ZA200510129B - Delivery of a drug via subconjuctival or periocular delivery of a prodrug in a polymeric microparticle - Google Patents
Delivery of a drug via subconjuctival or periocular delivery of a prodrug in a polymeric microparticle Download PDFInfo
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- ZA200510129B ZA200510129B ZA200510129A ZA200510129A ZA200510129B ZA 200510129 B ZA200510129 B ZA 200510129B ZA 200510129 A ZA200510129 A ZA 200510129A ZA 200510129 A ZA200510129 A ZA 200510129A ZA 200510129 B ZA200510129 B ZA 200510129B
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- prodrug
- active drug
- eye
- active
- delivery
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Classifications
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- 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
- A61K47/50—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K31/557—Eicosanoids, e.g. leukotrienes or prostaglandins
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- A—HUMAN NECESSITIES
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- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
- A61K31/203—Retinoic acids ; Salts thereof
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- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0048—Eye, e.g. artificial tears
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- A—HUMAN NECESSITIES
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- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0048—Eye, e.g. artificial tears
- A61K9/0051—Ocular inserts, ocular implants
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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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
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- 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
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- 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
- A61P27/12—Ophthalmic agents for cataracts
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
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- A61P37/08—Antiallergic agents
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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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1641—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, poloxamers
- A61K9/1647—Polyesters, e.g. poly(lactide-co-glycolide)
Landscapes
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
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- Public Health (AREA)
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- Life Sciences & Earth Sciences (AREA)
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- Ophthalmology & Optometry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/617,468 US20050009910A1 (en) | 2003-07-10 | 2003-07-10 | Delivery of an active drug to the posterior part of the eye via subconjunctival or periocular delivery of a prodrug |
Publications (1)
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| ZA200510129B true ZA200510129B (en) | 2007-02-28 |
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| ZA200510129A ZA200510129B (en) | 2003-07-10 | 2005-12-13 | Delivery of a drug via subconjuctival or periocular delivery of a prodrug in a polymeric microparticle |
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| EP (1) | EP1644047A2 (fr) |
| JP (1) | JP2007528851A (fr) |
| KR (1) | KR20060033008A (fr) |
| CN (1) | CN1882362A (fr) |
| AU (1) | AU2004260645B2 (fr) |
| BR (1) | BRPI0412496A (fr) |
| CA (1) | CA2531753A1 (fr) |
| IL (1) | IL172583A (fr) |
| MX (1) | MXPA06000408A (fr) |
| NO (1) | NO20056174L (fr) |
| NZ (2) | NZ582376A (fr) |
| PL (1) | PL380169A1 (fr) |
| RU (1) | RU2353393C2 (fr) |
| WO (1) | WO2005011741A2 (fr) |
| ZA (1) | ZA200510129B (fr) |
Families Citing this family (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050250737A1 (en) * | 2003-11-12 | 2005-11-10 | Allergan, Inc. | Therapeutic ophthalmic compositions containing retinal friendly excipients and related methods |
| US20050101582A1 (en) | 2003-11-12 | 2005-05-12 | Allergan, Inc. | Compositions and methods for treating a posterior segment of an eye |
| WO2005056010A1 (fr) * | 2003-12-02 | 2005-06-23 | Allergan, Inc. | Prevention et/ou reduction de la degeneration de photorecepteurs avec des retinoides |
| US8871224B2 (en) | 2003-12-09 | 2014-10-28 | Allergan, Inc. | Botulinum toxin therapy for skin disorders |
| AU2005221283C1 (en) * | 2004-03-17 | 2011-02-03 | Lars Michael Larsen | Prevention of retinopathy by inhibition of the visual cycle |
| US20050220734A1 (en) * | 2004-04-02 | 2005-10-06 | Allergan, Inc. | Therapy for melanin related afflictions |
| AU2011211380B9 (en) * | 2004-04-30 | 2014-05-08 | Allergan, Inc. | Biodegradable intravitreal tyrosine kinase inhibitor implants |
| US8512738B2 (en) | 2004-04-30 | 2013-08-20 | Allergan, Inc. | Biodegradable intravitreal tyrosine kinase implants |
| US7771742B2 (en) * | 2004-04-30 | 2010-08-10 | Allergan, Inc. | Sustained release intraocular implants containing tyrosine kinase inhibitors and related methods |
| AU2005240078A1 (en) * | 2004-04-30 | 2005-11-17 | Allergan, Inc. | Retinoid-containing sustained release intraocular drug delivery systems and related methods of manufacturing |
| US20060089590A1 (en) * | 2004-10-27 | 2006-04-27 | John Higuchi | Methods and devices for sustained in-vivo release of an active agent |
| ES2616296T3 (es) * | 2005-12-02 | 2017-06-12 | (Osi) Eyetech, Inc. | Micropartículas de liberación controlada |
| US20070202186A1 (en) | 2006-02-22 | 2007-08-30 | Iscience Interventional Corporation | Apparatus and formulations for suprachoroidal drug delivery |
| US8197435B2 (en) | 2006-05-02 | 2012-06-12 | Emory University | Methods and devices for drug delivery to ocular tissue using microneedle |
| CN101074935B (zh) * | 2006-05-19 | 2011-03-23 | 清华大学 | 探测器阵列及设备 |
| DK1864668T3 (da) * | 2006-06-01 | 2013-03-04 | Novagali Pharma Sa | Anvendelse af prodrug til okulær, intravitreal administration |
| US10022348B2 (en) | 2009-05-20 | 2018-07-17 | Sun Pharmaceutical Industries Limited | Topical solution of isotretinoin |
| SG176097A1 (en) | 2009-05-20 | 2011-12-29 | Ranbaxy Lab Ltd | Topical retinoid solutions |
| US8889193B2 (en) | 2010-02-25 | 2014-11-18 | The Johns Hopkins University | Sustained delivery of therapeutic agents to an eye compartment |
| WO2012039979A2 (fr) | 2010-09-10 | 2012-03-29 | The Johns Hopkins University | Diffusion rapide de grosses nanoparticules polymères dans le cerveau de mammifères |
| EP3520749A1 (fr) | 2010-10-15 | 2019-08-07 | Clearside Biomedical, Inc. | Dispositif d'accès oculaire |
| US9327037B2 (en) | 2011-02-08 | 2016-05-03 | The Johns Hopkins University | Mucus penetrating gene carriers |
| CA2863632C (fr) | 2012-01-19 | 2017-07-11 | The Johns Hopkins University | Formulations de nanoparticules presentant une penetration amelioree dans les muqueuses |
| EP2825206A1 (fr) | 2012-03-16 | 2015-01-21 | The Johns Hopkins University | Formulations à libération contrôlée pour l'administration d'inhibiteurs du hif-1 |
| US10159743B2 (en) | 2012-03-16 | 2018-12-25 | The Johns Hopkins University | Non-linear multiblock copolymer-drug conjugates for the delivery of active agents |
| EP2844295A1 (fr) | 2012-05-03 | 2015-03-11 | Kala Pharmaceuticals, Inc. | Nanoparticules pharmaceutiques permettant un transport muqueux amélioré |
| WO2013166408A1 (fr) | 2012-05-03 | 2013-11-07 | Kala Pharmaceuticals, Inc. | Nanoparticules pharmaceutiques présentant un transport muqueux amélioré |
| US11596599B2 (en) | 2012-05-03 | 2023-03-07 | The Johns Hopkins University | Compositions and methods for ophthalmic and/or other applications |
| US9827191B2 (en) | 2012-05-03 | 2017-11-28 | The Johns Hopkins University | Compositions and methods for ophthalmic and/or other applications |
| JP6392209B2 (ja) | 2012-05-04 | 2018-09-19 | ザ・ジョンズ・ホプキンス・ユニバーシティー | 粘液内層を通過する迅速な透過のための脂質ベース薬物キャリア |
| US20150258120A1 (en) | 2012-11-08 | 2015-09-17 | Clearside Biomedical, Inc. | Methods and devices for the treatment of ocular diseases in human subjects |
| US10568975B2 (en) | 2013-02-05 | 2020-02-25 | The Johns Hopkins University | Nanoparticles for magnetic resonance imaging tracking and methods of making and using thereof |
| JP6379183B2 (ja) | 2013-05-03 | 2018-08-22 | クリアサイド バイオメディカル，インコーポレイテッド | 眼球注射の装置および方法 |
| WO2014197317A1 (fr) | 2013-06-03 | 2014-12-11 | Clearside Biomedical, Inc. | Appareil et procédés pour une administration de médicament à l'aide de multiples réservoirs |
| US10010447B2 (en) | 2013-12-18 | 2018-07-03 | Novartis Ag | Systems and methods for subretinal delivery of therapeutic agents |
| WO2015116709A1 (fr) | 2014-01-28 | 2015-08-06 | Allergan, Inc. | Formulations topiques de rétinoïdes, et procédés d'utilisation |
| WO2015127389A1 (fr) | 2014-02-23 | 2015-08-27 | The Johns Hopkins University | Formulations de lavement hypotonique et méthodes d'utilisation |
| RU2710491C2 (ru) | 2014-06-20 | 2019-12-26 | Клиасайд Байомедикал, Инк. | Устройство для инъекции лекарственного средства в глазную ткань и способ инъекции лекарственного средства в глазную ткань |
| CA2974715C (fr) | 2015-01-27 | 2020-05-05 | The Johns Hopkins University | Formulations d'hydrogel hypotoniques pour le transport ameliore d'agents actifs au niveau de surfaces muqueuses |
| AR106018A1 (es) | 2015-08-26 | 2017-12-06 | Achillion Pharmaceuticals Inc | Compuestos de arilo, heteroarilo y heterocíclicos para el tratamiento de trastornos médicos |
| EP3340982B1 (fr) | 2015-08-26 | 2021-12-15 | Achillion Pharmaceuticals, Inc. | Composés pour le traitement de troubles immunitaires et inflammatoires |
| US10390901B2 (en) | 2016-02-10 | 2019-08-27 | Clearside Biomedical, Inc. | Ocular injection kit, packaging, and methods of use |
| JP2019514581A (ja) | 2016-05-02 | 2019-06-06 | クリアサイド バイオメディカル，インコーポレイテッド | 眼の薬物送達のためのシステムおよび方法 |
| CN109562113A (zh) | 2016-05-10 | 2019-04-02 | C4医药公司 | 用于靶蛋白降解的螺环降解决定子体 |
| EP3455218A4 (fr) | 2016-05-10 | 2019-12-18 | C4 Therapeutics, Inc. | Dégronimères de type glutarimide liés au carbone c3 pour la dégradation de protéines cibles |
| WO2017197055A1 (fr) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Dégronimères hétérocycliques pour la dégradation de protéines cibles |
| EP3939591A1 (fr) | 2016-06-27 | 2022-01-19 | Achillion Pharmaceuticals, Inc. | Composés de quinazoline et d'indole pour traiter des troubles médicaux |
| AU2017290748A1 (en) | 2016-07-01 | 2019-01-17 | G1 Therapeutics, Inc. | Pyrimidine-based antiproliferative agents |
| CN110177527B (zh) | 2016-08-12 | 2022-02-01 | 科尼尔赛德生物医学公司 | 用于调节药剂递送用针的插入深度的装置和方法 |
| US11931327B2 (en) | 2017-07-04 | 2024-03-19 | Daiichi Sankyo Company, Limited | Drug for retinal degenerative disease associated with photoreceptor degeneration |
| JP2021519337A (ja) | 2018-03-26 | 2021-08-10 | シー４ セラピューティクス， インコーポレイテッド | Ｉｋａｒｏｓの分解のためのセレブロン結合剤 |
| EP3841086A4 (fr) | 2018-08-20 | 2022-07-27 | Achillion Pharmaceuticals, Inc. | Composés pharmaceutiques pour le traitement de troubles médicaux du facteur d du complément |
| WO2020081723A1 (fr) | 2018-10-16 | 2020-04-23 | Georgia State University Research Foundation, Inc. | Promédicaments de monoxyde de carbone pour le traitement de troubles médicaux |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4853224A (en) * | 1987-12-22 | 1989-08-01 | Visionex | Biodegradable ocular implants |
| US4997652A (en) * | 1987-12-22 | 1991-03-05 | Visionex | Biodegradable ocular implants |
| US5164188A (en) * | 1989-11-22 | 1992-11-17 | Visionex, Inc. | Biodegradable ocular implants |
| US5275820A (en) * | 1990-12-27 | 1994-01-04 | Allergan, Inc. | Stable suspension formulations of bioerodible polymer matrix microparticles incorporating drug loaded ion exchange resin particles |
| US5384333A (en) * | 1992-03-17 | 1995-01-24 | University Of Miami | Biodegradable injectable drug delivery polymer |
| US5178635A (en) * | 1992-05-04 | 1993-01-12 | Allergan, Inc. | Method for determining amount of medication in an implantable device |
| WO1995003009A1 (fr) * | 1993-07-22 | 1995-02-02 | Oculex Pharmaceuticals, Inc. | Methode de traitement de la degenerescence maculaire |
| US5443505A (en) * | 1993-11-15 | 1995-08-22 | Oculex Pharmaceuticals, Inc. | Biocompatible ocular implants |
| US5420120A (en) * | 1993-12-17 | 1995-05-30 | Alcon Laboratories, Inc. | Anti-inflammatory glucocorticoid compounds for topical ophthalmic use |
| EP0754046A1 (fr) * | 1994-04-04 | 1997-01-22 | FREEMAN, William R. | Emploi de nucleosides de phosphonylemethoxyalkyle pour traiter la pression intra-oculaire elevee |
| WO1995027481A1 (fr) * | 1994-04-08 | 1995-10-19 | Atrix Laboratories, Inc. | Compositions liquides a diffusion |
| US5824685A (en) * | 1995-02-01 | 1998-10-20 | The Johns Hopkins University School Of Medicine | Method of preventing proliferation of retinal pigment epithelium by retinoic acid receptor agonists |
| US5718922A (en) * | 1995-05-31 | 1998-02-17 | Schepens Eye Research Institute, Inc. | Intravitreal microsphere drug delivery and method of preparation |
| US5675033A (en) * | 1995-06-06 | 1997-10-07 | Allergan | 2,4-pentadienoic acid derivatives having retinoid-like biological activity |
| US6277413B1 (en) * | 1998-07-17 | 2001-08-21 | Skyepharma, Inc. | Biodegradable compositions for the controlled release of encapsulated substances |
| US6017938A (en) * | 1998-07-28 | 2000-01-25 | Bershad; Susan | Short contact treatment for acne |
| US6378526B1 (en) * | 1998-08-03 | 2002-04-30 | Insite Vision, Incorporated | Methods of ophthalmic administration |
| US6416777B1 (en) * | 1999-10-21 | 2002-07-09 | Alcon Universal Ltd. | Ophthalmic drug delivery device |
| US6489335B2 (en) * | 2000-02-18 | 2002-12-03 | Gholam A. Peyman | Treatment of ocular disease |
| US20030018044A1 (en) * | 2000-02-18 | 2003-01-23 | Peyman Gholam A. | Treatment of ocular disease |
| EP1292285A4 (fr) * | 2000-06-02 | 2009-07-22 | Eisai Corp North America | Systemes de distribution d'agents bioactifs |
| AR030346A1 (es) * | 2000-08-14 | 2003-08-20 | Alcon Inc | Metodo de tratamiento de desordenes neurodegenerativos de la retina y cabeza de nervio optico |
| JP4061015B2 (ja) * | 2000-10-30 | 2008-03-12 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | レチノイン酸レセプターアゴニスト作用を有する薬剤含有組成物 |
| US6673802B2 (en) * | 2000-12-01 | 2004-01-06 | Osi Pharmaceuticals, Inc. | Compounds specific to adenosine A3 receptor and uses thereof |
| KR20040005936A (ko) * | 2001-04-26 | 2004-01-16 | 컨트롤 딜리버리 시스템즈 인코포레이티드 | 공동약물을 함유하는 서방 약물 전달 시스템 |
| GB0122318D0 (en) * | 2001-09-14 | 2001-11-07 | Novartis Ag | Organic compounds |
| US7381426B2 (en) * | 2002-01-24 | 2008-06-03 | Southwest Research Institute | Targeted delivery of bioactive factors to the systemic skeleton |
| JP2006507368A (ja) * | 2002-09-29 | 2006-03-02 | サーモディックス，インコーポレイティド | ステロイド含有治療剤の網膜下投与方法；脈絡膜及び網膜に薬力学作用を局在化するための方法；並びに網膜疾患の治療及び／又は予防のための関連する方法 |
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2003
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2004
- 2004-07-07 PL PL380169A patent/PL380169A1/pl not_active Application Discontinuation
- 2004-07-07 CA CA002531753A patent/CA2531753A1/fr not_active Abandoned
- 2004-07-07 AU AU2004260645A patent/AU2004260645B2/en not_active Ceased
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- 2004-07-07 NZ NZ582376A patent/NZ582376A/en not_active IP Right Cessation
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- 2004-07-07 WO PCT/US2004/021938 patent/WO2005011741A2/fr active Application Filing
- 2004-07-07 CN CNA2004800195540A patent/CN1882362A/zh active Pending
- 2004-07-07 MX MXPA06000408A patent/MXPA06000408A/es unknown
- 2004-07-07 NZ NZ544027A patent/NZ544027A/en not_active IP Right Cessation
- 2004-07-07 RU RU2006104983/14A patent/RU2353393C2/ru not_active IP Right Cessation
-
2005
- 2005-12-13 ZA ZA200510129A patent/ZA200510129B/en unknown
- 2005-12-14 IL IL172583A patent/IL172583A/en not_active IP Right Cessation
- 2005-12-23 NO NO20056174A patent/NO20056174L/no not_active Application Discontinuation
-
2012
- 2012-02-29 US US13/407,906 patent/US20120157499A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CA2531753A1 (fr) | 2005-02-10 |
| MXPA06000408A (es) | 2006-03-17 |
| AU2004260645A1 (en) | 2005-02-10 |
| CN1882362A (zh) | 2006-12-20 |
| KR20060033008A (ko) | 2006-04-18 |
| NO20056174L (no) | 2006-01-25 |
| WO2005011741A2 (fr) | 2005-02-10 |
| NZ544027A (en) | 2010-07-30 |
| EP1644047A2 (fr) | 2006-04-12 |
| AU2004260645B2 (en) | 2010-03-11 |
| NZ582376A (en) | 2012-02-24 |
| WO2005011741A3 (fr) | 2005-04-14 |
| IL172583A (en) | 2011-02-28 |
| PL380169A1 (pl) | 2007-01-08 |
| JP2007528851A (ja) | 2007-10-18 |
| BRPI0412496A (pt) | 2006-09-19 |
| US20120157499A1 (en) | 2012-06-21 |
| IL172583A0 (en) | 2006-04-10 |
| RU2353393C2 (ru) | 2009-04-27 |
| US20050009910A1 (en) | 2005-01-13 |
| RU2006104983A (ru) | 2006-06-27 |
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