tosylate
US9156789B2 (en) 2012-05-21 2015-10-13 Hetero Research Foundation Process for sorafenib tosylate polymorph III
WO2013175506A2 (en) 2012-05-21 2013-11-28 Hetero Research Foundation Process for sorafenib tosylate polymorph iii
WO2013175483A1 (en) * 2012-05-23 2013-11-28 Shilpa Medicare Limited Process for preparing crystalline sorafenib tosylate
WO2014118807A1 (en) * 2013-02-04 2014-08-07 Intas Pharmaceuticals Limited A novel process for the preparation of sorafenib tosylate form iii
WO2014138905A1 (en) * 2013-03-14 2014-09-18 Apotex Technologies Inc. Forms of sorafenib tosylate and processes for the preparation thereof
RU2568638C1 (en) * 2015-02-26 2015-11-20 Индивидуальный предприниматель Михайлов Олег Ростиславович CRYSTALLINE β-MODIFICATION OF 4-[4-({[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]CARBAMOYL}AMINO)PHENOXY]-N-METHYL-PYRIDINE-2-CARBOXAMIDE OF p-TOLUENE SULPHONATE, METHOD FOR PRODUCTION THEREOF AND PHARMACEUTICAL COMPOSITION BASED THEREON
EP3109236A1 (en) * 2015-06-23 2016-12-28 F.I.S.- Fabbrica Italiana Sintetici S.p.A. Scalable process for the preparation of sorafenib tosylate ethanol solvate and sorafenib tosylate form iii
US9738607B2 (en) 2015-06-23 2017-08-22 F.I.S.—Fabbrica Italiana Sintetici S.p.A. Scalable process for the preparation of Sorafenib tosylate ethanol solvate and Sorafenib tosylate form III
WO2018211336A2 (en) 2018-09-07 2018-11-22 Alvogen Malta Operations (Row) Ltd Solid dosage form containing sorafenib tosylate

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