PE20091032A1 - Composicion que contiene n-(3-metoxi-5-metilpirazin-2-il)-2-(4-[1,3,4-oxadiazol-2-il]fenil)piridin-3-sulfonamida (zibotentan) - Google Patents
Composicion que contiene n-(3-metoxi-5-metilpirazin-2-il)-2-(4-[1,3,4-oxadiazol-2-il]fenil)piridin-3-sulfonamida (zibotentan)Info
- Publication number
- PE20091032A1 PE20091032A1 PE2008001750A PE2008001750A PE20091032A1 PE 20091032 A1 PE20091032 A1 PE 20091032A1 PE 2008001750 A PE2008001750 A PE 2008001750A PE 2008001750 A PE2008001750 A PE 2008001750A PE 20091032 A1 PE20091032 A1 PE 20091032A1
- Authority
- PE
- Peru
- Prior art keywords
- zibotentan
- methylpyrazin
- oxadiazol
- sulfonamide
- pyridin
- Prior art date
Links
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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
-
- 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
-
- 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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- 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
- 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
-
- 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
- A61K9/1617—Organic compounds, e.g. phospholipids, fats
- A61K9/1623—Sugars or sugar alcohols, e.g. lactose; Derivatives thereof; Homeopathic globules
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
REFERIDA A UNA COMPOSICION FARMACEUTICA QUE CONTIENE N-(3-METOXI-5-METILPIRAZIN-2-IL)-2-(4-[1,3,4-OXADIAZOL-2-IL]FENIL)PIRIDIN-3-SULFONAMIDA (I) (ZIBOTENTAN) EN UNA CANTIDAD DE 2 A 20% EN PESO, MANITOL EN UNA CANTIDAD DE 65% A 75% EN PESO Y/O CELULOSA MICROCRISTALINA EN UNA CANTIDAD DE 10% A 15% EN PESO. TAMBIEN CONTIENE UNO O MAS AGLUTINANTES TAL COMO POVIDONA, UNO O MAS DESINTEGRANTES TAL COMO CROSCAMELOSA SODICA. EL COMPUESTO ZIBOTENTAN ES UN ANTAGONISTA DE LA ENDOTELINA Y ES UTIL EN EL TRATAMIENTO DEL CANCER
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US97973607P | 2007-10-12 | 2007-10-12 | |
US8911808P | 2008-08-15 | 2008-08-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20091032A1 true PE20091032A1 (es) | 2009-08-15 |
Family
ID=40534840
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2008001750A PE20091032A1 (es) | 2007-10-12 | 2008-10-10 | Composicion que contiene n-(3-metoxi-5-metilpirazin-2-il)-2-(4-[1,3,4-oxadiazol-2-il]fenil)piridin-3-sulfonamida (zibotentan) |
Country Status (35)
Country | Link |
---|---|
US (2) | US8168221B2 (es) |
EP (2) | EP2433620A1 (es) |
JP (1) | JP2011500548A (es) |
KR (1) | KR20100099113A (es) |
CN (1) | CN101896210A (es) |
AR (1) | AR068845A1 (es) |
AT (1) | ATE536893T1 (es) |
AU (1) | AU2008309385B2 (es) |
BR (1) | BRPI0818323A2 (es) |
CA (1) | CA2701385A1 (es) |
CL (1) | CL2008003022A1 (es) |
CO (1) | CO6270344A2 (es) |
CR (1) | CR11363A (es) |
CU (1) | CU20100064A7 (es) |
CY (1) | CY1112433T1 (es) |
DK (1) | DK2209501T3 (es) |
DO (1) | DOP2010000105A (es) |
EA (1) | EA201000545A1 (es) |
ES (1) | ES2377426T3 (es) |
HK (1) | HK1143095A1 (es) |
HR (1) | HRP20120085T1 (es) |
IL (1) | IL204953A0 (es) |
MX (1) | MX2010003989A (es) |
NI (1) | NI201000052A (es) |
NZ (1) | NZ585310A (es) |
PE (1) | PE20091032A1 (es) |
PL (1) | PL2209501T3 (es) |
PT (1) | PT2209501E (es) |
SG (1) | SG182138A1 (es) |
SI (1) | SI2209501T1 (es) |
SV (1) | SV2010003529A (es) |
TW (1) | TW200924768A (es) |
UY (1) | UY31385A1 (es) |
WO (1) | WO2009047565A2 (es) |
ZA (1) | ZA201002477B (es) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1816527A (zh) | 2003-06-06 | 2006-08-09 | 菲布罗根有限公司 | 含氮杂芳基化合物及其在增加内源性促红细胞生成素中的用途 |
WO2009047565A2 (en) | 2007-10-12 | 2009-04-16 | Astrazeneca Ab | Composition 064 |
CN101822796B (zh) * | 2010-03-17 | 2012-01-04 | 山西仟源制药有限公司 | 一种银冰含片及制备方法和应用 |
US9492395B2 (en) * | 2010-05-11 | 2016-11-15 | Sensient Colors Llc | Film coating composition and methods of making and using the same |
JO3753B1 (ar) * | 2011-10-14 | 2021-01-31 | Otsuka Pharma Co Ltd | قرص يتألف من 7-[4-(4-بينزو[بي]ثيوفين-4-ايل-ببرازين-1-1ايل)بوتكسيل]-1اتش-كوينولين-2-وان أو ملح منه |
MX369549B (es) * | 2012-04-27 | 2019-11-12 | Merck Patent Gmbh | Un proceso para la fabricación de núcleos de tabletas duros con recubrimiento. |
LT3470397T (lt) | 2012-07-16 | 2022-02-25 | Fibrogen, Inc. | Prolilo hidroksilazės inhibitoriaus kristalinės formos |
US8883823B2 (en) | 2012-07-16 | 2014-11-11 | Fibrogen, Inc. | Crystalline forms of a prolyl hydroxylase inhibitor |
SMT202000190T1 (it) | 2013-06-06 | 2020-05-08 | Fibrogen Inc | Formulazioni farmaceutiche di un inibitore di hif-idrossilasi |
TW202203971A (zh) * | 2020-03-31 | 2022-02-01 | 日商衛材R&D企管股份有限公司 | 錠劑、醫藥及其等之製造方法以及套組 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3674794A (en) * | 1970-03-18 | 1972-07-04 | Ciba Geigy Corp | Certain-3-pyridine-sulfonamide derivatives |
UA58494C2 (uk) * | 1995-06-07 | 2003-08-15 | Зенека Лімітед | Похідні n-гетероарилпіридинсульфонаміду, фармацевтична композиція, спосіб одержання та спосіб протидії впливам ендотеліну |
CN1179961C (zh) * | 1997-04-28 | 2004-12-15 | 安瑟希夫制药公司 | 用于治疗内皮肽介导之疾病的磺酰胺 |
US5783705A (en) * | 1997-04-28 | 1998-07-21 | Texas Biotechnology Corporation | Process of preparing alkali metal salys of hydrophobic sulfonamides |
JP2001058944A (ja) * | 1999-06-18 | 2001-03-06 | Takeda Chem Ind Ltd | 速崩壊性固形製剤 |
CA2374760A1 (en) * | 1999-06-18 | 2000-12-28 | Takeda Chemical Industries, Ltd. | Quickly disintegrating solid preparations |
CN1615135A (zh) | 2001-11-13 | 2005-05-11 | 法马西亚公司 | 磺酰胺前药如帕瑞考昔的口服剂型 |
GB0219660D0 (en) * | 2002-08-23 | 2002-10-02 | Astrazeneca Ab | Therapeutic use |
WO2004026233A2 (en) * | 2002-09-20 | 2004-04-01 | Merck & Co., Inc. | Mannitol formulation for integrin receptor antagonist |
GB0223854D0 (en) | 2002-10-12 | 2002-11-20 | Astrazeneca Ab | Therapeutic treatment |
GB0320806D0 (en) | 2003-09-05 | 2003-10-08 | Astrazeneca Ab | Therapeutic treatment |
US7772232B2 (en) | 2004-04-15 | 2010-08-10 | Bristol-Myers Squibb Company | Quinazolinyl compounds as inhibitors of potassium channel function |
GB0425854D0 (en) | 2004-11-25 | 2004-12-29 | Astrazeneca Ab | Therapeutic treatment |
CN101032464A (zh) * | 2007-04-01 | 2007-09-12 | 杨喜鸿 | 含有利莫那班和聚乙烯吡咯烷酮的组合物、固体分散体及其制备和药物应用 |
WO2009047565A2 (en) | 2007-10-12 | 2009-04-16 | Astrazeneca Ab | Composition 064 |
-
2008
- 2008-10-09 WO PCT/GB2008/050928 patent/WO2009047565A2/en active Application Filing
- 2008-10-09 ES ES08806744T patent/ES2377426T3/es active Active
- 2008-10-09 DK DK08806744.2T patent/DK2209501T3/da active
- 2008-10-09 EP EP11187017A patent/EP2433620A1/en not_active Withdrawn
- 2008-10-09 MX MX2010003989A patent/MX2010003989A/es active IP Right Grant
- 2008-10-09 PT PT08806744T patent/PT2209501E/pt unknown
- 2008-10-09 TW TW097139020A patent/TW200924768A/zh unknown
- 2008-10-09 AT AT08806744T patent/ATE536893T1/de active
- 2008-10-09 CN CN2008801210391A patent/CN101896210A/zh active Pending
- 2008-10-09 NZ NZ585310A patent/NZ585310A/en not_active IP Right Cessation
- 2008-10-09 PL PL08806744T patent/PL2209501T3/pl unknown
- 2008-10-09 SI SI200830529T patent/SI2209501T1/sl unknown
- 2008-10-09 EA EA201000545A patent/EA201000545A1/ru unknown
- 2008-10-09 AU AU2008309385A patent/AU2008309385B2/en not_active Ceased
- 2008-10-09 CA CA2701385A patent/CA2701385A1/en not_active Abandoned
- 2008-10-09 EP EP08806744A patent/EP2209501B1/en not_active Not-in-force
- 2008-10-09 JP JP2010528486A patent/JP2011500548A/ja active Pending
- 2008-10-09 BR BRPI0818323A patent/BRPI0818323A2/pt not_active IP Right Cessation
- 2008-10-09 SG SG2012039327A patent/SG182138A1/en unknown
- 2008-10-09 KR KR1020107010484A patent/KR20100099113A/ko not_active Withdrawn
- 2008-10-10 CL CL2008003022A patent/CL2008003022A1/es unknown
- 2008-10-10 UY UY31385A patent/UY31385A1/es not_active Application Discontinuation
- 2008-10-10 US US12/249,157 patent/US8168221B2/en not_active Expired - Fee Related
- 2008-10-10 AR ARP080104448A patent/AR068845A1/es not_active Application Discontinuation
- 2008-10-10 PE PE2008001750A patent/PE20091032A1/es not_active Application Discontinuation
-
2010
- 2010-04-08 ZA ZA2010/02477A patent/ZA201002477B/en unknown
- 2010-04-08 IL IL204953A patent/IL204953A0/en unknown
- 2010-04-12 CU CU20100064A patent/CU20100064A7/es unknown
- 2010-04-12 SV SV2010003529A patent/SV2010003529A/es not_active Application Discontinuation
- 2010-04-12 DO DO2010000105A patent/DOP2010000105A/es unknown
- 2010-04-12 CR CR11363A patent/CR11363A/es not_active Application Discontinuation
- 2010-04-12 NI NI201000052A patent/NI201000052A/es unknown
- 2010-05-07 CO CO10054830A patent/CO6270344A2/es not_active Application Discontinuation
- 2010-10-13 HK HK10109702.8A patent/HK1143095A1/xx not_active IP Right Cessation
-
2012
- 2012-01-24 HR HR20120085T patent/HRP20120085T1/hr unknown
- 2012-02-09 CY CY20121100136T patent/CY1112433T1/el unknown
- 2012-03-21 US US13/425,474 patent/US20120177705A1/en not_active Abandoned
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20091032A1 (es) | Composicion que contiene n-(3-metoxi-5-metilpirazin-2-il)-2-(4-[1,3,4-oxadiazol-2-il]fenil)piridin-3-sulfonamida (zibotentan) | |
CL2009000394A1 (es) | Compuestos derivados de n-(1h-indazol-5-il)pirrolidin-3-carboxamida sustituida, inhibidores de erk; composicion farmaceutica; y su uso en el tratamiento del cancer. | |
CL2011002706A1 (es) | Compuestos derivados de 4-(1,3-oxazol-2-il)-1h-indazol; composicion farmaceutica que los comprende; y sus usos en el tratamiento de enfermedades tales como epoc, autoinmunes, asma, entre otras. | |
AR112074A2 (es) | Derivados de 2-carboxamida-cicloamino-urea como inhibidores de pi-3 | |
PE20141682A1 (es) | Derivados de (4-fenilimidazol-2-il) etilamina utiles como moduladores de canal de sodio | |
PE20211700A1 (es) | Compuesto heterociclico y su uso | |
UY32547A (es) | Piperidinas sustituidas como antagonistas de ccr3 | |
UY32884A (es) | 1-sustituido-4-(5-(fenil o heteroaril)metoxi)-pirimidin-2-il)piperazinas y piperidinas | |
CR9214A (es) | 2-fenilindoles como antagonistas del receptor de la prostaglandina d2 | |
CR11683A (es) | Piridinas y pirazinas como inhibidores de p13k | |
PE20110298A1 (es) | Derivados de picolinamida como inhibidores de cinasa | |
PE20140105A1 (es) | Analogos deuterados de pridopidina utiles como estabilizadores dopaminergicos | |
ATE482210T1 (de) | Oxadiazolderivate als s1p1-rezeptor-agonisten | |
PE20141855A1 (es) | Benzotienilo-pirrolotriazinas disustituidas y sus usos | |
PE20090772A1 (es) | Derivados de bencimidazol | |
CO6541569A2 (es) | Inhibidores de n1-pirazoloespirocetona acetil-coa carboxilasa | |
CL2011001224A1 (es) | Compuestos derivados de benzofurano-3-carboxamida; composicion farmaceutica que los comprende; y su uso en tratamiento del virus de la hepatitis c. | |
CL2009001058A1 (es) | Compuestos derivados de oxazinas sustituidas, inhibidores de la 11b-hidroxiesteroide deshidrogenasa de tipo-1; composicion farmaceutica; y uso del compuesto para inhibir la actividad de 11b-hsd1, como en el tratamiento de la diabetes, dislipidemia, hipertension, obesidad, cancer, glaucoma, entre otras. | |
CL2011001082A1 (es) | Compuestos derivados de amino-tetrahidropiranos sustituidos con heterociclos, composicion farmaceutica; y uso en el tratamiento de una afeccion seleccionada de resistencia a la insulina, hiperglicemia y diabetes de tipo 2. | |
CL2011002115A1 (es) | Compuestos derivados de 5-fenil-1h-piridin-2-ona y 5-fenil-pirazin-2-ona, inhibidores de la tirosina-quinasa de bruton (btk); proceso de preparación de los compuestos, compuesto intermediario, composición farmacéutica y uso en el tratamiento de enfermedades inflamatorias y/o autoinmunes. | |
PE20130340A1 (es) | (r)-n-(3-(7-metil-1h-indazol-5-il)-1-(4-metilpiperidin-4-il)piperazin-1-il)-1-oxopropan-2-il)-4-(2-oxo-1,2-dihidroquinolin-3-il)piperidina-1-carboxamida como antagonista del receptor de peptido relacionado con el gen de la calcitonina (cgrp) | |
EA201071040A1 (ru) | Новые производные 1-бензил-3-гидроксиметилиндазола и их применение при лечении заболеваний, обусловленных экспрессией mcp-1, cx3cr1 и p40 | |
CL2009000368A1 (es) | 3-(amido o sulfamido)-4-(4-azinil sustituido) benzamidas o benzosulfonamidas; la composicion farmaceutica que los contiene; el uso de los compuestos; y un kit que contiene dichos compeustos; utiles como inhibidores del receptor de quimioquinas cxcr3. | |
PE20142318A1 (es) | Formulaciones de (+)-2-[1-(3-etoxi-4-metoxi-fenil)-2-metansulfonil-etil]-4-acetilaminoisoindolin-1,3-diona | |
GEP20135927B (en) | 1-benzyl-3-hydroxymethylindaz-ole derivatives and usage thereat treatment of diseases based on mcp-1, cx3cr1 and p40 expression |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant, registration | ||
FD | Application declared void or lapsed |