IL105366A - Vehicles for the treatment of diseases with interferon while reducing side effects - Google Patents
Vehicles for the treatment of diseases with interferon while reducing side effectsInfo
- Publication number
- IL105366A IL105366A IL10536693A IL10536693A IL105366A IL 105366 A IL105366 A IL 105366A IL 10536693 A IL10536693 A IL 10536693A IL 10536693 A IL10536693 A IL 10536693A IL 105366 A IL105366 A IL 105366A
- Authority
- IL
- Israel
- Prior art keywords
- ifn
- interferon
- use according
- treatment
- dose
- Prior art date
Links
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
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- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Organic Chemistry (AREA)
- Gastroenterology & Hepatology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Zoology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Oncology (AREA)
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- Communicable Diseases (AREA)
- Diabetes (AREA)
- Biochemistry (AREA)
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Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/868,916 US5372808A (en) | 1990-10-17 | 1992-04-15 | Methods and compositions for the treatment of diseases with consensus interferon while reducing side effect |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL105366A0 IL105366A0 (en) | 1993-08-18 |
| IL105366A true IL105366A (en) | 1999-11-30 |
Family
ID=25352556
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL10536693A IL105366A (en) | 1992-04-15 | 1993-04-13 | Vehicles for the treatment of diseases with interferon while reducing side effects |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US5372808A (cs) |
| EP (3) | EP0641359A4 (cs) |
| JP (2) | JPH07505894A (cs) |
| KR (1) | KR950701350A (cs) |
| CN (1) | CN1098103C (cs) |
| AT (1) | ATE254926T1 (cs) |
| AU (1) | AU683214B2 (cs) |
| CA (1) | CA2118121C (cs) |
| CZ (1) | CZ247194A3 (cs) |
| DE (1) | DE69333321T3 (cs) |
| DK (1) | DK0911033T4 (cs) |
| ES (1) | ES2210864T5 (cs) |
| HU (1) | HU227310B1 (cs) |
| IL (1) | IL105366A (cs) |
| MX (1) | MX9302160A (cs) |
| NO (1) | NO318643B1 (cs) |
| NZ (1) | NZ252871A (cs) |
| PT (1) | PT911033E (cs) |
| RO (1) | RO115700B1 (cs) |
| RU (1) | RU2128056C1 (cs) |
| SG (1) | SG52443A1 (cs) |
| SK (1) | SK284712B6 (cs) |
| TW (1) | TW265265B (cs) |
| UA (1) | UA44223C2 (cs) |
| WO (1) | WO1993021229A1 (cs) |
| ZA (1) | ZA932641B (cs) |
Families Citing this family (111)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6936694B1 (en) | 1982-05-06 | 2005-08-30 | Intermune, Inc. | Manufacture and expression of large structural genes |
| CA2006596C (en) * | 1988-12-22 | 2000-09-05 | Rika Ishikawa | Chemically-modified g-csf |
| US20020177688A1 (en) * | 1988-12-22 | 2002-11-28 | Kirin-Amgen, Inc., | Chemically-modified G-CSF |
| US6372206B1 (en) | 1989-03-02 | 2002-04-16 | University Of Florida | Orally-administered interferon-TAU compositions and methods |
| US5906816A (en) * | 1995-03-16 | 1999-05-25 | University Of Florida | Method for treatment of autoimmune diseases |
| US5372808A (en) † | 1990-10-17 | 1994-12-13 | Amgen Inc. | Methods and compositions for the treatment of diseases with consensus interferon while reducing side effect |
| US5676942A (en) * | 1992-02-10 | 1997-10-14 | Interferon Sciences, Inc. | Composition containing human alpha interferon species proteins and method for use thereof |
| ATE179330T1 (de) * | 1992-02-10 | 1999-05-15 | Interferon Sciences Inc | Verbesserte alpha-interferon-zusammensetzung und verfahren zu ihrer herstellung aus leukocyten des menschlichen peripheren blute |
| US6001589A (en) * | 1993-06-11 | 1999-12-14 | Pbl Biomedical Laboratories, Inc. | Method of identifying proteins modified by disease states related thereto |
| EP0751955A4 (en) | 1993-06-11 | 1998-10-07 | Pestka Biomedical Lab Inc | SUPER PROTEINS COMPRISING INTERFERONS AND INTERLEUKINS |
| AU1299295A (en) * | 1993-12-02 | 1995-06-19 | President And Fellows Of Harvard College | Improved efficacy of alpha-helical cytokines |
| ATE203415T1 (de) * | 1994-02-08 | 2001-08-15 | Amgen Inc | Orales verabreichungssystem von chemischmodifizierten proteinen g-csf |
| US20030053982A1 (en) * | 1994-09-26 | 2003-03-20 | Kinstler Olaf B. | N-terminally chemically modified protein compositions and methods |
| US5824784A (en) * | 1994-10-12 | 1998-10-20 | Amgen Inc. | N-terminally chemically modified protein compositions and methods |
| IL116730A0 (en) * | 1995-01-13 | 1996-05-14 | Amgen Inc | Chemically modified interferon |
| DE69636112T2 (de) * | 1995-08-30 | 2006-12-14 | Toray Industries, Inc. | Verfahren zum testen von myocarditis und cardiomyopathie |
| DK0858343T3 (da) | 1995-11-02 | 2004-05-10 | Schering Corp | Kontinuerlig lavdosis cytokininfusionsterapi |
| US5908621A (en) * | 1995-11-02 | 1999-06-01 | Schering Corporation | Polyethylene glycol modified interferon therapy |
| US5739313A (en) * | 1995-11-13 | 1998-04-14 | Regents Of The University Of Minnesota | Radionuclide labeling of vitamin B12 and coenzymes thereof |
| US20030026779A1 (en) * | 1999-10-15 | 2003-02-06 | Liming Yu | Treatment of tumors and viral infections with a hybrid conjugate of interferon and an immunoglobulin Fc |
| US5980884A (en) * | 1996-02-05 | 1999-11-09 | Amgen, Inc. | Methods for retreatment of patients afflicted with Hepatitis C using consensus interferon |
| AUPN976596A0 (en) * | 1996-05-09 | 1996-05-30 | Pharma Pacific Pty Ltd | Stimulation of host defence mechanisms |
| NZ332689A (en) | 1996-05-09 | 2000-07-28 | Pharma Pacific Pty Ltd | Using interferon to treat autoimmune, mycobacterial or neurodegenerative disease |
| US5831062A (en) * | 1996-05-09 | 1998-11-03 | Amgen Inc. | Use of the human interferon consensus gene for gene therapy |
| US20030190307A1 (en) * | 1996-12-24 | 2003-10-09 | Biogen, Inc. | Stable liquid interferon formulations |
| US6013253A (en) * | 1997-08-15 | 2000-01-11 | Amgen, Inc. | Treatment of multiple sclerosis using consensus interferon and IL-1 receptor antagonist |
| US6017876A (en) | 1997-08-15 | 2000-01-25 | Amgen Inc. | Chemical modification of granulocyte-colony stimulating factor (G-CSF) bioactivity |
| US6541033B1 (en) | 1998-06-30 | 2003-04-01 | Amgen Inc. | Thermosensitive biodegradable hydrogels for sustained delivery of leptin |
| WO2000018427A1 (en) * | 1998-09-29 | 2000-04-06 | Fleischmann W Robert | Methods of treating diseased cells |
| US6420339B1 (en) | 1998-10-14 | 2002-07-16 | Amgen Inc. | Site-directed dual pegylation of proteins for improved bioactivity and biocompatibility |
| US6451346B1 (en) * | 1998-12-23 | 2002-09-17 | Amgen Inc | Biodegradable pH/thermosensitive hydrogels for sustained delivery of biologically active agents |
| US6245740B1 (en) | 1998-12-23 | 2001-06-12 | Amgen Inc. | Polyol:oil suspensions for the sustained release of proteins |
| RU2140285C1 (ru) | 1999-01-25 | 1999-10-27 | Гапонюк Петр Яковлевич | Противовирусное средство - капли в нос "гриппферон" |
| ATE246202T1 (de) * | 1999-01-29 | 2003-08-15 | Hoffmann La Roche | Gcsf konjugate |
| US6806363B1 (en) | 1999-04-16 | 2004-10-19 | Mayo Foundation For Medical Education & Research | Cobalamin conjugates useful as antitumor agents |
| US8106098B2 (en) * | 1999-08-09 | 2012-01-31 | The General Hospital Corporation | Protein conjugates with a water-soluble biocompatible, biodegradable polymer |
| US7591995B2 (en) * | 1999-10-15 | 2009-09-22 | Mayo Foundation For Medical Education And Research | Cobalamin conjugates useful as imaging and therapeutic agents |
| MY164523A (en) | 2000-05-23 | 2017-12-29 | Univ Degli Studi Cagliari | Methods and compositions for treating hepatitis c virus |
| CA2410579C (en) | 2000-05-26 | 2010-04-20 | Jean-Pierre Sommadossi | Methods and compositions for treating flaviviruses and pestiviruses |
| US7105154B2 (en) * | 2000-07-19 | 2006-09-12 | Pepgen Corporation | Method of treatment using interferon-tau |
| US20030219405A1 (en) * | 2002-01-16 | 2003-11-27 | Yoshihiro Sokawa | Oral administration of interferon-tau |
| AU2002243438A1 (en) | 2000-10-25 | 2002-07-24 | Mayo Foundation For Medical Education And Research | Transcobalamin binding conjugates useful for treating abnormal cellular proliferation |
| WO2002044717A1 (en) * | 2000-12-01 | 2002-06-06 | Cornell Research Foundation | Animal model for flaviviridae infection |
| RU2179000C1 (ru) * | 2000-12-21 | 2002-02-10 | Тверская государственная медицинская академия | Способ комплексного лечения базалиом кожи |
| CN1245215C (zh) * | 2001-02-28 | 2006-03-15 | 四川省生物工程研究中心 | 重组高效复合干扰素用作乙型肝炎表面抗原和e抗原抑制剂 |
| US20060035327A1 (en) * | 2001-02-28 | 2006-02-16 | Guangwen Wei | Recombinant super-compound interferon and uses thereof |
| US8551469B2 (en) * | 2001-02-28 | 2013-10-08 | Superlab Far East Limited | Treatment of tumors and viral diseases with recombinant interferon alpha |
| US20050079579A1 (en) * | 2001-02-28 | 2005-04-14 | Guangwen Wei | Uses of spatial configuration to modulate protein function |
| US20030104996A1 (en) * | 2001-08-30 | 2003-06-05 | Tiansheng Li | L-methionine as a stabilizer for NESP/EPO in HSA-free formulations |
| JP2005508926A (ja) * | 2001-09-28 | 2005-04-07 | インターミューン インコーポレイテッド | 治療失敗例の患者においてｃ型肝炎ウイルス感染を治療するための方法 |
| PL369129A1 (en) * | 2001-09-28 | 2005-04-18 | Intermune, Inc. | Method for treating hepatitis c virus infection in treatment failure patients |
| WO2003026674A1 (en) * | 2001-09-28 | 2003-04-03 | Mayo Foundation For Medical Education And Research | Coadministration of transport protein with conjugated cobalamin to deliver agents |
| WO2003026589A2 (en) * | 2001-09-28 | 2003-04-03 | Idenix (Cayman) Limited | Methods and compositions for treating hepatitis c virus using 4'-modified nucleosides |
| US20050063949A1 (en) * | 2001-10-05 | 2005-03-24 | Gary Visor | Method of treating hepatitis virus infection with a multiphasic interferon delivery profile |
| EP1461067A1 (en) * | 2001-12-07 | 2004-09-29 | Intermune, Inc. | Compositions and method for treating hepatitis virus infection |
| US20040063912A1 (en) * | 2002-03-15 | 2004-04-01 | The Brigham And Women's Hospital, Inc. | Central airway administration for systemic delivery of therapeutics |
| US20030191056A1 (en) | 2002-04-04 | 2003-10-09 | Kenneth Walker | Use of transthyretin peptide/protein fusions to increase the serum half-life of pharmacologically active peptides/proteins |
| NZ537662A (en) | 2002-06-28 | 2007-10-26 | Idenix Cayman Ltd | 2'-C-methyl-3'-O-L-valine ester ribofuranosyl cytidine for treatment of flaviviridae infections |
| US7608600B2 (en) | 2002-06-28 | 2009-10-27 | Idenix Pharmaceuticals, Inc. | Modified 2′ and 3′-nucleoside prodrugs for treating Flaviviridae infections |
| BR0312278A (pt) | 2002-06-28 | 2007-06-19 | Idenix Cayman Ltd | éster 2'-c-metil-3'-o-l-valina de ribofuranosil citidina para tratamento de infecções por flaviviridae |
| ES2469569T3 (es) | 2002-06-28 | 2014-06-18 | Idenix Pharmaceuticals, Inc. | Prof�rmacos de nucle�sidos modificados en 2' y 3' para el tratamiento de infecciones de Flaviviridae |
| GB0215293D0 (en) * | 2002-07-03 | 2002-08-14 | Rega Foundation | Viral inhibitors |
| RU2005118421A (ru) | 2002-11-15 | 2006-01-20 | Айденикс (Кайман) Лимитед (Ky) | 2'-разветвленные нуклеозиды и мутация flaviviridae |
| US7314613B2 (en) | 2002-11-18 | 2008-01-01 | Maxygen, Inc. | Interferon-alpha polypeptides and conjugates |
| MXPA05006230A (es) | 2002-12-12 | 2005-09-20 | Idenix Cayman Ltd | Proceso para la produccion de nucleosidos ramificados-2'. |
| US20070072181A1 (en) * | 2003-02-28 | 2007-03-29 | Blatt Lawrence M | Combination therapy for treating alphavirus infection and liver fibrosis |
| US20070077225A1 (en) * | 2003-02-28 | 2007-04-05 | Blatt Lawrence M | Continuous delivery methods for treating hepatitis virus infection |
| PT3521297T (pt) | 2003-05-30 | 2022-03-18 | Gilead Pharmasset Llc | Análogos de nucleosídeo fluorados modificados |
| RU2006105640A (ru) * | 2003-07-25 | 2007-09-10 | Айденикс (Кайман) Лимитед (Ky) | Аналоги пуриновых нуклеозидов для лечения flaviviridae, включая гепатит с |
| US7585647B2 (en) * | 2003-08-28 | 2009-09-08 | Guangwen Wei | Nucleic acid encoding recombinant interferon |
| KR20060130009A (ko) | 2003-08-28 | 2006-12-18 | 휴이양테크 (유에스에이), 인크. | 변경된 공간 구조를 갖는 인터페론의 용도 |
| ES2473622T3 (es) * | 2003-08-28 | 2014-07-07 | Superlab Far East Limited | Usos de interferones con estructura espacial alterada |
| NZ546347A (en) | 2003-10-14 | 2009-11-27 | Intermune Inc | Macrocyclic carboxylic acids and acylsulfonamides as inhibitors of HCV replication |
| US7648998B2 (en) * | 2003-12-22 | 2010-01-19 | K.U. Leuven Research & Development | Imidazo 4,5-c pyridine compounds and methods of antiviral treatment |
| WO2005067889A1 (en) | 2003-12-30 | 2005-07-28 | Durect Corporation | Polymeric implants, preferably containing a mixture of peg and plg, for controlled release of active agents, preferably a gnrh |
| KR20070011451A (ko) | 2004-05-05 | 2007-01-24 | 예일 유니버시티 | 신규의 항바이러스 헬리오크산틴 유사체 |
| JP2008507298A (ja) | 2004-05-19 | 2008-03-13 | マキシジェン， インコーポレイテッド | インターフェロンαポリペプチドおよび結合体 |
| CN101023094B (zh) | 2004-07-21 | 2011-05-18 | 法莫赛特股份有限公司 | 烷基取代的2-脱氧-2-氟代-d-呋喃核糖基嘧啶和嘌呤及其衍生物的制备 |
| KR101177590B1 (ko) | 2004-09-14 | 2012-08-27 | 파마셋 인코포레이티드 | 2'-플루오로-2'-알킬 치환되거나 또는 다른 선택적으로치환된 리보퓨라노실 피리미딘 및 퓨린 및 그 유도체의제조 |
| EP1679065A1 (en) * | 2005-01-07 | 2006-07-12 | OctoPlus Sciences B.V. | Controlled release compositions for interferon based on PEGT/PBT block copolymers |
| CN101137391B (zh) * | 2005-03-09 | 2012-07-18 | 魏光文 | 重组高效复合干扰素的用途 |
| JP4516863B2 (ja) * | 2005-03-11 | 2010-08-04 | 株式会社ケンウッド | 音声合成装置、音声合成方法及びプログラム |
| BRPI0609809A2 (pt) | 2005-05-18 | 2011-10-11 | Maxygen Inc | polipeptìdeo isolado ou recombinante, conjugado, composição, polinucleotìdeo isolado ou recombinante, célula hospedeira, vetor, métodos para preparar o polipeptìdeo, para preparar um conjugado, para inibir replicação de um vìrus em células infectadas com o vìrus para reduzir o numero de cópias de um vìrus em células infectadas com o vìrus, para reduzir o nìvel de rna de hcv no soro de um paciente infectado com hcv, para reduzir o nìvel de dna de hbv em soro de um paciente infectado com hbv e para reduzir o nìvel de rna de hiv em soro de um paciente infectado com hiv, e, uso do polipeptìdeo ou do conjugado |
| ES2302402B1 (es) * | 2005-06-16 | 2009-05-08 | Proyecto De Biomedicina Cima, S.L. | Uso de una citoquina de la familia de interleuquina-6 en la preparacion de una composicion para administracion combinada con interferon-alfa. |
| US20090148407A1 (en) | 2005-07-25 | 2009-06-11 | Intermune, Inc. | Novel Macrocyclic Inhibitors of Hepatitis C Virus Replication |
| AU2006301966A1 (en) | 2005-10-11 | 2007-04-19 | Array Biopharma, Inc. | Compounds and methods for inhibiting hepatitis C viral replication |
| CU23432B6 (es) * | 2005-11-02 | 2009-10-16 | Ct Ingenieria Genetica Biotech | Formulaciones estabilizadas que contienen a los interferones gamma y alfa en proporciones potenciadoras |
| WO2007075876A2 (en) | 2005-12-23 | 2007-07-05 | Idenix Pharmaceuticals, Inc. | Process for preparing a synthetic intermediate for preparation of branched nucleosides |
| CA2648077A1 (en) * | 2006-03-31 | 2007-11-08 | Schering Corporation | Parenteral low dose type 1 interferons for bladder cancer |
| US7964580B2 (en) | 2007-03-30 | 2011-06-21 | Pharmasset, Inc. | Nucleoside phosphoramidate prodrugs |
| CN101525381B (zh) | 2008-03-04 | 2012-04-18 | 北京百川飞虹生物科技有限公司 | 一种重组复合干扰素及其表达载体的构建和表达 |
| TW200946541A (en) * | 2008-03-27 | 2009-11-16 | Idenix Pharmaceuticals Inc | Solid forms of an anti-HIV phosphoindole compound |
| US8173621B2 (en) | 2008-06-11 | 2012-05-08 | Gilead Pharmasset Llc | Nucleoside cyclicphosphates |
| MX2011006890A (es) * | 2008-12-23 | 2011-07-20 | Pharmasset Inc | Analogos de nucleosidos. |
| SG172359A1 (en) | 2008-12-23 | 2011-07-28 | Pharmasset Inc | Nucleoside phosphoramidates |
| AR074977A1 (es) | 2008-12-23 | 2011-03-02 | Pharmasset Inc | Sintesis de nucleosidos de purina |
| TWI598358B (zh) * | 2009-05-20 | 2017-09-11 | 基利法瑪席特有限責任公司 | 核苷磷醯胺 |
| US8618076B2 (en) | 2009-05-20 | 2013-12-31 | Gilead Pharmasset Llc | Nucleoside phosphoramidates |
| EP2440251A4 (en) * | 2009-06-09 | 2013-01-16 | Defyrus Inc | INTERFERON ADMINISTRATION FOR PROPHYLAXIS AGAINST PATHOGEN INFECTION OR TREATMENT OF PATHOGEN INFECTION |
| US20110027229A1 (en) | 2009-07-31 | 2011-02-03 | Medtronic, Inc. | Continuous subcutaneous administration of interferon-alpha to hepatitis c infected patients |
| CN102101886A (zh) | 2009-12-18 | 2011-06-22 | 四川辉阳生命工程股份有限公司 | 构象改变的重组干扰素晶体、其三维结构及应用 |
| PL3290428T3 (pl) | 2010-03-31 | 2022-02-07 | Gilead Pharmasset Llc | Tabletka zawierająca krystaliczny (S)-2-(((S)-(((2R,3R,4R,5R)-5-(2,4-diokso-3,4-dihydropirymidyn-1(2H)-ylo)-4-fluoro-3-hydroksy-4-metylotetrahydrofuran-2-ylo)metoksy)(fenoksy)fosforylo)amino)propanian izopropylu |
| DK2552930T3 (en) | 2010-03-31 | 2015-12-07 | Gilead Pharmasset Llc | Crystalline (S) -isopropyl 2 - (((S) - (((2R, 3R, 4R, 5R) -5- (2,4-dioxo-3,4-DIHYDROPYRIMIDIN- 1- (2 H) -yl) - 4-fluoro-3-hydroxy-4-methyltetrahydrofuran-2-yl) methoxy) (phenoxy) phosphoryl) amino) propanoate |
| US20120123338A1 (en) | 2010-06-16 | 2012-05-17 | Medtronic, Inc. | Damping systems for stabilizing medications in drug delivery devices |
| WO2012050925A2 (en) | 2010-09-28 | 2012-04-19 | Amylin Pharmaceuticals, Inc. | Highly soluble leptins |
| AR084044A1 (es) | 2010-11-30 | 2013-04-17 | Pharmasset Inc | Compuestos 2’-espiro-nucleosidos |
| BRPI1107312B1 (pt) * | 2011-11-25 | 2021-09-08 | Universidade Federal De Santa Catarina | Composto de acil-hidrazona |
| US8889159B2 (en) | 2011-11-29 | 2014-11-18 | Gilead Pharmasset Llc | Compositions and methods for treating hepatitis C virus |
| US8809354B2 (en) | 2011-12-31 | 2014-08-19 | Sheikh Riazuddin | 3-amino-2-(4-nitrophenyl)-4-(3H)-quinazolinone or derivatives thereof for treating or preventing antiviral infections |
| TWI726291B (zh) * | 2013-01-07 | 2021-05-01 | 英屬維爾京群島商遠東超級實驗室有限公司 | 通過干擾素的經皮和/或經粘膜給藥治療骨癌、皮膚癌、皮下癌、粘膜癌和/或粘膜下癌的方法和組合物 |
| PL3038601T3 (pl) | 2013-08-27 | 2020-08-24 | Gilead Pharmasset Llc | Formulacja złożona dwóch związków przeciwwirusowych |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES506955A0 (es) † | 1980-11-10 | 1983-02-01 | Genentech Inc | Un procedimiento para producir un polipeptido antiviral. |
| US6936694B1 (en) † | 1982-05-06 | 2005-08-30 | Intermune, Inc. | Manufacture and expression of large structural genes |
| SE8502430L (sv) † | 1985-05-15 | 1986-11-16 | Kabivitrum Ab | En cdna-molekyl som kodar for expressionen av en polypeptid av typen interferon alfa, en bakteriell eller celluler verd transformerad med en sadan molekyl och en polypeptid som uppvisar interferonaktivetet framstelld me |
| ATE78262T1 (de) † | 1985-06-11 | 1992-08-15 | Ciba Geigy Ag | Hybrid-interferone. |
| US5372808A (en) † | 1990-10-17 | 1994-12-13 | Amgen Inc. | Methods and compositions for the treatment of diseases with consensus interferon while reducing side effect |
| JP3496937B2 (ja) * | 1990-10-17 | 2004-02-16 | アムジエン・インコーポレーテツド | コンセンサスヒトインターフェロンを含有する細胞増殖障害治療用の医用組成物 |
-
1992
- 1992-04-15 US US07/868,916 patent/US5372808A/en not_active Expired - Lifetime
-
1993
- 1993-04-13 IL IL10536693A patent/IL105366A/en not_active IP Right Cessation
- 1993-04-14 EP EP93912363A patent/EP0641359A4/en not_active Withdrawn
- 1993-04-14 JP JP5518710A patent/JPH07505894A/ja active Pending
- 1993-04-14 DE DE69333321T patent/DE69333321T3/de not_active Expired - Lifetime
- 1993-04-14 MX MX9302160A patent/MX9302160A/es unknown
- 1993-04-14 SG SG1996004598A patent/SG52443A1/en unknown
- 1993-04-14 NZ NZ252871A patent/NZ252871A/xx not_active IP Right Cessation
- 1993-04-14 SK SK1247-94A patent/SK284712B6/sk not_active IP Right Cessation
- 1993-04-14 EP EP99100197A patent/EP0911033B2/en not_active Expired - Lifetime
- 1993-04-14 PT PT99100197T patent/PT911033E/pt unknown
- 1993-04-14 DK DK99100197.5T patent/DK0911033T4/da active
- 1993-04-14 WO PCT/US1993/004471 patent/WO1993021229A1/en not_active Ceased
- 1993-04-14 CA CA002118121A patent/CA2118121C/en not_active Expired - Lifetime
- 1993-04-14 HU HU9402979A patent/HU227310B1/hu unknown
- 1993-04-14 ES ES99100197T patent/ES2210864T5/es not_active Expired - Lifetime
- 1993-04-14 RU RU94046278A patent/RU2128056C1/ru active
- 1993-04-14 EP EP03026956A patent/EP1419782A1/en not_active Withdrawn
- 1993-04-14 AU AU42934/93A patent/AU683214B2/en not_active Expired
- 1993-04-14 AT AT99100197T patent/ATE254926T1/de active
- 1993-04-14 RO RO94-01665A patent/RO115700B1/ro unknown
- 1993-04-14 CZ CZ942471A patent/CZ247194A3/cs unknown
- 1993-04-14 UA UA94119017A patent/UA44223C2/uk unknown
- 1993-04-15 CN CN93105702A patent/CN1098103C/zh not_active Expired - Lifetime
- 1993-04-15 ZA ZA932641A patent/ZA932641B/xx unknown
- 1993-10-28 TW TW082109006A patent/TW265265B/zh not_active IP Right Cessation
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1994
- 1994-10-14 KR KR1019940703662A patent/KR950701350A/ko active Granted
- 1994-10-14 NO NO19943901A patent/NO318643B1/no not_active IP Right Cessation
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2004
- 2004-04-30 JP JP2004136025A patent/JP2005029561A/ja active Pending
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