SK27998A3 - Recombinant anti-cd4 antibodies for human therapy and methods for their production - Google Patents
Recombinant anti-cd4 antibodies for human therapy and methods for their production Download PDFInfo
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- SK27998A3 SK27998A3 SK279-98A SK27998A SK27998A3 SK 27998 A3 SK27998 A3 SK 27998A3 SK 27998 A SK27998 A SK 27998A SK 27998 A3 SK27998 A3 SK 27998A3
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- C07K16/462—Igs containing a variable region (Fv) from one specie and a constant region (Fc) from another
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- 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
- A61K38/00—Medicinal preparations containing peptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/21—Immunoglobulins specific features characterized by taxonomic origin from primates, e.g. man
-
- 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
- C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
- C07K2317/732—Antibody-dependent cellular cytotoxicity [ADCC]
-
- 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
- C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
- C07K2317/734—Complement-dependent cytotoxicity [CDC]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Immunology (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Peptides Or Proteins (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/523,894 US6136310A (en) | 1991-07-25 | 1995-09-06 | Recombinant anti-CD4 antibodies for human therapy |
| PCT/US1996/014324 WO1997009351A1 (fr) | 1995-09-06 | 1996-09-05 | Anticorps anti-cd4 recombinants pour therapie humaine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK27998A3 true SK27998A3 (en) | 1998-11-04 |
Family
ID=24086874
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK279-98A SK27998A3 (en) | 1995-09-06 | 1996-09-05 | Recombinant anti-cd4 antibodies for human therapy and methods for their production |
Country Status (23)
| Country | Link |
|---|---|
| US (5) | US6136310A (fr) |
| EP (1) | EP0854885B1 (fr) |
| JP (1) | JP3619866B2 (fr) |
| KR (1) | KR100491222B1 (fr) |
| CN (1) | CN100391978C (fr) |
| AP (1) | AP1193A (fr) |
| AT (1) | ATE348113T1 (fr) |
| AU (1) | AU717674B2 (fr) |
| BG (1) | BG64651B1 (fr) |
| BR (1) | BR9610404A (fr) |
| CA (1) | CA2231182A1 (fr) |
| CZ (1) | CZ291036B6 (fr) |
| DE (1) | DE69636760T2 (fr) |
| HU (1) | HU221351B1 (fr) |
| IL (1) | IL123447A0 (fr) |
| MX (1) | MX9801732A (fr) |
| NO (1) | NO324497B1 (fr) |
| NZ (1) | NZ316835A (fr) |
| OA (1) | OA10671A (fr) |
| RO (1) | RO120198B1 (fr) |
| RU (1) | RU2232773C2 (fr) |
| SK (1) | SK27998A3 (fr) |
| WO (1) | WO1997009351A1 (fr) |
Families Citing this family (156)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6136310A (en) * | 1991-07-25 | 2000-10-24 | Idec Pharmaceuticals Corporation | Recombinant anti-CD4 antibodies for human therapy |
| US6440418B1 (en) * | 1995-11-07 | 2002-08-27 | Idec Pharmaceuticals Corporation | Methods of treating autoimmune diseases with gp39-specific antibodies |
| EP0938334A4 (fr) * | 1996-07-26 | 2004-12-15 | Smithkline Beecham Corp | Methode amelioree de traitement de maladies de l'organisme induites par des cellules immunes |
| GB9624038D0 (en) * | 1996-11-19 | 1997-01-08 | Sandoz Ltd | Organic compounds |
| US7033589B1 (en) | 1997-02-20 | 2006-04-25 | Biogen Idec Ma Inc. | γ-1 anti-human CD23 monoclonal antibodies and use thereof as therapeutics |
| US6893636B2 (en) * | 1997-02-20 | 2005-05-17 | Biogen Idec Ma Inc. | Gamma-1 and gamma-3 anti-human CD23 monoclonal antibodies and use thereof as therapeutics |
| WO1998058966A1 (fr) * | 1997-06-24 | 1998-12-30 | Norman Godin | Composition pour immuniprotection specifique et procede d'obtention de ladite composition |
| US7189400B2 (en) | 1998-03-17 | 2007-03-13 | Genetics Institute, Llc | Methods of treatment with antagonists of MU-1 |
| US7198789B2 (en) * | 1998-03-17 | 2007-04-03 | Genetics Institute, Llc | Methods and compositions for modulating interleukin-21 receptor activity |
| US6057128A (en) | 1998-03-17 | 2000-05-02 | Genetics Institute, Inc. | MU-1, member of the cytokine receptor family |
| US6528624B1 (en) | 1998-04-02 | 2003-03-04 | Genentech, Inc. | Polypeptide variants |
| US7183387B1 (en) | 1999-01-15 | 2007-02-27 | Genentech, Inc. | Polypeptide variants with altered effector function |
| KR101077001B1 (ko) * | 1999-01-15 | 2011-10-26 | 제넨테크, 인크. | 효과기 기능이 변화된 폴리펩티드 변이체 |
| US6737056B1 (en) * | 1999-01-15 | 2004-05-18 | Genentech, Inc. | Polypeptide variants with altered effector function |
| US20020028178A1 (en) * | 2000-07-12 | 2002-03-07 | Nabil Hanna | Treatment of B cell malignancies using combination of B cell depleting antibody and immune modulating antibody related applications |
| WO2001068133A1 (fr) * | 2000-03-14 | 2001-09-20 | Genetics Institute, Inc. | Utilisation de la rapamycine et d'agents inhibiteurs de l'activite b7 en immunomodulation |
| JP2003535592A (ja) * | 2000-06-06 | 2003-12-02 | アイデック ファーマスーティカルズ コーポレイション | ヒトgp39に対する非アゴニスト抗体、含有する組成物、およびその治療的使用 |
| US20030211107A1 (en) * | 2002-01-31 | 2003-11-13 | Kandasamy Hariharan | Use of CD23 antagonists for the treatment of neoplastic disorders |
| US20030103971A1 (en) * | 2001-11-09 | 2003-06-05 | Kandasamy Hariharan | Immunoregulatory antibodies and uses thereof |
| US20070065436A1 (en) * | 2001-01-31 | 2007-03-22 | Biogen Idec Inc. | Anti-cd80 antibody having adcc activity for adcc mediated killing of b cell lymphoma cells alone or in combination with other therapies |
| US20020159996A1 (en) * | 2001-01-31 | 2002-10-31 | Kandasamy Hariharan | Use of CD23 antagonists for the treatment of neoplastic disorders |
| AR035779A1 (es) * | 2001-02-06 | 2004-07-14 | Genetics Inst Llc | Polipeptidos de fusion derivados de glicoproteina ib alfa de plaqueta y metodos de uso de los mismos |
| US6972324B2 (en) | 2001-05-18 | 2005-12-06 | Boehringer Ingelheim Pharmaceuticals, Inc. | Antibodies specific for CD44v6 |
| GB2376466A (en) * | 2001-06-14 | 2002-12-18 | Mark Frewin | TRX1 antibody |
| US7541443B2 (en) * | 2001-06-14 | 2009-06-02 | Tolerrx, Inc. | Anti-CD4 antibodies |
| DE60233738D1 (de) * | 2001-07-10 | 2009-10-29 | Biogen Idec Inc | Hemmung des apoptoseprozesses und verbesserung der zelleistung |
| GB2380127A (en) * | 2001-09-26 | 2003-04-02 | Isis Innovation | Treatment of chronic joint inflammation |
| DK1432431T3 (en) | 2001-10-04 | 2017-07-10 | Genetics Inst Llc | Methods and compositions for modulating interleukin-21 activity |
| DE60230918D1 (de) | 2001-11-16 | 2009-03-05 | Biogen Idec Inc | Polycistronische expression von antikörpern in cho zellen |
| EP2075256A2 (fr) | 2002-01-14 | 2009-07-01 | William Herman | Ligands ciblés |
| EP1572936A2 (fr) * | 2002-03-05 | 2005-09-14 | Eli Lilly And Company | Proteines hybrides g-csf heterologues |
| US20030180292A1 (en) * | 2002-03-14 | 2003-09-25 | Idec Pharmaceuticals | Treatment of B cell malignancies using anti-CD40L antibodies in combination with anti-CD20 antibodies and/or chemotherapeutics and radiotherapy |
| US20040016010A1 (en) * | 2002-04-17 | 2004-01-22 | Marion Kasaian | IL-21 receptor knockout animal and methods of use thereof |
| EP1517701A2 (fr) * | 2002-04-22 | 2005-03-30 | Recopharma AB | Vaccins a polypeptide hybride de mucine contenant un epitope de lewis y, compositions et procedes pour les utiliser |
| US8034351B2 (en) * | 2002-04-22 | 2011-10-11 | Recopharma Ab | Mucin fusion polypeptide vaccines, compositions and methods of use thereof |
| AU2003233008B2 (en) * | 2002-04-22 | 2008-04-24 | Recopharma Ab | Fusion polypeptides and methods for inhibiting microbial adhesion |
| EP1553982A4 (fr) * | 2002-07-15 | 2008-03-26 | Wyeth Corp | Techniques et compositions permettant de moduler la fonction et le developpement de cellules assistantes (t sb h /sb ) |
| NZ538629A (en) * | 2002-08-09 | 2008-05-30 | Recopharma Ab | Mucin-immunoglobulin fusion proteins |
| BR0314711A (pt) * | 2002-09-27 | 2005-07-26 | Tanox Inc | Composições sinérgicas para a prevenção e tratamento da sìndrome da imunodeficiência adquirida |
| DK1551876T3 (da) | 2002-10-16 | 2011-06-14 | Purdue Pharma Lp | Antistoffer, der binder til celle-associerede ca 125/0722P og fremgangsmåder til anvendelse deraf |
| KR100932340B1 (ko) * | 2002-10-17 | 2009-12-16 | 젠맵 에이/에스 | Cd20에 대한 인간 모노클로날 항체 |
| JP4033390B2 (ja) * | 2002-10-30 | 2008-01-16 | 独立行政法人科学技術振興機構 | 不死化ナチュラルキラー細胞株 |
| EP1460088A1 (fr) * | 2003-03-21 | 2004-09-22 | Biotest AG | Anticorps humanisé contre CD4 avec des caractéristiques immunosuppressives |
| EP1625165A2 (fr) * | 2003-04-03 | 2006-02-15 | Protein Design Labs, Inc. | Procedes de production et utilisation d'anticorps anti-integrine permettant d'inhiber la granulation tissulaire |
| JP2007537710A (ja) | 2003-06-11 | 2007-12-27 | ワイス | 血小板糖タンパク質IBα改変体融合ポリペプチドおよびその使用法 |
| GB2406094B (en) * | 2003-09-17 | 2007-06-06 | Antisoma Plc | Modified antibody comprising an amino acid substitution mutation which confers increased stability |
| JP2007534305A (ja) * | 2003-11-07 | 2007-11-29 | アムジェン インコーポレイテッド | サル免疫グロブリン配列 |
| EP1740946B1 (fr) * | 2004-04-20 | 2013-11-06 | Genmab A/S | Anticorps monoclonaux humains diriges contre cd20 |
| DOP2005000108A (es) * | 2004-06-04 | 2007-06-15 | Genentech Inc | Method for treating lupus |
| CA2574848A1 (fr) * | 2004-08-05 | 2006-12-21 | Wyeth | Inhibition de l'activite du recepteur d'interleukine 21 |
| CA2589422A1 (fr) * | 2004-10-14 | 2007-04-12 | Recopharma Ab | Compositions et procedes pour l'inhibition d'adherence et d'infection a h.pylori |
| US7589182B1 (en) | 2005-01-07 | 2009-09-15 | Los Alamos National Security, Llc | Anti-sulfotyrosine antibodies |
| US20060193849A1 (en) * | 2005-02-25 | 2006-08-31 | Antisoma Plc | Biological materials and uses thereof |
| EP3050963B1 (fr) | 2005-03-31 | 2019-09-18 | Chugai Seiyaku Kabushiki Kaisha | Procédé pour la production de polypeptide au moyen de la régulation d'un ensemble |
| GT200600148A (es) | 2005-04-14 | 2006-11-22 | Metodos para el tratamiento y la prevencion de fibrosis | |
| ES2400660T3 (es) * | 2005-11-01 | 2013-04-11 | Novartis Ag | Usos de anticuerpos anti-CD40 |
| WO2007053661A2 (fr) * | 2005-11-01 | 2007-05-10 | Novartis Ag | Utilisations d'anticorps anti-cd40 |
| CA2628928A1 (fr) * | 2005-11-10 | 2007-05-24 | Receptor Biologix, Inc. | Proteines de fusion a intron du facteur de croissance des hepatocytes |
| CA2633768A1 (fr) * | 2005-11-10 | 2007-05-18 | Bayer Schering Pharma Aktiengesellschaft | Reduction de restenose |
| US7495097B2 (en) * | 2005-11-23 | 2009-02-24 | Brown University | Rhodium quinonoid catalysts |
| EP1806365A1 (fr) | 2006-01-05 | 2007-07-11 | Boehringer Ingelheim International GmbH | Anticorps spécifiques pour la protéine alpha d'activation de fibroblastes et leurs immunoconjugués |
| EP2021366A2 (fr) * | 2006-01-23 | 2009-02-11 | Recopharma AB | Production de protéines portant de l'oligomannose ou des glycanes de type humain dans une levure et leurs procédés d'utilisation |
| US20090181041A1 (en) * | 2006-01-23 | 2009-07-16 | Jan Holgersson | Production of proteins carrying oligomannose or human-like glycans in yeast and methods of use thereof |
| DK2264060T3 (da) | 2006-01-26 | 2014-07-28 | Recopharma Ab | Sammensætninger og fremgangsmåder til inhibering af viral adhæsion |
| US20080279848A1 (en) * | 2006-03-16 | 2008-11-13 | Genentech, Inc. | Methods of treating lupus using CD4 antibodies |
| BRPI0708902A2 (pt) * | 2006-03-16 | 2011-06-14 | Genentech Inc | mÉtodos de tratar lupus usando anticorpos cd4 |
| TW200806317A (en) * | 2006-03-20 | 2008-02-01 | Wyeth Corp | Methods for reducing protein aggregation |
| EP2010920B1 (fr) * | 2006-03-23 | 2011-07-06 | Absorber AB | Antigènes de groupes sanguins de types différents pour applications diagnostiques et thérapeutiques |
| CA2647846C (fr) | 2006-03-31 | 2016-06-21 | Chugai Seiyaku Kabushiki Kaisha | Methodes de controle de la pharmacocinetique sanguine des anticorps |
| CN105177091A (zh) | 2006-03-31 | 2015-12-23 | 中外制药株式会社 | 用于纯化双特异性抗体的抗体修饰方法 |
| KR20090031897A (ko) * | 2006-06-12 | 2009-03-30 | 리셉터 바이오로직스 인크 | 전-세포 표면 수용체-특이적 치료제 |
| TW200817438A (en) * | 2006-08-17 | 2008-04-16 | Hoffmann La Roche | A conjugate of an antibody against CCR5 and an antifusogenic peptide |
| US20090143288A1 (en) * | 2007-03-13 | 2009-06-04 | Roche Palo Alto Llc | Peptide-complement conjugates |
| EP2125894B1 (fr) | 2007-03-22 | 2018-12-19 | Biogen MA Inc. | Protéines de liaison, incluant des anticorps, dérivés d'anticorps et fragments d'anticorps, qui se lient spécifiquement à cd154 et leurs utilisations |
| TW200902708A (en) * | 2007-04-23 | 2009-01-16 | Wyeth Corp | Methods of protein production using anti-senescence compounds |
| US20130195881A1 (en) | 2007-04-27 | 2013-08-01 | Sanjaya Singh | Potent, stable and non-immunosuppressive anti-cd4 antibodies |
| AR067584A1 (es) * | 2007-07-20 | 2009-10-14 | Hoffmann La Roche | Un conjugado de un anticuerpo contra la cd4 y peptidos antifusogenicos |
| 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 |
| KR102339457B1 (ko) | 2007-09-26 | 2021-12-14 | 추가이 세이야쿠 가부시키가이샤 | 항체 정상영역 개변체 |
| TW200932257A (en) * | 2007-10-16 | 2009-08-01 | Receptor Biologix Inc | Compositions comprising optimized Her1 and Her3 multimers and methods of use thereof |
| CA2708532C (fr) | 2007-12-05 | 2018-06-05 | Chugai Seiyaku Kabushiki Kaisha | Anticorps anti-nr10 et son utilisation |
| JP5795167B2 (ja) | 2008-03-13 | 2015-10-14 | バイオテスト・アクチエンゲゼルシヤフト | 疾患治療剤 |
| AU2009224690B2 (en) | 2008-03-13 | 2014-10-09 | Biotest Ag | Agent for treating disease |
| SG190598A1 (en) * | 2008-03-13 | 2013-06-28 | Biotest Ag | Agent for treating disease |
| JP2011519912A (ja) * | 2008-05-09 | 2011-07-14 | リコファーマ アーベー | 志賀毒素および志賀様毒素を阻害するための組成物および方法 |
| WO2009136297A2 (fr) * | 2008-05-09 | 2009-11-12 | Recopharma Ab | Compositions et procédés pour inhiber la toxine a de clostridium difficile |
| KR20160104101A (ko) * | 2008-05-23 | 2016-09-02 | 아고스 쎄라퓨틱스, 인코포레이티드 | 신규 가용성 cd83 폴리펩티드, 제형 및 사용 방법 |
| US20100021460A1 (en) * | 2008-07-15 | 2010-01-28 | Genentech, Inc. | Methods of Treating Autoimmune Diseases Using CD4 Antibodies |
| KR101671537B1 (ko) | 2008-08-11 | 2016-11-01 | 넥타르 테라퓨틱스 | 다분지형 중합체 알카노에이트 컨쥬게이트 |
| TWI440469B (zh) | 2008-09-26 | 2014-06-11 | Chugai Pharmaceutical Co Ltd | Improved antibody molecules |
| JP2012504110A (ja) * | 2008-09-29 | 2012-02-16 | バイオテスト・アクチエンゲゼルシヤフト | 疾患治療組成物 |
| ES2699434T3 (es) * | 2008-10-31 | 2019-02-11 | Wyeth Llc | Purificación de proteínas ácidas utilizando cromatografía de hidroxiapatita cerámica |
| WO2010074266A1 (fr) | 2008-12-26 | 2010-07-01 | 協和発酵キリン株式会社 | Anticorps anti-cd4 |
| US9228017B2 (en) | 2009-03-19 | 2016-01-05 | Chugai Seiyaku Kabushiki Kaisha | Antibody constant region variant |
| WO2010107109A1 (fr) | 2009-03-19 | 2010-09-23 | 中外製薬株式会社 | Variant d'une région constante d'anticorps |
| FR2945538B1 (fr) | 2009-05-12 | 2014-12-26 | Sanofi Aventis | Anticorps humanises specifiques de la forme protofibrillaire du peptide beta-amyloide. |
| RU2011151069A (ru) | 2009-05-15 | 2013-06-20 | Чугаи Сейяку Кабусики Кайся | Анти-axl антитело |
| JP5762408B2 (ja) | 2009-08-13 | 2015-08-12 | クルセル ホランド ベー ヴェー | ヒト呼吸器合胞体ウイルス(rsv)に対する抗体および使用方法 |
| WO2011035205A2 (fr) | 2009-09-18 | 2011-03-24 | Calmune Corporation | Anticorps dirigés contre candida, leurs collectes et procédés d'utilisation |
| US10150808B2 (en) | 2009-09-24 | 2018-12-11 | Chugai Seiyaku Kabushiki Kaisha | Modified antibody constant regions |
| EP2501800A4 (fr) | 2009-11-17 | 2013-05-22 | Musc Found For Res Dev | Anticorps monoclonaux humains pour nucléoline humaine |
| GB0920944D0 (en) | 2009-11-30 | 2010-01-13 | Biotest Ag | Agents for treating disease |
| EP2543730B1 (fr) | 2010-03-04 | 2018-10-31 | Chugai Seiyaku Kabushiki Kaisha | Variante de région constante d'anticorps |
| FR2958936A1 (fr) | 2010-04-14 | 2011-10-21 | Sanofi Aventis | Proteine de fusion robo1-fc et son utilisation dans le traitement des tumeurs |
| US8906374B2 (en) | 2010-04-20 | 2014-12-09 | Cedars-Sinai Medical Center | Combination therapy with CD4 lymphocyte depletion and mTOR inhibitors |
| TWI539963B (zh) | 2010-07-09 | 2016-07-01 | 庫賽爾荷蘭公司 | 抗-人類呼吸道融合性病毒(rsv)抗體及其使用方法 |
| UY33578A (es) * | 2010-08-31 | 2012-03-30 | Sanofi Sa | PÉPTIDO O COMPLEJO PEPTÍDICO QUE SE UNE A INTEGRINA a(ALFA) Y MÉTODOS Y USOS QUE IMPLICAN A LOS MISMOS |
| EP2471543A1 (fr) | 2010-12-02 | 2012-07-04 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Induction de tolérance ou immunosuppression pour empêcher en particulier la réaction du greffon contre l'hôte (GvHD) par une pré-incubation de courte durée des suspensions de cellules transplantées, tissus ou organes revêtus par les ligands sur les molécules à la surface des cellules |
| CA2821969A1 (fr) | 2010-12-21 | 2012-06-28 | Recopharma Ab | Substituts de larme |
| WO2012088422A1 (fr) | 2010-12-22 | 2012-06-28 | Nektar Therapeutics | Conjugués promédicaments polymères à plusieurs bras de composés à base de taxane |
| US10894087B2 (en) | 2010-12-22 | 2021-01-19 | Nektar Therapeutics | Multi-arm polymeric prodrug conjugates of cabazitaxel-based compounds |
| UY33833A (es) | 2010-12-23 | 2012-07-31 | Sanofi Sa | Proteína de fusión Robo1-Fc para su uso en el tratamiento del hepatocarcinoma |
| HUE041335T2 (hu) | 2011-03-29 | 2019-05-28 | Roche Glycart Ag | Antitest FC-variánsok |
| US20140088021A1 (en) | 2011-05-27 | 2014-03-27 | Nektar Therapeutics | Water-Soluble Polymer-Linked Binding Moiety and Drug Compounds |
| RU2623122C2 (ru) | 2011-10-26 | 2017-06-22 | Новартис Тиргезундхайт АГ | Моноклональные антитела и способы их применения |
| ES2743401T3 (es) * | 2012-07-05 | 2020-02-19 | Hoffmann La Roche | Sistema de expresión y secreción |
| MX361337B (es) | 2012-07-13 | 2018-12-04 | Roche Glycart Ag | Anticuerpos biespecificos anti-factor de crecimiento endotelial vascular humano (vegf) / anti-angiopoyetina-2 humana (ang-2) y su uso en el tratamiento de enfermedades vasculares oculares. |
| AU2013335004B2 (en) | 2012-10-22 | 2018-06-28 | Oneness Biotech Co. LTD | Antibodies to interleukin-6 and uses thereof |
| CA2899206C (fr) | 2013-01-24 | 2019-07-09 | Transderm, Inc. | Compositions pour une administration transdermique d'inhibiteurs de mtor |
| WO2014135984A2 (fr) | 2013-03-07 | 2014-09-12 | Recopharma Ab | Dispositif revêtu par une protéine de fusion mucine glycosylée-immunoglobuline |
| US20160108122A1 (en) * | 2013-05-23 | 2016-04-21 | Idac Theranostics, Inc. | Therapeutic or prophylactic agent for immunodeficiency virus infection |
| US20160158352A1 (en) * | 2013-07-10 | 2016-06-09 | The United States of America, as represented by the Secretary, Department of Health & Human Servic | Apoptotic cell-mediated induction of antigen specific regulatory t-cells for the therapy of autoimmune diseases in animals and humans |
| CN105764922B (zh) | 2013-09-27 | 2020-07-17 | 中外制药株式会社 | 多肽异源多聚体的制备方法 |
| CN105979961B (zh) | 2014-02-05 | 2020-12-18 | 西达-赛奈医疗中心 | 用于治疗癌症和感染性疾病的方法和组合物 |
| RU2730590C2 (ru) | 2015-02-27 | 2020-08-24 | Чугаи Сейяку Кабусики Кайся | Композиция для лечения заболеваний, связанных с ил-6 |
| WO2016159213A1 (fr) | 2015-04-01 | 2016-10-06 | 中外製薬株式会社 | Procédé pour la production d'un hétéro-oligomère polypeptidique |
| CN106188292B (zh) * | 2015-05-05 | 2019-09-24 | 北京傲锐东源生物科技有限公司 | 抗cd4蛋白单克隆抗体及其用途 |
| CA3004288C (fr) | 2015-12-28 | 2025-05-27 | Chugai Seiyaku Kabushiki Kaisha | Méthode de promotion de l’efficacité d’épuration d’un polypeptide contenant la région fc |
| SG10201607778XA (en) | 2016-09-16 | 2018-04-27 | Chugai Pharmaceutical Co Ltd | Anti-Dengue Virus Antibodies, Polypeptides Containing Variant Fc Regions, And Methods Of Use |
| IL302385B2 (en) | 2017-01-06 | 2024-06-01 | Palvella Therapeutics Inc | Non-aqueous preparations of mTOR inhibitors and methods of use |
| EP3354278A1 (fr) | 2017-01-31 | 2018-08-01 | Sanofi | Effet de protection des cellules neuronales d'anticorps spécifiques de la forme protofibrillaire du peptide bêta-amyloïde |
| CN108690138A (zh) * | 2017-04-12 | 2018-10-23 | 鸿运华宁(杭州)生物医药有限公司 | 一种能与人cd19或cd20和人cd3结合的双特异性抗体及其应用 |
| JP7185884B2 (ja) | 2017-05-02 | 2022-12-08 | 国立研究開発法人国立精神・神経医療研究センター | Il-6及び好中球の関連する疾患の治療効果の予測及び判定方法 |
| WO2019160907A1 (fr) * | 2018-02-14 | 2019-08-22 | University Of Virginia Patent Foundation | Régulation des cellules t cd4 + pour traiter une infection à clostridium difficile |
| IL277375B2 (en) | 2018-03-15 | 2025-08-01 | Chugai Pharmaceutical Co Ltd | Anti-dengue virus antibodies having cross-reactivity to zika virus and methods of use |
| JP2021530463A (ja) | 2018-07-02 | 2021-11-11 | パルヴェラ セラピューティクス、インク. | mTOR阻害剤の無水組成物および使用方法 |
| CN113248612A (zh) * | 2020-02-13 | 2021-08-13 | 上海君实生物医药科技股份有限公司 | 抗pd-1抗体在治疗神经内分泌瘤中的用途 |
| CN113244386A (zh) * | 2020-02-13 | 2021-08-13 | 上海君实生物医药科技股份有限公司 | 抗pd-1抗体在治疗肿瘤中的用途 |
| CN115197320A (zh) * | 2021-04-07 | 2022-10-18 | 中美冠科生物技术(太仓)有限公司 | 新型抗cd4抗体 |
| EP4381081A1 (fr) | 2021-08-04 | 2024-06-12 | Sana Biotechnology, Inc. | Utilisation de vecteurs viraux ciblant cd4 |
| US20250059560A1 (en) | 2021-12-16 | 2025-02-20 | Sana Biotechnology, Inc. | Methods and systems of particle production |
| WO2023133595A2 (fr) | 2022-01-10 | 2023-07-13 | Sana Biotechnology, Inc. | Méthodes de dosage et d'administration ex vivo de particules lipidiques ou de vecteurs viraux ainsi que systèmes et utilisations associés |
| WO2023150647A1 (fr) | 2022-02-02 | 2023-08-10 | Sana Biotechnology, Inc. | Procédés d'administration et de dosage répétés de particules lipidiques ou de vecteurs viraux et systèmes et utilisations connexes |
| WO2023168426A1 (fr) | 2022-03-03 | 2023-09-07 | Enosi Therapeutics Corporation | Compositions et cellules contenant des mélanges de protéines de fusion oligo-trap (ofps) et leurs utilisations |
| US20250222027A1 (en) | 2022-04-01 | 2025-07-10 | Sana Biotechnology, Inc. | Cytokine receptor agonist and viral vector combination therapies |
| WO2024026377A1 (fr) | 2022-07-27 | 2024-02-01 | Sana Biotechnology, Inc. | Procédés de transduction utilisant un vecteur viral et des inhibiteurs de facteurs de restriction antiviraux |
| WO2024044655A1 (fr) | 2022-08-24 | 2024-02-29 | Sana Biotechnology, Inc. | Administration de protéines hétérologues |
| EP4590688A1 (fr) | 2022-09-21 | 2025-07-30 | Sana Biotechnology, Inc. | Particules lipidiques comprenant des glycoprotéines fixant des paramyxovirus variants et leurs utilisations |
| CN120569191A (zh) | 2022-11-23 | 2025-08-29 | 乔治亚大学研究基金公司 | 用于增加免疫应答的组合物及其使用方法 |
| EP4627096A1 (fr) | 2022-12-02 | 2025-10-08 | Sana Biotechnology, Inc. | Particules lipidiques avec cofusogènes et leurs procédés de production et d'utilisation |
| WO2024186690A2 (fr) | 2023-03-03 | 2024-09-12 | Enosi Therapeutics Corporation | Protéines de fusion oligo-pièges (ofp) et leurs utilisations |
| WO2024220597A2 (fr) | 2023-04-18 | 2024-10-24 | Sana Biotechnology, Inc. | Dosage numérique utilisant des gouttelettes pour détecter un vecteur lentiviral compétent pour la réplication |
| WO2024243340A1 (fr) | 2023-05-23 | 2024-11-28 | Sana Biotechnology, Inc. | Fusogènes en tandem et particules lipidiques associées |
| WO2025104604A1 (fr) | 2023-11-14 | 2025-05-22 | Janssen Pharmaceuticals, Inc. | Anticorps anti-virus respiratoire syncytial et leurs utilisations |
| GB202401501D0 (en) | 2024-02-05 | 2024-03-20 | T Balance Therapeutics Gmbh | Medical use of regulatory t cell activator |
| WO2025184529A1 (fr) | 2024-03-01 | 2025-09-04 | Sana Biotechnology, Inc. | Particules virales à présentation fusogène et compositions et procédés associés |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8308235D0 (en) * | 1983-03-25 | 1983-05-05 | Celltech Ltd | Polypeptides |
| US4816567A (en) * | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
| DE3883899T3 (de) | 1987-03-18 | 1999-04-22 | Sb2, Inc., Danville, Calif. | Geänderte antikörper. |
| RU2014845C1 (ru) * | 1987-03-23 | 1994-06-30 | Хайвер Лимитед | Способ получения вакцины против спида |
| US4978745A (en) | 1987-11-23 | 1990-12-18 | Centocor, Inc. | Immunoreactive heterochain antibodies |
| US4975369A (en) * | 1988-04-21 | 1990-12-04 | Eli Lilly And Company | Recombinant and chimeric KS1/4 antibodies directed against a human adenocarcinoma antigen |
| DE3814887C1 (fr) * | 1988-05-02 | 1989-09-21 | Medice Chem.-Pharm. Fabrik Puetter Gmbh & Co Kg, 5860 Iserlohn, De | |
| IL162181A (en) * | 1988-12-28 | 2006-04-10 | Pdl Biopharma Inc | A method of producing humanized immunoglubulin, and polynucleotides encoding the same |
| AU4964290A (en) * | 1989-01-18 | 1990-08-13 | President And Fellows Of Harvard College | Compositions and methods for treating or preventing aids, arc and hiv infection |
| US5690933A (en) * | 1989-05-31 | 1997-11-25 | Glaxo Wellcome Inc. | Monoclonal antibodies for inducing tolerance |
| GB8912497D0 (en) * | 1989-05-31 | 1989-07-19 | Cobbold Stephen P | Monoclonal antibodies |
| JPH0353894A (ja) * | 1989-07-21 | 1991-03-07 | Calpis Food Ind Co Ltd:The | 抗ヒトcd4ペプチドに対するモノクローナル抗体 |
| US5120642A (en) * | 1989-11-28 | 1992-06-09 | Coulter Corporation | Monoclonal antibody which distinguishes helper inducer and suppressor inducer cd4+ lymphocytes |
| US5308839A (en) * | 1989-12-04 | 1994-05-03 | The Research Foundation Of State University Of New York | Composition comprising non-steroidal anti-inflammatory agent tenidap and effectively non-antibacterial tetracycline |
| IE65341B1 (en) * | 1990-11-08 | 1995-10-18 | Fujisawa Pharmaceutical Co | Suspensions containing tricyclic compounds |
| JP3502093B2 (ja) * | 1991-07-15 | 2004-03-02 | ザ・ウエルカム・ファウンデーション・リミテッド | 抗体の製造 |
| US6136310A (en) * | 1991-07-25 | 2000-10-24 | Idec Pharmaceuticals Corporation | Recombinant anti-CD4 antibodies for human therapy |
| SK285960B6 (sk) | 1991-07-25 | 2007-12-06 | Biogen Idec Inc. | Rekombinantné protilátky na liečenie ľudí |
| US5756096A (en) * | 1991-07-25 | 1998-05-26 | Idec Pharmaceuticals Corporation | Recombinant antibodies for human therapy |
| MX9204374A (es) * | 1991-07-25 | 1993-03-01 | Idec Pharma Corp | Anticuerpo recombinante y metodo para su produccion. |
| ATE155043T1 (de) * | 1992-10-08 | 1997-07-15 | Kennedy Inst Of Rheumatology | Behandlung von autoimmun- und entzundungskrankheiten |
| US6024957A (en) * | 1993-06-02 | 2000-02-15 | Research Corporation Technologies, Inc. | Immunomodulators and methods for the prevention and reversal of organ transplant rejection using same |
| US5691183A (en) * | 1993-07-07 | 1997-11-25 | University Technology Corporation | CD4+ T-lymphoctye proteases and genes encoding said proteases |
-
1995
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- 1996-09-05 CA CA002231182A patent/CA2231182A1/fr not_active Abandoned
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- 1996-09-05 AU AU69162/96A patent/AU717674B2/en not_active Ceased
- 1996-09-05 DE DE69636760T patent/DE69636760T2/de not_active Expired - Lifetime
- 1996-09-05 WO PCT/US1996/014324 patent/WO1997009351A1/fr not_active Ceased
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