ES2565063T3 - Anticuerpos para el tratamiento de un cáncer que expresa la claudina 6 - Google Patents

Anticuerpos para el tratamiento de un cáncer que expresa la claudina 6 Download PDF

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ES2565063T3
ES2565063T3 ES12715856.6T ES12715856T ES2565063T3 ES 2565063 T3 ES2565063 T3 ES 2565063T3 ES 12715856 T ES12715856 T ES 12715856T ES 2565063 T3 ES2565063 T3 ES 2565063T3
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cancer
cell
carcinoma
tumor
antibodies
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Ugur Sahin
Özlem TÜRECI
Michael Koslowski
Korden Walter
Stefan WÖLL
Maria Kreuzberg
Bernd Hubner
Michael Erdeljan
Michael WEICHEL
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Johannes Gutenberg Universitaet Mainz
Ganymed Pharmaceuticals GmbH
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Johannes Gutenberg Universitaet Mainz
Ganymed Pharmaceuticals GmbH
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    • 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
    • C07K16/30Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/395Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39591Stabilisation, fragmentation
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K2039/505Medicinal preparations containing antigens or antibodies comprising antibodies
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/20Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/24Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/30Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/33Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/30Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/34Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C07K2317/565Complementarity determining region [CDR]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C07K2317/567Framework region [FR]
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    • 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
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    • 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
    • C07K2317/732Antibody-dependent cellular cytotoxicity [ADCC]
    • 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
    • C07K2317/734Complement-dependent cytotoxicity [CDC]
    • 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
    • C07K2317/76Antagonist effect on antigen, e.g. neutralization or inhibition of binding
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/90Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
    • C07K2317/92Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value

Abstract

Anticuerpo que comprende: (i) una cadena pesada de anticuerpo que comprende una secuencia de cadena pesada de anticuerpo de SEC ID nº 36, y (ii) una cadena ligera de anticuerpo que comprende una secuencia de cadena ligera de anticuerpo seleccionada de entre SEC ID nº 35, nº 54 y nº 55.

Description

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de cáncer preferentemente son aquellas en las que las células tumorales o las células de cáncer expresan CLDN6 y se caracterizan por la asociación de CLDN6 con la superficie celular de las mismas.
Tal como se utiliza en la presente memoria, una "enfermedad tumoral", una "enfermedad de tipo tumoral" o una "enfermedad tumorigénica" se refiere a una enfermedad caracterizada por una multiplicación, proliferación, diferenciación, adhesión y/o migración celulares reguladas de manera aberrante, lo que puede resultar en la producción, o en la tendencia a producir, tumores y/o metástasis tumorales. La expresión "célula tumoral" se refiere a una célula anormal que se multiplica mediante una proliferación celular no controlada rápida y que continúa multiplicándose después de cesar los estímulos que iniciaron la nueva multiplicación.
El término "tumor" se refiere a un grupo anormal de células o a un tejido que crece mediante una proliferación celular no controlada rápida y que continúa creciendo tras cesar los estímulos que iniciaron el nuevo crecimiento. Los tumores muestran una falta parcial o total de organización estructural y coordinación funcional con el tejido normal, y habitualmente forman una masa diferenciada de tejido, que puede ser benigna, premaligna o maligna.
Preferentemente, una "enfermedad tumoral", "enfermedad de tipo tumoral" o "enfermedad tumorigénica" según la invención es una enfermedad de cáncer, es decir, una enfermedad maligna y una célula tumoral es una célula de cáncer. Preferentemente una "enfermedad tumoral", "enfermedad de tipo tumoral" o "enfermedad tumorigénica" se caracteriza por células que expresan CLDN6 y que se caracterizan por la asociación de CLDN6 con la superficie celular de las mismas y una célula tumoral expresa CLDN6 y se caracteriza por la asociación de CLDN6 con la superficie celular.
Una célula que expresa CLDN6 y que se caracteriza por la asociación de CLDN6 con la superficie celular preferentemente es una célula tumoral o una célula de cáncer, preferentemente de los tumores y cánceres indicados en la presente memoria. Preferentemente, dicha célula es una célula diferente de una célula placentaria.
Las enfermedades de cáncer preferentes o cánceres según la invención se seleccionan de entre el grupo que consiste de cáncer ovárico, en particular adenocarcinoma ovárico y teratocarcinoma ovárico, cáncer de pulmón, incluyendo el cáncer de pulmón microcítico (SCLC) y el cáncer de pulmón no microcítico (NSCLC), en particular el carcinoma y el adenocarcinoma pulmonares de células escamosas, cáncer gástrico, cáncer de mama, cáncer hepático, cáncer pancreático, cáncer de piel, en particular el carcinoma de células basales y el carcinoma de células escamosas, melanoma maligno, cáncer de cabeza y cuello, en particular el adenoma pleomórfico maligno, sarcoma, en particular el sarcoma y el carcinosarcoma sinoviales, cáncer de conductos biliares, cáncer de la vejiga urinaria, en particular el carcinoma de células transicionales y el carcinoma papilar, cáncer de riñón, en particular el carcinoma de células renales, incluyendo el carcinoma de células renales de células claras y el carcinoma de células renales papilar, cáncer de colon, cáncer de intestino delgado, incluyendo el cáncer del íleo, en particular el adenocarcinoma del intestino delgado y el adenocarcinoma del íleo, carcinoma embrionario testicular, coriocarcinoma placentario, cáncer cervical, cáncer testicular, en particular el seminoma testicular, teratoma testicular y cáncer testicular embrionario, cáncer uterino, un tumor de células germinativas tal como un teratocarcinoma o un carcinoma embrionario, en particular un tumor de células germinativas del testículo, y las formas metastásicas de los mismos.
Los tipos principales de cáncer de pulmón son el carcinoma de pulmón microcítico (SCLC) y el carcinoma de pulmón no microcítico (NSCLC). Existen tres subtipos principales de carcinoma de pulmón de células no pequeñas: el carcinoma de pulmón de células escamosas, el adenocarcinoma y el carcinoma de pulmón de células grandes. Los adenocarcinomas constituyen aproximadamente el 10% de los cánceres de pulmón. Este cáncer habitualmente se observa periféricamente en los pulmones, al contrario cáncer de pulmón microcítico (SCLC) y el cáncer de pulmón escamoso, los cuales tienden a localizarse más centralmente.
El cáncer de piel es un crecimiento maligno sobre la piel. Los cánceres de piel más comunes son el cáncer de células basales, el cáncer de células escamosas y el melanoma. El melanoma maligno es un tipo grave de cáncer de piel. Se debe a la multiplicación descontrolada de las células pigmentarias denominadas melanocitos.
Según la invención, un "carcinoma" es un cáncer que se inicia en la capa de revestimiento (células epiteliales) de los órganos.
El "carcinoma bronquiolar" es un carcinoma del pulmón que se cree que deriva del epitelio de los bronquiolos terminales, en los que el tejido neoplásico se extiende a lo largo de las paredes alveolares y crece en pequeñas masas dentro de los alveolos. Puede observarse mucina en algunas de las células y en el material en los alveolos, que también incluye células denudadas.
El "adenocarcinoma" es un cáncer que se origina en tejido glandular. Este tejido también es parte de una categoría más grande de tejidos conocida como tejido epitelial. El tejido epitelial incluye piel, glándulas y una diversidad de otros tejidos que revisten las cavidades y los órganos del cuerpo. El epitelio se deriva embriológicamente del ectodermo, endodermo y mesodermo. Para clasificarse como adenocarcinoma, las células no necesitan ser necesariamente una parte de una glándula, con la condición de que presenten propiedades secretorias. Esta forma de carcinoma puede producirse en algunos mamíferos superiores, incluyendo el ser humano. Los adenocarcinomas
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Claims (1)

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ES12715856.6T 2011-05-13 2012-04-20 Anticuerpos para el tratamiento de un cáncer que expresa la claudina 6 Active ES2565063T3 (es)

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US201161486071P 2011-05-13 2011-05-13
EP11004004 2011-05-13
EP11004004 2011-05-13
US201161486071P 2011-05-13
PCT/EP2012/001721 WO2012156018A1 (en) 2011-05-13 2012-04-20 Antibodies for treatment of cancer expressing claudin 6

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Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2011005630A (es) 2008-11-28 2011-09-28 Solazyme Inc Producción de aceites específicos en microorganismos heterótroficos recombinantes.
CN107028969A (zh) 2009-02-20 2017-08-11 加尼梅德药物公司 用于癌症诊断和治疗的方法和组合物
LT2499161T (lt) 2009-11-11 2017-11-27 Ganymed Pharmaceuticals Gmbh Specifiniai antikūnai, skirti klaudinui 6 (cldn6)
EP2404936A1 (en) 2010-07-06 2012-01-11 Ganymed Pharmaceuticals AG Cancer therapy using CLDN6 target-directed antibodies in vivo
GB201103955D0 (en) * 2011-03-09 2011-04-20 Antitope Ltd Antibodies
NZ724296A (en) 2011-05-13 2020-05-29 Ganymed Pharmaceuticals Ag Antibodies for treatment of cancer expressing claudin 6
KR102134088B1 (ko) 2012-08-24 2020-07-14 더 리젠츠 오브 더 유니버시티 오브 캘리포니아 Ror1 암을 치료하고 전이를 저해하는데 이용을 위한 항체와 백신
WO2015014376A1 (en) * 2013-07-31 2015-02-05 Biontech Ag Diagnosis and therapy of cancer involving cancer stem cells
KR20160070191A (ko) 2013-11-06 2016-06-17 스템센트알엑스 인코포레이티드 신규한 항-클라우딘 항체 및 사용 방법
CN105940107B (zh) 2013-11-11 2021-06-15 中外制药株式会社 含有改变了抗体可变区的抗原结合分子
JPWO2015108203A1 (ja) * 2014-01-15 2017-03-23 株式会社オーダーメードメディカルリサーチ 抗slc6a6抗体を用いたがん治療用医薬組成物
BR112016022727A8 (pt) * 2014-04-01 2018-12-04 Biontech Cell & Gene Therapies Gmbh imunorreceptores específicos de claudina-6 e epítopos de células t
JP7125248B2 (ja) 2014-11-11 2022-08-24 中外製薬株式会社 改変された抗体可変領域を含む抗原結合分子のライブラリ
CA2966753A1 (en) 2014-11-17 2016-05-26 Arno Therapeutics, Inc. Onapristone extended-release compositions and methods
CN106146666B (zh) * 2015-03-26 2019-09-06 科济生物医药(上海)有限公司 靶向cldn6的免疫效应细胞及其制备方法和应用
CN105504051B (zh) * 2015-12-17 2019-08-30 北京天成新脉生物技术有限公司 狂犬病毒核蛋白单克隆抗体及其应用
EP3474854A4 (en) 2016-06-27 2020-02-19 The Regents of The University of California DRUG ASSOCIATIONS FOR THE TREATMENT OF CANCER
US20180148471A1 (en) 2016-11-30 2018-05-31 Arno Therapeutics, Inc. Methods for onapristone synthesis dehydration and deprotection
CA3046092A1 (en) * 2016-12-28 2018-07-05 Genentech, Inc. Treatment of advanced her2 expressing cancer
WO2019048040A1 (en) 2017-09-06 2019-03-14 Ganymed Pharmaceuticals Gmbh ANTIBODIES USEFUL IN THE DIAGNOSIS OF CANCER
AU2018334434A1 (en) * 2017-09-18 2020-04-02 The Regents Of The University Of California Claudin6 antibodies and methods of treating cancer
CN111164208B (zh) 2017-09-29 2023-08-04 第一三共株式会社 抗体-吡咯并苯并二氮杂卓衍生物偶联物
TW201938194A (zh) 2017-12-05 2019-10-01 日商中外製藥股份有限公司 包含結合cd3及cd137的改變的抗體可變區之抗原結合分子
US20210054076A1 (en) * 2018-01-05 2021-02-25 Chugai Seiyaku Kabushiki Kaisha Cytotoxicity-inducing therapeutic agent
KR102340989B1 (ko) * 2018-03-28 2021-12-20 에이비온 주식회사 클라우딘 3의 ecl-2에 특이적으로 결합하는 항체, 이의 단편 및 이들의 용도
AU2020223293A1 (en) 2019-02-15 2021-08-19 Integral Molecular, Inc. Claudin 6 antibodies and uses thereof
WO2020168024A1 (en) 2019-02-15 2020-08-20 Integral Molecular, Inc. Antibodies comprising a common light chain and uses thereof
CN114174340A (zh) * 2019-03-20 2022-03-11 加利福尼亚大学董事会 密封蛋白-6抗体和药物缀合物
CN114206934A (zh) * 2019-03-20 2022-03-18 加利福尼亚大学董事会 密封蛋白-6双特异性抗体
WO2021006328A1 (en) 2019-07-10 2021-01-14 Chugai Seiyaku Kabushiki Kaisha Claudin-6 binding molecules and uses thereof
WO2021129927A1 (en) 2019-12-23 2021-07-01 Biontech Cell & Gene Therapies Gmbh Treatment with immune effector cells engineered to express an antigen receptor
CN111087465B (zh) * 2019-12-24 2020-12-08 广州医科大学 一种针对密蛋白6的抗体偶联药物及应用
JP6971419B2 (ja) 2020-03-31 2021-11-24 中外製薬株式会社 クローディン6を標的とする多重特異性抗原結合分子およびその使用
AU2021374036A1 (en) * 2020-11-06 2023-06-08 Amgen Inc. Polypeptide constructs selectively binding to cldn6 and cd3
CN117157319A (zh) 2021-03-09 2023-12-01 Xencor股份有限公司 结合cd3和cldn6的异二聚抗体
US20230008868A1 (en) * 2021-07-08 2023-01-12 Nippon Telegraph And Telephone Corporation User authentication device, user authentication method, and user authentication computer program
WO2023053282A1 (ja) 2021-09-29 2023-04-06 中外製薬株式会社 がんの治療に用いるための細胞傷害誘導治療剤
WO2023064899A1 (en) * 2021-10-14 2023-04-20 Health Research, Inc. Compositions and methods for use of recombinant t cell receptors against claudin 6
WO2024046572A1 (en) 2022-09-01 2024-03-07 BioNTech SE Chimeric antigen receptor-modified cells for the treatment of cldn6 expressing cancer
WO2023105005A1 (en) 2021-12-09 2023-06-15 BioNTech SE Chimeric antigen receptor-modified cells for the treatment of cldn6 expressing cancer
CN116064622B (zh) * 2023-02-13 2023-10-13 优睿赛思(武汉)生物科技有限公司 Claudin6-mCherry报告基因CHO-K1稳转细胞株制备及应用

Family Cites Families (72)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4946788A (en) 1985-06-11 1990-08-07 Ciba-Geigy Corporation Purified immunoglobulin-related factor, novel monoclonal antibodies, hybridoma cell lines, processes and applications
GB8601597D0 (en) 1986-01-23 1986-02-26 Wilson R H Nucleotide sequences
US4946778A (en) 1987-09-21 1990-08-07 Genex Corporation Single polypeptide chain binding molecules
WO1988007089A1 (en) 1987-03-18 1988-09-22 Medical Research Council Altered antibodies
GB8717430D0 (en) 1987-07-23 1987-08-26 Celltech Ltd Recombinant dna product
GB8809129D0 (en) 1988-04-18 1988-05-18 Celltech Ltd Recombinant dna methods vectors and host cells
US6255458B1 (en) 1990-08-29 2001-07-03 Genpharm International High affinity human antibodies and human antibodies against digoxin
GB9019812D0 (en) 1990-09-11 1990-10-24 Scotgen Ltd Novel antibodies for treatment and prevention of infection in animals and man
US5830755A (en) 1995-03-27 1998-11-03 The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services T-cell receptors and their use in therapeutic and diagnostic methods
US6121022A (en) 1995-04-14 2000-09-19 Genentech, Inc. Altered polypeptides with increased half-life
US5677139A (en) 1995-04-21 1997-10-14 President And Fellows Of Harvard College In vitro differentiation of CD34+ progenitor cells into T lymphocytes
UA56132C2 (uk) 1995-04-25 2003-05-15 Смітклайн Бічем Байолоджікалс С.А. Композиція вакцини (варіанти), спосіб стабілізації qs21 відносно гідролізу (варіанти), спосіб приготування композиції вакцини
WO2002008288A2 (en) 2000-07-20 2002-01-31 Genentech, Inc. Secreted and transmembrane polypeptides and nucleic acids encoding the same
US6277375B1 (en) 1997-03-03 2001-08-21 Board Of Regents, The University Of Texas System Immunoglobulin-like domains with increased half-lives
WO2000078961A1 (en) 1999-06-23 2000-12-28 Genentech, Inc. Secreted and transmembrane polypeptides and nucleic acids encoding the same
US5928631A (en) 1997-06-09 1999-07-27 The Procter & Gamble Company Methods for controlling environmental odors on the body using compositions comprising uncomplexed cyclodextrins
US20020127584A1 (en) 1997-09-18 2002-09-12 Genentech, Inc. Secreted and transmembrane polypeptides and nucleic acids encoding the same
US5932445A (en) 1997-11-07 1999-08-03 Incyte Pharmaceuticals, Inc. Signal peptide-containing proteins
US6194551B1 (en) 1998-04-02 2001-02-27 Genentech, Inc. Polypeptide variants
NZ531664A (en) 1998-09-01 2005-07-29 Genentech Inc Pro1317 polypeptides and sequences thereof with homology to the semaphorin B glycoprotein family
AU773028B2 (en) * 1998-11-03 2004-05-13 Adherex Technologies Inc. Compounds and methods for modulating claudin-mediated functions
AU3124000A (en) 1998-12-17 2000-07-03 Human Genome Sciences, Inc. 47 human secreted proteins
JP2002536995A (ja) 1999-02-22 2002-11-05 インサイト・ファーマスーティカルズ・インコーポレイテッド 結腸の疾患に関連する遺伝子
ES2287020T3 (es) 1999-06-02 2007-12-16 Genentech, Inc. Procedimiento y composiciones para inhibir el crecimiento de celulas neoplasicas.
EP1514933A1 (en) 1999-07-08 2005-03-16 Research Association for Biotechnology Secretory protein or membrane protein
EP1242443A4 (en) 1999-12-23 2005-06-22 Nuvelo Inc NEW NUCLEIC ACIDS AND POLYPEPTIDES
WO2001051513A2 (en) 2000-01-14 2001-07-19 Corixa Corporation Ovarian tumor-associated sequences
CA2404890C (en) 2000-03-30 2013-11-19 Whitehead Institute For Biomedical Research Rna sequence-specific mediators of rna interference
AU6531101A (en) 2000-06-02 2001-12-17 Genentech Inc Secreted and transmembrane polypeptides and nucleic acids encoding the same
JP2004506413A (ja) 2000-06-23 2004-03-04 ジェネンテック・インコーポレーテッド 血管形成に関与する疾患の診断と治療のための組成物と方法
CA2416538A1 (en) 2000-07-20 2002-01-31 Genentech, Inc. Compositions and methods for the diagnosis and treatment of disorders involving angiogenesis
EP2044839A3 (en) 2000-08-03 2009-07-01 Therapeutic Human Polyclonals, Inc. Production of humanized antibodies in transgenic animals
ES2295228T3 (es) 2000-11-30 2008-04-16 Medarex, Inc. Roedores transcromosomicos transgenicos para la preparacion de anticuerpos humanos.
US7754208B2 (en) 2001-01-17 2010-07-13 Trubion Pharmaceuticals, Inc. Binding domain-immunoglobulin fusion proteins
US20030133939A1 (en) 2001-01-17 2003-07-17 Genecraft, Inc. Binding domain-immunoglobulin fusion proteins
KR100788092B1 (ko) 2001-06-20 2007-12-21 제넨테크, 인크. 종양의 진단 및 치료를 위한 방법 및 이를 위한 조성물
CA2379661A1 (en) 2002-03-28 2003-09-28 Kursad Turksen Paracellular drug delivery system
EP2011886A3 (en) 2002-04-16 2009-02-11 Genentech, Inc. Compositions and methods for the diagnosis and treatment of tumor
AU2003225009A1 (en) * 2002-04-22 2003-11-03 Dyax Corporation Antibodies specific for mucin polypeptide
US20070207142A1 (en) 2002-05-08 2007-09-06 Genentech, Inc. Compositions and methods for the treatment of tumor of hematopoietic origin
JP2006516089A (ja) 2002-10-02 2006-06-22 ジェネンテック・インコーポレーテッド 腫瘍の診断と治療のための組成物と方法
KR100944575B1 (ko) 2002-10-17 2010-02-25 젠맵 에이/에스 Cd20에 대한 인간 모노클로날 항체
EP1578996A4 (en) 2002-10-18 2007-12-19 Genentech Inc COMPOSITIONS AND METHODS FOR DIAGNOSING AND TREATING TUMORS
AT500651B9 (de) 2003-05-27 2010-04-15 Altropus Gmbh Aktiv immunisierender antikörper
BRPI0410875A (pt) 2003-05-30 2006-07-04 Centocor Inc método de inibição do crescimento de tumor com anticorpos de fator antitecido
US20060019256A1 (en) 2003-06-09 2006-01-26 The Regents Of The University Of Michigan Compositions and methods for treating and diagnosing cancer
WO2006033664A1 (en) 2004-03-08 2006-03-30 Avalon Pharmaceuticals Determining cancer-linked genes and therapeutic targets using molecular cytogenetic methods
US7431927B2 (en) 2005-03-24 2008-10-07 Epitomics, Inc. TNFα-neutralizing antibodies
DE102005025041A1 (de) 2005-05-30 2006-12-07 Bell Flavors & Fragrances Duft Und Aroma Gmbh Mittel zur Anwendung in Spülmaschinen sowie Vorrichtung für dessen dosierte Einbringung während der Spül- und Trocknungsphasen
EP1790664A1 (en) 2005-11-24 2007-05-30 Ganymed Pharmaceuticals AG Monoclonal antibodies against claudin-18 for treatment of cancer
EP1970384A1 (en) * 2007-03-14 2008-09-17 Ganymed Pharmaceuticals AG Monoclonal antibodies for treatment of cancer
EP2138576A4 (en) 2007-03-16 2011-02-23 Kyowa Hakko Kirin Co Ltd ANTI-CLAUDIN-4 ANTIBODY
EP1997832A1 (en) 2007-05-29 2008-12-03 Ganymed Pharmaceuticals AG Monoclonal antibodies against Claudin-18 for treatment of cancer
WO2009025759A1 (en) 2007-08-17 2009-02-26 Progenics Pharmaceuticals (Nevada), Inc. Tight junction proteins associated with infection and entry of hepatitis c virus (hcv), methods and uses thereof
WO2009028663A1 (ja) * 2007-08-30 2009-03-05 Kyowa Hakko Kirin Co., Ltd. 抗Claudin-3抗体
EP2060583A1 (en) 2007-10-23 2009-05-20 Ganymed Pharmaceuticals AG Identification of tumor-associated markers for diagnosis and therapy
KR20100116179A (ko) * 2008-01-11 2010-10-29 고쿠리츠다이가쿠호우진 도쿄다이가쿠 항-cldn6 항체
CA2721072A1 (en) 2008-04-11 2009-10-15 Bionovo, Inc. Anticancer methods employing extracts of gleditsia sinensis lam
WO2010043650A2 (en) 2008-10-14 2010-04-22 Ablynx Nv Amino acid sequences directed against cellular receptors for viruses and bacteria
DE102009026966A1 (de) 2008-12-18 2010-07-01 Robert Bosch Gmbh Betrieb eines Bremskraftverstärkers als Pedalsimulator
JP2010178650A (ja) 2009-02-04 2010-08-19 Univ Of Tokyo 固形癌の再発予測のための試験方法および再発予防剤
EP2221063A1 (en) 2009-02-20 2010-08-25 Ganymed Pharmaceuticals AG Methods and compositions for diagnosis and treatment of cancer
CN107028969A (zh) 2009-02-20 2017-08-11 加尼梅德药物公司 用于癌症诊断和治疗的方法和组合物
LT2499161T (lt) 2009-11-11 2017-11-27 Ganymed Pharmaceuticals Gmbh Specifiniai antikūnai, skirti klaudinui 6 (cldn6)
EP2322555A1 (en) 2009-11-11 2011-05-18 Ganymed Pharmaceuticals AG Antibodies specific for claudin 6 (CLDN6)
WO2011105551A1 (ja) 2010-02-26 2011-09-01 国立大学法人大阪大学 癌幹細胞の検出方法、及び癌の治療剤または再発予防剤
EP2404936A1 (en) * 2010-07-06 2012-01-11 Ganymed Pharmaceuticals AG Cancer therapy using CLDN6 target-directed antibodies in vivo
NZ724296A (en) 2011-05-13 2020-05-29 Ganymed Pharmaceuticals Ag Antibodies for treatment of cancer expressing claudin 6
EP2749641B1 (en) 2011-09-07 2021-06-02 Chugai Seiyaku Kabushiki Kaisha Cancer stem cell isolation
EP2605017A1 (de) 2011-12-16 2013-06-19 Protagen AG Markersequenzen für gynäkologisches Malignom und deren Verwendung
WO2014015148A1 (en) 2012-07-19 2014-01-23 Amgen Inc. Human btnl3 proteins, nucleic acids, and antibodies and uses thereof
WO2015014376A1 (en) 2013-07-31 2015-02-05 Biontech Ag Diagnosis and therapy of cancer involving cancer stem cells

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