ES2545076T3 - Uso del inhibidor de HDAC panobinostat para el tratamiento de mieloma - Google Patents
Uso del inhibidor de HDAC panobinostat para el tratamiento de mieloma Download PDFInfo
- Publication number
- ES2545076T3 ES2545076T3 ES06789025.1T ES06789025T ES2545076T3 ES 2545076 T3 ES2545076 T3 ES 2545076T3 ES 06789025 T ES06789025 T ES 06789025T ES 2545076 T3 ES2545076 T3 ES 2545076T3
- Authority
- ES
- Spain
- Prior art keywords
- myeloma
- hdac inhibitor
- treatment
- panobinostat
- methyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
-
- 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
- A61K31/403—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 carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/4045—Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
-
- 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
-
- 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
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
El uso de un inhibidor de HDAC para la preparación de un medicamento para el tratamiento de mieloma, en el que el inhibidor de HDAC es N-hidroxi-3>=[4-[[[2-(2-metil-1H-indol-3-ilo)-etil]-amino]metil]fenil]-2E-2-propenamida que tiene la fórmula (III)**Fórmula** o una sal farmacéuticamente aceptable del mismo, y en el que el mieloma es resistente a quimioterapia convencional.
Description
Claims (1)
-
imagen1 imagen2
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US70522605P | 2005-08-03 | 2005-08-03 | |
US705226P | 2005-08-03 | ||
PCT/US2006/029801 WO2007019116A1 (en) | 2005-08-03 | 2006-08-01 | Use of hdac inhibitors for the treatment of myeloma |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2545076T3 true ES2545076T3 (es) | 2015-09-08 |
Family
ID=37307336
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES06789025.1T Active ES2545076T3 (es) | 2005-08-03 | 2006-08-01 | Uso del inhibidor de HDAC panobinostat para el tratamiento de mieloma |
Country Status (18)
Country | Link |
---|---|
US (2) | US20080221126A1 (es) |
EP (1) | EP1912640B1 (es) |
JP (2) | JP5665271B2 (es) |
KR (1) | KR101354237B1 (es) |
CN (2) | CN104324025A (es) |
AU (1) | AU2006278718B2 (es) |
BR (1) | BRPI0614090A2 (es) |
CA (1) | CA2617274C (es) |
DK (1) | DK1912640T3 (es) |
ES (1) | ES2545076T3 (es) |
HU (1) | HUE028025T2 (es) |
LT (1) | LTC1912640I2 (es) |
MX (1) | MX2008001610A (es) |
PL (1) | PL1912640T3 (es) |
PT (1) | PT1912640E (es) |
RU (1) | RU2420279C3 (es) |
SI (1) | SI1912640T1 (es) |
WO (1) | WO2007019116A1 (es) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5665271B2 (ja) * | 2005-08-03 | 2015-02-04 | ノバルティス アーゲー | 骨髄腫の処置のためのhdac阻害剤の使用 |
BRPI0807812A2 (pt) * | 2007-02-15 | 2020-06-23 | Novartis Ag | Combinações de lbh589 com outros agentes terapêuticos para tratar câncer |
KR101516446B1 (ko) * | 2007-05-30 | 2015-04-30 | 노파르티스 아게 | 골 파괴의 치료를 위한 hdac 억제제의 용도 |
WO2010075286A1 (en) * | 2008-12-24 | 2010-07-01 | University Of Washington | MOLECULAR ACTIVATORS OF THE Wnt/β-CATENIN PATHWAY |
CN102762100B (zh) † | 2009-11-13 | 2015-07-01 | 瑞塞普托斯公司 | 选择性的1-磷酸鞘氨醇受体调节剂及手性合成方法 |
KR20130101519A (ko) * | 2010-09-01 | 2013-09-13 | 노파르티스 아게 | Hdac 억제제와 혈소판감소증 약물의 조합물 |
MA41544A (fr) * | 2015-02-19 | 2017-12-26 | Novartis Ag | Dosages de panobinostat pour le traitement du myélome multiple |
US20180311257A1 (en) | 2015-11-03 | 2018-11-01 | Hochschule Darmstadt | Selective hdac8 inhibitors and their uses |
CN105348169B (zh) * | 2015-11-16 | 2018-03-30 | 青岛大学 | 一种组蛋白去乙酰酶抑制剂(e)‑3‑(2‑(1‑(4‑氯苯甲酰基)‑5‑甲氧基‑2‑甲基‑1氢‑吲哚‑3‑基)乙酰氨基)‑n‑羟基丁‑2‑烯酰胺及其制备方法和应用 |
CN109705057B (zh) * | 2017-10-25 | 2023-05-30 | 成都先导药物开发股份有限公司 | 组蛋白去乙酰化酶抑制剂及其制备方法与用途 |
US10537585B2 (en) | 2017-12-18 | 2020-01-21 | Dexcel Pharma Technologies Ltd. | Compositions comprising dexamethasone |
CN113164375A (zh) | 2018-07-18 | 2021-07-23 | 希成生物医药 | 包含盐霉素的聚合物纳米颗粒 |
WO2022251844A1 (en) | 2021-05-25 | 2022-12-01 | Hillstream Biopharma, Inc. | Polymeric nanoparticles comprising chemotherapeutic compounds and related methods |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PE20020354A1 (es) * | 2000-09-01 | 2002-06-12 | Novartis Ag | Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda) |
PL392652A1 (pl) * | 2001-05-16 | 2010-12-06 | Novartis Ag | Kombinacja zawierająca N-{5-[4-(4-metylo-piperazyno-metylo)-benzoiloamido]-2-metylofenylo}-4-(3-pirydylo)-2-pirymidyno-aminę oraz środek chemoterapeutyczny, jej zastosowanie, kompozycja farmaceutyczna ją zawierająca oraz zestaw zawierający taką kombinację |
JP2005511062A (ja) * | 2001-12-07 | 2005-04-28 | ノバルティス アクチエンゲゼルシャフト | タンパク質脱アセチル化酵素阻害剤についての生物マーカーとしてのアルファ−チューブリンアセチル化レベルの使用 |
US20040132825A1 (en) * | 2002-03-04 | 2004-07-08 | Bacopoulos Nicholas G. | Methods of treating cancer with HDAC inhibitors |
US20050043233A1 (en) * | 2003-04-29 | 2005-02-24 | Boehringer Ingelheim International Gmbh | Combinations for the treatment of diseases involving cell proliferation, migration or apoptosis of myeloma cells or angiogenesis |
JP2006528952A (ja) * | 2003-05-21 | 2006-12-28 | ノバルティス アクチエンゲゼルシャフト | ヒストンデアセチラーゼ阻害剤と化学療法剤の組み合わせ |
EP1667680A4 (en) * | 2003-08-29 | 2008-10-08 | Aton Pharma Inc | COMBINED METHODS OF TREATING CANCER |
WO2006102557A2 (en) | 2005-03-22 | 2006-09-28 | The President And Fellows Of Harvard College | Treatment of protein degradation disorders |
JP5665271B2 (ja) * | 2005-08-03 | 2015-02-04 | ノバルティス アーゲー | 骨髄腫の処置のためのhdac阻害剤の使用 |
-
2006
- 2006-08-01 JP JP2008525092A patent/JP5665271B2/ja active Active
- 2006-08-01 CA CA2617274A patent/CA2617274C/en active Active
- 2006-08-01 KR KR1020087002803A patent/KR101354237B1/ko active Protection Beyond IP Right Term
- 2006-08-01 DK DK06789025.1T patent/DK1912640T3/en active
- 2006-08-01 US US11/996,323 patent/US20080221126A1/en not_active Abandoned
- 2006-08-01 MX MX2008001610A patent/MX2008001610A/es active IP Right Grant
- 2006-08-01 SI SI200631952T patent/SI1912640T1/sl unknown
- 2006-08-01 CN CN201410610419.9A patent/CN104324025A/zh active Pending
- 2006-08-01 RU RU2008107871A patent/RU2420279C3/ru not_active IP Right Cessation
- 2006-08-01 EP EP06789025.1A patent/EP1912640B1/en active Active
- 2006-08-01 PT PT67890251T patent/PT1912640E/pt unknown
- 2006-08-01 BR BRPI0614090-4A patent/BRPI0614090A2/pt not_active Application Discontinuation
- 2006-08-01 CN CNA2006800281244A patent/CN101232880A/zh active Pending
- 2006-08-01 AU AU2006278718A patent/AU2006278718B2/en not_active Ceased
- 2006-08-01 ES ES06789025.1T patent/ES2545076T3/es active Active
- 2006-08-01 WO PCT/US2006/029801 patent/WO2007019116A1/en active Application Filing
- 2006-08-01 PL PL06789025T patent/PL1912640T3/pl unknown
- 2006-08-01 HU HUE06789025A patent/HUE028025T2/en unknown
-
2010
- 2010-03-04 US US12/717,373 patent/US8883842B2/en active Active
-
2013
- 2013-04-04 JP JP2013078867A patent/JP5876435B2/ja active Active
-
2016
- 2016-01-22 LT LTPA2016003C patent/LTC1912640I2/lt unknown
Also Published As
Publication number | Publication date |
---|---|
HUE028025T2 (en) | 2016-11-28 |
SI1912640T1 (sl) | 2015-10-30 |
EP1912640B1 (en) | 2015-06-17 |
KR20080031937A (ko) | 2008-04-11 |
PT1912640E (pt) | 2015-09-22 |
US8883842B2 (en) | 2014-11-11 |
RU2420279C2 (ru) | 2011-06-10 |
JP5876435B2 (ja) | 2016-03-02 |
JP2013173757A (ja) | 2013-09-05 |
CA2617274C (en) | 2017-10-10 |
RU2420279C3 (ru) | 2017-03-14 |
AU2006278718B2 (en) | 2010-10-07 |
BRPI0614090A2 (pt) | 2011-03-09 |
JP2009503087A (ja) | 2009-01-29 |
KR101354237B1 (ko) | 2014-01-22 |
MX2008001610A (es) | 2008-02-19 |
LTC1912640I2 (lt) | 2017-09-11 |
AU2006278718A1 (en) | 2007-02-15 |
CA2617274A1 (en) | 2007-02-15 |
EP1912640A1 (en) | 2008-04-23 |
RU2008107871A (ru) | 2009-09-10 |
DK1912640T3 (en) | 2015-09-14 |
WO2007019116A1 (en) | 2007-02-15 |
PL1912640T3 (pl) | 2015-11-30 |
US20080221126A1 (en) | 2008-09-11 |
CN101232880A (zh) | 2008-07-30 |
CN104324025A (zh) | 2015-02-04 |
JP5665271B2 (ja) | 2015-02-04 |
US20100160257A1 (en) | 2010-06-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ES2545076T3 (es) | Uso del inhibidor de HDAC panobinostat para el tratamiento de mieloma | |
ES2569477T3 (es) | Combinación de un inhibidor de HDAC y un antimetabolito | |
ES2525932T3 (es) | Derivados de dihidrotetrabenazina radiomarcados y su uso como agentes de imagenología | |
ES2545205T3 (es) | Combinación de azelastina y ciclesonida | |
ES2500068T3 (es) | Inhibidores heterocíclicos de MEK y métodos de uso de los mismos | |
ES2581331T3 (es) | Inhibidor de la progresión de una enfermedad atribuida a una acumulación anormal de grasa hepática | |
ES2665917T3 (es) | Endoxifeno para su uso en el tratamiento del cáncer | |
ES2551307T3 (es) | Composición de inhalación que contiene aclidinio para tratamiento de enfermedad pulmonar obstructiva crónica | |
ECSP066950A (es) | Combinaciones de glicopirrolato y agonistas del adrenoceptor-beta2 | |
ES2185606T3 (es) | Nuevo uso de una clase de compuestos peptidicos para tratamiento de la alodinia u otros tipos diferentes de dolor cronico o fantasma. | |
ES2485867T3 (es) | Compuestos opioides de carboxamido | |
ES2515168T3 (es) | Detección y tratamiento de la esquizofrenia | |
RS52214B (en) | HDAC INHIBITOR PHARMACEUTICAL FORMULATIONS | |
NI200500031A (es) | Nuevos procesos para la sintesis de ivabradine y ademas sales que la contienen con un acido aceptable farmaceuticamente. | |
RS53209B (en) | PHARMACEUTICAL COMPOSITION FOR VIRAL HEPATITIS C PROTEASE INHIBITOR | |
BRPI0113669B8 (pt) | n-hidróxi-3-[4-[[[2-(2-metil-1h-indol-3-il)etil]-amino]metil]fenil]-2e-2-propenamida, composição farmacêutica compreendendo o mesmo e uso | |
CO6321285A2 (es) | Uso de 3,11b-cis- dihidrotetrabenazina en el tratamiento de la esclerosis multiple y la mielitis autoinmunitaria | |
CL2009000882A1 (es) | Un compuesto n-(4-cloro-3-(piridin-2-il)fenil)-4-(2-hidroxi-2-metilpropilsulfonil)-2-metilbenzamida, inhibidor de la via de señalización hedgehog; composición farmacéutica que comprende a dicho compuesto; y su uso para tratar el cancer. | |
AR058433A1 (es) | Derivado de 1,1-dioxido de 1,4-benzotiazepina ,procedimiento para su preparacion ,medicamentos que comprenden este compuesto y su uso | |
AR082600A1 (es) | Polimorfos cristalinos de la sal de besilato de n-(3-(5-fluor-2-(4-(2-metoxietoxi)fenilamino)pirimidin-4-ilamino)fenil)acrilamida, composiciones farmaceuticas que los contienen y uso de los mismos para tratar canceres, enfermedades autoinmunes y oseas, entre otras | |
AR049274A1 (es) | Acido2-{[2-(2-metilaminopirimidin-4-il)-1h-indol-5-carbonil]amino}-3-(fenilpiridin-2-ilamino)propionico sustancialmente puro como inhibidor selectivo de la quinasa ikk-2 | |
CL2009000914A1 (es) | Compuestos derivados de 1-ciano-3-pirrolidinil-n-sustituidas-sulfonamidas, inhibidores de catepsina c; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento de una enfermedad pulmonar obstructiva cronica. | |
CL2008001868A1 (es) | Compuestos derivados de n-(2-(hetaril)aril)arilsulfonamidas y n-(2-(hetaril)hetaril)arilsulfonamidas; composicion farmaceutica que comprende a dicho compuesto; y uso para el tratamiento de enfermedades inflamatorias del intestino, enfermedad alergica | |
ATE440833T1 (de) | Antithrombotische diamide | |
AR079208A2 (es) | Inhibidores de la actividad de proteina tirosina quinasa, composicion y uso de dichos inhibidores para la preparacion de un medicamento para tratar una enfermedad, trastorno o condicion oftalmica |