JP2014523398A5 - - Google Patents

Download PDF

Info

Publication number
JP2014523398A5
JP2014523398A5 JP2014501258A JP2014501258A JP2014523398A5 JP 2014523398 A5 JP2014523398 A5 JP 2014523398A5 JP 2014501258 A JP2014501258 A JP 2014501258A JP 2014501258 A JP2014501258 A JP 2014501258A JP 2014523398 A5 JP2014523398 A5 JP 2014523398A5
Authority
JP
Japan
Prior art keywords
agent
integrin
beta
antibody
composition
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.)
Pending
Application number
JP2014501258A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014523398A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2012/030204 external-priority patent/WO2012129448A1/en
Publication of JP2014523398A publication Critical patent/JP2014523398A/ja
Publication of JP2014523398A5 publication Critical patent/JP2014523398A5/ja
Pending legal-status Critical Current

Links

JP2014501258A 2011-03-23 2012-03-22 抗−インテグリンを用いた抗血管新生療法を改良するための方法及び組成物 Pending JP2014523398A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161466791P 2011-03-23 2011-03-23
US61/466,791 2011-03-23
PCT/US2012/030204 WO2012129448A1 (en) 2011-03-23 2012-03-22 Methods and compositions for improving antiangiogenic therapy with anti-integrins

Publications (2)

Publication Number Publication Date
JP2014523398A JP2014523398A (ja) 2014-09-11
JP2014523398A5 true JP2014523398A5 (cg-RX-API-DMAC7.html) 2015-05-07

Family

ID=46879749

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014501258A Pending JP2014523398A (ja) 2011-03-23 2012-03-22 抗−インテグリンを用いた抗血管新生療法を改良するための方法及び組成物

Country Status (9)

Country Link
US (3) US20140079637A1 (cg-RX-API-DMAC7.html)
EP (1) EP2688585B1 (cg-RX-API-DMAC7.html)
JP (1) JP2014523398A (cg-RX-API-DMAC7.html)
KR (1) KR20140030153A (cg-RX-API-DMAC7.html)
CN (1) CN103561761A (cg-RX-API-DMAC7.html)
AU (1) AU2012230809B2 (cg-RX-API-DMAC7.html)
CA (1) CA2830908C (cg-RX-API-DMAC7.html)
ES (1) ES2699532T3 (cg-RX-API-DMAC7.html)
WO (1) WO2012129448A1 (cg-RX-API-DMAC7.html)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014523398A (ja) * 2011-03-23 2014-09-11 ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア 抗−インテグリンを用いた抗血管新生療法を改良するための方法及び組成物
EP2938359A4 (en) * 2012-12-26 2016-10-12 Oncosynergy Inc ANTI-INTEGRIN BETA1 ANTIBODY COMPOSITIONS AND METHODS OF USE
EP3067369A1 (en) 2015-03-11 2016-09-14 Institut d'Investigació Biomèdica de Bellvitge (IDIBELL) Methods and compositions for the treatment of anti-angiogenic resistant cancer
EP3067698A1 (en) 2015-03-11 2016-09-14 Institut d'Investigació Biomèdica de Bellvitge (IDIBELL) Pd-ecgf as biomarker of cancer
JP7056932B2 (ja) 2015-08-25 2022-04-19 ヒスタイド アクツィエンゲゼルシャフト 組織形成誘導用化合物及びその使用
HRP20211627T1 (hr) * 2015-09-17 2022-02-04 Histide Ag Farmaceutski pripravak koji se sastoji od agonista receptora čimbenika rasta i proteina inhibitora adhezije za pretvaranje neoplastične stanice u neneoplastičnu stanicu i njegova upotreba
WO2017046229A1 (en) * 2015-09-17 2017-03-23 Histide Ag Pharmaceutical association of growth factor receptor agonist and adhesion protein inhibitor for converting a neoplastic cell into a non-neoplastic cell and uses thereof
KR20180050744A (ko) * 2015-09-17 2018-05-23 히스티드 아게 신생물성 세포를 비-신생물성 세포로 전환시키기 위한 약제학적 회합물 및 이것의 용도
WO2020145669A1 (ko) * 2019-01-10 2020-07-16 에스지메디칼 주식회사 항 베타 1 인테그린 인간화 항체 및 이를 포함하는 암치료용 약학 조성물

Family Cites Families (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4816567A (en) 1983-04-08 1989-03-28 Genentech, Inc. Recombinant immunoglobin preparations
US5272263A (en) * 1989-04-28 1993-12-21 Biogen, Inc. DNA sequences encoding vascular cell adhesion molecules (VCAMS)
US6033665A (en) 1989-09-27 2000-03-07 Elan Pharmaceuticals, Inc. Compositions and methods for modulating leukocyte adhesion to brain endothelial cells
US6165467A (en) 1991-07-20 2000-12-26 Yoshihide Hagiwara Stabilized human monoclonal antibody preparation
US5840300A (en) 1995-09-11 1998-11-24 Trustees Of The University Of Pennsylvania Methods and compositions comprising single chain recombinant antibodies
US5846536A (en) * 1996-10-04 1998-12-08 The Regents Of The University Of California Restoration of normal phenotype in cancer cells
US6596276B1 (en) 1997-09-30 2003-07-22 Beth Israel Deaconess Medical Center Method for inhibiting tumor angiogenesis in a living subject
JP2002514605A (ja) * 1998-05-08 2002-05-21 ザ レジェンツ オブ ザ ユニヴァースティ オブ カリフォルニア 血管形成を検出および阻害する方法
EP1140840B1 (en) 1999-01-13 2006-03-22 Bayer Pharmaceuticals Corp. -g(v)-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
JP2002534468A (ja) 1999-01-13 2002-10-15 バイエル コーポレイション p38キナーゼ阻害剤としてのω−カルボキシアリール置換ジフェニル尿素
US7928239B2 (en) 1999-01-13 2011-04-19 Bayer Healthcare Llc Inhibition of RAF kinase using quinolyl, isoquinolyl or pyridyl ureas
US6949245B1 (en) 1999-06-25 2005-09-27 Genentech, Inc. Humanized anti-ErbB2 antibodies and treatment with anti-ErbB2 antibodies
US6716410B1 (en) 1999-10-26 2004-04-06 The Regents Of The University Of California Reagents and methods for diagnosing, imaging and treating atherosclerotic disease
JP3789066B2 (ja) 1999-12-08 2006-06-21 三菱電機株式会社 液晶表示装置
US8725620B2 (en) 2000-07-10 2014-05-13 Nobuyoshi Morimoto System and method for negotiating improved terms for products and services being purchased through the internet
US6995162B2 (en) 2001-01-12 2006-02-07 Amgen Inc. Substituted alkylamine derivatives and methods of use
US6878714B2 (en) 2001-01-12 2005-04-12 Amgen Inc. Substituted alkylamine derivatives and methods of use
WO2002097038A2 (en) * 2001-05-25 2002-12-05 Human Genome Sciences, Inc. Chemokine beta-1 fusion proteins
AU2002312566A1 (en) 2001-07-09 2003-01-29 Elan Pharmaceuticals, Inc. Methods of inhibiting amyloid toxicity
CA2466762A1 (en) 2001-12-04 2003-06-12 Onyx Pharmaceuticals, Inc. Raf-mek-erk pathway inhibitors to treat cancer
CN102816113B (zh) 2003-07-23 2015-05-13 拜耳医药保健有限责任公司 用于治疗和预防疾病和疾病症状的氟代ω-羧芳基二苯基脲
BRPI0507373A (pt) 2004-01-23 2007-07-10 Amgen Inc compostos e método de uso
US7618627B2 (en) * 2004-06-03 2009-11-17 The Regents Of The University Of California Method of increasing radiation sensitivity by inhibition of beta one integrin
EP1893647A2 (en) 2005-06-23 2008-03-05 MedImmune, Inc. Antibody formulations having optimized aggregation and fragmentation profiles
AR059066A1 (es) 2006-01-27 2008-03-12 Amgen Inc Combinaciones del inhibidor de la angiopoyetina -2 (ang2) y el inhibidor del factor de crecimiento endotelial vascular (vegf)
JP4997432B2 (ja) * 2006-02-10 2012-08-08 学校法人慶應義塾 神経幹細胞の増殖抑制剤
WO2008060645A2 (en) * 2006-03-21 2008-05-22 Genentech, Inc. Combinatorial therapy involving alpha5beta1 antagonists
CN101448858B (zh) * 2006-03-21 2013-06-12 健泰科生物技术公司 牵涉α5β1拮抗剂的联合疗法
EP2066689A4 (en) * 2006-09-07 2010-04-28 Univ South Florida HYD1-PEPTIDE AS ANTICREMENT
WO2009009114A2 (en) * 2007-07-12 2009-01-15 Oncomed Pharmaceuticals, Inc. Compositions and methods for treating and diagnosing cancer
WO2009018226A2 (en) * 2007-07-27 2009-02-05 Facet Biotech Corporation Pharmaceutical combinations comprising a tyrosine kinase inhibitor and an antibody against integrin alpha 1 beta 5 (cd49e)
EP2060287B1 (de) * 2007-11-14 2011-06-15 BrainLAB AG Medikamentenzuführungssystem für CED (Convection Enhanced Delivery)-Katheterinfusionen
CA2734863A1 (en) * 2008-08-20 2010-02-25 New York Blood Center, Inc. Regulation of integrin surface expression
CA2748161A1 (en) * 2008-12-23 2010-07-01 Astrazeneca Ab Targeted binding agents directed to .alpha.5.beta.1 and uses thereof
AR075925A1 (es) * 2009-03-25 2011-05-04 Genentech Inc Anticuerpos anti-alfa5beta1 (alfa5beta1: glicoproteina integrina) y sus usos
JP2014523398A (ja) * 2011-03-23 2014-09-11 ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア 抗−インテグリンを用いた抗血管新生療法を改良するための方法及び組成物
EP2938359A4 (en) * 2012-12-26 2016-10-12 Oncosynergy Inc ANTI-INTEGRIN BETA1 ANTIBODY COMPOSITIONS AND METHODS OF USE

Similar Documents

Publication Publication Date Title
JP2014523398A5 (cg-RX-API-DMAC7.html)
Ohri et al. Radiotherapy for hepatocellular carcinoma: new indications and directions for future study
Gingis-Velitski et al. Host response to short-term, single-agent chemotherapy induces matrix metalloproteinase-9 expression and accelerates metastasis in mice
Adamali et al. Current and novel drug therapies for idiopathic pulmonary fibrosis
Ning et al. Therapeutic strategies targeting cancer stem cells
Cho et al. Therapeutic potential of metformin in papillary thyroid cancer in vitro and in vivo
US12350302B2 (en) Dosing regime and formulations for type B adenoviruses
JP2012067116A5 (cg-RX-API-DMAC7.html)
Liu et al. 177Lu-labeled antibodies for EGFR-targeted SPECT/CT imaging and radioimmunotherapy in a preclinical head and neck carcinoma model
RU2016129287A (ru) Лечение злокачественных опухолей с применением комбинаций ингибиторов erk и raf
RU2016109811A (ru) Лечение рака комбинацией антагониста pd-1 и динациклиба
JP2016530323A5 (cg-RX-API-DMAC7.html)
JP2011116755A5 (cg-RX-API-DMAC7.html)
TR201807411T4 (tr) DNA-PK inhibitörleri.
JP2008507536A5 (cg-RX-API-DMAC7.html)
ME02470B (me) Nanočesтice nabijene sa hemoterapeutskim anтitumorskim lekom
JP2017506662A5 (cg-RX-API-DMAC7.html)
Cho et al. Phase Ib/II study of the pan-cyclin-dependent kinase inhibitor roniciclib in combination with chemotherapy in patients with extensive-disease small-cell lung cancer
JP2014511383A5 (cg-RX-API-DMAC7.html)
Specenier et al. Recurrent head and neck cancer: current treatment and future prospects
JP2019532047A5 (cg-RX-API-DMAC7.html)
Mayer et al. SABRE-B: an evaluation of paclitaxel and bevacizumab with or without sunitinib as first-line treatment of metastatic breast cancer
WO2012154587A3 (en) Methods for preventing toxic drug-drug interactions in combination therapies comprising anti-erbb3 agents
CN104623663B (zh) 评估癌症于治疗后情况的方法及其相关应用
Zhang et al. Management of castrate resistant prostate cancer—recent advances and optimal sequence of treatments