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 PDF

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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
Application number
ES06789025.1T
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English (en)
Inventor
Peter W. Atadja
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Novartis AG
Original Assignee
Novartis AG
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Filing date
Publication date
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=37307336&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ES2545076(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis AG filed Critical Novartis AG
Application granted granted Critical
Publication of ES2545076T3 publication Critical patent/ES2545076T3/es
Anticipated expiration legal-status Critical
Active legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic 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
    • A61K31/403Heterocyclic 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
    • A61K31/404Indoles, e.g. pindolol
    • A61K31/4045Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/4965Non-condensed pyrazines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/498Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (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)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (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

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Claims (1)

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    imagen2
ES06789025.1T 2005-08-03 2006-08-01 Uso del inhibidor de HDAC panobinostat para el tratamiento de mieloma Active ES2545076T3 (es)

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)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL1912640T3 (pl) * 2005-08-03 2015-11-30 Novartis Ag Zastosowanie inhibitora HDAC panobinostatu w leczeniu szpiczaka
EP2491923A3 (en) * 2007-02-15 2012-12-26 Novartis AG Combinations of therapeutic agents for treating cancer
CA2687274A1 (en) * 2007-05-30 2008-12-11 Novartis Ag Use of hdac inhibitors for the treatment of bone destruction
US20120046242A1 (en) * 2008-12-24 2012-02-23 Massachusetts Institute Of Technology Molecular activators of the wnt/beta-catenin pathway
SI2498610T2 (sl) 2009-11-13 2024-10-30 Receptos Llc Selektivni modulatorji receptorja sfingozin-1-fosfata in postopki kiralne sinteze
RU2013114246A (ru) * 2010-09-01 2014-10-20 Новартис Аг Комбинация hdac ингибиторов с лекарственными средствами против тромбоцитопении
MA41544A (fr) * 2015-02-19 2017-12-26 Novartis Ag Dosages de panobinostat pour le traitement du myélome multiple
JP6923219B2 (ja) 2015-11-03 2021-08-18 ホーホシューレ ダルムシュタット 選択的hdac8阻害剤およびこれらの使用
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
AU2019307629A1 (en) 2018-07-18 2021-02-18 Hillstream Biopharma Inc. Polymeric nanoparticles comprising salinomycin
WO2022251844A1 (en) 2021-05-25 2022-12-01 Hillstream Biopharma, Inc. Polymeric nanoparticles comprising chemotherapeutic compounds and related methods

Family Cites Families (9)

* Cited by examiner, † Cited by third party
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)
BR0209647A (pt) * 2001-05-16 2004-07-27 Novartis Ag Combinação que compreende n-{5-[4-(4-metil-piperazino-metil)-benzoilamido]-2-metil fenil}-4-(3-piridil)-2-pirimidina-amina e um agente quimioterapêutico
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
MXPA05012464A (es) * 2003-05-21 2006-01-30 Novartis Ag Combinacion de inhibidores de deacetilasa de histona con agentes quimioterapeuticos.
JP2007504131A (ja) 2003-08-29 2007-03-01 エートン ファーマ インコーポレーティッド 癌の組み合わせ処置法
US8999289B2 (en) 2005-03-22 2015-04-07 President And Fellows Of Harvard College Treatment of protein degradation disorders
PL1912640T3 (pl) * 2005-08-03 2015-11-30 Novartis Ag Zastosowanie inhibitora HDAC panobinostatu w leczeniu szpiczaka

Also Published As

Publication number Publication date
JP2013173757A (ja) 2013-09-05
WO2007019116A1 (en) 2007-02-15
HUE028025T2 (en) 2016-11-28
KR20080031937A (ko) 2008-04-11
LTC1912640I2 (lt) 2017-09-11
AU2006278718B2 (en) 2010-10-07
BRPI0614090A2 (pt) 2011-03-09
RU2420279C3 (ru) 2017-03-14
CN104324025A (zh) 2015-02-04
EP1912640B1 (en) 2015-06-17
US20080221126A1 (en) 2008-09-11
EP1912640A1 (en) 2008-04-23
JP5876435B2 (ja) 2016-03-02
CA2617274C (en) 2017-10-10
PL1912640T3 (pl) 2015-11-30
CN101232880A (zh) 2008-07-30
CA2617274A1 (en) 2007-02-15
JP2009503087A (ja) 2009-01-29
DK1912640T3 (en) 2015-09-14
PT1912640E (pt) 2015-09-22
US8883842B2 (en) 2014-11-11
SI1912640T1 (sl) 2015-10-30
US20100160257A1 (en) 2010-06-24
JP5665271B2 (ja) 2015-02-04
RU2420279C2 (ru) 2011-06-10
MX2008001610A (es) 2008-02-19
KR101354237B1 (ko) 2014-01-22
RU2008107871A (ru) 2009-09-10
AU2006278718A1 (en) 2007-02-15

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