AU2014238105B2 - Methods for achieving therapeutically effective doses of anti-CD47 agents - Google Patents
Methods for achieving therapeutically effective doses of anti-CD47 agents Download PDFInfo
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- AU2014238105B2 AU2014238105B2 AU2014238105A AU2014238105A AU2014238105B2 AU 2014238105 B2 AU2014238105 B2 AU 2014238105B2 AU 2014238105 A AU2014238105 A AU 2014238105A AU 2014238105 A AU2014238105 A AU 2014238105A AU 2014238105 B2 AU2014238105 B2 AU 2014238105B2
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3722317B1 (en) * | 2008-01-15 | 2024-08-07 | The Board of Trustees of the Leland Stanford Junior University | Markers of acute myeloid leukemia stem cells |
| JP5547656B2 (ja) | 2008-01-15 | 2014-07-16 | 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 | Ｃｄ４７によって媒介される食作用を操作するための方法 |
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| US9221908B2 (en) | 2012-12-12 | 2015-12-29 | Vasculox, Inc. | Therapeutic CD47 antibodies |
| HK1216647A1 (zh) | 2012-12-12 | 2016-11-25 | Vasculox Inc. | 治疗性cd47抗体 |
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| ES2901501T3 (es) * | 2015-01-21 | 2022-03-22 | Univ Leland Stanford Junior | Uso de agonistas de TLR y agente anti-CD47 para mejorar la fagocitosis de las células cancerosas |
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| CN108348589B (zh) | 2015-09-18 | 2022-09-23 | 安驰肿瘤公司 | 治疗性cd47抗体 |
| CA2999277A1 (en) | 2015-09-21 | 2017-03-30 | Surface Oncology, Inc. | Anti-cd47 antibodies and methods of use |
| US10344094B2 (en) | 2015-12-11 | 2019-07-09 | The Board Of Trustees Of The Leland Stanford Junior University | Treatment of cancer with dual targeting of CD47 and EGFR |
| KR102833922B1 (ko) * | 2016-01-21 | 2025-07-15 | 더 보드 어브 트러스티스 어브 더 리랜드 스탠포드 주니어 유니버시티 | 면역조절제의 조합물에 의한 암의 치료 |
| CN117695387A (zh) * | 2016-04-15 | 2024-03-15 | 小利兰·斯坦福大学托管委员会 | 用于确定和实现抗cd47药剂治疗癌症的治疗有效剂量的方法 |
| US9957576B2 (en) | 2016-04-21 | 2018-05-01 | The Board Of Trustees Of The Leland Stanford Junior University | Methods for determining responsiveness to an anti-CD47 agent |
| PL3448421T3 (pl) | 2016-04-29 | 2022-03-28 | The Board Of Trustees Of The Leland Stanford Junior University | Sposoby i kompozycje do zapobiegania i leczenia zrostów chirurgicznych |
| EP3487522A4 (en) | 2016-07-19 | 2020-04-01 | Teva Pharmaceuticals Australia Pty Ltd | Anti-cd47 combination therapy |
| JOP20190009A1 (ar) | 2016-09-21 | 2019-01-27 | Alx Oncology Inc | أجسام مضادة ضد بروتين ألفا منظم للإشارات وطرق استخدامها |
| EP3529276A4 (en) | 2016-10-21 | 2020-06-17 | Arch Oncology, Inc. | CD47 THERAPEUTIC ANTIBODIES |
| EP3532497B1 (en) * | 2016-10-26 | 2024-07-24 | The Board of Trustees of the Leland Stanford Junior University | Modified immunoglobulin hinge regions to reduce hemagglutination |
| US11779631B2 (en) | 2016-11-03 | 2023-10-10 | Pfizer Inc. | CD47 blockade therapy by HDAC inhibitors |
| WO2018160739A1 (en) | 2017-02-28 | 2018-09-07 | The Board Of Trustees Of The Leland Stanford Junior University | Antifibrotic activity of cd47 blockade |
| WO2018165015A1 (en) | 2017-03-09 | 2018-09-13 | The Board Of Trustees Of The Leland Stanford Junior University | Treatment of pediatric brain tumors with targeting of cd47 pathway |
| PT3642242T (pt) | 2017-06-21 | 2024-04-16 | Univ Leland Stanford Junior | Parâmetros de dosagem para terapias de direcionamento de cd47 para malignidades hematológicas |
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| EP4194470A1 (en) | 2017-10-18 | 2023-06-14 | Forty Seven, Inc. | Treatment of ovarian cancer with anti-cd47 and anti-pd-l1 |
| MA51208A (fr) | 2017-12-01 | 2020-10-07 | Seattle Genetics Inc | Anticorps (masqués) contre cd47 et leurs utilisations pour le traîtement du cancer |
| US11891450B2 (en) * | 2018-02-12 | 2024-02-06 | Forty Seven, Inc. | Anti-CD47 agent-based treatment of CD20-positive cancer |
| CN118344481A (zh) | 2018-03-21 | 2024-07-16 | Alx肿瘤生物技术公司 | 针对信号调控蛋白α的抗体和使用方法 |
| JP7266670B2 (ja) | 2018-09-27 | 2023-04-28 | セルジーン コーポレイション | ＳＩＲＰα結合タンパク質及びその使用方法 |
| US11591390B2 (en) | 2018-09-27 | 2023-02-28 | Celgene Corporation | SIRP-α binding proteins and methods of use thereof |
| US20220119523A1 (en) * | 2019-02-08 | 2022-04-21 | The Board Of Trustees Of The Leland Stanford Junior University | Treatment of cutaneous t cell lymphoma with targeting of cd47 pathway |
| EP3976658A4 (en) * | 2019-05-24 | 2023-06-07 | Forty Seven, Inc. | Regimes for co-administration of immunotherapeutic agents against c-kit and cd47 |
| AU2020282791A1 (en) | 2019-05-31 | 2021-12-09 | ALX Oncology Inc. | Methods of treating cancer with SIRP alpha Fc fusion in combination with an immune checkpoint inhibitor |
| WO2020247820A1 (en) * | 2019-06-07 | 2020-12-10 | ALX Oncology Inc. | Methods and reagents for reducing the interference of drugs that bind cd47 in serological assays |
| PL4045083T3 (pl) | 2019-10-18 | 2024-05-13 | Forty Seven, Inc. | Terapie skojarzone do leczenia zespołów mielodysplastycznych i ostrej białaczki szpikowej |
| US11702474B2 (en) | 2019-12-17 | 2023-07-18 | Pfizer Inc. | Antibodies specific for CD47, PD-L1, and uses thereof |
| IL301972A (en) * | 2020-10-09 | 2023-06-01 | Sana Biotechnology Inc | Methods for activating safe killing mechanisms using the CD47–SIRPα blocking factor |
| WO2022130016A1 (en) | 2020-12-18 | 2022-06-23 | Instil Bio (Uk) Limited | Tumor infiltrating lymphocytes and anti-cd47 therapeutics |
| US12098214B2 (en) | 2021-05-13 | 2024-09-24 | ALX Oncology Inc. | Combination therapies for treating cancer |
| EP4376856A1 (en) * | 2021-07-28 | 2024-06-05 | Actinium Pharmaceuticals, Inc. | Combination radioimmunotherapy and cd47 blockade in the treatment of cancer |
| US12234294B2 (en) | 2021-11-05 | 2025-02-25 | Kiniksa Pharmaceuticals, Gmbh | Pharmaceutical composition of a humanized anti-CD40 antibody |
| EP4670792A2 (en) | 2021-11-19 | 2025-12-31 | KIST (Korea Institute of Science and Technology) | THERAPEUTIC COMPOUNDS FOR RED BLOOD CELL MEDIATED ADMINISTRATION OF AN ACTIVE PHARMACEUTICAL TO A TARGET CELL |
| WO2023133577A1 (en) * | 2022-01-10 | 2023-07-13 | Kiniksa Pharmaceuticals, Ltd. | Methods of treating or reducing risk of transplant rejection |
| US20250302953A1 (en) | 2022-02-14 | 2025-10-02 | Sana Biotechnology, Inc. | Methods of treating patients exhibiting a prior failed therapy with hypoimmunogenic cells |
| 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 |
| CN120202222A (zh) | 2022-11-16 | 2025-06-24 | 勃林格殷格翰国际有限公司 | 抗SIRPa抗体的疗效预测性生物标志物 |
| CN120344257A (zh) | 2022-12-09 | 2025-07-18 | 美国辉瑞有限公司 | Cd47阻断剂和抗cd20/抗cd3双特异性抗体组合疗法 |
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Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009091601A1 (en) * | 2008-01-15 | 2009-07-23 | The Board Of Trustees Of The Leland Stanford Junior University | Methods for manipulating phagocytosis mediated by cd47 |
| US20120282174A1 (en) * | 2009-09-15 | 2012-11-08 | Weissman Irving L | Synergistic Anti-CD47 Therapy for Hematologic Cancers |
| WO2013109752A1 (en) * | 2012-01-17 | 2013-07-25 | The Board Of Trustees Of The Leland Stanford Junior University | High affinity sirp-alpha reagents |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20020052309A1 (en) * | 1996-09-11 | 2002-05-02 | Athanasius A. Anagnostou | Method of treating endothelial injury |
| WO2002092784A2 (en) * | 2001-05-15 | 2002-11-21 | Emory University | POLYNUCLEOTIDES AND POLYPEPTIDES RELATING TO THE MODULATION OF SIRP α-CD47 |
| US20040213792A1 (en) | 2003-04-24 | 2004-10-28 | Clemmons David R. | Method for inhibiting cellular activation by insulin-like growth factor-1 |
| US20070113297A1 (en) * | 2005-09-13 | 2007-05-17 | Yongguang Yang | Methods and compositions for inhibition of immune responses |
| US8377448B2 (en) | 2006-05-15 | 2013-02-19 | The Board Of Trustees Of The Leland Standford Junior University | CD47 related compositions and methods for treating immunological diseases and disorders |
| EP2388270A3 (en) * | 2007-10-11 | 2012-04-25 | The Hospital For Sick Children | Modulation of SIRPa - CD47 interaction for increasing human hematopoietic stem cell engraftment and compounds therefor |
| CN101456911A (zh) * | 2007-12-12 | 2009-06-17 | 江苏豪森药业股份有限公司 | 促红细胞生成素模拟肽衍生物及其可药用盐和其制备方法与用途 |
| EP3722317B1 (en) | 2008-01-15 | 2024-08-07 | The Board of Trustees of the Leland Stanford Junior University | Markers of acute myeloid leukemia stem cells |
| EP2111869A1 (en) | 2008-04-23 | 2009-10-28 | Stichting Sanquin Bloedvoorziening | Compositions and methods to enhance the immune system |
| WO2011041453A1 (en) * | 2009-09-29 | 2011-04-07 | The Board Of Trustees Of The Leland Stanford Junior University | Isolation and use of melanoma cancer stem cells |
| DK2569013T3 (da) | 2010-05-14 | 2017-02-13 | Univ Leland Stanford Junior | Humaniserede og kimære monoklonale antistoffer til cd47 |
| EP2812443B1 (en) * | 2012-02-06 | 2019-05-29 | Inhibrx, Inc. | Cd47 antibodies and methods of use thereof |
| 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 |
| SG11201408646VA (en) | 2012-07-06 | 2015-01-29 | Genmab Bv | Dimeric protein with triple mutations |
| EA036963B1 (ru) * | 2013-02-06 | 2021-01-20 | Инхибркс, Инк. | Применение эпитопа cd47 для получения антитела к cd47 |
| AU2014238105B2 (en) | 2013-03-15 | 2018-11-15 | The Board Of Trustees Of The Leland Stanford Junior University | Methods for achieving therapeutically effective doses of anti-CD47 agents |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009091601A1 (en) * | 2008-01-15 | 2009-07-23 | The Board Of Trustees Of The Leland Stanford Junior University | Methods for manipulating phagocytosis mediated by cd47 |
| US20120282174A1 (en) * | 2009-09-15 | 2012-11-08 | Weissman Irving L | Synergistic Anti-CD47 Therapy for Hematologic Cancers |
| WO2013109752A1 (en) * | 2012-01-17 | 2013-07-25 | The Board Of Trustees Of The Leland Stanford Junior University | High affinity sirp-alpha reagents |
Non-Patent Citations (1)
| Title |
|---|
| WILLINGHAM S.B. et al., "The CD47-signal regulatory protein alpha (SIRPa) interactions a therapeutic target for human solid tumors", Proceedings of the National Academy of Sciences, 2012, Vol. 109, No. 17, pages 6662-6667 * |
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