TR201806761T4 - THE USE OF ALL IN THE PREPARATION OF A MEDICINE FOR THE TREATMENT OF IRON HOMEOSTASIS DISORDERS. - Google Patents
THE USE OF ALL IN THE PREPARATION OF A MEDICINE FOR THE TREATMENT OF IRON HOMEOSTASIS DISORDERS. Download PDFInfo
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- TR201806761T4 TR201806761T4 TR2018/06761T TR201806761T TR201806761T4 TR 201806761 T4 TR201806761 T4 TR 201806761T4 TR 2018/06761 T TR2018/06761 T TR 2018/06761T TR 201806761 T TR201806761 T TR 201806761T TR 201806761 T4 TR201806761 T4 TR 201806761T4
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- 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
- G01N33/90—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving iron binding capacity of blood
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
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- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Gastroenterology & Hepatology (AREA)
- Epidemiology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Biomedical Technology (AREA)
- Zoology (AREA)
- Molecular Biology (AREA)
- Cardiology (AREA)
- Endocrinology (AREA)
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- Obesity (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP01401377 | 2001-05-25 | ||
| EP01401537A EP1262187A1 (en) | 2001-05-25 | 2001-06-14 | Use of hepcidin for preparing a medicament for treating disorders of iron homeostasis |
| EP02290795 | 2002-03-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TR201806761T4 true TR201806761T4 (en) | 2018-06-21 |
Family
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| Application Number | Title | Priority Date | Filing Date |
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| TR2018/06761T TR201806761T4 (en) | 2001-05-25 | 2002-05-24 | THE USE OF ALL IN THE PREPARATION OF A MEDICINE FOR THE TREATMENT OF IRON HOMEOSTASIS DISORDERS. |
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| Country | Link |
|---|---|
| US (4) | US7169758B2 (https=) |
| EP (2) | EP1392345B2 (https=) |
| JP (4) | JP4944360B2 (https=) |
| CN (2) | CN1612746B (https=) |
| AT (1) | ATE427114T1 (https=) |
| AU (1) | AU2002321105A1 (https=) |
| CA (1) | CA2448382C (https=) |
| CY (1) | CY1120241T1 (https=) |
| DE (1) | DE60231804D1 (https=) |
| ES (2) | ES2326469T5 (https=) |
| TR (1) | TR201806761T4 (https=) |
| WO (1) | WO2002098444A2 (https=) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JP4944360B2 (ja) * | 2001-05-25 | 2012-05-30 | アンスティテュ ナシオナル ド ラ サント エ ド ラ ルシュルシェ メディカル（アンセルム） | 鉄ホメオスタシスの障害を治療するための医薬品を製造するためのヘプシジンの使用 |
| CA2506668C (en) | 2002-11-19 | 2014-08-19 | Drg International, Inc. | Diagnostic method for diseases by screening for hepcidin in human or animal tissues, blood or body fluids and therapeutic uses therefor |
| US7411048B2 (en) | 2002-11-19 | 2008-08-12 | Drg International, Inc. | Diagnostic method for diseases by screening for hepcidin in human or animal tissues, blood or body fluids |
| US8017737B2 (en) | 2002-11-19 | 2011-09-13 | Hasan Kulaksiz | Diagnostic methods for diseases by screening for hepcidin in human or animal tissues, blood or body fluids; monoclonal antibodies specific to human hepcidin and associated uses therefor |
| DE10349124A1 (de) | 2003-10-22 | 2005-05-19 | Roche Diagnostics Gmbh | Differenzialdiagnostik mit Hepcidin |
| US20060063208A1 (en) | 2004-08-02 | 2006-03-23 | Woolf Clifford J | DRG11-responsive (DRAGON) gene and uses thereof |
| KR100679100B1 (ko) * | 2004-10-29 | 2007-02-06 | 엘지.필립스 엘시디 주식회사 | 수평 전계 인가형 액정 표시 패널 및 그 제조방법 |
| US7968091B2 (en) | 2005-02-16 | 2011-06-28 | The General Hospital Corporation | Methods and compositions to regulate iron metabolism |
| WO2007120883A2 (en) * | 2006-04-12 | 2007-10-25 | Isis Pharmaceuticals, Inc. | Compositions and their uses directed to hepcidin |
| MX2009000685A (es) * | 2006-07-21 | 2009-01-30 | Amgen Inc | Metodo para detectar y/o cuantificar hepcidina en una muestra. |
| AU2007299629C1 (en) | 2006-09-21 | 2012-05-10 | Alnylam Pharmaceuticals, Inc. | Compositions and methods for inhibiting expression of the HAMP gene |
| US20110053268A1 (en) * | 2006-10-17 | 2011-03-03 | Naohisa Tomosugi | Method for diagnosis of abnormal iron metabolism using active hepcidin as indicator |
| TW201307390A (zh) * | 2007-02-02 | 2013-02-16 | Amgen Inc | 海帕西啶（ｈｅｐｃｉｄｉｎ）、海帕西啶拮抗劑及使用方法 |
| WO2008124768A1 (en) | 2007-04-09 | 2008-10-16 | The General Hospital Corporation | Hemojuvelin fusion proteins and uses thereof |
| WO2008146903A1 (ja) * | 2007-05-31 | 2008-12-04 | Naohisa Tomosugi | 活性型ヘプシジンを指標とした、急性虚血性疾患の診断方法 |
| WO2009044284A1 (en) | 2007-10-02 | 2009-04-09 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | Antibodies specific for human hepcidin |
| WO2009055078A2 (en) | 2007-10-26 | 2009-04-30 | University Of Utah Research Foundation | Identification of the hepcidin binding site on ferroportin |
| PE20091261A1 (es) * | 2007-11-02 | 2009-08-17 | Lilly Co Eli | Anticuerpos anti-hepcidina |
| CA2722600C (en) | 2008-05-01 | 2014-01-21 | Amgen Inc. | Anti-hepcidin antibodies and methods of use |
| EA201170312A1 (ru) * | 2008-08-06 | 2012-03-30 | Эли Лилли Энд Компани | Селективные антитела к гепцидину-25 и их применение |
| US20100068737A1 (en) * | 2008-09-16 | 2010-03-18 | University Of Tennessee Research Foundation | Enzyme-linked Immunosorbent Assay (ELISA) for Canine Hepcidin |
| JP6018753B2 (ja) | 2008-11-13 | 2016-11-02 | ザ・ジェネラル・ホスピタル・コーポレイションＴｈｅ Ｇｅｎｅｒａｌ Ｈｏｓｐｉｔａｌ Ｃｏｒｐｏｒａｔｉｏｎ | Ｂｍｐ−６の調節によって鉄の恒常性を制御するための方法および組成物 |
| US8999935B2 (en) * | 2009-02-11 | 2015-04-07 | New York University | Treatment of osteoporosis in peri- and post-menopausal women with hepcidin |
| DE102009034150A1 (de) | 2009-07-20 | 2011-01-27 | Fresenius Medical Care Deutschland Gmbh | Adsorbens zur Adsorption von Hepcidin |
| AR077892A1 (es) | 2009-08-20 | 2011-09-28 | Vifor Int Ag | Quinolinas antagonistas de la hepcidina |
| AR077958A1 (es) | 2009-08-27 | 2011-10-05 | Vifor Int Ag | Quinoxalinonas antagonistas de la hepcidina |
| AR077999A1 (es) | 2009-09-02 | 2011-10-05 | Vifor Int Ag | Antagonistas de pirimidin y triazin-hepcidina |
| JP2013503835A (ja) | 2009-09-07 | 2013-02-04 | ヴィフォール （インターナショナル） アクチェンゲゼルシャフト | 新規なエタンジアミン系ヘプシジン拮抗薬 |
| TW201111379A (en) | 2009-09-09 | 2011-04-01 | Vifor Int Ag | Novel thiazole-and oxazole-hepcidine-antagonists |
| US20120214803A1 (en) | 2011-02-18 | 2012-08-23 | Vifor (International) Ag | Novel Sulfonaminoquinoline Hepcidin Antagonists |
| EP2723861A4 (en) | 2011-06-21 | 2014-12-10 | Alnylam Pharmaceuticals Inc | COMPOSITIONS AND METHODS FOR INHIBITING HEPCIDINE ANTIMICROBIAL PEPTIDE (HAMP) OR THE ASSOCIATED GENE EXPRESSION |
| EP2574669B1 (en) * | 2011-06-29 | 2018-10-17 | Kabushiki Kaisha Dnaform | Biological sample pretreatment method, method for detecting rna, and pretreatment kit |
| EP2780364A2 (en) | 2011-11-18 | 2014-09-24 | Eleven Biotherapeutics, Inc. | Proteins with improved half-life and other properties |
| US9657098B2 (en) | 2013-03-15 | 2017-05-23 | Intrinsic Lifesciences, Llc | Anti-hepcidin antibodies and uses thereof |
| EP2976085A1 (en) | 2013-03-21 | 2016-01-27 | INSERM - Institut National de la Santé et de la Recherche Médicale | Method and pharmaceutical composition for use in the treatment of chronic liver diseases associated with a low hepcidin expression |
| AU2015321462B2 (en) | 2014-09-22 | 2020-04-30 | Intrinsic Lifesciences Llc | Humanized anti-hepcidin antibodies and uses thereof |
| US10098878B2 (en) | 2014-10-10 | 2018-10-16 | The Board Of Regents Of The University Of Texas System | HIF-2α inhibitors for treating iron overload disorders |
| AU2017205633A1 (en) * | 2016-01-08 | 2018-08-16 | La Jolla Pharmaceutial Company | Methods of administering hepcidin |
| WO2018165186A1 (en) * | 2017-03-07 | 2018-09-13 | Intrinsic Lifesciences Llc | Assessment of chronic iron deficiency |
| WO2019165252A1 (en) * | 2018-02-23 | 2019-08-29 | La Jolla Pharmaceutical Company | Compositions comprising hepcidin and methods of use thereof |
| US12011489B2 (en) | 2022-03-30 | 2024-06-18 | Christopher Key | Compositions and methods for treating inflammatory disease |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
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| FR2766207B1 (fr) * | 1997-07-11 | 2000-12-08 | Rhone Poulenc Agrochimie | Gene chimere codant pour la drosomycine, vecteur le contenant pour la transformation des cellules vegetales et plantes transformees obtenues resistantes aux maladies |
| FR2770853B1 (fr) * | 1997-11-07 | 1999-12-31 | Rhone Poulenc Agrochimie | Gene codant pour la thanatine, vecteur le contenant et plantes transformees obtenues resistantes aux maladies |
| US7109292B2 (en) * | 1999-03-08 | 2006-09-19 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
| AU3269399A (en) * | 1999-03-22 | 2000-10-09 | Universitat Zurich | Transforming growth factor (tfg) beta superfamily antagonists |
| JP4944360B2 (ja) * | 2001-05-25 | 2012-05-30 | アンスティテュ ナシオナル ド ラ サント エ ド ラ ルシュルシェ メディカル（アンセルム） | 鉄ホメオスタシスの障害を治療するための医薬品を製造するためのヘプシジンの使用 |
| CA2506668C (en) † | 2002-11-19 | 2014-08-19 | Drg International, Inc. | Diagnostic method for diseases by screening for hepcidin in human or animal tissues, blood or body fluids and therapeutic uses therefor |
| US8017737B2 (en) † | 2002-11-19 | 2011-09-13 | Hasan Kulaksiz | Diagnostic methods for diseases by screening for hepcidin in human or animal tissues, blood or body fluids; monoclonal antibodies specific to human hepcidin and associated uses therefor |
| US7411048B2 (en) * | 2002-11-19 | 2008-08-12 | Drg International, Inc. | Diagnostic method for diseases by screening for hepcidin in human or animal tissues, blood or body fluids |
| US7968091B2 (en) * | 2005-02-16 | 2011-06-28 | The General Hospital Corporation | Methods and compositions to regulate iron metabolism |
| CN101522022B (zh) * | 2006-09-16 | 2013-05-08 | 大豆实验室公司 | 利用大豆肽降低总胆固醇水平和ldl胆固醇水平的产品和方法 |
| TW201307390A (zh) † | 2007-02-02 | 2013-02-16 | Amgen Inc | 海帕西啶（ｈｅｐｃｉｄｉｎ）、海帕西啶拮抗劑及使用方法 |
| WO2009044284A1 (en) † | 2007-10-02 | 2009-04-09 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | Antibodies specific for human hepcidin |
| WO2009097461A1 (en) | 2008-01-29 | 2009-08-06 | Neoguide Systems Inc. | Apparatus and methods for automatically controlling an endoscope |
| WO2013086143A1 (en) | 2011-12-09 | 2013-06-13 | The Regents Of The University Of California | Modified mini-hepcidin peptides and methods of using thereof |
| CN102245626A (zh) † | 2008-12-05 | 2011-11-16 | 加利福尼亚大学董事会 | 微型铁调素肽及其使用方法 |
| US9315545B2 (en) | 2014-04-07 | 2016-04-19 | Merganser Biotech, Inc. | Hepcidin mimetic peptides and uses thereof |
| KR20170043509A (ko) | 2014-06-27 | 2017-04-21 | 프로타고니스트 테라퓨틱스, 인코포레이티드 | 헵시딘 및 미니-헵시딘 유사체 및 그의 용도 |
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- 2002-05-24 WO PCT/EP2002/006924 patent/WO2002098444A2/en not_active Ceased
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- 2002-05-24 CA CA2448382A patent/CA2448382C/en not_active Expired - Lifetime
- 2002-05-24 EP EP02754742.1A patent/EP1392345B2/en not_active Expired - Lifetime
- 2002-05-24 CN CN028148150A patent/CN1612746B/zh not_active Expired - Fee Related
- 2002-05-24 DE DE60231804T patent/DE60231804D1/de not_active Expired - Lifetime
- 2002-05-24 EP EP09004579.0A patent/EP2186524B1/en not_active Expired - Lifetime
- 2002-05-24 AT AT02754742T patent/ATE427114T1/de not_active IP Right Cessation
- 2002-05-24 ES ES02754742.1T patent/ES2326469T5/es not_active Expired - Lifetime
- 2002-05-24 US US10/478,987 patent/US7169758B2/en not_active Expired - Lifetime
- 2002-05-24 CN CN201010232752.2A patent/CN101884780B/zh not_active Expired - Fee Related
- 2002-05-24 TR TR2018/06761T patent/TR201806761T4/en unknown
- 2002-05-24 ES ES09004579.0T patent/ES2693050T3/es not_active Expired - Lifetime
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2006
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2018
- 2018-05-18 CY CY20181100516T patent/CY1120241T1/el unknown
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