KR20080090406A - 재조합 1가 항체 및 그의 제조 방법 - Google Patents
재조합 1가 항체 및 그의 제조 방법 Download PDFInfo
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- KR20080090406A KR20080090406A KR1020087015774A KR20087015774A KR20080090406A KR 20080090406 A KR20080090406 A KR 20080090406A KR 1020087015774 A KR1020087015774 A KR 1020087015774A KR 20087015774 A KR20087015774 A KR 20087015774A KR 20080090406 A KR20080090406 A KR 20080090406A
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| EP2121745A2 (en) | 2007-02-26 | 2009-11-25 | Oxford Genome Sciences (UK) Limited | Proteins |
| WO2008104803A2 (en) | 2007-02-26 | 2008-09-04 | Oxford Genome Sciences (Uk) Limited | Proteins |
| ES2667863T3 (es) * | 2007-03-29 | 2018-05-14 | Genmab A/S | Anticuerpos biespecíficos y métodos de producción de los mismos |
| US20130195881A1 (en) * | 2007-04-27 | 2013-08-01 | Sanjaya Singh | Potent, stable and non-immunosuppressive anti-cd4 antibodies |
| AU2008255350B2 (en) * | 2007-05-31 | 2014-07-10 | Genmab A/S | Transgenic animals producing monovalent human antibodies and antibodies obtainable from these animals |
| WO2008145137A2 (en) * | 2007-05-31 | 2008-12-04 | Genmab A/S | Recombinant non glycosylated monovalent half-antibodies obtained by molecular engineering |
| WO2008145138A1 (en) * | 2007-05-31 | 2008-12-04 | Genmab A/S | Recombinant fucose modified monovalent half-antibodies obtained by molecular engineering |
| JP6071165B2 (ja) | 2007-05-31 | 2017-02-01 | ゲンマブ エー/エス | 安定なIgG4抗体 |
| US20110045007A1 (en) * | 2007-05-31 | 2011-02-24 | Genmab A/S | Fusion or linked proteins with extended half life |
| US9273134B2 (en) | 2007-06-05 | 2016-03-01 | Yale University | Inhibitors of receptor tyrosine kinases and methods of use thereof |
| JP5588866B2 (ja) | 2007-08-10 | 2014-09-10 | メダレックス エル.エル.シー. | Hco32およびhco27、ならびに関連実施例 |
| EP2190987B1 (en) * | 2007-08-21 | 2012-11-14 | MorphoSys AG | Methods for the formation of disulphide bonds |
| US8865875B2 (en) | 2007-08-22 | 2014-10-21 | Medarex, L.L.C. | Site-specific attachment of drugs or other agents to engineered antibodies with C-terminal extensions |
| CA2699394C (en) | 2007-09-17 | 2020-03-24 | The Regents Of The University Of California | Internalizing human monoclonal antibodies targeting prostate cancer cells in situ |
| CN103880965B (zh) | 2007-09-21 | 2018-02-16 | 加利福尼亚大学董事会 | 被导靶的干扰素显示强的细胞凋亡和抗肿瘤活性 |
| US20110245473A1 (en) | 2007-09-26 | 2011-10-06 | Chugai Seiyaku Kabushiki Kaisha | Anti-IL-6 Receptor Antibody |
| CN106519025B (zh) | 2007-09-26 | 2021-04-23 | 中外制药株式会社 | 利用cdr的氨基酸取代来改变抗体等电点的方法 |
| AR066172A1 (es) * | 2007-09-28 | 2009-07-29 | Chugai Pharmaceutical Co Ltd | Metodo para la preparacion de un anticuerpo antiglipicano 3 con modulada cinetica plasmatica mediante variacion de la semivida plasmatica. |
| WO2009054001A1 (en) * | 2007-10-22 | 2009-04-30 | Biocon Limited | A pharmaceutical composition and a process thereof |
| UY31504A1 (es) | 2007-11-30 | 2009-07-17 | Construcciones de union de antigenos | |
| SG186656A1 (en) | 2007-12-14 | 2013-01-30 | Bristol Myers Squibb Co | Binding molecules to the human ox40 receptor |
| EP2080770A1 (en) * | 2008-01-21 | 2009-07-22 | MorphoSys AG | Proteinaceous binding molecules comprising purification tags |
| CA2721052C (en) | 2008-04-11 | 2023-02-21 | Chugai Seiyaku Kabushiki Kaisha | Antigen-binding molecule capable of binding to two or more antigen molecules repeatedly |
| KR20110036638A (ko) | 2008-07-25 | 2011-04-07 | 리차드 더블유. 와그너 | 단백질 스크리닝 방법 |
| AU2009324092A1 (en) | 2008-12-03 | 2011-06-23 | Genmab A/S | Antibody variants having modifications in the constant region |
| UA109633C2 (uk) | 2008-12-09 | 2015-09-25 | Антитіло людини проти тканинного фактора | |
| CA2750581A1 (en) | 2009-01-21 | 2010-07-29 | Oxford Biotherapeutics Ltd. | Pta089 protein |
| US20100260752A1 (en) | 2009-01-23 | 2010-10-14 | Biosynexus Incorporated | Opsonic and protective antibodies specific for lipoteichoic acid of gram positive bacteria |
| CA2753332A1 (en) | 2009-02-24 | 2010-09-02 | Glaxo Group Limited | Antigen-binding constructs |
| JP2012518400A (ja) | 2009-02-24 | 2012-08-16 | グラクソ グループ リミテッド | 多価および/または複数特異的rankl結合性構築物 |
| JP2012518398A (ja) | 2009-02-24 | 2012-08-16 | グラクソ グループ リミテッド | 抗原結合性構築物 |
| CA2753702C (en) | 2009-03-05 | 2017-01-03 | Medarex, Inc. | Fully human antibodies specific to cadm1 |
| SG10201401604VA (en) | 2009-04-20 | 2014-08-28 | Oxford Biotherapeutics Ltd | Antibodies Specific To Cadherin-17 |
| CA2758842A1 (en) | 2009-04-24 | 2010-10-28 | Glaxo Group Limited | Fgfr1c antibody combinations |
| EP2470569A1 (en) | 2009-10-13 | 2012-07-04 | Oxford Biotherapeutics Ltd. | Antibodies against epha10 |
| WO2011050001A2 (en) | 2009-10-20 | 2011-04-28 | The Regents Of The University Of California | Anti-botulinum neurotoxin antibodies |
| WO2011054007A1 (en) | 2009-11-02 | 2011-05-05 | Oxford Biotherapeutics Ltd. | Ror1 as therapeutic and diagnostic target |
| EP2496944A2 (en) | 2009-11-05 | 2012-09-12 | Novartis AG | Biomarkers predictive of progression of fibrosis |
| MY172472A (en) | 2009-12-10 | 2019-11-26 | Regeneron Pharma | Mice that make heavy chain antibodies |
| JP2013519869A (ja) | 2010-02-10 | 2013-05-30 | ノバルティス アーゲー | 筋肉成長のための方法および化合物 |
| EP3511342B1 (en) | 2010-03-10 | 2024-01-17 | Genmab A/S | Monoclonal antibodies against c-met |
| HUE027760T2 (en) | 2010-04-09 | 2016-11-28 | Critical Care Diagnostics Inc | Soluble human ST-2 antibodies and assays |
| US9150663B2 (en) | 2010-04-20 | 2015-10-06 | Genmab A/S | Heterodimeric antibody Fc-containing proteins and methods for production thereof |
| ES2949159T3 (es) | 2010-05-06 | 2023-09-26 | Novartis Ag | Composiciones y métodos de uso para anticuerpos terapéuticos de proteína 6 relacionada con lipoproteínas de baja densidad (LRP6) |
| BR112012028326A2 (pt) | 2010-05-06 | 2017-03-21 | Novartis Ag | anticorpo multivalente isolado, anticorpos biparatópicos isolados, ácido nucleico, vetor, composição farmacêutica, método de obtenção dos referidos anticorpos, bem como uso do dos mesmos |
| WO2011147986A1 (en) | 2010-05-27 | 2011-12-01 | Genmab A/S | Monoclonal antibodies against her2 |
| JP6082344B2 (ja) | 2010-05-27 | 2017-02-15 | ゲンマブ エー/エス | Her2エピトープに対するモノクローナル抗体 |
| EP2580243B1 (en) | 2010-06-09 | 2019-10-16 | Genmab A/S | Antibodies against human cd38 |
| RS56599B1 (sr) | 2010-06-15 | 2018-02-28 | Genmab As | Konjugati humanog antitela sa lekom protiv tkivnog faktora |
| US8822663B2 (en) | 2010-08-06 | 2014-09-02 | Moderna Therapeutics, Inc. | Engineered nucleic acids and methods of use thereof |
| CA2808154A1 (en) | 2010-08-13 | 2012-02-16 | Medimmmune Limited | Monomeric polypeptides comprising variant fc regions and methods of use |
| PH12013500333A1 (en) | 2010-08-20 | 2013-04-22 | Novartis Ag | Antibodies for epidermal growth factor receptor 3 (her3) |
| JP5978212B2 (ja) | 2010-08-24 | 2016-08-24 | アボット・ラボラトリーズAbbott Laboratories | Hivコアタンパク質に特異的な抗体及びその使用 |
| SG10201912092VA (en) | 2010-09-09 | 2020-02-27 | Pfizer | 4-1bb binding molecules |
| CN103328511B (zh) | 2010-09-10 | 2016-01-20 | 埃派斯进有限公司 | 抗-IL-1β抗体及其使用方法 |
| SG10201508118WA (en) | 2010-09-30 | 2015-11-27 | Agency Science Tech & Res | Methods and reagents for detection and treatment of esophageal metaplasia |
| CA2821992A1 (en) | 2010-10-01 | 2012-04-05 | Moderna Therapeutics, Inc. | Engineered nucleic acids and methods of use thereof |
| EP2853542A1 (en) | 2010-11-24 | 2015-04-01 | Glaxo Group Limited | Multispecific antigen binding proteins targeting HGF |
| RU2013144392A (ru) | 2011-03-03 | 2015-04-10 | Апексиджен, Инк. | Антитела к рецептору il-6 и способы применения |
| EP2683740B1 (en) | 2011-03-10 | 2018-07-04 | Omeros Corporation | Generation of anti-fn14 monoclonal antibodies by ex-vivo accelerated antibody evolution |
| DE12722942T1 (de) | 2011-03-31 | 2021-09-30 | Modernatx, Inc. | Freisetzung und formulierung von manipulierten nukleinsäuren |
| US9499610B2 (en) | 2011-04-08 | 2016-11-22 | H. Lundbeck A/S | Antibodies specific to pyroglutamated Aβ |
| CN103796677B (zh) | 2011-04-20 | 2019-08-16 | 健玛保 | 针对her2和cd3的双特异性抗体 |
| EP2699260B1 (en) | 2011-04-20 | 2024-11-20 | Genmab A/S | Bispecifc antibodies against her2 |
| JP6177231B2 (ja) | 2011-04-20 | 2017-08-09 | ゲンマブ エー/エス | Her2に対する二重特異性抗体 |
| CN106928362B (zh) | 2011-04-29 | 2021-10-26 | 埃派斯进有限公司 | 抗-cd40抗体及其使用方法 |
| SI2726094T1 (sl) | 2011-06-28 | 2017-04-26 | Oxford Biotherapeutics Ltd | Terapevtski in diagnostični cilj |
| NZ618503A (en) | 2011-06-28 | 2016-03-31 | Oxford Biotherapeutics Ltd | Antibodies to adp-ribosyl cyclase 2 |
| US20130004484A1 (en) | 2011-06-30 | 2013-01-03 | Genentech, Inc. | Anti-c-met antibody formulations |
| US9150846B2 (en) | 2011-07-05 | 2015-10-06 | Bioasis Technologies, Inc. | P97-antibody conjugates and methods of use |
| UA117901C2 (uk) | 2011-07-06 | 2018-10-25 | Ґенмаб Б.В. | Спосіб посилення ефекторної функції вихідного поліпептиду, його варіанти та їх застосування |
| DK2739649T3 (en) | 2011-08-05 | 2018-01-08 | Bioasis Technologies Inc | P97 FRAGMENTS WITH TRANSFER ACTIVITY |
| US9102724B2 (en) | 2011-08-12 | 2015-08-11 | Omeros Corporation | Anti-FZD10 monoclonal antibodies and methods for their use |
| US9464124B2 (en) | 2011-09-12 | 2016-10-11 | Moderna Therapeutics, Inc. | Engineered nucleic acids and methods of use thereof |
| GB201116092D0 (en) | 2011-09-16 | 2011-11-02 | Bioceros B V | Antibodies and uses thereof |
| WO2013043452A1 (en) | 2011-09-20 | 2013-03-28 | Eli Lilly And Company | Anti-c-met antibodies |
| HRP20220250T1 (hr) | 2011-10-03 | 2022-04-29 | Modernatx, Inc. | Modificirani nukleozidi, nukleotidi i nukleinske kiseline, te njihove uporabe |
| SI2771364T1 (sl) | 2011-10-27 | 2019-10-30 | Genmab As | Produkcija heterodimernih proteinov |
| CA2854153A1 (en) | 2011-11-02 | 2013-05-10 | Apexigen, Inc. | Anti-kdr antibodies and methods of use |
| JP2015502741A (ja) | 2011-11-04 | 2015-01-29 | ノバルティス アーゲー | 低比重リポタンパク質関連タンパク質6(lrp6)−半減期延長構築物 |
| BR112014012005A2 (pt) | 2011-11-21 | 2017-12-19 | Genentech Inc | composições, métodos, formulação farmacêutica e artigo |
| WO2013079973A1 (en) | 2011-12-02 | 2013-06-06 | Di Cara Danielle Marie | Antibodies against hgf - receptor and uses |
| TW201328706A (zh) | 2011-12-05 | 2013-07-16 | Novartis Ag | 表皮生長因子受體3(her3)之抗體 |
| US20130273029A1 (en) | 2011-12-05 | 2013-10-17 | Novartis Ag | Antibodies for epidermal growth factor receptor 3 (her3) directed to domain ii of her3 |
| SI2791160T1 (sl) | 2011-12-16 | 2022-07-29 | Modernatx, Inc. | Sestave modificirane MRNA |
| ES2693593T3 (es) | 2012-03-15 | 2018-12-12 | Omeros Corporation | Composición y método para la diversificación de secuencias diana |
| US9283287B2 (en) | 2012-04-02 | 2016-03-15 | Moderna Therapeutics, Inc. | Modified polynucleotides for the production of nuclear proteins |
| AU2013243952A1 (en) | 2012-04-02 | 2014-10-30 | Modernatx, Inc. | Modified polynucleotides for the production of cytoplasmic and cytoskeletal proteins |
| US10501512B2 (en) | 2012-04-02 | 2019-12-10 | Modernatx, Inc. | Modified polynucleotides |
| US9572897B2 (en) | 2012-04-02 | 2017-02-21 | Modernatx, Inc. | Modified polynucleotides for the production of cytoplasmic and cytoskeletal proteins |
| CN120383672A (zh) | 2012-04-20 | 2025-07-29 | 美勒斯公司 | 用于产生免疫球蛋白样分子的方法和手段 |
| EP3632462A1 (en) | 2012-07-06 | 2020-04-08 | Genmab B.V. | Dimeric protein with triple mutations |
| JP6514103B2 (ja) | 2012-07-06 | 2019-05-15 | ゲンマブ ビー.ブイ. | 三重変異を有する二量体タンパク質 |
| AU2013296557B2 (en) | 2012-07-31 | 2019-04-18 | Bioasis Technologies Inc. | Dephosphorylated lysosomal storage disease proteins and methods of use thereof |
| GB201213652D0 (en) | 2012-08-01 | 2012-09-12 | Oxford Biotherapeutics Ltd | Therapeutic and diagnostic target |
| WO2014037419A1 (en) * | 2012-09-04 | 2014-03-13 | Vib Vzw | Immunoglobulin single variable domains directed against cd74 and uses derived thereof |
| ES2773107T3 (es) | 2012-10-05 | 2020-07-09 | Kyowa Kirin Co Ltd | Composición de proteína heterodimérica |
| KR102270618B1 (ko) | 2012-10-30 | 2021-06-30 | 아펙시젠, 인코포레이티드 | 항-cd40 항체 및 사용 방법 |
| SMT202200337T1 (it) | 2012-11-26 | 2022-09-14 | Modernatx Inc | Rna modificato al livello del terminale |
| JP6396313B2 (ja) | 2012-12-07 | 2018-09-26 | ファイザー・インク | 操作された単量体抗体断片 |
| TWI693073B (zh) | 2012-12-21 | 2020-05-11 | 日商中外製藥股份有限公司 | 對gpc3標的治療劑療法為有效之患者投與的gpc3標的治療劑 |
| US9856319B2 (en) | 2012-12-28 | 2018-01-02 | Abbvie Inc. | Monovalent binding proteins |
| KR20220156667A (ko) | 2013-01-10 | 2022-11-25 | 젠맵 비. 브이 | 인간 IgG1 Fc 영역 변이체 및 그의 용도 |
| TWI682941B (zh) | 2013-02-01 | 2020-01-21 | 美商再生元醫藥公司 | 含嵌合恆定區之抗體 |
| GB201302447D0 (en) | 2013-02-12 | 2013-03-27 | Oxford Biotherapeutics Ltd | Therapeutic and diagnostic target |
| CA2902068C (en) | 2013-02-28 | 2023-10-03 | Caprion Proteomics Inc. | Tuberculosis biomarkers and uses thereof |
| EP2970433B1 (en) | 2013-03-13 | 2019-09-18 | Bioasis Technologies Inc. | Fragments of p97 and uses thereof |
| JP2016514130A (ja) | 2013-03-14 | 2016-05-19 | ノバルティス アーゲー | Notch3に対する抗体 |
| US20140363433A1 (en) | 2013-03-15 | 2014-12-11 | Omeros Corporation | Methods of Generating Bioactive Peptide-bearing Antibodies and Compositions Comprising the Same |
| WO2014144542A2 (en) | 2013-03-15 | 2014-09-18 | Omeros Corporation | Methods of generating bioactive peptide-bearing antibodies and compositions comprising the same |
| US8980864B2 (en) | 2013-03-15 | 2015-03-17 | Moderna Therapeutics, Inc. | Compositions and methods of altering cholesterol levels |
| MD20180107A2 (ro) | 2013-03-18 | 2019-06-30 | Biocerox Products B.V. | Anticorpi anti-CD134 (OX40) umanizaţi şi utilizarea acestora |
| US20160108122A1 (en) * | 2013-05-23 | 2016-04-21 | Idac Theranostics, Inc. | Therapeutic or prophylactic agent for immunodeficiency virus infection |
| ES2776706T3 (es) | 2013-07-05 | 2020-07-31 | Genmab As | Anticuerpos contra CD3 humanizados o quiméricos |
| BR112016002219A2 (pt) * | 2013-07-31 | 2017-09-12 | Amgen Inc | estabilização de polipeptídeos contendo fc |
| EP3027653A2 (en) | 2013-08-02 | 2016-06-08 | Pfizer Inc | Anti-cxcr4 antibodies and antibody-drug conjugates |
| EP3038657A2 (en) | 2013-08-28 | 2016-07-06 | Bioasis Technologies Inc. | Cns-targeted conjugates having modified fc regions and methods of use thereof |
| US10023626B2 (en) | 2013-09-30 | 2018-07-17 | Modernatx, Inc. | Polynucleotides encoding immune modulating polypeptides |
| US10323076B2 (en) | 2013-10-03 | 2019-06-18 | Modernatx, Inc. | Polynucleotides encoding low density lipoprotein receptor |
| MX376623B (es) | 2013-10-11 | 2025-03-07 | Regeneron Pharma | Cultivo celular metabolicamente optimizado. |
| JP6590803B2 (ja) | 2013-11-21 | 2019-10-16 | ゲンマブ エー/エス | 抗体−薬物コンジュゲート凍結乾燥製剤 |
| EP3102608B1 (en) | 2014-02-03 | 2019-09-18 | Bioasis Technologies Inc. | P97 fusion proteins |
| EP3107562B1 (en) | 2014-02-19 | 2019-09-18 | Bioasis Technologies Inc. | P97-ids fusion proteins |
| BR112016021572A2 (pt) | 2014-03-21 | 2017-10-03 | Regeneron Pharma | Métodos para preparar um animal não humano geneticamente modificado e para produzir proteínas de ligação, hibridoma, ácido nucleico, célula, e, proteína de ligação |
| JP6847664B2 (ja) | 2014-05-01 | 2021-03-24 | バイオアシス テクノロジーズ インコーポレイテッド | P97−ポリヌクレオチド複合体 |
| US11760807B2 (en) | 2014-05-08 | 2023-09-19 | Chugai Seiyaku Kabushiki Kaisha | GPC3-targeting drug which is administered to patient responsive to GPC3-targeting drug therapy |
| CN107073297B (zh) | 2014-07-08 | 2021-09-14 | 纽约大学 | Tau显像配体和其在Tau蛋白病的诊断和治疗中的用途 |
| AU2015286569B2 (en) | 2014-07-11 | 2021-04-15 | Genmab A/S | Antibodies binding AXL |
| JO3568B1 (ar) | 2014-09-05 | 2020-07-05 | Janssen Pharmaceutica Nv | عوامل ربط cd123 واستخداماتها |
| MA40764A (fr) | 2014-09-26 | 2017-08-01 | Chugai Pharmaceutical Co Ltd | Agent thérapeutique induisant une cytotoxicité |
| DK3233907T3 (da) | 2014-12-19 | 2021-06-07 | Genmab As | Bispecifikke heterodimeriske proteiner hos gnavere |
| WO2016102588A1 (en) | 2014-12-22 | 2016-06-30 | Genmab A/S | Method for the production of antibodies |
| CN107847594B (zh) | 2015-05-06 | 2022-04-15 | 詹森生物科技公司 | 前列腺特异性膜抗原(psma)双特异性结合剂及其用途 |
| EP3318879B1 (en) | 2015-07-01 | 2020-10-21 | Chugai Seiyaku Kabushiki Kaisha | Gpc3-targeting therapeutic agent which is administered to patient for whom the gpc3-targeting therapeutic agent is effective |
| CA2991805A1 (en) | 2015-07-10 | 2017-01-19 | Genmab A/S | Axl-specific antibody-drug conjugates for cancer treatment |
| GB201512215D0 (en) | 2015-07-13 | 2015-08-19 | Lundbeck & Co As H | Agents,uses and methods |
| JO3711B1 (ar) | 2015-07-13 | 2021-01-31 | H Lundbeck As | أجسام مضادة محددة لبروتين تاو وطرق استعمالها |
| GB201512203D0 (en) | 2015-07-13 | 2015-08-19 | Lundbeck & Co As H | Agents,uses and methods |
| HK1255383A1 (zh) | 2015-07-31 | 2019-08-16 | The Research Institute At Nationwide Children's Hospital | 去除生物膜的肽及抗體 |
| EP3334761B1 (en) | 2015-08-13 | 2023-07-19 | New York University | Antibody-based molecules selective for the {p}ser404 epitope of tau and their uses in the diagnosis and treatment of tauopathy |
| JP6913078B2 (ja) | 2015-08-13 | 2021-08-04 | ニューヨーク・ユニバーシティ | タウの短縮型Asp421エピトープに特異的な、抗体を基にした分子、ならびにタウ異常症の診断および治療におけるそれらの使用 |
| PT3337824T (pt) | 2015-08-17 | 2020-09-10 | Janssen Pharmaceutica Nv | Anticorpos anti-bcma, moléculas de ligação a antigénio biespecíficas que ligam bcma e cd3, e suas utilizações |
| US20190030178A1 (en) | 2015-09-11 | 2019-01-31 | Genmab A/S | Dosing regimens for anti-tf-antibody drug-conjugates |
| AR106189A1 (es) | 2015-10-02 | 2017-12-20 | Hoffmann La Roche | ANTICUERPOS BIESPECÍFICOS CONTRA EL A-b HUMANO Y EL RECEPTOR DE TRANSFERRINA HUMANO Y MÉTODOS DE USO |
| EP3365027B1 (en) | 2015-10-14 | 2022-03-30 | Research Institute at Nationwide Children's Hospital | Hu specific antibodies and their use in inhibiting biofilm |
| JP2018534933A (ja) | 2015-11-02 | 2018-11-29 | ヤンセン ファーマシューティカ エヌ.ベー. | 抗il1rap抗体、il1rapとcd3を結合する二重特異性抗原結合分子、及びその使用 |
| DK3383920T3 (da) | 2015-11-30 | 2024-04-02 | Univ California | Levering af tumorspecifik nyttelast og immunaktivering ved hjælp af et humant antistof rettet mod et meget specifikt tumorcelleoverfladeantigen |
| KR20180101479A (ko) | 2016-01-13 | 2018-09-12 | 젠맵 에이/에스 | 항체 및 그의 약물 접합체를 위한 제제 |
| US20170210799A1 (en) | 2016-01-22 | 2017-07-27 | Janssen Biotech, Inc. | Anti-ror1, antibodies, ror1 x cd3 bispecific antibodies, and methods of using the same |
| EP3411406B1 (en) | 2016-02-05 | 2025-04-09 | Genmab A/S | Multispecific antigen-binding molecule with improved internalization characteristics |
| UA126115C2 (uk) | 2016-03-08 | 2022-08-17 | Янссен Байотек, Інк. | Антитіло до gitr |
| US20190233522A1 (en) | 2016-07-08 | 2019-08-01 | Genmab A/S | New dosage regimens for antibody drug conjugates based on anti-axl antibodies |
| MA56165A (fr) | 2016-07-12 | 2022-04-20 | H Lundbeck As | Anticorps spécifiques de la protéine tau hyperphosphorylée et leurs procédés d'utilisation |
| BR112019000512A2 (pt) | 2016-07-14 | 2019-04-24 | Genmab A/S | anticorpo, ácido nucleico, vetor de expressão, célula hospedeira, composição, métodos de tratamento de uma doença, para produzir um anticorpo biespecífico e para detectar se a reticulação entre as células que expressam cd40 e cd137 ocorre em uma amostra, uso de um anticorpo multiespecífico, e, kit |
| TWI781108B (zh) | 2016-07-20 | 2022-10-21 | 比利時商健生藥品公司 | 抗gprc5d抗體、結合gprc5d與cd3之雙特異性抗原結合分子及其用途 |
| US11186634B2 (en) | 2016-07-29 | 2021-11-30 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Antibodies targeting tumor associated macrophages and uses thereof |
| EP3494143B1 (en) | 2016-08-03 | 2022-10-05 | Cipla USA, Inc. | Plazomicin antibodies and methods of use |
| US11161909B2 (en) | 2016-08-15 | 2021-11-02 | Novartis Ag | Regimens and methods of treating multiple sclerosis using ofatumumab |
| EP3500302A4 (en) | 2016-08-16 | 2020-03-25 | University of Maryland, Baltimore | METHODS OF TREATING CANCER WITH BIFUNCTIONAL MOLECULES TARGETING GROWTH FACTORS |
| EP3535291A1 (en) | 2016-11-01 | 2019-09-11 | Genmab B.V. | Polypeptide variants and uses thereof |
| WO2018089829A1 (en) | 2016-11-10 | 2018-05-17 | Fortis Therapeutics, Inc. | Cd46-specific effector cells and uses thereof |
| US10889635B2 (en) | 2016-11-15 | 2021-01-12 | H. Lundbeck A/S | Agents, uses and methods for the treatment of synucleinopathy |
| EP4545070A3 (en) | 2016-11-22 | 2025-06-18 | Elektrofi, Inc | Particles comprising a therapeutic or diagnostic agent and suspensions and methods of use thereof |
| JP2020503857A (ja) | 2016-12-12 | 2020-02-06 | セファイド | 自動反応カートリッジにおける統合化イムノpcr及び核酸分析 |
| CN110072888B (zh) | 2016-12-16 | 2023-07-18 | H.隆德贝克有限公司 | 药剂、用途和方法 |
| US10364286B2 (en) | 2016-12-22 | 2019-07-30 | H. Lundbeck A/S | Monoclonal anti-alpha-synuclein antibodies for preventing tau aggregation |
| AU2018206552C1 (en) | 2017-01-04 | 2025-04-10 | Research Institute At Nationwide Children's Hospital | DNABII vaccines and antibodies with enhanced activity |
| CN110267985B (zh) | 2017-01-04 | 2023-05-23 | H.隆德贝克有限公司 | 用于治疗眼科疾病的特异性针对过度磷酸化τ蛋白的抗体 |
| JP7577446B2 (ja) | 2017-02-10 | 2024-11-05 | ジェンマブ ビー.ブイ. | ポリペプチドバリアントおよびそれらの使用 |
| TW201834688A (zh) | 2017-02-24 | 2018-10-01 | 日商中外製藥股份有限公司 | 藥學組成物、抗原結合分子、治療方法以及篩選方法 |
| US11274160B2 (en) | 2017-03-02 | 2022-03-15 | INSERM (Institut National de la Santé et de la Recherche Médicale | Antibodies having specificity to Nectin-4 and uses thereof |
| FI3592769T3 (fi) | 2017-03-09 | 2024-07-30 | Genmab As | Vasta-aineita PD-L1:tä vastaan |
| US11746136B2 (en) | 2017-03-15 | 2023-09-05 | Research Institute At Nationwide Children's Hospital | Composition and methods for disruption of bacterial biofilms without accompanying inflammation |
| KR102706161B1 (ko) | 2017-03-31 | 2024-09-19 | 젠맵 홀딩 비.브이. | 이중특이적 항-cd37 항체, 모노클로날 항-cd37 항체 및 그의 사용 방법 |
| JP7679175B2 (ja) | 2017-04-20 | 2025-05-19 | エータイアー ファーマ, インコーポレイテッド | 肺の炎症を治療するための組成物および方法 |
| KR102869563B1 (ko) | 2017-07-17 | 2025-10-10 | 얀센 바이오테크 인코포레이티드 | 피브로넥틴 iii형 도메인에 대한 항원 결합 영역 및 이의 사용 방법 |
| US10894833B2 (en) | 2017-07-20 | 2021-01-19 | H. Lundbeck A/S | Agents, uses and methods for treatment |
| EP3658581A1 (en) | 2017-07-24 | 2020-06-03 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Antibodies and peptides to treat hcmv related diseases |
| KR102758346B1 (ko) | 2017-08-04 | 2025-01-24 | 젠맵 에이/에스 | Pd-l1 및 cd137에 결합하는 결합제 및 그의 용도 |
| WO2019036855A1 (en) | 2017-08-21 | 2019-02-28 | Adagene Inc. | Anti-cd137 molecules and use thereof |
| US11746150B2 (en) | 2017-12-19 | 2023-09-05 | Surrozen Operating, Inc. | Anti-LRP5/6 antibodies and methods of use |
| JP7418332B2 (ja) | 2017-12-19 | 2024-01-19 | スロゼン オペレーティング, インコーポレイテッド | 抗フリズルド抗体及び使用方法 |
| CN118271444A (zh) | 2017-12-19 | 2024-07-02 | 瑟罗泽恩奥普瑞汀公司 | Wnt替代分子和其用途 |
| WO2019139987A1 (en) | 2018-01-09 | 2019-07-18 | Elstar Therapeutics, Inc. | Calreticulin binding constructs and engineered t cells for the treatment of diseases |
| US20210107988A1 (en) | 2018-01-24 | 2021-04-15 | Genmab B.V. | Polypeptide variants and uses thereof |
| WO2019148444A1 (en) | 2018-02-02 | 2019-08-08 | Adagene Inc. | Anti-ctla4 antibodies and methods of making and using the same |
| WO2019148445A1 (en) | 2018-02-02 | 2019-08-08 | Adagene Inc. | Precision/context-dependent activatable antibodies, and methods of making and using the same |
| EP3749360A1 (en) | 2018-02-09 | 2020-12-16 | Genmab A/S | Pharmaceutical compositions comprising bispecific antibodies directed against cd3 and cd20 and their uses |
| AU2019233523A1 (en) | 2018-03-12 | 2020-10-01 | Genmab A/S | Antibodies |
| WO2019178362A1 (en) | 2018-03-14 | 2019-09-19 | Elstar Therapeutics, Inc. | Multifunctional molecules that bind to calreticulin and uses thereof |
| TWI841554B (zh) | 2018-03-21 | 2024-05-11 | 丹麥商珍美寶股份有限公司 | 以鉑為主之劑與抗組織因子抗體-藥物共軛物的組合治療癌症之方法 |
| EA202092448A1 (ru) | 2018-04-10 | 2021-03-05 | Генмаб А/С | Axl-специфичные антитела для лечения онкологических заболеваний |
| BR112020022179A2 (pt) | 2018-05-03 | 2021-02-02 | Genmab B.V. | primeiro anticorpo, anticorpo, composição, métodos para tratar um indivíduo tendo uma doença, para esgotar uma população de célula e para induzir a proliferação em uma população de célula, e, kit. |
| CN112739716B (zh) | 2018-05-07 | 2025-05-27 | 展马博联合股份有限公司 | 使用抗pd-1抗体与抗组织因子抗体-药物偶联物的组合治疗癌症的方法 |
| JOP20200292A1 (ar) | 2018-05-16 | 2020-11-15 | Stichting Vumc | Bcma / cd3 و gprdc5d / cd3 مضادات غير محددة للاستخدام في علاج السرطان |
| US12115262B2 (en) | 2018-05-24 | 2024-10-15 | Elektrofi, Inc. | Particles comprising a therapeutic or diagnostic agent and suspensions and methods of use thereof |
| JP7513530B2 (ja) | 2018-06-22 | 2024-07-09 | ジェンマブ ホールディング ビー.ブイ. | 抗cd37抗体および抗cd20抗体、組成物、ならびにそれらの使用方法 |
| AU2019297451A1 (en) | 2018-07-03 | 2021-01-28 | Marengo Therapeutics, Inc. | Anti-TCR antibody molecules and uses thereof |
| DK3820906T3 (da) | 2018-07-05 | 2025-12-15 | Surrozen Operating Inc | Multispecifikke wnt-surrogatmolekyler og anvendelser deraf |
| MA53122A (fr) | 2018-07-13 | 2021-05-19 | Genmab As | Variants d'anticorps cd38 et leurs utilisations |
| WO2020012038A1 (en) | 2018-07-13 | 2020-01-16 | Genmab A/S | Trogocytosis-mediated therapy using cd38 antibodies |
| CA3107332A1 (en) | 2018-07-22 | 2020-01-30 | Bioasis Technologies Inc. | Treatment of lymphatic metastases |
| TW202021618A (zh) | 2018-08-17 | 2020-06-16 | 美商23與我有限公司 | 抗il1rap抗體及其使用方法 |
| WO2020053122A1 (en) | 2018-09-10 | 2020-03-19 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Combination of her2/neu antibody with heme for treating cancer |
| US20220111043A1 (en) | 2018-09-19 | 2022-04-14 | Lava Therapeutics B.V. | Dual acting cd1d immunoglobulin |
| EP3856783A1 (en) | 2018-09-26 | 2021-08-04 | Genmab A/S | Axl-specific antibodies for treatment of non-small cell lung cancer |
| EP3860715A1 (en) | 2018-10-04 | 2021-08-11 | Genmab Holding B.V. | Pharmaceutical compositions comprising bispecific anti-cd37 antibodies |
| US12161701B2 (en) | 2018-10-05 | 2024-12-10 | Research Institute At Nationwide Children's Hospital | Compositions and methods for enzymatic disruption of bacterial biofilms |
| SG11202103124WA (en) | 2018-10-23 | 2021-04-29 | Glycardial Diagnostics S L | Antibodies specific for glycosylated apoj and uses thereof |
| EP3870608A1 (en) | 2018-10-25 | 2021-09-01 | Polpharma Biologics Utrecht B.V. | Anti-human cd89 antibodies and uses thereof |
| TWI844571B (zh) | 2018-10-30 | 2024-06-11 | 丹麥商珍美寶股份有限公司 | 使用抗血管內皮生長因子(vegf)抗體與抗組織因子(tf)抗體-藥物共軛體之組合以治療癌症之方法 |
| JP7410143B2 (ja) | 2018-11-01 | 2024-01-09 | 山▲東▼新▲時▼代▲薬▼▲業▼有限公司 | 二重特異性抗体及びその用途 |
| CN120983617A (zh) | 2018-11-06 | 2025-11-21 | 健玛保 | 抗体配制剂 |
| TWI874341B (zh) | 2018-12-18 | 2025-03-01 | 美商健生生物科技公司 | 產生異二聚體抗體之方法 |
| AR117327A1 (es) | 2018-12-20 | 2021-07-28 | 23Andme Inc | Anticuerpos anti-cd96 y métodos de uso de estos |
| EP4647436A2 (en) | 2018-12-21 | 2025-11-12 | Sapreme Technologies B.V. | Biologically active cluster of molecules |
| AU2019405782A1 (en) | 2018-12-21 | 2021-06-17 | 23Andme, Inc. | Anti-IL-36 antibodies and methods of use thereof |
| JP2022519082A (ja) | 2019-02-01 | 2022-03-18 | ラヴァ・セラピューティクス・ベー・フェー | 新規cd40結合抗体 |
| NL2022494B1 (en) | 2019-02-01 | 2020-08-19 | Lava Therapeutics B V | Novel CD40-binding antibodies |
| GB2599228B (en) | 2019-02-21 | 2024-02-07 | Marengo Therapeutics Inc | Multifunctional molecules that bind to T cell related cancer cells and uses thereof |
| AU2020224681A1 (en) | 2019-02-21 | 2021-09-16 | Marengo Therapeutics, Inc. | Antibody molecules that bind to NKp30 and uses thereof |
| GB201903767D0 (en) * | 2019-03-19 | 2019-05-01 | Quadrucept Bio Ltd | Multimers, tetramers & octamers |
| EP3733707A1 (en) | 2019-04-30 | 2020-11-04 | Celyad S.A. | Car t-cells targeting bcma and uses thereof |
| WO2020225456A1 (en) | 2019-05-09 | 2020-11-12 | Genmab B.V. | Dosage regimens for a combination of anti-dr5 antibodies for use in treating cancer |
| US12209118B2 (en) | 2019-07-08 | 2025-01-28 | Research Institute At Nationwide Children's Hospital | Antibody compositions for disrupting biofilms |
| WO2021009081A1 (en) | 2019-07-12 | 2021-01-21 | Janssen Pharmaceutica Nv | Binding agents and uses thereof |
| US20220273809A1 (en) | 2019-07-19 | 2022-09-01 | Genmab A/S | Axl antibody-drug conjugates for use in treating cancer |
| US20220249674A1 (en) | 2019-07-25 | 2022-08-11 | Sapreme Technologies B.V. | Bioactive saponin linked to a functional moiety |
| MX2022001721A (es) | 2019-08-15 | 2022-03-11 | Genmab As | Composiciones farmaceuticas que comprenden anticuerpos biespecificos dirigidos contra cd3 y cd20 y sus usos. |
| EP4028424A1 (en) | 2019-09-12 | 2022-07-20 | Genmab A/S | Bispecific antibodies binding to 5t4 and cd3 for use in treatment of cancer |
| EP4027978A1 (en) | 2019-09-13 | 2022-07-20 | Elektrofi, Inc. | Compositions and methods for the delivery of therapeutic biologics for treatment of disease |
| EP3792283A1 (en) | 2019-09-16 | 2021-03-17 | Lava Therapeutics B.V. | Treatment of cancer comprising administration of vgamma9vdelta2 t cell receptor binding antibodies |
| WO2021058729A1 (en) | 2019-09-27 | 2021-04-01 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Anti-müllerian inhibiting substance type i receptor antibodies and uses thereof |
| WO2021058763A1 (en) | 2019-09-27 | 2021-04-01 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Anti-müllerian inhibiting substance antibodies and uses thereof |
| EP4055046A1 (en) | 2019-11-06 | 2022-09-14 | Genmab B.V. | Antibody variant combinations and uses thereof |
| US20230040928A1 (en) | 2019-12-09 | 2023-02-09 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Antibodies having specificity to her4 and uses thereof |
| BR112022012725A2 (pt) | 2019-12-24 | 2022-11-16 | Jjp Biologics Sp Z O O | Anticorpos hvem (tnfrsf14) anti-humanos e usos dos mesmos |
| JP2023509708A (ja) | 2020-01-03 | 2023-03-09 | マレンゴ・セラピューティクス,インコーポレーテッド | 抗tcr抗体分子およびその使用 |
| PE20230113A1 (es) | 2020-01-16 | 2023-01-27 | Genmab As | Formulaciones de anticuerpos anti-cd38 y usos de las mismas |
| WO2021155916A1 (en) | 2020-02-04 | 2021-08-12 | BioNTech SE | Treatment involving antigen vaccination and binding agents binding to pd-l1 and cd137 |
| EP4100059A1 (en) | 2020-02-04 | 2022-12-14 | Genmab A/S | Antibodies for use in therapy |
| CA3168613A1 (en) | 2020-03-18 | 2021-09-23 | Genmab A/S | Antibodies binding to b7h4 |
| WO2021212019A1 (en) | 2020-04-17 | 2021-10-21 | Elektrofi, Inc. | Methods of forming particles by continuous droplet formation and dehydration |
| CN115698078A (zh) | 2020-04-21 | 2023-02-03 | Jjp佰优罗机克斯有限公司 | 人源化抗人cd89抗体及其用途 |
| US20230265204A1 (en) | 2020-04-24 | 2023-08-24 | Hoffmann-La Roche Inc. | Enzyme and pathway modulation with sulfhydryl compounds and their derivatives |
| EP4146175A1 (en) | 2020-05-08 | 2023-03-15 | Genmab A/S | Bispecific antibodies against cd3 and cd20 |
| MX2022014166A (es) | 2020-05-11 | 2022-12-02 | Janssen Biotech Inc | Metodos para tratar el mieloma multiple. |
| JP2023525053A (ja) | 2020-05-12 | 2023-06-14 | インサーム(インスティテュ ナシオナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシェ メディカル) | 皮膚t細胞リンパ腫及びtfh由来リンパ腫を処置する新しい方法 |
| EP4559477A3 (en) | 2020-05-13 | 2025-08-13 | Adagene AG | Compositions and methods for treating cancer |
| CN116323665A (zh) | 2020-05-29 | 2023-06-23 | 23和我公司 | 抗cd200r1抗体及其使用方法 |
| US20230235040A1 (en) | 2020-06-22 | 2023-07-27 | Almirall, S.A. | Anti-il-36 antibodies and methods of use thereof |
| JP2023532807A (ja) | 2020-07-08 | 2023-07-31 | ラヴァ・セラピューティクス・エヌ・ヴイ | Psma及びガンマ-デルタt細胞受容体に結合する抗体 |
| EP3939999A1 (en) | 2020-07-14 | 2022-01-19 | Fundación del Sector Público Estatal Centro Nacional de Investigaciones Oncológicas Carlos III (F.S.P. CNIO) | Interleukin 11 receptor alpha subunit (il11ra) neutralizing antibodies and uses thereof |
| WO2022018294A1 (en) | 2020-07-23 | 2022-01-27 | Genmab B.V. | A combination of anti-dr5 antibodies and an immunomodulatory imide drug for use in treating multiple myeloma |
| KR20230065256A (ko) | 2020-08-06 | 2023-05-11 | 비온테크 에스이 | 코로나바이러스 s 단백질용 결합제 |
| US11484604B2 (en) | 2020-08-07 | 2022-11-01 | Fortis Therapeutics, Inc. | Immunoconjugates targeting CD46 and methods of use thereof |
| WO2022049220A2 (en) | 2020-09-02 | 2022-03-10 | Genmab A/S | Antibody therapy |
| BR112023004351A2 (pt) | 2020-09-10 | 2023-04-04 | Genmab As | Método para tratar linfoma folicular em um sujeito humano |
| EP4210744A1 (en) | 2020-09-10 | 2023-07-19 | Genmab A/S | Bispecific antibody against cd3 and cd20 in combination therapy for treating diffuse large b-cell lymphoma |
| CA3192251A1 (en) | 2020-09-10 | 2022-03-17 | Genmab A/S | Bispecific antibody against cd3 and cd20 in combination therapy for treating diffuse large b-cell lymphoma |
| WO2022053658A1 (en) | 2020-09-10 | 2022-03-17 | Genmab A/S | Bispecific antibody against cd3 and cd20 in combination therapy for treating diffuse large b-cell lymphoma |
| EP4210743A1 (en) | 2020-09-10 | 2023-07-19 | Genmab A/S | Bispecific antibody against cd3 and cd20 in combination therapy for treating follicular lymphoma |
| WO2022053653A1 (en) | 2020-09-10 | 2022-03-17 | Genmab A/S | Bispecific antibodies against cd3 and cd20 for treating chronic lymphocytic leukemia |
| IL301269A (en) | 2020-09-14 | 2023-05-01 | Ichnos Sciences S A | Antibodies that bind to IL1RAP and their uses |
| TW202227478A (zh) | 2020-09-15 | 2022-07-16 | 德商拜恩迪克公司 | 對細胞靶向遞送的藥劑及方法 |
| MX2023003749A (es) | 2020-10-02 | 2023-04-24 | Genmab As | Anticuerpos capaces de unirse al receptor huerfano 2 similar a tirosina-cinasa receptora (ror2) y anticuerpos biespecificos que se unen a ror2 y al cumulo de diferenciacion 3 (cd3). |
| AU2021393908A1 (en) | 2020-12-07 | 2023-06-22 | BioNTech SE | Antibody and taxane combination therapy |
| EP4259660A1 (en) | 2020-12-10 | 2023-10-18 | LAVA Therapeutics N.V. | Antibodies that bind gamma-delta t cell receptors |
| EP4276466A4 (en) | 2021-01-08 | 2024-12-18 | Beijing Hanmi Pharmaceutical Co., Ltd. | ANTIBODY SPECIFICALLY BINDING WITH PD-L1 AND ANTIGEN-BINDING FRAGMENT OF ANTIBODY |
| EP4276111A4 (en) | 2021-01-08 | 2025-04-30 | Beijing Hanmi Pharmaceutical Co., Ltd. | Antibody specifically binding to 4-1bb and antigen-binding fragment of antibody |
| JP7699210B2 (ja) | 2021-01-08 | 2025-06-26 | 北京韓美薬品有限公司 | Cd47と特異的に結合する抗体及びその抗原結合フラグメント |
| EP4281566A1 (en) | 2021-01-20 | 2023-11-29 | Coding Bio Limited | Methods for high throughput screening of chimeric antigen receptors |
| GB202100754D0 (en) | 2021-01-20 | 2021-03-03 | Coding Bio Ltd | Methods for high throughput screening of chimeric antigen receptors |
| CA3211114A1 (en) | 2021-02-16 | 2022-08-25 | Janssen Biotech, Inc. | Materials and methods for enhanced linker targeting |
| TW202302636A (zh) | 2021-02-16 | 2023-01-16 | 比利時商健生藥品公司 | 靶向bcma、gprc5d及cd3之三特異性抗體 |
| CA3209454A1 (en) | 2021-02-26 | 2022-09-01 | Robertus Cornelis ROOVERS | Antibodies that bind cd123 and gamma-delta t cell receptors |
| IL305681A (en) | 2021-03-09 | 2023-11-01 | Genmab As | Multispecific binding agents against cd40 and cd137 in therapy |
| BR112023017887A2 (pt) | 2021-03-12 | 2023-10-10 | Genmab As | Proteína compreendendo um primeiro polipeptídeo e um segundo polipeptídeo, anticorpo biespecífico, ácido nucleico de codificação do dito primeiro ou segundo polipeptídeo, célula hospedeira, composição farmacêutica, proteína, anticorpo biespecífico ou composição farmacêutica para uso, e, métodos de tratamento e de preparo de um anticorpo biespecífico |
| MX2023011267A (es) | 2021-03-24 | 2023-12-14 | Janssen Biotech Inc | Anticuerpo triespecífico dirigido a cd79b, cd20, y cd3. |
| WO2022216993A2 (en) | 2021-04-08 | 2022-10-13 | Marengo Therapeutics, Inc. | Multifuntional molecules binding to tcr and uses thereof |
| JP2024519212A (ja) | 2021-05-07 | 2024-05-09 | ジェンマブ エー/エス | B7h4およびcd3に結合する二重特異性抗体を含む薬学的組成物 |
| US20240255517A1 (en) | 2021-06-04 | 2024-08-01 | Elektrofi, Inc. | Methods For Screening Particle Formulations Comprising Proteins |
| JP2024522179A (ja) | 2021-06-08 | 2024-06-11 | バイオエヌテック セル アンド ジーン セラピーズ ゲーエムベーハー | 免疫エフェクタ細胞の活性化および標的化のための薬剤および方法 |
| US20240262924A1 (en) | 2021-06-21 | 2024-08-08 | Genmab A/S | Combination dosage regime of cd137 and pd-l1 binding agents |
| AU2022312698A1 (en) | 2021-07-13 | 2024-01-25 | BioNTech SE | Multispecific binding agents against cd40 and cd137 in combination therapy for cancer |
| IL309495A (en) | 2021-07-15 | 2024-02-01 | BioNTech SE | Agents encoding cldn6 and cd3 binding elements for treating cldn6-positive cancers |
| WO2023023227A1 (en) | 2021-08-20 | 2023-02-23 | Alexion Pharmaceuticals, Inc. | Methods for treating sickle cell disease or beta thalassemia using complement alternative pathway inhibitors |
| WO2023023220A1 (en) | 2021-08-20 | 2023-02-23 | Alexion Pharmaceuticals, Inc. | Methods for treating sickle cell disease or beta thalassemia using a complement alternative pathway inhibitor |
| JP2024532620A (ja) | 2021-08-30 | 2024-09-05 | ラッセン・セラピューティクス1・インコーポレイテッド | 抗IL-11Rα抗体 |
| IL311141A (en) | 2021-09-06 | 2024-04-01 | Genmab As | Antibodies capable of binding to CD27, their variants and uses thereof |
| JP2024536383A (ja) | 2021-10-06 | 2024-10-04 | ジェンマブ エー/エス | 併用におけるpd-l1およびcd137に対する多重特異性結合剤 |
| JP2024538755A (ja) | 2021-10-06 | 2024-10-23 | ジェンマブ エー/エス | がんを処置するための、抗pd-1抗体との組合せにおけるpd-l1及びcd137に対する多特異性結合剤 |
| KR20240082397A (ko) | 2021-10-08 | 2024-06-10 | 젠맵 에이/에스 | Cd30 및 cd3에 결합하는 항체 |
| WO2023067138A1 (en) | 2021-10-21 | 2023-04-27 | LAVA Therapeutics N.V. | Uses of gamma delta t cell activating antibodies |
| IL312503A (en) | 2021-11-03 | 2024-07-01 | Janssen Biotech Inc | Methods of treating cancers and enhancing efficacy of bcmaxcd3 bispecific antibodies |
| WO2023083439A1 (en) | 2021-11-09 | 2023-05-19 | BioNTech SE | Tlr7 agonist and combinations for cancer treatment |
| GB202116514D0 (en) | 2021-11-16 | 2021-12-29 | Coding Bio Ltd | Computational methods for the design and optimisation of chimeric antigen receptors (cars) |
| JP2025503176A (ja) | 2022-01-28 | 2025-01-30 | ジェンマブ エー/エス | びまん性大細胞型b細胞リンパ腫を治療するための併用療法におけるcd3及びcd20に対する二重特異性抗体 |
| AU2023213099A1 (en) | 2022-01-28 | 2024-07-18 | Genmab A/S | Bispecific antibody against cd3 and cd20 in combination therapy for treating diffuse large b-cell lymphoma |
| EP4472672A1 (en) | 2022-02-02 | 2024-12-11 | BioNTech SE | Agents and methods for targeted delivery to cells |
| US20250154202A1 (en) | 2022-02-02 | 2025-05-15 | BioNTech SE | Cyclic epitope tags |
| WO2023148277A1 (en) | 2022-02-02 | 2023-08-10 | BioNTech SE | Agents and methods for targeted delivery of nucleic acids to cells |
| EP4238988A1 (en) | 2022-03-01 | 2023-09-06 | Consejo Superior De Investigaciones Científicas | Antibodies against sars-cov-2 and uses thereof |
| WO2023174521A1 (en) | 2022-03-15 | 2023-09-21 | Genmab A/S | Binding agents binding to epcam and cd137 |
| WO2023175171A1 (en) | 2022-03-18 | 2023-09-21 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Bk polyomavirus antibodies and uses thereof |
| WO2023186905A1 (en) | 2022-03-29 | 2023-10-05 | LAVA Therapeutics N.V. | A method of treating a hematological cancer following screening for cd1d positive tumor cells |
| WO2023198839A2 (en) | 2022-04-13 | 2023-10-19 | Genmab A/S | Bispecific antibodies against cd3 and cd20 |
| CA3248272A1 (en) | 2022-04-29 | 2023-11-02 | Elektrofi, Inc. | INJECTABLE SUSPENSION |
| US20250325643A1 (en) | 2022-05-12 | 2025-10-23 | Genmab A/S | Binding agents capable of binding to cd27 in combination therapy |
| IL316628A (en) | 2022-05-12 | 2024-12-01 | Genmab As | Binding agents capable of binding to CD27 in combination therapy |
| EP4285926A1 (en) | 2022-05-30 | 2023-12-06 | LAVA Therapeutics N.V. | Combination treatment for chronic lymphocytic leukemia |
| EP4292610A1 (en) | 2022-06-15 | 2023-12-20 | LAVA Therapeutics N.V. | Variant antibodies that bind gamma-delta t cell receptors |
| EP4292609A1 (en) | 2022-06-15 | 2023-12-20 | LAVA Therapeutics N.V. | Compositions comprising antibodies that bind gamma-delta t cell receptors |
| NL2032398B1 (en) | 2022-07-06 | 2024-01-23 | Academisch Ziekenhuis Leiden | Bispecific antibody and uses thereof |
| AU2023317702A1 (en) | 2022-08-01 | 2025-01-09 | BioNTech SE | Nucleic acid compositions comprising amphiphilic oligo ethylene glycol (oeg)-conjugated compounds and methods of using such compounds and compositions |
| CN117586388A (zh) | 2022-08-09 | 2024-02-23 | 深圳智源生物医药有限公司 | 改进的β淀粉样蛋白寡聚体特异性结合抗体 |
| TW202417490A (zh) | 2022-08-31 | 2024-05-01 | 美商艾力克森製藥公司 | 用於治療鐮狀細胞病的融合多肽之劑量及投與 |
| JP2025531832A (ja) | 2022-09-08 | 2025-09-25 | アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル | LTBP2(潜在的形質転換増殖因子β結合タンパク質2)に対する特異性を有する抗体及びその使用 |
| EP4587473A1 (en) | 2022-09-12 | 2025-07-23 | Institut National de la Santé et de la Recherche Médicale | New anti-itgb8 antibodies and its uses thereof |
| GB202214132D0 (en) | 2022-09-27 | 2022-11-09 | Coding Bio Ltd | CLL1 binding molecules |
| EP4628505A1 (en) | 2022-10-28 | 2025-10-08 | Genor Biopharma Co., Ltd. | Novel anti-ctla4 antibody |
| TW202432177A (zh) | 2022-10-31 | 2024-08-16 | 丹麥商珍美寶股份有限公司 | Cd38抗體及其用途 |
| EP4612179A1 (en) | 2022-11-02 | 2025-09-10 | Genmab A/S | Bispecific antibodies against cd3 and cd20 for treating richter's syndrome |
| AU2023401158A1 (en) | 2022-12-01 | 2025-05-29 | BioNTech SE | Multispecific antibody against cd40 and cd137 in combination therapy with anti-pd1 ab and chemotherapy |
| WO2024148241A1 (en) | 2023-01-06 | 2024-07-11 | Lassen Therapeutics 1, Inc. | Anti-il-18bp antibodies |
| IL321948A (en) | 2023-01-06 | 2025-09-01 | Lassen Therapeutics Inc | Anti-IL-18 BP antibodies |
| KR20250133727A (ko) | 2023-01-06 | 2025-09-08 | 라센 테라퓨틱스, 인코포레이티드 | 갑상선 안구 질환을 치료하기 위한 항-IL-11Rα 항체 |
| WO2024165146A1 (en) | 2023-02-07 | 2024-08-15 | Biontech Cell & Gene Therapies Gmbh | Immune effector cells stably and transiently expressing nucleic acids |
| GB202301949D0 (en) | 2023-02-10 | 2023-03-29 | Coding Bio Ltd | CLL1 and/or CD33 binding molecules |
| EP4438624A1 (en) | 2023-03-27 | 2024-10-02 | LAVA Therapeutics N.V. | Antibodies that bind nectin-4 and gamma-delta t cell receptors |
| AR132290A1 (es) | 2023-04-05 | 2025-06-11 | Genmab As | Composiciones farmacéuticas que comprenden anticuerpos que se unen a cd30 y cd3 |
| WO2024209072A1 (en) | 2023-04-06 | 2024-10-10 | Genmab A/S | Multispecific binding agents against pd-l1 and cd137 for treating cancer |
| WO2024213754A1 (en) | 2023-04-13 | 2024-10-17 | Genmab A/S | Methods of treating lymphoma with bispecific antibodies against cd3 and cd20 |
| TW202509071A (zh) | 2023-05-12 | 2025-03-01 | 丹麥商珍美寶股份有限公司 | 能夠與ox40結合之抗體、其變異體及其用途 |
| AR133071A1 (es) | 2023-06-30 | 2025-08-20 | Genmab As | ANTICUERPOS QUE SE UNEN A LA PROTEÍNA DE ACTIVACIÓN DE FIBROBLASTOS a Y AL RECEPTOR DE MUERTE 4 |
| WO2025012417A1 (en) | 2023-07-13 | 2025-01-16 | Institut National de la Santé et de la Recherche Médicale | Anti-neurotensin long fragment and anti-neuromedin n long fragment antibodies and uses thereof |
| WO2025021277A1 (en) | 2023-07-21 | 2025-01-30 | BioNTech SE | Agents and methods for targeted delivery of cytokines to immune cells |
| TW202519261A (zh) | 2023-07-27 | 2025-05-16 | 荷蘭商拉法醫療公司 | 用於治療癌症之結合γ-δ T細胞受體之抗體 |
| WO2025027077A1 (en) | 2023-08-02 | 2025-02-06 | BioNTech SE | Agents and methods for targeted delivery of immune effector cells |
| WO2025026553A1 (en) | 2023-08-02 | 2025-02-06 | BioNTech SE | Agents and methods for targeted delivery to cells |
| WO2025032158A1 (en) | 2023-08-08 | 2025-02-13 | Institut National de la Santé et de la Recherche Médicale | Method to treat tauopathies |
| WO2025038492A1 (en) | 2023-08-11 | 2025-02-20 | Abalytics Oncology, Inc. | Anti-ctla-4 antibodies and related binding molecules and methods and uses thereof |
| US20250082736A1 (en) | 2023-09-08 | 2025-03-13 | Elektrofi, Inc. | Particles and suspensions comprising hyaluronan degrading agents and methods of use thereof |
| WO2025056180A1 (en) | 2023-09-15 | 2025-03-20 | BioNTech SE | Methods of treatment using agents binding to epcam and cd137 in combination with pd-1 axis binding antagonists |
| WO2025073890A1 (en) | 2023-10-06 | 2025-04-10 | Institut National de la Santé et de la Recherche Médicale | Method to capture circulating tumor extracellular vesicles |
| TW202535921A (zh) | 2023-10-11 | 2025-09-16 | 德商拜恩迪克公司 | 用於靶向遞送免疫效應子細胞之試劑及方法 |
| GB202317065D0 (en) | 2023-11-07 | 2023-12-20 | Coding Bio Ltd | BCMA binding molecules |
| WO2025111402A1 (en) | 2023-11-21 | 2025-05-30 | Board Of Regents Of The University Of Nebraska | Anti-amyloid beta antibodies and related compositions and methods thereof |
| WO2025114411A1 (en) | 2023-11-29 | 2025-06-05 | Institut National de la Santé et de la Recherche Médicale | New method to treat brain or neurologic disorders |
| WO2025114541A1 (en) | 2023-11-30 | 2025-06-05 | Genmab A/S | Antibodies capable of binding to ox40 in combination therapy |
| US20250230251A1 (en) | 2023-12-20 | 2025-07-17 | Bristol-Myers Squibb Company | Antibodies targeting il-18 receptor beta (il-18rb) and related methods |
| WO2025134049A1 (en) | 2023-12-21 | 2025-06-26 | Janssen Biotech, Inc | Trispecific antibody targeting bcma, gprc5d and cd3 for the treatment of al amyloidosis |
| WO2025134050A1 (en) | 2023-12-21 | 2025-06-26 | Janssen Biotech, Inc | Trispecific antibody targeting bcma, gprc5d and cd3 for the treatment of multiple myeloma |
| WO2025224297A1 (en) | 2024-04-26 | 2025-10-30 | Institut National de la Santé et de la Recherche Médicale | Antibodies having specificity to tgfbi and uses thereof |
| WO2025233825A1 (en) | 2024-05-06 | 2025-11-13 | Janssen Pharmaceutica Nv | Enrichment of cells expressing a bird linker |
| WO2025240670A2 (en) | 2024-05-15 | 2025-11-20 | Abalytics Oncology, Inc. | Anti-pd-1 antibodies and related binding molecules and methods and uses thereof |
| WO2025242732A1 (en) | 2024-05-21 | 2025-11-27 | Institut National de la Santé et de la Recherche Médicale | Pan antibodies against sars-cov-2 spike protein and uses thereof for therapeutical purposes |
| WO2025242827A1 (en) | 2024-05-22 | 2025-11-27 | Genmab A/S | Bispecific antibody against pd-l1 and cd137 in combination therapy |
| EP4653460A1 (en) | 2024-05-23 | 2025-11-26 | Egle Therapeutics | Il18r agonist antibodies and uses thereof |
| WO2025242910A1 (en) | 2024-05-23 | 2025-11-27 | Egle Therapeutics | Il18r agonist antibodies and uses thereof |
| US20250361317A1 (en) | 2024-05-24 | 2025-11-27 | Janssen Biotech, Inc. | Bispecific antibody targeting emr2 (cd312) and the t-cell receptor trbv19 |
| WO2025248097A2 (en) | 2024-05-31 | 2025-12-04 | Gamamabs Pharma | Humanized anti-human her3 antibodies and uses thereof |
| WO2025257181A1 (en) | 2024-06-11 | 2025-12-18 | Institut National de la Santé et de la Recherche Médicale | Antibodies targeting trans-active response dna-binding protein-43 (tdp-43) |
Family Cites Families (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3883899T3 (de) | 1987-03-18 | 1999-04-22 | Sb2, Inc., Danville, Calif. | Geänderte antikörper. |
| ATE139258T1 (de) | 1990-01-12 | 1996-06-15 | Cell Genesys Inc | Erzeugung xenogener antikörper |
| US6046310A (en) * | 1996-03-13 | 2000-04-04 | Protein Design Labs., Inc. | FAS ligand fusion proteins and their uses |
| EP0953639A1 (en) * | 1998-04-30 | 1999-11-03 | Boehringer Ingelheim International GmbH | FAPalpha-specific antibody with improved producibility |
| JP4282906B2 (ja) * | 1998-08-10 | 2009-06-24 | アジェンシス,インコーポレイテッド | Bpc−1:前立腺および膀胱の癌細胞によって発現および分泌がなされる分泌型の脳特異的蛋白質 |
| DK1355919T3 (da) | 2000-12-12 | 2011-03-14 | Medimmune Llc | Molekyler med længere halveringstider, sammensætninger og anvendelser deraf |
| US7754208B2 (en) * | 2001-01-17 | 2010-07-13 | Trubion Pharmaceuticals, Inc. | Binding domain-immunoglobulin fusion proteins |
| US7829084B2 (en) * | 2001-01-17 | 2010-11-09 | Trubion Pharmaceuticals, Inc. | Binding constructs and methods for use thereof |
| EP2316951A1 (en) * | 2001-01-17 | 2011-05-04 | Trubion Pharmaceuticals, Inc. | Binding domain-immunoglobulin fusion proteins |
| US7300916B2 (en) | 2001-02-27 | 2007-11-27 | Yoshiko Yasuda | Preventives/remedies for thickened scar, keloid or chronic arthritic diseases |
| US7595378B2 (en) | 2001-06-13 | 2009-09-29 | Genmab A/S | Human monoclonal antibodies to epidermal growth factor receptor (EGFR) |
| AU2002305478A1 (en) | 2001-06-20 | 2003-01-08 | Molecular Staging, Inc. | Conjugates of reduced antibodies and biomolecules |
| US7053202B2 (en) * | 2001-10-19 | 2006-05-30 | Millennium Pharmaceuticals, Inc. | Immunoglobulin DNA cassette molecules, monobody constructs, methods of production, and methods of use therefor |
| US7317091B2 (en) | 2002-03-01 | 2008-01-08 | Xencor, Inc. | Optimized Fc variants |
| JP2006508062A (ja) | 2002-09-17 | 2006-03-09 | ジーティーシー バイオセラピューティックス インコーポレイテッド | 重鎖間ジスルフィド結合を欠く免疫グロブリン分子の単離 |
| US7608429B2 (en) | 2002-10-31 | 2009-10-27 | Genentech, Inc. | Methods and compositions for increasing antibody production |
| BRPI0316282B8 (pt) | 2002-11-15 | 2021-05-25 | Genmab As | anticorpo humano isolado monoclonal, composição, imunoconjugado, molécula biespecífica ou multiespecífica, método e conjunto de diagnóstico para detectar a presença de antígeno cd25 ou uma célula que expressa cd25, e, vetor de expressão |
| PT1606318E (pt) * | 2003-03-26 | 2009-11-10 | Deutsches Krebsforsch | Proteínas de fusão de fc melhoradas |
| AU2004263823B2 (en) * | 2003-05-30 | 2008-09-18 | Agensys, Inc. | Prostate stem cell antigen (PSCA) variants and subsequences thereof |
| US20050069521A1 (en) * | 2003-08-28 | 2005-03-31 | Emd Lexigen Research Center Corp. | Enhancing the circulating half-life of interleukin-2 proteins |
| AR045614A1 (es) | 2003-09-10 | 2005-11-02 | Hoffmann La Roche | Anticuerpos contra el recepctor de la interleuquina- 1 y los usos de los mismos |
| US20060134105A1 (en) * | 2004-10-21 | 2006-06-22 | Xencor, Inc. | IgG immunoglobulin variants with optimized effector function |
| WO2005063815A2 (en) | 2003-11-12 | 2005-07-14 | Biogen Idec Ma Inc. | Fcϝ receptor-binding polypeptide variants and methods related thereto |
| JP4762904B2 (ja) * | 2003-11-13 | 2011-08-31 | ハンミ ホールディングス カンパニー リミテッド | 免疫グロブリン不変領域の量産方法 |
| CN1922210A (zh) | 2003-12-19 | 2007-02-28 | 健泰科生物技术公司 | 可用作治疗剂的单价抗体片段 |
| CA2563333A1 (en) * | 2004-04-06 | 2005-10-27 | The Regents Of The University Of California | Orphan receptor tyrosine kinase as a target in breast cancer |
| CA2578613A1 (en) | 2004-08-11 | 2007-01-25 | Trubion Pharmaceuticals, Inc. | Binding domain fusion proteins |
| WO2006031994A2 (en) | 2004-09-14 | 2006-03-23 | Xencor, Inc. | Monomeric immunoglobulin fc domains |
| JP4958555B2 (ja) | 2004-09-22 | 2012-06-20 | 協和発酵キリン株式会社 | 安定化されたヒトIgG4抗体 |
| ES2416136T3 (es) | 2005-09-26 | 2013-07-30 | Medarex, Inc. | Conjugados de anticuerpo-fármaco y su uso |
| TW200732350A (en) | 2005-10-21 | 2007-09-01 | Amgen Inc | Methods for generating monovalent IgG |
| US10155816B2 (en) * | 2005-11-28 | 2018-12-18 | Genmab A/S | Recombinant monovalent antibodies and methods for production thereof |
| EP1960431B1 (en) | 2005-12-15 | 2014-10-01 | Genmab A/S | Use of effector-function-deficient antibodies for treatment of auto-immune diseases |
| WO2008145137A2 (en) | 2007-05-31 | 2008-12-04 | Genmab A/S | Recombinant non glycosylated monovalent half-antibodies obtained by molecular engineering |
| US20110045007A1 (en) | 2007-05-31 | 2011-02-24 | Genmab A/S | Fusion or linked proteins with extended half life |
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| US20190169298A1 (en) | 2019-06-06 |
| US10155816B2 (en) | 2018-12-18 |
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| JP6341954B2 (ja) | 2018-06-13 |
| BRPI0619056A2 (pt) | 2011-09-20 |
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| EP1973576A1 (en) | 2008-10-01 |
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| AU2006317242A1 (en) | 2007-05-31 |
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| CA2631184A1 (en) | 2007-05-31 |
| SG10201600950TA (en) | 2016-03-30 |
| JP5525729B2 (ja) | 2014-06-18 |
| JP2016182138A (ja) | 2016-10-20 |
| WO2007059782A1 (en) | 2007-05-31 |
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