CA3015839A1 - Connexin (cx)43 hemichannel-binding antibodies and uses thereof - 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
-
- 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
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
-
- 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
- C07K2317/75—Agonist effect on antigen
-
- 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)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Physical Education & Sports Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
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- Neurology (AREA)
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- Oncology (AREA)
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- Psychiatry (AREA)
- Communicable Diseases (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Epidemiology (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662300492P | 2016-02-26 | 2016-02-26 | |
| US62/300,492 | 2016-02-26 | ||
| PCT/US2017/019605 WO2017147561A1 (en) | 2016-02-26 | 2017-02-27 | CONNEXIN (Cx) 43 HEMICHANNEL-BINDING ANTIBODIES AND USES THEREOF |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA3015839A1 true CA3015839A1 (en) | 2017-08-31 |
Family
ID=59685694
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA3015839A Pending CA3015839A1 (en) | 2016-02-26 | 2017-02-27 | Connexin (cx)43 hemichannel-binding antibodies and uses thereof |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US10889637B2 (enExample) |
| EP (1) | EP3419998A4 (enExample) |
| JP (1) | JP7098527B2 (enExample) |
| CN (2) | CN116672445A (enExample) |
| AU (2) | AU2017224122B2 (enExample) |
| CA (1) | CA3015839A1 (enExample) |
| WO (1) | WO2017147561A1 (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11912762B2 (en) | 2013-08-21 | 2024-02-27 | Board Of Regents Of The University Of Texas System | Method of treating osteoarthritis by administering an anti-connexin 43 antibody |
| US11912758B2 (en) | 2016-02-26 | 2024-02-27 | The Board Of Regents Of The University Of Texas System | Methods of treating metastasis, including inhibiting bone cancer metastasis, by administering an antibody which binds connexin 43 (Cx43) hemichannel |
| US12503500B2 (en) | 2024-02-09 | 2025-12-23 | Board Of Regents, The University Of Texas System | Connexin 43 (Cx43) hemichannel-binding antibodies |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2710220A1 (es) * | 2017-10-19 | 2019-04-23 | Fund Profesor Novoa Santos | Compuestos anti-conexina para su uso en la prevención y/o el tratamiento de enfermedades degenerativas de las articulaciones |
| AU2019249427A1 (en) * | 2018-04-02 | 2020-10-29 | Alamab Therapeutics, Inc. | Connexin 43 antibodies and use thereof |
| WO2019222800A1 (en) * | 2018-05-21 | 2019-11-28 | Hudson Institute of Medical Research | Methods for the treatment or prevention of autoimmune or autoinflammatory diseases |
| US12187794B2 (en) * | 2019-02-04 | 2025-01-07 | Alamab Therapeutics, Inc. | Connexin 43 antibodies and use thereof |
| JP7710374B2 (ja) * | 2019-02-28 | 2025-07-18 | ボード オブ リージェンツ ザ ユニヴァーシティ オブ テキサス システム | 骨肉腫を治療するための組成物及び使用方法 |
| AU2020358101A1 (en) | 2019-10-02 | 2022-04-28 | Alamab Therapeutics, Inc. | Anto-connexin antibody formulations |
| WO2022026914A1 (en) * | 2020-07-31 | 2022-02-03 | Alamab Therapeutics, Inc. | Anti-connexin antibody formulations |
| EP3981421A1 (en) * | 2020-10-06 | 2022-04-13 | Fundación Profesor Novoa Santos | Connexin 43 for use in the treatment of a cancer type characterized by the activation of a mitogen-activated protein kinase |
| CN117377686A (zh) * | 2021-01-13 | 2024-01-09 | 德克萨斯大学体系董事会 | 用于治疗骨关节炎、类风湿性关节炎以及关节和肌腱病症的组合物和方法 |
| WO2023212727A1 (en) * | 2022-04-29 | 2023-11-02 | Board Of Regents, The University Of Texas System | Compositions and methods for treating eye diseases |
| JP2025515029A (ja) * | 2022-05-04 | 2025-05-13 | ブイエスティー バイオ コーポレーション | 血管透過性の選択的調節のための組成物及び方法 |
| WO2024145461A2 (en) * | 2022-12-30 | 2024-07-04 | Board Of Regents, The University Of Texas System | Compositions for treating osteoporosis and bone loss and methods of use thereof |
| WO2024206157A1 (en) * | 2023-03-24 | 2024-10-03 | Board Of Regents, The University Of Texas System | Compositions and methods for treating obesity and reducing fat accumulation |
| WO2025199516A1 (en) * | 2024-03-22 | 2025-09-25 | Board Of Regents, The University Of Texas System | Compositions and methods for preserving or increasing lean muscle mass |
| CN118791620B (zh) * | 2024-07-02 | 2025-04-04 | 北京市华信行生物科技有限公司 | 抗糖原磷酸化酶gpbb单克隆抗体及其应用 |
Family Cites Families (74)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL154598B (nl) | 1970-11-10 | 1977-09-15 | Organon Nv | Werkwijze voor het aantonen en bepalen van laagmoleculire verbindingen en van eiwitten die deze verbindingen specifiek kunnen binden, alsmede testverpakking. |
| US3817837A (en) | 1971-05-14 | 1974-06-18 | Syva Corp | Enzyme amplification assay |
| US3939350A (en) | 1974-04-29 | 1976-02-17 | Board Of Trustees Of The Leland Stanford Junior University | Fluorescent immunoassay employing total reflection for activation |
| US3996345A (en) | 1974-08-12 | 1976-12-07 | Syva Company | Fluorescence quenching with immunological pairs in immunoassays |
| US4196265A (en) | 1977-06-15 | 1980-04-01 | The Wistar Institute | Method of producing antibodies |
| US4277437A (en) | 1978-04-05 | 1981-07-07 | Syva Company | Kit for carrying out chemically induced fluorescence immunoassay |
| US4275149A (en) | 1978-11-24 | 1981-06-23 | Syva Company | Macromolecular environment control in specific receptor assays |
| US4366241A (en) | 1980-08-07 | 1982-12-28 | Syva Company | Concentrating zone method in heterogeneous immunoassays |
| US4957939A (en) | 1981-07-24 | 1990-09-18 | Schering Aktiengesellschaft | Sterile pharmaceutical compositions of gadolinium chelates useful enhancing NMR imaging |
| US4867973A (en) | 1984-08-31 | 1989-09-19 | Cytogen Corporation | Antibody-therapeutic agent conjugates |
| US4472509A (en) | 1982-06-07 | 1984-09-18 | Gansow Otto A | Metal chelate conjugated monoclonal antibodies |
| US4606855A (en) | 1982-07-26 | 1986-08-19 | Mex Research Associates C/O Leon Reimer | Monoclonal antibody to digoxin |
| US4469797A (en) | 1982-09-23 | 1984-09-04 | Miles Laboratories, Inc. | Digoxigenin immunogens, antibodies, labeled conjugates, and related derivatives |
| US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
| DE3330160A1 (de) | 1983-08-20 | 1985-03-07 | Boehringer Ingelheim KG, 6507 Ingelheim | Monoklonaler antikoerper mit hoher affinitaet zum digoxin |
| DE3342870A1 (de) | 1983-11-26 | 1985-06-05 | Boehringer Mannheim Gmbh, 6800 Mannheim | Digitalis-antikoerper, verfahren zu ihrer herstellung und ihre verwendung zur therapie von digitalis-intoxikationen |
| US4767720A (en) | 1985-08-29 | 1988-08-30 | Hsc Research Development Corporation | Antidigoxin antibodies |
| US4938948A (en) | 1985-10-07 | 1990-07-03 | Cetus Corporation | Method for imaging breast tumors using labeled monoclonal anti-human breast cancer antibodies |
| US4946778A (en) | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
| US5091513A (en) | 1987-05-21 | 1992-02-25 | Creative Biomolecules, Inc. | Biosynthetic antibody binding sites |
| US5824311A (en) | 1987-11-30 | 1998-10-20 | Trustees Of The University Of Pennsylvania | Treatment of tumors with monoclonal antibodies against oncogene antigens |
| JP3040121B2 (ja) | 1988-01-12 | 2000-05-08 | ジェネンテク,インコーポレイテッド | 増殖因子レセプターの機能を阻害することにより腫瘍細胞を処置する方法 |
| US4870287A (en) | 1988-03-03 | 1989-09-26 | Loma Linda University Medical Center | Multi-station proton beam therapy system |
| US5223409A (en) | 1988-09-02 | 1993-06-29 | Protein Engineering Corp. | Directed evolution of novel binding proteins |
| JPH049249A (ja) | 1990-04-27 | 1992-01-14 | Kusuda:Kk | 塗型剤吹き付け機 |
| GB9015198D0 (en) | 1990-07-10 | 1990-08-29 | Brien Caroline J O | Binding substance |
| WO1992002551A1 (en) | 1990-08-02 | 1992-02-20 | B.R. Centre Limited | Methods for the production of proteins with a desired function |
| US5164296A (en) | 1990-08-31 | 1992-11-17 | University Of Maryland At Baltimore | Assay methods involving ouabain |
| US5656434A (en) | 1990-12-28 | 1997-08-12 | Suntory Limited | Monoclonal antibody against cardiac glycoside and utilization thereof |
| US5858657A (en) | 1992-05-15 | 1999-01-12 | Medical Research Council | Methods for producing members of specific binding pairs |
| DE69230142T2 (de) | 1991-05-15 | 2000-03-09 | Cambridge Antibody Technology Ltd. | Verfahren zur herstellung von spezifischen bindungspaargliedern |
| WO1994004679A1 (en) | 1991-06-14 | 1994-03-03 | Genentech, Inc. | Method for making humanized antibodies |
| EP0590058B1 (en) | 1991-06-14 | 2003-11-26 | Genentech, Inc. | HUMANIZED Heregulin ANTIBODy |
| US5565332A (en) | 1991-09-23 | 1996-10-15 | Medical Research Council | Production of chimeric antibodies - a combinatorial approach |
| US5770376A (en) | 1992-12-02 | 1998-06-23 | Biomedical Sciences Research Laboratories, Inc. | Method of diagnosing and treating myocardial infarction and hypertension |
| US5846945A (en) | 1993-02-16 | 1998-12-08 | Onyx Pharmaceuticals, Inc. | Cytopathic viruses for therapy and prophylaxis of neoplasia |
| US5801005A (en) | 1993-03-17 | 1998-09-01 | University Of Washington | Immune reactivity to HER-2/neu protein for diagnosis of malignancies in which the HER-2/neu oncogene is associated |
| US5420253A (en) | 1993-09-09 | 1995-05-30 | Willmar Poultry Company, Inc. | Method for purifying egg yolk immunoglobulins |
| GB9325182D0 (en) | 1993-12-08 | 1994-02-09 | T Cell Sciences Inc | Humanized antibodies or binding proteins thereof specific for t cell subpopulations exhibiting select beta chain variable regions |
| DK1231268T3 (da) | 1994-01-31 | 2005-11-21 | Univ Boston | Polyklonale antistofbiblioteker |
| US5861499A (en) | 1994-02-10 | 1999-01-19 | Imclone Systems Incorporated | Nucleic acid molecules encoding the variable or hypervariable region of a monoclonal antibody that binds to an extracellular domain |
| GB9506466D0 (en) | 1994-08-26 | 1995-05-17 | Prolifix Ltd | Cell cycle regulated repressor and dna element |
| US5760395A (en) | 1996-04-18 | 1998-06-02 | Universities Research Assoc., Inc. | Method and apparatus for laser-controlled proton beam radiology |
| US5739169A (en) | 1996-05-31 | 1998-04-14 | Procept, Incorporated | Aromatic compounds for inhibiting immune response |
| US6709659B1 (en) | 1996-08-02 | 2004-03-23 | Zymogenetics, Inc. | Antibodies that bind testis-specific insulin homolog polypeptides |
| US6406867B1 (en) | 1996-08-16 | 2002-06-18 | Human Genome Sciences, Inc. | Antibody to human endokine alpha and methods of use |
| US6709873B1 (en) | 1997-04-09 | 2004-03-23 | Isodiagnostika Inc. | Method for production of antibodies to specific sites of rapamycin |
| US6861572B1 (en) | 1997-11-14 | 2005-03-01 | Origen Therapeutics, Inc. | Production of proteins in eggs |
| US6913745B1 (en) | 1997-12-02 | 2005-07-05 | Neuralab Limited | Passive immunization of Alzheimer's disease |
| HUP0102782A3 (en) | 1998-06-19 | 2002-12-28 | Smithkline Beecham Corp | Salycilanilide as inhibitors of transcription factor nf-kb |
| US6432673B1 (en) | 1998-12-07 | 2002-08-13 | Zymogenetics, Inc. | Growth factor homolog ZVEGF3 |
| PT1146908E (pt) * | 1999-01-27 | 2005-10-31 | David Dr Becker | Formulacoes que contem nucleotidos de anti-sentido para conexinas |
| US20020064528A1 (en) | 2000-01-28 | 2002-05-30 | Zhenping Zhu | Antibodies specific to KDR and uses thereof |
| US6946546B2 (en) | 2000-03-06 | 2005-09-20 | Cambridge Antibody Technology Limited | Human antibodies against eotaxin |
| US6849259B2 (en) | 2000-06-16 | 2005-02-01 | Symphogen A/S | Polyclonal antibody composition for treating allergy |
| US6753407B2 (en) | 2000-08-15 | 2004-06-22 | North Carolina State University | Antimicrobial peptides isolated from fish |
| US8178098B2 (en) | 2001-04-03 | 2012-05-15 | National Jewish Health | Method to inhibit airway hyperresponsiveness using aerosolized T cell receptor antibodies |
| US6891024B2 (en) | 2001-05-24 | 2005-05-10 | The Curators Of The University Of Missouri | Monoclonal antibodies to Sarcocystis neurona and uses therefor |
| WO2004006955A1 (en) | 2001-07-12 | 2004-01-22 | Jefferson Foote | Super humanized antibodies |
| US6906131B2 (en) | 2001-09-17 | 2005-06-14 | Stockhausen Gmbh & Co. Kg | Cellulose material with improved absorbency |
| US7153822B2 (en) | 2002-01-29 | 2006-12-26 | Wyeth | Compositions and methods for modulating connexin hemichannels |
| KR101215701B1 (ko) | 2002-07-19 | 2012-12-26 | 베스 이스라엘 데코니스 메디칼 센터 | 자간전증 또는 자간의 진단 및 치료 방법 |
| AU2004294824A1 (en) | 2003-12-03 | 2005-06-16 | Coda Therapeutics (Nz) Ltd | Antisense compounds targeted to connexins and methods of use thereof |
| WO2005085423A1 (en) | 2004-02-27 | 2005-09-15 | Michigan State University | Oct-4 and gjic expression as markers for adult human stem cells and cancer cell precursors |
| EP1753880A4 (en) | 2004-05-14 | 2010-07-14 | Univ California | METHOD FOR THE TREATMENT OF CANCER USING MONOCLONAL ANTI-WNT2 ANTIBODIES AND siRNA |
| CA2596412A1 (en) | 2005-02-03 | 2006-12-21 | Coda Therapeutics Limited | Anti-connexin compounds and uses thereof |
| CA2710382A1 (en) | 2007-12-21 | 2009-07-09 | Coda Therapeutics, Inc. | Treatment of orthopedic conditions |
| KR101745394B1 (ko) | 2008-12-22 | 2017-06-09 | 노보 노르디스크 에이/에스 | 조직 인자 경로 억제자에 대한 항체 |
| RU2408728C1 (ru) | 2009-07-28 | 2011-01-10 | Федеральное государственное учреждение "Государственный Научный Центр Социальной и Судебной Психиатрии им. В.П. Сербского" (ФГУ "ГНЦССП Росздрава") | Способ получения иммуногенного рекомбинантного экстраклеточного фрагмента коннексина-43 |
| EP2700652B1 (en) | 2011-04-18 | 2018-12-19 | The University of Tokyo | Diagnosis and treatment of cancer using anti-itm2a antibody |
| RU2457862C1 (ru) | 2011-07-07 | 2012-08-10 | Федеральное государственное учреждение "Государственный научный центр социальной и судебной психиатрии им. В.П. Сербского" Министерства здравоохранения и социального развития Российской Федерации | Способ лечения низкодифференцированных глиом |
| WO2013163423A1 (en) | 2012-04-25 | 2013-10-31 | Musc Foundation For Research Development | Compositions and methods for wound healing and tissue repair |
| EP3036005A4 (en) | 2013-08-21 | 2017-04-26 | The Board Of Regents Of The University Of Texas System | Compositions and methods for targeting connexin hemichannels |
| WO2017147561A1 (en) | 2016-02-26 | 2017-08-31 | The Board Of Regents Of The University Of Texas System | CONNEXIN (Cx) 43 HEMICHANNEL-BINDING ANTIBODIES AND USES THEREOF |
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2017
- 2017-02-27 WO PCT/US2017/019605 patent/WO2017147561A1/en not_active Ceased
- 2017-02-27 JP JP2018545296A patent/JP7098527B2/ja active Active
- 2017-02-27 CN CN202210879114.2A patent/CN116672445A/zh active Pending
- 2017-02-27 CA CA3015839A patent/CA3015839A1/en active Pending
- 2017-02-27 EP EP17757405.0A patent/EP3419998A4/en active Pending
- 2017-02-27 CN CN201780025896.0A patent/CN109071642B/zh active Active
- 2017-02-27 US US16/078,990 patent/US10889637B2/en active Active
- 2017-02-27 AU AU2017224122A patent/AU2017224122B2/en active Active
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2021
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2024
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11912762B2 (en) | 2013-08-21 | 2024-02-27 | Board Of Regents Of The University Of Texas System | Method of treating osteoarthritis by administering an anti-connexin 43 antibody |
| US12162937B2 (en) | 2013-08-21 | 2024-12-10 | Board Of Regents Of The University Of Texas System | Methods of treating an inflammatory disorder by administering an antibody which binds to a connexin CX43 hemichannel |
| US11912758B2 (en) | 2016-02-26 | 2024-02-27 | The Board Of Regents Of The University Of Texas System | Methods of treating metastasis, including inhibiting bone cancer metastasis, by administering an antibody which binds connexin 43 (Cx43) hemichannel |
| US12503500B2 (en) | 2024-02-09 | 2025-12-23 | Board Of Regents, The University Of Texas System | Connexin 43 (Cx43) hemichannel-binding antibodies |
Also Published As
| Publication number | Publication date |
|---|---|
| US20190359696A1 (en) | 2019-11-28 |
| JP7098527B2 (ja) | 2022-07-11 |
| US20240254212A1 (en) | 2024-08-01 |
| AU2017224122A1 (en) | 2018-09-20 |
| EP3419998A4 (en) | 2019-09-25 |
| CN109071642B (zh) | 2022-08-09 |
| WO2017147561A1 (en) | 2017-08-31 |
| AU2017224122B2 (en) | 2024-04-11 |
| AU2024204761A1 (en) | 2024-08-01 |
| EP3419998A1 (en) | 2019-01-02 |
| US10889637B2 (en) | 2021-01-12 |
| US11912758B2 (en) | 2024-02-27 |
| US20210253680A1 (en) | 2021-08-19 |
| CN109071642A (zh) | 2018-12-21 |
| JP2019509283A (ja) | 2019-04-04 |
| CN116672445A (zh) | 2023-09-01 |
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