HUP0302726A2 - Eljárások rák kezelésére szolgáló epotilon analógokat tartalmazó gyógyszerkészítmények előállítására és beadására - Google Patents
Eljárások rák kezelésére szolgáló epotilon analógokat tartalmazó gyógyszerkészítmények előállítására és beadásáraInfo
- Publication number
- HUP0302726A2 HUP0302726A2 HU0302726A HUP0302726A HUP0302726A2 HU P0302726 A2 HUP0302726 A2 HU P0302726A2 HU 0302726 A HU0302726 A HU 0302726A HU P0302726 A HUP0302726 A HU P0302726A HU P0302726 A2 HUP0302726 A2 HU P0302726A2
- Authority
- HU
- Hungary
- Prior art keywords
- patient
- involving
- treating cancer
- optionally substituted
- alkyl
- Prior art date
Links
- 206010028980 Neoplasm Diseases 0.000 title abstract 6
- 201000011510 cancer Diseases 0.000 title abstract 6
- 229930013356 epothilone Natural products 0.000 title abstract 4
- 150000003883 epothilone derivatives Chemical class 0.000 title abstract 4
- 238000000034 method Methods 0.000 title abstract 4
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 3
- 239000000203 mixture Substances 0.000 abstract 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 4
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 238000001035 drying Methods 0.000 abstract 4
- 239000002736 nonionic surfactant Substances 0.000 abstract 4
- 238000007911 parenteral administration Methods 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 206010029350 Neurotoxicity Diseases 0.000 abstract 2
- 206010044221 Toxic encephalopathy Diseases 0.000 abstract 2
- 239000003085 diluting agent Substances 0.000 abstract 2
- 230000007135 neurotoxicity Effects 0.000 abstract 2
- 231100000228 neurotoxicity Toxicity 0.000 abstract 2
- 238000004806 packaging method and process Methods 0.000 abstract 2
- 239000000243 solution Substances 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- 230000003442 weekly effect Effects 0.000 abstract 2
- 230000003288 anthiarrhythmic effect Effects 0.000 abstract 1
- 230000003266 anti-allergic effect Effects 0.000 abstract 1
- 230000000567 anti-anemic effect Effects 0.000 abstract 1
- 230000002456 anti-arthritic effect Effects 0.000 abstract 1
- 230000001430 anti-depressive effect Effects 0.000 abstract 1
- 230000003178 anti-diabetic effect Effects 0.000 abstract 1
- 230000036436 anti-hiv Effects 0.000 abstract 1
- 230000003110 anti-inflammatory effect Effects 0.000 abstract 1
- 230000000648 anti-parkinson Effects 0.000 abstract 1
- 230000002682 anti-psoriatic effect Effects 0.000 abstract 1
- 230000003356 anti-rheumatic effect Effects 0.000 abstract 1
- 230000000259 anti-tumor effect Effects 0.000 abstract 1
- 239000003416 antiarrhythmic agent Substances 0.000 abstract 1
- 239000000935 antidepressant agent Substances 0.000 abstract 1
- 229940005513 antidepressants Drugs 0.000 abstract 1
- 239000003472 antidiabetic agent Substances 0.000 abstract 1
- 239000000939 antiparkinson agent Substances 0.000 abstract 1
- 239000003435 antirheumatic agent Substances 0.000 abstract 1
- 229940076005 apoptosis modulator Drugs 0.000 abstract 1
- 230000001966 cerebroprotective effect Effects 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 239000000824 cytostatic agent Substances 0.000 abstract 1
- 230000001085 cytostatic effect Effects 0.000 abstract 1
- 229960000935 dehydrated alcohol Drugs 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 238000009472 formulation Methods 0.000 abstract 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- -1 heterocyclo Chemical group 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 230000001506 immunosuppresive effect Effects 0.000 abstract 1
- 238000001802 infusion Methods 0.000 abstract 1
- 238000001990 intravenous administration Methods 0.000 abstract 1
- 238000010253 intravenous injection Methods 0.000 abstract 1
- 230000010534 mechanism of action Effects 0.000 abstract 1
- 230000000324 neuroprotective effect Effects 0.000 abstract 1
- 230000001777 nootropic effect Effects 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000011877 solvent mixture Substances 0.000 abstract 1
- 239000012873 virucide Substances 0.000 abstract 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0087—Galenical forms not covered by A61K9/02 - A61K9/7023
- A61K9/0095—Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
-
- 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
- A61K31/427—Thiazoles not condensed and containing further heterocyclic 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/19—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
-
- 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
- A61P35/00—Antineoplastic agents
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Dermatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Hospice & Palliative Care (AREA)
- Otolaryngology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
A találmány tárgyát epotilon analógokat tartalmazó, orális vagyintravénás infúziós alkalmazásra szolgáló gyógyszerkészítményformázása és a készítmény rákos beteg intravénás vagy oráliskezelésére szolgáló eljárás képezi. Az analógot legalább 50 térfogat%terc-butil-alkoholt vízben tartalmazó oldószerelegyben oldják, majdliofilizálják és a kapott liofilizátumot egy fiolában, vízmentesetanol és egy nemionos felületaktív anyag elegyét tartalmazó másodikfiolával együtt csomagolják. Minden lépést fénytől védett körülményekközötti hajtanak végre. Alkalmazáskor a második fiola tartamátegyesítik a liofilizált termékkel, azt így feloldva. Ezt az oldatotmegfelelő hígítószerrel az analóg koncentrációjának körülbelül 0,1mg/ml és 0,9 mg/ml közötti értékre hígítják. A betegnek az émelygés,hányás, túlérzékenység vagy gyomorirritáció meggátlására egy vagy többtovábbi terápiás szert, így H1 vagy H2 antihisztamint is beadnak. Azepotilon analógot orálisan körülbelül 0,05 mg/kg és 200mg/kg közötti,intravénásan körülbelül 1 mg/m2 és 65 mg/m2 közötti adagbanalkalmazzák. Az epotilon analógot intravénásan általában 3 hetesciklusban alkalmazzák, orálisan e ciklus előtt vagy után adják be. Másmódszer szerint az analógot egy vagy több olyan 28 napos ciklusbanalkalmazzák, amelyben az intravénás infúziót az 1., 7. és 14. napon,45 és 90 perc közötti ideig, és orálisan a 21. napon adják be. Ó
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US26422801P | 2001-01-25 | 2001-01-25 | |
US29000801P | 2001-05-11 | 2001-05-11 | |
PCT/US2002/001813 WO2002058700A1 (en) | 2001-01-25 | 2002-01-22 | Methods of administering epothilone analogs for the treatment of cancer |
Publications (3)
Publication Number | Publication Date |
---|---|
HUP0302726A2 true HUP0302726A2 (hu) | 2003-11-28 |
HUP0302726A3 HUP0302726A3 (en) | 2007-08-28 |
HU229349B1 HU229349B1 (en) | 2013-11-28 |
Family
ID=28678063
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU0302726A HU229349B1 (en) | 2001-01-25 | 2002-01-22 | Methods for preparation of pharmaceutical composition containing epothilone analogs useful for treatment of cancer |
Country Status (25)
Country | Link |
---|---|
US (1) | US6670384B2 (hu) |
EP (2) | EP1938821B1 (hu) |
KR (1) | KR100851719B1 (hu) |
CN (1) | CN100341505C (hu) |
AR (1) | AR032409A1 (hu) |
AT (1) | ATE389401T1 (hu) |
BG (1) | BG66494B1 (hu) |
BR (1) | BRPI0206509B8 (hu) |
CY (1) | CY1108114T1 (hu) |
CZ (1) | CZ20032021A3 (hu) |
DE (1) | DE60225666T2 (hu) |
DK (1) | DK1353668T3 (hu) |
EE (1) | EE05301B1 (hu) |
ES (1) | ES2304240T3 (hu) |
HK (2) | HK1065946A1 (hu) |
HU (1) | HU229349B1 (hu) |
IS (1) | IS2865B (hu) |
NO (1) | NO20130070L (hu) |
NZ (1) | NZ526870A (hu) |
PE (1) | PE20020734A1 (hu) |
PT (1) | PT1353668E (hu) |
SK (1) | SK288098B6 (hu) |
TW (1) | TWI342211B (hu) |
UY (1) | UY27137A1 (hu) |
YU (1) | YU58203A (hu) |
Families Citing this family (32)
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US6867305B2 (en) | 1996-12-03 | 2005-03-15 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
EP1386922B1 (en) | 1996-12-03 | 2012-04-11 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereof, analogues and uses thereof |
US6204388B1 (en) * | 1996-12-03 | 2001-03-20 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
US6605599B1 (en) | 1997-07-08 | 2003-08-12 | Bristol-Myers Squibb Company | Epothilone derivatives |
UA75365C2 (en) | 2000-08-16 | 2006-04-17 | Bristol Myers Squibb Co | Epothilone analog polymorph modifications, a method for obtaining thereof (variants), a pharmaceutical composition based thereon |
IL156580A0 (en) * | 2001-01-25 | 2004-01-04 | Bristol Myers Squibb Co | A method for formulating an epothilone analog for parenteral use and pharmaceutical preparations including an epothilone analog |
BR0207487A (pt) | 2001-02-20 | 2004-08-10 | Brystol Myers Squibb Company | Método de tratamento de tumores em mamìferos e uso de compostos de epotilona |
RU2321400C2 (ru) * | 2001-03-14 | 2008-04-10 | Бристол-Маерс Сквибб Компани | Композиция аналога эпотилона в сочетании с химиотерапевтическими агентами для лечения рака |
WO2003077903A1 (en) * | 2002-03-12 | 2003-09-25 | Bristol-Myers Squibb Company | C12-cyano epothilone derivatives |
TW200400191A (en) * | 2002-05-15 | 2004-01-01 | Bristol Myers Squibb Co | Pharmaceutical compositions and methods of using C-21 modified epothilone derivatives |
US6921769B2 (en) | 2002-08-23 | 2005-07-26 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
US7649006B2 (en) | 2002-08-23 | 2010-01-19 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
DK1506203T3 (da) | 2002-08-23 | 2007-05-14 | Sloan Kettering Inst Cancer | Syntese af epothiloner, mellemprodukter deraf, analoger deraf og anvendelser deraf |
EP1663214A1 (en) * | 2003-09-02 | 2006-06-07 | Novartis AG | Cancer treatment with epothilones |
US20050171167A1 (en) * | 2003-11-04 | 2005-08-04 | Haby Thomas A. | Process and formulation containing epothilones and analogs thereof |
US20090004277A1 (en) * | 2004-05-18 | 2009-01-01 | Franchini Miriam K | Nanoparticle dispersion containing lactam compound |
BRPI0518286A2 (pt) * | 2004-11-18 | 2008-11-11 | Bristol Myers Squibb Co | microesfera com revestimento entÉrico contendo ixabepilona e sua preparaÇço |
EP1824458A1 (en) * | 2004-11-18 | 2007-08-29 | Bristol-Myers Squibb Company | Enteric coated bead comprising epothilone or an epothilone analog, and preparation and administration thereof |
EP1674098A1 (en) * | 2004-12-23 | 2006-06-28 | Schering Aktiengesellschaft | Stable and tolerable parental formulations of highly reactive organic drug substances with low or no solubility in water |
WO2007086879A2 (en) | 2005-02-11 | 2007-08-02 | University Of Southern California | Method of expressing proteins with disulfide bridges |
CN1870631B (zh) * | 2005-11-11 | 2010-04-14 | 华为技术有限公司 | 媒体网关的门控方法 |
US8158152B2 (en) * | 2005-11-18 | 2012-04-17 | Scidose Llc | Lyophilization process and products obtained thereby |
EP2029156A4 (en) | 2006-05-01 | 2010-07-21 | Univ Southern California | POLY THERAPY FOR TREATING CANCER |
WO2010056901A2 (en) | 2008-11-13 | 2010-05-20 | University Of Southern California | Method of expressing proteins with disulfide bridges with enhanced yields and activity |
US8263581B2 (en) * | 2009-07-03 | 2012-09-11 | Jdp Therapeutics, Inc. | Non-sedating antihistamine injection formulations and methods of use thereof |
US8513259B2 (en) | 2009-07-03 | 2013-08-20 | Jdp Therapeutics, Inc. | Non-sedating antihistamine injection formulations and methods of use thereof |
MX2012013100A (es) | 2010-05-18 | 2013-01-22 | Cerulean Pharma Inc | Composiciones y metodos para el tratamiento de enfermedades autoinmunes y otras enfermedades. |
WO2012170384A1 (en) | 2011-06-06 | 2012-12-13 | Chevron Phillips Chemical Company Lp | Use of metallocene compounds for cancer treatment |
PL401116A1 (pl) * | 2012-10-09 | 2014-04-14 | Ryszka Florian Farmaceutyczny Zakład Naukowo-Produkcyjny Biochefa | Kompozycja dodawana do płynów infuzyjnych |
CN107041886A (zh) * | 2016-02-06 | 2017-08-15 | 北京华昊中天生物技术有限公司 | 脱环氧埃坡霉素衍生物制剂、制备及其治疗肿瘤的应用 |
EP4087545A1 (en) | 2020-01-10 | 2022-11-16 | R-Pharm US Operating LLC | Compositions of ixabepilone |
CN114727995B (zh) * | 2020-09-02 | 2024-06-11 | 北京华昊中天生物医药股份有限公司 | 优替德隆的固体口服制剂 |
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FR2775187B1 (fr) * | 1998-02-25 | 2003-02-21 | Novartis Ag | Utilisation de l'epothilone b pour la fabrication d'une preparation pharmaceutique antiproliferative et d'une composition comprenant l'epothilone b comme agent antiproliferatif in vivo |
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EP1140944B1 (en) | 1998-12-22 | 2003-08-27 | Novartis AG | Epothilone derivatives and their use as antitumor agents |
EA009206B1 (ru) | 1999-02-18 | 2007-12-28 | Шеринг Акциенгезельшафт | Производные 16-галогенэпотилона и их фармацевтическое использование |
US6211412B1 (en) | 1999-03-29 | 2001-04-03 | The University Of Kansas | Synthesis of epothilones |
AR023792A1 (es) | 1999-04-30 | 2002-09-04 | Bayer Schering Pharma Ag | Derivados 6-alquenilo- y 6-alquinilo-epotilona, los procedimientos para prepararlos y su empleo en productos farmaceuticos |
US20020045609A1 (en) * | 2000-05-26 | 2002-04-18 | Gary Ashley | Epothilone derivatives and methods for making and using the same |
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2002
- 2002-01-22 ES ES02713446T patent/ES2304240T3/es not_active Expired - Lifetime
- 2002-01-22 EP EP08152923.2A patent/EP1938821B1/en not_active Expired - Lifetime
- 2002-01-22 NZ NZ526870A patent/NZ526870A/en not_active IP Right Cessation
- 2002-01-22 EE EEP200300320A patent/EE05301B1/xx not_active IP Right Cessation
- 2002-01-22 AT AT02713446T patent/ATE389401T1/de active
- 2002-01-22 HU HU0302726A patent/HU229349B1/hu not_active IP Right Cessation
- 2002-01-22 DE DE60225666T patent/DE60225666T2/de not_active Expired - Lifetime
- 2002-01-22 PT PT02713446T patent/PT1353668E/pt unknown
- 2002-01-22 YU YU58203A patent/YU58203A/sh unknown
- 2002-01-22 DK DK02713446T patent/DK1353668T3/da active
- 2002-01-22 BR BR0206509A patent/BRPI0206509B8/pt not_active IP Right Cessation
- 2002-01-22 CZ CZ20032021A patent/CZ20032021A3/cs unknown
- 2002-01-22 KR KR1020037009825A patent/KR100851719B1/ko not_active IP Right Cessation
- 2002-01-22 SK SK856-2003A patent/SK288098B6/sk not_active IP Right Cessation
- 2002-01-22 CN CNB028040902A patent/CN100341505C/zh not_active Expired - Fee Related
- 2002-01-22 EP EP02713446A patent/EP1353668B1/en not_active Expired - Lifetime
- 2002-01-23 TW TW091101089A patent/TWI342211B/zh not_active IP Right Cessation
- 2002-01-23 US US10/055,653 patent/US6670384B2/en not_active Expired - Lifetime
- 2002-01-25 AR ARP020100287A patent/AR032409A1/es not_active Application Discontinuation
- 2002-01-25 UY UY27137A patent/UY27137A1/es not_active Application Discontinuation
- 2002-01-25 PE PE2002000062A patent/PE20020734A1/es active IP Right Grant
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2003
- 2003-07-24 IS IS6891A patent/IS2865B/is unknown
- 2003-08-19 BG BG108112A patent/BG66494B1/bg unknown
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2004
- 2004-11-10 HK HK04108838A patent/HK1065946A1/xx not_active IP Right Cessation
- 2004-11-10 HK HK08106497.7A patent/HK1116339A1/xx not_active IP Right Cessation
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2008
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2013
- 2013-01-14 NO NO20130070A patent/NO20130070L/no not_active Application Discontinuation
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