WO1997023230A1 - Method of treating disorders characterized by overexpression of cytidine deaminase or deoxycytidine deaminase - Google Patents
Method of treating disorders characterized by overexpression of cytidine deaminase or deoxycytidine deaminase Download PDFInfo
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- WO1997023230A1 WO1997023230A1 PCT/US1996/020649 US9620649W WO9723230A1 WO 1997023230 A1 WO1997023230 A1 WO 1997023230A1 US 9620649 W US9620649 W US 9620649W WO 9723230 A1 WO9723230 A1 WO 9723230A1
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- dideoxycytidine
- deaminase
- dideoxy
- azidocytidine
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- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
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- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
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- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/12—Triazine radicals
Definitions
- the present invention relates to a method of treating a disorder characterized in part by the overexpression of cytidine deaminase or deoxycytidine deaminase, in a subject in need of such treatment, by administering 5-methyl-2' , 3 ' -dideoxy-3 ' -azidocytidine
- CD cytidine deaminase
- araC araC
- Lack of response to araC is found to be due primarily either to inactivation of the deoxycytidine kinase gene locus (whose product is required for activation of araC to its cancer-killing form) , or to overexpression of cytidine deaminase or deoxycytidine deaminase (which deactivates araC by deaminating it to an inactive form, araUracil) .
- HIV human immunodeficiency virus
- AZT 3' -azido-3'deoxythymidine
- Inflammatory cells associated with the symptoms of arthritis have also been shown to overexpress cytidine deaminase.
- a relatively non-toxic prodrug that would be preferentially activated to a metabolite that is toxic to the inflammatory cells mediating arthritis would therefore be useful.
- a method of treating a disorder characterized by the overexpression of cytidine deaminase or deoxycytidine deaminase in a subject in need of such treatment is disclosed.
- 5-methyl- 2' , 3 ' -dideoxy-3 ' -azidocytidine (5mAZC) or an analog thereof (hereinafter referred to as the "active compound") , is administered to a subject in need of such treatment, in an amount effective to treat the disorder.
- a first aspect of the invention is a method of treating a disorder characterized by the overexpression of cytidine deaminase or deoxycytidine deaminase in a subject in need of such treatment, comprising administering a compound of Formula I:
- X and X j ⁇ are each independently C or N;
- R- L is lower alkyl, lower alkenyl, lower alkynyl, halogen, or haloalkyl; and
- R 2 is H, -N 3 , -OH, amino, or halogen; or a pharmaceutically acceptable salt thereof, to the subject in an amount effective to treat the disorder.
- a method of combatting leukemia resistant to cytosine arabinoside (araC) in a subject in need of such treatment by administering a compound of Formula I to said subject in an amount effective to combat araC- resistant leukemia is another particular aspect of the foregoing method.
- a method of combatting HIV-infection in a subject in need of such treatment by administering a compound of Formula I to said subject in an amount effective to treat HIV infection i ⁇ yet another particular aspect of the foregoing.
- a method of combatting arthritis in a subject in need of such treatment by administering a compound of
- Formula I to said subject in an amount effective to treat arthritis is still another more particular aspect of the foregoing.
- a second aspect of the present invention is a method of combatting cancer in a subject in need of such -4 - treatment, wherein said cancer is characterized by the overexpression of cytidine deaminase, by administering a compound of Formula I to said subject in an amount effective to combat said cancer, is one particular aspect of the foregoing method.
- a third aspect of the present invention is a pharmaceutical composition containing an active compound as disclosed herein, in an amount effective to treat a disorder characterized by the overexpression of cytidine deaminase or deoxycytidine deaminase, in a pharmaceutically acceptable carrier (e.g., a sterile liquid or solid carrier) .
- a pharmaceutically acceptable carrier e.g., a sterile liquid or solid carrier
- a fourth aspect of the present invention is the use of an active compound as disclosed herein for the preparation of a medicament for carrying out the methods given above.
- Figure 1 is a graph of a dose response curve comparing the efficacy of 5mAZC in HT-29SF CD cells, which overexpress cytidine deaminase, and HT-29SF cells, which do not.
- HT-29SF cells were plated in the bottom compartment, and HT-29SF CD cells in the top compartment of a "Transwell" culture dish (1,000 cells each) .
- a semipermeable membrane separated the two compartments of the Transwell, such that drugs administered in the tissue culture media bathed both compartments equally.
- the numbers on the x-axis indicate the concentrations (in ⁇ M) at which 5mAZC was administered continuously for 72 hours; the numbers on the y-axis indicate the number of surviving cells.
- the circular (•) data points represent the dose response for the HT-29SF CD cells.
- the square ( ⁇ ) data points represent the dose response for the HT-29SF cells .
- the method of the present invention can be used to treat a subject suffering from a disorder characterized by overexpression of cytidine deaminase or deoxycytidine deaminase by administering 5-methyl-2' , 3' - dideoxy-3 ' -azidocytidine (5mAZC) , or an analog thereof, or pharmaceutically acceptable salts thereof (i.e. "active compounds”) .
- a disorder characterized by overexpression of cytidine deaminase or deoxycytidine deaminase by administering 5-methyl-2' , 3' - dideoxy-3 ' -azidocytidine (5mAZC) , or an analog thereof, or pharmaceutically acceptable salts thereof (i.e. "active compounds”) .
- disorders include, but are not limited to, cancer, leukemia that is resistant to cytosine arabinoside (araC) , HIV infection, and arthritis.
- the method of the present invention is used to treat a subject suffering from a cancer that is characterized by the overexpression of cytidine deaminase.
- these cancers include adenocarcinoma of the colon, adenocarcinoma of the lung, adenocarcinoma of the stomach, adenocarcinoma of the breast, Wilm' s tumor, chondrocarcinoma, chondrosarcoma, leukemia, prostate tumors, brain tumors (e.g., glioma, astrocytoma) , kidney tumors, pancreatic tumors, cervical tumors, liver tumors (e.g., hepatoblastoma, hepatocarcinoma) , neuroblastoma, retinoblastoma, melanoma, basal cell carcinoma, sarcoma, and cancers metastatic to the liver (e.g., colon cancer) .
- the present invention is concerned primarily with the treatment of human subjects but may also be employed for the treatment of other mammalian subjects, such as dogs and cats, for veterinary purposes.
- lower alkyl refers to Cl to C4 linear or branched alkyl, such as methyl, ethyl, propyl, butyl, isopropyl, sec-butyl, and tert- butyl. Methyl is currently preferred.
- lower alkenyl refers to C2 to C5 linear or branched alkenyl, such as ethenyl, propenyl, and butenyl .
- lower alkynyl refers to C2 to C5 linear or branched alkynyl, such as propynyl and butynyl .
- haloalkyl refers to a lower alkyl as defined above wherein one or more hydrogens is substituted with a halo-group (e.g., a chloro-, fluor-, bromo- or iodo-group) , with -CF 3 being currently preferred.
- a halo-group e.g., a chloro-, fluor-, bromo- or iodo-group
- Active compounds useful in the practice of the present invention include compounds of Formula I:
- X and X x are each independently C or N;
- R- t is lower alkyl, lower alkenyl, lower alkynyl, halogen, or haloalkyl;
- R 2 is H, -N 3 , -OH, amino, or halogen.
- R x is methyl or -CF 3
- R 2 is -N 3 or -OH.
- R x is methyl and R 2 is -N 3 .
- Analogs of 5mAZC useful in the practice of the present invention include, but are not limited to, 5- methyl - 2 ' , 3 ' -dideoxycyt idine , 5 - ethyl - 2 ' , 3 ' - dideoxycytidine, 5-ethyl-2' , 3' -dideoxy-3 ' -azidocytidine, 5-propyl-2' , 3 ' -dideoxycytidine, 5-propyl-2' , 3' -dideoxy- 3' -azidocytidine, 5-propene-2', 3' -dideoxycytidine, 5- propene-2 ' , 3 ' -dideoxy-3' -azidocytidine, 5-propyne-2' , 3' - dideoxycytidine, and 5-propyne-2 ' , 3 ' -dideoxy-3 ' - azidocytidine.
- 5mAZC The structure of 5mAZC is known. See, e . g. , T.S. Lin et al. , J. Med. Chem . 26, 1691-1696 (1983) . 5mAZC is available from ChemSyn Laboratories (Lenexa, Kansas, USA) . Compounds useful for carrying out the present invention may be synthesized in accordance with known procedures which will be apparent to those skilled in the art. See, e . g. , T.S. Lin et al . , supra ; T. Kulikowski et al., Acta Biochim . Polonica 16, 201-217 (1969) ; J.J. Fox et al . , J. Amer. Chem . Soc . 81, 178-187 (1959) .
- the active compounds disclosed herein can, as noted above, be prepared in the form of their pharmaceutically acceptable salts.
- Pharmaceutically acceptable salts are salts that retain the desired biological activity of the parent compound and do not impart undesired toxicological effects.
- Examples of such salts are (a) acid addition salts formed with inorganic acids, for example hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, nitric acid and the like; and salts formed with organic acids such as, for example, acetic acid, oxalic acid, tartaric acid, succinic acid, maleic acid, fumaric acid, gluconic acid, citric acid, malic acid, ascorbic acid, benzoic acid, tannic acid, palmitic acid, alginic acid, polyglutamic acid, naphthalenesulfonic acid, methanesul onic acid, p- toluenesulfonic acid, naphthalenedisulfonic acid, polygalacturonic acid,
- the dosage of the active compound may generally be as high as 1000 ⁇ mol/kg, but more preferably is less than 500 ⁇ mol/kg and most preferably is less than 100 ⁇ mol/kg. Depending on the solubility of the particular formulation of active compound administered, the daily dose may be divided among one or several unit dose administrations. Administration of the active compounds may be carried out therapeutically (i.e., as a rescue treatment) or prophylactically.
- compositions for use in the present method of treating disorders characterized by the overexpression of cytidine deaminase include those suitable for inhalation, oral, rectal, parenteral (including subcutaneous, intradermal, intramuscular, intravenous) and transdermal administration.
- the compositions may conveniently be presented in unit dosage form and may be prepared by any of the methods well known in the art. The most suitable route of administration in any given case may depend upon the anatomic location of the disorder in the subject, the nature and severity of the condition being treated, and the particular formulation that is being used.
- the formulations may conveniently be presented in unit dosage form and may be prepared by any of the methods well known in the art .
- the active compound is administered in a dose range as given above.
- the dose of active agent will vary according to the condition being treated and the dose at which adverse pharmacological effects occur. One skilled in the art will take such factors into account when determining dosage .
- the active compound is administered to the subject with araC- resistant leukemia in an amount sufficient to be metabolized by cytidine deaminase or deoxycytidine deaminase to AZT in sufficient concentration to kill the araC-resistant cancer cells.
- the active compound may be used alone or in combination with one or more anti-leukemia agents for the prophylaxis or treatment of araC-resistant leukemia.
- active agents or the physiologically acceptable salts thereof are typically admixed with, inter alia, an acceptable carrier.
- the carrier must, of course, be acceptable in the sense of being compatible with any other ingredients in the formulation and must not be deleterious to the patient.
- the carrier may be a solid or a liquid, or both, and is preferably formulated with the compound as a unit-dose formulation, for example, a tablet, which may contain from 0.5% to 99% by weight of the active compound.
- One or more active compounds may be incorporated in the formulations of the invention (e.g., the formulation may contain one or more additional agents as noted above) , which formulations may be prepared by any of the well known techniques of pharmacy consisting essentially of admixing the components, optionally including one or more accessory therapeutic ingredients.
- Formulations suitable for oral administration may be presented in discrete units, such as capsules, cachets, lozenges, or tablets, each containing a predetermined amount of the active compound; as a powder or granules; as a solution or a suspension in an aqueous or non-aqueous liquid; or as an oil-in-water or water-in- oil emulsion.
- Such formulations may be prepared by any suitable method of pharmacy which includes the step of bringing into association the active compound and a suitable carrier (which may contain one or more accessory ingredients as noted above) .
- the formulations of the invention are prepared by uniformly and intimately admixing the active compound with a liquid or finely divided solid carrier, or both, and then, if necessary, shaping the resulting mixture.
- a tablet may be prepared by compressing or molding a powder or granules containing the active compound, optionally with one or more accessory ingredients.
- Compressed tablets may be prepared by compressing, in a suitable machine, the compound in a free-flowing form, such as a powder or granules optionally mixed with a binder, lubricant, inert diluent, and/or surface active/dispersing agent (s) .
- Molded tablets may be made by molding, in a suitable machine, the powdered compound moistened with an inert liquid binder.
- Formulations for oral administration may optionally include enteric coatings known in the art to prevent degradation of the formulation in the stomach and provide release of the drug in the small intestine.
- Formulations suitable for buccal (sub-lingual) administration include lozenges comprising the active compound in a flavored base, usually sucrose and acacia or tragacanth; and pastilles comprising the compound in an inert base such as gelatin and glycerin or sucrose and acacia.
- Formulations of the present invention suitable for parenteral administration comprise sterile aqueous and non-aqueous injection solutions of the active compound, which preparations are preferably isotonic with the blood of the intended recipient. These preparations may contain anti-oxidants, buffers, bacteriostats and solutes which render the formulation isotonic with the blood of the intended recipient.
- Aqueous and non-aqueous sterile suspensions may include suspending agents and thickening agents.
- the formulations may be presented in unit ⁇ dose or multi-dose containers, for example sealed ampoules and vials, and may be stored in a freeze-dried (lyophilized) condition requiring only the addition of the sterile liquid carrier, for example, saline or water- for-injection immediately prior to use.
- sterile liquid carrier for example, saline or water- for-injection immediately prior to use.
- Extemporaneous injection solutions and suspensions may be prepared from sterile powders, granules and tablets of the kind previously described.
- Formulations suitable for rectal administration are preferably presented as unit dose suppositories. These may be prepared by admixing the active compound with one or more conventional solid carriers, for example, cocoa butter, and then shaping the resulting mixture .
- Formulations suitable for transdermal administration may be presented as discrete patches adapted to remain in intimate contact with the epidermis of the recipient for a prolonged period of time. Formulations suitable for transdermal administration may also be delivered by iontophoresis (see, e.g., Pharmaceutical Research 3, 318 (1986)) and typically take the form of an optionally buffered aqueous solution of the active compound.
- g grams
- h hours
- kg means kilogram
- ml means milliliter
- M means molar
- ⁇ g means microgram
- ⁇ mol means micromoles
- nmol means nanomoles
- pmol means picomoles
- ⁇ Ci microCuries.
- HT-29SF human adenocarcinoma cells naturally express a high level of cytidine deaminase (CD) .
- HT-29SF CD cells are a subline of the HT-29SF line that express even higher CD levels than normal (about 5.4 times the expression level of HT-29SF cells) .
- HT-29SF CD cells were plated in the top compartment of a Transwell culture dish, while HT-29SF cells were placed in the bottom compartment (1000 cells each) .
- a semipermeable membrane separated the two compartments of the Transwell, such that drugs administered in the tissue culture media bathe both compartments equally.
- 5mAZC was administered continuously for 72 h at concentrations ranging from 0 ⁇ M to 50 ⁇ M. The results of this experiment are shown in Figure 1. The results of this experiment confirm the idea that cells that highly overexpress CD are sensitive to 5mAZC.
- Example 2 Based upon the results obtained above in Example 1, the dose of 50 ⁇ M 5mAZC was selected for more in-depth analysis. Two experiments were performed, in quintuplicate, in the same Transwell dishes, containing the HT-29SF cells and the HT-29SF CD cells in compartments separated only by a membrane permeable to 5mAZC. The results are given below in Table 1: Experiment 1 Experiment 2 Number of viable cells Number of viable cells
- Example 3 In vivo activity of 5mAZC: Human tumor xenograft model To determine if 5mAZC exhibits in vivo activity, three sixteen-week old female Balb/C nu/nu mice were subcutaneously inoculated with 2.0 x IO 6 HT-29SF cells in the left scapular region, and 2.0 x 10 6 HT-29SF CD cells in the right scapular region. One mouse received twice daily intraperitoneal doses of 150 mg/kg of 5mAZC. The other mouse received saline only. This treatment continued for 5 weeks, at which time the animals were euthanized and the solid tumors were dissected free and weighed. The examined tumors had the following weight characteristics:
- mice received subcutaneous injections of 5 x 10 6 HT-29SF cells. Twelve of the animals received 600 mg/kg/day 5mAZC in the flank for 28 days. Eighteen animals received saline injections on the same schedule. On Day 29, the animals were sacrificed and the tumor volume was quantified by standard methods. The average tumor volume for the control group receiving saline was 509 ⁇ 292 mm 3 . In contrast, the animals treated with 5mAZC had an average tumor volume of 273 ⁇ 97 mm 3 , an average 46% reduction in size.
- CD cytidine deaminase
- colon tumors and adjacent mucosa from surgical specimens were homogenized in 5mM Tris-Cl, pH 7.4, sonicated on ice in three 5-second pulses, and then adjusted to 50mM Tris-HCl, pH 7.4.
- the homogenates were centrifuged at 12,000 x g for 15 minutes at 4°C, and the homogenates stored at -70°C until analysis. Protein concentration was determined using a BioRad protein assay kit and bovine gamma globulin was used as a standard.
- the reaction mixture (lOO ⁇ L) contained 25 mM Tris-Cl, pH 7.4, 0.5 ⁇ Ci of [ 3 H] -cytidine and 0.02-0.05 mg of homogenate tissue. Reactions were carried out at 37°C for 30 minutes, then stoped with 3 L of cold 0.001 N HCl. The reaction mixture was placed on Whatman P-81 phosphocellulose discs that were washed with 3 mL of H 2 0, 1 mL of 0.1 N HCl, and 3 mL of H 2 0 twice before use. The mixture was allowed to flow gently by gravity for 1 hr and then assayed for radioactivity. The results were normalized for protein content and expressed as nmol/min/mg protein. The results of this experiment are presented below in Table 2.
- Example 5 Preferential Deamination of 5mAZC to AZT in Colonic Tumors:
- Each reaction mixture contained 0.26 ⁇ Ci of [ 3 H]-5mAZC.
- the reactions were terminated with 50 ⁇ L of 2M perchloric acid and the mixture separated by HPLC using a 4.6 x 25 cm Beckman Ultrasphere ODS with a mobile phase of 12.5% acetonitrile in 40 mM sodium acetate pH 7.0. Unlabeled 5mAZC and AZT were used to authenticate the resulting peaks.
- the fractions corresponding to radiolabeled 5mAZC and AZT were collected and assayed for radioactivity by scintillation counting. The results were normalized for protein content and expressed as pmol/min/mg protein, and are provided below in Table 3.
Abstract
Description
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Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
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JP9523869A JPH11513992A (en) | 1995-12-22 | 1996-12-23 | Agents and methods for treating diseases involving overexpression of cytidine deaminase or deoxycytidine deaminase |
EP96945043A EP0876149A4 (en) | 1995-12-22 | 1996-12-23 | Method of treating disorders characterized by overexpression of cytidine deaminase or deoxycytidine deaminase |
KR1019980704809A KR19990076695A (en) | 1995-12-22 | 1996-12-23 | Active Agents and Methods for Treating Diseases Associated with Overexpression of Cytidine Deaminase or Deoxycytidine Deaminase |
AU13501/97A AU728377C (en) | 1995-12-22 | 1996-12-23 | Method of treating disorders characterized by overexpression of cytidine deaminase or deoxycytidine deaminase |
Applications Claiming Priority (2)
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US57718595A | 1995-12-22 | 1995-12-22 | |
US08/577,185 | 1995-12-22 |
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WO1997023230A1 true WO1997023230A1 (en) | 1997-07-03 |
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PCT/US1996/020649 WO1997023230A1 (en) | 1995-12-22 | 1996-12-23 | Method of treating disorders characterized by overexpression of cytidine deaminase or deoxycytidine deaminase |
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US (1) | US6136791A (en) |
EP (1) | EP0876149A4 (en) |
JP (1) | JPH11513992A (en) |
KR (1) | KR19990076695A (en) |
AU (1) | AU728377C (en) |
CA (1) | CA2241255A1 (en) |
RU (1) | RU98113785A (en) |
WO (1) | WO1997023230A1 (en) |
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WO2017158396A1 (en) * | 2016-03-16 | 2017-09-21 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Cytidine deaminase inhibitors for the treatment of pancreatic cancer |
US11209421B2 (en) * | 2016-03-31 | 2021-12-28 | Centre National De La Recherche Scientifique | Cytidine deaminase expression level in cancer as a new therapeutic target |
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- 1996-12-23 EP EP96945043A patent/EP0876149A4/en not_active Withdrawn
- 1996-12-23 KR KR1019980704809A patent/KR19990076695A/en not_active Application Discontinuation
- 1996-12-23 WO PCT/US1996/020649 patent/WO1997023230A1/en not_active Application Discontinuation
- 1996-12-23 RU RU98113785/14A patent/RU98113785A/en not_active Application Discontinuation
- 1996-12-23 AU AU13501/97A patent/AU728377C/en not_active Ceased
- 1996-12-23 CA CA002241255A patent/CA2241255A1/en not_active Abandoned
- 1996-12-23 JP JP9523869A patent/JPH11513992A/en not_active Ceased
- 1996-12-23 US US08/772,455 patent/US6136791A/en not_active Expired - Fee Related
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US5215971A (en) * | 1986-12-19 | 1993-06-01 | Medivir Ab | Antiviral pharmaceutical composition comprising 5-substituted pyrimidine nucleosides |
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Cited By (16)
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US7250416B2 (en) | 2005-03-11 | 2007-07-31 | Supergen, Inc. | Azacytosine analogs and derivatives |
US7700567B2 (en) | 2005-09-29 | 2010-04-20 | Supergen, Inc. | Oligonucleotide analogues incorporating 5-aza-cytosine therein |
US8461123B2 (en) | 2005-09-29 | 2013-06-11 | Astex Pharmaceuticals, Inc. | Oligonucleotide analogues incorporating 5-aza-cytosine therein |
US9358248B2 (en) | 2005-09-29 | 2016-06-07 | Astex Pharmaceuticals, Inc. | Oligonucleotide analogues incorporating 5-aza-cytosine therein |
US10933079B2 (en) | 2005-09-29 | 2021-03-02 | Astex Pharmaceuticals, Inc. | Oligonucleotide analogues incorporating 5-aza-cytosine therein |
US9480698B2 (en) | 2005-09-29 | 2016-11-01 | Astex Pharmaceuticals, Inc. | Oligonucleotide analogues incorporating 5-aza-cytosine therein |
US10456415B2 (en) | 2005-09-29 | 2019-10-29 | Astex Pharmaceuticals, Inc. | Oligonucleotide analogues incorporating 5-aza-cytosine therein |
US9913856B2 (en) | 2011-08-30 | 2018-03-13 | Astex Pharmaceuticals, Inc. | Drug formulations |
US10517886B2 (en) | 2011-08-30 | 2019-12-31 | Astex Pharmaceuticals, Inc. | Drug formulations |
US9381207B2 (en) | 2011-08-30 | 2016-07-05 | Astex Pharmaceuticals, Inc. | Drug formulations |
US9605197B2 (en) * | 2012-02-29 | 2017-03-28 | Global Green Products Llc | System and method for inhibiting scale formation in oil wells |
US9914869B2 (en) | 2012-02-29 | 2018-03-13 | Global Green Products Llc | System and method for inhibiting scale formation in oil wells |
WO2016195353A1 (en) * | 2015-06-01 | 2016-12-08 | Kainos Medicine, Inc. | A use of 1'-cyano-cytarabine for cancer treatment |
US10485764B2 (en) | 2015-07-02 | 2019-11-26 | Otsuka Pharmaceutical Co., Ltd. | Lyophilized pharmaceutical compositions |
US10519190B2 (en) | 2017-08-03 | 2019-12-31 | Otsuka Pharmaceutical Co., Ltd. | Drug compound and purification methods thereof |
US11963973B2 (en) | 2019-02-01 | 2024-04-23 | Hemispherian As | Deoxy-cytidine or uridine derivatives for use in cancer therapies |
Also Published As
Publication number | Publication date |
---|---|
RU98113785A (en) | 2000-06-10 |
EP0876149A1 (en) | 1998-11-11 |
CA2241255A1 (en) | 1997-07-03 |
AU728377B2 (en) | 2001-01-11 |
EP0876149A4 (en) | 2001-09-26 |
US6136791A (en) | 2000-10-24 |
JPH11513992A (en) | 1999-11-30 |
AU1350197A (en) | 1997-07-17 |
AU728377C (en) | 2003-10-30 |
KR19990076695A (en) | 1999-10-15 |
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