AR046222A1 - Composiciones farmaceuticas de liberacion sostenida que incluyen aplindore y sus derivados - Google Patents
Composiciones farmaceuticas de liberacion sostenida que incluyen aplindore y sus derivadosInfo
- Publication number
- AR046222A1 AR046222A1 ARP040103986A ARP040103986A AR046222A1 AR 046222 A1 AR046222 A1 AR 046222A1 AR P040103986 A ARP040103986 A AR P040103986A AR P040103986 A ARP040103986 A AR P040103986A AR 046222 A1 AR046222 A1 AR 046222A1
- Authority
- AR
- Argentina
- Prior art keywords
- optionally substituted
- alkyl
- defined above
- hydrogen
- controlled release
- Prior art date
Links
- DYJIKHYBKVODAC-ZDUSSCGKSA-N (2s)-2-[(benzylamino)methyl]-2,3,7,9-tetrahydro-[1,4]dioxino[2,3-e]indol-8-one Chemical compound C([C@H]1COC=2C=CC3=C(C=2O1)CC(N3)=O)NCC1=CC=CC=C1 DYJIKHYBKVODAC-ZDUSSCGKSA-N 0.000 title 1
- 229950001748 aplindore Drugs 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 230000002459 sustained effect Effects 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 5
- 238000013270 controlled release Methods 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 150000002431 hydrogen Chemical class 0.000 abstract 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 abstract 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 abstract 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 abstract 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 abstract 2
- 238000009472 formulation Methods 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 125000005553 heteroaryloxy group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 1
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 abstract 1
- CJRPBMIZIBLPDX-UHFFFAOYSA-N 1h-imidazole;1h-indazole Chemical compound C1=CNC=N1.C1=CC=C2C=NNC2=C1 CJRPBMIZIBLPDX-UHFFFAOYSA-N 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 abstract 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 abstract 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 abstract 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 abstract 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 abstract 1
- 125000004423 acyloxy group Chemical group 0.000 abstract 1
- 125000001118 alkylidene group Chemical group 0.000 abstract 1
- 125000002102 aryl alkyloxo group Chemical group 0.000 abstract 1
- -1 bencisoxazole Chemical compound 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- VZWXIQHBIQLMPN-UHFFFAOYSA-N chromane Chemical compound C1=CC=C2CCCOC2=C1 VZWXIQHBIQLMPN-UHFFFAOYSA-N 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 229960003638 dopamine Drugs 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 abstract 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 abstract 1
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000005186 naphthyloxy group Chemical group C1(=CC=CC2=CC=CC=C12)O* 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229930192474 thiophene Natural products 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
-
- 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
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- 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
- A61K9/20—Pills, tablets, discs, rods
-
- 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
- A61K9/2806—Coating materials
- A61K9/2833—Organic macromolecular compounds
- A61K9/286—Polysaccharides, e.g. gums; Cyclodextrin
- A61K9/2866—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Neurology (AREA)
- Organic Chemistry (AREA)
- Biomedical Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Indole Compounds (AREA)
Abstract
Reivindicación 1: Una formulación de dosis de liberación controlada, caracterizada porque comprende un compuesto de la fórmula (1), en la cual: R1y R2 son, independientemente, hidrógeno, alquilo C1-6, fenilo o bencilo; o R1 y R2, tomados en conjunto, son bencilideno opcionalmente sustituido con R3 como se define más adelante o alquilideno de hasta 6 átomos de carbono; o R1 y R2, tomados en conjunto con el átomo de carbono al cual están unidos, forman un residuo carbonilo o un grupo cicloalquilo que tiene hasta 6 átomos de carbono; R3 es hidrógeno, hidroxi, halógeno, trifluorometilo, trifluorometoxi, alquilo C1-6, alcoxi C1-6, arilalcoxi C7-12, alcanoiloxi C2-6, amino, mono- o di-alquilamino en el cual cada grupo alquilo C1-6, alcanamido C2-6 o alcanosulfonamido C1-6; R4 es hidrógeno o alquilo C1-6; n es uno de los números enteros 0, 1, 2, 3, 4, 5, ó 6; Z es hidrógeno, hidroxi, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, cicloalquilo C3-8, alquilo policíclico C7-15, fenilo opcionalmente sustituido con R3 como se ha definido antes, fenoxi, opcionalmente sustituido con R3 como se ha definido antes, naftilo opcionalmente sustituido con R3 como se ha definido antes o naftiloxi opcionalmente sustituido con R3 como se ha definido antes, heteroarilo o heteroariloxi, en donde el anillo heterocíclico del grupo heteroarilo o heteroariloxi es seleccionado de tiofeno, furano, piridina, pirazina, pirimidina, indol, indazol imidazol, cromano, cumarina, carboestirilo, quinolina, bencisoxazol, benzoxazol, pirazol, pirrol, tiazol, oxazol, o isoxazol y el anillo heterocíclico está opcionalmente sustituido por R3 como se ha definido antes; o una sal farmacéuticamente aceptable de lo mismo. Reivindicación 22: Un método de tratamiento para un desorden del sistema dopaminérgico, caracterizado porque comprende administrar a un paciente que necesita de dicho tratamiento una formulación de dosis de liberación controlada de acuerdo a cualquiera de las reivindicaciones 1-21. Reivindicación 53: Un conjunto de formas de dosis de liberación controlada, caracterizado porque comprende una pluralidad de formas de dosis de liberación controlada individuales, en donde cada forma de dosis individual comprende una cantidad diferente de dicho compuesto de acuerdo a las reivindicaciones 1, 7 o 17.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US51531503P | 2003-10-29 | 2003-10-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR046222A1 true AR046222A1 (es) | 2005-11-30 |
Family
ID=34572826
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP040103986A AR046222A1 (es) | 2003-10-29 | 2004-10-29 | Composiciones farmaceuticas de liberacion sostenida que incluyen aplindore y sus derivados |
Country Status (21)
| Country | Link |
|---|---|
| US (5) | US20050095292A1 (es) |
| EP (1) | EP1675583B1 (es) |
| JP (1) | JP5547865B2 (es) |
| KR (1) | KR101409724B1 (es) |
| CN (2) | CN102335116A (es) |
| AR (1) | AR046222A1 (es) |
| AU (1) | AU2004286855B2 (es) |
| BR (1) | BRPI0415953B8 (es) |
| CA (1) | CA2543045C (es) |
| ES (1) | ES2405404T3 (es) |
| GT (1) | GT200400218A (es) |
| IL (1) | IL174958A (es) |
| MX (1) | MXPA06004752A (es) |
| NO (1) | NO20062004L (es) |
| PA (1) | PA8616201A1 (es) |
| PE (1) | PE20050484A1 (es) |
| RU (1) | RU2376988C2 (es) |
| SG (1) | SG147450A1 (es) |
| TW (1) | TW200517106A (es) |
| WO (1) | WO2005044262A1 (es) |
| ZA (1) | ZA200603409B (es) |
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| JP5547865B2 (ja) | 2003-10-29 | 2014-07-16 | ワイス・エルエルシー | アプリンドルおよびその誘導体を含む持続放出型医薬組成物 |
| US8858993B2 (en) * | 2005-07-25 | 2014-10-14 | Metrics, Inc. | Coated tablet with zero-order or near zero-order release kinetics |
| CN101247790A (zh) * | 2005-08-26 | 2008-08-20 | Bpsi控股公司 | 含有控释羟丙甲纤维素基质的药物组合物 |
| US20070134322A1 (en) * | 2005-12-14 | 2007-06-14 | Forest Laboratories, Inc. | Modified and pulsatile release pharmaceutical formulations of escitalopram |
| US8148414B2 (en) | 2008-08-19 | 2012-04-03 | Xenoport, Inc. | Prodrugs of methyl hydrogen fumarate, pharmaceutical compositions thereof, and methods of use |
| MX367667B (es) * | 2008-12-22 | 2019-08-30 | Novartis Ag | Régimen de dosificación de un agonista de los receptores de s1p. |
| EP3061821B1 (en) | 2009-07-22 | 2019-07-10 | Puretech Health LLC | Compositions for treatment of disorders ameliorated by muscarinic receptor activation |
| EP2468264A1 (en) * | 2010-12-27 | 2012-06-27 | Laboratorios Liconsa, S.A. | Oral pharmaceutical tablet for controled release of mesalazine and process for obtaining it |
| HUE045612T2 (hu) | 2011-01-07 | 2020-01-28 | Novartis Ag | Immunszuppresszáns készítmények |
| EP3718546A1 (en) | 2011-08-16 | 2020-10-07 | Cardiora Pty Ltd | Controlled-release formulation |
| WO2014031844A1 (en) | 2012-08-22 | 2014-02-27 | Xenoport, Inc. | Methods of administering monomethyl fumarate and prodrugs thereof having reduced side effects |
| AU2013305684B2 (en) | 2012-08-22 | 2016-11-24 | Xenoport, Inc. | Oral dosage forms of methyl hydrogen fumarate and prodrugs thereof |
| US10179118B2 (en) | 2013-03-24 | 2019-01-15 | Arbor Pharmaceuticals, Llc | Pharmaceutical compositions of dimethyl fumarate |
| US9302977B2 (en) | 2013-06-07 | 2016-04-05 | Xenoport, Inc. | Method of making monomethyl fumarate |
| US9421182B2 (en) | 2013-06-21 | 2016-08-23 | Xenoport, Inc. | Cocrystals of dimethyl fumarate |
| EP3041467A1 (en) | 2013-09-06 | 2016-07-13 | XenoPort, Inc. | Crystalline forms of (n,n-diethylcarbamoyl)methyl methyl (2e)but-2-ene-1,4-dioate, methods of synthesis and use |
| EP3105238A4 (en) | 2014-02-13 | 2017-11-08 | Ligand Pharmaceuticals, Inc. | Prodrug compounds and their uses |
| US9999672B2 (en) | 2014-03-24 | 2018-06-19 | Xenoport, Inc. | Pharmaceutical compositions of fumaric acid esters |
| EP3236963B1 (en) | 2014-12-22 | 2020-01-29 | Cardiora Pty Ltd | Method of treatment |
| US11434200B2 (en) | 2017-03-09 | 2022-09-06 | Novartis Ag | Solid forms comprising an oxime ether compound and a coformer, compositions and methods of use thereof |
| PE20200732A1 (es) | 2017-06-21 | 2020-07-23 | Minerva Neurosciences Inc | Formas de dosificacion oral y de liberacion controlada gastrorresistentes |
| US10980747B2 (en) * | 2017-11-27 | 2021-04-20 | Shin-Etsu Chemical Co., Ltd. | Composition for solid preparation, solid preparation, and method for producing the same |
| JP6983139B2 (ja) * | 2017-11-27 | 2021-12-17 | 信越化学工業株式会社 | 固形製剤用組成物並びに固形製剤及びその製造方法 |
| CN111788196A (zh) | 2018-01-09 | 2020-10-16 | 配体药物公司 | 缩醛化合物及其治疗用途 |
| EP3856182B1 (en) | 2018-09-28 | 2025-12-24 | Karuna Therapeutics, Inc. | Compositions and methods for treating disorders ameliorated by muscarnic receptor activation |
| TWI841545B (zh) * | 2018-12-12 | 2024-05-11 | 日商田邊三菱製藥股份有限公司 | 耐胃性控制釋放經口劑型 |
| CN115710224A (zh) * | 2020-06-28 | 2023-02-24 | 海创药业股份有限公司 | 一种喹啉类化合物晶型及其制备方法 |
| CN116549406B (zh) * | 2023-05-23 | 2023-12-19 | 北京丰科睿泰医药科技有限公司 | 一种盐酸曲唑酮缓释片剂 |
| US12466883B1 (en) | 2024-05-13 | 2025-11-11 | Lumen Bioscience, Inc. | Leptin compositions and methods of making and using the same to support weight loss and/or maintenance |
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| GB9704948D0 (en) | 1997-03-11 | 1997-04-30 | Knoll Ag | Therapeutic agents |
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| US6350773B1 (en) | 1999-12-10 | 2002-02-26 | American Home Products Corporation | Therapeutic combinations of (S)-2-(benzylamino-methyl)-2,3,8,9,-tetrahydro 7H-1,4-dioxino{2,3-e}indol-8-one and neuroleptics for the treatment or prevention of psychotic disorders |
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| TW200811182A (en) | 2006-05-25 | 2008-03-01 | Wyeth Corp | Oxindoledioxans, synthesis thereof, and intermediates thereto |
-
2004
- 2004-10-28 JP JP2006538307A patent/JP5547865B2/ja not_active Expired - Lifetime
- 2004-10-28 RU RU2006118321/15A patent/RU2376988C2/ru active
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- 2004-10-28 KR KR1020067008178A patent/KR101409724B1/ko not_active Expired - Lifetime
- 2004-10-28 BR BRPI0415953A patent/BRPI0415953B8/pt not_active IP Right Cessation
- 2004-10-28 AU AU2004286855A patent/AU2004286855B2/en not_active Ceased
- 2004-10-28 ES ES04818331T patent/ES2405404T3/es not_active Expired - Lifetime
- 2004-10-28 PA PA20048616201A patent/PA8616201A1/es unknown
- 2004-10-28 TW TW093132737A patent/TW200517106A/zh unknown
- 2004-10-28 CN CN2011102045501A patent/CN102335116A/zh active Pending
- 2004-10-28 US US10/975,254 patent/US20050095292A1/en not_active Abandoned
- 2004-10-28 CN CNA2004800319308A patent/CN1874767A/zh active Pending
- 2004-10-28 CA CA2543045A patent/CA2543045C/en not_active Expired - Fee Related
- 2004-10-28 WO PCT/US2004/036013 patent/WO2005044262A1/en not_active Ceased
- 2004-10-28 PE PE2004001037A patent/PE20050484A1/es not_active Application Discontinuation
- 2004-10-28 GT GT200400218A patent/GT200400218A/es unknown
- 2004-10-28 MX MXPA06004752A patent/MXPA06004752A/es active IP Right Grant
- 2004-10-28 SG SG200807793-5A patent/SG147450A1/en unknown
- 2004-10-29 AR ARP040103986A patent/AR046222A1/es unknown
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- 2006-04-11 IL IL174958A patent/IL174958A/en active IP Right Grant
- 2006-04-28 ZA ZA200603409A patent/ZA200603409B/xx unknown
- 2006-05-04 NO NO20062004A patent/NO20062004L/no not_active Application Discontinuation
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2018
- 2018-03-05 US US15/912,438 patent/US10292966B2/en not_active Expired - Lifetime
- 2018-08-08 US US16/058,769 patent/US10463648B2/en not_active Expired - Lifetime
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2019
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