NZ552476A - Tumor specific antibody - Google Patents
Tumor specific antibodyInfo
- Publication number
- NZ552476A NZ552476A NZ552476A NZ55247605A NZ552476A NZ 552476 A NZ552476 A NZ 552476A NZ 552476 A NZ552476 A NZ 552476A NZ 55247605 A NZ55247605 A NZ 55247605A NZ 552476 A NZ552476 A NZ 552476A
- Authority
- NZ
- New Zealand
- Prior art keywords
- protein
- seq
- amino acid
- acid sequence
- cancer
- Prior art date
Links
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/31—Immunoglobulins specific features characterized by aspects of specificity or valency multispecific
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/54—F(ab')2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/55—Fab or Fab'
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
- C07K2317/565—Complementarity determining region [CDR]
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
- C07K2317/62—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising only variable region components
- C07K2317/622—Single chain antibody (scFv)
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
- C07K2317/62—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising only variable region components
- C07K2317/624—Disulfide-stabilized antibody (dsFv)
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
- C07K2317/62—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising only variable region components
- C07K2317/626—Diabody or triabody
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/77—Internalization into the cell
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
- C07K2319/55—Fusion polypeptide containing a fusion with a toxin, e.g. diphteria toxin
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
- G01N2333/46—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans from vertebrates
- G01N2333/47—Assays involving proteins of known structure or function as defined in the subgroups
- G01N2333/4701—Details
- G01N2333/471—Pregnancy proteins, e.g. placenta proteins, alpha-feto-protein, pregnancy specific beta glycoprotein
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
- G01N2333/705—Assays involving receptors, cell surface antigens or cell surface determinants
- G01N2333/70585—CD44
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- Biomedical Technology (AREA)
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- Proteomics, Peptides & Aminoacids (AREA)
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Applications Claiming Priority (2)
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| US57829104P | 2004-06-10 | 2004-06-10 | |
| PCT/CA2005/000899 WO2005121341A1 (en) | 2004-06-10 | 2005-06-10 | Tumor specific antibody |
Publications (1)
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| NZ552476A true NZ552476A (en) | 2009-09-25 |
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Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2382990B1 (en) | 2003-04-30 | 2014-09-17 | Universität Zürich | Methods for treating cancer using an immunotoxin |
| JP5025460B2 (ja) | 2004-03-19 | 2012-09-12 | メルク パテント ゲーエムベーハー | 修飾ブーゲニンタンパク質、サイトトキシン、ならびにそれらの方法および使用 |
| CA2633138A1 (en) * | 2005-12-23 | 2007-06-28 | Viventia Biotech Inc. | Methods for generating and screening fusion protein libraries and uses thereof |
| US8263744B2 (en) | 2007-04-19 | 2012-09-11 | Viventia Biotechnologies Inc. | Binding proteins that bind to EpCAM linked to an effector molecule |
| GB0718045D0 (en) | 2007-09-14 | 2007-10-24 | Peptcell Ltd | Pharmaceutical compound |
| US8318472B2 (en) | 2007-09-27 | 2012-11-27 | Viventia Biotechnologies Inc. | Optimized nucleic acid sequences for the expression of VB4-845 |
| CA2709380A1 (en) * | 2007-12-21 | 2009-07-09 | University Of Rochester | Cd24 as a brain tumor stem cell marker and a diagnostic and therapeutic target in primary neural and glial tumors of the brain |
| US20100008978A1 (en) * | 2008-05-09 | 2010-01-14 | The Regents Of The University Of California | Nanoparticles effective for internalization into cells |
| US20100009390A1 (en) * | 2008-05-09 | 2010-01-14 | The Regents Of The University Of California | Mutant antibodies with high affinity for egfr |
| TWI404931B (zh) * | 2009-02-20 | 2013-08-11 | Nat Synchrotron Radiation Res Ct | 癌化生物樣本之檢測方法及其使用之檢驗試劑 |
| JP6041333B2 (ja) * | 2011-01-13 | 2016-12-07 | 学校法人近畿大学 | 抗腫瘍剤 |
| EP2966985B1 (en) * | 2013-03-15 | 2018-09-19 | Mayo Foundation for Medical Education and Research | Identification and monitoring of monoclonal immunoglobulins by molecular mass |
| EP3024456A4 (en) | 2013-07-26 | 2017-04-12 | Update Pharma Inc. | Combinatorial methods to improve the therapeutic benefit of bisantrene |
| US9822182B2 (en) | 2013-10-02 | 2017-11-21 | Viventia Bio Inc. | Anti-EPCAM antibodies and methods of use |
| BR112016023046A8 (pt) | 2014-04-04 | 2021-05-11 | Mayo Found Medical Education & Res | kit compreendendo anticorpos e agentes redutores |
| WO2016018978A1 (en) | 2014-07-29 | 2016-02-04 | Mayo Foundation For Medical Education And Research | Quantifying monoclonal antibody therapeutics by lc-ms/ms |
| WO2016068294A1 (ja) * | 2014-10-31 | 2016-05-06 | 株式会社カネカ | タンパク質合成阻害タンパク質毒素を含むポリペプチドの製造方法 |
| CN108513547A (zh) | 2015-03-12 | 2018-09-07 | 维文蒂亚生物公司 | 用于epcam阳性膀胱癌的治疗方法 |
| EP3268041A4 (en) | 2015-03-12 | 2018-09-05 | Viventia Bio Inc. | Dosing strategies for targeting epcam positive bladder cancer |
| WO2016187571A2 (en) * | 2015-05-20 | 2016-11-24 | Viventia Bio Inc. | Her2 immunotoxins and methods of using the same |
| CN112961213A (zh) * | 2015-08-12 | 2021-06-15 | 肿瘤疗法科学股份有限公司 | Depdc1衍生的肽和包含它们的疫苗 |
| WO2017053932A1 (en) | 2015-09-24 | 2017-03-30 | Mayo Foundation For Medical Education And Research | Identification of immunoglobulin free light chains by mass spectrometry |
| CN105510586B (zh) * | 2015-12-22 | 2017-09-12 | 湖北鹊景生物医学有限公司 | 用于肺癌诊断的试剂盒及其使用方法 |
| EP3523647B1 (en) | 2016-09-07 | 2024-06-26 | Mayo Foundation for Medical Education and Research | Identification and monitoring of cleaved immunoglobulins by molecular mass |
| EP3681907A4 (en) | 2017-09-13 | 2021-07-07 | Mayo Foundation for Medical Education and Research | IDENTIFICATION AND MONITORING OF IMMUNOGLOBULIN J-CHAINS |
| WO2019055634A1 (en) | 2017-09-13 | 2019-03-21 | Mayo Foundation For Medical Education And Research | IDENTIFICATION AND MONITORING OF A MACROPHAGE APOPTOSIS INHIBITOR |
| CN109324189B (zh) * | 2018-08-15 | 2021-10-01 | 泰达国际心血管病医院 | 多蛋白组合物的应用及先天性心脏病筛查试剂盒 |
| CN111138521B (zh) * | 2018-11-06 | 2022-10-28 | 香雪生命科学技术(广东)有限公司 | 源自于afp抗原的短肽 |
| BR112021016121A2 (pt) * | 2019-02-15 | 2022-01-04 | Atreca Inc | Anticorpo isolado que se liga a tecidos tumorais, anticorpo que se liga ao tecido tumoral, método para induzir uma resposta imune, método para tratar um paciente com câncer com um tumor, método para identificar um paciente que tem um tumor, vetor de expressão, célula hospedeira, método para produzir um anticorpo, método para identificar um anticorpo com atividade antitumoral, uso de um anticorpo e polipeptídeo |
| CN112300261B (zh) * | 2019-07-23 | 2023-03-17 | 香雪生命科学技术(广东)有限公司 | 一种衍生自afp的肿瘤抗原短肽 |
| CN112851811B (zh) * | 2021-01-28 | 2022-08-09 | 姜国胜 | 一种cd44v6纳米抗体及其作为白血病研究试剂的应用 |
| CN114773478B (zh) * | 2022-03-14 | 2023-05-23 | 深圳市国创纳米抗体技术有限公司 | 抗afp抗原vhh结构域及含有其的双特异性抗体 |
| WO2024040194A1 (en) | 2022-08-17 | 2024-02-22 | Capstan Therapeutics, Inc. | Conditioning for in vivo immune cell engineering |
| CN116297727B (zh) * | 2022-09-13 | 2024-01-23 | 山东大学齐鲁医院 | 一种甲胎蛋白和异常凝血酶原电致发光传感器的制备及其应用 |
| US12311033B2 (en) | 2023-05-31 | 2025-05-27 | Capstan Therapeutics, Inc. | Lipid nanoparticle formulations and compositions |
| US20250127728A1 (en) | 2023-10-05 | 2025-04-24 | Capstan Therapeutics, Inc. | Constrained Ionizable Cationic Lipids and Lipid Nanoparticles |
| WO2025076113A1 (en) | 2023-10-05 | 2025-04-10 | Capstan Therapeutics, Inc. | Ionizable cationic lipids with conserved spacing and lipid nanoparticles |
| WO2025179294A2 (en) | 2024-02-22 | 2025-08-28 | Capstan Therapeutics, Inc. | Immune engineering amplification |
| WO2025217452A1 (en) | 2024-04-11 | 2025-10-16 | Capstan Therapeutics, Inc. | Constrained ionizable cationic lipids and lipid nanoparticles |
| WO2025217454A2 (en) | 2024-04-11 | 2025-10-16 | Capstan Therapeutics, Inc. | Ionizable cationic lipids and lipid nanoparticles |
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| US4736866A (en) | 1984-06-22 | 1988-04-12 | President And Fellows Of Harvard College | Transgenic non-human mammals |
| CN1042940A (zh) * | 1988-12-01 | 1990-06-13 | 中国农业科学院哈尔滨兽医研究所 | 马传贫病马与接种弱毒疫苗马的血清抗体鉴别诊断试剂 |
| WO1990010457A1 (en) | 1989-03-14 | 1990-09-20 | New York University | Method of treating hiv infections using immunotoxins |
| US5863540A (en) * | 1991-03-15 | 1999-01-26 | Duke University | Adhesion molecule |
| CN1075208A (zh) * | 1992-12-02 | 1993-08-11 | 张昌卿 | 一种检测eb病毒抗体的显色试剂及其制造方法 |
| US6197582B1 (en) | 1998-03-18 | 2001-03-06 | The Trustees Of Columbia University In The City Of New York | Development of human monoclonal antibodies and uses thereof |
| JP2003299497A (ja) * | 2002-02-05 | 2003-10-21 | Masayoshi Kachi | ムコ多糖類及びその製造方法 |
| WO2003066830A2 (en) * | 2002-02-08 | 2003-08-14 | Genetastix Corporation | Human monoclonal antibodies against membrane proteins |
| EP2341067A1 (en) * | 2003-07-18 | 2011-07-06 | Amgen, Inc | Specific binding agents to hepatocyte growth factor |
| JP5025460B2 (ja) | 2004-03-19 | 2012-09-12 | メルク パテント ゲーエムベーハー | 修飾ブーゲニンタンパク質、サイトトキシン、ならびにそれらの方法および使用 |
| US8802442B2 (en) | 2011-11-30 | 2014-08-12 | Eric B. Wheeldon | Apparatus and method for the remote sensing of blood in human feces and urine |
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2005
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- 2005-06-10 EP EP14198378.3A patent/EP2927322A1/en not_active Withdrawn
- 2005-06-10 WO PCT/CA2005/000899 patent/WO2005121341A1/en not_active Ceased
- 2005-06-10 PL PL05754865T patent/PL1766017T3/pl unknown
- 2005-06-10 US US11/570,198 patent/US8383117B2/en not_active Expired - Fee Related
- 2005-06-10 AU AU2005252275A patent/AU2005252275B2/en not_active Ceased
- 2005-06-10 NZ NZ552476A patent/NZ552476A/en not_active IP Right Cessation
- 2005-06-10 EP EP05754865.3A patent/EP1766017B1/en not_active Expired - Lifetime
- 2005-06-10 CA CA2569788A patent/CA2569788C/en not_active Expired - Fee Related
- 2005-06-10 ES ES05754865.3T patent/ES2535229T3/es not_active Expired - Lifetime
- 2005-06-10 JP JP2007526144A patent/JP5026268B2/ja not_active Expired - Fee Related
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2006
- 2006-12-06 IL IL179891A patent/IL179891A/en not_active IP Right Cessation
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2012
- 2012-03-30 JP JP2012078467A patent/JP2012187104A/ja active Pending
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2013
- 2013-01-17 US US13/743,672 patent/US8969540B2/en not_active Expired - Lifetime
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2015
- 2015-01-23 US US14/604,047 patent/US20150197575A1/en not_active Abandoned
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| US20070292441A1 (en) | 2007-12-20 |
| US8969540B2 (en) | 2015-03-03 |
| PL1766017T3 (pl) | 2015-08-31 |
| CA2569788A1 (en) | 2005-12-22 |
| CN101044242A (zh) | 2007-09-26 |
| US20130217865A1 (en) | 2013-08-22 |
| CN101044242B (zh) | 2013-10-30 |
| EP1766017B1 (en) | 2015-01-21 |
| JP2012187104A (ja) | 2012-10-04 |
| US20150197575A1 (en) | 2015-07-16 |
| ES2535229T3 (es) | 2015-05-06 |
| EP1766017A4 (en) | 2009-12-02 |
| US8383117B2 (en) | 2013-02-26 |
| AU2005252275B2 (en) | 2011-07-21 |
| IL179891A (en) | 2014-07-31 |
| JP5026268B2 (ja) | 2012-09-12 |
| EP2927322A1 (en) | 2015-10-07 |
| AU2005252275A1 (en) | 2005-12-22 |
| WO2005121341A1 (en) | 2005-12-22 |
| EP1766017A1 (en) | 2007-03-28 |
| CA2569788C (en) | 2014-03-18 |
| IL179891A0 (en) | 2007-05-15 |
| JP2008508903A (ja) | 2008-03-27 |
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Legal Events
| Date | Code | Title | Description |
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| RENW | Renewal (renewal fees accepted) | ||
| PSEA | Patent sealed | ||
| ASS | Change of ownership |
Owner name: VIVENTIA BIOTECHNOLOGIES INC., CA Free format text: OLD OWNER(S): VIVENTIA BIOTECH INC.; VIVENTIA BIOTECH INC. |
|
| RENW | Renewal (renewal fees accepted) | ||
| LAPS | Patent lapsed |