AU2003249014B2 - Compositions and methods for the diagnosis and treatment of tumor - Google Patents
Compositions and methods for the diagnosis and treatment of tumor Download PDFInfo
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- AU2003249014B2 AU2003249014B2 AU2003249014A AU2003249014A AU2003249014B2 AU 2003249014 B2 AU2003249014 B2 AU 2003249014B2 AU 2003249014 A AU2003249014 A AU 2003249014A AU 2003249014 A AU2003249014 A AU 2003249014A AU 2003249014 B2 AU2003249014 B2 AU 2003249014B2
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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
- C07K16/30—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
-
- 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
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
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- Biomedical Technology (AREA)
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- Proteomics, Peptides & Aminoacids (AREA)
- Genetics & Genomics (AREA)
- Hematology (AREA)
- Analytical Chemistry (AREA)
- Toxicology (AREA)
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- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Testing Resistance To Weather, Investigating Materials By Mechanical Methods (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US39499802P | 2002-07-09 | 2002-07-09 | |
| US60/394,998 | 2002-07-09 | ||
| PCT/US2003/021606 WO2004004662A2 (en) | 2002-07-09 | 2003-07-08 | Compositions and methods for the diagnosis and treatment of tumor |
Publications (2)
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| AU2003249014A1 AU2003249014A1 (en) | 2004-01-23 |
| AU2003249014B2 true AU2003249014B2 (en) | 2009-07-02 |
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|---|---|---|---|
| AU2003249014A Expired - Fee Related AU2003249014B2 (en) | 2002-07-09 | 2003-07-08 | Compositions and methods for the diagnosis and treatment of tumor |
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|---|---|
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| EP (1) | EP1572091A4 (enExample) |
| JP (1) | JP2006500009A (enExample) |
| AU (1) | AU2003249014B2 (enExample) |
| CA (1) | CA2491488A1 (enExample) |
| IL (1) | IL165950A0 (enExample) |
| WO (1) | WO2004004662A2 (enExample) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6737056B1 (en) | 1999-01-15 | 2004-05-18 | Genentech, Inc. | Polypeptide variants with altered effector function |
| US7183387B1 (en) | 1999-01-15 | 2007-02-27 | Genentech, Inc. | Polypeptide variants with altered effector function |
| KR101155191B1 (ko) | 1999-01-15 | 2012-06-13 | 제넨테크, 인크. | 효과기 기능이 변화된 폴리펩티드 변이체 |
| US20040132101A1 (en) | 2002-09-27 | 2004-07-08 | Xencor | Optimized Fc variants and methods for their generation |
| US7317091B2 (en) | 2002-03-01 | 2008-01-08 | Xencor, Inc. | Optimized Fc variants |
| US7662925B2 (en) | 2002-03-01 | 2010-02-16 | Xencor, Inc. | Optimized Fc variants and methods for their generation |
| US8188231B2 (en) | 2002-09-27 | 2012-05-29 | Xencor, Inc. | Optimized FC variants |
| KR100980065B1 (ko) * | 2002-09-27 | 2010-09-03 | 젠코어 인코포레이티드 | 최적화된 Fc 변이체 및 그의 제조 방법 |
| US8388955B2 (en) | 2003-03-03 | 2013-03-05 | Xencor, Inc. | Fc variants |
| US8084582B2 (en) | 2003-03-03 | 2011-12-27 | Xencor, Inc. | Optimized anti-CD20 monoclonal antibodies having Fc variants |
| US20090010920A1 (en) | 2003-03-03 | 2009-01-08 | Xencor, Inc. | Fc Variants Having Decreased Affinity for FcyRIIb |
| US9051373B2 (en) | 2003-05-02 | 2015-06-09 | Xencor, Inc. | Optimized Fc variants |
| US8101720B2 (en) | 2004-10-21 | 2012-01-24 | Xencor, Inc. | Immunoglobulin insertions, deletions and substitutions |
| US9714282B2 (en) | 2003-09-26 | 2017-07-25 | Xencor, Inc. | Optimized Fc variants and methods for their generation |
| US7276585B2 (en) | 2004-03-24 | 2007-10-02 | Xencor, Inc. | Immunoglobulin variants outside the Fc region |
| US20150010550A1 (en) | 2004-07-15 | 2015-01-08 | Xencor, Inc. | OPTIMIZED Fc VARIANTS |
| EP2314618A3 (en) | 2004-11-12 | 2011-10-19 | Xencor Inc. | Fc variants with altered binding to FcRn |
| US8546543B2 (en) | 2004-11-12 | 2013-10-01 | Xencor, Inc. | Fc variants that extend antibody half-life |
| US8802820B2 (en) | 2004-11-12 | 2014-08-12 | Xencor, Inc. | Fc variants with altered binding to FcRn |
| US8367805B2 (en) | 2004-11-12 | 2013-02-05 | Xencor, Inc. | Fc variants with altered binding to FcRn |
| DK1931709T3 (en) | 2005-10-03 | 2017-03-13 | Xencor Inc | FC VARIETIES WITH OPTIMIZED FC RECEPTOR BINDING PROPERTIES |
| JP4860703B2 (ja) | 2005-10-06 | 2012-01-25 | ゼンコー・インコーポレイテッド | 最適化された抗cd30抗体 |
| ES2402591T3 (es) | 2006-08-14 | 2013-05-07 | Xencor Inc. | Anticuerpos optimizados que seleccionan como diana CD19 |
| WO2008036688A2 (en) | 2006-09-18 | 2008-03-27 | Xencor, Inc. | Optimized antibodies that target hm1.24 |
| KR101616758B1 (ko) | 2007-12-26 | 2016-04-29 | 젠코어 인코포레이티드 | FcRn에 대한 변경된 결합성을 갖는 Fc 변이체 |
| SG187457A1 (en) * | 2008-01-11 | 2013-02-28 | Univ Tokyo | Anti-cldn6 antibody |
| US12492253B1 (en) | 2008-02-25 | 2025-12-09 | Xencor, Inc. | Anti-human C5 antibodies |
| US9493578B2 (en) | 2009-09-02 | 2016-11-15 | Xencor, Inc. | Compositions and methods for simultaneous bivalent and monovalent co-engagement of antigens |
| US8362210B2 (en) | 2010-01-19 | 2013-01-29 | Xencor, Inc. | Antibody variants with enhanced complement activity |
| KR20160044598A (ko) | 2011-03-29 | 2016-04-25 | 로슈 글리카트 아게 | 항체 Fc 변이체 |
| UA120029C2 (uk) | 2012-07-13 | 2019-09-25 | Рош Глікарт Аг | Спосіб зниження в'язкості біспецифічного антитіла до vegf/ang-2 та застосування такого антитіла для лікування судинних очних захворювань |
| IL315729A (en) | 2016-08-02 | 2024-11-01 | Visterra Inc | Fc region containing polypeptides and uses thereof |
| US11180535B1 (en) | 2016-12-07 | 2021-11-23 | David Gordon Bermudes | Saccharide binding, tumor penetration, and cytotoxic antitumor chimeric peptides from therapeutic bacteria |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1994018227A2 (en) * | 1993-02-04 | 1994-08-18 | Denzyme Aps | Improved method for the refolding of proteins |
| WO2002022677A2 (en) * | 2000-09-12 | 2002-03-21 | Consiglio Nazionale Delle Ricerche | Variants of allergenic proteins of the group 2 of dermatophagoides |
| WO2003086307A2 (en) * | 2002-04-12 | 2003-10-23 | The Board Of Trustees Of The University Of Arkansas | β2-MICROGLOBILIN (β2m) AND ANTI-β2m BINDING AGENTS AS ANTI-CANCER THERAPEUTICS |
-
2003
- 2003-07-08 CA CA002491488A patent/CA2491488A1/en not_active Abandoned
- 2003-07-08 WO PCT/US2003/021606 patent/WO2004004662A2/en not_active Ceased
- 2003-07-08 JP JP2004520117A patent/JP2006500009A/ja not_active Withdrawn
- 2003-07-08 US US10/521,053 patent/US20060062727A1/en not_active Abandoned
- 2003-07-08 EP EP03763455A patent/EP1572091A4/en not_active Withdrawn
- 2003-07-08 AU AU2003249014A patent/AU2003249014B2/en not_active Expired - Fee Related
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2004
- 2004-12-23 IL IL16595004A patent/IL165950A0/xx unknown
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2006
- 2006-09-29 US US11/537,292 patent/US20090181014A1/en not_active Abandoned
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1994018227A2 (en) * | 1993-02-04 | 1994-08-18 | Denzyme Aps | Improved method for the refolding of proteins |
| WO2002022677A2 (en) * | 2000-09-12 | 2002-03-21 | Consiglio Nazionale Delle Ricerche | Variants of allergenic proteins of the group 2 of dermatophagoides |
| WO2003086307A2 (en) * | 2002-04-12 | 2003-10-23 | The Board Of Trustees Of The University Of Arkansas | β2-MICROGLOBILIN (β2m) AND ANTI-β2m BINDING AGENTS AS ANTI-CANCER THERAPEUTICS |
Non-Patent Citations (9)
| Title |
|---|
| Cinningham et al. Biochemistry 1973, 12(24), 4811-4821 * |
| GeneCore AN AB021288 * |
| Klein et al. European Journal of Immunogenics 1996, 23(6), 417-423 * |
| Nomura et al. Journal of Urology 2007, 178(1), 292-300 * |
| Saito et al. Surgical Nerology 1988, 29(6), 435-442 * |
| Shields et al. J. Biol. Chem. 2001, 276(9), 6591-6604 * |
| Suzuki et al. Brain and Nerve 1987, 39(10), 965-970 * |
| Weiner et al. Seminars in Oncology 1999, 26(4, Suppl 12), 41-50 * |
| Yang Jing et al. Cancer Cell 2006, 10(4), 295-307 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2491488A1 (en) | 2004-01-15 |
| EP1572091A4 (en) | 2008-03-05 |
| US20090181014A1 (en) | 2009-07-16 |
| JP2006500009A (ja) | 2006-01-05 |
| IL165950A0 (en) | 2006-01-15 |
| US20060062727A1 (en) | 2006-03-23 |
| AU2003249014A1 (en) | 2004-01-23 |
| EP1572091A2 (en) | 2005-09-14 |
| WO2004004662A2 (en) | 2004-01-15 |
| WO2004004662A3 (en) | 2005-08-11 |
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