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WO2009020094A1 - 疎水性分子で修飾した抗体 - Google Patents

疎水性分子で修飾した抗体 Download PDF

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Publication number
WO2009020094A1
WO2009020094A1 PCT/JP2008/063959 JP2008063959W WO2009020094A1 WO 2009020094 A1 WO2009020094 A1 WO 2009020094A1 JP 2008063959 W JP2008063959 W JP 2008063959W WO 2009020094 A1 WO2009020094 A1 WO 2009020094A1
Authority
WO
WIPO (PCT)
Prior art keywords
hydrophobic molecule
antibody modified
antibody
immunoliposome
modified
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.)
Ceased
Application number
PCT/JP2008/063959
Other languages
English (en)
French (fr)
Inventor
Koji Morita
Takako Niwa
Yuji Kasuya
Kimihisa Ichikawa
Hiroko Yoshida
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Daiichi Sankyo Co Ltd
Original Assignee
Daiichi Sankyo Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Daiichi Sankyo Co Ltd filed Critical Daiichi Sankyo Co Ltd
Priority to US12/672,861 priority Critical patent/US20110269942A1/en
Priority to JP2009526447A priority patent/JPWO2009020094A1/ja
Priority to EP08792163A priority patent/EP2184355A4/en
Publication of WO2009020094A1 publication Critical patent/WO2009020094A1/ja
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2878Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the NGF-receptor/TNF-receptor superfamily, e.g. CD27, CD30, CD40, CD95
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/69Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
    • A61K47/6905Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit the form being a colloid or an emulsion
    • A61K47/6911Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit the form being a colloid or an emulsion the form being a liposome
    • A61K47/6913Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit the form being a colloid or an emulsion the form being a liposome the liposome being modified on its surface by an antibody
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/10Dispersions; Emulsions
    • A61K9/127Synthetic bilayered vehicles, e.g. liposomes or liposomes with cholesterol as the only non-phosphatidyl surfactant
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/70Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/73Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Immunology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Organic Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Dispersion Chemistry (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Medicinal Preparation (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

本発明は、癌、自己免疫疾患または炎症性疾患に対して治療効果を有するイムノリポソーム製剤または疎水性分子修飾抗体に関する。すなわち、本発明は、デスドメイン含有受容体発現細胞にアポトーシスを誘導可能な抗体を構成成分とするイムノリポソームまたは疎水性分子修飾抗体に関する。
PCT/JP2008/063959 2007-08-09 2008-08-04 疎水性分子で修飾した抗体 Ceased WO2009020094A1 (ja)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US12/672,861 US20110269942A1 (en) 2007-08-09 2008-08-04 Antibodies modified with hydrophobic molecule
JP2009526447A JPWO2009020094A1 (ja) 2007-08-09 2008-08-04 疎水性分子で修飾した抗体
EP08792163A EP2184355A4 (en) 2007-08-09 2008-08-04 WITH A HYDROPHOBIC MOLECULE MODIFIED ANTIBODY

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2007-208664 2007-08-09
JP2007208664 2007-08-09

Publications (1)

Publication Number Publication Date
WO2009020094A1 true WO2009020094A1 (ja) 2009-02-12

Family

ID=40341326

Family Applications (2)

Application Number Title Priority Date Filing Date
PCT/JP2008/063959 Ceased WO2009020094A1 (ja) 2007-08-09 2008-08-04 疎水性分子で修飾した抗体
PCT/JP2008/063958 Ceased WO2009020093A1 (ja) 2007-08-09 2008-08-04 デスドメイン含有受容体発現細胞にアポトーシスを誘導するイムノリポソーム

Family Applications After (1)

Application Number Title Priority Date Filing Date
PCT/JP2008/063958 Ceased WO2009020093A1 (ja) 2007-08-09 2008-08-04 デスドメイン含有受容体発現細胞にアポトーシスを誘導するイムノリポソーム

Country Status (8)

Country Link
US (2) US20100209490A1 (ja)
EP (2) EP2177230A4 (ja)
JP (2) JPWO2009020094A1 (ja)
KR (1) KR20100046185A (ja)
CN (1) CN101820913A (ja)
CA (1) CA2695991A1 (ja)
TW (2) TW200916477A (ja)
WO (2) WO2009020094A1 (ja)

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US20100209490A1 (en) * 2007-08-09 2010-08-19 Daiichi Sankyo Company, Limited Immunoliposome inducing apoptosis into cell expressing death domain-containing receptor
JPWO2012093733A1 (ja) * 2011-01-07 2014-06-09 セイコーエプソン株式会社 抗シグナルペプチド抗体の製造方法
EP2480230A4 (en) * 2009-09-24 2015-06-10 Seattle Genetics Inc DR5 Ligand-HEILMITTELKONJUGATE
US9238796B2 (en) 2010-06-04 2016-01-19 Toagosei Co. Ltd. Cell growth-promoting peptide and use thereof
US9370182B2 (en) 2012-05-28 2016-06-21 Toagosei Co., Ltd. Antimicrobial peptide and use thereof
US9480727B2 (en) 2012-10-18 2016-11-01 Toagosei Co. Ltd. Synthetic peptide for inhibiting expression of type 2 TNF receptor and use thereof
JP2020040983A (ja) * 2014-03-31 2020-03-19 ハンミ ファーマシューティカル カンパニー リミテッド 免疫グロブリンFcフラグメント結合を用いたタンパク質及びペプチドの溶解度を改善する方法
JP2021512622A (ja) * 2018-02-06 2021-05-20 シアトル チルドレンズ ホスピタル ディー/ビー/エー シアトル チルドレンズ リサーチ インスティテュート フルオレセイン結合エーテルリン脂質(fl−ple)で標識された腫瘍に対して最適なt細胞機能を示すフルオレセイン特異的car
US11168109B2 (en) 2012-03-08 2021-11-09 Hanmi Science Co., Ltd. Process for preparation of physiologically active polypeptide complex
WO2022136939A1 (en) * 2020-12-21 2022-06-30 Samarth Zarad A method for preparation of a drug encapsulated liposome in an organic solvent emulsion
US11434271B2 (en) 2011-11-04 2022-09-06 Hanmi Science Co., Ltd. Method for preparing physiologically active polypeptide complex

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JP7282521B2 (ja) 2016-04-08 2023-05-29 パーデュー・リサーチ・ファウンデイション Car t細胞療法のための方法および組成物
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US20200230159A1 (en) * 2017-08-09 2020-07-23 The Regents Of The University Of Michigan Apoptosis-mimicking structures
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IT202000004846A1 (it) * 2020-03-06 2021-09-06 Univ Degli Studi G Dannunzio Chieti Pescara Pro-drug innovativo micellare su backbone polimerico del Killer TNF-apoptosis induced ligand.
IT202000013042A1 (it) * 2020-06-01 2021-12-01 Univ Degli Studi G Dannunzio Chieti Pescara Sistema liposomiale con killer tnf-apoptosis induced ligand (killertrail), pro-apoptotico-direzionante.
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WO2023204290A1 (ja) * 2022-04-21 2023-10-26 愛知県 多重特異性ナノ粒子
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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110269942A1 (en) * 2007-08-09 2011-11-03 Daiichi Sankyo Company, Limited Antibodies modified with hydrophobic molecule
US20100209490A1 (en) * 2007-08-09 2010-08-19 Daiichi Sankyo Company, Limited Immunoliposome inducing apoptosis into cell expressing death domain-containing receptor
EP2480230A4 (en) * 2009-09-24 2015-06-10 Seattle Genetics Inc DR5 Ligand-HEILMITTELKONJUGATE
US9238796B2 (en) 2010-06-04 2016-01-19 Toagosei Co. Ltd. Cell growth-promoting peptide and use thereof
JPWO2012093733A1 (ja) * 2011-01-07 2014-06-09 セイコーエプソン株式会社 抗シグナルペプチド抗体の製造方法
US9309307B2 (en) 2011-01-07 2016-04-12 Seiko Epson Corporation Antibody against amyloid precursor protein signal peptide
US11434271B2 (en) 2011-11-04 2022-09-06 Hanmi Science Co., Ltd. Method for preparing physiologically active polypeptide complex
US11168109B2 (en) 2012-03-08 2021-11-09 Hanmi Science Co., Ltd. Process for preparation of physiologically active polypeptide complex
US9370182B2 (en) 2012-05-28 2016-06-21 Toagosei Co., Ltd. Antimicrobial peptide and use thereof
US9480727B2 (en) 2012-10-18 2016-11-01 Toagosei Co. Ltd. Synthetic peptide for inhibiting expression of type 2 TNF receptor and use thereof
JP2020040983A (ja) * 2014-03-31 2020-03-19 ハンミ ファーマシューティカル カンパニー リミテッド 免疫グロブリンFcフラグメント結合を用いたタンパク質及びペプチドの溶解度を改善する方法
JP2021512622A (ja) * 2018-02-06 2021-05-20 シアトル チルドレンズ ホスピタル ディー/ビー/エー シアトル チルドレンズ リサーチ インスティテュート フルオレセイン結合エーテルリン脂質(fl−ple)で標識された腫瘍に対して最適なt細胞機能を示すフルオレセイン特異的car
JP2024012513A (ja) * 2018-02-06 2024-01-30 シアトル チルドレンズ ホスピタル (ディービーエイ シアトル チルドレンズ リサーチ インスティテュート) フルオレセイン結合エーテルリン脂質(fl-ple)で標識された腫瘍に対して最適なt細胞機能を示すフルオレセイン特異的car
JP7774961B2 (ja) 2018-02-06 2025-11-25 シアトル チルドレンズ ホスピタル ディー/ビー/エイ シアトル チルドレンズ リサーチ インスティテュート フルオレセイン結合エーテルリン脂質(fl-ple)で標識された腫瘍に対して最適なt細胞機能を示すフルオレセイン特異的car
WO2022136939A1 (en) * 2020-12-21 2022-06-30 Samarth Zarad A method for preparation of a drug encapsulated liposome in an organic solvent emulsion

Also Published As

Publication number Publication date
CN101820913A (zh) 2010-09-01
EP2184355A1 (en) 2010-05-12
TW200914064A (en) 2009-04-01
KR20100046185A (ko) 2010-05-06
WO2009020093A1 (ja) 2009-02-12
CA2695991A1 (en) 2009-02-12
US20110269942A1 (en) 2011-11-03
EP2177230A1 (en) 2010-04-21
JPWO2009020093A1 (ja) 2010-11-04
JPWO2009020094A1 (ja) 2010-11-04
US20100209490A1 (en) 2010-08-19
TW200916477A (en) 2009-04-16
EP2184355A4 (en) 2011-04-27
EP2177230A4 (en) 2011-04-27

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