DK1912640T3 - Anvendelse af hdac-hæmmeren panobinostat til behandling af myelom - Google Patents

Anvendelse af hdac-hæmmeren panobinostat til behandling af myelom Download PDF

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Publication number
DK1912640T3
DK1912640T3 DK06789025.1T DK06789025T DK1912640T3 DK 1912640 T3 DK1912640 T3 DK 1912640T3 DK 06789025 T DK06789025 T DK 06789025T DK 1912640 T3 DK1912640 T3 DK 1912640T3
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Prior art keywords
myeloma
combination
hdac inhibitor
cells
iii
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DK06789025.1T
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English (en)
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Peter W Atadja
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Novartis Ag
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    • 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

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  • 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)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Indole Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Claims (8)

  1. ANVENDELSE AF HDAC-HÆMMEREN PANOBINOSTAT TIL BEHANDLING AF MYELOM PATENTKRAV
    1. Anvendelse af en HDAC-hæmmer til fremstilling af et medikament til behandling af myelom, hvor HDAC-hæmmeren er V-hydroxy-3-[4-[[[2-(2-methyl-l//-indol-3-yl)-cthyl]-amino]mcthyl]phcnyl]-2L'-2-propenamid med formlen (III)
    (Hl) > eller et farmaceutisk acceptabelt salt deraf, og hvor myelomet er resistent over for traditionel kemoterapi.
  2. 2. Anvendelse ifølge krav 1, hvor sygdommen er multipelt myelom.
  3. 3. HDAC-inhibitor, der er A-hydroxy-3-[4-[[[2-(2-methyl-l//-indol-3-yl)-ethyl]- amino]methyl]phenyl]-2£'-2-propenamid med formlen (III)
    (III) i eller et farmaceutisk acceptabelt salt deraf, til anvendelse i behandlingen af myelom, hvor myelomet er resistent over for traditionel kemoterapi.
  4. 4. HDAC-hæmmer ifølge krav 3 til anvendelse ifølge krav 3, hvor sygdommen er multipelt myelom.
  5. 5. Kombination til anvendelse i behandlingen af myelom, hvilken kombination omfatter en HDAC-hæmmer og en forbindelse, der bevirker apoptose af myelomceller, hvori de aktive bestanddele er til stede i hvert tilfælde i fri form eller i form af et farmaceutisk acceptabelt salt og eventuelt mindst én farmaceutisk acceptabel bærer, hvor HD AC-hæmmeren er V-hydroxy-3-[4-[[[2-(2-methyl-lF/-indol-3-yl)-ethyl]-amino]methyl]phenyl]-2ii-2-propenamid med formlen (III)
    (III) * og hvor forbindelsen, der bevirker apoptose af myelomceller, er bortezomib.
  6. 6. Kombination ifølge krav 5 til anvendelse ifølge krav 5, hvor anvendelsen er en simultan, separat eller sekventiel anvendelse.
  7. 7. Kombination ifølge krav 5 til anvendelse ifølge krav 5 eller 6, hvor myelomet er multipelt myelom.
  8. 8. Farmaceutisk sammensætning omfattende en kvantitet, der sammen er terapeutisk effektiv mod myelom, af en kombination ifølge krav 5 og mindst én farmaceutisk acceptabel bærer, til anvendelse i behandlingen af myelom.
DK06789025.1T 2005-08-03 2006-08-01 Anvendelse af hdac-hæmmeren panobinostat til behandling af myelom DK1912640T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US70522605P 2005-08-03 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
DK1912640T3 true DK1912640T3 (da) 2015-09-14

Family

ID=37307336

Family Applications (1)

Application Number Title Priority Date Filing Date
DK06789025.1T DK1912640T3 (da) 2005-08-03 2006-08-01 Anvendelse af hdac-hæmmeren panobinostat til behandling af myelom

Country Status (18)

Country Link
US (2) US20080221126A1 (da)
EP (1) EP1912640B1 (da)
JP (2) JP5665271B2 (da)
KR (1) KR101354237B1 (da)
CN (2) CN104324025A (da)
AU (1) AU2006278718B2 (da)
BR (1) BRPI0614090A2 (da)
CA (1) CA2617274C (da)
DK (1) DK1912640T3 (da)
ES (1) ES2545076T3 (da)
HU (1) HUE028025T2 (da)
LT (1) LTC1912640I2 (da)
MX (1) MX2008001610A (da)
PL (1) PL1912640T3 (da)
PT (1) PT1912640E (da)
RU (1) RU2420279C3 (da)
SI (1) SI1912640T1 (da)
WO (1) WO2007019116A1 (da)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080221126A1 (en) * 2005-08-03 2008-09-11 Atadja Peter W Use of Hdac Inhibitors for the Treatment of Myeloma
RU2009134223A (ru) * 2007-02-15 2011-03-20 Новартис АГ (CH) Комбинация lbh589 с другими терапевтическими средствами, предназначенная для лечения рака
WO2008150782A1 (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
EP3868377A1 (en) 2009-11-13 2021-08-25 Receptos Llc Selective sphingosine 1 phosphate receptor modulators and methods of chiral synthesis
US20130171141A1 (en) * 2010-09-01 2013-07-04 Novartis Ag Combination of hdac inhibitors with thrombocytopenia drugs
MA41544A (fr) * 2015-02-19 2017-12-26 Novartis Ag Dosages de panobinostat pour le traitement du myélome multiple
WO2017077008A1 (en) 2015-11-03 2017-05-11 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
WO2020018778A1 (en) 2018-07-18 2020-01-23 Surender Kharbanda 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)
EP2253319A1 (en) * 2001-05-16 2010-11-24 Novartis AG Combination comprising N-{5-[4-(4-methyl-piperazino-methyl)-benzoylamido]-2-methylphenyl}-4-(3-pyridyl)-2pyrimidine-amine and a chemotherapeutic agent.
WO2003048774A1 (en) 2001-12-07 2003-06-12 Novartis Ag Use of alpha-tubulin acetylation levels as a biomarker for protein deacetylase inhibitors
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
AU2004241729A1 (en) * 2003-05-21 2004-12-02 Novartis Ag Combination of histone deacetylase inhibitors with chemotherapeutic agents
CN101856348A (zh) 2003-08-29 2010-10-13 斯隆-凯特林癌症研究所 联合治疗癌症的方法
EP2491926B1 (en) 2005-03-22 2018-05-09 President and Fellows of Harvard College Treatment of protein degradation disorders
US20080221126A1 (en) * 2005-08-03 2008-09-11 Atadja Peter W Use of Hdac Inhibitors for the Treatment of Myeloma

Also Published As

Publication number Publication date
KR20080031937A (ko) 2008-04-11
US8883842B2 (en) 2014-11-11
RU2420279C2 (ru) 2011-06-10
LTC1912640I2 (lt) 2017-09-11
EP1912640B1 (en) 2015-06-17
JP5876435B2 (ja) 2016-03-02
CA2617274A1 (en) 2007-02-15
ES2545076T3 (es) 2015-09-08
PT1912640E (pt) 2015-09-22
CA2617274C (en) 2017-10-10
RU2008107871A (ru) 2009-09-10
AU2006278718A1 (en) 2007-02-15
CN104324025A (zh) 2015-02-04
JP2009503087A (ja) 2009-01-29
KR101354237B1 (ko) 2014-01-22
SI1912640T1 (sl) 2015-10-30
JP5665271B2 (ja) 2015-02-04
US20100160257A1 (en) 2010-06-24
EP1912640A1 (en) 2008-04-23
PL1912640T3 (pl) 2015-11-30
RU2420279C3 (ru) 2017-03-14
HUE028025T2 (en) 2016-11-28
MX2008001610A (es) 2008-02-19
AU2006278718B2 (en) 2010-10-07
BRPI0614090A2 (pt) 2011-03-09
US20080221126A1 (en) 2008-09-11
CN101232880A (zh) 2008-07-30
JP2013173757A (ja) 2013-09-05
WO2007019116A1 (en) 2007-02-15

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