EP0687179A1 - APPLICATION D'ANTICONVULSIVANTS COMME LA CARBAMAZEPINE ET l'OXCARBAZEPINE, DANS LE TRAITEMENT DU NEURO-SIDA - Google Patents

APPLICATION D'ANTICONVULSIVANTS COMME LA CARBAMAZEPINE ET l'OXCARBAZEPINE, DANS LE TRAITEMENT DU NEURO-SIDA

Info

Publication number
EP0687179A1
EP0687179A1 EP94908375A EP94908375A EP0687179A1 EP 0687179 A1 EP0687179 A1 EP 0687179A1 EP 94908375 A EP94908375 A EP 94908375A EP 94908375 A EP94908375 A EP 94908375A EP 0687179 A1 EP0687179 A1 EP 0687179A1
Authority
EP
European Patent Office
Prior art keywords
oxcarbazepine
carbamazepine
treatment
pharmaceutically acceptable
aids
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP94908375A
Other languages
German (de)
English (en)
French (fr)
Inventor
Anne Bousseau
Adam Doble
Erik Louvel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Aventis Pharma SA
Original Assignee
Rhone Poulenc Rorer SA
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
Application filed by Rhone Poulenc Rorer SA filed Critical Rhone Poulenc Rorer SA
Publication of EP0687179A1 publication Critical patent/EP0687179A1/fr
Withdrawn legal-status Critical Current

Links

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
    • A61K31/425—Thiazoles
    • A61K31/428—Thiazoles condensed with carbocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425—Thiazoles
    • 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
    • A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • 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
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • 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
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/04—Immunostimulants

Definitions

  • anti-convulsants such as carbamazepine and oxcarbazepine, in the treatment of neuro-AIDS.
  • the present invention relates to a new therapeutic application of the anticonvulsants chosen from carbamazepine and oxcarbazepine or the pharmaceutically acceptable salts of these compounds.
  • Carbamazepine and oxcarbazepine or the pharmaceutically acceptable salts of these compounds are described as anticonvulsants and antiepileptics in particular in patent EP 50589.
  • neuro-AIDS includes dementia, cognitive impairment, neuropathy, myopathy, eye disorders and all neurological symptoms associated with the HIV-1 virus.
  • Cortical cell cultures are prepared according to the method described by SINDOU et al., Brain Res., 572, 242-246 (1992). After 8 to 10 days of culture, the neurons having acquired a correct neuritic form are used for the tests. The cells are kept at 37 ° C. in a CO2 oven for the entire experiment.
  • Neuronal survival is assessed before and after 24 hours of application of the product to be tested by a colorimetric technique using Tuspan Blue, counting predetermined fields (semi-quantitative method). A minimum of 4 dishes of cultures per concentration (100 neurons per dish) was analyzed.
  • GP120 was applied to the culture medium for 24 hours alone at a concentration of 20 pmol and causes neuronal death of the order of 43%.
  • the product to be tested in solution in dimethyl sulfoxide (10 " 3M) is applied 5 minutes before the application of GP120 and then incubated for 24 hours at concentrations of 10" 7 to 10 " 8 mol. Neuronal survival is greater than 80%.
  • salts with mineral acids such as hydrochloride, sulfate, nitrate, phosphate or organic salts such as acetate, propionate, succinate, oxalate, benzoate, fumarate, maleate, methanesulfonate, isethionate, theophillin- acetate, salicylate, phenolphthalinate, methylene-bis- ⁇ -oxynaphthoate or substitution derivatives of these derivatives.
  • mineral acids such as hydrochloride, sulfate, nitrate, phosphate or organic salts such as acetate, propionate, succinate, oxalate, benzoate, fumarate, maleate, methanesulfonate, isethionate, theophillin- acetate, salicylate, phenolphthalinate, methylene-bis- ⁇ -oxynaphthoate or substitution derivatives of these derivatives.
  • the medicaments consist of at least one anticonvulsant chosen from carbamazepine and oxcarbazepine in free form or in the form of an addition salt with a pharmaceutically acceptable acid, in the pure state or in the form of a composition in which it is associated with any other pharmaceutically compatible product, which may be inert or physiologically active.
  • the medicaments according to the invention can be used orally or parenterally.
  • compositions for oral administration tablets, pills, powders (gelatin capsules, cachets) or granules can be used.
  • the active principle according to the invention is mixed with one or more inert diluents, such as starch, cellulose, sucrose, lactose or silica, under a stream of argon.
  • inert diluents such as starch, cellulose, sucrose, lactose or silica
  • These compositions can also comprise substances other than diluents, for example one or more lubricants such as magnesium stearate or talc, a dye, a coating (dragees) or a varnish.
  • compositions for oral administration solutions, suspensions, emulsions, syrups and pharmaceutically acceptable elixirs containing inert diluents such as water, ethanol, glycerol, vegetable oils or paraffin oil.
  • inert diluents such as water, ethanol, glycerol, vegetable oils or paraffin oil.
  • These compositions can include substances other than diluents, for example wetting, sweetening, thickening, flavoring or stabilizing products.
  • the sterile compositions for parenteral administration can preferably be aqueous or non-aqueous solutions, suspensions or emulsions.
  • solvent or vehicle water, propylene glycol, polyethylene glycol, vegetable oils, in particular olive oil, injectable organic esters, for example ethyl oleate or other organic solvents can be used. suitable.
  • These compositions can also contain adjuvants, in particular wetting agents, isotonizers, emulsifiers, dispersants and stabilizers. Sterilization can be done in several ways, for example by aseptic filtration, by incorporating sterilizing agents into the composition, by irradiation or by heating. They can also be prepared in the form of sterile solid compositions which can be dissolved at the time of use in sterile water or any other sterile injectable medium.
  • the doses depend on the desired effect, on the duration of the treatment and on the route of administration used; they are generally between 50 and 400 mg per day orally for an adult with unit doses ranging from 25 to 200 mg of active substance.
  • the doctor will determine the appropriate dosage based on age, weight and all other factors specific to the subject to be treated.
  • Tablets containing 50 mg of active product having the following composition are prepared according to the usual technique:
  • capsules containing 50 mg of active product having the following composition are prepared:
  • a solution for injection containing 10 mg of active product having the following composition is prepared:
  • the invention also relates to the process for the preparation of medicaments useful in the treatment of neuro-AIDS consisting in mixing an anticonvulsant chosen from carbamazepine and oxcarbazepine or the pharmaceutically acceptable salts of these compounds with one or more compatible diluents and / or adjuvants and pharmaceutically acceptable.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Neurology (AREA)
  • Virology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Molecular Biology (AREA)
  • Hospice & Palliative Care (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Psychiatry (AREA)
  • AIDS & HIV (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
EP94908375A 1993-03-05 1994-02-25 APPLICATION D'ANTICONVULSIVANTS COMME LA CARBAMAZEPINE ET l'OXCARBAZEPINE, DANS LE TRAITEMENT DU NEURO-SIDA Withdrawn EP0687179A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR9302568A FR2702148B1 (fr) 1993-03-05 1993-03-05 Application d'anticonvulsivants dans le traitement du neuro-sida.
FR9302568 1993-03-05
PCT/FR1994/000209 WO1994020110A1 (fr) 1993-03-05 1994-02-25 APPLICATION D'ANTICONVULSIVANTS COMME LA CARBAMAZEPINE ET l'OXCARBAZEPINE, DANS LE TRAITEMENT DU NEURO-SIDA

Publications (1)

Publication Number Publication Date
EP0687179A1 true EP0687179A1 (fr) 1995-12-20

Family

ID=9444690

Family Applications (3)

Application Number Title Priority Date Filing Date
EP94908376A Expired - Lifetime EP0687177B1 (fr) 1993-03-05 1994-02-25 Application de la lamotrigine dans le traitement du neuro-sida
EP94908374A Expired - Lifetime EP0687176B1 (fr) 1993-03-05 1994-02-25 Application du riluzole dans le traitement du neuro-sida
EP94908375A Withdrawn EP0687179A1 (fr) 1993-03-05 1994-02-25 APPLICATION D'ANTICONVULSIVANTS COMME LA CARBAMAZEPINE ET l'OXCARBAZEPINE, DANS LE TRAITEMENT DU NEURO-SIDA

Family Applications Before (2)

Application Number Title Priority Date Filing Date
EP94908376A Expired - Lifetime EP0687177B1 (fr) 1993-03-05 1994-02-25 Application de la lamotrigine dans le traitement du neuro-sida
EP94908374A Expired - Lifetime EP0687176B1 (fr) 1993-03-05 1994-02-25 Application du riluzole dans le traitement du neuro-sida

Country Status (23)

Country Link
US (2) US5629312A (ko)
EP (3) EP0687177B1 (ko)
JP (3) JPH08507509A (ko)
KR (3) KR100318168B1 (ko)
AT (2) ATE147981T1 (ko)
AU (3) AU6143894A (ko)
CA (3) CA2154571A1 (ko)
CZ (3) CZ284423B6 (ko)
DE (2) DE69401577T2 (ko)
DK (2) DK0687177T3 (ko)
ES (2) ES2157252T3 (ko)
FR (1) FR2702148B1 (ko)
GR (2) GR3022356T3 (ko)
HU (3) HU9502584D0 (ko)
IL (3) IL108844A (ko)
NO (3) NO307687B1 (ko)
PL (3) PL310475A1 (ko)
PT (1) PT687176E (ko)
RU (1) RU2157205C2 (ko)
SK (3) SK279659B6 (ko)
UA (1) UA41355C2 (ko)
WO (3) WO1994020108A1 (ko)
ZA (2) ZA941525B (ko)

Families Citing this family (25)

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US5866597A (en) * 1993-03-19 1999-02-02 Glaxo Wellcome Inc. Use of triazine compounds for the treatment of memory and learning disorders
GB9424766D0 (en) * 1994-12-07 1995-02-08 Wellcome Found Pharmaceutical composition
GB9512854D0 (en) * 1995-06-23 1995-08-23 Wellcome Found Novel formulation
DE19603984A1 (de) * 1996-02-05 1997-08-07 Bayer Ag Granulate von Triazinen
US20020022056A1 (en) 1997-02-14 2002-02-21 Burkhard Schlutermann Oxacarbazepine film-coated tablets
CO4920215A1 (es) * 1997-02-14 2000-05-29 Novartis Ag Tabletas de oxacarbazepina recubiertas de una pelicula y metodo para la produccion de estas formulaciones
US5922746A (en) * 1997-03-27 1999-07-13 Allergan Inhibition of noninactivating Na channels of mammalian optic nerve as a means of preventing optic nerve degeneration associated with glaucoma
GB9721497D0 (en) 1997-10-09 1997-12-10 Ciba Geigy Ag Organic compounds
FR2774592B1 (fr) * 1998-02-06 2000-03-17 Rhone Poulenc Rorer Sa Application du 2-amino-6-trifluoromethoxybenzothiazole pour la prevention ou le traitement des dysfonctionnements du cervelet
FR2774908B1 (fr) * 1998-02-17 2000-06-23 Centre Nat Rech Scient Utilisation d'inhibiteur de la liberation du glutamate dans le traitement de l'ischemie retinienne
FR2787028B1 (fr) 1998-12-15 2002-10-18 Aventis Pharma Sa Utilisation du riluzole dans le traitement des traumatismes acoustiques
WO2000066121A1 (en) * 1999-04-29 2000-11-09 Centre National De La Recherche Scientifique (C.N.R.S.) A method for the prevention of ischemic spinal cord injury caused by aortic crossclamping
US7479498B2 (en) * 1999-08-23 2009-01-20 Phoenix Biosciences, Inc. Treatments for viral infections
GB9925962D0 (en) * 1999-11-02 1999-12-29 Novartis Ag Organic compounds
FR2801217B1 (fr) * 1999-11-24 2002-12-06 Aventis Pharma Sa Association de riluzole et de gabapentine et son utilisation comme medicament
GB9930058D0 (en) 1999-12-20 2000-02-09 Novartis Ag Organic compounds
US6207179B1 (en) * 2000-05-18 2001-03-27 Phoenix Scientific, Inc. Parasiticidal formulation for animals and a method of making this formulation
CA2471666C (en) 2004-06-18 2009-10-13 Apotex Pharmachem Inc. An improved process for the preparation of oxcarbazepine and related intermediates
EP3753561A1 (en) * 2005-04-05 2020-12-23 Yale University Glutamate modulating agents in the treatment of mental disorders
US20060252745A1 (en) 2005-05-06 2006-11-09 Almeida Jose L D Methods of preparing pharmaceutical compositions comprising eslicarbazepine acetate and methods of use
FR2910811B1 (fr) * 2007-01-03 2009-07-10 Ass Pour Le Dev De La Biothera Utilisation du riluzole et de ses derives pour fabriquer de nouveaux medicaments
GB0700773D0 (en) 2007-01-15 2007-02-21 Portela & Ca Sa Drug therapies
FR2957077B1 (fr) * 2010-03-02 2012-04-13 Univ Dauvergne Clermont I Utilisation du riluzole pour traiter ou prevenir les effets indesirables d'agents anti-cancereux
CN107249567B (zh) * 2014-11-21 2021-08-03 拜尔哈文制药股份有限公司 利鲁唑的舌下给药
EP4298191A4 (en) * 2021-02-24 2024-07-03 Vgp Ipco Llc FOAMING EVAPORATOR COIL CLEANER

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FR2492258A1 (fr) * 1980-10-17 1982-04-23 Pharmindustrie Nouveau medicament a base d'amino-2 trifluoromethoxy-6 benzothiazole
US4431641A (en) * 1980-10-17 1984-02-14 Ciba-Geigy Corporation Pharmaceutical compositions having antiepileptic and antineuralgic action
GB8613183D0 (en) * 1986-05-30 1986-07-02 Wellcome Found Triazine salt
US4826860A (en) * 1987-03-16 1989-05-02 Warner-Lambert Company Substituted 2-aminobenzothiazoles and derivatives useful as cerebrovascular agents
US4918090A (en) * 1988-01-25 1990-04-17 Warner-Lambert Company Substituted 2-aminbenzothiazoles and derivatives useful as cerebrovascular agents
EP0435826A1 (de) * 1989-12-27 1991-07-03 Ciba-Geigy Ag Intravenöse Lösungen für Status Epilepticus
US5326570A (en) * 1991-07-23 1994-07-05 Pharmavene, Inc. Advanced drug delivery system and method of treating psychiatric, neurological and other disorders with carbamazepine
FR2688138B1 (fr) * 1992-03-06 1995-05-05 Rhone Poulenc Rorer Sa Application de l'amino-2 trifluoromethoxy-6 benzothiazole pour obtenir un medicament destine au traitement de la sclerose laterale amyotrophique.
JPH07308499A (ja) * 1994-05-20 1995-11-28 Brother Ind Ltd 衣類乾燥機

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See references of WO9420110A1 *

Also Published As

Publication number Publication date
SK107695A3 (en) 1996-06-05
HUT73433A (en) 1996-07-29
CA2154573A1 (fr) 1994-09-15
HUT73434A (en) 1996-07-29
AU675118B2 (en) 1997-01-23
NO307687B1 (no) 2000-05-15
HU9502583D0 (en) 1995-11-28
ZA941530B (en) 1994-10-06
US5624945A (en) 1997-04-29
NO953372L (no) 1995-08-28
DE69401577T2 (de) 1997-05-15
ZA941525B (en) 1994-11-09
GR3022356T3 (en) 1997-04-30
JPH08507507A (ja) 1996-08-13
FR2702148B1 (fr) 1995-04-07
WO1994020103A1 (fr) 1994-09-15
ES2157252T3 (es) 2001-08-16
NO953372D0 (no) 1995-08-28
EP0687177A1 (fr) 1995-12-20
HU9502584D0 (en) 1995-11-28
DE69427344D1 (de) 2001-07-05
DK0687176T3 (da) 2001-07-30
CZ226095A3 (en) 1995-12-13
CA2154572C (fr) 2006-06-06
WO1994020110A1 (fr) 1994-09-15
KR960700723A (ko) 1996-02-24
WO1994020108A1 (fr) 1994-09-15
FR2702148A1 (fr) 1994-09-09
NO953371D0 (no) 1995-08-28
CZ284423B6 (cs) 1998-11-11
AU6143794A (en) 1994-09-26
HU217132B (hu) 1999-11-29
SK279659B6 (sk) 1999-02-11
NO953370D0 (no) 1995-08-28
SK107595A3 (en) 1996-06-05
ATE201597T1 (de) 2001-06-15
EP0687176A1 (fr) 1995-12-20
AU675119B2 (en) 1997-01-23
PL310475A1 (en) 1995-12-11
PT687176E (pt) 2001-09-28
RU2157205C2 (ru) 2000-10-10
CA2154571A1 (fr) 1994-09-15
US5629312A (en) 1997-05-13
UA41355C2 (uk) 2001-09-17
EP0687176B1 (fr) 2001-05-30
GR3035957T3 (en) 2001-08-31
IL108844A0 (en) 1994-06-24
SK107495A3 (en) 1996-06-05
JPH08507509A (ja) 1996-08-13
KR100318168B1 (ko) 2002-06-20
CZ226195A3 (en) 1995-12-13
CA2154572A1 (fr) 1994-09-15
ES2096455T3 (es) 1997-03-01
KR960700721A (ko) 1996-02-24
HU9502585D0 (en) 1995-11-28
JP3578174B2 (ja) 2004-10-20
AU6143994A (en) 1994-09-26
ATE147981T1 (de) 1997-02-15
AU6143894A (en) 1994-09-26
IL108844A (en) 1998-01-04
DE69427344T2 (de) 2002-04-25
CZ225995A3 (en) 1995-12-13
DK0687177T3 (da) 1997-02-10
IL108846A0 (en) 1994-06-24
NO953370L (no) 1995-08-28
EP0687177B1 (fr) 1997-01-22
IL108845A0 (en) 1994-06-24
JPH08507508A (ja) 1996-08-13
CZ285339B6 (cs) 1999-07-14
DE69401577D1 (de) 1997-03-06
KR960700716A (ko) 1996-02-24
NO953371L (no) 1995-08-28
PL310476A1 (en) 1995-12-11
PL310474A1 (en) 1995-12-11

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Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

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