NO316667B1 - Anvendelsen av 40-O-(2-hydroksy)etyl-rapamycin ved fremstilling av medikamenter - Google Patents
Anvendelsen av 40-O-(2-hydroksy)etyl-rapamycin ved fremstilling av medikamenter Download PDFInfo
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- NO316667B1 NO316667B1 NO19984340A NO984340A NO316667B1 NO 316667 B1 NO316667 B1 NO 316667B1 NO 19984340 A NO19984340 A NO 19984340A NO 984340 A NO984340 A NO 984340A NO 316667 B1 NO316667 B1 NO 316667B1
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- Prior art keywords
- rejection
- graft
- rapamycin
- compound
- animals
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- 125000002345 steroid group Chemical group 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 231100000041 toxicology testing Toxicity 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 231100000216 vascular lesion Toxicity 0.000 description 1
- 238000007631 vascular surgery Methods 0.000 description 1
- 210000005166 vasculature Anatomy 0.000 description 1
- 210000001631 vena cava inferior Anatomy 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/436—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
- 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)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Transplantation (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Saccharide Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9606452.2A GB9606452D0 (en) | 1996-03-27 | 1996-03-27 | Organic compounds |
| PCT/EP1997/001548 WO1997035575A1 (fr) | 1996-03-27 | 1997-03-26 | Utilisation de la rapamicine dans les vasculopathies et les xenotransplantations |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO984340L NO984340L (no) | 1998-09-18 |
| NO984340D0 NO984340D0 (no) | 1998-09-18 |
| NO316667B1 true NO316667B1 (no) | 2004-03-29 |
Family
ID=10791127
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19984340A NO316667B1 (no) | 1996-03-27 | 1998-09-18 | Anvendelsen av 40-O-(2-hydroksy)etyl-rapamycin ved fremstilling av medikamenter |
Country Status (30)
| Country | Link |
|---|---|
| US (5) | US6384046B1 (fr) |
| EP (3) | EP1149581A3 (fr) |
| JP (2) | JP2000507226A (fr) |
| KR (2) | KR100836971B1 (fr) |
| CN (1) | CN1124135C (fr) |
| AT (1) | ATE224194T1 (fr) |
| AU (1) | AU716514B2 (fr) |
| BR (1) | BR9708358A (fr) |
| CA (1) | CA2247275C (fr) |
| CY (1) | CY2404B1 (fr) |
| CZ (1) | CZ292483B6 (fr) |
| DE (1) | DE69715611T2 (fr) |
| DK (2) | DK0893996T3 (fr) |
| ES (2) | ES2184078T3 (fr) |
| GB (1) | GB9606452D0 (fr) |
| HK (1) | HK1018688A1 (fr) |
| HU (1) | HU226422B1 (fr) |
| ID (1) | ID17195A (fr) |
| IL (1) | IL125812A (fr) |
| MY (1) | MY117798A (fr) |
| NO (1) | NO316667B1 (fr) |
| NZ (1) | NZ331463A (fr) |
| PL (1) | PL187732B1 (fr) |
| PT (2) | PT893996E (fr) |
| RU (1) | RU2214247C2 (fr) |
| SI (1) | SI2008657T1 (fr) |
| SK (1) | SK284343B6 (fr) |
| TR (1) | TR199801919T2 (fr) |
| WO (1) | WO1997035575A1 (fr) |
| ZA (1) | ZA972719B (fr) |
Families Citing this family (69)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9606452D0 (en) * | 1996-03-27 | 1996-06-05 | Sandoz Ltd | Organic compounds |
| NZ333657A (en) | 1996-07-30 | 2000-05-26 | Novartis Ag | A pharmaceutical composition comprising cyclosporin A and 40-O-(2-hydroxyethyl)-rapamycin |
| US6890546B2 (en) | 1998-09-24 | 2005-05-10 | Abbott Laboratories | Medical devices containing rapamycin analogs |
| ATE474590T1 (de) * | 1999-05-10 | 2010-08-15 | Paolo Brenner | Kombination von immunsuppressiven substanzen zur behandlung oder vorbeugung von transplantat abstossungen |
| US20070032853A1 (en) | 2002-03-27 | 2007-02-08 | Hossainy Syed F | 40-O-(2-hydroxy)ethyl-rapamycin coated stent |
| US6790228B2 (en) | 1999-12-23 | 2004-09-14 | Advanced Cardiovascular Systems, Inc. | Coating for implantable devices and a method of forming the same |
| US7807211B2 (en) | 1999-09-03 | 2010-10-05 | Advanced Cardiovascular Systems, Inc. | Thermal treatment of an implantable medical device |
| ATE362382T1 (de) | 2000-03-15 | 2007-06-15 | Orbusneich Medical Inc | Beschichtung welche ein anhaften von endothelzellen stimuliert |
| US8460367B2 (en) * | 2000-03-15 | 2013-06-11 | Orbusneich Medical, Inc. | Progenitor endothelial cell capturing with a drug eluting implantable medical device |
| US8088060B2 (en) | 2000-03-15 | 2012-01-03 | Orbusneich Medical, Inc. | Progenitor endothelial cell capturing with a drug eluting implantable medical device |
| US20030229393A1 (en) * | 2001-03-15 | 2003-12-11 | Kutryk Michael J. B. | Medical device with coating that promotes cell adherence and differentiation |
| US9522217B2 (en) | 2000-03-15 | 2016-12-20 | Orbusneich Medical, Inc. | Medical device with coating for capturing genetically-altered cells and methods for using same |
| US20070141107A1 (en) * | 2000-03-15 | 2007-06-21 | Orbusneich Medical, Inc. | Progenitor Endothelial Cell Capturing with a Drug Eluting Implantable Medical Device |
| US20070055367A1 (en) * | 2000-03-15 | 2007-03-08 | Orbus Medical Technologies, Inc. | Medical device with coating that promotes endothelial cell adherence and differentiation |
| US20050002986A1 (en) * | 2000-05-12 | 2005-01-06 | Robert Falotico | Drug/drug delivery systems for the prevention and treatment of vascular disease |
| US8236048B2 (en) | 2000-05-12 | 2012-08-07 | Cordis Corporation | Drug/drug delivery systems for the prevention and treatment of vascular disease |
| US6670355B2 (en) * | 2000-06-16 | 2003-12-30 | Wyeth | Method of treating cardiovascular disease |
| EP1709974A3 (fr) * | 2000-06-16 | 2006-12-06 | Wyeth | Methode pour le traitement de maladies cardio-vasculaires en utilisant de la rapamycine |
| US20020013335A1 (en) * | 2000-06-16 | 2002-01-31 | American Home Products Corporation | Method of treating cardiovascular disease |
| JP5100951B2 (ja) | 2000-09-29 | 2012-12-19 | コーディス・コーポレイション | 被覆医用器具 |
| EP2762140B1 (fr) | 2001-02-19 | 2017-03-22 | Novartis AG | Traitement de tumeurs solides du cerveau avec un dérivé de la rapamycine |
| US8741378B1 (en) | 2001-06-27 | 2014-06-03 | Advanced Cardiovascular Systems, Inc. | Methods of coating an implantable device |
| US7682387B2 (en) | 2002-04-24 | 2010-03-23 | Biosensors International Group, Ltd. | Drug-delivery endovascular stent and method for treating restenosis |
| US6939376B2 (en) | 2001-11-05 | 2005-09-06 | Sun Biomedical, Ltd. | Drug-delivery endovascular stent and method for treating restenosis |
| US20040024450A1 (en) * | 2002-04-24 | 2004-02-05 | Sun Biomedical, Ltd. | Drug-delivery endovascular stent and method for treating restenosis |
| JP2005525911A (ja) * | 2002-05-20 | 2005-09-02 | オーバス メディカル テクノロジーズ インク． | 移植可能な薬物溶出医療用デバイス |
| US8109987B2 (en) | 2003-04-14 | 2012-02-07 | Tryton Medical, Inc. | Method of treating a lumenal bifurcation |
| US7279174B2 (en) * | 2003-05-08 | 2007-10-09 | Advanced Cardiovascular Systems, Inc. | Stent coatings comprising hydrophilic additives |
| US20050118344A1 (en) | 2003-12-01 | 2005-06-02 | Pacetti Stephen D. | Temperature controlled crimping |
| US7220755B2 (en) | 2003-11-12 | 2007-05-22 | Biosensors International Group, Ltd. | 42-O-alkoxyalkyl rapamycin derivatives and compositions comprising same |
| US9114198B2 (en) | 2003-11-19 | 2015-08-25 | Advanced Cardiovascular Systems, Inc. | Biologically beneficial coatings for implantable devices containing fluorinated polymers and methods for fabricating the same |
| WO2005107817A2 (fr) * | 2004-04-30 | 2005-11-17 | Orbus Medical Technologies, Inc. | Dispositif medical comprenant un revetement permettant de capturer des cellules genetiquement modifiees et ses procedes d'utilisation |
| CA2571710A1 (fr) | 2004-06-24 | 2006-11-02 | Nicholas Valiante | Immuno-potentialisateurs a petites molecules et analyses visant a detecter leur presence |
| US8709469B2 (en) | 2004-06-30 | 2014-04-29 | Abbott Cardiovascular Systems Inc. | Anti-proliferative and anti-inflammatory agent combination for treatment of vascular disorders with an implantable medical device |
| US7901451B2 (en) * | 2004-09-24 | 2011-03-08 | Biosensors International Group, Ltd. | Drug-delivery endovascular stent and method for treating restenosis |
| EP1838288A4 (fr) * | 2004-12-20 | 2010-08-04 | Ariad Pharma Inc | Materiels et procedes therapeutiques |
| JP5709354B2 (ja) | 2005-11-14 | 2015-04-30 | アリアド・ファーマシューティカルズ・インコーポレイテッド | ｍＴＯＲ阻害剤投与によるがん患者の治療 |
| US20080317814A1 (en) * | 2005-11-17 | 2008-12-25 | Access Plus Co., Ltd. | Tube for Connecting Marteriovenous and Interposition for Medical Operation |
| US20070173923A1 (en) * | 2006-01-20 | 2007-07-26 | Savage Douglas R | Drug reservoir stent |
| WO2008033956A2 (fr) | 2006-09-13 | 2008-03-20 | Elixir Medical Corporation | Composés de lactone macrocyclique et leurs procédés d'utilisation |
| US8067055B2 (en) * | 2006-10-20 | 2011-11-29 | Biosensors International Group, Ltd. | Drug-delivery endovascular stent and method of use |
| US20080097591A1 (en) | 2006-10-20 | 2008-04-24 | Biosensors International Group | Drug-delivery endovascular stent and method of use |
| US20080103584A1 (en) | 2006-10-25 | 2008-05-01 | Biosensors International Group | Temporal Intraluminal Stent, Methods of Making and Using |
| KR100930167B1 (ko) * | 2007-09-19 | 2009-12-07 | 삼성전기주식회사 | 초광각 광학계 |
| US8661630B2 (en) | 2008-05-21 | 2014-03-04 | Abbott Cardiovascular Systems Inc. | Coating comprising an amorphous primer layer and a semi-crystalline reservoir layer |
| EP2219700B1 (fr) | 2007-11-14 | 2024-03-20 | Biosensors International Group, Ltd. | Appareil et procédé de revêtement automatisé |
| WO2009089549A1 (fr) * | 2008-01-11 | 2009-07-16 | Massachusetts Eye & Ear Infirmary | Animaux transgéniques de caspase dimérisable d'arrêt conditionnel |
| JP2012504654A (ja) * | 2008-10-03 | 2012-02-23 | エリクシアー メディカル コーポレイション | 多環状ラクトン化合物およびその使用方法 |
| US8366763B2 (en) | 2009-07-02 | 2013-02-05 | Tryton Medical, Inc. | Ostium support for treating vascular bifurcations |
| US8685433B2 (en) | 2010-03-31 | 2014-04-01 | Abbott Cardiovascular Systems Inc. | Absorbable coating for implantable device |
| UA104738C2 (ru) | 2011-05-18 | 2014-03-11 | Олег Миколайович Лазаренко | Композиция для повышения биосовместимости имплантатов и клеток для трансплантации с организмом реципиента и способ ее приготовления |
| CN102268015B (zh) * | 2011-08-30 | 2013-08-28 | 成都摩尔生物医药有限公司 | 一种依维莫司的合成方法 |
| US10682415B2 (en) | 2013-07-22 | 2020-06-16 | Wisconsin Alumni Research Foundation | Thermogel formulation for combination drug delivery |
| KR101723265B1 (ko) | 2013-08-16 | 2017-04-04 | 가톨릭대학교 산학협력단 | mTOR/STAT3 신호억제제 처리된 면역조절능을 갖는 간엽줄기세포 및 이를 포함하는 면역질환의 예방 또는 치료용 세포치료제 조성물 |
| CN110101485B (zh) | 2013-09-24 | 2021-07-06 | 吉纳生命科学公司 | 用于细胞植入物的气体处理的系统 |
| WO2015054280A1 (fr) | 2013-10-08 | 2015-04-16 | Lam Therapeutics, Inc. | Rapamycine pour le traitement de la lymphangioléiomyomatose |
| US10307371B2 (en) | 2014-02-11 | 2019-06-04 | AI Therapeutics, Inc. | Rapamycin for the treatment of lymphangioleiomyomatosis |
| KR20160120739A (ko) | 2014-02-11 | 2016-10-18 | 램 테라퓨틱스, 인코포레이티드 | 림프관평활근종증의 치료를 위한 라파마이신 |
| HRP20230863T1 (hr) | 2014-04-04 | 2023-11-10 | AI Therapeutics, Inc. | Inhalacijska formulacija rapamicina, namijenjena liječenju stanja povezanih sa starenjem |
| MX2017004440A (es) | 2014-10-07 | 2017-11-01 | Lam Therapeutics Inc | Una formulacion de rapamicina inhalable para el tratamiento de hipertension pulmonar. |
| MA40910A (fr) | 2014-11-07 | 2017-09-12 | Civitas Therapeutics Inc | Poudres de rapamycine pour administration pulmonaire |
| WO2016130645A1 (fr) | 2015-02-10 | 2016-08-18 | Lam Therapeutics, Inc. | Rapamycine destinée au traitement de la lymphangioléiomyomatose |
| MX2019001670A (es) | 2016-08-10 | 2019-07-04 | Univ Texas | Terapia con rapamicina topica. |
| AU2017328714B2 (en) | 2016-09-19 | 2022-05-12 | Biotronik Ag | Polymer-free drug eluting vascular stents |
| RU2019114817A (ru) | 2016-11-15 | 2020-11-16 | Джинер Лайф Сайенс, Инк. | Устройство чрезкожной диффузии газов, подходящее для применения с подкожным имплантатом |
| US11826492B2 (en) | 2016-12-22 | 2023-11-28 | Biotronik Ag | Intratumoral drug delivery materials and methods for treating breast cancer |
| CA3062412A1 (fr) | 2017-05-04 | 2018-11-08 | Giner Life Sciences, Inc. | Dispositif implantable de distribution robuste, de gaz et procedes, systemes et dispositifs l'utilisant |
| AR112834A1 (es) | 2017-09-26 | 2019-12-18 | Novartis Ag | Derivados de rapamicina |
| US20200261427A1 (en) | 2019-02-20 | 2020-08-20 | Al Therapeutics, Inc. | Topical rapamycin formulations and their use in treating facial angiofibromas and other skin disorders |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5639724A (en) * | 1984-07-24 | 1997-06-17 | Sandoz Ltd. | Cyclosporin galenic forms |
| US5364612A (en) * | 1991-05-06 | 1994-11-15 | Immunomedics, Inc. | Detection of cardiovascular lesions |
| CA2086642C (fr) * | 1992-01-09 | 2004-06-15 | Randall E. Morris | Methode de traitement des maladies vasculaires hyperproliferatives |
| US5516781A (en) * | 1992-01-09 | 1996-05-14 | American Home Products Corporation | Method of treating restenosis with rapamycin |
| CA2094858C (fr) * | 1992-04-28 | 2004-06-15 | Robert D. Mitchell | Methode de traitement des maladies vasculaires hyperproliferatives |
| US5747034A (en) * | 1992-07-09 | 1998-05-05 | Chiron Corporation | Methods and materials for the induction of T cell anergy |
| US5283257A (en) * | 1992-07-10 | 1994-02-01 | The Board Of Trustees Of The Leland Stanford Junior University | Method of treating hyperproliferative vascular disease |
| GB9221220D0 (en) * | 1992-10-09 | 1992-11-25 | Sandoz Ag | Organic componds |
| WO1995016691A1 (fr) * | 1993-12-17 | 1995-06-22 | Sandoz Ltd. | Derives de rapamycine utilises comme immonosuppresseurs |
| US5362718A (en) * | 1994-04-18 | 1994-11-08 | American Home Products Corporation | Rapamycin hydroxyesters |
| US6265427B1 (en) * | 1995-06-07 | 2001-07-24 | The Proctor & Gamble Company | Pharmaceutical composition for the method of treating leukemia |
| CA2219659C (fr) * | 1995-06-09 | 2008-03-18 | Novartis Ag | Derives de rapamycine |
| GB9606452D0 (en) * | 1996-03-27 | 1996-06-05 | Sandoz Ltd | Organic compounds |
-
1996
- 1996-03-27 GB GBGB9606452.2A patent/GB9606452D0/en active Pending
-
1997
- 1997-03-25 ID IDP970980A patent/ID17195A/id unknown
- 1997-03-25 MY MYPI97001258A patent/MY117798A/en unknown
- 1997-03-26 JP JP9532077A patent/JP2000507226A/ja not_active Withdrawn
- 1997-03-26 AT AT97915441T patent/ATE224194T1/de not_active IP Right Cessation
- 1997-03-26 KR KR1020057005463A patent/KR100836971B1/ko not_active IP Right Cessation
- 1997-03-26 KR KR1020077008212A patent/KR20070083654A/ko not_active Application Discontinuation
- 1997-03-26 DK DK97915441T patent/DK0893996T3/da active
- 1997-03-26 ES ES97915441T patent/ES2184078T3/es not_active Expired - Lifetime
- 1997-03-26 CN CN97193278A patent/CN1124135C/zh not_active Expired - Lifetime
- 1997-03-26 PT PT97915441T patent/PT893996E/pt unknown
- 1997-03-26 CZ CZ19983070A patent/CZ292483B6/cs not_active IP Right Cessation
- 1997-03-26 CA CA2247275A patent/CA2247275C/fr not_active Expired - Lifetime
- 1997-03-26 DK DK08017336.2T patent/DK2008657T3/da active
- 1997-03-26 EP EP01116262A patent/EP1149581A3/fr not_active Withdrawn
- 1997-03-26 DE DE69715611T patent/DE69715611T2/de not_active Revoked
- 1997-03-26 NZ NZ331463A patent/NZ331463A/en not_active IP Right Cessation
- 1997-03-26 ES ES08017336T patent/ES2421455T3/es not_active Expired - Lifetime
- 1997-03-26 PT PT80173362T patent/PT2008657E/pt unknown
- 1997-03-26 PL PL97328659A patent/PL187732B1/pl unknown
- 1997-03-26 HU HU0001267A patent/HU226422B1/hu unknown
- 1997-03-26 SI SI9730801T patent/SI2008657T1/sl unknown
- 1997-03-26 EP EP08017336.2A patent/EP2008657B1/fr not_active Expired - Lifetime
- 1997-03-26 SK SK1327-98A patent/SK284343B6/sk not_active IP Right Cessation
- 1997-03-26 AU AU22918/97A patent/AU716514B2/en not_active Expired
- 1997-03-26 TR TR1998/01919T patent/TR199801919T2/xx unknown
- 1997-03-26 BR BR9708358A patent/BR9708358A/pt not_active Application Discontinuation
- 1997-03-26 IL IL12581297A patent/IL125812A/en not_active IP Right Cessation
- 1997-03-26 RU RU98119312/14A patent/RU2214247C2/ru active
- 1997-03-26 WO PCT/EP1997/001548 patent/WO1997035575A1/fr not_active Application Discontinuation
- 1997-03-26 EP EP97915441A patent/EP0893996B1/fr not_active Revoked
- 1997-03-27 ZA ZA972719A patent/ZA972719B/xx unknown
-
1998
- 1998-09-18 NO NO19984340A patent/NO316667B1/no not_active IP Right Cessation
-
1999
- 1999-08-31 HK HK99103744A patent/HK1018688A1/xx not_active IP Right Cessation
-
2000
- 2000-11-14 US US09/712,359 patent/US6384046B1/en not_active Expired - Lifetime
-
2002
- 2002-03-07 US US10/092,639 patent/US20020127248A1/en not_active Abandoned
-
2004
- 2004-01-08 CY CY0400004A patent/CY2404B1/xx unknown
-
2008
- 2008-12-10 JP JP2008314494A patent/JP5124431B2/ja not_active Expired - Lifetime
-
2010
- 2010-03-01 US US12/715,007 patent/US20100152105A1/en not_active Abandoned
-
2012
- 2012-01-24 US US13/357,199 patent/US20120177690A1/en not_active Abandoned
-
2014
- 2014-03-05 US US14/197,368 patent/US20140187574A1/en not_active Abandoned
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| MK1K | Patent expired |