JP2013540734A5 - - Google Patents

Download PDF

Info

Publication number
JP2013540734A5
JP2013540734A5 JP2013528366A JP2013528366A JP2013540734A5 JP 2013540734 A5 JP2013540734 A5 JP 2013540734A5 JP 2013528366 A JP2013528366 A JP 2013528366A JP 2013528366 A JP2013528366 A JP 2013528366A JP 2013540734 A5 JP2013540734 A5 JP 2013540734A5
Authority
JP
Japan
Prior art keywords
mll
romidepsin
pharmaceutical composition
composition
dose
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.)
Granted
Application number
JP2013528366A
Other languages
English (en)
Other versions
JP5948332B2 (ja
JP2013540734A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2011/051173 external-priority patent/WO2012037008A2/en
Publication of JP2013540734A publication Critical patent/JP2013540734A/ja
Publication of JP2013540734A5 publication Critical patent/JP2013540734A5/ja
Application granted granted Critical
Publication of JP5948332B2 publication Critical patent/JP5948332B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Description

Figure 2013540734

Claims (14)

  1. ロミデプシンを含む、MLL再構成急性リンパ性白血病(ALL)の治療に使用するための医薬組成物。
  2. 前記ロミデプシンが、約0.5mg/m2から約28mg/m2の範囲の用量、若しくは約5mg/m2から約15mg/m2の範囲、若しくは約8mg/m2の用量、若しくは約10mg/m2の用量、若しくは約12mg/m2の用量、若しくは約14mg/m2の用量での静脈内投与に適したものであり、4時間かけて注入される、請求項1記載の医薬組成物。
  3. 28日周期の第1、8、及び15日に投与され、該周期が28日毎に繰り返される、請求項2記載の医薬組成物。
  4. 前記ロミデプシンが、約1mg/m2から約300mg/m2の範囲の用量、若しくは約15mg/m2から約100mg/m2の範囲の用量、若しくは25mg/m2から約75mg/m2の範囲の用量での経口投与に適したものである、請求項1記載の医薬組成物。
  5. 前記MLL再構成ALLが、MLL再構成乳児ALLである、請求項1記載の医薬組成物。
  6. 細胞をロミデプシンと接触させることにより細胞を処理するための組成物であって、該ロミデプシンの濃度が、該細胞の成長を阻害するか又は該細胞を死滅させるのに十分なものであり、該細胞が、MLL再構成ALL細胞である、前記組成物。
  7. 前記細胞が、MLL再構成乳児ALL細胞株である、請求項6記載の組成物。
  8. 前記細胞株が、SEM又はRS4:11細胞株である、請求項7記載の組成物。
  9. 前記ロミデプシンの濃度が、約0.01nMから500nMの範囲であるか、又は約0.1nMから100nMの範囲であるか、又は約1nMから5nMの範囲である、請求項6記載の組成物。
  10. 前記細胞が、MLL再構成乳児ALL細胞である、請求項6記載の組成物。
  11. MLL再構成乳児ALLの治療に使用するための医薬組成物であって、こうした治療を必要とする患者に、28日周期の第1、8、及び15日に、4時間かけて静脈内注入することによって、14mg/m2の用量で投与されることに適したものであり、該周期が、28日毎に繰り返される、前記医薬組成物。
  12. ロミデプシン及び医薬として許容し得る担体、賦形剤又は希釈剤を含む、MLL再構成ALLを治療するための医薬組成物。
  13. ロミデプシン又はその医薬組成物を装入した1以上の容器を含む、MLL再構成ALLを治療するためのキット。
  14. 前記MLL再構成ALLが、MLL再構成乳児ALLである、請求項13記載のキット。
JP2013528366A 2010-09-13 2011-09-12 Mll再構成白血病の治療法 Active JP5948332B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US38245910P 2010-09-13 2010-09-13
US61/382,459 2010-09-13
PCT/US2011/051173 WO2012037008A2 (en) 2010-09-13 2011-09-12 Therapy for mll-rearranged leukemia

Publications (3)

Publication Number Publication Date
JP2013540734A JP2013540734A (ja) 2013-11-07
JP2013540734A5 true JP2013540734A5 (ja) 2015-01-08
JP5948332B2 JP5948332B2 (ja) 2016-07-06

Family

ID=44653606

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2013528366A Active JP5948332B2 (ja) 2010-09-13 2011-09-12 Mll再構成白血病の治療法

Country Status (4)

Country Link
US (1) US8859502B2 (ja)
EP (1) EP2616054A2 (ja)
JP (1) JP5948332B2 (ja)
WO (1) WO2012037008A2 (ja)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100093610A1 (en) * 2006-12-29 2010-04-15 Vrolijk Nicholas H Romidepsin-based treatments for cancer
CA2912973A1 (en) * 2013-05-24 2014-11-27 4Sc Ag Gene expression biomarkers and their use for diagnostic and prognostic application in patients potentially in need of hdac inhibitor treatment
NZ630311A (en) 2013-12-27 2016-03-31 Celgene Corp Romidepsin formulations and uses thereof
GB2530470A (en) * 2014-04-17 2016-03-30 Imp Innovations Ltd Methods
KR20170044097A (ko) * 2014-07-07 2017-04-24 에이스틸론 파마수티컬스 인코포레이티드 히스톤 탈아세틸화효소 저해제에 의한 백혈병의 치료

Family Cites Families (107)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2927352A1 (de) 1979-07-06 1981-02-05 Thomae Gmbh Dr K In 6-stellung substituierte benzothiazol-2(3h)-one enthaltende arzneimittel
US4410545A (en) 1981-02-13 1983-10-18 Syntex (U.S.A.) Inc. Carbonate diester solutions of PGE-type compounds
US4328245A (en) 1981-02-13 1982-05-04 Syntex (U.S.A.) Inc. Carbonate diester solutions of PGE-type compounds
US4409239A (en) 1982-01-21 1983-10-11 Syntex (U.S.A.) Inc. Propylene glycol diester solutions of PGE-type compounds
GB8817743D0 (en) 1988-07-26 1988-09-01 Fujisawa Pharmaceutical Co Fr901228 substance & preparation thereof
US5143854A (en) 1989-06-07 1992-09-01 Affymax Technologies N.V. Large scale photolithographic solid phase synthesis of polypeptides and receptor binding screening thereof
US5545522A (en) 1989-09-22 1996-08-13 Van Gelder; Russell N. Process for amplifying a target polynucleotide sequence using a single primer-promoter complex
US5817667A (en) * 1991-04-17 1998-10-06 University Of Georgia Research Foudation Compounds and methods for the treatment of cancer
JPH064872A (ja) 1992-06-19 1994-01-14 Sony Corp 光ディスク再生装置
JPH0764872A (ja) 1993-08-26 1995-03-10 Fujitsu Ten Ltd データ記憶制御装置
US5578832A (en) 1994-09-02 1996-11-26 Affymetrix, Inc. Method and apparatus for imaging a sample on a device
US5605793A (en) 1994-02-17 1997-02-25 Affymax Technologies N.V. Methods for in vitro recombination
US6117679A (en) 1994-02-17 2000-09-12 Maxygen, Inc. Methods for generating polynucleotides having desired characteristics by iterative selection and recombination
US5837458A (en) 1994-02-17 1998-11-17 Maxygen, Inc. Methods and compositions for cellular and metabolic engineering
US5556752A (en) 1994-10-24 1996-09-17 Affymetrix, Inc. Surface-bound, unimolecular, double-stranded DNA
US6777217B1 (en) 1996-03-26 2004-08-17 President And Fellows Of Harvard College Histone deacetylases, and uses related thereto
US5776905A (en) 1996-08-08 1998-07-07 The Board Of Trustees Of The Leland Stamford Junior University Apoptotic regression of intimal vascular lesions
US6030961A (en) 1997-03-11 2000-02-29 Bar-Ilan Research & Development Co., Ltd. Oxyalkylene phosphate compounds and uses thereof
US6124495A (en) 1997-03-11 2000-09-26 Beacon Laboratories, Inc. Unsaturated oxyalkylene esters and uses thereof
JP3494624B2 (ja) 1997-09-02 2004-02-09 住友製薬株式会社 新規な環状テトラペプチド誘導体とその医薬用途
US6350458B1 (en) 1998-02-10 2002-02-26 Generex Pharmaceuticals Incorporated Mixed micellar drug deliver system and method of preparation
JPH11335375A (ja) 1998-05-20 1999-12-07 Mitsui Chem Inc ヒストン脱アセチル化酵素阻害作用を有するベンズアミド誘導体
US6214986B1 (en) 1998-10-07 2001-04-10 Isis Pharmaceuticals, Inc. Antisense modulation of bcl-x expression
US20070148228A1 (en) 1999-02-22 2007-06-28 Merrion Research I Limited Solid oral dosage form containing an enhancer
US6723338B1 (en) 1999-04-01 2004-04-20 Inex Pharmaceuticals Corporation Compositions and methods for treating lymphoma
WO2001018171A2 (en) 1999-09-08 2001-03-15 Sloan-Kettering Institute For Cancer Research Novel class of cytodifferentiating agents and histone deacetylase inhibitors, and methods of use thereof
EP1246839B1 (en) 1999-12-08 2004-06-16 Xcyte Therapies, Inc. Depsipeptide and congeners thereof for use as immunosuppressants
US6828302B1 (en) 1999-12-08 2004-12-07 Xcyte Therapies, Inc. Therapeutic uses of depsipeptides and congeners thereof
CA2317003A1 (en) 2000-02-28 2001-08-28 Hidenori Nakajima Gene expression potentiator
JP2001348340A (ja) 2000-06-07 2001-12-18 Yamanouchi Pharmaceut Co Ltd ヒストン脱アセチル化酵素阻害剤
EP1302476B1 (en) 2000-07-17 2009-03-11 Astellas Pharma Inc. Reduced fk228 and use thereof
AU2001285042A1 (en) 2000-08-18 2002-03-04 The Governement Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services Methods of treating cutaneous and peripheral t-cell lymphoma by a histone deacetylase inhibitor
JP2004508049A (ja) 2000-09-01 2004-03-18 藤沢薬品工業株式会社 Fr901228物質の製造法
AU2002243231A1 (en) 2000-11-21 2002-07-24 Wake Forest University Method of treating autoimmune diseases
WO2002055688A2 (en) 2001-01-10 2002-07-18 Us Gov Health & Human Serv Histone deacetylase inhibitors in diagnosis and treatment of thyroid neoplasms
US7219016B2 (en) 2001-04-20 2007-05-15 Yale University Systems and methods for automated analysis of cells and tissues
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
DE60227658D1 (de) 2001-05-02 2008-08-28 Univ California Verfahren zur behandlung neurodegenerativer, psychiatrischer und anderer störungen mit deacetylaseinhibitoren
AU2002305769B2 (en) 2001-05-30 2007-07-19 Georgetown University Small molecule antagonists of Bcl2 family proteins
US7171311B2 (en) 2001-06-18 2007-01-30 Rosetta Inpharmatics Llc Methods of assigning treatment to breast cancer patients
HU229521B1 (hu) 2001-08-21 2014-01-28 Astellas Pharma Inc A hiszton-dezacetiláz inhibitor gyógyászati alkalmazása, és eljárás tumorellenes hatásának kiértékelésére
WO2003017763A1 (en) 2001-08-24 2003-03-06 The Government Of The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Use of a histone deacetylase inhibitor to increase the entry of an adenoviral agent into a cell
EP1293205A1 (en) 2001-09-18 2003-03-19 G2M Cancer Drugs AG Valproic acid and derivatives thereof for the combination therapy of human cancers, for the treatment of tumour metastasis and minimal residual disease
US6706686B2 (en) 2001-09-27 2004-03-16 The Regents Of The University Of Colorado Inhibition of histone deacetylase as a treatment for cardiac hypertrophy
AU2002353891A1 (en) 2001-10-25 2003-05-06 Buck Institute For Age Research Screening system for modulators of her2 mediated transcription and her2 modulators identifed thereby
WO2003038060A2 (en) 2001-11-01 2003-05-08 The Regents Of The University Of Michigan Small molecule inhibitors targeted at bcl-2
WO2003053468A1 (en) 2001-12-21 2003-07-03 Universite Libre De Bruxelles Method for obtaining the elimination of integrated and functional viruses from infected mammal cells
US20030134423A1 (en) 2002-01-04 2003-07-17 Chu Yong Liang Compounds for delivering substances into cells
JP2005525345A (ja) 2002-02-15 2005-08-25 スローン−ケッタリング・インスティテュート・フォー・キャンサー・リサーチ Trx媒介性疾患を処置する方法
WO2003070754A1 (fr) 2002-02-20 2003-08-28 Minoru Yoshida Inhibiteurs d'histone desacetylase et procede de production de ces inhibiteurs
US20040132825A1 (en) 2002-03-04 2004-07-08 Bacopoulos Nicholas G. Methods of treating cancer with HDAC inhibitors
NZ567758A (en) 2002-03-04 2009-07-31 Merck Hdac Res Llc Methods of inducing terminal differentiation using suberoylanilide hydrozmic acid (SAHA)
AU2003226014A1 (en) 2002-03-28 2003-10-13 Brigham And Women's Hospital, Inc. Histone deacetylase inhibitors for the treatment of multiple sclerosis, amyotrophic lateral sclerosis and alzheimer's disease
CN1649645A (zh) 2002-04-05 2005-08-03 藤泽药品工业株式会社 用于治疗肾癌的缩酚肽
AU2003226408B2 (en) 2002-04-15 2007-06-14 Sloan-Kettering Institute For Cancer Research Combination therapy for the treatment of cancer
US6809118B2 (en) 2002-07-25 2004-10-26 Yih-Lin Chung Methods for therapy of radiation cutaneous syndrome
US20040002447A1 (en) 2002-06-04 2004-01-01 Regents Of The University Of California Induction of insulin expression
US20050065596A1 (en) 2002-07-24 2005-03-24 Xufan Tseng Stents capable of controllably releasing histone deacetylase inhibitors
ES2342378T3 (es) 2002-08-20 2010-07-06 Astellas Pharma Inc. Inhibidor de degradacion de matriz extracelular del cartilago artrodial.
BR0314112A (pt) 2002-09-13 2005-07-12 Univ Virginia Commonwealth Combinação de a) n-{5-[4-(4-metil-piperazino-metil)-benzoilamido]-2-metil fenil}-4-(3-piridil)-2-pirimidina-amina e b) um inibidor de desacetilase de histona para o tratamento de leucemia
SE0300098D0 (sv) 2003-01-15 2003-01-15 Forskarpatent I Syd Ab Use of cyclin D1 inhibitors
WO2004064727A2 (en) 2003-01-16 2004-08-05 Georgetown University Method of cancer treatment using hdac inhibitors
KR20050106438A (ko) 2003-02-19 2005-11-09 아스텔라스세이야쿠 가부시키가이샤 히스톤 디아세틸라제 저해제의 항종양 효과의 예측방법
WO2004096289A1 (ja) 2003-04-25 2004-11-11 Fujisawa Pharmaceutical Co 遺伝子導入効率増強剤
US20040213826A1 (en) 2003-04-28 2004-10-28 Marx Steven O. Medical devices and methods for inhibiting proliferation of smooth muscle cells
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
PL2238982T3 (pl) 2003-06-27 2013-03-29 Astellas Pharma Inc Środek do terapii mięsaka tkanek miękkich
BR122016015715B8 (pt) 2003-07-23 2021-05-25 Bayer Healthcare Llc composições farmacêuticas de metilamida de ácido 4[4-[3-(4-cloro-3-trifluorometilfenil)-ureido]-3-fluorofenóxi)-piridina-2-carboxílico
AU2003268185A1 (en) * 2003-08-25 2005-04-11 Dana-Farber Cancer Institute Inc. Method of treating mixed lineage leukemia gene-rearranged acute lymphoblastic leukemias
AU2004266169B9 (en) 2003-08-26 2007-05-10 Merck Hdac Research, Llc Method of treating cancer with HDAC inhibitors
EP2226072A1 (en) 2003-08-29 2010-09-08 Aton Pharma, Inc. Combinations of suberoylanilide hydroxamic acid and antimetbolic agents for treating cancer
US20050059682A1 (en) 2003-09-12 2005-03-17 Supergen, Inc., A Delaware Corporation Compositions and methods for treatment of cancer
KR20070012618A (ko) 2003-09-18 2007-01-26 콤비네이토릭스, 인코포레이티드 신생물 치료용 약의 조합
DE602004027824D1 (de) 2003-09-25 2010-08-05 Astellas Pharma Inc Antitumorales mittel mit einem histon-deacetylase-hemmer und einem topoisomerase-ii-hemmer
US8614318B2 (en) 2003-11-13 2013-12-24 Abbvie Inc. Apoptosis promoters
JP2007511211A (ja) 2003-11-14 2007-05-10 ホルム,ペル・ゾンネ アデノウイルスおよびそれをコードしている核酸の新たな使用
CA2590257A1 (en) 2003-11-14 2005-06-09 Per Sonne Holm Novel adenoviruses, nucleic acids that code for the same and the use of said viruses
WO2005053609A2 (en) 2003-11-26 2005-06-16 Guilford Pharmaceuticals Inc. Methods of nad+-dependent deacetylase inhibitors
WO2005058298A2 (en) 2003-12-10 2005-06-30 Wisconsin Alumni Research Foundation Fk228 analogs and their use as hdac-inhibitors
US7951780B2 (en) 2004-02-25 2011-05-31 Astellas Pharma Inc. Antitumor agent
US20050187148A1 (en) 2004-02-25 2005-08-25 Yoshinori Naoe Antitumor agent
CA2557568C (en) 2004-02-27 2014-05-27 Jane Trepel Pharmacodynamic assays using flow cytometry
GB0405349D0 (en) 2004-03-10 2004-04-21 Univ Birmingham Cancer therapy and medicaments therefor
PL1591109T3 (pl) 2004-04-30 2008-11-28 Topotarget Germany Ag Preparat zawierający inhibitor deacetylazy histonów wykazujący dwufazowe uwalnianie”
ITMI20040876A1 (it) 2004-04-30 2004-07-30 Univ Degli Studi Milano Inibitori delle istone deacetilasi-hdac-quali agenti ipolipidemizzati per la terapia e la prevenzione dell'arteriosclerosi e malattie cardiovascolari
WO2005115149A2 (en) 2004-05-20 2005-12-08 Dow Agrosciences Llc Insectidal activity of a cyclic peptide
WO2005117930A2 (en) 2004-06-04 2005-12-15 Sloan-Kettering Institute For Cancer Research Use of thioredoxin measurements for diagnostics and treatments
WO2005123089A2 (en) 2004-06-10 2005-12-29 Kalypsys, Inc. Multicyclic sulfonamide compounds as inhibitors of histone deacetylase for the treatment of disease
US20060018921A1 (en) 2004-07-16 2006-01-26 Baylor College Of Medicine Histone deacetylase inhibitors and cognitive applications
US7745446B2 (en) 2004-09-06 2010-06-29 Bayer Schering Pharma Aktiengesellschaft Pyrazolo[1,5-c]pyrimidines
CA2586228A1 (en) 2004-11-17 2006-05-26 The University Of Chicago Histone deacetylase inhibitors and methods of use
US8889742B2 (en) 2004-11-30 2014-11-18 The Trustees Of The University Of Pennsylvania Use of HDAC and/or DNMT inhibitors for treatment of ischemic injury
WO2006060429A2 (en) 2004-12-03 2006-06-08 Novartis Ag Identification of variants in histone deacetylase 1 (hdac1) to predict drug response
US20060128660A1 (en) 2004-12-10 2006-06-15 Wisconsin Alumni Research Foundation FK228 analogs and methods of making and using the same
GB0511266D0 (en) 2005-06-02 2005-07-13 Trust Chemical compounds
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
US7943568B2 (en) 2005-09-30 2011-05-17 The Ohio State University Research Foundation Antitumor agents
JP2009515524A (ja) 2005-11-10 2009-04-16 アメリカ合衆国 Abcb1多型バリアントスクリーニング、診断及び処置のための物質及び方法
EP1965824A4 (en) 2005-11-18 2011-10-19 Gloucester Pharmaceuticals Inc METABOLITENE DERIVATIVES OF HDAC INHIBITOR FK228
EP2049139A4 (en) 2006-04-24 2009-06-24 Gloucester Pharmaceuticals Inc TREATMENT OF TUMORS EXPRESSING RAS
US8957027B2 (en) 2006-06-08 2015-02-17 Celgene Corporation Deacetylase inhibitor therapy
JP2009539862A (ja) 2006-06-09 2009-11-19 メリオン リサーチ Iii リミテッド 強化剤を含む固体経口投与剤形
US7857804B2 (en) 2006-09-01 2010-12-28 Mccaffrey Timothy A Use of Bcl inhibitors for the prevention of fibroproliferative reclosure of dilated blood vessels and other iatrogenic fibroproliferative disorders
US20100093610A1 (en) * 2006-12-29 2010-04-15 Vrolijk Nicholas H Romidepsin-based treatments for cancer
MX2009006969A (es) 2006-12-29 2010-04-07 Gloucester Pharmaceuticals Purificacion de romidepsina.
WO2009064300A1 (en) * 2007-11-15 2009-05-22 The Johns Hopkins University Combinations of hdac inhibitors and cytokines/growth factors
MX2011001132A (es) * 2008-07-30 2011-08-17 Gloucester Pharmaceuticals Inc Tratamiento acelerado.

Similar Documents

Publication Publication Date Title
PH12014502447A1 (en) Use of high dose laquinimod for treating multiple sclerosis
BRPI0607168A2 (pt) terapia de combinação parenteral, composição farmacêutica, processo para preparar uma composição farmacêutica e método de tratamento
JP2009539769A5 (ja)
JP2013505205A5 (ja)
JP2015212268A5 (ja)
JP2008519047A5 (ja)
JP2010507567A5 (ja)
JP2013540734A5 (ja)
JP2012193216A5 (ja)
JP2006504795A5 (ja)
RU2017134443A (ru) Способ лечения с применением традипитанта
US20150231198A1 (en) Combination therapy for hematological malignancies
NZ595767A (en) Composition for the treatment of prostate cancer
RU2013111954A (ru) Способ лечения от бокового амиотрофического склероза
JP2013541583A5 (ja)
JP2013516493A5 (ja)
RU2013123646A (ru) Комбинированная композиция
JP2015522033A5 (ja)
JP2019511496A5 (ja)
JP2016505050A5 (ja)
JP2013541587A5 (ja)
JP2019526559A5 (ja)
MX2015009546A (es) Dosificacion aumentada de efavirenz para el tratamiento de cancer.
RU2015115398A (ru) N-ацетил-L-цистеин для применения в экстракорпоральном оплодотворении
PE20130782A1 (es) Composiciones farmaceuticas que consisten de paracetamol y el proceso para la preparacion del mismo