JP2005525345A5 - - Google Patents
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- JP2005525345A5 JP2005525345A5 JP2003569148A JP2003569148A JP2005525345A5 JP 2005525345 A5 JP2005525345 A5 JP 2005525345A5 JP 2003569148 A JP2003569148 A JP 2003569148A JP 2003569148 A JP2003569148 A JP 2003569148A JP 2005525345 A5 JP2005525345 A5 JP 2005525345A5
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- JP
- Japan
- Prior art keywords
- pharmaceutical composition
- composition according
- cancer
- saha
- pharmaceutically acceptable
- Prior art date
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- 239000008194 pharmaceutical composition Substances 0.000 claims 46
- WAEXFXRVDQXREF-UHFFFAOYSA-N Vorinostat Chemical compound ONC(=O)CCCCCCC(=O)NC1=CC=CC=C1 WAEXFXRVDQXREF-UHFFFAOYSA-N 0.000 claims 14
- 229960000237 Vorinostat Drugs 0.000 claims 14
- 201000011510 cancer Diseases 0.000 claims 13
- 150000007529 inorganic bases Chemical class 0.000 claims 8
- 150000003839 salts Chemical class 0.000 claims 8
- 239000011780 sodium chloride Substances 0.000 claims 8
- 150000001412 amines Chemical class 0.000 claims 6
- 239000000203 mixture Substances 0.000 claims 6
- 150000007530 organic bases Chemical class 0.000 claims 5
- 229910052783 alkali metal Inorganic materials 0.000 claims 4
- 150000001340 alkali metals Chemical class 0.000 claims 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 4
- 150000001342 alkaline earth metals Chemical class 0.000 claims 4
- 150000001413 amino acids Chemical class 0.000 claims 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims 4
- MIJDSYMOBYNHOT-UHFFFAOYSA-N 2-(ethylamino)ethanol Chemical compound CCNCCO MIJDSYMOBYNHOT-UHFFFAOYSA-N 0.000 claims 2
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-Methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 claims 2
- 239000004475 Arginine Substances 0.000 claims 2
- JUHORIMYRDESRB-UHFFFAOYSA-N Benzathine Chemical compound C=1C=CC=CC=1CNCCNCC1=CC=CC=C1 JUHORIMYRDESRB-UHFFFAOYSA-N 0.000 claims 2
- 206010005003 Bladder cancer Diseases 0.000 claims 2
- 206010006187 Breast cancer Diseases 0.000 claims 2
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 claims 2
- MBBZMMPHUWSWHV-BDVNFPICSA-N Meglumine Chemical compound CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO MBBZMMPHUWSWHV-BDVNFPICSA-N 0.000 claims 2
- MFDFERRIHVXMIY-UHFFFAOYSA-N Procaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 claims 2
- 206010038389 Renal cancer Diseases 0.000 claims 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Tris Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims 2
- 239000004480 active ingredient Substances 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 2
- 229910052791 calcium Inorganic materials 0.000 claims 2
- 239000011575 calcium Substances 0.000 claims 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N ethanolamine Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims 2
- 229910052744 lithium Inorganic materials 0.000 claims 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 2
- 229910052749 magnesium Inorganic materials 0.000 claims 2
- 239000011777 magnesium Substances 0.000 claims 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 2
- 229910052700 potassium Inorganic materials 0.000 claims 2
- 239000011591 potassium Substances 0.000 claims 2
- 229960004919 procaine Drugs 0.000 claims 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims 2
- 229910052708 sodium Inorganic materials 0.000 claims 2
- 239000011734 sodium Substances 0.000 claims 2
- 206010009944 Colon cancer Diseases 0.000 claims 1
- 206010024324 Leukaemias Diseases 0.000 claims 1
- 210000000265 Leukocytes Anatomy 0.000 claims 1
- 206010035226 Plasma cell myeloma Diseases 0.000 claims 1
- 206010060862 Prostate cancer Diseases 0.000 claims 1
- 210000003491 Skin Anatomy 0.000 claims 1
- 201000001531 bladder carcinoma Diseases 0.000 claims 1
- 239000002775 capsule Substances 0.000 claims 1
- 238000001764 infiltration Methods 0.000 claims 1
- 201000010982 kidney cancer Diseases 0.000 claims 1
- 201000000050 myeloid neoplasm Diseases 0.000 claims 1
- 210000000056 organs Anatomy 0.000 claims 1
- 201000010174 renal carcinoma Diseases 0.000 claims 1
- 201000005112 urinary bladder cancer Diseases 0.000 claims 1
Claims (42)
- 前記SAHAが、有機塩基または無機塩基との薬学的に受容可能な塩として処方される、請求項1または2に記載の薬学的組成物。
- 前記有機塩基が、有機アミンである、請求項3に記載の薬学的組成物。
- 前記有機アミンが、ピコリン、エタノールアミン、トリエタノールアミン、2−エチルアミノエタノール、プロカインおよびN,N’−ジベンジルエチレンジアミンからなる群より選択される、請求項4に記載の薬学的組成物。
- 前記有機アミンが、トリエチルアミン、ピリジン、ジシクロヘキシルアミンおよびN−メチル−D−グルカミンからなる群より選択される、請求項4に記載の薬学的組成物。
- 前記有機塩基が塩基性アミノ酸である、請求項3に記載の薬学的組成物。
- 前記塩基性アミノ酸がアルギニンである、請求項7に記載の薬学的組成物。
- 前記無機塩基がアルカリ金属である、請求項3に記載の薬学的組成物。
- 前記アルカリ金属が、リチウム、ナトリウムおよびカリウムからなる群より選択される、請求項9に記載の薬学的組成物。
- 前記無機塩基がアルカリ土類金属である、請求項3に記載の薬学的組成物。
- 前記アルカリ土類金属が、カルシウムおよびマグネシウムからなる群より選択される、請求項11に記載の薬学的組成物。
- 前記無機塩基がアンモニウムである、請求項3に記載の薬学的組成物。
- 前記組成物がカプセル内に包含される、請求項1または2に記載の薬学的組成物。
- 前記組成物が錠剤として処方される、請求項1または2に記載の薬学的組成物。
- SAHAが前記組成物中の活性成分である、請求項1または2に記載の薬学的組成物。
- 前記有機塩基が、有機アミンである、請求項17に記載の薬学的組成物。
- 前記有機アミンが、ピコリン、エタノールアミン、トリエタノールアミン、2−エチルアミノエタノール、プロカインおよびN,N’−ジベンジルエチレンジアミンからなる群より選択される、請求項18に記載の薬学的組成物。
- 前記有機アミンが、トリエチルアミン、ピリジン、ジシクロヘキシルアミンおよびN−メチル−D−グルカミンからなる群より選択される、請求項18に記載の薬学的組成物。
- 前記有機塩基が塩基性アミノ酸である、請求項17に記載の薬学的組成物。
- 前記塩基性アミノ酸がアルギニンである、請求項21に記載の薬学的組成物。
- 前記無機塩基がアルカリ金属である、請求項17に記載の薬学的組成物。
- 前記アルカリ金属が、リチウム、ナトリウムおよびカリウムからなる群より選択される、請求項23に記載の薬学的組成物。
- 前記無機塩基がアルカリ土類金属である、請求項17に記載の薬学的組成物。
- 前記アルカリ土類金属が、カルシウムおよびマグネシウムからなる群より選択される、請求項25に記載の薬学的組成物。
- 前記無機塩基がアンモニウムである、請求項17に記載の薬学的組成物。
- 前記癌が膀胱癌である、請求項28に記載の薬学的組成物。
- 前記癌が膀胱癌腫である、請求項28に記載の薬学的組成物。
- 前記癌が乳癌である、請求項28に記載の薬学的組成物。
- 前記癌が乳癌腫である、請求項28に記載の薬学的組成物。
- 前記癌が前立腺癌である、請求項28に記載の薬学的組成物。
- 前記癌が結腸癌である、請求項28に記載の薬学的組成物。
- 前記癌が白血病である、請求項28に記載の薬学的組成物。
- 前記癌が骨髄腫である、請求項28に記載の薬学的組成物。
- 前記癌が皮膚または器官の白血球浸潤を伴う癌である、請求項28に記載の薬学的組成物。
- 前記癌が腎臓癌である、請求項28に記載の薬学的組成物。
- 前記癌が腎臓癌腫である、請求項28に記載の薬学的組成物。
- 前記SAHAまたはその薬学的に受容可能な塩または水和物が、1日2回、200mgの用量で経口投与される、請求項28〜39のいずれか1項に記載の薬学的組成物。
- 前記SAHAまたはその薬学的に受容可能な塩または水和物が、1日1回、400mgの用量で経口投与される、請求項28〜39のいずれか1項に記載の薬学的組成物。
- SAHAが前記薬学的組成物中の活性成分である、請求項40または41のいずれか1項に記載の薬学的組成物。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US35738302P | 2002-02-15 | 2002-02-15 | |
PCT/US2003/004924 WO2003070188A2 (en) | 2002-02-15 | 2003-02-14 | Method of treating trx mediated diseases |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2005525345A JP2005525345A (ja) | 2005-08-25 |
JP2005525345A5 true JP2005525345A5 (ja) | 2006-03-30 |
Family
ID=27757609
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2003569148A Pending JP2005525345A (ja) | 2002-02-15 | 2003-02-14 | Trx媒介性疾患を処置する方法 |
Country Status (6)
Country | Link |
---|---|
US (3) | US20030235588A1 (ja) |
EP (1) | EP1482962A4 (ja) |
JP (1) | JP2005525345A (ja) |
AU (1) | AU2003219803B8 (ja) |
CA (1) | CA2476434A1 (ja) |
WO (1) | WO2003070188A2 (ja) |
Families Citing this family (79)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1231919B1 (en) * | 1999-09-08 | 2015-09-30 | Sloan-Kettering Institute For Cancer Research | Derivatives of 1-amino-1-(hetero)arylaminocarbonyl-6-hydroxyaminocarbonylhexane useful in the treatment of tumors |
AU2002230049A1 (en) * | 2001-01-30 | 2002-08-12 | The Provost, Fellows And Scholars Of The College Of The Holy And Unidivided Trinity Of Queen Elizabe | Thioredoxin derived from h. pylori, which is capable of inhibiting nf-kappa b activation |
AU2002340253C1 (en) * | 2001-10-16 | 2011-03-31 | Sloan-Kettering Institute For Cancer Research | Treatment of neurodegenerative diseases and cancer of the brain |
EP1482962A4 (en) * | 2002-02-15 | 2009-12-23 | Sloan Kettering Inst Cancer | METHOD OF TREATING THIOREDOXIN-MEDIATED DISEASES (TRX) |
US7456219B2 (en) * | 2002-03-04 | 2008-11-25 | Merck Hdac Research, Llc | Polymorphs of suberoylanilide hydroxamic acid |
US20070060614A1 (en) * | 2002-03-04 | 2007-03-15 | Bacopoulos Nicholas G | Methods of treating cancer with hdac inhibitors |
EP2266552A3 (en) * | 2002-03-04 | 2011-03-02 | Merck HDAC Research, LLC | Methods of inducing terminal differentiation |
US7148257B2 (en) | 2002-03-04 | 2006-12-12 | Merck Hdac Research, Llc | Methods of treating mesothelioma with suberoylanilide hydroxamic acid |
US20060276547A1 (en) * | 2002-03-04 | 2006-12-07 | Bacopoulos Nicholas G | Methods of treating cancer with HDAC inhibitors |
US20040132825A1 (en) * | 2002-03-04 | 2004-07-08 | Bacopoulos Nicholas G. | Methods of treating cancer with HDAC inhibitors |
WO2003083067A2 (en) * | 2002-03-28 | 2003-10-09 | Brigham And Women's Hospital, Inc. | Histone deacetylase inhibitors for the treatment of multiple sclerosis, amyotrophic lateral sclerosis and alzheimer's disease |
AU2003226408B2 (en) * | 2002-04-15 | 2007-06-14 | Sloan-Kettering Institute For Cancer Research | Combination therapy for the treatment of cancer |
US8946295B2 (en) * | 2002-07-25 | 2015-02-03 | Sunny Pharmtech Inc. | Histone hyperacetylating agents for promoting wound healing and preventing scar formation |
CN1839121A (zh) * | 2003-04-01 | 2006-09-27 | 斯隆-凯特林癌症研究所 | 异羟肟酸化合物及其使用方法 |
EP1491188A1 (en) * | 2003-06-25 | 2004-12-29 | G2M Cancer Drugs AG | Topical use of valproic acid for the prevention or treatment of skin disorders |
US20050037992A1 (en) * | 2003-07-22 | 2005-02-17 | John Lyons | Composition and method for treating neurological disorders |
DK1663194T3 (da) * | 2003-08-26 | 2010-07-19 | Merck Hdac Res Llc | Anvendelse af SAHA til behandling af mesotheliom |
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 |
JP2007508318A (ja) * | 2003-10-09 | 2007-04-05 | エートン ファーマ インコーポレーティッド | チオフェンおよびベンゾチオフェンヒドロキサム酸誘導体 |
CA2547356A1 (en) * | 2003-11-26 | 2005-06-16 | Aton Pharma, Inc. | Diamine and iminodiacetic acid hydroxamic acid derivatives |
US20050197336A1 (en) * | 2004-03-08 | 2005-09-08 | Miikana Therapeutics Corporation | Inhibitors of histone deacetylase |
US7345043B2 (en) * | 2004-04-01 | 2008-03-18 | Miikana Therapeutics | Inhibitors of histone deacetylase |
AU2005230682B2 (en) * | 2004-04-05 | 2010-10-21 | Merck Hdac Research, Llc | Histone deacetylase inhibitor prodrugs |
US8029815B2 (en) | 2004-04-28 | 2011-10-04 | Elford Howard L | Methods for treating or preventing restenosis and other vascular proliferative disorders |
WO2005117930A2 (en) * | 2004-06-04 | 2005-12-15 | Sloan-Kettering Institute For Cancer Research | Use of thioredoxin measurements for diagnostics and treatments |
US7132454B2 (en) * | 2004-08-27 | 2006-11-07 | Regents Of The University Of California | HEXIM1 as a suppressor of HIV replication and cardiac hypertrophy |
WO2006060382A2 (en) * | 2004-11-30 | 2006-06-08 | Trustees Of The University Of Pennsylvania | Use of hdac and/or dnmt inhibitors for treatment of ischemic injury |
JP2008523138A (ja) * | 2004-12-14 | 2008-07-03 | バイオランクス カンパニー リミテッド | Runx2をアセチル化してRunx2活性を増加させることによって、BMPによる骨形成経路を活性化させる方法 |
US8999944B2 (en) | 2005-01-20 | 2015-04-07 | University Of Rochester | Thioredoxin interacting protein (TXNIP) as regulator of vascular function |
EP1855760A2 (en) | 2005-02-03 | 2007-11-21 | TopoTarget UK Limited | Combination therapies using hdac inhibitors |
CA2596015A1 (en) * | 2005-02-14 | 2006-08-24 | Sampath K. Anandan | Fused heterocyclic compounds useful as inhibitors of histone deacetylase |
US20090280100A1 (en) * | 2005-02-25 | 2009-11-12 | Redox Bioscience Inc. | Preventive or Therapeutic Agent for Inflammatory Ocular-Surface Diseases |
EP1719543A1 (en) * | 2005-05-04 | 2006-11-08 | Asan Labs., Ltd. | Use of histone deacetylase inhibitors for the treatment of gastrointestinal distress |
GB0509225D0 (en) | 2005-05-05 | 2005-06-15 | Chroma Therapeutics Ltd | Inhibitors of enzymatic activity |
KR101329437B1 (ko) * | 2005-05-13 | 2013-11-14 | 토포타겟 유케이 리미티드 | Hdac 억제제의 약학 제형 |
TWI365068B (en) | 2005-05-20 | 2012-06-01 | Merck Sharp & Dohme | Formulations of suberoylanilide hydroxamic acid and methods for producing same |
EA200800321A1 (ru) | 2005-07-14 | 2008-06-30 | Такеда Сан Диего, Инк. | Ингибиторы гистондеацетилазы |
EP1743654A1 (en) * | 2005-07-15 | 2007-01-17 | TopoTarget Germany AG | Use of inhibitors of histone deacetylases in combination with NSAID for the therapy of cancer and/or inflammatory diseases |
WO2007021682A1 (en) * | 2005-08-10 | 2007-02-22 | Novartis Ag | Method of use of deacetylase inhibitors |
WO2007117272A2 (en) * | 2005-09-30 | 2007-10-18 | The Henry M. Jackson Foundation For The Advancement Of Military Medicine | Methods for treatment of hemorrhagic shock and related disorders |
EP1954284A4 (en) * | 2005-11-04 | 2010-01-06 | Merck & Co Inc | ANTICANCER TREATMENT OF SAHA AND PEMETREXED |
EP1942907A2 (en) * | 2005-11-04 | 2008-07-16 | Merck and Co., Inc. | Methods of using saha and erlotinib for treating cancer |
CA2626679C (en) * | 2005-11-04 | 2011-08-16 | Merck & Co., Inc. | Methods of treating cancers with saha, carboplatin, and paclitaxel and other combination therapies |
EP2361619A1 (en) | 2005-11-10 | 2011-08-31 | TopoTarget UK Limited | Histone deacetylase (hdac) inhibitors (pxd-101) alone for the treatment of hematological cancer |
WO2007145704A2 (en) | 2006-04-24 | 2007-12-21 | Gloucester Pharmaceuticals | Gemcitabine combination therapy |
US8957027B2 (en) | 2006-06-08 | 2015-02-17 | Celgene Corporation | Deacetylase inhibitor therapy |
AU2007317921A1 (en) * | 2006-11-03 | 2008-05-15 | University Of Maryland, Baltimore | Methods of using SAHA and Bortezomib for treating multiple myeloma |
US8088951B2 (en) * | 2006-11-30 | 2012-01-03 | Massachusetts Institute Of Technology | Epigenetic mechanisms re-establish access to long-term memory after neuronal loss |
EP2102230A2 (en) | 2006-12-29 | 2009-09-23 | Gloucester Pharmaceuticals, Inc. | Purifiction of romidepsin |
US20110015168A1 (en) * | 2007-01-19 | 2011-01-20 | Mitchell Keegan | Methods for increasing levels of human fetal hemoglobin |
WO2008113056A2 (en) | 2007-03-14 | 2008-09-18 | Knopp Neurosciences, Inc. | Synthesis of chirally purified substituted benzothiazole diamines |
EP2170311A4 (en) * | 2007-05-16 | 2011-10-19 | Avalon Pharmaceuticals | COMPOSITIONS AND METHODS FOR TREATING OR PREVENTING AUTOIMMUNE DISEASES |
AU2008269154B2 (en) | 2007-06-27 | 2014-06-12 | Merck Sharp & Dohme Llc | 4-carboxybenzylamino derivatives as histone deacetylase inhibitors |
EP2030615A3 (en) * | 2007-08-13 | 2009-12-02 | ELFORD, Howard L. | Ribonucleotide reductase inhibitors for use in the treatment or prevention of neuroinflammatory or autoimmune diseases |
EP2203421B1 (en) * | 2007-09-25 | 2014-05-07 | TopoTarget UK Limited | Methods of synthesis of certain n-hydroxy-3-(3-phenylsulfamoyl-phenyl)-acrylamide compounds |
US20100216796A1 (en) * | 2007-10-04 | 2010-08-26 | Solomon Kattar | N-hydroxy-naphthalene dicarboxamide and n-hydroxy-biphenyl-dicarboxamide compounds as histone deacetylase inhibitors |
CN102083428A (zh) * | 2008-03-07 | 2011-06-01 | 顶标公司 | 采用长时间连续输液Belinostat进行治疗的方法 |
ES2332687B1 (es) * | 2008-03-13 | 2011-01-10 | Proyecto De Biomedicina Cima, S.L. | Nuevos usos de 4pba y sus sales farmaceuticamente aceptables. |
EP2334185A4 (en) * | 2008-08-19 | 2011-09-21 | Knopp Neurosciences Inc | COMPOSITIONS AND METHODS FOR USE OF (R) -PRAMIPEXOL |
GB0900555D0 (en) * | 2009-01-14 | 2009-02-11 | Topotarget As | New methods |
WO2011053876A1 (en) * | 2009-10-30 | 2011-05-05 | Massachusetts Institute Of Technology | The use of ci-994 and dinaline for the treatment of memory/cognition and anxiety disorders |
CN103108648A (zh) | 2010-07-12 | 2013-05-15 | 细胞基因公司 | 罗米地辛固体形式及其用途 |
US8859502B2 (en) | 2010-09-13 | 2014-10-14 | Celgene Corporation | Therapy for MLL-rearranged leukemia |
WO2013041407A1 (en) * | 2011-09-19 | 2013-03-28 | Cellzome Ag | Hydroxamic acids as hdac6 inhibitors |
WO2013096816A1 (en) | 2011-12-22 | 2013-06-27 | Biogen Idec Ma Inc. | Improved synthesis of amine substituted 4,5,6,7-tetrahydrobenzothiazole compounds |
AU2013202506B2 (en) | 2012-09-07 | 2015-06-18 | Celgene Corporation | Resistance biomarkers for hdac inhibitors |
AU2013202507B9 (en) | 2012-11-14 | 2015-08-13 | Celgene Corporation | Inhibition of drug resistant cancer cells |
US9662313B2 (en) | 2013-02-28 | 2017-05-30 | Knopp Biosciences Llc | Compositions and methods for treating amyotrophic lateral sclerosis in responders |
EP2976425B1 (en) * | 2013-03-18 | 2019-11-06 | Qiagen GmbH | Stabilization and isolation of extracellular nucleic acids |
US9468630B2 (en) | 2013-07-12 | 2016-10-18 | Knopp Biosciences Llc | Compositions and methods for treating conditions related to increased eosinophils |
PL3019167T3 (pl) | 2013-07-12 | 2021-06-14 | Knopp Biosciences Llc | Leczenie podwyższonych poziomów eozynofili i/lub bazofili |
HUE055850T2 (hu) | 2013-08-13 | 2022-01-28 | Knopp Biosciences Llc | Készítmények és módszerek a krónikus urticaria (csalánkiütés) kezelésére |
ES2813674T3 (es) | 2013-08-13 | 2021-03-24 | Knopp Biosciences Llc | Composiciones y métodos para el tratamiento de trastornos de células plasmáticas y trastornos prolinfocíticos de células b |
NZ630311A (en) | 2013-12-27 | 2016-03-31 | Celgene Corp | Romidepsin formulations and uses thereof |
CN104490854A (zh) * | 2014-12-27 | 2015-04-08 | 中国人民解放军第四军医大学 | 丁酸钠的治疗变态反应性鼻炎的应用 |
US11291693B2 (en) | 2015-06-25 | 2022-04-05 | Synlogic Operating Company, Inc. | Bacteria engineered to treat metabolic diseases |
CN107698464A (zh) * | 2017-10-12 | 2018-02-16 | 江苏师范大学 | 具有组蛋白去乙酰化酶抑制作用的贝利司他结构类似物及其应用 |
KR102187148B1 (ko) * | 2018-08-20 | 2020-12-04 | 주식회사 휴젝스 | 산발적 파킨슨병 진단의 정보제공방법 및 약물 스크리닝 방법 |
CN110790686B (zh) * | 2019-10-08 | 2022-03-08 | 南开大学 | 一种化合物及其在制备抗炎以及治疗急性肺损伤、慢阻肺、哮喘或肺纤维化药物中的应用 |
Family Cites Families (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61176523A (ja) * | 1985-01-30 | 1986-08-08 | Teruhiko Beppu | 制癌剤 |
US5330744A (en) * | 1988-11-14 | 1994-07-19 | Sloan-Kettering Institute For Cancer Research | Method for increasing sensitivity to chemically induced terminal differentiation |
US5608108A (en) * | 1988-11-14 | 1997-03-04 | Sloan-Kettering Institute For Cancer Research | Potent inducers of terminal differentiation and method of use thereof |
US5055608A (en) * | 1988-11-14 | 1991-10-08 | Sloan-Kettering Institute For Cancer Research | Novel potent inducers of thermal differentiation and method of use thereof |
US5175191A (en) * | 1988-11-14 | 1992-12-29 | Sloan-Kettering Institute For Cancer Research | Potent inducers of terminal differentiation and methods of use thereof |
US5098899A (en) * | 1989-03-06 | 1992-03-24 | Trustees Of Boston University | Method for therapeutically treating psoriatic arthritis using vitamin D analogues and metabolites |
US5369108A (en) * | 1991-10-04 | 1994-11-29 | Sloan-Kettering Institute For Cancer Research | Potent inducers of terminal differentiation and methods of use thereof |
US5700811A (en) * | 1991-10-04 | 1997-12-23 | Sloan-Kettering Institute For Cancer Research | Potent inducers of terminal differentiation and method of use thereof |
USRE38506E1 (en) * | 1991-10-04 | 2004-04-20 | Sloan-Kettering Institute For Cancer Research | Potent inducers of terminal differentiation and methods of use thereof |
US5635532A (en) * | 1991-10-21 | 1997-06-03 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Compositions and methods for therapy and prevention of pathologies including cancer, AIDS and anemia |
US5888511A (en) * | 1993-02-26 | 1999-03-30 | Advanced Biotherapy Concepts, Inc. | Treatment of autoimmune diseases, including AIDS |
US5724983A (en) * | 1994-08-01 | 1998-03-10 | New England Center Hospitals, Inc. | Continuous monitoring using a predictive instrument |
EP0827742A1 (en) * | 1996-09-04 | 1998-03-11 | Vrije Universiteit Brussel | Use of histone deacetylase inhibitors for treating fribosis or cirrhosis |
US6043389A (en) * | 1997-03-11 | 2000-03-28 | Mor Research Applications, Ltd. | Hydroxy and ether-containing oxyalkylene esters and uses thereof |
US6231880B1 (en) * | 1997-05-30 | 2001-05-15 | Susan P. Perrine | Compositions and administration of compositions for the treatment of blood disorders |
US6262116B1 (en) * | 1998-01-23 | 2001-07-17 | Sloan-Kettering Institute For Cancer Research | Transcription therapy for cancers |
CZ20011342A3 (cs) * | 1998-10-13 | 2001-09-12 | Fujisawa Pharmaceutical Co., Ltd. | Cyklické tetrapeptidy |
JP2002528391A (ja) * | 1998-10-19 | 2002-09-03 | メチルジェン,インク. | 組合せ治療による遺伝子発現の修飾 |
EP1231919B1 (en) * | 1999-09-08 | 2015-09-30 | Sloan-Kettering Institute For Cancer Research | Derivatives of 1-amino-1-(hetero)arylaminocarbonyl-6-hydroxyaminocarbonylhexane useful in the treatment of tumors |
US20050004007A1 (en) * | 2000-09-12 | 2005-01-06 | Steven Grant | Promotion of adoptosis in cancer cells by co-administration of cyclin dependent kinase inhibitiors and cellular differentiation agents |
GB0023983D0 (en) * | 2000-09-29 | 2000-11-15 | Prolifix Ltd | Therapeutic compounds |
WO2002055017A2 (en) * | 2000-11-21 | 2002-07-18 | Wake Forest University | Method of treating autoimmune diseases |
US6495719B2 (en) * | 2001-03-27 | 2002-12-17 | Circagen Pharmaceutical | Histone deacetylase inhibitors |
US6905669B2 (en) * | 2001-04-24 | 2005-06-14 | Supergen, Inc. | Compositions and methods for reestablishing gene transcription through inhibition of DNA methylation and histone deacetylase |
AU2002318364A1 (en) * | 2001-06-14 | 2003-01-02 | Bristol-Myers Squibb Company | Novel human histone deacetylases |
ITMI20011733A1 (it) * | 2001-08-07 | 2003-02-07 | Italfarmaco Spa | Derivati dell'acido idrossamico inibitori degli enzimi istone deacetilasi, quali nuovi farmaci antiinfiammatori inibenti la sintesi di citoc |
US20040132643A1 (en) * | 2002-01-09 | 2004-07-08 | Fojo Antonio Tito | Histone deacelylase inhibitors in diagnosis and treatment of thyroid neoplasms |
EP1482962A4 (en) * | 2002-02-15 | 2009-12-23 | Sloan Kettering Inst Cancer | METHOD OF TREATING THIOREDOXIN-MEDIATED DISEASES (TRX) |
US7148257B2 (en) * | 2002-03-04 | 2006-12-12 | Merck Hdac Research, Llc | Methods of treating mesothelioma with suberoylanilide hydroxamic acid |
US7456219B2 (en) * | 2002-03-04 | 2008-11-25 | Merck Hdac Research, Llc | Polymorphs of suberoylanilide hydroxamic acid |
US20040132825A1 (en) * | 2002-03-04 | 2004-07-08 | Bacopoulos Nicholas G. | Methods of treating cancer with HDAC inhibitors |
EP2266552A3 (en) * | 2002-03-04 | 2011-03-02 | Merck HDAC Research, LLC | Methods of inducing terminal differentiation |
AU2003226408B2 (en) * | 2002-04-15 | 2007-06-14 | Sloan-Kettering Institute For Cancer Research | Combination therapy for the treatment of cancer |
JP2006508986A (ja) * | 2002-11-20 | 2006-03-16 | エルラント ゲネ セラペウチクス エルエルシー | ヒストンデアセチラーゼ阻害剤による肺細胞の治療方法 |
CN1839121A (zh) * | 2003-04-01 | 2006-09-27 | 斯隆-凯特林癌症研究所 | 异羟肟酸化合物及其使用方法 |
-
2003
- 2003-02-14 EP EP03716078A patent/EP1482962A4/en not_active Withdrawn
- 2003-02-14 US US10/369,094 patent/US20030235588A1/en not_active Abandoned
- 2003-02-14 WO PCT/US2003/004924 patent/WO2003070188A2/en active IP Right Grant
- 2003-02-14 AU AU2003219803A patent/AU2003219803B8/en not_active Ceased
- 2003-02-14 JP JP2003569148A patent/JP2005525345A/ja active Pending
- 2003-02-14 CA CA002476434A patent/CA2476434A1/en not_active Abandoned
-
2005
- 2005-09-09 US US11/223,405 patent/US20060009526A1/en not_active Abandoned
- 2005-09-09 US US11/223,547 patent/US20060009527A1/en not_active Abandoned
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