AR128483A2 - Formas sólidas de ácido {[5-(3-clorofenil)-3-hidroxipiridin-2-carbonil]amino}acético, sus composiciones y usos - Google Patents
Formas sólidas de ácido {[5-(3-clorofenil)-3-hidroxipiridin-2-carbonil]amino}acético, sus composiciones y usosInfo
- Publication number
- AR128483A2 AR128483A2 ARP230100302A ARP230100302A AR128483A2 AR 128483 A2 AR128483 A2 AR 128483A2 AR P230100302 A ARP230100302 A AR P230100302A AR P230100302 A ARP230100302 A AR P230100302A AR 128483 A2 AR128483 A2 AR 128483A2
- Authority
- AR
- Argentina
- Prior art keywords
- compound
- crystalline compound
- solid forms
- crystalline
- hydroxypyridin
- Prior art date
Links
- 239000007787 solid Substances 0.000 title abstract 4
- JGRXMPYUTJLTKT-UHFFFAOYSA-N 2-[[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino]acetic acid Chemical compound C1=C(O)C(C(=O)NCC(=O)O)=NC=C1C1=CC=CC(Cl)=C1 JGRXMPYUTJLTKT-UHFFFAOYSA-N 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 12
- 238000000034 method Methods 0.000 abstract 3
- 239000013078 crystal Substances 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 238000000634 powder X-ray diffraction Methods 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D495/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4418—Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
-
- 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
-
- 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
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4866—Organic macromolecular compounds
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
- C07D213/803—Processes of preparation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
Formas sólidas que comprenden el ácido {[5-(3-clorofenil)-3-hidroxipiridin-2-carbonil]amino}acético, las composiciones que comprenden las formas sólidas, los métodos de elaboración de las formas sólidas y los métodos de uso para el tratamiento de diversas enfermedades o trastornos. Reivindicación 1: Un compuesto cristalino (I) caracterizado porque tiene la fórmula: (1), que tiene un patrón de difracción de polvos por rayos X que comprende uno, dos, tres, cuatro o cinco picos a alrededor de 18,1, 20,3, 22,9, 24,0, y 26,3º 2q; y en donde el compuesto cristalino (I) está de manera considerable libre de cualquier otro compuesto cristalino (I). Reivindicación 26: Una composición farmacéutica caracterizada porque comprende un compuesto cristalino de una cualquiera de las reivindicaciones 1 a 25. Reivindicación 32: Un método para la elaboración de un compuesto cristalino (I), caracterizado porque comprende, a) la preparación de una solución del compuesto (I) en un solvente orgánico; b) el cambio de la condición de la solución hasta sobresaturación para provocar la formación de cristales; y c) la separación de los cristales; en donde el compuesto cristalino (I) está de manera considerable libre de cualquier forma cristalina del compuesto (I); o en donde el compuesto cristalino (I), está de manera considerable libre de un compuesto de fórmula (2); determinado por CG / EM; o en donde el compuesto cristalino (I), está de manera considerable libre de compuesto (I) amorfo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361904803P | 2013-11-15 | 2013-11-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR128483A2 true AR128483A2 (es) | 2024-05-15 |
Family
ID=53058045
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP140104298A AR099354A1 (es) | 2013-11-15 | 2014-11-14 | Formas sólidas de ácido {[5-(3-clorofenil)-3-hidroxipiridin-2-carbonil]amino}acético, composiciones, y sus usos |
ARP230100302A AR128483A2 (es) | 2013-11-15 | 2023-02-08 | Formas sólidas de ácido {[5-(3-clorofenil)-3-hidroxipiridin-2-carbonil]amino}acético, sus composiciones y usos |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP140104298A AR099354A1 (es) | 2013-11-15 | 2014-11-14 | Formas sólidas de ácido {[5-(3-clorofenil)-3-hidroxipiridin-2-carbonil]amino}acético, composiciones, y sus usos |
Country Status (24)
Country | Link |
---|---|
US (7) | US9701636B2 (es) |
EP (2) | EP3068394A4 (es) |
JP (4) | JP2016537365A (es) |
KR (2) | KR102381295B1 (es) |
CN (2) | CN114890943A (es) |
AR (2) | AR099354A1 (es) |
AU (4) | AU2014348523B2 (es) |
BR (1) | BR112016011065B1 (es) |
CA (1) | CA2930128A1 (es) |
CL (1) | CL2016001150A1 (es) |
CR (2) | CR20200220A (es) |
DO (1) | DOP2016000109A (es) |
IL (2) | IL245634A0 (es) |
MA (1) | MA39033A1 (es) |
MX (3) | MX2021001169A (es) |
MY (1) | MY180626A (es) |
PE (1) | PE20160945A1 (es) |
PH (1) | PH12016500866A1 (es) |
RU (2) | RU2016123382A (es) |
SA (1) | SA516371129B1 (es) |
SG (2) | SG10202012791TA (es) |
TW (4) | TWI788702B (es) |
WO (1) | WO2015073779A1 (es) |
ZA (2) | ZA201603189B (es) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PT3357911T (pt) | 2006-06-26 | 2022-07-11 | Akebia Therapeutics Inc | Inibidores da prolil-hidroxilase e métodos de utilização |
NO2686520T3 (es) | 2011-06-06 | 2018-03-17 | ||
ES2974273T3 (es) | 2013-06-13 | 2024-06-26 | Akebia Therapeutics Inc | Composiciones y métodos para tratar la anemia |
KR102381295B1 (ko) | 2013-11-15 | 2022-03-31 | 아케비아 테라퓨틱스 인코포레이티드 | {[5-(3-클로로페닐)-3-하이드록시피리딘-2-카보닐]아미노}아세트산의 고체형, 이의 조성물 및 용도 |
CA2937349A1 (en) * | 2014-01-23 | 2015-07-30 | Akebia Therapeutics, Inc. | Compositions and methods for treating ocular diseases |
JP2018502882A (ja) | 2015-01-23 | 2018-02-01 | アケビア セラピューティクス インコーポレイテッドAkebia Therapeutics Inc. | 2−(5−(3−フルオロフェニル)−3−ヒドロキシピコリンアミド)酢酸の固体形態、その組成物及び使用 |
PL3277270T3 (pl) | 2015-04-01 | 2022-02-14 | Akebia Therapeutics, Inc. | Kompozycje i sposoby leczenia niedokrwistości |
CN105837502A (zh) * | 2016-04-05 | 2016-08-10 | 湖南欧亚生物有限公司 | 一种Vadadustat的合成方法 |
MX2019006883A (es) * | 2016-12-13 | 2019-10-21 | Crystal Pharmaceutical Suzhou Co Ltd | Formas cristalinas novedosas de ácido {[5-(3-clorofenil)-3-idroxip iridina-2-carbonilo] amino} acético y procedimientos para la preparación del mismo. |
WO2019028150A1 (en) * | 2017-08-01 | 2019-02-07 | Akebia Therapeutics, Inc. | COMPOSITIONS FOR USE IN METHODS OF TREATING HEMOGLOBINOPATHIES |
CA3097219A1 (en) | 2018-05-09 | 2019-11-14 | Akebia Therapeutics, Inc. | Process for preparing 2-[[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino]acetic acid |
WO2020075199A1 (en) | 2018-10-12 | 2020-04-16 | Mylan Laboratories Limited | Polymorphic forms of vadadustat |
US11970450B2 (en) | 2018-11-28 | 2024-04-30 | Sandoz Ag | Multi-component crystals of an orally available HIF prolyl hydroxylase inhibitor |
US11524939B2 (en) | 2019-11-13 | 2022-12-13 | Akebia Therapeutics, Inc. | Solid forms of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino} acetic acid |
IT202000014116A1 (it) | 2020-06-12 | 2021-12-12 | Olon Spa | Nuovo composto cristallino di vadadustat |
WO2021257800A1 (en) * | 2020-06-19 | 2021-12-23 | Akebia Therapeutics, Inc. | Modulation of drug-drug interactions of vadadustat |
GB202011431D0 (en) * | 2020-07-23 | 2020-09-09 | Johnson Matthey Plc | Polymorphs of vadadustat and methods for preparing the polymorphs |
CN115996720A (zh) * | 2020-09-04 | 2023-04-21 | 广东东阳光药业有限公司 | 一种低氧诱导因子脯氨酰羟化酶抑制剂的晶型及其制备方法 |
JP2024503377A (ja) | 2021-01-08 | 2024-01-25 | アケビア セラピューティクス インコーポレイテッド | バダデュスタットを使用した治療方法 |
WO2022179967A1 (en) | 2021-02-23 | 2022-09-01 | Glaxosmithkline Intellectual Property (No.2) Limited | Vadadustat for treating covid-19 in a hospitalized subject |
WO2022187142A1 (en) * | 2021-03-01 | 2022-09-09 | Akebia Therapeutics, Inc. | Modulation of drug-drug interactions of vadadustat |
Family Cites Families (194)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3894920A (en) | 1971-12-21 | 1975-07-15 | Sagami Chem Res | Process for preparing alkyl-substituted 3,6-dihydro-o-dioxin derivatives |
US4016287A (en) | 1972-07-17 | 1977-04-05 | Boehringer Ingelheim Gmbh | Dermatological compositions containing an acylamino-carboxylic acid or an alkyl ester thereof |
BR8807740A (pt) | 1988-07-25 | 1990-10-16 | V Kurgansky Nauchny Ts Vosstan | Aparelho de tracao para reconstrucao plastica da mao |
TW219933B (es) | 1990-02-26 | 1994-02-01 | Lilly Co Eli | |
US5405613A (en) | 1991-12-11 | 1995-04-11 | Creative Nutrition Canada Corp. | Vitamin/mineral composition |
TW352384B (en) | 1992-03-24 | 1999-02-11 | Hoechst Ag | Sulfonamido- or sulfonamidocarbonylpyridine-2-carboxamides, process for their preparation and their use as pharmaceuticals |
DE4219158A1 (de) | 1992-06-11 | 1993-12-16 | Thomae Gmbh Dr K | Biphenylderivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
ES2101421T3 (es) | 1993-11-02 | 1997-07-01 | Hoechst Ag | Amidas de acidos carboxilicos heterociclicos sustituidos, su preparacion y su utilizacion como medicamentos. |
EP0650960B1 (de) | 1993-11-02 | 1997-03-05 | Hoechst Aktiengesellschaft | Substituierte heterocyclische Carbonsäureamidester, ihre Herstellung und ihre Verwendung als Arzneimittel |
TW406076B (en) | 1993-12-30 | 2000-09-21 | Hoechst Ag | Substituted heterocyclic carboxamides, their preparation and their use as pharmaceuticals |
DE4410480A1 (de) | 1994-03-25 | 1995-09-28 | Hoechst Ag | Sulfonamidocarbonylpyridin-2-carbonsäureesteramide sowie ihre Pyridin-N-oxide, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
DE4410423A1 (de) | 1994-03-25 | 1995-09-28 | Hoechst Ag | Sulfonamidocarbonylpyridin-2-carbonsäureamide sowie ihre Pyridin-N-oxide, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
IL135495A (en) | 1995-09-28 | 2002-12-01 | Hoechst Ag | Intermediate compounds for the preparation of quinoline-converted amines - 2 - carboxylic acid |
JPH09221476A (ja) | 1995-12-15 | 1997-08-26 | Otsuka Pharmaceut Co Ltd | 医薬組成物 |
CA2253282A1 (en) | 1996-04-30 | 1997-11-06 | Hoechst Aktiengesellschaft | 3-alkoxypyridine-2-carboxylic acid amide esters, their preparation and their use as drugs |
DE19620041A1 (de) | 1996-05-17 | 1998-01-29 | Merck Patent Gmbh | Adhäsionsrezeptor-Antagonisten |
DE19650215A1 (de) | 1996-12-04 | 1998-06-10 | Hoechst Ag | 3-Hydroxypyridin-2-carbonsäureamidester, ihre Herstellung und ihre Verwendung als Arzneimittel |
CN1282319A (zh) | 1997-10-09 | 2001-01-31 | 小野药品工业株式会社 | 氨基丁酸衍生物 |
DE19746287A1 (de) | 1997-10-20 | 1999-04-22 | Hoechst Marion Roussel De Gmbh | Substituierte Isochinolin-2-Carbonsäureamide, ihre Herstellung und ihre Verwendung als Arzneimittel |
AU757868B2 (en) | 1998-03-23 | 2003-03-06 | Aventis Pharmaceuticals Inc. | Piperididinyl and N-amidinopiperidinyl derivatives |
EP1107974B1 (en) | 1998-08-27 | 2006-08-02 | Teva Pharmaceutical Industries Ltd. | Novel hydrate forms of alendronate sodium, processes for manufacture thereof, and pharmaceutical compositions thereof |
US6500987B1 (en) | 1998-11-27 | 2002-12-31 | Teva Pharmaceutical Industries Ltd. | Sertraline hydrochloride polymorphs |
DE69929462T2 (de) | 1998-11-27 | 2006-09-07 | Teva Pharmaceutical Industries Ltd. | Sertralin hydrochlorid form |
US6159379A (en) | 1999-05-04 | 2000-12-12 | Baker Hughes Incorporated | Organic ammonium salts for the removal of water soluble organics in produced water |
JP2001048786A (ja) | 1999-08-05 | 2001-02-20 | Yamanouchi Pharmaceut Co Ltd | 三環式ヘテロアリール誘導体 |
CZ2002404A3 (cs) | 1999-08-11 | 2002-06-12 | Teva Pharmaceutical Industries Ltd. | Polymorfní formy torsemidu |
EP2206497A1 (en) | 1999-11-17 | 2010-07-14 | Teva Pharmaceutical Industries Ltd. | Polymorphic form of atorvastatin calcium |
AU779306B2 (en) | 1999-12-14 | 2005-01-13 | Teva Gyogyszergyar Reszvenytarsasag | Novel forms of pravastatin sodium |
JP2003517011A (ja) | 1999-12-16 | 2003-05-20 | テバ ファーマシューティカル インダストリーズ リミティド | レフルノミドの新規な製法及び新しい結晶形態 |
WO2001044262A1 (en) | 1999-12-16 | 2001-06-21 | Teva Pharmaceutical Industries Ltd. | Processes for preparing clarithromycin polymorphs and novel polymorph iv |
ES2281374T3 (es) | 1999-12-21 | 2007-10-01 | Teva Pharmaceutical Industries Ltd. | Nuevos polimorfos de hidrocloruro de sertralina, procedimientos para su preparacion, composiciones que los contienen y metodos para su utilizacion. |
CZ20022332A3 (cs) | 2000-01-07 | 2003-01-15 | Transform Pharmaceuticals, Inc. | Sestava vzorků |
SI1280535T1 (es) | 2000-01-11 | 2005-08-31 | Teva Pharma | |
US6589758B1 (en) | 2000-05-19 | 2003-07-08 | Amgen Inc. | Crystal of a kinase-ligand complex and methods of use |
KR100729298B1 (ko) | 2000-07-27 | 2007-06-18 | 테바 파마슈티컬 인더스트리즈 리미티드 | 결정질의 순수한 모다피닐 및 이의 제조 방법 |
AU2002241764A1 (en) | 2000-10-19 | 2002-06-18 | Teva Pharmaceutical Industries Ltd. | Crystalline venlafaxine base and novel polymorphs of venlafaxine hydrochloride, processes for preparing thereof |
US20020183553A1 (en) | 2000-10-19 | 2002-12-05 | Ben-Zion Dolitzky | Crystalline venlafaxine base and novel polymorphs of venlafaxine hydrochloride, processes for preparing thereof |
KR20030042038A (ko) | 2000-10-30 | 2003-05-27 | 테바 파마슈티컬 인더스트리즈 리미티드 | 온단세트론 히드로클로라이드의 신규한 결정 형태 및용매화물 형태와 이들의 제조 방법 |
US6605636B2 (en) | 2000-11-03 | 2003-08-12 | Teva Pharmaceutical Industries Ltd. | Atorvastatin hemi-calcium form VII |
US7501450B2 (en) | 2000-11-30 | 2009-03-10 | Teva Pharaceutical Industries Ltd. | Crystal forms of atorvastatin hemi-calcium and processes for their preparation as well as novel processes for preparing other forms |
IL156055A0 (en) | 2000-11-30 | 2003-12-23 | Teva Pharma | Novel crystal forms of atorvastatin hemi calcium and processes for their preparation as well as novel processes for preparing other forms |
JP2004526706A (ja) | 2001-02-12 | 2004-09-02 | テバ ファーマシューティカル インダストリーズ リミティド | オクスカルバゼピンの新しい結晶形態及びそれらの調製方法 |
US6855510B2 (en) | 2001-03-20 | 2005-02-15 | Dana Farber Cancer Institute, Inc. | Pharmaceuticals and methods for treating hypoxia and screening methods therefor |
US6849718B2 (en) | 2001-03-20 | 2005-02-01 | Dana Farber Cancer Institute, Inc. | Muteins of hypoxia inducible factor alpha and methods of use thereof |
AU2002241154A1 (en) | 2001-03-21 | 2002-10-03 | Isis Innovation Ltd. | Assays, methods and means relating to hypoxia inducible factor (hif) hydroxylase |
WO2002080857A2 (en) | 2001-04-09 | 2002-10-17 | Teva Pharmaceutical Industries Ltd. | Polymorphs of fexofenadine hydrochloride |
SE0101327D0 (sv) | 2001-04-12 | 2001-04-12 | Astrazeneca Ab | New crystalline forms |
JP2005523874A (ja) | 2001-08-01 | 2005-08-11 | テバ ジョジセルジャール レースベニュタールシャシャーグ | N−〔3−(3−シアノピラゾロ〔1,5−a〕ピリミジン−7−イル)フェニル〕−N−エチルアセタミド(ザレプロン)の精製方法、及び当該方法により得られうるザレプロンの結晶型 |
KR100774271B1 (ko) | 2001-09-07 | 2007-11-08 | 테바 파마슈티컬 인더스트리즈 리미티드 | 발라사이클로비르 염산염의 결정질 형태 |
WO2003028664A2 (en) | 2001-10-03 | 2003-04-10 | Teva Pharmaceutical Industries Ltd. | Preparation of levofloxacin and forms thereof |
US6566088B1 (en) | 2001-10-04 | 2003-05-20 | Board Of Regents, The University Of Texas System | Prolyl-4-hydroxylases |
GB0124941D0 (en) | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
CA2465913A1 (en) | 2001-11-08 | 2003-05-15 | Judith Aronhime | Polymorphs of fexofenadine base |
CN1612866A (zh) | 2001-11-14 | 2005-05-04 | 特瓦制药工业有限公司 | 无定形和结晶形的氯沙坦钾及其制备方法 |
AU2002362061A1 (en) | 2001-12-04 | 2003-06-17 | Biogal Gyogyszergyar Rt | Preparation of orlistat and orlistat crystalline forms |
CN102552263A (zh) | 2001-12-06 | 2012-07-11 | 法布罗根股份有限公司 | 提高内源性红细胞生成素(epo)的方法 |
PL370802A1 (en) | 2001-12-18 | 2005-05-30 | Teva Pharmaceutical Industries Ltd. | Polymorphs of clopidogrel hydrogensulfate |
WO2003065975A2 (en) | 2001-12-28 | 2003-08-14 | Biogal Gyogyszergyar Rt | Processes for preparing crystalline and amorphous mupirocin calcium |
CN1298322C (zh) | 2002-01-15 | 2007-02-07 | 特瓦制药工业有限公司 | 卡维地洛的结晶固体及其制备方法 |
CA2475864A1 (en) | 2002-02-15 | 2003-08-28 | Teva Pharmaceutical Industries Ltd. | Novel crystal forms of atorvastatin hemi-calcium and processes for their preparation, as well as novel processes for preparing atorvastatin hemi-calcium forms i, viii and ix |
CA2479668A1 (en) | 2002-03-20 | 2003-10-02 | Teva Pharmaceutical Industries Ltd. | Crystalline forms of quetiapine hemifumarate |
EP1476442A2 (en) | 2002-03-27 | 2004-11-17 | Teva Pharmaceutical Industries Ltd. | Lansoprazole polymorphs and processes for preparation thereof |
JP3803672B2 (ja) | 2002-04-11 | 2006-08-02 | テバ ファーマシューティカル インダストリーズ リミティド | 新規多形及び偽多形 |
EP1499581A1 (en) | 2002-04-29 | 2005-01-26 | Teva Pharmaceutical Industries Ltd. | Process for preparation of polymorphic form ii of sertraline hydrochloride, pharmaceutical formulations and methods of administration thereof |
PL373192A1 (en) | 2002-04-30 | 2005-08-22 | Teva Gyogyszergyar Reszvenytarsasag | Novel crystal forms of ondansetron, processes for their preparation, pharmaceutical compositions containing the novel forms and methods for treating nausea using them |
KR20040106518A (ko) | 2002-05-10 | 2004-12-17 | 테바 파마슈티컬 인더스트리즈 리미티드 | 가티플록사신의 신규한 결정 형태 |
DE03757471T1 (de) | 2002-06-10 | 2005-09-01 | Teva Pharmaceutical Industries Ltd. | Polymorphe form xvi von fexofenadin-hydrochlorid |
CN1674902A (zh) | 2002-06-14 | 2005-09-28 | 特瓦制药工业有限公司 | 新晶型的加替沙星 |
WO2004009532A1 (en) | 2002-07-18 | 2004-01-29 | Teva Pharmaceutical Industries Ltd. | Polymorphic forms of nateglinide |
US7534913B2 (en) | 2002-07-18 | 2009-05-19 | Teva Pharmaceutica Industries Ltd. | Crystalline form of nateglinide |
US20040022764A1 (en) * | 2002-07-31 | 2004-02-05 | Hanan Polansky | Inhibition of microcompetition with a foreign polynucleotide as treatment of chronic disease |
EP1545530A1 (en) | 2002-08-06 | 2005-06-29 | Teva Pharmaceutical Industries Limited | Novel crystalline forms of gatifloxacin |
WO2004018470A2 (en) | 2002-08-26 | 2004-03-04 | Teva Pharmaceutical Industries Ltd. | Crystalline solid famciclovir forms i, ii, iii and preparation thereof |
US20050043329A1 (en) | 2002-09-06 | 2005-02-24 | Shlomit Wizel | Crystalline forms of valacyclovir hydrochloride |
EP1572643A2 (en) | 2002-11-28 | 2005-09-14 | Teva Pharmaceutical Industries Ltd. | Crystalline form f of atorvastatin hemi-calcium salt |
US7618940B2 (en) | 2002-12-06 | 2009-11-17 | Fibrogen, Inc. | Fat regulation |
US8124582B2 (en) | 2002-12-06 | 2012-02-28 | Fibrogen, Inc. | Treatment of diabetes |
WO2004054583A1 (en) | 2002-12-12 | 2004-07-01 | Teva Pharmaceutical Industries Ltd. | Crystalline forms of gatifloxacin and processes for preparation |
US7323459B2 (en) | 2002-12-24 | 2008-01-29 | Teva Pharmaceutical Industries Ltd. | Crystal forms, methods for their preparation and method for preparation of olanzapine |
US20040242619A1 (en) | 2003-03-12 | 2004-12-02 | Toth Zoltan G. | Processes for preparation of polymorphic forms of desloratadine |
EP1601667A2 (en) | 2003-03-12 | 2005-12-07 | Teva Pharmaceutical Industries Limited | Crystalline and amorphous solids of pantoprazole and processes for their preparation |
EP1511739B1 (en) | 2003-03-17 | 2008-04-30 | Teva Pharmaceutical Industries Ltd. | Polymorphs of valsartan |
WO2004103999A1 (en) | 2003-05-15 | 2004-12-02 | TEVA Gyógyszergyár Részvénytársaság | AZTREONAM β POLYMORPH WITH VERY LOW RESIDUAL SOLVENT CONTENT |
EP1638972A2 (en) | 2003-06-02 | 2006-03-29 | Teva Pharmaceutical Industries Limited | Novel crystalline forms of valacyclovir hydrochloride |
EP1546146A1 (en) | 2003-06-03 | 2005-06-29 | Teva Pharmaceutical Industries Limited | POLYMORPHIC FORMS OF ZIPRASIDONE HCl AND PROCESSES FOR THEIR PREPARATION |
PT1644336E (pt) | 2003-06-06 | 2011-04-21 | Fibrogen Inc | Compostos de heteroarilo que contêm azoto e sua utilização no aumento da eritropoetina endógena |
US7368468B2 (en) | 2003-06-18 | 2008-05-06 | Teva Pharmaceutical Industries Ltd. | Fluvastatin sodium crystal forms XIV, LXXIII, LXXIX, LXXX and LXXXVII, processes for preparing them, compositions containing them and methods of using them |
EP1790634A3 (en) | 2003-06-18 | 2007-06-13 | Teva Pharmaceutical Industries Ltd. | Fluvastatin sodium crystal form and processes for preparing it |
GB0314129D0 (en) | 2003-06-18 | 2003-07-23 | Astrazeneca Ab | Therapeutic agents |
EP1567533B1 (en) | 2003-07-03 | 2009-03-11 | Teva Pharmaceutical Industries Ltd. | Zoledronic acid crystal forms, zoledronate sodium salt crystal forms, amorphous zoledronate sodium salt, and processes for their preparation |
WO2005051921A1 (en) | 2003-11-24 | 2005-06-09 | Teva Pharmaceutical Industries Ltd. | Crystalline ammonium salts of rosuvastatin |
ES2374922T3 (es) | 2003-12-16 | 2012-02-23 | Teva Pharmaceutical Industries Ltd. | Procedimientos de preparación de formas cristalinas de aripiprazol. |
WO2005058819A2 (en) | 2003-12-16 | 2005-06-30 | Teva Pharmaceutical Industries Ltd. | Polymorphic forms of tegaserod base and salts thereof |
EP1592688A2 (en) | 2003-12-18 | 2005-11-09 | Teva Pharmaceutical Industries Ltd. | Polymorphic form b2 of ziprasidone base |
EP1708708A1 (en) | 2004-01-30 | 2006-10-11 | Teva Pharmaceutical Industries Ltd. | Montelukast free acid polymorphs |
US20050187244A1 (en) | 2004-01-30 | 2005-08-25 | Entire Interest. | Montelukast sodium polymorphs |
EP1713795A2 (en) | 2004-02-11 | 2006-10-25 | Teva Pharmaceutical Industries Ltd. | Candesartan cilexetil polymorphs |
WO2005108370A1 (ja) | 2004-04-16 | 2005-11-17 | Ajinomoto Co., Inc. | ベンゼン化合物 |
JP2007532687A (ja) | 2004-04-26 | 2007-11-15 | テバ ファーマシューティカル インダストリーズ リミティド | フェキソフェナジン塩酸塩の結晶形およびその製造方法 |
EP1656339A1 (en) | 2004-05-07 | 2006-05-17 | Teva Pharmaceutical Industries Ltd | Polymorphic forms of nateglinide |
WO2005116031A1 (en) | 2004-05-18 | 2005-12-08 | Teva Pharmaceutical Industries Ltd. | Drying process for preparing crystalline solid famciclovir |
CA2556920A1 (en) | 2004-05-20 | 2005-12-01 | Teva Pharmaceutical Fine Chemicals S.R.L. | Levalbuterol hydrochloride polymorph a |
MX2007000087A (es) | 2004-06-23 | 2007-11-06 | Teva Pharma | Acido ibandronico solido y cristalino. |
WO2006004922A1 (en) | 2004-06-29 | 2006-01-12 | Teva Pharmaceutical Industries Ltd. | Crystalline form iv of linezolid |
WO2006025939A1 (en) | 2004-07-01 | 2006-03-09 | Teva Pharmaceutical Industries Ltd. | Crystalline forms of 1,24(s)-dihydroxy vitamin d2 |
CA2573784A1 (en) | 2004-07-20 | 2006-02-02 | Teva Gyogyszergyar Zartkoruen Mukodo Reszvenytarsasag | Crystalline mycophenolate sodium |
JP2007505944A (ja) | 2004-07-22 | 2007-03-15 | テバ ファーマシューティカル インダストリーズ リミティド | アトルバスタチンヘミカルシウム及びその調製の方法 |
CN1976894A (zh) | 2004-07-22 | 2007-06-06 | 特瓦药物精化学品股份有限公司 | 阿托莫西汀盐酸盐的多形体 |
JP4559431B2 (ja) | 2004-08-23 | 2010-10-06 | テバ ファーマシューティカル インダストリーズ リミティド | 固体及び結晶イバンドロネートナトリウム及びその調製方法 |
KR20070052780A (ko) | 2004-09-21 | 2007-05-22 | 테바 파마슈티컬 인더스트리즈 리미티드 | 결정질 클로피도그렐 브롬산염 및 이의 제조 방법 |
JP2008514641A (ja) | 2004-09-28 | 2008-05-08 | テバ ファーマシューティカル インダストリーズ リミティド | 結晶形フェキソフェナジン、およびその調製方法 |
US20060111571A1 (en) | 2004-11-02 | 2006-05-25 | Shlomit Wizel | Tadalafil crystal forms and processes for preparing them |
WO2006050509A2 (en) | 2004-11-03 | 2006-05-11 | Teva Pharmaceutical Industries Ltd. | Amorphous and polymorphic forms of telmisartan sodium |
EP1812428A2 (en) | 2004-11-19 | 2007-08-01 | Teva Pharmaceutical Industries Ltd | Zolmitriptan crystal forms |
CA2584365A1 (en) | 2004-12-01 | 2006-06-08 | Teva Gyogyszergyar Zartkoeruen Mukoedo Reszvenytarsasag | Ascomycin crystalline forms and preparation thereof |
WO2006060808A1 (en) | 2004-12-03 | 2006-06-08 | Teva Pharmaceutical Industries Ltd. | Ezetimibe polymorphs |
EP1836154A1 (en) | 2005-01-11 | 2007-09-26 | Teva Pharmaceutical Fine Chemicals S.R.L. | Polymorphs of memantine hydrochloride |
WO2006081515A2 (en) | 2005-01-27 | 2006-08-03 | Teva Pharmaceutical Industries Ltd. | Duloxetine hydrochloride polymorphs |
US20080213404A1 (en) | 2005-02-04 | 2008-09-04 | Johnson Randall S | Hif Modulating Compounds and Methods of Use Thereof |
EP1866295A2 (en) | 2005-02-24 | 2007-12-19 | Teva Pharmaceutical Industries Ltd | Processes for the preparation of linezolid intermediate |
MX2007010392A (es) | 2005-02-24 | 2007-10-17 | Teva Pharma | Cristales de ladostigil tratrato, metodos de produccion y composiciones farmaceuticas de los mismos. |
US7399871B2 (en) | 2005-03-08 | 2008-07-15 | Teva Pharmaceutical Industries Ltd. | Crystal forms of (S)-(+)-N,N-dimethyl-3-(1-naphthalenyloxy)-3-(2-thienyl)propanamine oxalate and the preparation thereof |
US20060270684A1 (en) | 2005-03-14 | 2006-11-30 | Judith Aronhime | Crystalline forms of ziprasidone mesylate |
MX2007012396A (es) | 2005-04-06 | 2007-11-20 | Teva Pharma | Formas cristalinas de pregabalina. |
DE102005019712A1 (de) | 2005-04-28 | 2006-11-09 | Bayer Healthcare Ag | Dipyridyl-dihydropyrazolone und ihre Verwendung |
CA2604760C (en) | 2005-05-23 | 2012-06-26 | Cadbury Adams Usa Llc | Taste potentiator compositions and beverages containing same |
EP1975150A1 (en) | 2005-05-23 | 2008-10-01 | Teva Pharmaceutical Industries Ltd. | Cinacalcet salts |
WO2006133391A2 (en) | 2005-06-06 | 2006-12-14 | Fibrogen, Inc. | Improved treatment for anemia using a hif-alpha stabilising agent |
EP1893559A2 (en) | 2005-06-09 | 2008-03-05 | Teva Pharmaceutical Industries Ltd | Process for preparation of sertraline hydrochloride form i |
KR20070088507A (ko) | 2005-06-09 | 2007-08-29 | 테바 파마슈티컬 인더스트리즈 리미티드 | 카베딜올의 결정질 형태 및 이것의 제조 방법 |
JP5410751B2 (ja) | 2005-06-15 | 2014-02-05 | ファイブローゲン、インコーポレーテッド | がん治療のための化合物および方法 |
US20070112057A1 (en) | 2005-06-22 | 2007-05-17 | Santiago Ini | Polymorphic forms of tegaserod maleate |
WO2007033216A2 (en) | 2005-09-12 | 2007-03-22 | Beth Israel Deaconess Medical Center | Methods and compositions for the treatment and diagnosis of diseases characterized by vascular leak, hypotension, or a procoagulant state |
WO2007038571A2 (en) | 2005-09-26 | 2007-04-05 | Smithkline Beecham Corporation | Prolyl hydroxylase antagonists |
WO2007038676A2 (en) | 2005-09-28 | 2007-04-05 | Teva Pharmaceutical Industries Ltd. | Polymorphic forms of ladostigil tartrate |
WO2007047194A2 (en) | 2005-10-11 | 2007-04-26 | Dana-Farber Cancer Institute, Inc. | Methods for treating mitf-related disorders |
CN101291911B (zh) | 2005-10-19 | 2014-08-13 | 泰华制药工业有限公司 | 拉奎尼莫钠晶体及其制备方法 |
WO2007053722A2 (en) | 2005-10-31 | 2007-05-10 | Teva Pharmaceutical Industries Ltd. | Crystalline form of cefdinir cesium salt |
WO2007053724A2 (en) | 2005-10-31 | 2007-05-10 | Teva Pharmaceutical Industries Ltd. | Crystalline forms of cefdinir potassium salt |
WO2007059307A2 (en) | 2005-11-15 | 2007-05-24 | Teva Pharmaceutical Industries Ltd. | Crystalline and amorphous forms of telithromycin |
EP1828098A1 (en) | 2005-11-22 | 2007-09-05 | Teva Pharmaceutical Industries Ltd | Crystal forms of cinacalcet hci and processes for their preparation |
ES2446416T3 (es) | 2005-12-09 | 2014-03-07 | Amgen, Inc. | Compuestos basados en quinolona que presentan actividad inhibidora de prolil hidroxilasa, composiciones y usos de los mismos |
EP1966133A2 (en) | 2005-12-13 | 2008-09-10 | Teva Pharmaceutical Industries Ltd. | Crystal form of atorvastatin hemi-calcium and processes for preparation thereof |
WO2007081889A2 (en) | 2006-01-05 | 2007-07-19 | Teva Gyógyszergyár Zártkörüen Müködö Részvénytársaság | Production of dolasetron |
BRPI0706377A2 (pt) | 2006-01-09 | 2011-03-22 | Btg Int Ltd | moduladores de fator -1 induzìvel por hipoxia e usos relacionados |
WO2007082899A1 (en) | 2006-01-17 | 2007-07-26 | Vib Vzw | Inhibitors of prolyl-hydroxylase 1 for the treatment of skeletal muscle degeneration |
WO2007084697A2 (en) | 2006-01-18 | 2007-07-26 | Teva Pharmaceutical Industries Ltd. | Process for preparing a crystalline form of tegaserod maleate |
JP4801451B2 (ja) | 2006-01-19 | 2011-10-26 | 株式会社日立ハイテクノロジーズ | 走査電子顕微鏡等に用いる電子銃の制御装置及び制御方法 |
US20070208053A1 (en) | 2006-01-19 | 2007-09-06 | Arnold Lee D | Fused heterobicyclic kinase inhibitors |
ITMI20060179A1 (it) | 2006-02-02 | 2007-08-03 | Abiogen Pharma Spa | Procedimento per la risoluzione di miscele racemiche e complesso diastereoisomerico di un agente risolvente e di unantiomero di interesse |
US20070293702A1 (en) | 2006-02-21 | 2007-12-20 | Viviana Braude | Novel crystalline forms of armodafinil and preparation thereof |
CA2642180A1 (en) | 2006-02-27 | 2007-09-07 | Teva Pharmaceutical Industries Ltd. | Fluvastatin sodium novel forms and preparation therof |
US7588924B2 (en) | 2006-03-07 | 2009-09-15 | Procter & Gamble Company | Crystal of hypoxia inducible factor 1 alpha prolyl hydroxylase |
TW200808793A (en) | 2006-03-07 | 2008-02-16 | Smithkline Beecham Corp | Prolyl hydroxylase inhibitors |
WO2007109799A2 (en) | 2006-03-23 | 2007-09-27 | Teva Pharmaceutical Industries Ltd. | Polymorphs of eszopiclone malate |
JP2009537558A (ja) | 2006-05-16 | 2009-10-29 | スミスクライン・ビーチャム・コーポレイション | プロリルヒドロキシラーゼ阻害剤 |
TWI394747B (zh) | 2006-06-23 | 2013-05-01 | Smithkline Beecham Corp | 脯胺醯基羥化酶抑制劑 |
PT3357911T (pt) | 2006-06-26 | 2022-07-11 | Akebia Therapeutics Inc | Inibidores da prolil-hidroxilase e métodos de utilização |
TW200845994A (en) | 2007-01-12 | 2008-12-01 | Smithkline Beecham Corp | N-substituted glycine derivatives: prolyl hydroxylase inhibitors |
CL2008000066A1 (es) | 2007-01-12 | 2008-08-01 | Smithkline Beecham Corp | Compuestos derivados de (5-hidroxi-3-oxo-2,3-dihidropiridazina-4-carbonil)glicina, inhibidores de hif prolil hidroxilasas; procedimiento de preparacion; composicion farmaceutica que comprende a dichos compuestos; y su uso en el tratamiento de la anem |
CA2683758A1 (en) | 2007-04-18 | 2008-10-30 | Merck & Co., Inc. | Novel 1,8-naphthyridine compounds |
AU2008241577B2 (en) | 2007-04-18 | 2011-04-07 | Amgen Inc. | Indanone derivatives that inhibit prolyl hydroxylase |
EP2150251B9 (en) | 2007-05-04 | 2013-02-27 | Amgen, Inc | Thienopyridine and thiazolopyridine derivatives that inhibit prolyl hydroxylase activity |
CA2685942A1 (en) | 2007-05-16 | 2008-11-27 | Merck & Co., Inc. | Spiroindalones |
TW200908984A (en) | 2007-08-07 | 2009-03-01 | Piramal Life Sciences Ltd | Pyridyl derivatives, their preparation and use |
WO2009037570A2 (en) | 2007-08-10 | 2009-03-26 | Crystalgenomics, Inc. | Pyridine derivatives and methods of use thereof |
WO2009039323A1 (en) | 2007-09-19 | 2009-03-26 | Smithkline Beecham Corporation | Prolyl hydroxylase inhibitors |
WO2009039321A1 (en) | 2007-09-19 | 2009-03-26 | Smithkline Beecham Corporation | Prolyl hydroxylase inhibitors |
WO2009043093A1 (en) | 2007-10-04 | 2009-04-09 | Newsouth Innovations Pty Limited | Hif inhibition |
WO2009049112A1 (en) | 2007-10-10 | 2009-04-16 | Smithkline Beecham Corporation | Prolyl hydroxylase inhibitors |
JP2011503094A (ja) | 2007-11-08 | 2011-01-27 | ジェネンテック, インコーポレイテッド | 抗b因子抗体およびそれらの使用 |
WO2009067790A1 (en) | 2007-11-26 | 2009-06-04 | Uti Limited Partnership | STIMULATION OF HYPOXIA INDUCIBLE FACTOR -1 ALPHA (HIF-1α) FOR THE TREATMENT OF CLOSTRIDIUM DIFFICILE ASSOCIATED DISEASE (CDAD), FOR INTESTINAL MOTILITY AND FOR DETECTING INFECTION |
WO2009073497A2 (en) | 2007-11-30 | 2009-06-11 | Smithkline Beecham Corporation | Prolyl hydroxylase inhibitors |
WO2009070644A1 (en) | 2007-11-30 | 2009-06-04 | Smithkline Beecham Corporation | Prolyl hydroxylase inhibitors |
US8269008B2 (en) | 2007-12-03 | 2012-09-18 | Fibrogen, Inc. | Oxazolopyridine and isoxazolopyridine derivatives for use in the treatment of HIF-mediated conditions |
JP2011507894A (ja) | 2007-12-19 | 2011-03-10 | グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー | プロリルヒドロキシラーゼ阻害剤 |
US20110003013A1 (en) | 2008-01-04 | 2011-01-06 | Garvan Institute Of Medical Research | Method of increasing metabolism |
WO2009089547A1 (en) | 2008-01-11 | 2009-07-16 | Fibrogen, Inc. | Isothiazole-pyridine derivatives as modulators of hif (hypoxia inducible factor) activity |
AR071997A1 (es) | 2008-06-04 | 2010-07-28 | Bristol Myers Squibb Co | Forma cristalina de 6-((4s)-2-metil-4-(2-naftil)-1,2,3,4-tetrahidroisoquinolin-7-il)piridazin-3-amina |
NO2686520T3 (es) | 2011-06-06 | 2018-03-17 | ||
EP2717870B1 (en) | 2011-06-06 | 2017-09-27 | Akebia Therapeutics Inc. | Composition for stabilizing hypoxia inducible factor-2 alpha useful for treating cancer |
US9206134B2 (en) | 2011-07-22 | 2015-12-08 | Beijing Betta Pharmaceuticals Co. Ltd. | Polymorphic forms of compounds as prolyl hydroxylase inhibitor, and uses thereof |
US8772895B2 (en) | 2011-11-28 | 2014-07-08 | Taiwan Semiconductor Manufacturing Company, Ltd. | Dark current reduction for back side illuminated image sensor |
EP2637274B1 (en) | 2012-03-05 | 2022-05-04 | Vetco Gray Scandinavia AS | Power cable termination arrangement |
ES2974273T3 (es) | 2013-06-13 | 2024-06-26 | Akebia Therapeutics Inc | Composiciones y métodos para tratar la anemia |
KR102381295B1 (ko) | 2013-11-15 | 2022-03-31 | 아케비아 테라퓨틱스 인코포레이티드 | {[5-(3-클로로페닐)-3-하이드록시피리딘-2-카보닐]아미노}아세트산의 고체형, 이의 조성물 및 용도 |
CA2937349A1 (en) | 2014-01-23 | 2015-07-30 | Akebia Therapeutics, Inc. | Compositions and methods for treating ocular diseases |
JP2018502882A (ja) | 2015-01-23 | 2018-02-01 | アケビア セラピューティクス インコーポレイテッドAkebia Therapeutics Inc. | 2−(5−(3−フルオロフェニル)−3−ヒドロキシピコリンアミド)酢酸の固体形態、その組成物及び使用 |
CA2979985A1 (en) | 2015-03-20 | 2016-09-29 | Akebia Therapeutics, Inc. | Deuterium-enriched hypoxia-inducible factor prolyl hydroxylase enzyme inhibitors |
PL3277270T3 (pl) | 2015-04-01 | 2022-02-14 | Akebia Therapeutics, Inc. | Kompozycje i sposoby leczenia niedokrwistości |
MX2019006883A (es) | 2016-12-13 | 2019-10-21 | Crystal Pharmaceutical Suzhou Co Ltd | Formas cristalinas novedosas de ácido {[5-(3-clorofenil)-3-idroxip iridina-2-carbonilo] amino} acético y procedimientos para la preparación del mismo. |
CA3097219A1 (en) | 2018-05-09 | 2019-11-14 | Akebia Therapeutics, Inc. | Process for preparing 2-[[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino]acetic acid |
WO2021087144A1 (en) | 2019-10-31 | 2021-05-06 | Akebia Therapeutics, Inc. | Therapeutic methods using vadadustat |
US11524939B2 (en) | 2019-11-13 | 2022-12-13 | Akebia Therapeutics, Inc. | Solid forms of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino} acetic acid |
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