CA2998644A1 - Therapeutic cd47 antibodies - Google Patents
Therapeutic cd47 antibodies Download PDFInfo
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- CA2998644A1 CA2998644A1 CA2998644A CA2998644A CA2998644A1 CA 2998644 A1 CA2998644 A1 CA 2998644A1 CA 2998644 A CA2998644 A CA 2998644A CA 2998644 A CA2998644 A CA 2998644A CA 2998644 A1 CA2998644 A1 CA 2998644A1
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Families Citing this family (90)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2786083T3 (es) | 2012-12-12 | 2020-10-08 | Arch Oncology Inc | Anticuerpos terapéuticos CD47 |
| US9221908B2 (en) | 2012-12-12 | 2015-12-29 | Vasculox, Inc. | Therapeutic CD47 antibodies |
| KR102489471B1 (ko) | 2014-12-30 | 2023-01-18 | 셀진 코포레이션 | 항-cd47 항체 및 그 용도 |
| BR112018005322A2 (pt) | 2015-09-18 | 2018-12-11 | Arch Oncology, Inc. | anticorpo monoclonal ou seu fragmento de ligação a antígenos, composição farmacêutica, anticorpo monoclonal ou seu fragmento de ligação a antígenos para uso, método de tratamento de lesão de isquemia-reperfusão, método de tratamento de câncer em um paciente humano, método de avaliação da expressão de cd47 em células tumorais e/ou imunes usando um anticorpo monoclonal ou seu fragmento de ligação a antígenos |
| WO2018075960A1 (en) * | 2016-10-21 | 2018-04-26 | Tioma Therapeutics, Inc. | Therapeutic cd47 antibodies |
| SG11201908602UA (en) * | 2017-03-22 | 2019-10-30 | Arch Oncology Inc | Combination therapy for the treatment of solid and hematological cancers |
| CA3058966A1 (en) | 2017-04-14 | 2018-10-18 | Tollnine, Inc. | Immunomodulating polynucleotides, antibody conjugates thereof, and methods of their use |
| CA3071860A1 (en) | 2017-08-02 | 2019-02-07 | Phanes Therapeutics, Inc. | Anti-cd47 antibodies and uses thereof |
| MX2020001873A (es) * | 2017-08-18 | 2020-10-22 | Ultrahuman Four Ltd | Agentes de union. |
| CN109422811A (zh) | 2017-08-29 | 2019-03-05 | 信达生物制药(苏州)有限公司 | 抗cd47抗体及其用途 |
| AU2018351006B2 (en) * | 2017-10-18 | 2024-08-29 | Forty Seven, LLC | Anti-CD47 agent-based ovarian cancer therapy |
| KR20200070341A (ko) * | 2017-10-18 | 2020-06-17 | 포티 세븐, 인코포레이티드 | 항-cd47 및 항-pd-l1로 난소암의 치료 |
| WO2019086574A1 (en) * | 2017-11-01 | 2019-05-09 | Hummingbird Bioscience Holdings Pte. Ltd. | Cd47 and cd33 antigen-binding molecules |
| KR20200079511A (ko) * | 2017-11-01 | 2020-07-03 | 허밍버드 바이오사이언스 홀딩스 피티이. 엘티디. | Cd47 항원-결합 분자 |
| GB201720426D0 (en) * | 2017-12-07 | 2018-01-24 | Hummingbird Bioscience Pte Ltd | CD47 and BCMA antigen-binding molecules |
| MX2020005463A (es) | 2017-12-01 | 2020-09-07 | Seattle Genetics Inc | Anticuerpos anti grupo de diferenciacion 47 (anti-cd47) y sus usos para tratar cancer. |
| EA202091364A1 (ru) * | 2017-12-04 | 2020-10-13 | Бейджин Ханми Фармасьютикал Ко., Лтд. | Анти-pd-l1/анти-cd47 биспецифическое антитело с подобной природному антителу структурой и в форме гетеродимера и способ его получения |
| CN110144009B (zh) * | 2018-02-14 | 2020-01-21 | 上海洛启生物医药技术有限公司 | Cd47单域抗体及其用途 |
| WO2019179366A1 (en) * | 2018-03-20 | 2019-09-26 | Wuxi Biologics (Shanghai) Co. Ltd. | Novel anti-cd47 antibodies |
| CN110305212A (zh) | 2018-03-27 | 2019-10-08 | 信达生物制药(苏州)有限公司 | 抗cd47抗体及其用途 |
| GB201804860D0 (en) * | 2018-03-27 | 2018-05-09 | Ultrahuman Two Ltd | CD47 Binding agents |
| CN110577597B (zh) | 2018-06-11 | 2021-10-22 | 康诺亚生物医药科技（成都）有限公司 | 一种阻断CD47和SIRPα相互作用的抗体 |
| CN108872569A (zh) * | 2018-06-19 | 2018-11-23 | 浠思（上海）生物技术有限公司 | 利用HTRF一步法筛选CD47/SIRP alpha阻断剂的方法 |
| WO2020009725A1 (en) * | 2018-07-05 | 2020-01-09 | Trican Biotechnology Co., Ltd | Human anti-cd47 antibodies and uses thereof |
| WO2020019135A1 (zh) * | 2018-07-23 | 2020-01-30 | 中国科学院微生物研究所 | 一种抗cd47抗体及其应用 |
| CN112805029A (zh) * | 2018-08-13 | 2021-05-14 | 安驰肿瘤公司 | 治疗性cd47抗体 |
| US12331320B2 (en) | 2018-10-10 | 2025-06-17 | The Research Foundation For The State University Of New York | Genome edited cancer cell vaccines |
| BR112021009325A2 (pt) * | 2018-11-14 | 2021-09-14 | Arch Oncology, Inc. | Anticorpo monoclonal, ou fragmento de ligação ao antígeno do mesmo; anticorpo biespecífico; método para prevenir ou tratar um câncer suscetível em um ser humano; método de ensaio de expressão de sirp¿ em células tumorais e/ou imunes; e; composição farmacêutica |
| MX2021007043A (es) * | 2018-12-14 | 2021-08-11 | Boehringer Ingelheim Io Canada Inc | Anticuerpos antiperiostina y usos de estos. |
| CN109550047A (zh) * | 2019-01-16 | 2019-04-02 | 中国药科大学 | 抗cd47抗体在制备防治心力衰竭的药物中的应用 |
| US20220144943A1 (en) * | 2019-02-08 | 2022-05-12 | Integrity Bioventures, Inc. | Anti-cd47 antibodies and uses thereof |
| WO2020210719A1 (en) | 2019-04-10 | 2020-10-15 | Elevatebio Management, Inc. | Flt3-specific chimeric antigen receptors and methods of using the same |
| US10858442B2 (en) | 2019-04-18 | 2020-12-08 | Qlsf Biotherapeutics Inc. | Antibodies that target human CD47 |
| US20200400662A1 (en) | 2019-06-07 | 2020-12-24 | ALX Oncology Inc. | Methods and reagents for reducing the interference of drugs that bind cd47 in serological assays |
| KR20220024211A (ko) * | 2019-06-19 | 2022-03-03 | 레푸 바이오파마 컴퍼니 리미티드 | 항-cd47 항체 및 그것의 사용 |
| US11795210B2 (en) | 2019-07-16 | 2023-10-24 | Gilead Sciences, Inc. | HIV vaccines and methods of making and using |
| CN112239507A (zh) | 2019-07-17 | 2021-01-19 | 鸿运华宁（杭州）生物医药有限公司 | ETA抗体与TGF-β Trap的融合蛋白质，以及其药物组合物和应用 |
| WO2021043220A1 (zh) * | 2019-09-03 | 2021-03-11 | 中山康方生物医药有限公司 | 抗cd47的单克隆抗体及其用途 |
| WO2021046216A1 (en) * | 2019-09-03 | 2021-03-11 | Arch Oncology, Inc. | Methods for identifying biomarkers to predict treatment response |
| KR20220062500A (ko) * | 2019-09-16 | 2022-05-17 | 서피스 온콜로지, 인크. | 항-cd39 항체 조성물 및 방법 |
| US11795223B2 (en) | 2019-10-18 | 2023-10-24 | Forty Seven, Inc. | Combination therapies for treating myelodysplastic syndromes and acute myeloid leukemia |
| CN114901364A (zh) * | 2019-10-23 | 2022-08-12 | 安驰肿瘤公司 | 用于治疗实体癌和血液癌的组合疗法 |
| AU2020372522B2 (en) | 2019-10-25 | 2024-08-15 | WuXi Biologics Ireland Limited | Novel anti-CD47 antibodies and uses thereof |
| MX2022005123A (es) | 2019-10-31 | 2022-05-30 | Forty Seven Inc | Tratamiento basado en anti-cd47 y anti-cd20 para cancer hematologico. |
| PE20230160A1 (es) | 2019-12-17 | 2023-02-01 | Pfizer | Anticuerpos especificos para cd47, pd-l1 y sus usos |
| KR20220131918A (ko) | 2019-12-24 | 2022-09-29 | 카나 바이오사이언스, 인코포레이션 | 다이아실글리세롤 키나제 조절 화합물 |
| BR112022014623A2 (pt) | 2020-02-14 | 2022-09-13 | Jounce Therapeutics Inc | Anticorpos e proteínas de fusão que se ligam a ccr8 e usos dos mesmos |
| CN115427458A (zh) | 2020-02-28 | 2022-12-02 | 塔拉克治疗公司 | 转谷氨酰胺酶介导的缀合 |
| CA3169301A1 (en) * | 2020-03-18 | 2021-09-23 | Shyr Jiann Li | Anti-il4 receptor antibodies for veterinary use |
| US12091681B2 (en) | 2020-03-27 | 2024-09-17 | Mendus B.V. | Ex vivo use of modified cells of leukemic origin for enhancing the efficacy of adoptive cell therapy |
| AR121805A1 (es) * | 2020-04-10 | 2022-07-13 | Hutchison Medipharma Ltd | Anticuerpo anti-cd47 y usos del mismo |
| JP2023531678A (ja) | 2020-06-22 | 2023-07-25 | ザ ボード オブ トラスティーズ オブ ザ レランド スタンフォード ジュニア ユニバーシティー | 加齢筋肉、萎縮性筋肉、または異栄養性筋肉の処置のためのｔｓｐ－１阻害物質 |
| EP4171617A1 (en) | 2020-06-30 | 2023-05-03 | Mendus B.V. | Use of leukemia-derived cells in ovarian cancer vaccines |
| WO2022022662A1 (zh) * | 2020-07-31 | 2022-02-03 | 百奥泰生物制药股份有限公司 | Cd47抗体及其应用 |
| JP2023552375A (ja) | 2020-12-06 | 2023-12-15 | エーエルエックス オンコロジー インコーポレイテッド | 血清学的アッセイにおいてｃｄ４７に結合する薬物の干渉を低減するための多量体 |
| US20220305100A1 (en) | 2021-03-12 | 2022-09-29 | Dcprime B.V. | Methods of vaccination and use of cd47 blockade |
| US20240190993A1 (en) | 2021-04-14 | 2024-06-13 | INSERM (Institut National de la Santé et de la Recherche Médicale) | New method to improve the anti-tumoral activity of macrophages |
| TW202302145A (zh) | 2021-04-14 | 2023-01-16 | 美商基利科學股份有限公司 | ＣＤ４７／ＳＩＲＰα結合及ＮＥＤＤ８活化酶Ｅ１調節次單元之共抑制以用於治療癌症 |
| PE20242071A1 (es) | 2021-06-23 | 2024-10-18 | Gilead Sciences Inc | Compuestos moduladores de diacilglicerol quinasa |
| AU2022297367B2 (en) | 2021-06-23 | 2025-04-10 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
| CA3222439A1 (en) | 2021-06-23 | 2022-12-29 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
| US11976072B2 (en) | 2021-06-23 | 2024-05-07 | Gilead Sciences, Inc. | Diacylglycerol kinase modulating compounds |
| EP4362968A4 (en) * | 2021-06-30 | 2025-07-23 | Ohio State Innovation Foundation | METHODS AND COMPOSITIONS FOR INHIBITING DIHYDROOROTATE DEHYDROGENASE IN COMBINATION WITH AN ANTI-CD47-SIRPA THERAPEUTIC AGENT |
| US20240368279A1 (en) * | 2021-08-24 | 2024-11-07 | Shanghai Sinobay Biotechnology Co., Ltd. | Antibody Specifically Binding to CD47, Recombinant Oncolytic Virus Thereof and Use Thereof |
| JP2024539252A (ja) | 2021-10-28 | 2024-10-28 | ギリアード サイエンシーズ， インコーポレイテッド | ピリジジン－３（２ｈ）－オン誘導体 |
| PE20241186A1 (es) | 2021-10-29 | 2024-06-03 | Gilead Sciences Inc | Compuestos de cd73 |
| EP4452414A2 (en) | 2021-12-22 | 2024-10-30 | Gilead Sciences, Inc. | Ikaros zinc finger family degraders and uses thereof |
| US12122764B2 (en) | 2021-12-22 | 2024-10-22 | Gilead Sciences, Inc. | IKAROS zinc finger family degraders and uses thereof |
| TW202340168A (zh) | 2022-01-28 | 2023-10-16 | 美商基利科學股份有限公司 | Ｐａｒｐ７抑制劑 |
| US20250302953A1 (en) | 2022-02-14 | 2025-10-02 | Sana Biotechnology, Inc. | Methods of treating patients exhibiting a prior failed therapy with hypoimmunogenic cells |
| CA3253296A1 (en) | 2022-03-17 | 2023-09-21 | Gilead Sciences Inc | Zinc Finger Degradation Agents of the Ikaros Family and Their Uses |
| WO2023183313A1 (en) | 2022-03-22 | 2023-09-28 | Sana Biotechnology, Inc. | Engineering cells with a transgene in b2m or ciita locus and associated compositions and methods |
| CN119031937A (zh) | 2022-03-24 | 2024-11-26 | 吉利德科学公司 | 用于治疗表达Trop-2的癌症的联合疗法 |
| TWI876305B (zh) | 2022-04-05 | 2025-03-11 | 美商基利科學股份有限公司 | 用於治療結腸直腸癌之組合療法 |
| CR20240451A (es) | 2022-04-21 | 2024-12-04 | Gilead Sciences Inc | Compuestos de modulación de kras g12d |
| JP2025522762A (ja) | 2022-07-01 | 2025-07-17 | ギリアード サイエンシーズ， インコーポレイテッド | Ｃｄ７３化合物 |
| CA3259040A1 (en) | 2022-07-12 | 2024-01-18 | Gilead Sciences Inc | HIV Immunogenic Polypeptides and Vaccines and Their Uses |
| US20240091351A1 (en) | 2022-09-21 | 2024-03-21 | Gilead Sciences, Inc. | FOCAL IONIZING RADIATION AND CD47/SIRPa DISRUPTION ANTICANCER COMBINATION THERAPY |
| EP4638436A1 (en) | 2022-12-22 | 2025-10-29 | Gilead Sciences, Inc. | Prmt5 inhibitors and uses thereof |
| WO2024215754A1 (en) | 2023-04-11 | 2024-10-17 | Gilead Sciences, Inc. | Kras modulating compounds |
| AU2024259556A1 (en) | 2023-04-21 | 2025-10-23 | Gilead Sciences, Inc. | Prmt5 inhibitors and uses thereof |
| US20250042922A1 (en) | 2023-06-30 | 2025-02-06 | Gilead Sciences, Inc. | Kras modulating compounds |
| US20250066328A1 (en) | 2023-07-26 | 2025-02-27 | Gilead Sciences, Inc. | Parp7 inhibitors |
| TW202519517A (zh) | 2023-07-26 | 2025-05-16 | 美商基利科學股份有限公司 | Ｐａｒｐ７抑制劑 |
| WO2025054347A1 (en) | 2023-09-08 | 2025-03-13 | Gilead Sciences, Inc. | Kras g12d modulating compounds |
| WO2025054530A1 (en) | 2023-09-08 | 2025-03-13 | Gilead Sciences, Inc. | Pyrimidine-containing polycyclic derivatives as kras g12d modulating compounds |
| US20250154172A1 (en) | 2023-11-03 | 2025-05-15 | Gilead Sciences, Inc. | Prmt5 inhibitors and uses thereof |
| WO2025137640A1 (en) | 2023-12-22 | 2025-06-26 | Gilead Sciences, Inc. | Azaspiro wrn inhibitors |
| WO2025201450A1 (zh) * | 2024-03-27 | 2025-10-02 | 康方汇科(上海)生物有限公司 | 药物组合及用途 |
| US20250376484A1 (en) | 2024-05-21 | 2025-12-11 | Gilead Sciences, Inc. | Prmt5 inhibitors and uses thereof |
Family Cites Families (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE143052T1 (de) | 1986-07-07 | 1996-10-15 | Centocor Inc | Chimärisches murine-mensch-immunoglobulin, spezifisch für tumorassoziertes 17-1a antigen |
| US7531643B2 (en) | 1997-09-11 | 2009-05-12 | Chugai Seiyaku Kabushiki Kaisha | Monoclonal antibody inducing apoptosis |
| DE69839492D1 (de) | 1997-09-11 | 2008-06-26 | Chugai Pharmaceutical Co Ltd | Monoklonale antikörper zur apoptosis-induzierung |
| CA2226962A1 (en) | 1998-02-16 | 1999-08-16 | Marie Sarfati | Use of binding agents to cd47 and its ligands in the treatment or the prophylaxis of various inflammatory, autoimmune and allergic diseases and in the treatment of graft rejection |
| DE19813759C1 (de) | 1998-03-27 | 1999-07-15 | Gsf Forschungszentrum Umwelt | Verfahren zur Induktion einer durch NK-Zellen vermittelten Immunantwort |
| US7696325B2 (en) | 1999-03-10 | 2010-04-13 | Chugai Seiyaku Kabushiki Kaisha | Polypeptide inducing apoptosis |
| AU2940900A (en) * | 1999-03-10 | 2000-09-28 | Chugai Seiyaku Kabushiki Kaisha | Single-stranded fv inducing apoptosis |
| EP1109900A1 (en) | 1999-06-21 | 2001-06-27 | Inkine Pharmaceutical Company Inc. | Angiocidin: a cys-ser-val-thr-cys-gly specific tumor cell adhesion receptor |
| AU6698900A (en) | 1999-07-16 | 2001-02-05 | Agricultural Research Service | Live recombinant vaccine against avian leukosis virus using a marek's disease virus (mdv) virus as vector |
| US20010041670A1 (en) | 1999-12-06 | 2001-11-15 | Ronit Simantov | Thrombospondin-binding region of histidine-rich glycoprotein and method of use |
| AU2002315052A1 (en) * | 2001-05-15 | 2002-11-25 | Emory University | Polynucleotides and polypeptides relating to the modulation of sirp alpha-cd47 |
| JP2005520795A (ja) | 2001-12-12 | 2005-07-14 | コンフォーマ・セラピューティクス・コーポレイション | Ｈｓｐ９０阻害活性を有するプリン類似体 |
| US20040213792A1 (en) | 2003-04-24 | 2004-10-28 | Clemmons David R. | Method for inhibiting cellular activation by insulin-like growth factor-1 |
| CA2545166A1 (en) | 2003-11-11 | 2005-05-19 | Chugai Seiyaku Kabushiki Kaisha | Humanized anti-cd47 antibody |
| RU2007108716A (ru) | 2004-09-10 | 2008-10-20 | Вайет (Us) | Гуманизированные антитела к антигену 5т4 и конъюгаты гуманизированного антитела к антигену 5т4 с калихеамицином |
| JP2007008895A (ja) | 2005-07-04 | 2007-01-18 | Chugai Pharmaceut Co Ltd | 抗ｃｄ４７抗体とインテグリンリガンドとの併用 |
| US7514229B2 (en) | 2005-09-29 | 2009-04-07 | The Board Of Trustees Of The Leland Stanford Junior University | Methods for diagnosing and evaluating treatment of blood disorders |
| DK2368914T3 (en) | 2006-03-10 | 2019-03-04 | Wyeth Llc | Anti-5T4 antibodies and uses thereof |
| WO2008043072A2 (en) | 2006-10-05 | 2008-04-10 | Biogen Idec Inc. | Cd80 antagonists for treating neoplastic disorders |
| AU2007319576B2 (en) | 2006-10-06 | 2014-01-16 | The Government Of The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Prevention of tissue ischemia, related methods and compositions |
| CA2711938C (en) | 2008-01-15 | 2019-11-12 | The Board Of Trustees Of The Leland Stanford Junior University | Methods for manipulating phagocytosis mediated by cd47 |
| AU2014201010B2 (en) * | 2008-01-15 | 2016-03-03 | The Board Of Trustees Of The Leland Stanford Junior University | Methods for manipulating phagocytosis mediated by CD47 |
| ES2988620T3 (es) | 2008-01-15 | 2024-11-21 | The Board Of Trustees Of The Leland Stanfordjunior Univ | Marcadores de las células madre de la leucemia mieloide aguda |
| CA2715166C (en) | 2008-02-11 | 2017-05-16 | Curetech Ltd. | Monoclonal antibodies for tumor treatment |
| KR101604515B1 (ko) * | 2008-03-14 | 2016-03-17 | 알러간, 인코포레이티드 | 면역-기반 보툴리눔 독소 세로타입 ａ 활성 검정 |
| EP3031825B1 (en) * | 2008-03-14 | 2019-07-24 | Allergan, Inc. | Immuno-based botulinum toxin serotype a activity assays |
| EP2111869A1 (en) | 2008-04-23 | 2009-10-28 | Stichting Sanquin Bloedvoorziening | Compositions and methods to enhance the immune system |
| WO2010017332A2 (en) | 2008-08-07 | 2010-02-11 | The Government Of The United States Of America, As Represented By The Secretary Of The Department Of Health & Human Services | Radioprotectants targeting thrombospondin-1 and cd47 |
| ES2927646T3 (es) | 2009-09-15 | 2022-11-08 | Univ Leland Stanford Junior | Terapia anti-CD47 sinérgica para cánceres hematológicos |
| WO2011083141A2 (en) * | 2010-01-08 | 2011-07-14 | Ablynx Nv | Method for generation of immunoglobulin sequences by using lipoprotein particles |
| WO2011091286A1 (en) | 2010-01-21 | 2011-07-28 | Immunogen, Inc. | Compositions and methods for treatment of ovarian cancer |
| EP2569013B1 (en) | 2010-05-14 | 2016-11-23 | The Board of Trustees of the Leland Stanford Junior University | Humanized and chimeric monoclonal antibodies to cd47 |
| WO2012047427A2 (en) * | 2010-08-31 | 2012-04-12 | The Regents Of The University Of California | Antibodies for botulinum neurotoxins |
| US20140271683A1 (en) | 2010-12-21 | 2014-09-18 | The Board Of Trustees Of The Leland Stanford Junior University | Therapeutic and Diagnostic Methods for Manipulating Phagocytosis Through Calreticulin and Low Density Lipoprotein-Related Receptor |
| US20140140989A1 (en) | 2012-02-06 | 2014-05-22 | Inhibrx Llc | Non-Platelet Depleting and Non-Red Blood Cell Depleting CD47 Antibodies and Methods of Use Thereof |
| ES2743203T3 (es) * | 2012-02-06 | 2020-02-18 | Inhibrx Inc | Anticuerpos CD47 y métodos de uso de los mismos |
| SG10201704992SA (en) | 2012-06-21 | 2017-07-28 | Compugen Ltd | Lsr antibodies, and uses thereof for treatment of cancer |
| RU2019118257A (ru) * | 2012-12-03 | 2019-06-24 | Новиммун С.А. | Анти-cd47 антитела и способы их применения |
| US9221908B2 (en) | 2012-12-12 | 2015-12-29 | Vasculox, Inc. | Therapeutic CD47 antibodies |
| ES2786083T3 (es) | 2012-12-12 | 2020-10-08 | Arch Oncology Inc | Anticuerpos terapéuticos CD47 |
| EP4137518A1 (en) * | 2013-02-06 | 2023-02-22 | Inhibrx, Inc. | Non-platelet depleting and non-red blood cell depleting cd47 antibodies and methods of use thereof |
| DK2970493T3 (da) | 2013-03-15 | 2019-05-13 | Univ Leland Stanford Junior | Fremgangsmåder til opnåelse af terapeutisk effektive doser af anti-cd47-midler |
| CN103665165B (zh) * | 2013-08-28 | 2016-02-24 | 江苏匡亚生物医药科技有限公司 | 一种靶向人CD47-SIRPα信号通路的双特异性抗体及其制备方法和用途 |
| EP3089993A1 (en) | 2013-12-31 | 2016-11-09 | Development Center for Biotechnology | Anti-vegf antibodies and use thereof |
| BR112018005322A2 (pt) | 2015-09-18 | 2018-12-11 | Arch Oncology, Inc. | anticorpo monoclonal ou seu fragmento de ligação a antígenos, composição farmacêutica, anticorpo monoclonal ou seu fragmento de ligação a antígenos para uso, método de tratamento de lesão de isquemia-reperfusão, método de tratamento de câncer em um paciente humano, método de avaliação da expressão de cd47 em células tumorais e/ou imunes usando um anticorpo monoclonal ou seu fragmento de ligação a antígenos |
| US10946042B2 (en) | 2015-12-01 | 2021-03-16 | The Trustees Of The University Of Pennsylvania | Compositions and methods for selective phagocytosis of human cancer cells |
| WO2018075960A1 (en) | 2016-10-21 | 2018-04-26 | Tioma Therapeutics, Inc. | Therapeutic cd47 antibodies |
| SG11201908602UA (en) | 2017-03-22 | 2019-10-30 | Arch Oncology Inc | Combination therapy for the treatment of solid and hematological cancers |
| US20190309066A1 (en) | 2017-03-22 | 2019-10-10 | Arch Oncology, Inc. | Combination therapy for the treatment of solid and hematological cancers |
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2016
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- 2016-09-17 EP EP16847511.9A patent/EP3349787A4/en not_active Withdrawn
- 2016-09-17 CN CN202211086845.8A patent/CN116425875A/zh not_active Withdrawn
- 2016-09-17 CA CA2998644A patent/CA2998644A1/en not_active Withdrawn
- 2016-09-17 AU AU2016324316A patent/AU2016324316B2/en not_active Revoked
- 2016-09-17 MX MX2018003374A patent/MX2018003374A/es unknown
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- 2016-09-17 NZ NZ740686A patent/NZ740686A/en not_active IP Right Cessation
- 2016-09-17 CN CN201680062144.7A patent/CN108348589B/zh not_active Withdrawn - After Issue
- 2016-09-17 WO PCT/US2016/052383 patent/WO2017049251A2/en not_active Ceased
- 2016-09-17 UA UAA201808714A patent/UA126146C2/uk unknown
- 2016-09-17 RU RU2018124859A patent/RU2748401C2/ru active
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2017
- 2017-11-21 US US15/820,054 patent/US10239945B2/en active Active
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2018
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- 2018-06-27 ZA ZA2018/04326A patent/ZA201804326B/en unknown
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| JP6885606B2 (ja) | 2021-06-16 |
| US10239945B2 (en) | 2019-03-26 |
| CN108348589B (zh) | 2022-09-23 |
| RU2018124859A (ru) | 2020-01-14 |
| MX2018003374A (es) | 2018-11-09 |
| PH12018500515A1 (en) | 2018-08-29 |
| RU2748401C2 (ru) | 2021-05-25 |
| IL258168A (en) | 2018-05-31 |
| EP3349787A2 (en) | 2018-07-25 |
| AU2016324316A1 (en) | 2018-04-05 |
| WO2017049251A2 (en) | 2017-03-23 |
| US20210070865A1 (en) | 2021-03-11 |
| BR112018005322A2 (pt) | 2018-12-11 |
| US10844124B2 (en) | 2020-11-24 |
| NZ740686A (en) | 2021-12-24 |
| JP2018536624A (ja) | 2018-12-13 |
| RU2018124859A3 (enExample) | 2020-06-05 |
| US20190300611A1 (en) | 2019-10-03 |
| CN116425875A (zh) | 2023-07-14 |
| AU2016324316B2 (en) | 2023-02-09 |
| WO2017049251A3 (en) | 2017-04-20 |
| EP3349787A4 (en) | 2019-03-27 |
| CN108348589A (zh) | 2018-07-31 |
| ZA201804326B (en) | 2019-09-25 |
| UA126146C2 (uk) | 2022-08-25 |
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