WO2024105180A1 - Biomarqueurs d'efficacité prédictive pour anticorps anti-sirpa - Google Patents
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2803—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
- C07K2317/565—Complementarity determining region [CDR]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Genetics & Genomics (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Peptides Or Proteins (AREA)
Abstract
L'application concerne de manière générale le traitement du cancer chez des patients qui présentent des cellules immunitaires, en particulier des cellules myéloïdes, par exemple des macrophages associés à une tumeur, des monocytes, des cellules dendritiques myéloïdes, des MDSC et/ou une tumeur associant des neutrophiles, qui expriment les marqueurs biologiques CD11b et SIRPα dans le microenvironnement d'une tumeur. Ces patients ont été identifiés comme étant les sujets répondant le mieux à des thérapies qui comprennent l'administration d'un anticorps antagoniste anti-SIRPα.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP22306687.9 | 2022-11-16 | ||
EP22306687 | 2022-11-16 |
Publications (1)
Publication Number | Publication Date |
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WO2024105180A1 true WO2024105180A1 (fr) | 2024-05-23 |
Family
ID=84370637
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/EP2023/082095 WO2024105180A1 (fr) | 2022-11-16 | 2023-11-16 | Biomarqueurs d'efficacité prédictive pour anticorps anti-sirpa |
Country Status (1)
Country | Link |
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WO (1) | WO2024105180A1 (fr) |
Citations (53)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997048723A2 (fr) | 1996-06-17 | 1997-12-24 | MAX-PLANCK-GESELLSCHAFT ZUR FÖRDERUNG DER WISSENSCHAFTEN E.V. Hofgartenstrasse 2 | Nouvelles proteines ptp20, pcp-2, bdp1, clk et sirp, produits et procedes connexes |
WO2000066159A1 (fr) | 1999-04-28 | 2000-11-09 | Faculteit Der Geneeskunde Van De Vrije Universiteit | Methode d'inhibition du fonctionnement des cellules s'utilisant dans des therapies anti-inflammatoires et anti-tumorales |
WO2001040307A1 (fr) | 1999-11-30 | 2001-06-07 | Eberhard-Karls-Universität Tübingen Universitätsklinikum | Anticorps diriges contre les proteines regulatrices de signal |
WO2006121168A1 (fr) | 2005-05-09 | 2006-11-16 | Ono Pharmaceutical Co., Ltd. | Anticorps monoclonaux humains pour mort programmee 1 (mp-1) et procedes pour traiter le cancer en utilisant des anticorps anti-mp-1 seuls ou associes a d’autres immunotherapies |
WO2009131453A1 (fr) | 2008-04-23 | 2009-10-29 | Stichting Sanquin Bloedvoorziening | Compositions et procédés pour renforcer le système immunitaire |
WO2013056352A1 (fr) | 2011-10-19 | 2013-04-25 | University Health Network | Anticorps et fragments d'anticorps ciblant sirp-alpha et leur utilisation pour le traitement de cancers hématologiques |
WO2014149477A1 (fr) | 2013-03-15 | 2014-09-25 | The Board Of Trustees Of The Leland Stanford Junior University | Procédés d'obtention de doses thérapeutiquement efficaces d'agents anti-cd47 |
WO2014186761A2 (fr) | 2013-05-17 | 2014-11-20 | The Board Of Trustes Of The Leland Stanford Junior University | Procédés pour déterminer la réactivité à un agent anti-cd47 |
WO2014194302A2 (fr) | 2013-05-31 | 2014-12-04 | Sorrento Therapeutics, Inc. | Protéines de liaison à l'antigène qui se lient à pd-1 |
WO2015138600A2 (fr) | 2014-03-11 | 2015-09-17 | The Board Of Trustees Of The Leland Stanford Junior University | Anticorps anti-sirp-alpha et anticorps bispécifiques de stimulation des macrophages |
WO2016063233A1 (fr) | 2014-10-24 | 2016-04-28 | Effimune | Procédé et compositions permettant l'induction d'une différenciation des cellules myéloïdes suppressives pour traiter le cancer et les maladies infectieuses |
WO2016205042A1 (fr) | 2015-06-16 | 2016-12-22 | The Board Of Trustees Of The Leland Stanford Junior University | Anticorps agonistes de sirpα |
WO2017019846A1 (fr) | 2015-07-30 | 2017-02-02 | Macrogenics, Inc. | Molécules se liant à pd-1 et méthodes d'utilisation correspondantes |
WO2017025016A1 (fr) | 2015-08-10 | 2017-02-16 | Innovent Biologics (Suzhou) Co., Ltd. | Anticorps anti-pd-1 |
WO2017040790A1 (fr) | 2015-09-01 | 2017-03-09 | Agenus Inc. | Anticorps anti-pd1 et méthodes d'utilisation de ceux-ci |
WO2017132825A1 (fr) | 2016-02-02 | 2017-08-10 | 华为技术有限公司 | Procédé de vérification de puissance d'émission, équipement utilisateur et station de base |
WO2017133540A1 (fr) | 2016-02-02 | 2017-08-10 | Innovent Biologics (Suzhou) Co., Ltd. | Anticorps anti-pd-1 |
WO2017178653A2 (fr) | 2016-04-14 | 2017-10-19 | Ose Immunotherapeutics | Nouveaux anticorps anti-sirpa et leurs applications thérapeutiques |
WO2018008470A1 (fr) | 2016-07-05 | 2018-01-11 | 国立大学法人神戸大学 | Agent antitumoral |
WO2018026600A1 (fr) | 2016-08-03 | 2018-02-08 | The Board Of Trustees Of The Leland Stanford Junior University | L'interruption de l'engagement du récepteur fc sur les macrophages améliore l'efficacité de la thérapie par anticorps anti-sirpalpha |
WO2018057669A1 (fr) | 2016-09-21 | 2018-03-29 | Alexo Therapeutics Inc. | Anticorps contre la protéine régulatrice de signal alpha et procédés d'utilisation |
WO2018107058A1 (fr) | 2016-12-09 | 2018-06-14 | Alector Llc | Anticorps anti-sirp-alpha et leurs procédés d'utilisation |
WO2018141964A1 (fr) | 2017-02-06 | 2018-08-09 | Orionis Biosciences Nv | Protéines chimériques ciblées et leurs utilisations |
WO2018160739A1 (fr) | 2017-02-28 | 2018-09-07 | The Board Of Trustees Of The Leland Stanford Junior University | Activité antifibrotique du blocage de cd47 |
WO2018190719A2 (fr) | 2017-04-13 | 2018-10-18 | Aduro Biotech Holdings, Europe B.V. | Anticorps anti-sirp alpha |
WO2018210793A2 (fr) | 2017-05-16 | 2018-11-22 | Synthon Biopharmaceuticals B.V. | ANTICORPS ANTI-SIRPα |
WO2019023347A1 (fr) | 2017-07-26 | 2019-01-31 | Forty Seven, Inc. | Anticorps anti-sirp-alpha et méthodes associées |
WO2019073080A1 (fr) * | 2017-10-13 | 2019-04-18 | Ose Immunotherapeutics | Anticorps anti-sirpa modifiés et leurs utilisations |
WO2019183266A1 (fr) | 2018-03-21 | 2019-09-26 | ALX Oncology Inc. | Anticorps contre la protéine régulatrice de signal alpha et procédés d'utilisation |
WO2019200462A1 (fr) | 2018-04-16 | 2019-10-24 | Adaerata, Limited Partnership | Méthodes de prévention ou de traitement de cancers positifs pour slamf7 et négatifs pour slamf7 |
WO2019226973A1 (fr) | 2018-05-25 | 2019-11-28 | Alector Llc | Anticorps anti-sirpa et leurs procédés d'utilisation |
WO2020006374A2 (fr) | 2018-06-29 | 2020-01-02 | Alector Llc | Anticorps anti-sirp-bêta1 et procédés d'utilisation associés |
WO2020013170A1 (fr) | 2018-07-10 | 2020-01-16 | 国立大学法人神戸大学 | ANTIBODY ANTI-SIRPα |
WO2020033646A1 (fr) | 2018-08-08 | 2020-02-13 | Orionis Biosciences, Inc. | PROTÉINES CHIMÈRES CIBLÉES SUR SIRP1α ET LEURS UTILISATIONS |
WO2020068752A1 (fr) | 2018-09-27 | 2020-04-02 | Celgene Corporation | PROTÉINES DE LIAISON SIRPα ET MÉTHODES D'UTILISATION DE CELLES-CI |
WO2020099653A1 (fr) | 2018-11-15 | 2020-05-22 | Byondis B.V. | ANTICORPS ANTI-SIRPα HUMANISÉS |
WO2020102422A1 (fr) | 2018-11-14 | 2020-05-22 | Arch Oncology, Inc. | ANTICORPS SIRPα THÉRAPEUTIQUES |
WO2020107115A1 (fr) | 2018-11-29 | 2020-06-04 | Trillium Therapeutics Inc. | Biomarqueurs pour une thérapie de blocage de cd47 |
CN111635458A (zh) | 2020-03-20 | 2020-09-08 | 上海健信生物医药科技有限公司 | 靶向Sirpα的抗体或其抗原结合片段及其制备和应用 |
WO2020180811A1 (fr) | 2019-03-04 | 2020-09-10 | Qilu Puget Sound Biotherapeutics Corporation | ANTICORPS ANTI-SIRPα |
CN111995682A (zh) | 2020-08-21 | 2020-11-27 | 博奥信生物技术(南京)有限公司 | 抗人SIRPα单克隆抗体及其用途 |
CN112010979A (zh) | 2020-08-21 | 2020-12-01 | 博奥信生物技术(南京)有限公司 | 一种抗人SIRPα单克隆抗体及其用途 |
WO2020247820A1 (fr) | 2019-06-07 | 2020-12-10 | ALX Oncology Inc. | Procédés et réactifs pour réduire les interférences de médicaments se liant au cd47 dans des dosages sérologiques |
WO2021022044A1 (fr) | 2019-07-31 | 2021-02-04 | Forty Seven, Inc. | Régimes d'appauvrissement pour une thérapie à lymphocytes t ou à cellules nk modifiés |
WO2021032078A1 (fr) | 2019-08-20 | 2021-02-25 | Elpiscience (Suzhou) Biopharma, Ltd. | Nouveaux anticorps anti-sirpa |
CN112574310A (zh) | 2020-12-11 | 2021-03-30 | 浙江博锐生物制药有限公司 | 抗SIRPα抗体及其用途 |
WO2021076908A1 (fr) | 2019-10-18 | 2021-04-22 | Forty Seven, Inc. | Polythérapies pour le traitement de syndromes myélodysplasiques et de la leucémie myéloïde aiguë |
WO2021129697A1 (fr) | 2019-12-24 | 2021-07-01 | Lanova Medicines Limited Company | ANTICORPS MONOCLONAUX ANTI-SIRPα ET LEURS UTILISATIONS |
WO2021174127A1 (fr) | 2020-02-28 | 2021-09-02 | Apexigen, Inc. | Anticorps anti-sirpa et méthodes d'utilisation |
WO2021222746A2 (fr) | 2020-04-30 | 2021-11-04 | Arch Oncology, Inc. | ANTICORPS SIRPα THÉRAPEUTIQUES |
WO2021226591A1 (fr) | 2020-05-08 | 2021-11-11 | Electra Therapeutics, Inc. | Anticorps dirigés contre sirp alpha, sirp bêta 1, et sirp gamma et leurs utilisations |
CN113735973A (zh) | 2020-05-28 | 2021-12-03 | 中国科学院微生物研究所 | 一种抗SIRPα抗体及其应用 |
WO2022254379A1 (fr) | 2021-06-04 | 2022-12-08 | Boehringer Ingelheim International Gmbh | Anticorps anti-sirp-alpha |
-
2023
- 2023-11-16 WO PCT/EP2023/082095 patent/WO2024105180A1/fr unknown
Patent Citations (58)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997048723A2 (fr) | 1996-06-17 | 1997-12-24 | MAX-PLANCK-GESELLSCHAFT ZUR FÖRDERUNG DER WISSENSCHAFTEN E.V. Hofgartenstrasse 2 | Nouvelles proteines ptp20, pcp-2, bdp1, clk et sirp, produits et procedes connexes |
WO2000066159A1 (fr) | 1999-04-28 | 2000-11-09 | Faculteit Der Geneeskunde Van De Vrije Universiteit | Methode d'inhibition du fonctionnement des cellules s'utilisant dans des therapies anti-inflammatoires et anti-tumorales |
WO2001040307A1 (fr) | 1999-11-30 | 2001-06-07 | Eberhard-Karls-Universität Tübingen Universitätsklinikum | Anticorps diriges contre les proteines regulatrices de signal |
WO2006121168A1 (fr) | 2005-05-09 | 2006-11-16 | Ono Pharmaceutical Co., Ltd. | Anticorps monoclonaux humains pour mort programmee 1 (mp-1) et procedes pour traiter le cancer en utilisant des anticorps anti-mp-1 seuls ou associes a d’autres immunotherapies |
WO2009131453A1 (fr) | 2008-04-23 | 2009-10-29 | Stichting Sanquin Bloedvoorziening | Compositions et procédés pour renforcer le système immunitaire |
WO2013056352A1 (fr) | 2011-10-19 | 2013-04-25 | University Health Network | Anticorps et fragments d'anticorps ciblant sirp-alpha et leur utilisation pour le traitement de cancers hématologiques |
WO2014149477A1 (fr) | 2013-03-15 | 2014-09-25 | The Board Of Trustees Of The Leland Stanford Junior University | Procédés d'obtention de doses thérapeutiquement efficaces d'agents anti-cd47 |
WO2014186761A2 (fr) | 2013-05-17 | 2014-11-20 | The Board Of Trustes Of The Leland Stanford Junior University | Procédés pour déterminer la réactivité à un agent anti-cd47 |
WO2014194302A2 (fr) | 2013-05-31 | 2014-12-04 | Sorrento Therapeutics, Inc. | Protéines de liaison à l'antigène qui se lient à pd-1 |
WO2015138600A2 (fr) | 2014-03-11 | 2015-09-17 | The Board Of Trustees Of The Leland Stanford Junior University | Anticorps anti-sirp-alpha et anticorps bispécifiques de stimulation des macrophages |
WO2016063233A1 (fr) | 2014-10-24 | 2016-04-28 | Effimune | Procédé et compositions permettant l'induction d'une différenciation des cellules myéloïdes suppressives pour traiter le cancer et les maladies infectieuses |
WO2016205042A1 (fr) | 2015-06-16 | 2016-12-22 | The Board Of Trustees Of The Leland Stanford Junior University | Anticorps agonistes de sirpα |
WO2017019846A1 (fr) | 2015-07-30 | 2017-02-02 | Macrogenics, Inc. | Molécules se liant à pd-1 et méthodes d'utilisation correspondantes |
WO2017024465A1 (fr) | 2015-08-10 | 2017-02-16 | Innovent Biologics (Suzhou) Co., Ltd. | Anticorps anti-pd-1 |
WO2017025016A1 (fr) | 2015-08-10 | 2017-02-16 | Innovent Biologics (Suzhou) Co., Ltd. | Anticorps anti-pd-1 |
WO2017040790A1 (fr) | 2015-09-01 | 2017-03-09 | Agenus Inc. | Anticorps anti-pd1 et méthodes d'utilisation de ceux-ci |
WO2017132825A1 (fr) | 2016-02-02 | 2017-08-10 | 华为技术有限公司 | Procédé de vérification de puissance d'émission, équipement utilisateur et station de base |
WO2017133540A1 (fr) | 2016-02-02 | 2017-08-10 | Innovent Biologics (Suzhou) Co., Ltd. | Anticorps anti-pd-1 |
WO2017178653A2 (fr) | 2016-04-14 | 2017-10-19 | Ose Immunotherapeutics | Nouveaux anticorps anti-sirpa et leurs applications thérapeutiques |
WO2018008470A1 (fr) | 2016-07-05 | 2018-01-11 | 国立大学法人神戸大学 | Agent antitumoral |
WO2018026600A1 (fr) | 2016-08-03 | 2018-02-08 | The Board Of Trustees Of The Leland Stanford Junior University | L'interruption de l'engagement du récepteur fc sur les macrophages améliore l'efficacité de la thérapie par anticorps anti-sirpalpha |
WO2018057669A1 (fr) | 2016-09-21 | 2018-03-29 | Alexo Therapeutics Inc. | Anticorps contre la protéine régulatrice de signal alpha et procédés d'utilisation |
WO2018107058A1 (fr) | 2016-12-09 | 2018-06-14 | Alector Llc | Anticorps anti-sirp-alpha et leurs procédés d'utilisation |
US20190275150A1 (en) * | 2016-12-09 | 2019-09-12 | Alector Llc | Anti-SIRP-Alpha Antibodies and Methods of Use Thereof |
WO2018141964A1 (fr) | 2017-02-06 | 2018-08-09 | Orionis Biosciences Nv | Protéines chimériques ciblées et leurs utilisations |
WO2018160739A1 (fr) | 2017-02-28 | 2018-09-07 | The Board Of Trustees Of The Leland Stanford Junior University | Activité antifibrotique du blocage de cd47 |
WO2018190719A2 (fr) | 2017-04-13 | 2018-10-18 | Aduro Biotech Holdings, Europe B.V. | Anticorps anti-sirp alpha |
WO2018210793A2 (fr) | 2017-05-16 | 2018-11-22 | Synthon Biopharmaceuticals B.V. | ANTICORPS ANTI-SIRPα |
WO2019023347A1 (fr) | 2017-07-26 | 2019-01-31 | Forty Seven, Inc. | Anticorps anti-sirp-alpha et méthodes associées |
WO2019073080A1 (fr) * | 2017-10-13 | 2019-04-18 | Ose Immunotherapeutics | Anticorps anti-sirpa modifiés et leurs utilisations |
WO2019183266A1 (fr) | 2018-03-21 | 2019-09-26 | ALX Oncology Inc. | Anticorps contre la protéine régulatrice de signal alpha et procédés d'utilisation |
WO2019200462A1 (fr) | 2018-04-16 | 2019-10-24 | Adaerata, Limited Partnership | Méthodes de prévention ou de traitement de cancers positifs pour slamf7 et négatifs pour slamf7 |
WO2019226973A1 (fr) | 2018-05-25 | 2019-11-28 | Alector Llc | Anticorps anti-sirpa et leurs procédés d'utilisation |
WO2020006374A2 (fr) | 2018-06-29 | 2020-01-02 | Alector Llc | Anticorps anti-sirp-bêta1 et procédés d'utilisation associés |
WO2020013170A1 (fr) | 2018-07-10 | 2020-01-16 | 国立大学法人神戸大学 | ANTIBODY ANTI-SIRPα |
WO2020033646A1 (fr) | 2018-08-08 | 2020-02-13 | Orionis Biosciences, Inc. | PROTÉINES CHIMÈRES CIBLÉES SUR SIRP1α ET LEURS UTILISATIONS |
WO2020068752A1 (fr) | 2018-09-27 | 2020-04-02 | Celgene Corporation | PROTÉINES DE LIAISON SIRPα ET MÉTHODES D'UTILISATION DE CELLES-CI |
WO2020102422A1 (fr) | 2018-11-14 | 2020-05-22 | Arch Oncology, Inc. | ANTICORPS SIRPα THÉRAPEUTIQUES |
WO2020099653A1 (fr) | 2018-11-15 | 2020-05-22 | Byondis B.V. | ANTICORPS ANTI-SIRPα HUMANISÉS |
WO2020107115A1 (fr) | 2018-11-29 | 2020-06-04 | Trillium Therapeutics Inc. | Biomarqueurs pour une thérapie de blocage de cd47 |
WO2020180811A1 (fr) | 2019-03-04 | 2020-09-10 | Qilu Puget Sound Biotherapeutics Corporation | ANTICORPS ANTI-SIRPα |
WO2020247820A1 (fr) | 2019-06-07 | 2020-12-10 | ALX Oncology Inc. | Procédés et réactifs pour réduire les interférences de médicaments se liant au cd47 dans des dosages sérologiques |
WO2021022044A1 (fr) | 2019-07-31 | 2021-02-04 | Forty Seven, Inc. | Régimes d'appauvrissement pour une thérapie à lymphocytes t ou à cellules nk modifiés |
US20210347908A1 (en) | 2019-08-20 | 2021-11-11 | Elpiscience (Suzhou) Biopharma, Ltd. | Novel anti-sirpa antibodies |
WO2021032078A1 (fr) | 2019-08-20 | 2021-02-25 | Elpiscience (Suzhou) Biopharma, Ltd. | Nouveaux anticorps anti-sirpa |
WO2021076908A1 (fr) | 2019-10-18 | 2021-04-22 | Forty Seven, Inc. | Polythérapies pour le traitement de syndromes myélodysplasiques et de la leucémie myéloïde aiguë |
WO2021129697A1 (fr) | 2019-12-24 | 2021-07-01 | Lanova Medicines Limited Company | ANTICORPS MONOCLONAUX ANTI-SIRPα ET LEURS UTILISATIONS |
WO2021174127A1 (fr) | 2020-02-28 | 2021-09-02 | Apexigen, Inc. | Anticorps anti-sirpa et méthodes d'utilisation |
WO2021185273A1 (fr) | 2020-03-20 | 2021-09-23 | 上海健信生物医药科技有限公司 | ANTICORPS CIBLANT SIRPα OU FRAGMENT DE LIAISON À L'ANTIGÈNE DE CELUI-CI, PRÉPARATION ET UTILISATION ASSOCIÉES |
CN111635458A (zh) | 2020-03-20 | 2020-09-08 | 上海健信生物医药科技有限公司 | 靶向Sirpα的抗体或其抗原结合片段及其制备和应用 |
WO2021222746A2 (fr) | 2020-04-30 | 2021-11-04 | Arch Oncology, Inc. | ANTICORPS SIRPα THÉRAPEUTIQUES |
WO2021226591A1 (fr) | 2020-05-08 | 2021-11-11 | Electra Therapeutics, Inc. | Anticorps dirigés contre sirp alpha, sirp bêta 1, et sirp gamma et leurs utilisations |
WO2021226576A1 (fr) | 2020-05-08 | 2021-11-11 | Electra Therapeutics, Inc. | Anticorps anti sirp alpha et anti sirp bêta 1 humanisés et leurs utilisations |
CN113735973A (zh) | 2020-05-28 | 2021-12-03 | 中国科学院微生物研究所 | 一种抗SIRPα抗体及其应用 |
CN112010979A (zh) | 2020-08-21 | 2020-12-01 | 博奥信生物技术(南京)有限公司 | 一种抗人SIRPα单克隆抗体及其用途 |
CN111995682A (zh) | 2020-08-21 | 2020-11-27 | 博奥信生物技术(南京)有限公司 | 抗人SIRPα单克隆抗体及其用途 |
CN112574310A (zh) | 2020-12-11 | 2021-03-30 | 浙江博锐生物制药有限公司 | 抗SIRPα抗体及其用途 |
WO2022254379A1 (fr) | 2021-06-04 | 2022-12-08 | Boehringer Ingelheim International Gmbh | Anticorps anti-sirp-alpha |
Non-Patent Citations (14)
Title |
---|
"UniProt", Database accession no. P11215 |
"Uniprot", Database accession no. P78324 |
ARNOUK SANA ET AL: "Imaging and therapeutic targeting of the tumor immune microenvironment with biologics", ADVANCED DRUG DELIVERY REVIEWS, ELSEVIER, AMSTERDAM , NL, vol. 184, 26 March 2022 (2022-03-26), XP087025783, ISSN: 0169-409X, [retrieved on 20220326], DOI: 10.1016/J.ADDR.2022.114239 * |
BARCLAY, A.N.BROWN, M.H., NAT REV IMMUNOL, vol. 6, 2006, pages 457 - 64 |
CHAMPIAT S ET AL: "Predictive response biomarkers from Phase I clinical trial of a SIRPalpha inhibitor BI765063, stand-alone and in combination with ezabenlimab, a PD1 inhibitor, in patients with advanced solid tumors | Cancer Research | American Association for Cancer Research", CANCER RESEARCH, 1 April 2023 (2023-04-01), POSTER PRESENTATIONS - PROFFERED ABSTRACTS| APRIL 04 2023 Abstract 2129:, XP093124511, Retrieved from the Internet <URL:https://aacrjournals.org/cancerres/article/83/7_Supplement/2129/724367/Abstract-2129-Predictive-response-biomarkers-from> [retrieved on 20240126] * |
DIZMAN NAZLI ET AL: "Cancer Therapy Targeting CD47/SIRP[alpha]", CANCERS, 11 December 2021 (2021-12-11), pages 1 - 17, XP093034401, DOI: 10.3390/cancers13246229 * |
GAUTTIER V ET AL: "Supplemental data", 19 October 2020 (2020-10-19), pages 1 - 28, XP093035269, Retrieved from the Internet <URL:https://www.jci.org/articles/view/135528/sd/1> [retrieved on 20230328] * |
GAUTTIER VANESSA ET AL, vol. 130, no. 11, 2 November 2020 (2020-11-02), GB, pages 6109 - 6123, XP055832928, ISSN: 0021-9738, Retrieved from the Internet <URL:https://ose-immuno.com/wp-content/uploads/2020/10/SIRPa_JCI-2020.pdf> DOI: 10.1172/JCI135528 * |
HUBERT M ET AL: "IFN-III is selectively produced by cDC1 and predicts good clinical outcome in breast cancer", SCIENCE IMMUNOLOGY, AAAS, US, vol. 5, no. 46, 17 April 2020 (2020-04-17), pages eaav3942 - 1, XP009523096, ISSN: 2470-9468, DOI: 10.1126/SCIIMMUNOL.AAV3942 * |
KALATHIL SURESH GOPI ET AL: "Importance of myeloid derived suppressor cells in cancer from a biomarker perspective", CELLULAR IMMUNOLOGY, ACADEMIC PRESS, SAN DIEGO, CA, US, vol. 361, 31 December 2020 (2020-12-31), XP086484911, ISSN: 0008-8749, [retrieved on 20201231], DOI: 10.1016/J.CELLIMM.2020.104280 * |
MAUTE R. ET AL: "CD47-SIRP[alpha]-targeted therapeutics: status and prospects", IOTECH, vol. 13, 1 March 2022 (2022-03-01), pages 100070, XP093028949, DOI: 10.1016/j.iotech.2022.100070 * |
SHULTZ, L.D. ET AL., J IMMUNOL, vol. 154, 1995, pages 180 - 91 |
SI-YANG LIU ET AL., J. HEMATOL. ONCOL., vol. 10, 2017, pages 136 |
TADAHIKO YANAGITA ET AL: "Anti-SIRP? antibodies as a potential new tool for cancer immunotherapy", vol. 2, no. 1, 12 January 2017 (2017-01-12), pages 1 - 15, XP055421877, ISSN: 2379-3708, Retrieved from the Internet <URL:https://insight.jci.org/articles/view/89140> DOI: 10.1172/jci.insight.89140 * |
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