AR081364A1 - Composiciones farmaceuticas de pazopanib y metodos para su elaboracion - Google Patents
Composiciones farmaceuticas de pazopanib y metodos para su elaboracionInfo
- Publication number
- AR081364A1 AR081364A1 ARP110101514A ARP110101514A AR081364A1 AR 081364 A1 AR081364 A1 AR 081364A1 AR P110101514 A ARP110101514 A AR P110101514A AR P110101514 A ARP110101514 A AR P110101514A AR 081364 A1 AR081364 A1 AR 081364A1
- Authority
- AR
- Argentina
- Prior art keywords
- pazopanib
- solution
- modified cyclodextrin
- milligrams
- milliliter
- Prior art date
Links
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
- A61K31/41—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
- A61K31/415—1,2-Diazoles
-
- 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
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
- A61K47/40—Cyclodextrins; Derivatives thereof
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61K47/50—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
- A61K47/69—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 the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
- A61K47/6949—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 the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
- A61K47/6951—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 the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
-
- 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
- A61K9/0048—Eye, e.g. artificial tears
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
Abstract
Reivindicacion 1: Una composicion farmacéutica, la cual comprende: una cantidad de una sal de adicion de ácido de pazopanib equivalente a aproximadamente 10 miligramos de base libre de pazopanib/mililitro de la composicion; de aproximadamente el 2.0 a aproximadamente el 13.0 por ciento en peso/peso de una ciclodextrina modificada que es adecuada para utilizarse en una formulacion oftálmica, seleccionándose la ciclodextrina modificada de tal manera que la ciclodextrina modificada dé como resultado la pKa de pazopanib en una solucion de 10 miligramos de pazopanib/mililitro de agua con una cantidad dada de ciclodextrina modificada que sea más baja que la pKa de pazopanib en una solucion de 10 miligramos de pazopanib/mililitro de agua; si es necesario, un agente de ajuste del pH para proporcionar un pH de 3.5 a 5.7; si es necesario, un agente de ajuste de tonicidad para proporcionar una osmolaridad de 200 a 400 mOsm; y agua; en donde la composicion es estable durante cuando menos 2 meses. Reivindicacion 38: Un método para la preparacion de una solucion super- saturada de pazopanib, comprendiendo este método: 5 formar una solucion acuosa de una sal de adicion de ácido de pazopanib y una ciclodextrina modificada adecuada para utilizarse en una formulacion oftálmica; y ajustar el pH de la solucion entre 3.5 a 5.7, para obtener una solucion super-saturada de pazopanib, en donde la lo concentracion de la sal de adicion de ácido de pazopanib solubilizada en la solucion super-saturada es equivalente a aproximadamente 10 miligramos/mililitro de la base libre de pazopanib.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US33171510P | 2010-05-05 | 2010-05-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR081364A1 true AR081364A1 (es) | 2012-08-29 |
Family
ID=44851507
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP110101514A AR081364A1 (es) | 2010-05-05 | 2011-05-03 | Composiciones farmaceuticas de pazopanib y metodos para su elaboracion |
Country Status (26)
Country | Link |
---|---|
US (3) | US20120028918A1 (es) |
EP (1) | EP2566331B1 (es) |
JP (1) | JP5835717B2 (es) |
KR (1) | KR20130071434A (es) |
CN (1) | CN102970871A (es) |
AR (1) | AR081364A1 (es) |
AU (1) | AU2011247995B2 (es) |
BR (1) | BR112012028291A2 (es) |
CA (1) | CA2798386A1 (es) |
CL (1) | CL2012003075A1 (es) |
CO (1) | CO6640262A2 (es) |
CR (1) | CR20120556A (es) |
DO (1) | DOP2012000281A (es) |
EA (1) | EA201291168A1 (es) |
ES (1) | ES2519615T3 (es) |
HK (1) | HK1175947A1 (es) |
IL (1) | IL222751A0 (es) |
MA (1) | MA34286B1 (es) |
MX (1) | MX2012012837A (es) |
NZ (1) | NZ603411A (es) |
PE (1) | PE20130217A1 (es) |
SG (1) | SG185087A1 (es) |
TW (1) | TW201206908A (es) |
UY (1) | UY33367A (es) |
WO (1) | WO2011140343A1 (es) |
ZA (1) | ZA201208265B (es) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070020299A1 (en) | 2003-12-31 | 2007-01-25 | Pipkin James D | Inhalant formulation containing sulfoalkyl ether cyclodextrin and corticosteroid |
ES2493641T3 (es) * | 2007-06-28 | 2014-09-12 | Cydex Pharmaceuticals, Inc. | Administración nasal de soluciones acuosas de corticosteroides |
US8623395B2 (en) | 2010-01-29 | 2014-01-07 | Forsight Vision4, Inc. | Implantable therapeutic device |
WO2013022801A1 (en) | 2011-08-05 | 2013-02-14 | Forsight Vision4, Inc. | Small molecule delivery with implantable therapeutic device |
TW201206908A (en) * | 2010-05-05 | 2012-02-16 | Glaxo Wellcome Mfg Pte Ltd | Pharmaceutical compositions and methods of making same |
PT2600930T (pt) | 2010-08-05 | 2021-03-22 | Forsight Vision4 Inc | Aparelho injetor e método para distribuição de fármacos |
WO2012068549A2 (en) | 2010-11-19 | 2012-05-24 | Forsight Vision4, Inc. | Therapeutic agent formulations for implanted devices |
EP3903733A1 (en) | 2011-09-16 | 2021-11-03 | ForSight Vision4, Inc. | Fluid exchange apparatus |
JP2015507020A (ja) * | 2012-02-17 | 2015-03-05 | ファーマサイクリックス,インク. | ヒストンデアセチラーゼ阻害剤とパゾパニブの組み合わせおよびその使用 |
EP3509387B1 (en) * | 2012-03-08 | 2021-07-28 | Samsung Electronics Co., Ltd. | Method for controlling services in wireless communication system |
US9968603B2 (en) | 2013-03-14 | 2018-05-15 | Forsight Vision4, Inc. | Systems for sustained intraocular delivery of low solubility compounds from a port delivery system implant |
US11136625B2 (en) | 2013-08-28 | 2021-10-05 | Crown Bioscience, Inc. (Taicang) | Gene expression signatures predictive of subject response to a multi-kinase inhibitor and methods of using the same |
AU2015301054B2 (en) | 2014-08-08 | 2020-05-14 | Forsight Vision4, Inc. | Stable and soluble formulations of receptor tyrosine kinase inhibitors, and methods of preparation thereof |
AU2015346450B2 (en) | 2014-11-10 | 2020-01-30 | Forsight Vision4, Inc. | Expandable drug delivery devices and method of use |
US11129900B2 (en) | 2014-12-25 | 2021-09-28 | Kyoto University | Cytophilic peptide-fused high-density lipoprotein, and delivery of drug to posterior segment of eye by ocular installation of said fusion |
ES2837524T3 (es) | 2016-04-05 | 2021-06-30 | Forsight Vision4 Inc | Dispositivos de administración de fármacos oculares implantables |
CN110769853B (zh) * | 2017-04-17 | 2022-06-03 | 北京生命科学研究所 | 治疗雄性衰老 |
WO2019028104A1 (en) * | 2017-08-02 | 2019-02-07 | Alphala Co., Ltd. | NOVEL COMPOUND AND PHARMACEUTICAL COMPOSITION CONTAINING THE SAME |
MX2020013238A (es) * | 2018-06-07 | 2021-02-22 | Pfizer | Formulacion acuosa que comprende 1-(4-{[4-(dimetilamino)piperidin- 1-il]carbonil}fenil)-3-[4-(4,6-dimorfolin-4-il-1,3,5-triazin-2-il )fenil]urea. |
CN113350351A (zh) * | 2020-03-13 | 2021-09-07 | 青晓制药公司 | 帕唑帕尼的应用、药物组合物、注射液及制备方法和应用 |
US20240050429A1 (en) * | 2022-08-10 | 2024-02-15 | Qx Therapeutics, Inc. | Pazopanib pharmaceutical composition, injection and preparation method and use thereof |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE8904296D0 (sv) * | 1989-12-21 | 1989-12-21 | Pharmacia Ab | Transdermal system |
US7893040B2 (en) * | 2005-07-22 | 2011-02-22 | Oculis Ehf | Cyclodextrin nanotechnology for ophthalmic drug delivery |
BRPI0619057A2 (pt) * | 2005-11-29 | 2011-09-20 | Smithkline Beecham Corp | formulação farmacêutica de uso tópico, uso de um ou mais compostos, e, compostos |
AR059066A1 (es) * | 2006-01-27 | 2008-03-12 | Amgen Inc | Combinaciones del inhibidor de la angiopoyetina -2 (ang2) y el inhibidor del factor de crecimiento endotelial vascular (vegf) |
CN101484136A (zh) * | 2006-04-18 | 2009-07-15 | Ekr治疗公司 | 预混合的、立即可用的药物组合物 |
CA3105972A1 (en) * | 2007-10-19 | 2009-04-30 | Novartis Ag | Compositions and methods for treatment of diabetic retinopathy |
WO2009097446A1 (en) * | 2008-01-30 | 2009-08-06 | Genentech, Inc. | Pyrazolopyrimidine pi3k inhibitor compounds and methods of use |
BR112012001030A2 (pt) * | 2009-07-16 | 2019-09-24 | Glaxo Wellcome Mfg Pte Ltd | método para tratar a degeneração macular, e, uso de um composto. |
WO2011039648A1 (en) * | 2009-09-30 | 2011-04-07 | Glaxo Wellcome Manufacturing Pte Ltd. | Methods of administration and treatment |
UY33164A (es) * | 2010-01-06 | 2011-08-31 | Glaxo Wellcome Mfg Pte Ltd | Metodo de tratamiento |
US20130023550A1 (en) * | 2010-05-05 | 2013-01-24 | Glaxo Wellcome Manufacturing Pte, Ltd | Pharmaceutical compositions and methods of making same |
TW201206908A (en) * | 2010-05-05 | 2012-02-16 | Glaxo Wellcome Mfg Pte Ltd | Pharmaceutical compositions and methods of making same |
-
2011
- 2011-05-03 TW TW100115488A patent/TW201206908A/zh unknown
- 2011-05-03 UY UY0001033367A patent/UY33367A/es unknown
- 2011-05-03 AR ARP110101514A patent/AR081364A1/es unknown
- 2011-05-05 MX MX2012012837A patent/MX2012012837A/es active IP Right Grant
- 2011-05-05 ES ES11778348.0T patent/ES2519615T3/es active Active
- 2011-05-05 JP JP2013509268A patent/JP5835717B2/ja not_active Expired - Fee Related
- 2011-05-05 AU AU2011247995A patent/AU2011247995B2/en not_active Ceased
- 2011-05-05 CA CA2798386A patent/CA2798386A1/en not_active Abandoned
- 2011-05-05 MA MA35417A patent/MA34286B1/fr unknown
- 2011-05-05 EP EP11778348.0A patent/EP2566331B1/en active Active
- 2011-05-05 CN CN2011800333447A patent/CN102970871A/zh active Pending
- 2011-05-05 BR BR112012028291A patent/BR112012028291A2/pt not_active IP Right Cessation
- 2011-05-05 SG SG2012079968A patent/SG185087A1/en unknown
- 2011-05-05 EA EA201291168A patent/EA201291168A1/ru unknown
- 2011-05-05 US US13/133,030 patent/US20120028918A1/en not_active Abandoned
- 2011-05-05 KR KR1020127031739A patent/KR20130071434A/ko not_active Application Discontinuation
- 2011-05-05 WO PCT/US2011/035363 patent/WO2011140343A1/en active Application Filing
- 2011-05-05 NZ NZ603411A patent/NZ603411A/en not_active IP Right Cessation
- 2011-05-05 US US13/101,689 patent/US20110281901A1/en not_active Abandoned
- 2011-05-05 PE PE2012002115A patent/PE20130217A1/es not_active Application Discontinuation
-
2012
- 2012-10-29 IL IL222751A patent/IL222751A0/en unknown
- 2012-10-31 CL CL2012003075A patent/CL2012003075A1/es unknown
- 2012-11-01 CR CR20120556A patent/CR20120556A/es unknown
- 2012-11-02 DO DO2012000281A patent/DOP2012000281A/es unknown
- 2012-11-02 ZA ZA2012/08265A patent/ZA201208265B/en unknown
- 2012-12-05 CO CO12221016A patent/CO6640262A2/es not_active Application Discontinuation
-
2013
- 2013-03-14 HK HK13103191.6A patent/HK1175947A1/xx not_active IP Right Cessation
-
2015
- 2015-05-06 US US14/705,298 patent/US20150231265A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
JP2013525501A (ja) | 2013-06-20 |
JP5835717B2 (ja) | 2015-12-24 |
AU2011247995A1 (en) | 2012-12-13 |
TW201206908A (en) | 2012-02-16 |
HK1175947A1 (en) | 2013-07-19 |
CR20120556A (es) | 2013-02-20 |
KR20130071434A (ko) | 2013-06-28 |
EP2566331A1 (en) | 2013-03-13 |
DOP2012000281A (es) | 2013-05-31 |
US20110281901A1 (en) | 2011-11-17 |
MA34286B1 (fr) | 2013-06-01 |
US20120028918A1 (en) | 2012-02-02 |
MX2012012837A (es) | 2013-01-24 |
AU2011247995B2 (en) | 2014-07-31 |
ES2519615T3 (es) | 2014-11-07 |
EP2566331A4 (en) | 2013-09-18 |
EA201291168A1 (ru) | 2013-06-28 |
NZ603411A (en) | 2014-10-31 |
UY33367A (es) | 2011-10-31 |
ZA201208265B (en) | 2013-07-31 |
EP2566331B1 (en) | 2014-09-03 |
US20150231265A1 (en) | 2015-08-20 |
PE20130217A1 (es) | 2013-03-21 |
CL2012003075A1 (es) | 2013-03-08 |
CO6640262A2 (es) | 2013-03-22 |
IL222751A0 (en) | 2012-12-31 |
BR112012028291A2 (pt) | 2015-09-15 |
WO2011140343A1 (en) | 2011-11-10 |
CN102970871A (zh) | 2013-03-13 |
SG185087A1 (en) | 2012-12-28 |
CA2798386A1 (en) | 2011-11-10 |
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