PL212660B1 - Zasadniczo niewodna zelowa kompozycja farmaceutyczna do podawania na skóre oraz jej zastosowanie - Google Patents
Zasadniczo niewodna zelowa kompozycja farmaceutyczna do podawania na skóre oraz jej zastosowanieInfo
- Publication number
- PL212660B1 PL212660B1 PL360941A PL36094101A PL212660B1 PL 212660 B1 PL212660 B1 PL 212660B1 PL 360941 A PL360941 A PL 360941A PL 36094101 A PL36094101 A PL 36094101A PL 212660 B1 PL212660 B1 PL 212660B1
- Authority
- PL
- Poland
- Prior art keywords
- dihydroxy
- vitamin
- composition
- composition according
- hydroxy
- Prior art date
Links
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- 235000019166 vitamin D Nutrition 0.000 claims abstract description 36
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- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 description 1
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- OFHCOWSQAMBJIW-AVJTYSNKSA-N alfacalcidol Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)C[C@H](O)C1=C OFHCOWSQAMBJIW-AVJTYSNKSA-N 0.000 description 1
- 229960002535 alfacalcidol Drugs 0.000 description 1
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- 229960003957 dexamethasone Drugs 0.000 description 1
- BIABMEZBCHDPBV-UHFFFAOYSA-N dipalmitoyl phosphatidylglycerol Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(COP(O)(=O)OCC(O)CO)OC(=O)CCCCCCCCCCCCCCC BIABMEZBCHDPBV-UHFFFAOYSA-N 0.000 description 1
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- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
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- 238000002844 melting Methods 0.000 description 1
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Classifications
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/59—Compounds containing 9, 10- seco- cyclopenta[a]hydrophenanthrene ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/44—Oils, fats or waxes according to two or more groups of A61K47/02-A61K47/42; Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24347100P | 2000-10-27 | 2000-10-27 | |
| PCT/DK2001/000613 WO2002034235A1 (en) | 2000-10-27 | 2001-09-26 | Topical composition containing at least one vitamin d or one vitamin d analogue and at least one corticosteroid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL360941A1 PL360941A1 (en) | 2004-09-20 |
| PL212660B1 true PL212660B1 (pl) | 2012-11-30 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL360941A PL212660B1 (pl) | 2000-10-27 | 2001-09-26 | Zasadniczo niewodna zelowa kompozycja farmaceutyczna do podawania na skóre oraz jej zastosowanie |
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| EP (1) | EP1331927B1 (enExample) |
| JP (3) | JP4451061B2 (enExample) |
| KR (1) | KR100844285B1 (enExample) |
| CN (1) | CN100382803C (enExample) |
| AT (1) | ATE380542T1 (enExample) |
| AU (2) | AU9163701A (enExample) |
| BR (1) | BRPI0114927B8 (enExample) |
| CA (1) | CA2423930C (enExample) |
| CY (1) | CY1107294T1 (enExample) |
| CZ (1) | CZ305984B6 (enExample) |
| DE (1) | DE60131881T2 (enExample) |
| DK (1) | DK1331927T3 (enExample) |
| ES (1) | ES2298264T3 (enExample) |
| HU (1) | HU230005B1 (enExample) |
| IL (2) | IL154888A0 (enExample) |
| MX (1) | MXPA03003511A (enExample) |
| PL (1) | PL212660B1 (enExample) |
| PT (1) | PT1331927E (enExample) |
| RU (1) | RU2271810C2 (enExample) |
| WO (1) | WO2002034235A1 (enExample) |
Families Citing this family (53)
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| US8263580B2 (en) * | 1998-09-11 | 2012-09-11 | Stiefel Research Australia Pty Ltd | Vitamin formulation |
| US20090098065A1 (en) * | 2000-01-11 | 2009-04-16 | Avikam Harel | Composition and methods for the treatment of skin disorders |
| WO2006120682A2 (en) * | 2005-05-10 | 2006-11-16 | Dermipsor Ltd. | Compositions and methods for treating hyperproliferative epidermal diseases |
| DK1331927T3 (da) * | 2000-10-27 | 2008-05-05 | Leo Pharma As | Topisk komposition der indeholder mindst et D-vitamin eller en D-vitamin analog og mindst et kosttikosteroid |
| US20090143328A1 (en) * | 2001-08-13 | 2009-06-04 | Mcdonald George | Method of Treating Cancer by Administration of Topical Active Corticosteroids |
| MXPA05003805A (es) * | 2002-12-17 | 2005-06-08 | Galderma Sa | Composiciones farmaceuticas que comprenden una combinacion de calcitriol y propionato de clobetasol. |
| FR2854802B1 (fr) * | 2003-05-12 | 2005-06-24 | Galderma Res & Dev | Procede de preparation d'une formulation contenant un principe actif microdose |
| US8404667B2 (en) * | 2006-12-29 | 2013-03-26 | Wisconsin Alumni Research Foundation | Compounds, compositions, kits and methods of use to orally and topically treat acne and other skin conditions by 19-Nor vitamin D analog |
| FR2871700B1 (fr) * | 2004-06-17 | 2006-11-17 | Galderma Sa | Composition sous forme de spray comprenant une association d'actifs pharmaceutiques, une phase alcoolique, et une phase huileuse |
| FR2871696B1 (fr) * | 2004-06-17 | 2006-11-10 | Galderma Sa | Composition topique pour le traitement du psoriasis |
| FR2871697B1 (fr) * | 2004-06-17 | 2007-06-29 | Galderma Sa | Composition sous forme de spray comprenant une association d'actifs pharmaceutiques, une phase alcoolique, au moins un silicone volatile et une phase huileuse non volatile |
| FR2871693B1 (fr) * | 2004-06-17 | 2006-08-25 | Galderma Sa | Utilisation d'une composition pharmaceutique comprenant du calcitriol et du propionate de clobetasol pour le traitement du psoriasis |
| FR2871698B1 (fr) * | 2004-06-17 | 2008-07-04 | Galderma Sa | Composition sous forme de spray comprenant une association d'actifs pharmaceutiques et une phase huileuse |
| FR2871694B1 (fr) * | 2004-06-17 | 2008-07-04 | Galderma Sa | Composition pharmaceutique comprenant un onguent oleagineux et deux principes actifs solubilises |
| EP1781302A4 (en) * | 2004-07-28 | 2010-02-17 | Lipopeptide Ab | NEW USE |
| US7740875B2 (en) * | 2004-10-08 | 2010-06-22 | Mediquest Therapeutics, Inc. | Organo-gel formulations for therapeutic applications |
| US20060078580A1 (en) | 2004-10-08 | 2006-04-13 | Mediquest Therapeutics, Inc. | Organo-gel formulations for therapeutic applications |
| WO2006129161A2 (en) | 2005-06-01 | 2006-12-07 | Stiefel Research Australia Pty Ltd | Vitamin formulation |
| WO2006131401A2 (en) * | 2005-06-10 | 2006-12-14 | Galderma S.A. | Controlled release of a drug through skin on the basis of a topical composition comprising a drug, a film-forming silicone and at least one volatile solvent |
| MXPA05009381A (es) * | 2005-09-02 | 2007-03-01 | Fernando Ahumada Ayala | Preparaciones para el cuidado de la piel que contienen mupirocina y dipropionato de betametasona. |
| US8497258B2 (en) | 2005-11-12 | 2013-07-30 | The Regents Of The University Of California | Viscous budesonide for the treatment of inflammatory diseases of the gastrointestinal tract |
| US8679545B2 (en) | 2005-11-12 | 2014-03-25 | The Regents Of The University Of California | Topical corticosteroids for the treatment of inflammatory diseases of the gastrointestinal tract |
| US8324192B2 (en) | 2005-11-12 | 2012-12-04 | The Regents Of The University Of California | Viscous budesonide for the treatment of inflammatory diseases of the gastrointestinal tract |
| BRPI0621471A2 (pt) | 2006-03-17 | 2012-09-11 | Leo Pharma As | métodos de isomerização de uma solução de um derivado de vitamina d, para produzir e preparar calcipotriol ou monoidrato de calcipotriol, e para a fabricação de uma formulação farmacêutica ou medicamento, e, uso de um reator foto-reator de fluxo direto ou foto-reator de fluxo contìnuo |
| US20080064669A1 (en) * | 2006-08-29 | 2008-03-13 | Rakefet Cohen | Stable pharmacologically active compositions including vitamin D-containing and corticosteroid compounds with low pH compatibility |
| FR2909284B1 (fr) * | 2006-11-30 | 2012-09-21 | Galderma Sa | Nouvelles compositions sous forme d'onguent sans vaseline comprenant un derive de vitamine d et eventuellement un anti-inflammatoire steroidien |
| ES2272198B1 (es) * | 2006-12-28 | 2008-06-01 | Laboratorios Viñas S.A. | Procedimiento para la obtencion de hidrato de calcipotriol. |
| US10265265B2 (en) | 2007-03-15 | 2019-04-23 | Drug Delivery Solutions Limited | Topical composition |
| EP1970048A1 (en) * | 2007-03-15 | 2008-09-17 | Drug Delivery Solutions Limited | Polyaphron topical composition with vitamin D |
| EP1970049A1 (en) * | 2007-03-15 | 2008-09-17 | Drug Delivery Solutions Limited | Polyaphron topical composition with vitamin D and corticosteroid |
| EP2008651A1 (en) | 2007-06-26 | 2008-12-31 | Drug Delivery Solutions Limited | A bioerodible patch |
| US20100216754A1 (en) * | 2007-11-13 | 2010-08-26 | Meritage Pharma, Inc. | Compositions for the treatment of inflammation of the gastrointestinal tract |
| US20090131386A1 (en) * | 2007-11-13 | 2009-05-21 | Meritage Pharma, Inc. | Compositions for the treatment of inflammation of the gastrointestinal tract |
| CA2704949A1 (en) | 2007-11-13 | 2009-05-22 | Meritage Pharma, Inc. | Gastrointestinal delivery systems |
| US20090123551A1 (en) * | 2007-11-13 | 2009-05-14 | Meritage Pharma, Inc. | Gastrointestinal delivery systems |
| US20090264392A1 (en) * | 2008-04-21 | 2009-10-22 | Meritage Pharma, Inc. | Treating eosinophilic esophagitis |
| PL2515874T3 (pl) * | 2009-12-22 | 2015-01-30 | Leo Pharma As | Nanokryształy jednowodnego kalcypotriolu |
| US9254296B2 (en) * | 2009-12-22 | 2016-02-09 | Leo Pharma A/S | Pharmaceutical composition comprising vitamin D analogue and cosolvent-surfactant mixture |
| AU2010335654B2 (en) * | 2009-12-22 | 2015-04-09 | Leo Pharma A/S | Cutaneous composition comprising vitamin D analogue and a mixture of solvent and surfactants |
| JP5945268B2 (ja) | 2010-06-11 | 2016-07-05 | レオ ファーマ アクティーゼルスカブ | ビタミンｄ類似体およびコルチコステロイドを含むスプレー医薬組成物 |
| RU2429818C1 (ru) * | 2010-06-28 | 2011-09-27 | Государственное учреждение здравоохранения "Кемеровская областная клиническая больница" | Лечебное средство |
| RU2442565C1 (ru) * | 2010-08-27 | 2012-02-20 | Государственное учреждение здравоохранения "Кемеровская областная клиническая больница" | Лечебная мазь |
| US8685381B2 (en) * | 2010-10-23 | 2014-04-01 | Joel Schlessinger | Topical base and active agent-containing compositions, and methods for improving and treating skin |
| US8968755B2 (en) | 2010-10-23 | 2015-03-03 | Joel Schlessinger | Topical base and active agent-containing compositions, and methods for improving and treating skin |
| WO2012123515A1 (en) | 2011-03-14 | 2012-09-20 | Drug Delivery Solutions Limited | An ophthalmic composition |
| JP5897299B2 (ja) * | 2011-10-14 | 2016-03-30 | 岩城製薬株式会社 | ローション剤 |
| CN104138352B (zh) * | 2013-04-19 | 2018-02-27 | 江苏知原药业有限公司 | 卡泊三醇非水凝胶 |
| TW201636025A (zh) * | 2015-04-15 | 2016-10-16 | Maruho Kk | 皮膚用之醫藥組成物 |
| LT3310389T (lt) * | 2015-06-18 | 2020-11-10 | Bausch Health Ireland Limited | Vietinio vartojimo kompozicijos, apimančios kortikosteroidą ir retinoidą, skirtos psoriazės gydymui |
| EP3542788A1 (en) | 2018-03-19 | 2019-09-25 | MC2 Therapeutics Limited | Topical composition comprising calcipotriol and betamethasone dipropionate |
| KR102354028B1 (ko) | 2020-05-13 | 2022-01-24 | 동국대학교 경주캠퍼스 산학협력단 | 건선 예방, 개선 또는 치료용 피부 외용제 조성물 |
| CN114159567B (zh) * | 2020-09-10 | 2023-03-31 | 南京海融医药科技股份有限公司 | 一种治疗皮肤病的混悬凝胶剂 |
| CN115569199B (zh) * | 2022-02-14 | 2024-08-20 | 海勃(上海)医药科技有限公司 | 一种药物组合物及其制备方法和应用 |
Family Cites Families (22)
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| US4569935A (en) * | 1983-03-17 | 1986-02-11 | University Of Tennessee Research Corp. | Topical treatment of psoriasis with imidazole antibiotics |
| US4610978A (en) * | 1983-03-22 | 1986-09-09 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Compositions containing 1α-hydroxycholecalciferol for topical treatment of skin disorders and methods employing same |
| SE457055B (sv) * | 1986-08-18 | 1988-11-28 | Ferring Ab | Topisk straalskyddsgel foer mukosa innehaallande kaerlsammandragande substanser |
| IL86170A (en) * | 1987-05-01 | 1992-12-01 | Elan Transdermal Ltd | Preparations and compositions comprising nicotine for percutaneous administration |
| US4847071A (en) | 1987-10-22 | 1989-07-11 | The Procter & Gamble Company | Photoprotection compositions comprising tocopherol sorbate and an anti-inflammatory agent |
| US5002938A (en) | 1988-03-21 | 1991-03-26 | Bristol-Myers Squibb Company | Antifungal gel formulations |
| EP0437225B1 (de) * | 1990-01-10 | 1994-04-20 | F. Hoffmann-La Roche Ag | Topische Präparate |
| US5185150A (en) * | 1990-08-24 | 1993-02-09 | Wisconsin Alumni Research Fdn. | Cosmetic compositions containing 19-nor-vitamin D compounds |
| US5763428A (en) * | 1990-09-21 | 1998-06-09 | Bone Care International, Inc. | Methods of treating skin disorders with novel 1a-hydroxy vitamin D4 compounds and derivatives thereof |
| JP2571493B2 (ja) * | 1992-06-04 | 1997-01-16 | 株式会社資生堂 | 皮膚外用剤 |
| AU4841193A (en) * | 1992-08-28 | 1994-03-29 | Lunar Corporation | 1alpha,24(S)-dihydroxy vitamin D2, its formation and use |
| GB9226860D0 (en) * | 1992-12-23 | 1993-02-17 | Leo Pharm Prod Ltd | Novel treatment |
| DE4328217C2 (de) * | 1993-08-21 | 1996-01-11 | Lohmann Therapie Syst Lts | Therapeutisches System zur Behandlung der Psoriasis |
| US5708017A (en) * | 1995-04-04 | 1998-01-13 | Merck & Co., Inc. | Stable, ready-to-use pharmaceutical paste composition containing proton pump inhibitors |
| FR2740042B1 (fr) * | 1995-10-23 | 1997-11-14 | Oreal | Support, et composition contenant ce support et un actif cosmetique ou dermatologique stabilise |
| JPH10158147A (ja) * | 1996-11-29 | 1998-06-16 | Kenji Nakamura | 皮膚保護用の被膜組成物とそれを用いた製品 |
| EP0971743B1 (de) * | 1997-04-18 | 2006-07-12 | Fritz Stanislaus | Stabilisiertes arzneimittel enthaltend cysteinylderivate |
| JPH11188054A (ja) * | 1997-12-25 | 1999-07-13 | Lion Corp | 皮膚外用部材 |
| US5990100A (en) * | 1998-03-24 | 1999-11-23 | Panda Pharmaceuticals, L.L.C. | Composition and method for treatment of psoriasis |
| FR2785284B1 (fr) * | 1998-11-02 | 2000-12-01 | Galderma Res & Dev | Analogues de la vitamine d |
| CA2370565C (en) * | 1999-04-23 | 2008-11-25 | Leo Pharmaceutical Products Ltd. A/S (Lovens Kemiske Fabrik Produktionsaktieselskab) | Dermally applicable vitamin d-containing pharmaceutical compositions |
| DK1331927T3 (da) * | 2000-10-27 | 2008-05-05 | Leo Pharma As | Topisk komposition der indeholder mindst et D-vitamin eller en D-vitamin analog og mindst et kosttikosteroid |
-
2001
- 2001-09-26 DK DK01971719T patent/DK1331927T3/da active
- 2001-09-26 CN CNB018177964A patent/CN100382803C/zh not_active Expired - Lifetime
- 2001-09-26 JP JP2002537289A patent/JP4451061B2/ja not_active Expired - Lifetime
- 2001-09-26 MX MXPA03003511A patent/MXPA03003511A/es active IP Right Grant
- 2001-09-26 RU RU2003115616/15A patent/RU2271810C2/ru active
- 2001-09-26 IL IL15488801A patent/IL154888A0/xx unknown
- 2001-09-26 PT PT01971719T patent/PT1331927E/pt unknown
- 2001-09-26 HU HU0302881A patent/HU230005B1/hu unknown
- 2001-09-26 ES ES01971719T patent/ES2298264T3/es not_active Expired - Lifetime
- 2001-09-26 PL PL360941A patent/PL212660B1/pl unknown
- 2001-09-26 CZ CZ2003-1162A patent/CZ305984B6/cs not_active IP Right Cessation
- 2001-09-26 CA CA002423930A patent/CA2423930C/en not_active Expired - Lifetime
- 2001-09-26 BR BRPI0114927A patent/BRPI0114927B8/pt not_active IP Right Cessation
- 2001-09-26 WO PCT/DK2001/000613 patent/WO2002034235A1/en not_active Ceased
- 2001-09-26 KR KR1020037005809A patent/KR100844285B1/ko not_active Expired - Lifetime
- 2001-09-26 AU AU9163701A patent/AU9163701A/xx active Pending
- 2001-09-26 AT AT01971719T patent/ATE380542T1/de active
- 2001-09-26 DE DE60131881T patent/DE60131881T2/de not_active Expired - Lifetime
- 2001-09-26 AU AU2001291637A patent/AU2001291637B2/en not_active Expired
- 2001-09-26 EP EP01971719A patent/EP1331927B1/en not_active Expired - Lifetime
- 2001-10-26 US US09/984,072 patent/US6787529B2/en not_active Expired - Lifetime
-
2003
- 2003-03-12 IL IL154888A patent/IL154888A/en not_active IP Right Cessation
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2008
- 2008-03-03 CY CY20081100243T patent/CY1107294T1/el unknown
- 2008-07-24 JP JP2008191184A patent/JP5721927B2/ja not_active Expired - Lifetime
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2013
- 2013-01-29 JP JP2013014295A patent/JP5699169B2/ja not_active Expired - Lifetime
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