NO317003B1 - Anvendelse av hepariner med lav molekylvekt for fremstilling av et medikament for terapi av cerebrale odemer - Google Patents
Anvendelse av hepariner med lav molekylvekt for fremstilling av et medikament for terapi av cerebrale odemer Download PDFInfo
- Publication number
- NO317003B1 NO317003B1 NO19995539A NO995539A NO317003B1 NO 317003 B1 NO317003 B1 NO 317003B1 NO 19995539 A NO19995539 A NO 19995539A NO 995539 A NO995539 A NO 995539A NO 317003 B1 NO317003 B1 NO 317003B1
- Authority
- NO
- Norway
- Prior art keywords
- molecular weight
- low molecular
- heparin
- lesion
- weight heparins
- Prior art date
Links
- 229940127215 low-molecular weight heparin Drugs 0.000 title claims abstract description 35
- 206010048962 Brain oedema Diseases 0.000 title claims abstract description 10
- 208000006752 brain edema Diseases 0.000 title claims abstract description 8
- 239000003814 drug Substances 0.000 title claims description 5
- 238000002560 therapeutic procedure Methods 0.000 title claims description 4
- 229940079593 drug Drugs 0.000 title description 4
- 238000004519 manufacturing process Methods 0.000 title description 2
- 239000003055 low molecular weight heparin Substances 0.000 claims abstract description 16
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 claims description 28
- 229920000669 heparin Polymers 0.000 claims description 19
- 229960002897 heparin Drugs 0.000 claims description 11
- 229960000610 enoxaparin Drugs 0.000 claims description 6
- -1 heparin ester Chemical class 0.000 claims description 5
- 229960000899 nadroparin Drugs 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 229940090880 ardeparin Drugs 0.000 claims description 2
- 229940107792 certoparin Drugs 0.000 claims description 2
- 229960003828 danaparoid Drugs 0.000 claims description 2
- XEKSTYNIJLDDAZ-JASSWCPGSA-D decasodium;(2s,3s,4r,5r,6r)-6-[(2r,3r,4r,5r,6r)-6-[(2r,3s,4s,5r,6r)-2-carboxylato-4-hydroxy-6-[(2r,3s,4r,5r,6s)-4-hydroxy-6-methoxy-5-(sulfonatoamino)-2-(sulfonatooxymethyl)oxan-3-yl]oxy-5-sulfonatooxyoxan-3-yl]oxy-5-(sulfonatoamino)-4-sulfonatooxy-2-(sul Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].O[C@@H]1[C@@H](NS([O-])(=O)=O)[C@@H](OC)O[C@H](COS([O-])(=O)=O)[C@H]1O[C@H]1[C@H](OS([O-])(=O)=O)[C@@H](O)[C@H](O[C@@H]2[C@@H]([C@@H](OS([O-])(=O)=O)[C@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O[C@@H]4[C@@H]([C@@H](O)[C@H](O)[C@@H](COS([O-])(=O)=O)O4)NS([O-])(=O)=O)[C@H](O3)C([O-])=O)O)[C@@H](COS([O-])(=O)=O)O2)NS([O-])(=O)=O)[C@H](C([O-])=O)O1 XEKSTYNIJLDDAZ-JASSWCPGSA-D 0.000 claims description 2
- 229920001542 oligosaccharide Polymers 0.000 claims description 2
- 150000002482 oligosaccharides Chemical class 0.000 claims description 2
- 229960005496 reviparin Drugs 0.000 claims description 2
- 229960005062 tinzaparin Drugs 0.000 claims description 2
- 229960004762 parnaparin Drugs 0.000 claims 1
- 230000003902 lesion Effects 0.000 description 25
- 206010030113 Oedema Diseases 0.000 description 14
- 241001465754 Metazoa Species 0.000 description 9
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 230000002490 cerebral effect Effects 0.000 description 6
- 241000700159 Rattus Species 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 210000003625 skull Anatomy 0.000 description 4
- 210000001519 tissue Anatomy 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000037396 body weight Effects 0.000 description 3
- 210000004556 brain Anatomy 0.000 description 3
- 238000005194 fractionation Methods 0.000 description 3
- 210000001320 hippocampus Anatomy 0.000 description 3
- 210000002966 serum Anatomy 0.000 description 3
- 238000013222 sprague-dawley male rat Methods 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 208000032843 Hemorrhage Diseases 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000007799 cork Substances 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 210000001951 dura mater Anatomy 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 230000023597 hemostasis Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 238000000034 method Methods 0.000 description 2
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- 229940081623 rose bengal Drugs 0.000 description 2
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000008223 sterile water Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 230000009424 thromboembolic effect Effects 0.000 description 2
- 230000008733 trauma Effects 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 208000035143 Bacterial infection Diseases 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 206010008111 Cerebral haemorrhage Diseases 0.000 description 1
- 206010010071 Coma Diseases 0.000 description 1
- 208000010496 Heart Arrest Diseases 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 208000030852 Parasitic disease Diseases 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 206010038669 Respiratory arrest Diseases 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 241000282887 Suidae Species 0.000 description 1
- 208000007536 Thrombosis Diseases 0.000 description 1
- 208000036142 Viral infection Diseases 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 238000001042 affinity chromatography Methods 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000001858 anti-Xa Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
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- 210000003169 central nervous system Anatomy 0.000 description 1
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- 229940110456 cocoa butter Drugs 0.000 description 1
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- 239000003479 dental cement Substances 0.000 description 1
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- 230000002874 effect on oedema Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
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- 150000002148 esters Chemical class 0.000 description 1
- 239000003889 eye drop Substances 0.000 description 1
- 229940012356 eye drops Drugs 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 239000007903 gelatin capsule Substances 0.000 description 1
- 238000002523 gelfiltration Methods 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- BCQZXOMGPXTTIC-UHFFFAOYSA-N halothane Chemical compound FC(F)(F)C(Cl)Br BCQZXOMGPXTTIC-UHFFFAOYSA-N 0.000 description 1
- 229960003132 halothane Drugs 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 210000004347 intestinal mucosa Anatomy 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000008141 laxative Substances 0.000 description 1
- 229940125722 laxative agent Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 229940118179 lovenox Drugs 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 230000003211 malignant effect Effects 0.000 description 1
- 210000004379 membrane Anatomy 0.000 description 1
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- 239000002324 mouth wash Substances 0.000 description 1
- 239000007923 nasal drop Substances 0.000 description 1
- 229940100662 nasal drops Drugs 0.000 description 1
- 208000018389 neoplasm of cerebral hemisphere Diseases 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 230000001936 parietal effect Effects 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 238000009527 percussion Methods 0.000 description 1
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000002685 pulmonary effect Effects 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000003206 sterilizing agent Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- HFFLGKNGCAIQMO-UHFFFAOYSA-N trichloroacetaldehyde Chemical compound ClC(Cl)(Cl)C=O HFFLGKNGCAIQMO-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 208000003663 ventricular fibrillation Diseases 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
-
- 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
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/726—Glycosaminoglycans, i.e. mucopolysaccharides
- A61K31/727—Heparin; Heparan
-
- 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
- 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
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- 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
- A61P7/10—Antioedematous agents; Diuretics
-
- 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
-
- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Dermatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9706551A FR2763849B1 (fr) | 1997-05-28 | 1997-05-28 | Utilisation des heparines de bas poids moleculaire pour la prevention et le traitement des oedemes cerebraux |
PCT/FR1998/001035 WO1998053834A1 (fr) | 1997-05-28 | 1998-05-25 | Utilisation des heparines de bas poids moleculaire pour la prevention et le traitement des oedemes cerebraux |
Publications (3)
Publication Number | Publication Date |
---|---|
NO995539D0 NO995539D0 (no) | 1999-11-12 |
NO995539L NO995539L (no) | 1999-11-12 |
NO317003B1 true NO317003B1 (no) | 2004-07-19 |
Family
ID=9507336
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO19995539A NO317003B1 (no) | 1997-05-28 | 1999-11-12 | Anvendelse av hepariner med lav molekylvekt for fremstilling av et medikament for terapi av cerebrale odemer |
Country Status (24)
Country | Link |
---|---|
US (1) | US6579858B1 (es) |
EP (1) | EP0984787B1 (es) |
JP (1) | JP2002502387A (es) |
KR (1) | KR100562425B1 (es) |
CN (1) | CN1223351C (es) |
AT (1) | ATE225181T1 (es) |
AU (1) | AU742995B2 (es) |
BR (1) | BR9809180A (es) |
CA (1) | CA2290682A1 (es) |
DE (1) | DE69808455T2 (es) |
DK (1) | DK0984787T3 (es) |
ES (1) | ES2182321T3 (es) |
FR (1) | FR2763849B1 (es) |
IL (2) | IL132670A0 (es) |
MA (1) | MA24554A1 (es) |
NO (1) | NO317003B1 (es) |
NZ (1) | NZ501366A (es) |
PE (1) | PE73099A1 (es) |
PT (1) | PT984787E (es) |
RU (1) | RU2195287C2 (es) |
TN (1) | TNSN98072A1 (es) |
TW (1) | TW546141B (es) |
WO (1) | WO1998053834A1 (es) |
ZA (1) | ZA984433B (es) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2787329B1 (fr) * | 1998-12-17 | 2001-02-09 | Aventis Pharma Sa | Nouvelle application therapeutique des heparines de bas poids moleculaire |
CA2458852A1 (en) * | 2001-08-28 | 2003-03-06 | Leo Pharma A/S | Antithrombotic compositions comprising low molecular weight heparin and low molecular weight dermatan sulphate |
ITMI20031023A1 (it) * | 2003-05-21 | 2004-11-22 | Umberto Cornelli | Glicosaminoglicani aventi peso molecolare medio 2400 d atti al trattamento delle disfunzioni emozionali. |
US11840565B2 (en) | 2016-12-29 | 2023-12-12 | University Of Miami | Methods and compositions for treating virus-associated inflammation |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2013092C1 (ru) * | 1989-02-27 | 1994-05-30 | Дагестанский государственный медицинский институт | Способ лечения отека мозга при туберкулезном менингоэнцефалите |
-
1997
- 1997-05-28 FR FR9706551A patent/FR2763849B1/fr not_active Expired - Fee Related
-
1998
- 1998-05-19 PE PE1998000385A patent/PE73099A1/es not_active Application Discontinuation
- 1998-05-25 AU AU77760/98A patent/AU742995B2/en not_active Ceased
- 1998-05-25 EP EP98925774A patent/EP0984787B1/fr not_active Expired - Lifetime
- 1998-05-25 IL IL13267098A patent/IL132670A0/xx unknown
- 1998-05-25 JP JP50031199A patent/JP2002502387A/ja not_active Ceased
- 1998-05-25 DE DE69808455T patent/DE69808455T2/de not_active Expired - Lifetime
- 1998-05-25 BR BR9809180-8A patent/BR9809180A/pt not_active Application Discontinuation
- 1998-05-25 NZ NZ501366A patent/NZ501366A/xx unknown
- 1998-05-25 MA MA25089A patent/MA24554A1/fr unknown
- 1998-05-25 ES ES98925774T patent/ES2182321T3/es not_active Expired - Lifetime
- 1998-05-25 AT AT98925774T patent/ATE225181T1/de not_active IP Right Cessation
- 1998-05-25 PT PT98925774T patent/PT984787E/pt unknown
- 1998-05-25 RU RU99128103/14A patent/RU2195287C2/ru not_active IP Right Cessation
- 1998-05-25 DK DK98925774T patent/DK0984787T3/da active
- 1998-05-25 ZA ZA984433A patent/ZA984433B/xx unknown
- 1998-05-25 KR KR1019997011052A patent/KR100562425B1/ko not_active IP Right Cessation
- 1998-05-25 TW TW087108064A patent/TW546141B/zh not_active IP Right Cessation
- 1998-05-25 CN CNB988054906A patent/CN1223351C/zh not_active Expired - Fee Related
- 1998-05-25 CA CA002290682A patent/CA2290682A1/fr not_active Abandoned
- 1998-05-25 WO PCT/FR1998/001035 patent/WO1998053834A1/fr active IP Right Grant
- 1998-05-27 TN TNTNSN98072A patent/TNSN98072A1/fr unknown
-
1999
- 1999-11-01 IL IL132670A patent/IL132670A/en not_active IP Right Cessation
- 1999-11-12 NO NO19995539A patent/NO317003B1/no not_active IP Right Cessation
- 1999-11-29 US US09/450,110 patent/US6579858B1/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US6579858B1 (en) | 2003-06-17 |
NZ501366A (en) | 2000-11-24 |
EP0984787A1 (fr) | 2000-03-15 |
DE69808455D1 (de) | 2002-11-07 |
DK0984787T3 (da) | 2003-02-03 |
FR2763849A1 (fr) | 1998-12-04 |
IL132670A0 (en) | 2001-03-19 |
CA2290682A1 (fr) | 1998-12-03 |
KR20010013073A (ko) | 2001-02-26 |
CN1223351C (zh) | 2005-10-19 |
ES2182321T3 (es) | 2003-03-01 |
CN1257429A (zh) | 2000-06-21 |
WO1998053834A1 (fr) | 1998-12-03 |
FR2763849B1 (fr) | 2000-09-15 |
IL132670A (en) | 2010-05-31 |
ATE225181T1 (de) | 2002-10-15 |
DE69808455T2 (de) | 2003-07-03 |
EP0984787B1 (fr) | 2002-10-02 |
JP2002502387A (ja) | 2002-01-22 |
NO995539D0 (no) | 1999-11-12 |
NO995539L (no) | 1999-11-12 |
KR100562425B1 (ko) | 2006-03-17 |
PT984787E (pt) | 2003-01-31 |
AU742995B2 (en) | 2002-01-17 |
RU2195287C2 (ru) | 2002-12-27 |
BR9809180A (pt) | 2000-08-01 |
TNSN98072A1 (fr) | 2005-03-15 |
ZA984433B (en) | 1998-12-28 |
TW546141B (en) | 2003-08-11 |
MA24554A1 (fr) | 1998-12-31 |
PE73099A1 (es) | 1999-10-21 |
AU7776098A (en) | 1998-12-30 |
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MM1K | Lapsed by not paying the annual fees |