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WO1997005873A2 - Utilisation de fluconazole pour inhiber la croissance de cancers - Google Patents

Utilisation de fluconazole pour inhiber la croissance de cancers Download PDF

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Publication number
WO1997005873A2
WO1997005873A2 PCT/US1996/012474 US9612474W WO9705873A2 WO 1997005873 A2 WO1997005873 A2 WO 1997005873A2 US 9612474 W US9612474 W US 9612474W WO 9705873 A2 WO9705873 A2 WO 9705873A2
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WO
WIPO (PCT)
Prior art keywords
agents
triazol
propan
pharmaceutical composition
bis
Prior art date
Application number
PCT/US1996/012474
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English (en)
Other versions
WO1997005873A3 (fr
Inventor
James Berger Camden
Original Assignee
The Procter & Gamble Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US08/674,180 external-priority patent/US5908855A/en
Priority to BR9609966A priority Critical patent/BR9609966A/pt
Priority to SK141-98A priority patent/SK14198A3/sk
Priority to HU9903420A priority patent/HUP9903420A3/hu
Priority to MX9800998A priority patent/MX9800998A/es
Priority to JP9508494A priority patent/JPH11510187A/ja
Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to PL96324904A priority patent/PL324904A1/xx
Priority to IL12309596A priority patent/IL123095A0/xx
Priority to NZ315184A priority patent/NZ315184A/xx
Priority to EP96926806A priority patent/EP0841921A2/fr
Priority to AU66833/96A priority patent/AU711966B2/en
Publication of WO1997005873A2 publication Critical patent/WO1997005873A2/fr
Publication of WO1997005873A3 publication Critical patent/WO1997005873A3/fr
Priority to NO980473A priority patent/NO980473L/no

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4196—1,2,4-Triazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

Definitions

  • This invention is a pharmaceutical composition that is useful for the treatment of cancers and tumors, particularly in human and warm blooded animals containing 2-(2,4-difluorophenyl)- l,3-bis(lH-l,2,4-triazol-l-yl)propan-2-ol and its derivatives. It can be used in combination with other chemotherapeutic agents and potentiators. The same composition can be used to treat viral infections.
  • cancers including leukemia, are the leading cause of death in animals and humans.
  • the exact cause of leukemia is not known, but links between certain activities such as smoking or exposure to carcinogens and the incidence of certain types of leukemia and tumors has been shown by a number of researchers.
  • chemotherapeutic agents Many types have been shown to be effective against cancers, tumors and leukemia, but not all types of cancer and tumor cells respond to these agents. Unfortunately, many of these agents also destroy normal cells. The exact mechanism for the action of these chemotherapeutic agents are not always known.
  • cytocidal or cytostatic agents work best on cancers with large growth factors, i.e., ones whose cells are rapidly dividing.
  • hormones in particular estrogen, progesterone and testosterone, and some antibiotics produced by a variety of microbes, alkylating agents, and anti-metabolites form the bulk of therapies available to oncologists.
  • cytotoxic agents that have specificity for leukemia, cancer and tumor cells while not affecting normal cells would be extremely desirable. Unfortunately, none have been found and instead agents which target especially rapidly dividing cells (both diseased and normal) have been used.
  • 2-(2,4-difluorophenyl)-l,3-bis(lH-l,2,4-triazol-l-yl)propan-2-ol and its derivatives in combination with other chemotherapeutic agents which are effective in destroying the tumor is a novel method of treatment.
  • 2-(2,4-Difluorophenyl)-l,3-bis(lH-l,2,4-triazol-l- yl)propan-2-ol and its derivatives can also be used to treat viral infections either alone or in the presence of a potentiator.
  • a pharmaceutical composition for treatment of mammals, and in particular, warm blooded animals and humans, which are affected by leukemia comprising a pharmaceutical carrier and an effective amount of 2-(2,4-difluorophenyl)-l,3-bis(lH-l,2,4-triazol-l-yl)propan-2-ol (Fluconazole®) and its derivatives.
  • 2-(2,4-Difluorophenyl)-l,3-bis(lH-l,2,4-triazol-l-yl)propan- 2-ol has the formula:
  • compositions can be used to inhibit the growth of leukemia, tumors and cancer cells in humans or animals by administration of an effective amount either orally, rectally, topically or parenterally, or intravenously. These compositions do not significantly affect healthy cells.
  • Potentiators can also be used in combination with 2-(2,4-difluorophenyl)-l,3-bis(lH- l,2,4-triazol-l-yl)propan-2-ol and its derivatives as can chemotherapeutic agents.
  • compositions are particularly effective against the influenza virus.
  • the term “comprising” means various components can be conjointly employed in the pharmaceutical composition of this invention. Accordingly, the terms “consisting essentially o and “consisting o are embodied in the term comprising.
  • a "pharmaceutically acceptable” component is one that is suitable for use with humans and/or animals without undue adverse side effects (such as toxicity, irritation, and allergic response) commensurate with a reasonable benefit/risk ratio.
  • safe and effective amount refers to the quantity of a component which is sufficient to yield a desired therapeutic response without undue adverse side effects (such as toxicity, irritation, or allergic response) commensurate with a reasonable benefit/risk ratio when used in the manner of this invention.
  • the specific "safe and effective amount” will, obviously, vary with such factors as the particular condition being treated, the physical condition of the patient, the type of mammal being treated, the duration of the treatment, the nature of concurrent therapy (if any), and the specific formulations employed and the structure ofthe compounds or its derivatives.
  • a "2-(2,4-difluorophenyl)-l,3-bis(lH-l,2,4-triazol-l-yl)propan-2-ol derivative” includes its esters and ethers and its pharmaceutically acceptable salts.
  • a "pharmaceutical addition salts” are salts of 2-(2,4-difluorophenyl)-l,3- bis(lH-l,2,4-triazol-l-yl)propan-2-ol with an organic or inorganic acid.
  • These preferred acid addition salts are chlorides, bromides, sulfates, nitrates, phosphates, sulfonates, formates, tartrates, maleates, malates, citrates, benzoates, salicylates, ascorbates, and the like.
  • a "pharmaceutical carrier” is a pharmaceutically acceptable solvent, suspending agent or vehicle for delivering the anti-leukemia agent to the animal or human.
  • the carrier may be liquid or solid and is selected with the planned manner of administration in mind.
  • cancer or “leukemia” refers to all types of cancers or neoplasm or malignant disease which attack normal healthy blood cells or bone marrow which produces blood cells which are found in mammals.
  • viruses includes viruses which cause diseases in warm blooded animals including HTV, influenza, rhinoviruses, herpes and the like.
  • 2-(2,4-difluorophenyl)-l,3-bis(lH-l,2,4-triazol-l-yl)propan-2-ol and its derivatives includes esters and ethers as well as addition salts.
  • potentiators are materials such as triprolidine and its cis-isomer or 1H- Benzimidazole-2-propanoic acid which are used in combination with 2-(2,4-difluorophenyl)-l,3- bis(lH-l,2,4-triazol-l-yl)propan-2-ol and its derivatives. Potentiators can affect the immune system or enhance the effectiveness of the drugs.
  • chemotherapeutic agents includes DNA-interactive Agents, Antime ⁇ tabolites, Tubulin-Interactive Agents, Hormonal agents and others, such as Asparaginase or hydroxyurea.
  • the derivatives include the lower carboxylic acid esters of the propanol group, for example, acetyl, propanoyl, butyl, pentyl and hexyl esters. Particularly preferred are the esters of carboxylic acids having less than seven carbons, and most preferably propyl esters.
  • Aryl carboxylic acids such as salicylic acid, benzoic acid, and related acids can also be used to esterify the propanol group.
  • Alkyl ethers having less than 7 carbons are also useful derivatives.
  • the pharmaceutical addition salts are salts of 2-(2,4-difluorophenyl)-l,3-bis(lH-l,2,4- triazol-l-yl)propan-2*ol with an organic or inorganic acid.
  • These preferred acid addition salts are chlorides, bromides, sulfates, nitrates, phosphates, sulfonates, formates, tartrates, maleates, malates, citrates, benzoates, salicylates, ascorbates, and the like.
  • These compounds are part of a more generic class of fungicides with the formula:
  • the chemotherapeutic agents are generally grouped as DNA-interactive Agents, Antimetabolites, Tubulin-Interactive Agents, Hormonal agents and others such as Asparaginase or hydroxyurea. Each of the groups of chemotherapeutic agents can be further divided by type of activity or compound.
  • the chemotherapeutic agents used in combination with 2-(2,4- d ⁇ luorophenyl)-l,3-bis(lH-l,2,4-triazol-l-yl)propan-2-ol and its derivatives include members of all of these groups.
  • DNA-interactive Agents include the alkylating agents, e.g. Cisplatin, Cyclophosphamide, Altretamine; the DNA strand-breakage agents, such as Bleomycin; the intercalating topoisomerase II inhibitors, e.g., Dactinomycin and Doxorubicin); the nonintercalating topoisomerase II inhibitors such as, Etoposide and Teniposde; and the DNA minor groove binder
  • the alkylating agents form covalent chemical adducts with cellular DNA, RNA, and protein molecules and with smaller amino acids, glutathione and similar chemicals. Generally, these alkylating agents react with a nucleophilic atom in a cellular constituent, such as an amino, carboxyl, phosphate, sulfhydryl group in nucleic acids, proteins, amino acids, or glutathione. The mechamsm and the role of these alkylating agents in cancer therapy is not well understood.
  • Typical alkylating agents include: Nitrogen mustards, such as Chlorambucil, Cyclophosphamide, Isofamide,
  • Aziridine such as Thiotepa methanesulphonate esters such as Busulfan; nitroso ureas, such as Carmustine, Lomustine, Streptozocin; platinum complexes, such as Cisplatin, Carboplatin; bioreductive alkylator, such as Mitomycin, and Procarbazine, dacarbazine and Altretamine;
  • DNA strand breaking agents include Bleomycin
  • DNA topoisomerase II inhibitors include the following: Intercalators, such as A sacrine, Dactinomycin, Daunorubicin, Doxorubicin,
  • the DNA minor groove binder is Plicamycin.
  • the antimetabolites interfere with the production of nucleic acids by one or the other of two major mechanisms. Some of the drugs inhibit production of the deoxyribonucleoside triphosphates that are the immediate precursors for DNA synthesis, thus inhibiting DNA replication. Some of the compounds are sufficiently like purines or pyrimidines to be able to substitute for them in the anabolic nucleotide pathways. These analogs can then be substituted into the DNA and RNA instead of their normal counte ⁇ arts.
  • the antimetabolites useful herein include: folate antagonists such as Methotrexate and trimetrexate pyrimidine antagonists, such as Fluorouracil, Fluorodeoxyuridine, CB3717, Azacitidine, Cytarabine, and Floxuridine purine antagonists include Mercaptopurine, 6-Thioguanine, Fludarabine, Pentostatin; sugar modified analogs include Cyctrabine, Fludarabine; ribonucleotide reductase inhibitors include hydroxyurea.
  • folate antagonists such as Methotrexate and trimetrexate pyrimidine antagonists, such as Fluorouracil, Fluorodeoxyuridine, CB3717, Azacitidine, Cytarabine, and Floxuridine purine antagonists include Mercaptopurine, 6-Thioguanine, Fludarabine, Pentostatin
  • sugar modified analogs include Cyctrabine, Fludarabine
  • Tubulin Interactive agents act by binding to specific sites on tubulin, a protein that polymerizes to form cellular microtubules. Microtubules are critical cell structure units. When the interactive agents bind on the protein, the cell can not form microtubules
  • Tubulin Interactive agents include Vincristine and Vinblastine, both alkaloids and Paclitaxel.
  • Hormonal agents are also useful in the treatment of cancers and tumors. They are used in hormonally susceptible tumors and are usually derived from natural sources.
  • estrogens conjugated estrogens and Ethinyl Estradiol and Diethylstilbesterol, Chlortrianisen and Idenestrol
  • progestins such as Hydroxyprogesterone caproate, Medroxyprogesterone, and Megestrol
  • androgens such as testosterone, testosterone propionate
  • Adrenal corticosteroids are derived from natural adrenal cortisol or hydrocortisone. They are used because of their anti inflammatory benefits as well as the ability of some to inhibit mitotic divisions and to halt DNA synthesis. These compounds include, Prednisone, Dexamethasone, Methylprednisolone, and Prednisolone.
  • Leutinizing hormone releasing hormone agents or gonadotropin-releasing hormone antagonists are used primarily the treatment of prostate cancer. These include leuprolide acetate and goserelin acetate. They prevent the biosynthesis of steroids in the testes.
  • Antihormonal antigens include: antiestrogenic agents such as Tamosifen, antiandrogen agents such as Flutamide ; and antiadrenal agents such as Mitotane and Aminoglutethimide. Hydroxyurea appears to act primarily through inhibition of the enzyme ribonucleotide reductase.
  • Asparaginase is an enzyme which converts asparagine to nonfunctional aspartic acid and thus blocks protein synthesis in the tumor.
  • Taxol is preferred chemotherapeutic agent.
  • potentiators can be any material which improves or increase the efficacy of the pharmaceutical composition or acts on the immune system.
  • One such potentiator is triprolidine and its cis-isomer which are used in combination with the chemotherapeutic agents and 2-(2,4- difluorophenyl)-l,3-bis(lH-l,2,4-triazol-l-yl)propan-2-ol and its derivatives.
  • Triprolidine is described in US 5,114,951 (1992).
  • Procodazole is a non-specific active immunoprotective agent against viral and bacterial infections and can be used with the compositions claimed herein. It is effective with 2-(2,4-difluorophenyl)- l,3-bis(lH-l,2,4-triazol-l-yl)propan-2-ol and its derivatives alone in treating cancers, tumors, leukemia and viral infections or combined with chemotherapeutic agents.
  • Propionic acid and its salts and esters can also be used in combination with the pharmaceutical compositions claimed herein.
  • Antioxidant vitamins such as vitamins A, C and E and beta-carotene can be added to these compositions.
  • any suitable dosage may be given in the method of the invention.
  • the type of compoimd and the carrier and the amount will vary widely depending on the species of the warm blooded animal or human, body weight, and the type of cancer or tumor or viral infection being treated. Generally a dosage of between about 1 milligram (mg) per kilogram (kg) of body weight and about 1000 mg per kg of body weight is suitable for either the 2-(2,4-difluorophenyl)-l,3-bis(lH-l,2,4- triazol-l-yl)propan-2-ol and its derivatives or the chemotherapeutic agent. Preferably from 15 mg to about 800 mg/kg of body weight is used.
  • a dosage unit may comprise a single compound or mixtures thereof with other compounds or other cancer inhibiting compounds.
  • the dosage unit can also comprise diluents, extenders, carriers, liposomes and the like.
  • the unit may be in solid or gel form such as pills, tablets, capsules and the like or in liquid form suitable for oral, rectal, topical, intravenous injection or parenteral administration or injection into or around the bone marrow.
  • chemotherapeutic agents 2-(2,4-difiuorophenyI)-l,3-bis(lH-l,2,4-triazol-l- yl)propan-2-ol and its derivatives and, optionally, the potentiators are typically mixed with a pharmaceutically acceptable carrier.
  • This carrier can be a solid or liquid and the type is generally chosen based on the type of administration being used.
  • the active agent can be coadministered in the form of a tablet or capsule, liposome, as an agglomerated powder or in a liquid form.
  • suitable solid carriers include lactose, sucrose, gelatin and agar.
  • Capsule or tablets can be easily formulated and can be made easy to swallow or chew; other solid forms include granules, and bulk powders. Tablets may contain suitable binders, lubricants, diluents, disintegrating agents, coloring agents, flavoring agents, flow-inducing agents, and melting agents.
  • suitable liquid dosage forms include solutions or suspensions in water, pharmaceutically acceptable fats and oils, alcohols or other organic solvents, including esters, emulsions, syrups or elixirs, suspensions, solutions and/or suspensions reconstituted from non- effervescent granules and effervescent preparations reconstituted from effervescent granules.
  • Such liquid dosage forms may contain, for example, suitable solvents, preservatives, emulsifying agents, suspending agents, diluents, sweeteners, thickeners, and melting agents.
  • Oral dosage forms optionally contain flavorants and coloring agents.
  • Parenteral and intravenous forms would also include minerals and other materials to make them compatible with the type of injection or delivery system chosen.
  • the method of treatment can be any suitable method which is effective in the treatment of the particular cancer or tumor type being treated. Treatment may be oral, rectal, topical, parenteral or intravenous admimstration or by injection into the tumor or cancer. The method of applying an effective amount also varies depending on the leukemia, cancer, tumor or virus being treated.
  • parenteral treatment by intravenous, subcutaneous, or intramuscular application of the 2-(2,4-d ⁇ luorophenyl)-l,3-bis(lH-l,2,4-triazol-l-yl)propan-2-ol and its derivatives, formulated with an appropriate carrier, additional cancer inhibiting compound or compounds or diluent to facilitate application will be the preferred method of administering the compounds to warm blooded animals.
  • 2-(2,4- difluorophenyl)-l,3-bis(lH-l,2,4-triazol-l-yl)propan-2-ol and its derivatives can be combined with fungicides, herbicides or other antiviral agents.
  • Preferred herbicides and fungicides include carbendazim, fluoconazole, benomyl, glyphosate and propicodazole.
  • compositions When used for treatment of viral infection, they can be combined with other anti-viral agents.
  • mice Female CD (mice Charles River Breeding Laboratories, Portage, MI) 5 to 7 weeks old of age at the time of receipt are used. Mice are approximately 6 to 9 weeks old and weigh approximately 20 to 28 grams at the time test initiation. All mice used in the study do not vary in age by more than 10 days. The mice are housed 6 per cage with bedding. The mice are fed rodent diet 5002 (PMI, St. Louis Missouri) adlibitum. Fresh water is supplied to the mice adlibitum.
  • PMI rodent diet
  • Human influenza virus strain AT2 Taiwan/l/64 is used to challenge the mice.
  • the organism is stored at approximately -70°C.
  • Prior to infectious challenge a vial of frozen stock is thawed and diluted to the appropriate concentration in buffered saline solution.
  • the mice are anesthetized with Halothane and the virus challenge dose is administered intra-nasally in volume of 50 microlitres.
  • Test materials are administered at the concentration and volume as provided below.
  • 10 mice per group receive the test articles by oral lavage.
  • Saline control animals 10 receive a comparable volume of saline as compared to the test article-dosed mice.
  • Test article dosing is accomplished at approximately 24 hour intervals.
  • day 0 approximately 4 hours after the second dosing of test articles or saline, all mice are challenged intra-nasally with an infective dose of virus calculated to produce approximately 90% lethality. Animals are observed daily for 21 days after infectious challenge for mortality or moribundity.
  • Solid tumors removed from patients are minced into 2 to 5 mm fragments and immediately placed in McCoy's Medium 5A plus 10% heat inactivated newborn calf serum plus 1% penicillin streptomycin. Within 4 hours, these solid tumors are mechanically disassociated with scissors, forced through No. 100 stainless steel mesh, through 25 gauge needles, and then washed with McCoys medium as described above. Ascitic, pleural, pericardial fluids and bone marrow are obtained by standard techniques. The fluid or marrow is placed in sterile containers containing 10 units of preservative free heparin per ml. of malignant fluid or marrow. After centrifugation at 150 x g for 10 minutes, the cells are harvested and washed with McCoy's medium plus 10% heat inactivated calf serum. The viability of cell suspensions is determined on a hemocytometer with trypan blue.
  • Cells to be cloned are suspended in 0.3% agar in enriched CMRL1066 supplemented with 15% heat inactivated horse serum, penicillin (100 units/ml), streptomycin (2mg/ml), glutamine (2mM), insulin (3 units ml), asparagine (0.6 mg/ml), and HEPES buffer (2mM).
  • penicillin 100 units/ml
  • streptomycin 2mg/ml
  • glutamine 2mM
  • insulin 3 units ml
  • asparagine 0.6 mg/ml
  • HEPES buffer HEPES buffer
  • the number of colomes (defined as 50 cells) formed in the 3 compound treated plates is compared to the number of colonies formed in the 3 control plates, and the percent colonies surviving at the concentration of compound can be tabulated.
  • Three positive control plates are used to determine survival rate. Orthosodium vanadate at 200 ⁇ g/ml is used as the positive control. If there is ⁇ 30% cells in the positive control when compared to the untreated control, the test is evaluated.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
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  • Medicinal Chemistry (AREA)
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Epidemiology (AREA)
  • Virology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Une composition pharmaceutique pour le traitement de cancers ou de tumeurs chez les mammifères contient du 2-(2,4-difluorophényl)-1,3-bis(1H-1,2,4-triazol-1-yl)propan-2-ol et ses dérivés. On peut utiliser un agent chimiothérapeutique en combinaison avec le 2-(2,4-difluorophényl)-1,3-bis(1H-1,2,4-triazol-1-yl)propan-2-ol et ses dérivés, ainsi que des agents de potentialisation. Le 2-(2,4-difluorophényl)-1,3-bis(1H-1,2,4-triazol-1-yl)propan-2-ol et ses dérivés peuvent également être utilisés pour traiter des infections virales, soit seul(s), soit en association avec d'autres agents antiviraux ou avec un agent de potentialisation.
PCT/US1996/012474 1995-08-04 1996-07-30 Utilisation de fluconazole pour inhiber la croissance de cancers WO1997005873A2 (fr)

Priority Applications (11)

Application Number Priority Date Filing Date Title
AU66833/96A AU711966B2 (en) 1995-08-04 1996-07-30 Use of fluconazole for inhibiting the growth of cancers
IL12309596A IL123095A0 (en) 1995-08-04 1996-07-30 Pharmaceutical compositions containing fluconazole for inhibiting the growth of cancers
HU9903420A HUP9903420A3 (en) 1995-08-04 1996-07-30 Use of fluconazole for the preparation of pharmaceutical compositions, inhibiting the growth of cancers and treating viral infections
MX9800998A MX9800998A (es) 1995-08-04 1996-07-30 Uso de fluconazol para inhibir el crecimiento de canceres.
JP9508494A JPH11510187A (ja) 1995-08-04 1996-07-30 癌の成長を阻害するためのフルコナゾールの使用
BR9609966A BR9609966A (pt) 1995-08-04 1996-07-30 Uso de fluconazol para a inibição do desenvolvimento de cânceres
PL96324904A PL324904A1 (en) 1995-08-04 1996-07-30 Application of fluconazole in carcinoma development inhibition
SK141-98A SK14198A3 (en) 1995-08-04 1996-07-30 Use of fluconazole for inhibiting the growth of cancers
NZ315184A NZ315184A (en) 1995-08-04 1996-07-30 Use of fluconazole for inhibiting the growth of cancers and viral infections
EP96926806A EP0841921A2 (fr) 1995-08-04 1996-07-30 Utilisation de fluconazole pour inhiber la croissance de cancers
NO980473A NO980473L (no) 1995-08-04 1998-02-03 Anvendelse av flukonazol for å inhibere cancervekst

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US188995P 1995-08-04 1995-08-04
US60/001,889 1995-08-04
US08/674,180 1996-07-16
US08/674,180 US5908855A (en) 1996-07-16 1996-07-16 Compositions for treating viral infections

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WO1997005873A2 true WO1997005873A2 (fr) 1997-02-20
WO1997005873A3 WO1997005873A3 (fr) 1997-03-27

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PCT/US1996/012474 WO1997005873A2 (fr) 1995-08-04 1996-07-30 Utilisation de fluconazole pour inhiber la croissance de cancers

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EP (1) EP0841921A2 (fr)
JP (1) JPH11510187A (fr)
KR (1) KR19990036138A (fr)
CN (1) CN1195288A (fr)
AR (1) AR003175A1 (fr)
AU (1) AU711966B2 (fr)
BR (1) BR9609966A (fr)
CA (1) CA2229024A1 (fr)
CZ (1) CZ33798A3 (fr)
HU (1) HUP9903420A3 (fr)
IL (1) IL123095A0 (fr)
MX (1) MX9800998A (fr)
NO (1) NO980473L (fr)
NZ (2) NZ503921A (fr)
PL (1) PL324904A1 (fr)
SK (1) SK14198A3 (fr)
TR (2) TR199800270T1 (fr)
WO (1) WO1997005873A2 (fr)

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998051303A1 (fr) * 1997-05-16 1998-11-19 The Procter & Gamble Company Traitement du vih et du cancer
US6138783A (en) * 1995-12-13 2000-10-31 Compagnie Generale D'enterprises Automobiles "C.G.E.A." Drive unit suitable for coupling to a wheeled body, and resulting vehicle
US6228876B1 (en) 1995-06-07 2001-05-08 The Procter & Gamble Company Pharmaceutical composition for inhibiting the growth of cancers
US6245789B1 (en) 1998-05-19 2001-06-12 The Procter & Gamble Company HIV and viral treatment
US6262093B1 (en) 1995-04-12 2001-07-17 The Proctor & Gamble Company Methods of treating cancer with benzimidazoles
US6265427B1 (en) 1995-06-07 2001-07-24 The Proctor & Gamble Company Pharmaceutical composition for the method of treating leukemia
US6271217B1 (en) 1997-01-28 2001-08-07 The Procter & Gamble Company Method of treating cancer with a benzimidazole and a chemotherapeutic agent
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US6407131B1 (en) 1997-05-16 2002-06-18 The Procter & Gamble Company Compounds and method for use thereof in the treatment of cancer or viral infections
US6423734B1 (en) 1999-08-13 2002-07-23 The Procter & Gamble Company Method of preventing cancer
JP2002529426A (ja) * 1998-11-09 2002-09-10 アイデック・ファーマシューティカルズ・コーポレイション キメラ抗ｃｄ２０抗体を用いた、循環腫瘍細胞に関連した血液学的悪性疾患の治療
US6462062B1 (en) 2000-09-26 2002-10-08 The Procter & Gamble Company Compounds and methods for use thereof in the treatment of cancer or viral infections
US6479526B1 (en) 1995-04-12 2002-11-12 The Procter & Gamble Company Pharmaceutical composition for inhibiting the growth of viruses and cancers
US6498188B1 (en) 1995-04-12 2002-12-24 The Procter & Gamble Company Methods of treatment for cancer or viral infections
RU2201230C1 (ru) * 2001-12-24 2003-03-27 Закрытое акционерное общество "Брынцалов-А" Лекарственное средство флузол, обладающее противогрибковым действием
US6608096B1 (en) 2000-09-26 2003-08-19 University Of Arizona Foundation Compounds and methods for use thereof in the treatment of cancer or viral infections
US6686391B2 (en) 1995-08-04 2004-02-03 University Of Arizona Foundation N-chlorophenylcarbamate and N-chlorophenylthiocarbamate compositions
EP1895012A1 (fr) * 2006-08-30 2008-03-05 Universitätsklinikum Freiburg Méthode de l'induction de l'apoptose de cellules tumorales par l'augmentation du niveau d'oxyde d'azote
AU2002329844B2 (en) * 2001-08-24 2008-05-22 3M Innovative Properties Company Vacuum assisted tissue treatment system
WO2008073961A2 (fr) * 2006-12-12 2008-06-19 Emory University Composés et procédés de modulation de la mise ai silence d'un polynucléotide d'intérêt
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US6262093B1 (en) 1995-04-12 2001-07-17 The Proctor & Gamble Company Methods of treating cancer with benzimidazoles
US6362207B1 (en) 1995-04-12 2002-03-26 The Procter & Gamble Company Methods of treating viral infections with benzimidazoles
US6498188B1 (en) 1995-04-12 2002-12-24 The Procter & Gamble Company Methods of treatment for cancer or viral infections
US6228876B1 (en) 1995-06-07 2001-05-08 The Procter & Gamble Company Pharmaceutical composition for inhibiting the growth of cancers
US6265427B1 (en) 1995-06-07 2001-07-24 The Proctor & Gamble Company Pharmaceutical composition for the method of treating leukemia
US6552059B2 (en) 1995-06-07 2003-04-22 University Of Arizona Foundation Pharmaceutical composition for and method of treating leukemia
US6686391B2 (en) 1995-08-04 2004-02-03 University Of Arizona Foundation N-chlorophenylcarbamate and N-chlorophenylthiocarbamate compositions
US6138783A (en) * 1995-12-13 2000-10-31 Compagnie Generale D'enterprises Automobiles "C.G.E.A." Drive unit suitable for coupling to a wheeled body, and resulting vehicle
US6271217B1 (en) 1997-01-28 2001-08-07 The Procter & Gamble Company Method of treating cancer with a benzimidazole and a chemotherapeutic agent
US6329355B1 (en) 1997-01-28 2001-12-11 The Procter & Gamble Company Method for inhibiting the growth of cancers
US6420411B1 (en) 1997-05-16 2002-07-16 The Procter & Gamble Company Compounds and methods for use thereof in the treatment of cancer or viral infections
US6900235B1 (en) 1997-05-16 2005-05-31 Uaf Technologies And Research, Llc Benzimidazole compounds, and pharmaceutical compositions and unit dosages thereof
US6710065B1 (en) 1997-05-16 2004-03-23 Uaf Technologies And Research, Llc Compounds and methods for use thereof in the treatment of cancer
US6423736B1 (en) 1997-05-16 2002-07-23 The Proctor & Gamble Company Compounds and methods for use thereof in the treatment of cancer or viral infections
US6864275B1 (en) 1997-05-16 2005-03-08 Uaf Technologies And Research, Llc Compounds and methods for use thereof in the treatment of cancer
US6407131B1 (en) 1997-05-16 2002-06-18 The Procter & Gamble Company Compounds and method for use thereof in the treatment of cancer or viral infections
US6482843B1 (en) 1997-05-16 2002-11-19 The Procter & Gamble Company Compounds and methods for use thereof in the treatment of cancer or viral infections
WO1998051303A1 (fr) * 1997-05-16 1998-11-19 The Procter & Gamble Company Traitement du vih et du cancer
US6506783B1 (en) 1997-05-16 2003-01-14 The Procter & Gamble Company Cancer treatments and pharmaceutical compositions therefor
US6245789B1 (en) 1998-05-19 2001-06-12 The Procter & Gamble Company HIV and viral treatment
JP2002529426A (ja) * 1998-11-09 2002-09-10 アイデック・ファーマシューティカルズ・コーポレイション キメラ抗ｃｄ２０抗体を用いた、循環腫瘍細胞に関連した血液学的悪性疾患の治療
US8206711B2 (en) 1998-11-09 2012-06-26 Biogen Idec Inc. Treatment of chronic lymphocytic leukemia using anti-CD20 antibodies
JP2010285439A (ja) * 1998-11-09 2010-12-24 Biogen Idec Inc キメラ抗ｃｄ２０抗体を用いた、循環腫瘍細胞に関連した血液学的悪性疾患の治療
JP4842435B2 (ja) * 1998-11-09 2011-12-21 バイオジェン・アイデック・インコーポレイテッド キメラ抗ｃｄ２０抗体を用いた、循環腫瘍細胞に関連した血液学的悪性疾患の治療
US6423734B1 (en) 1999-08-13 2002-07-23 The Procter & Gamble Company Method of preventing cancer
US6407105B1 (en) 2000-09-26 2002-06-18 The Procter & Gamble Company Compounds and methods for use thereof in the treatment of cancer or viral infections
US6462062B1 (en) 2000-09-26 2002-10-08 The Procter & Gamble Company Compounds and methods for use thereof in the treatment of cancer or viral infections
US6608096B1 (en) 2000-09-26 2003-08-19 University Of Arizona Foundation Compounds and methods for use thereof in the treatment of cancer or viral infections
US6380232B1 (en) 2000-09-26 2002-04-30 The Procter & Gamble Company Benzimidazole urea derivatives, and pharmaceutical compositions and unit dosages thereof
US6720349B2 (en) 2000-09-26 2004-04-13 Uaf Technologies And Research, Llc Compounds for use in the treatment of cancer or viral infections
AU2002329844B2 (en) * 2001-08-24 2008-05-22 3M Innovative Properties Company Vacuum assisted tissue treatment system
RU2201230C1 (ru) * 2001-12-24 2003-03-27 Закрытое акционерное общество "Брынцалов-А" Лекарственное средство флузол, обладающее противогрибковым действием
WO2008071242A1 (fr) 2006-08-30 2008-06-19 Universitätsklinikum Freiburg Procédé d'induction d'une apoptose tumorale par augmentation des niveaux d'oxyde nitrique
EP1895012A1 (fr) * 2006-08-30 2008-03-05 Universitätsklinikum Freiburg Méthode de l'induction de l'apoptose de cellules tumorales par l'augmentation du niveau d'oxyde d'azote
US8288088B2 (en) 2006-08-30 2012-10-16 Universitatsklinikum Freiburg Method for inducing tumor apoptosis by increasing nitric oxide levels
US8829004B2 (en) 2006-08-30 2014-09-09 Universitaetsklinikum Freiburg Method for inducing tumor apoptosis by increasing nitric oxide levels
WO2008073961A3 (fr) * 2006-12-12 2009-02-26 Univ Emory Composés et procédés de modulation de la mise ai silence d'un polynucléotide d'intérêt
WO2008073961A2 (fr) * 2006-12-12 2008-06-19 Emory University Composés et procédés de modulation de la mise ai silence d'un polynucléotide d'intérêt
WO2019185521A1 (fr) * 2018-03-26 2019-10-03 Westfälische Wilhelms-Universität Münster Inhibiteur de biosynthèse d'ergostérol et infection par le virus de la grippe

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HUP9903420A3 (en) 2001-12-28
JPH11510187A (ja) 1999-09-07
CN1195288A (zh) 1998-10-07
AR003175A1 (es) 1998-07-08
PL324904A1 (en) 1998-06-22
NZ315184A (en) 2000-05-26
TR199800270T1 (xx) 1998-05-21
HUP9903420A2 (hu) 2000-03-28
SK14198A3 (en) 1999-03-12
CZ33798A3 (cs) 1998-06-17
BR9609966A (pt) 1999-02-02
EP0841921A2 (fr) 1998-05-20
NZ503921A (en) 2002-03-01
IL123095A0 (en) 1998-09-24
NO980473L (no) 1998-04-03
WO1997005873A3 (fr) 1997-03-27
MX9800998A (es) 1998-04-30
AU6683396A (en) 1997-03-05
NO980473D0 (no) 1998-02-03
AU711966B2 (en) 1999-10-28
CA2229024A1 (fr) 1997-02-20
TR199801739T2 (xx) 1998-12-21
KR19990036138A (ko) 1999-05-25

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