PT107925A - Tratamento de combinação de daa (eg. com abt-072 ou abt-333) para utilização no tratamento de hcv - Google Patents
Tratamento de combinação de daa (eg. com abt-072 ou abt-333) para utilização no tratamento de hcv Download PDFInfo
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- PT107925A PT107925A PT107925A PT10792512A PT107925A PT 107925 A PT107925 A PT 107925A PT 107925 A PT107925 A PT 107925A PT 10792512 A PT10792512 A PT 10792512A PT 107925 A PT107925 A PT 107925A
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- treatment
- hcv
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Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US10201584B1 (en) | 2011-05-17 | 2019-02-12 | Abbvie Inc. | Compositions and methods for treating HCV |
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| US9629841B2 (en) * | 2012-10-18 | 2017-04-25 | Abbvie Inc. | Formulations of pyrimidinedione derivative compounds |
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| SI2968301T1 (sl) | 2013-03-14 | 2017-07-31 | Abb Vie Inc. | Kombinacija dveh antivirusnih sredstev za zdravljenje hepatitisa C |
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| CN105451736A (zh) * | 2013-07-02 | 2016-03-30 | 艾伯维公司 | 用于治疗hcv的方法 |
| US20150023913A1 (en) | 2013-07-02 | 2015-01-22 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
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| US9775831B2 (en) | 2013-07-17 | 2017-10-03 | Bristol-Myers Squibb Company | Combinations comprising biphenyl derivatives for use in the treatment of HCV |
| SI3038601T1 (sl) | 2013-08-27 | 2020-07-31 | Gilead Pharmasset Llc | Formulacija kombinacije dveh protivirusnih spojin |
| US20150141351A1 (en) * | 2013-11-18 | 2015-05-21 | AbbVie Deutschland GmbH & Co. KG | Solid Pharmaceutical Compositions |
| WO2015095572A1 (en) * | 2013-12-19 | 2015-06-25 | Abbvie Inc. | Methods for treating liver transplant recipients |
| EP3089757A1 (en) | 2014-01-03 | 2016-11-09 | AbbVie Inc. | Solid antiviral dosage forms |
| CN106413711A (zh) | 2014-04-02 | 2017-02-15 | 艾伯维公司 | 治疗hcv的方法 |
| US11311519B2 (en) | 2014-05-01 | 2022-04-26 | Eiger Biopharmaceuticals, Inc. | Treatment of hepatitis delta virus infection |
| US10076512B2 (en) | 2014-05-01 | 2018-09-18 | Eiger Biopharmaceuticals, Inc. | Treatment of hepatitis delta virus infection |
| WO2016089814A1 (en) | 2014-12-02 | 2016-06-09 | Concert Pharmaceuticals, Inc. | Deuterated analogues of daclatasvir |
| JP2017536403A (ja) * | 2014-12-04 | 2017-12-07 | アイガー・バイオファーマシューティカルズ・インコーポレイテッドEiger Biopharmaceuticals, Inc. | デルタ肝炎ウイルス感染の治療 |
| EP3227319B1 (en) | 2014-12-04 | 2019-11-27 | Novartis AG | Methods and compositions using klotho variant polypeptides |
| CN104546780A (zh) * | 2014-12-12 | 2015-04-29 | 安徽一灵药业有限公司 | 一种达卡他韦薄膜包衣片制剂及其制备方法 |
| WO2016172342A1 (en) | 2015-04-21 | 2016-10-27 | Eiger Biopharmaceuticals, Inc. | Pharmaceutical compositions comprising lonafarnib and ritonavir |
| US20160375017A1 (en) | 2015-06-26 | 2016-12-29 | Abbvie Inc. | Solid Pharmaceutical Compositions for Treating HCV |
| WO2017004053A1 (en) * | 2015-06-29 | 2017-01-05 | Abbvie Inc. | Methods for treating hcv |
| US20180177779A1 (en) | 2015-07-08 | 2018-06-28 | Abbvie Inc. | Methods for Treating HCV |
| US10617675B2 (en) | 2015-08-06 | 2020-04-14 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| CN109689063A (zh) | 2016-04-28 | 2019-04-26 | 埃默里大学 | 含有炔烃的核苷酸和核苷治疗组合物及其相关用途 |
| CA2994496A1 (en) | 2017-02-14 | 2018-08-14 | Abbvie Inc. | Methods for treating hcv |
| CA2981993A1 (en) | 2017-08-02 | 2019-02-02 | Abbvie Inc. | Methods for treating hcv |
| JP2020536909A (ja) | 2017-10-12 | 2020-12-17 | アッヴィ・インコーポレイテッド | Hcvを処置するための方法 |
Family Cites Families (403)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5026687A (en) | 1990-01-03 | 1991-06-25 | The United States Of America As Represented By The Department Of Health And Human Services | Treatment of human retroviral infections with 2',3'-dideoxyinosine alone and in combination with other antiviral compounds |
| AU4671193A (en) | 1992-07-13 | 1994-01-31 | Kenneth E. Sherman | Composition and method of treating hepatitis b |
| US6107027A (en) | 1994-12-14 | 2000-08-22 | University Of Washington | Ribozymes for treating hepatitis C |
| GB9505025D0 (en) | 1995-03-13 | 1995-05-03 | Medical Res Council | Chemical compounds |
| US6387365B1 (en) | 1995-05-19 | 2002-05-14 | Schering Corporation | Combination therapy for chronic hepatitis C infection |
| US5980884A (en) | 1996-02-05 | 1999-11-09 | Amgen, Inc. | Methods for retreatment of patients afflicted with Hepatitis C using consensus interferon |
| GB9605293D0 (en) | 1996-03-13 | 1996-05-15 | Glaxo Group Ltd | Medicaments |
| US5922757A (en) | 1996-09-30 | 1999-07-13 | The Regents Of The University Of California | Treatment and prevention of hepatic disorders |
| AU5157998A (en) | 1996-11-01 | 1998-05-29 | Thomas Najarian | Methods and compositions for treatment of hepatitis c infection |
| IL119833A (en) | 1996-12-15 | 2001-01-11 | Lavie David | Hypericum perforatum extracts for the preparation of pharmaceutical compositions for the treatment of hepatitis |
| US6010890A (en) | 1997-04-29 | 2000-01-04 | New York Blood Center, Inc. | Method for viral inactivation and compositions for use in same |
| US6103706A (en) | 1997-04-29 | 2000-08-15 | New York Blood Center, Inc. | Methods for treating viral infections |
| US6143752A (en) | 1997-08-01 | 2000-11-07 | Oren; Ran | Method for preventing or arresting liver damage in humans |
| DE69801970T2 (de) | 1997-09-21 | 2002-06-13 | Schering Corp., Kenilworth | Kombinationstherapie zur Entfernung von nachweisbarer HCV-RNS in Patienten mit chronischer Hepatitis C-Infektion |
| JP3838034B2 (ja) | 1997-10-13 | 2006-10-25 | 大塚製薬株式会社 | C型肝炎治療効果の改善剤及びその応用 |
| FR2771637B1 (fr) | 1997-12-01 | 2003-10-24 | Hutchinson | Utilisation d'un halogenure de dialkyldialkylammonium par voie parenterale dans les infections bacteriennes et virales |
| CN1290168A (zh) | 1997-12-11 | 2001-04-04 | 牛津大学院长校长专家委员会 | 膜相关病毒复制的抑制 |
| CA2313049A1 (en) | 1997-12-17 | 1999-06-24 | Cornell Research Foundation, Inc. | Cyclooxygenase-2 inhibition |
| US7462605B2 (en) | 1998-01-23 | 2008-12-09 | Celmed Oncology (Usa), Inc. | Phosphoramidate compounds and methods of use |
| CA2326535A1 (en) | 1998-03-27 | 1999-10-07 | Regents Of The University Of Minnesota | Nucleosides with antiviral and anticancer activity |
| JP2000007578A (ja) | 1998-06-24 | 2000-01-11 | Hiroaki Okushin | C型肝炎ウイルスの陰性化のための投薬システム |
| ATE312843T1 (de) | 1998-07-01 | 2005-12-15 | Debiopharm Sa | Neues cyclosporin mit verbesserter wirkung |
| RU2158604C2 (ru) | 1998-07-03 | 2000-11-10 | Толоконская Наталья Петровна | Способ лечения вирусного гепатита c |
| US6323180B1 (en) | 1998-08-10 | 2001-11-27 | Boehringer Ingelheim (Canada) Ltd | Hepatitis C inhibitor tri-peptides |
| JP2002527522A (ja) | 1998-10-16 | 2002-08-27 | シェリング・コーポレーション | 慢性C型肝炎感染を有する患者における検出可能HCV−RNA根絶用リバビリン−インターフェロン−α併用療法 |
| US6403564B1 (en) | 1998-10-16 | 2002-06-11 | Schering Corporation | Ribavirin-interferon alfa combination therapy for eradicating detectable HCV-RNA in patients having chronic hepatitis C infection |
| US20080275005A1 (en) | 1998-11-25 | 2008-11-06 | Murphy Michael P | Mitochondrially targeted antioxidants |
| EP1140143A2 (en) | 1998-12-18 | 2001-10-10 | Schering Corporation | Ribavirin-pegylated interferon alfa induction hcv combination therapy |
| AU2156900A (en) | 1998-12-18 | 2000-07-12 | Schering Corporation | Ribavirin-interferon alfa induction hcv combination therapy |
| US6824768B2 (en) | 1998-12-18 | 2004-11-30 | Schering Corporation | Ribavirin-pegylated interferon alfa induction HCV combination therapy |
| JP2000212099A (ja) | 1999-01-19 | 2000-08-02 | Mochida Pharmaceut Co Ltd | ウイルス性肝炎治療剤 |
| ATE286407T1 (de) | 1999-02-13 | 2005-01-15 | Purepulse Technologies Inc | Verfahren zur inaktivierung von pathogenen mittels breitspektrum-pulslicht |
| JP2002541204A (ja) | 1999-04-12 | 2002-12-03 | ユニバーシティ オブ マドラス | B型肝炎、c型肝炎及びその他の肝臓の関連ウイルス感染の治療に有用な医薬製剤及びその調製方法 |
| US6849254B1 (en) | 1999-04-19 | 2005-02-01 | Schering Corporation | HCV combination therapy |
| KR20020092896A (ko) | 1999-07-22 | 2002-12-12 | 뉴바이오틱스 인코퍼레이티드 | 효소 촉매된 치료요법 활성화 |
| BR0013252A (pt) | 1999-08-13 | 2002-04-16 | Hoffmann La Roche | Micofenolato mofetila em associação com peg-ifn-alfa |
| US20050245502A1 (en) | 1999-08-23 | 2005-11-03 | Phoenix Biosciences | Treatments for viral infections |
| KR100392292B1 (ko) | 2000-01-07 | 2003-07-22 | 주식회사 펩트론 | 5원환 융합 방향족 헤테로사이클릭 화합물을 유효성분으로 하는 hcv 치료제 조성물 |
| US6727267B2 (en) | 2000-04-05 | 2004-04-27 | Tularik Inc. | NS5B HVC polymerase inhibitors |
| WO2001077371A1 (fr) | 2000-04-07 | 2001-10-18 | Shionogi & Co., Ltd. | Procede de dosage de preincubation |
| ES2312436T3 (es) | 2000-04-18 | 2009-03-01 | Virco Bvba | Metodos para medir la resitencia a los farmacos. |
| US6415797B1 (en) | 2000-07-07 | 2002-07-09 | First Circle Medical, Inc. | Treatment of human herpesviruses using hyperthermia |
| MY139078A (en) | 2000-07-21 | 2009-08-28 | Schering Corp | Peptides as ns3-serine protease inhibitors of hepatitis c virus |
| US7244721B2 (en) | 2000-07-21 | 2007-07-17 | Schering Corporation | Peptides as NS3-serine protease inhibitors of hepatitis C virus |
| CN1466680A (zh) | 2000-08-02 | 2004-01-07 | ����-������ҩƷ��˾ | 给予促红细胞生成素改善抗病毒及抗肿瘤化疗 |
| SV2003000617A (es) | 2000-08-31 | 2003-01-13 | Lilly Co Eli | Inhibidores de la proteasa peptidomimetica ref. x-14912m |
| DK1326632T3 (da) | 2000-10-12 | 2007-01-15 | Viromics Gmbh | Protease-inhibitorer til behandling af infektioner af hepatitisvirus |
| EP1363703A4 (en) | 2000-10-13 | 2006-06-07 | Univ Monash | PREVENTION OF DISEASES BY REACTIVATION OF THYMUS |
| HK1052878A1 (zh) | 2000-10-18 | 2003-10-03 | Schering Corporation | 利巴传林-聚乙二醇化干扰素α:丙型肝炎病毒的联合治疗 |
| FR2815543B1 (fr) | 2000-10-19 | 2003-10-24 | Sedat | Seringue d'auto-injection d'un melange extemporane |
| DE60135481D1 (de) | 2000-10-20 | 2008-10-02 | Genetics Inst | Verwendung von il-13 inhibitoren zur behandlung von tumoren |
| EP1337504A4 (en) | 2000-11-08 | 2005-10-05 | Cellgate Inc | NEW POLYAMINE ANALOGON AMINOIC ACID CONJUGATES FOR USE AS CANCER |
| WO2002053096A2 (en) | 2000-12-06 | 2002-07-11 | The Trustees Of The University Of Pennsylvania | Single therapy and combination therapy involving drugs with target cellular proteins and drugs which target pathogen-encoded proteins |
| EA007491B1 (ru) | 2001-01-22 | 2006-10-27 | Мерк Энд Ко., Инк. | Производные нуклеозидов в качестве ингибиторов рнк-зависимой рнк вирусной полимеразы |
| US7105499B2 (en) | 2001-01-22 | 2006-09-12 | Merck & Co., Inc. | Nucleoside derivatives as inhibitors of RNA-dependent RNA viral polymerase |
| 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 |
| GB0107924D0 (en) | 2001-03-29 | 2001-05-23 | Angeletti P Ist Richerche Bio | Inhibitor of hepatitis C virus NS3 protease |
| US6673775B2 (en) | 2001-04-18 | 2004-01-06 | Schering Corporation | Ribavirin-interferon alfa combination therapy for eradicating detectable HCV-RNA in patients having chronic hepatitis C infection |
| WO2002089731A2 (en) | 2001-05-03 | 2002-11-14 | Stanford University | Agents for treatment of hcv and methods of use |
| US6833351B2 (en) | 2001-05-21 | 2004-12-21 | Douglas T. Dieterich | Method of treating anemia caused by ribavirin treatment of hepatitis C using erythropoietin alpha |
| RU2004102500A (ru) | 2001-06-29 | 2005-04-10 | Максиген Апс (Dk) | Композиции интерферонов |
| US20030138403A1 (en) | 2001-06-29 | 2003-07-24 | Maxygen Aps | Interferon formulations |
| HUP0401156A2 (hu) | 2001-07-20 | 2004-12-28 | Intermune, Inc. | Májfibrózis kezelésére szolgáló módszerek |
| WO2003024461A1 (en) | 2001-09-20 | 2003-03-27 | Schering Corporation | Hcv combination therapy |
| WO2003028754A1 (en) | 2001-09-28 | 2003-04-10 | Intermune, Inc. | Method for treating hepatitis c virus infection in treatment failure patients |
| PL369129A1 (en) | 2001-09-28 | 2005-04-18 | Intermune, Inc. | Method for treating hepatitis c virus infection in treatment failure patients |
| IL160965A0 (en) | 2001-10-05 | 2004-08-31 | Intermune Inc | Method of treating hepatitis virus infection with a multiphasic interferon delivery profile |
| PE20030545A1 (es) | 2001-10-31 | 2003-06-19 | Schering Corp | Formulaciones de jarabe de ribavirina |
| WO2003037908A1 (en) | 2001-10-31 | 2003-05-08 | Ribapharm Inc. | Antiviral combination therapy and compositions |
| JP2005536982A (ja) | 2001-11-07 | 2005-12-08 | 麒麟麦酒株式会社 | インビトロにおけるt細胞増幅および増幅されたt細胞集団 |
| AUPR879601A0 (en) | 2001-11-09 | 2001-12-06 | Biota Scientific Management Pty Ltd | Novel chemical compounds and their use |
| WO2003049760A1 (en) | 2001-12-07 | 2003-06-19 | Intermune, Inc. | Compositions and method for treating hepatitis virus infection |
| EP1321463B1 (en) | 2001-12-21 | 2007-08-08 | Virochem Pharma Inc. | Thiazole derivatives and their use for the treatment or prevention of Flavivirus infections |
| US6906190B2 (en) | 2002-01-04 | 2005-06-14 | Ribapharm Inc. | Inhibitors for de novo-RNA polymerases and methods of identifying targets for same |
| RU2212248C1 (ru) | 2002-01-21 | 2003-09-20 | Государственное образовательное учреждение высшего профессионального образования Санкт-Петербургская государственная медицинская академия им. И.И. Мечникова | Способ лечения больных хроническим вирусным гепатитом c |
| WO2003072135A2 (en) | 2002-02-26 | 2003-09-04 | North Shore-Long Island Jewish Research Insitute | Inhibition of inflammatory cytokine production by stimulation of brain muscarinic receptors |
| CA2383243A1 (en) | 2002-04-23 | 2003-10-23 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | Method for inhibiting fibrogenesis |
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| WO2003101199A1 (en) | 2002-05-31 | 2003-12-11 | Schering Corporation | Combination therapy for rna virus infections involving ribavirin and impdh inhibitors |
| TWI334785B (en) | 2002-06-03 | 2010-12-21 | Serono Lab | Use of recombinant ifn-β1a and pharmaceutical composition comprising recombinant ifn-β1a for the treatment of hcv infection in patients of asian race |
| US7608600B2 (en) | 2002-06-28 | 2009-10-27 | Idenix Pharmaceuticals, Inc. | Modified 2′ and 3′-nucleoside prodrugs for treating Flaviviridae infections |
| ES2350687T3 (es) | 2002-07-03 | 2011-01-26 | Ono Pharmaceutical Co., Ltd. | Composiciones de inmunopotenciación. |
| ITMI20021860A1 (it) | 2002-08-28 | 2004-02-29 | Scalia Antonio Cassar | Impiego dei triptani come agenti antivirali. |
| US20060223145A1 (en) | 2002-11-01 | 2006-10-05 | Lohray Braj B | Method for producing recombinant human interferon alpha 2b polypeptide in pichia pastoris |
| AU2003287666A1 (en) | 2002-11-13 | 2004-06-03 | Control Delivery Systems, Inc. | Systemic delivery of antiviral agents |
| WO2004047673A2 (en) | 2002-11-21 | 2004-06-10 | Novacea, Inc. | Treatment of liver disease with active vitamin d compounds |
| WO2004073599A2 (en) | 2003-02-18 | 2004-09-02 | Pfizer Inc. | Inhibitors of hepatitis c virus, compositions and treatments using the same |
| WO2004078127A2 (en) | 2003-02-28 | 2004-09-16 | Intermune, Inc. | Continuous delivery methods for treating hepatitis virus infection |
| AU2003225670A1 (en) | 2003-02-28 | 2004-09-28 | Intermune, Inc. | Interferon drug therapy for the treatment of viral diseases and liver fibrosis |
| EP1601368A2 (en) | 2003-02-28 | 2005-12-07 | Intermune, Inc. | Methods and compositions for treatment of viral diseases |
| TWI269656B (en) | 2003-03-05 | 2007-01-01 | Original Image Co Ltd | Therapeutical composition for hepatitis C |
| UA64191A (en) | 2003-03-14 | 2004-02-16 | Yevhenii Mykhailovych Neiko | Method for treating chronic hepatitises of various etiology |
| US20040198840A1 (en) | 2003-04-02 | 2004-10-07 | Deloach Reuben Edwin | Hydrazide substrate safely shuts down disease activated protease to halt viral replication, cancerous cell division, and toxic protein generation |
| DE602004019518D1 (de) | 2003-04-16 | 2009-04-02 | Bristol Myers Squibb Co | Makrocyclische isochinolinpeptidinhibitoren des hepatitis-c-virus |
| US20040258663A1 (en) | 2003-05-08 | 2004-12-23 | Nastech Pharmaceutical Company Inc. | Compositions and methods for enhanced mucosal delivery of interferon alpha |
| WO2005000308A2 (en) | 2003-05-15 | 2005-01-06 | Rigel Pharmaceuticals, Inc. | Methods of identifying hcv ns5b polymerase inhibitors and use against hepatitis c |
| KR101115294B1 (ko) | 2003-05-21 | 2012-04-12 | 베링거 인겔하임 인터내셔날 게엠베하 | C형 간염 억제제 화합물 |
| PT1633766T (pt) | 2003-05-30 | 2019-06-04 | Gilead Pharmasset Llc | Análogos de nucleósido fluorado modificado |
| US20050187170A1 (en) | 2003-06-16 | 2005-08-25 | Biocryst Pharmaceuticals, Inc. | Enhancing the efficiency of RNA polymerase inhibitors by using inosine monophosphate dehydrogenase inhibitors |
| EP1643981A2 (en) | 2003-06-20 | 2006-04-12 | Viral Genomix, Inc. | Antiviral compositions and methods of using the same |
| AU2004260009A1 (en) | 2003-07-11 | 2005-02-03 | Oregon Health And Science University | Methods of treatment and disgnosis using modulators of virus-induced cellular gene sequences |
| MD2549G2 (ro) | 2003-07-18 | 2005-08-31 | Национальный Научно-Практический Центр Превентивной Медицины Министерства Здравоохранения Республики Молдова | Metodă de tratament a hepatitei virale cronice C. |
| GB0317009D0 (en) | 2003-07-21 | 2003-08-27 | Univ Cardiff | Chemical compounds |
| WO2005018330A1 (en) | 2003-08-18 | 2005-03-03 | Pharmasset, Inc. | Dosing regimen for flaviviridae therapy |
| WO2005025583A2 (en) | 2003-09-05 | 2005-03-24 | Anadys Pharmaceuticals, Inc. | Tlr7 ligands for the treatment of hepatitis c |
| EP1671643A1 (en) | 2003-09-08 | 2006-06-21 | Intellectual Property Consulting Inc. | Medicinal composition for treating chronic hepatitis c |
| AR045870A1 (es) | 2003-10-11 | 2005-11-16 | Vertex Pharma | Terapia de combinacion para la infeccion de virus de hepatitis c |
| US7491794B2 (en) | 2003-10-14 | 2009-02-17 | Intermune, Inc. | Macrocyclic compounds as inhibitors of viral replication |
| WO2005038056A1 (en) | 2003-10-14 | 2005-04-28 | Intermune, Inc. | Combination therapy for the treatment of viral diseases |
| CN103145715B (zh) | 2003-10-14 | 2016-08-03 | F·霍夫曼-罗须公司 | 作为hcv复制抑制剂的巨环羧酸和酰基磺酰胺 |
| US20050085528A1 (en) | 2003-10-17 | 2005-04-21 | Pfizer Inc. | Parmaceutical |
| EP1692516B1 (en) | 2003-10-24 | 2010-12-01 | Immunaid Pty Ltd | Method of therapy |
| MXPA06004723A (es) | 2003-10-27 | 2006-07-05 | Vertex Pharma | Combinacion para el tratamiento del hcv. |
| WO2005043118A2 (en) | 2003-10-27 | 2005-05-12 | Vertex Pharmaceuticals Incorporated | Drug discovery method |
| UA68233A (en) | 2003-11-25 | 2004-07-15 | Univ Zaporizhia State Medical | Method for treating chronic hepatitis c |
| US7078064B2 (en) | 2003-12-03 | 2006-07-18 | George Zabrecky | Compositions and methods useful for treating and preventing chronic liver disease, chronic HCV infection and non-alcoholic steatohepatitis |
| EP2546254A1 (en) | 2003-12-22 | 2013-01-16 | K.U.Leuven Research & Development | Imidazo[4,5-C]pyridine compounds and methods of antiviral treatment |
| WO2005062949A2 (en) | 2003-12-23 | 2005-07-14 | Intermune, Inc. | Method for treating hepatitis virus infection |
| US20070258946A1 (en) | 2003-12-23 | 2007-11-08 | Blatt Lawrence M | Combination Therapy for Treating Hepatitis C Virus Infection |
| WO2005067963A1 (en) | 2003-12-23 | 2005-07-28 | Intermune, Inc. | Use of polyethylene glycol-modified interferon-alpha in therapeutic dosing regimens |
| DE10361944A1 (de) | 2003-12-31 | 2005-07-28 | Viromics Gmbh | Mittel zur Hemmung der Virusreplikation durch Regulation der Proteinfaltung |
| EP1718315A4 (en) | 2004-02-06 | 2008-08-13 | Univ Monash | HIGH DOSE USE OF SULFATED POLYSACCHARIDES IN SHORT INTERVALS FOR THE TREATMENT OF INFECTIONS |
| EP1730165A1 (en) | 2004-02-27 | 2006-12-13 | Schering Corporation | Inhibitors of hepatitis c virus ns3 protease |
| CA2563058C (en) | 2004-04-22 | 2012-10-16 | Howard J. Smith & Associates Pty Ltd | Supportive treatment of liver disease |
| JP4943322B2 (ja) | 2004-05-04 | 2012-05-30 | ボード オブ トラスティーズ オブ ザ レランド スタンフォード ジュニア ユニバーシティ | 標的細胞中のウイルスゲノム量を減少させるための方法および組成物 |
| WO2005107745A1 (en) | 2004-05-06 | 2005-11-17 | Schering Corporation | An inhibitor of hepatitis c |
| CA2565658A1 (en) | 2004-05-06 | 2005-11-17 | Conjuchem Biotechnologies Inc. | Compounds for specific viral target |
| WO2006016930A2 (en) | 2004-05-14 | 2006-02-16 | Intermune, Inc. | Methods for treating hcv infection |
| EP1753775B1 (en) | 2004-05-25 | 2012-12-26 | Boehringer Ingelheim International GmbH | Process for preparing acyclic hcv protease inhibitors |
| SG153800A1 (en) | 2004-06-08 | 2009-07-29 | Vertex Pharma | Pharmaceutical compositions |
| DE602005026294D1 (de) | 2004-07-14 | 2011-03-24 | Novartis Ag | Verwendung einer kombination von cyclosporin und pegylierten interferonen zur behandlung von hepatitis c (hcv) |
| 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 |
| EP1627641A1 (en) | 2004-08-04 | 2006-02-22 | Victor Eluwa | Pharmaceutical compositions comprising metal oxides and uses thereof |
| US7153848B2 (en) | 2004-08-09 | 2006-12-26 | Bristol-Myers Squibb Company | Inhibitors of HCV replication |
| US7348425B2 (en) | 2004-08-09 | 2008-03-25 | Bristol-Myers Squibb Company | Inhibitors of HCV replication |
| AU2005289453A1 (en) | 2004-09-27 | 2006-04-06 | Government of the United States of America, as represented by the Secretary of the Department of Health and Human Services, National Institutes of Health | Modulating MxA expression |
| CN101056648B (zh) | 2004-10-01 | 2012-08-15 | 德比奥法姆股份有限公司 | [d-meala]3-[etval]4环孢菌素用于丙型肝炎感染治疗的应用以及包含所述[d-meala]3-[etval]4-环孢菌素的药物组合物 |
| BRPI0516825A (pt) | 2004-10-01 | 2008-09-23 | Vertex Pharma | inibição da protease ns3-ns4a do vìrus da hepatite c (vhc) |
| US7723310B2 (en) | 2004-10-18 | 2010-05-25 | Three Rivers Pharmaceuticals, Llc | Large dose ribavirin formulations |
| US20060228333A1 (en) | 2004-10-20 | 2006-10-12 | Kye-Hyung Paik | Methods for control of tumors and chronic infections by modulating immunologically informed carriers homing to tolerogenic organs or tissues |
| WO2006043153A2 (en) | 2004-10-20 | 2006-04-27 | Michel Xilinas | Use of zinc and copper chelators for the treatment of viral diseases |
| AU2005298412B2 (en) | 2004-10-26 | 2011-06-09 | Istituto Di Ricerche Di Biologia Molecolare P Angeletti Spa | Tetracyclic indole derivatives as antiviral agents |
| MY141025A (en) | 2004-10-29 | 2010-02-25 | Vertex Pharma | Dose forms |
| US7592315B2 (en) | 2004-11-02 | 2009-09-22 | Schering Corporation | Peptide viral entry inhibitors |
| US20060105063A1 (en) | 2004-11-18 | 2006-05-18 | Kent Hann | Synergic combination of compositions containing aloe vera isolates and their therapeutic application |
| CA2589935A1 (en) | 2004-12-09 | 2006-06-15 | Regents Of The University Of Minnesota | Nucleosides with antiviral and anticancer activity |
| TW200633718A (en) | 2004-12-16 | 2006-10-01 | Applied Research Systems | Treatment of hepatitis c in the asian population |
| DE102004061746A1 (de) | 2004-12-22 | 2006-07-06 | Bayer Healthcare Ag | Alkinyl-substituierte Thiophene |
| EP1674104A1 (en) | 2004-12-24 | 2006-06-28 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | Uridine derivatives as antiviral drugs against a flaviviridae, especially HCV |
| EP1679065A1 (en) | 2005-01-07 | 2006-07-12 | OctoPlus Sciences B.V. | Controlled release compositions for interferon based on PEGT/PBT block copolymers |
| CA2594934A1 (en) | 2005-01-17 | 2006-07-20 | Jerini Ag | C5a receptor antagonists |
| EP2361630A1 (en) | 2005-02-03 | 2011-08-31 | Intarcia Therapeutics, Inc | Implantable drug delivery device comprising particles and an osmotic pump |
| MX2007009561A (es) | 2005-02-09 | 2008-01-14 | Migenix Inc | Composiciones y metodos para tratar o evitar infecciones de flaviviridae. |
| US20060198787A1 (en) | 2005-02-18 | 2006-09-07 | Larry Blatt | Biomarkers for predicting liver fibrosis treatment efficacy |
| US8232240B2 (en) | 2005-02-23 | 2012-07-31 | The Brigham And Women's Hospital, Inc. | Inhibitors of enveloped virus infectivity |
| US20090156545A1 (en) | 2005-04-01 | 2009-06-18 | Hostetler Karl Y | Substituted Phosphate Esters of Nucleoside Phosphonates |
| US20060229293A1 (en) | 2005-04-06 | 2006-10-12 | Addiction Research Institute, Inc. | Compositions for the treatment of hepatitis C and methods for using compositions for the treatment of hepatitis C |
| WO2006110656A2 (en) | 2005-04-08 | 2006-10-19 | Chimerix, Inc. | Compounds, compositions and methods for the treatment of viral infections and other medical disorders |
| WO2006113431A2 (en) | 2005-04-13 | 2006-10-26 | University Of Massachusetts | Dual functional oligonucleotides for use as anti-viral agents |
| US20060241144A1 (en) | 2005-04-20 | 2006-10-26 | Albert Cha | Method for treating apathy syndrome |
| BRPI0610283A2 (pt) | 2005-05-13 | 2010-10-19 | Virochem Pharma Inc | composto, uso do mesmo na preparação de um medicamento para o tratamento ou prevenção de uma infecção por vìrus de hepatite c, composição farmacêutica e combinação farmacêutica |
| WO2006127289A1 (en) | 2005-05-20 | 2006-11-30 | Valeant Research & Development | Treatment of hcv with subtherapeutic doses of ribavirin |
| WO2006127482A1 (en) | 2005-05-20 | 2006-11-30 | Bioenvision, Inc. | Methylene blue therapy of viral disease |
| CN101184771A (zh) | 2005-05-26 | 2008-05-21 | 先灵公司 | 干扰素-IgG融合体 |
| KR101174966B1 (ko) | 2005-05-31 | 2012-08-17 | 노파르티스 아게 | 철이 발병에 관여하는 간질환의 치료 |
| US7793040B2 (en) | 2005-06-01 | 2010-09-07 | Microsoft Corporation | Content addressable memory architecture |
| PE20070011A1 (es) | 2005-06-02 | 2007-03-08 | Schering Corp | Formulaciones farmaceuticas de compuestos inhibidores de proteasa del vhc o catepsina |
| WO2006130688A2 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Compounds for inhibiting cathepsin activity |
| WO2006130553A2 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Hcv protease inhibitors |
| US8119602B2 (en) | 2005-06-02 | 2012-02-21 | Schering Corporation | Administration of HCV protease inhibitors in combination with food to improve bioavailability |
| US20060281689A1 (en) | 2005-06-02 | 2006-12-14 | Schering Corporation | Method for modulating activity of HCV protease through use of a novel HCV protease inhibitor to reduce duration of treatment period |
| US20060276407A1 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Methods of treating hepatitis C virus |
| US20060276404A1 (en) | 2005-06-02 | 2006-12-07 | Anima Ghosal | Medicaments and methods combining a HCV protease inhibitor and an AKR competitor |
| WO2006130552A2 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Methods of treating hepatitis c virus |
| US20060275366A1 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Controlled-release formulation |
| US20070207949A1 (en) | 2005-06-02 | 2007-09-06 | Anima Ghosal | Medicaments and methods combining a HCV protease inhibitor and an AKR competitor |
| US20070237818A1 (en) | 2005-06-02 | 2007-10-11 | Malcolm Bruce A | Controlled-release formulation of HCV protease inhibitor and methods using the same |
| US20070232527A1 (en) | 2005-06-02 | 2007-10-04 | Anima Ghosal | Medicaments and methods combining a HCV protease inhibitor and an AKR competitor |
| US20070021351A1 (en) | 2005-06-02 | 2007-01-25 | Schering Corporation | Liver/plasma concentration ratio for dosing hepatitis C virus protease inhibitor |
| JP5149168B2 (ja) | 2005-06-07 | 2013-02-20 | エール ユニヴァーシティ | Lfmauおよびldtを用いる癌および他の症状または病状の処置方法 |
| RU2293572C1 (ru) | 2005-07-18 | 2007-02-20 | Гюнтер Хаазе | Способ лечения хронического вирусного гепатита с генотип-2 с умеренной активностью |
| TWI387603B (zh) | 2005-07-20 | 2013-03-01 | Merck Sharp & Dohme | Hcv ns3蛋白酶抑制劑 |
| PE20070211A1 (es) | 2005-07-29 | 2007-05-12 | Medivir Ab | Compuestos macrociclicos como inhibidores del virus de hepatitis c |
| EP2402331A1 (en) | 2005-08-02 | 2012-01-04 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases |
| MX2008001865A (es) | 2005-08-12 | 2008-04-15 | Human Genome Sciences Inc | Proteinas de fusion de albumina. |
| DE102005038768A1 (de) | 2005-08-16 | 2007-02-22 | Toximed Gmbh | Pharmazeutischer Wirkstoff gegen Borreliose |
| PT2194043E (pt) | 2005-08-19 | 2014-03-04 | Vertex Pharma | Processos |
| US8193328B2 (en) | 2005-09-08 | 2012-06-05 | Philadelphia Health & Education Corporation | Identification of modulators of serine protease inhibitor Kazal and their use as anti-cancer and anti-viral agents |
| US7531164B2 (en) | 2005-10-21 | 2009-05-12 | Duke University | Preventing bacterial or viral infectivity and composition containing infection preventing additive |
| IE20050723A1 (en) | 2005-10-28 | 2007-05-30 | Patrick T Prendergast | Anti-mineralocorticoid therapy of infection |
| WO2007056016A2 (en) | 2005-11-02 | 2007-05-18 | Kemia, Inc. | Bisamide cytokine inhibitors |
| RU2306134C2 (ru) | 2005-11-07 | 2007-09-20 | Государственное образовательное учреждение высшего профессионального образования "Самарский Государственный медицинский университет" | Способ базисного лечения хронического вирусного гепатита c |
| EP2392590A3 (en) | 2005-11-11 | 2012-03-14 | Vertex Pharmaceuticals Incorporated | Hepatitis C virus variants |
| WO2007058384A1 (en) | 2005-11-17 | 2007-05-24 | Osaka University | Method of suppressing replication of hepatitis c virus, inhibitor of replication of the virus and method of screening for the same |
| RU2326115C2 (ru) | 2005-11-21 | 2008-06-10 | Ефаг АО | Соли 1-алкиламино-1-дезоксиполиолов с 9-оксоакридин-10-уксусной кислотой, лекарственные препараты на их основе, применение, способы профилактики и лечения |
| AR057623A1 (es) | 2005-11-28 | 2007-12-05 | Omega Bio Pharma H K Ltd | Materiales y metodos para el tratamiento de las infecciones virales |
| CA2632903C (en) | 2005-12-02 | 2015-11-24 | Vianova Labs, Inc. | Treatment of cancer and other diseases |
| NZ568909A (en) | 2005-12-09 | 2011-10-28 | Hoffmann La Roche | Antiviral 4-fluoro-4-methyl nucleoside prodrugs |
| WO2007075896A2 (en) | 2005-12-22 | 2007-07-05 | Kemia, Inc. | Heterocyclic cytokine inhibitors |
| RU2306934C1 (ru) | 2005-12-28 | 2007-09-27 | ГОУ ВПО Омская Государственная Медицинская Академия | Способ лечения больных хроническим вирусным гепатитом c |
| UA100840C2 (ru) | 2006-01-09 | 2013-02-11 | РОМАРК ЛЕБОРЕТЕРИЗ, Эл.Си. | Композиция для лечения вирусного гепатита |
| MD20060037A (ro) | 2006-01-24 | 2007-07-31 | Национальный Научно-Практический Центр Превентивной Медицины Министерства Здравоохранения Республики Молдова | Metodă de tratament al hepatitei virale acute C |
| MX2008010355A (es) | 2006-02-09 | 2008-10-31 | Schering Corp | Combinaciones que comprenden inhibidores de proteasa del virus de la hepatitis c e inhibidores de polimerasa del virus de la hepatitis c, y metodos de tratamiento relacionados con los mismos. |
| US20070224167A1 (en) | 2006-02-09 | 2007-09-27 | Schering Corporation | Novel HCV inhibitor combinations and methods |
| EP1991229A2 (en) | 2006-02-27 | 2008-11-19 | Vertex Pharmaceuticals Incorporated | Co-crystals and pharmaceutical compositions comprising the same |
| US20070225297A1 (en) | 2006-03-16 | 2007-09-27 | Perni Robert B | Deuterated hepatitis C protease inhibitors |
| CA2646335A1 (en) | 2006-03-20 | 2007-09-27 | Vertex Pharmaceuticals Incorporated | Pharmaceutical compositions |
| WO2007109604A2 (en) | 2006-03-20 | 2007-09-27 | Vertex Pharmaceuticals Incorporated | Pharmaceutical compositions |
| US8895531B2 (en) | 2006-03-23 | 2014-11-25 | Rfs Pharma Llc | 2′-fluoronucleoside phosphonates as antiviral agents |
| WO2007111866A2 (en) | 2006-03-23 | 2007-10-04 | Schering Corporation | Combinations of hcv protease inhibitor(s) and cyp3a4 inhibitor(s), and methods of treatment related thereto |
| US8021835B2 (en) | 2006-05-04 | 2011-09-20 | The Rockefeller University | HCV coreceptor and methods of use thereof |
| WO2008060695A2 (en) | 2006-05-22 | 2008-05-22 | The Trustees Of The University Of Pennsylvania | Antiviral inhibition of casein kinase ii |
| DE102006026464A1 (de) | 2006-06-01 | 2007-12-06 | Virologik Gmbh Innovationszentrum Medizintechnik Und Pharma | Pharmazeutische Zusammensetzung zur Behandlung von Virusinfektionen und / oder Tumorerkrankungen durch Inhibition der Proteinfaltung und des Proteinabbaus |
| WO2007143164A1 (en) | 2006-06-02 | 2007-12-13 | San Diego State University Research Foundation | Compositions and methods for ameliorating hyperlipidemia |
| US20080019950A1 (en) | 2006-06-04 | 2008-01-24 | Cellartis Ab | Novel hepatocyte-like cells and hepatoblast-like cells derived from hBS cells |
| WO2007146712A2 (en) | 2006-06-09 | 2007-12-21 | Kemia, Inc. | Therapy using cytokine inhibitors |
| WO2007149382A2 (en) | 2006-06-19 | 2007-12-27 | The Cleveland Clinic Foundation | Therapeutic compositions and methods useful in treating hepatitis |
| KR20090024834A (ko) | 2006-07-05 | 2009-03-09 | 인터뮨, 인크. | C형 간염 바이러스 복제의 신규 억제제 |
| US20080081791A1 (en) | 2006-07-06 | 2008-04-03 | Weida Huang | Methods of using combinations of siRNAs for treating a disease or a disorder, and for enhancing siRNA efficacy in RNAi |
| US20090227491A1 (en) | 2006-07-07 | 2009-09-10 | Gilead Sciences, Inc. | Antiviral phosphinate compounds |
| US7906619B2 (en) | 2006-07-13 | 2011-03-15 | Achillion Pharmaceuticals, Inc. | 4-amino-4-oxobutanoyl peptides as inhibitors of viral replication |
| US8329159B2 (en) | 2006-08-11 | 2012-12-11 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| EP1886685A1 (en) | 2006-08-11 | 2008-02-13 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods, uses and compositions for modulating replication of hcv through the farnesoid x receptor (fxr) activation or inhibition |
| WO2008022006A2 (en) | 2006-08-11 | 2008-02-21 | Enanta Pharmaceuticals, Inc. | Arylalkoxyl hepatitis c virus protease inhibitors |
| US20100158862A1 (en) | 2006-08-11 | 2010-06-24 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| US20080131398A1 (en) | 2006-08-21 | 2008-06-05 | United Therapeutics Corporation | Combination therapy for treatment of viral infections |
| WO2008024763A2 (en) | 2006-08-25 | 2008-02-28 | Wyeth | Identification and characterization of hcv replicon variants with reduced susceptibility to hcv-796, and methods related thereto |
| US7655419B2 (en) | 2006-08-25 | 2010-02-02 | The Board Of Trustees Of The Leland Stanford Junior University | Methods and compositions for identifying anti-HCV agents |
| TW200815384A (en) | 2006-08-25 | 2008-04-01 | Viropharma Inc | Combination therapy method for treating hepatitis C virus infection and pharmaceutical compositions for use therein |
| WO2008032227A2 (en) | 2006-09-11 | 2008-03-20 | Biomas, Ltd. | Topical formulations of tellurium-containing compounds |
| WO2008033466A2 (en) | 2006-09-14 | 2008-03-20 | Combinatorx (Singapore) Pre. Ltd. | Compositions and methods for treatment of viral diseases |
| MX2009002816A (es) | 2006-09-14 | 2009-05-28 | Human Genome Sciences Inc | Proteinas de fusion de albumina. |
| WO2008039179A1 (en) | 2006-09-26 | 2008-04-03 | Addiction Research Institute, Inc. | Compositions for the treatment of hepatitis c and methods for using compositions for the treatment of hepatitis c |
| JP5252459B2 (ja) | 2006-10-10 | 2013-07-31 | ギリアド ファーマセット エルエルシー | リボフラノシルピリミジンヌクレオシドの調製 |
| US7777395B2 (en) | 2006-10-12 | 2010-08-17 | Eastman Kodak Company | Continuous drop emitter with reduced stimulation crosstalk |
| KR101615500B1 (ko) | 2006-10-27 | 2016-04-27 | 머크 샤프 앤드 돔 코포레이션 | Hcv ns3 프로테아제 억제제 |
| AU2007321677B2 (en) | 2006-11-15 | 2013-04-11 | Vertex Pharmaceuticals (Canada) Incorporated | Thiophene analogues for the treatment or prevention of flavivirus infections |
| US20100093824A1 (en) | 2006-11-29 | 2010-04-15 | Judith Frydman | Methods of treating viral infection |
| US20100081672A1 (en) | 2006-12-07 | 2010-04-01 | Schering Corporation | Ph sensitive matrix formulation |
| RU2336096C1 (ru) | 2006-12-14 | 2008-10-20 | ООО Медицинский центр "Столица" | Способ лечения гепатита с |
| RU2345787C2 (ru) | 2006-12-25 | 2009-02-10 | Государственное образовательное учреждение высшего профессионального образования "Самарский Государственный медицинский университет" | Способ лечения хронического вирусного гепатита с |
| US20080261913A1 (en) | 2006-12-28 | 2008-10-23 | Idenix Pharmaceuticals, Inc. | Compounds and pharmaceutical compositions for the treatment of liver disorders |
| CN101668538A (zh) | 2007-01-08 | 2010-03-10 | 芬诺密克斯公司 | 大环类丙型肝炎蛋白酶抑制剂 |
| WO2008089034A2 (en) | 2007-01-11 | 2008-07-24 | Kemia, Inc. | Cytokine inhibitors |
| US7645732B2 (en) | 2007-01-24 | 2010-01-12 | Board Of Regents, The University Of Texas System | Treating hepatitis C virus infection |
| ES2524784T3 (es) | 2007-02-01 | 2014-12-12 | Janssen R&D Ireland | Formas polimórficas de un inhibidor macrocíclico del VHC |
| TWI426918B (zh) | 2007-02-12 | 2014-02-21 | Merck Sharp & Dohme | Il-23拮抗劑於治療感染之用途 |
| DK2125026T3 (en) | 2007-02-21 | 2014-12-08 | Allaccem Inc | FORMATIONS BASED ON bridged POLYCYCLIC COMPOUNDS FOR INHIBITION AND RELIEF OF DISEASES |
| DK2114924T3 (da) | 2007-02-27 | 2012-04-10 | Vertex Pharma | Co-krystaller og farmaceutiske sammensætninger omfattende disse |
| WO2008106167A1 (en) | 2007-02-28 | 2008-09-04 | Conatus Pharmaceuticals, Inc. | Combination therapy comprising matrix metalloproteinase inhibitors and caspase inhibitors for the treatment of liver diseases |
| MD3477G2 (ro) | 2007-03-21 | 2008-08-31 | Николае БОДРУГ | Metodă de tratament al hepatitei virale cronice C |
| WO2008116194A2 (en) | 2007-03-22 | 2008-09-25 | Innovative Biologics, Inc. | Blockers of pore-forming virulence factors and their use as anti-infectives |
| PL2308514T3 (pl) | 2007-03-23 | 2013-11-29 | To Bbb Holding B V | Koniugaty do ukierunkowanego dostarczania leku poprzez barierę krew-mózg |
| US7964580B2 (en) | 2007-03-30 | 2011-06-21 | Pharmasset, Inc. | Nucleoside phosphoramidate prodrugs |
| WO2008124384A2 (en) | 2007-04-03 | 2008-10-16 | Aegerion Pharmaceuticals, Inc. | Combinations of mtp inhibitors with cholesterol absorption inhibitors or interferon for treating hepatitis c |
| CA2685285A1 (en) | 2007-04-27 | 2008-11-06 | Chimerix, Inc. | Methods of reducing nephrotoxicity in subjects administered with nucleoside phosphonates |
| US20080269205A1 (en) | 2007-04-27 | 2008-10-30 | Ondine International, Ltd. | Methods to prevent vertical transmission of infectious diseases |
| BRPI0811020A2 (pt) | 2007-05-03 | 2015-07-21 | Intermune Inc | Composto, composição farmacêutica e métodos de inibição da atividade da protease ns3/ns4, de tratamento da fibrose hepática, de intensificação da função hepática em indivíduo com infecção do vírus da hepatite c e métodos de síntese de compostos, de administração de inibidor da infecção do vírus da hepatite c (hcv) e de distribuição de forma de dosagem oral. |
| MX2009011930A (es) | 2007-05-04 | 2009-11-18 | Vertex Pharma | Terapia de combinacion para el tratamiento de infeccion de virus de hepatitis c. |
| KR20100027134A (ko) | 2007-05-10 | 2010-03-10 | 인터뮨, 인크. | C형 간염 바이러스 복제의 신규 펩티드 억제제 |
| WO2008144072A1 (en) | 2007-05-21 | 2008-11-27 | Vertex Pharmaceuticals Incorporated | Dose forms comprising vx- 950 and their dosage regimen |
| RU2348412C1 (ru) | 2007-06-01 | 2009-03-10 | Лариса Леонидовна Попова | Способ профилактики рецидива хронического вирусного гепатита с после достижения вирусологической ремиссии |
| WO2008154248A1 (en) | 2007-06-06 | 2008-12-18 | Inova Health System | Prognostic chronic hepatitis c biomarkers |
| EP2162431B1 (en) | 2007-06-29 | 2017-06-07 | Gilead Sciences, Inc. | Antiviral compounds |
| CN100532388C (zh) | 2007-07-16 | 2009-08-26 | 郑州大学 | 2’-氟-4’-取代-核苷类似物、其制备方法及应用 |
| EP2175865A4 (en) | 2007-07-25 | 2012-01-11 | Biolex Therapeutics Inc | INTERFERON DRUG PRODUCTS WITH CONTROLLED RELEASE AND TREATMENT OF HCV INFECTIONS THEREWITH |
| WO2009015389A2 (en) | 2007-07-26 | 2009-01-29 | Entra Pharmaceuticals Inc. | Skin-patch pump comprising a changing-volume electrochemical actuator |
| ES2563477T3 (es) | 2007-08-03 | 2016-03-15 | Biotron Limited | Composiciones antivirales para tratar la hepatitis C a base de 5-(1-metilpirazol-4-il)2-naftoilguanidina y 2'-C-metiladenosina o 2'-C-metilcitidina |
| US7728027B2 (en) | 2007-08-08 | 2010-06-01 | Bristol-Myers Squibb Company | Process for synthesizing compounds useful for treating hepatitis C |
| US8629171B2 (en) | 2007-08-08 | 2014-01-14 | Bristol-Myers Squibb Company | Crystalline form of methyl ((1S)-1-((25)-2-(5-(4'-(2-((25)-1((2S)-2-((methoxycarbonyl)amino)-3-methylbutanoyl)-2-pyrrolidinyl)-1H-imidazol-2-yl)-1-pyrrolidinyl)carbonyl)-2-methylpropyl)carbamate dihydrochloride salt |
| WO2009026292A1 (en) | 2007-08-20 | 2009-02-26 | Anadys Pharmaceuticals, Inc. | Dosing methods for treating disease |
| MX2010002407A (es) | 2007-08-30 | 2010-03-26 | Vertex Pharma | Cocristales y composiciones farmaceuticas que los comprenden. |
| WO2009033183A2 (en) | 2007-09-08 | 2009-03-12 | University Of Florida Research Foundation | Compounds and methods for treatment of hcv and conditions associated with cd81 binding |
| US20090076100A1 (en) | 2007-09-13 | 2009-03-19 | Protia, Llc | Deuterium-enriched gsk625433 |
| NZ583825A (en) | 2007-09-14 | 2012-06-29 | Schering Corp | Method of treating hepatitis C patients comprising an HCV protease inhibitor, an antiviral compound and an interferon |
| AU2008302448B2 (en) | 2007-09-17 | 2014-11-06 | Abbvie Ireland Unlimited Company | Uracil or thymine derivative for treating hepatitis C |
| PL2639226T3 (pl) * | 2007-09-17 | 2017-02-28 | Abbvie Bahamas Ltd. | Pirymidyny o działaniu przeciw zakaźnym oraz ich zastosowania |
| WO2009039248A2 (en) | 2007-09-18 | 2009-03-26 | Stanford University | Methods of treating a flaviviridae family viral infection and compositions for treating a flaviviridae family viral infection |
| US20090082414A1 (en) | 2007-09-26 | 2009-03-26 | Protia, Llc | Deuterium-enriched viramidine |
| US20090082366A1 (en) | 2007-09-26 | 2009-03-26 | Protia, Llc | Deuterium-enriched telaprevir |
| MX2010003726A (es) | 2007-10-03 | 2010-09-14 | Sabell Corp | Composiciones herbarias y metodos de tratamiento de trastornos hepaticos. |
| EP2211895A2 (en) | 2007-10-05 | 2010-08-04 | Medtronic, Inc. | Use of a specific dosage regimen of ifn-alpha and ribavirin for treating hepatitis c |
| JP2011503060A (ja) | 2007-11-05 | 2011-01-27 | バーテックス ファーマシューティカルズ インコーポレイテッド | Vx−950、peg−ifnおよびリババリンを含むhcv併用治療剤 |
| ES2374117T3 (es) | 2007-11-15 | 2012-02-13 | Madaus Gmbh | Componente de silibinina para el tratamiento de la hepatitis. |
| CA2709032C (en) | 2007-12-21 | 2016-02-23 | F. Hoffmann-La Roche Ag | Process for the preparation of a macrocycle |
| US8202996B2 (en) * | 2007-12-21 | 2012-06-19 | Bristol-Myers Squibb Company | Crystalline forms of N-(tert-butoxycarbonyl)-3-methyl-L-valyl-(4R)-4-((7-chloro-4-methoxy-1-isoquinolinyl)oxy)-N- ((1R,2S)-1-((cyclopropylsulfonyl)carbamoyl)-2-vinylcyclopropyl)-L-prolinamide |
| EP2237666A4 (en) | 2007-12-21 | 2012-05-16 | Avila Therapeutics Inc | HCV PROTEASE INHIBITORS AND USES THEREOF |
| CN102137676A (zh) | 2007-12-27 | 2011-07-27 | 伊皮芬尼生物科学公司 | 抗病毒化合物 |
| CA2717792A1 (en) | 2008-03-07 | 2009-09-11 | Santaris Pharma A/S | Pharmaceutical compositions for treatment of microrna related diseases |
| JP5283106B2 (ja) | 2008-03-14 | 2013-09-04 | 国立大学法人 熊本大学 | C型肝炎ウイルス阻害剤 |
| US20100009970A1 (en) | 2008-03-19 | 2010-01-14 | Combinatorx (Singapore) Pte. Ltd. | Compositions and methods for treatment of viral diseases |
| US20110045001A1 (en) | 2008-03-28 | 2011-02-24 | Biontex Laboratories Gmbh | Transfection results of non-viral gene delivery systems by influencing of the innate immune system |
| MX2010011307A (es) | 2008-04-15 | 2010-11-09 | Intermune Inc | Nuevos inhibidores de la replicacion del virus de hepatitis c. |
| HUE038946T2 (hu) * | 2008-04-23 | 2018-12-28 | Gilead Sciences Inc | 1'-szubsztituált carba-nukleozid analógok antivirális kezelésre |
| SG190569A1 (en) | 2008-04-23 | 2013-06-28 | Vertex Pharma | Treatment of hepatitis c virus infections with telaprevir (vx-950) in patients non-responsive to treatment with pegylated interferon-alpha-2a/2b and ribavirin |
| DE102008029669A1 (de) | 2008-05-16 | 2009-11-19 | Schlaak, Jörg Friedrich, Prof. Dr. med. | Neue Therapeutika für die Hepatitis-Therapie |
| WO2009149179A2 (en) | 2008-06-03 | 2009-12-10 | Aethlon Medical Inc. | Enhanced antiviral therapy methods and devices |
| AU2009255994B2 (en) | 2008-06-05 | 2014-07-17 | Bristol-Myers Squibb Company | Use of pegylated Type III Interferons for the treatment of hepatitis C |
| EP2293796A1 (en) | 2008-06-10 | 2011-03-16 | Janssen Pharmaceutica, N.V. | Telaprevir dosing regimen |
| WO2009152589A1 (en) | 2008-06-17 | 2009-12-23 | Universidade Federal De Minas Gerais-Ufmg | Use of paf receptor for treating infections caused by flaviviridae |
| PT2310095E (pt) | 2008-07-22 | 2012-11-16 | Angeletti P Ist Richerche Bio | Compostos de quinoxalina macrocílicos como inibidores da protease ns3 do hcv |
| CA2737144A1 (en) | 2008-07-25 | 2010-01-28 | The Regents Of The University Of Colorado | Methods for treating viral disorders |
| RU2373952C1 (ru) | 2008-07-30 | 2009-11-27 | Юрий Михайлович Амбалов | Способ лечебного питания больных хроническим гепатитом с, получающих комплексную противовирусную терапию |
| EP2323979A4 (en) | 2008-08-06 | 2012-03-07 | Sciclone Pharmaceuticals Inc | TREATMENT OR PREVENTION OF HEPATITIS C WITH IMMUNOMODULATOR COMPOUNDS |
| CA2732091A1 (en) | 2008-08-07 | 2010-02-11 | F. Hoffmann-La Roche Ag | Process for the preparation of a macrocycle |
| JP2011530532A (ja) | 2008-08-07 | 2011-12-22 | シェーリング コーポレイション | 固体分子分散物中のhcvプロテアーゼインヒビターの薬学的処方物 |
| WO2010021681A2 (en) | 2008-08-18 | 2010-02-25 | Combinatorx (Singapore) Pte. Ltd. | Compositions and methods for treatment of viral diseases |
| WO2010020676A1 (en) | 2008-08-20 | 2010-02-25 | Vib Vzw | The use of topoisomerase type i inhibitors to treat viral infections |
| JP2012501345A (ja) | 2008-08-28 | 2012-01-19 | バーテックス ファーマシューティカルズ インコーポレイテッド | Hcv遺伝子型の分析 |
| US8580759B2 (en) | 2008-08-29 | 2013-11-12 | Osaka University | Anti-hepatitis C virus composition |
| WO2010027921A1 (en) | 2008-09-03 | 2010-03-11 | Vertex Pharmaceuticals Incorporated | Co-crystals and pharmaceutical formulations comprising the same |
| UY32099A (es) | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | Inhibidores macrocíclicos de serina proteasas de hepatitis c |
| KR101653550B1 (ko) | 2008-09-16 | 2016-09-02 | 베링거 인겔하임 인터내셔날 게엠베하 | 강력한 hcv 억제제인 2-티아졸릴-4-퀴놀리닐-옥시 유도체의 결정 형태 |
| BRPI0918653A2 (pt) | 2008-09-17 | 2015-12-01 | Boehringer Ingelheim Int | combinação de inibidor de ns3 protese de hcv com interferon e ribavirina. |
| WO2010031832A2 (en) | 2008-09-18 | 2010-03-25 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc | Synergistic combinations of a macrocyclic inhibitor of hcv and a thiophene-2-carboxylic acid derivative |
| AU2009296653A1 (en) | 2008-09-24 | 2010-04-01 | Janssen Pharmaceutica Nv | Therapeutic regimen comprising peg- interferon, ribavirin and VX-950 for the treatment of Hepatitis " |
| CN102227237A (zh) | 2008-09-26 | 2011-10-26 | 国家健康与医学研究院 | 作为针对hcv感染的抗病毒治疗的靶标的宿主细胞激酶 |
| CA2738985A1 (en) | 2008-09-30 | 2010-04-08 | Mochida Pharmaceutical Co., Ltd. | Therapeutic agent for hepatitis c |
| EP2341924A4 (en) | 2008-10-02 | 2013-01-23 | David Gladstone Inst | METHOD FOR THE TREATMENT OF HEPATITIS C VIRUS INFECTIONS |
| MX2011003813A (es) | 2008-10-08 | 2011-07-28 | Carolinas Medical Ct The Charlotte Mecklenburg Hospital Authority D B A | Tratamiento de la infeccion del virus de la hepatitis c con la sobreexpresion de arnmicro-196. |
| CA2740728A1 (en) | 2008-10-15 | 2010-04-22 | Intermune, Inc. | Therapeutic antiviral peptides |
| WO2010049438A2 (en) | 2008-10-30 | 2010-05-06 | Innate Pharma | Improved methods of using phosphoantigens for the treatment of diseases |
| WO2010053942A1 (en) | 2008-11-05 | 2010-05-14 | Vertex Pharmaceuticals Incorporated | Methods for treating hepatitis c virus infection |
| HRP20140097T1 (hr) | 2008-11-21 | 2014-03-14 | Boehringer Ingelheim International Gmbh | Farmaceutski sastav jakog hcv-inhibitora za oralnu primjenu |
| NZ592668A (en) | 2008-12-10 | 2013-12-20 | Achillion Pharmaceuticals Inc | New 4-amino-4-oxobutanoyl peptides as inhibitors of viral replication |
| EP2356236B1 (en) | 2008-12-11 | 2015-07-29 | Xiangxue Group (Hong Kong) Company Limited | siRNA COMPOSITIONS AND METHODS FOR POTENTLY INHIBITING VIRAL INFECTION |
| WO2010069809A1 (en) | 2008-12-18 | 2010-06-24 | F. Hoffmann-La Roche Ag | Biomarkers for hcv treatment response |
| CN102753563A (zh) | 2008-12-23 | 2012-10-24 | 吉利德制药有限责任公司 | 核苷类似物 |
| US20120009148A1 (en) | 2008-12-29 | 2012-01-12 | Yissum Research Development Company Of The Hebrew University Of Jerusalem, Ltd. | Methods of predicting responsiveness to interferon treatment and treating hepatitis c infection |
| US8840934B2 (en) | 2009-01-02 | 2014-09-23 | Rainbow Pharmaceutical Sa | Uses of ammonium chloride |
| JP2012514657A (ja) | 2009-01-09 | 2012-06-28 | ユニバーシテイ・カレツジ・オブ・カーデイフ・コンサルタンツ・リミテツド | ウィルス感染を治療するためのグアノシンヌクレオシド化合物のホスホルアミダート誘導体 |
| RU2398582C1 (ru) | 2009-01-19 | 2010-09-10 | Государственное образовательное учреждение высшего профессионального образования "Санкт-Петербургская государственная медицинская академия им. И.М. Мечникова Федерального агентства по здравоохранению и социальному развитию" | Способ лечения хронического вирусного гепатита с 1-генотипа с умеренной активностью и репликативностью |
| EP2396028A2 (en) | 2009-02-12 | 2011-12-21 | Vertex Pharmceuticals Incorporated | Hcv combination therapies comprising pegylated interferon, ribavirin and telaprevir |
| US8101643B2 (en) | 2009-02-27 | 2012-01-24 | Enanta Pharmaceuticals, Inc. | Benzimidazole derivatives |
| AR075584A1 (es) | 2009-02-27 | 2011-04-20 | Intermune Inc | COMPOSICIONES TERAPEUTICAS QUE COMPRENDEN beta-D-2'-DESOXI-2'-FLUORO-2'-C-METILCITIDINA Y UN DERIVADO DE ACIDO ISOINDOL CARBOXILICO Y SUS USOS. COMPUESTO. |
| WO2010101649A2 (en) | 2009-03-05 | 2010-09-10 | Pablo Gastaminza | Sigma 1 receptor inhibition as a novel therapeutical approach against hepatitis c virus infection |
| MX2011008963A (es) | 2009-03-05 | 2012-02-01 | Ascendis Pharma As | Profarmacos portadores de interferon alfa. |
| US9034837B2 (en) | 2009-04-24 | 2015-05-19 | Roche Innovation Center Copenhagen A/S | Pharmaceutical compositions for treatment of HCV patients that are poor-responders to interferon |
| PT2421527T (pt) | 2009-04-25 | 2018-08-02 | Hoffmann La Roche | Métodos de melhoria farmacocinética |
| KR101503752B1 (ko) | 2009-05-13 | 2015-03-18 | 길리애드 파마셋 엘엘씨 | 항바이러스 화합물 |
| US8618076B2 (en) | 2009-05-20 | 2013-12-31 | Gilead Pharmasset Llc | Nucleoside phosphoramidates |
| TWI576352B (zh) * | 2009-05-20 | 2017-04-01 | 基利法瑪席特有限責任公司 | 核苷磷醯胺 |
| WO2010135649A1 (en) | 2009-05-21 | 2010-11-25 | Schering Corporation | Genetic markers associated with interferon-alpha response |
| US8691938B2 (en) * | 2009-06-11 | 2014-04-08 | Abbvie Inc. | Anti-viral compounds |
| TW201113279A (en) | 2009-06-23 | 2011-04-16 | Gilead Sciences Inc | Pharmaceutical compositions useful for treating HCV |
| WO2010151488A1 (en) | 2009-06-23 | 2010-12-29 | Gilead Sciences, Inc. | Combination of boceprevir with 5- ( { 6- [2, 4- bis (trifluoromethyl) phenyl] pyridazin-3 -yl } methyl) -2- (2 -fluorophenyl) -5h- imidazo [4, 5-c] pyridine for the treatment of hcv |
| TW201111381A (en) | 2009-06-23 | 2011-04-01 | Gilead Sciences Inc | Pharmaceutical combinations useful for treating HCV |
| AU2010264479B2 (en) | 2009-06-26 | 2017-06-01 | Romark Laboratories L.C. | Compounds and methods for treating influenza |
| PE20120322A1 (es) | 2009-07-07 | 2012-04-14 | Boehringer Ingelheim Int | Composicion farmaceutica que comprende faldaprevir o una sal del mismo en un vehiculo auto-emulsionante |
| RU2400229C1 (ru) | 2009-07-13 | 2010-09-27 | Государственное образовательное учреждение высшего профессионального образования "Санкт-Петербургская государственная медицинская академия им. И.И. Мечникова Федерального агентства по здравоохранению и социальному развитию" | СПОСОБ ЛЕЧЕНИЯ БОЛЬНЫХ ХРОНИЧЕСКИМ ВИРУСНЫМ ГЕПАТИТОМ С, ГЕНОТИПОМ 3а |
| EP2467144A1 (en) | 2009-07-24 | 2012-06-27 | ViroLogik GmbH | Combination of proteasome inhibitors and anti-hepatitis medication for treating hepatitis |
| WO2011014882A1 (en) | 2009-07-31 | 2011-02-03 | Medtronic, Inc. | CONTINUOUS SUBCUTANEOUS ADMINISTRATION OF INTERFERON-α TO HEPATITIS C INFECTED PATIENTS |
| JP2013500713A (ja) | 2009-07-31 | 2013-01-10 | サントル オスピタリエ ウニヴェルシテール ヴォドア | Hcv感染患者においてc型肝炎の転帰を診断又は予測する方法 |
| CN102470158A (zh) | 2009-08-27 | 2012-05-23 | 默沙东公司 | 制备丙型肝炎病毒的蛋白酶抑制剂的工艺方法 |
| WO2011038224A1 (en) | 2009-09-24 | 2011-03-31 | Trustees Of Boston University | Methods for treating viral disorders |
| WO2011041551A1 (en) | 2009-10-01 | 2011-04-07 | Intermune, Inc. | Therapeutic antiviral peptides |
| US8415374B2 (en) | 2009-10-12 | 2013-04-09 | Bristol-Myers Squibb Company | Combinations of hepatitis C virus inhibitors |
| US8729058B2 (en) | 2009-10-27 | 2014-05-20 | Michael Zasloff | Methods and compositions for treating and preventing viral infections |
| US9174988B2 (en) | 2009-10-27 | 2015-11-03 | Trustees Of Boston University | Small molecule inhibitors of hepatitis C virus |
| KR20120106942A (ko) | 2009-10-30 | 2012-09-27 | 베링거 인겔하임 인터내셔날 게엠베하 | Bi201335, 인터페론 알파 및 리바비린을 포함하는 hcv 병용 치료요법을 위한 투여 용법 |
| AU2010325065A1 (en) | 2009-11-09 | 2012-05-24 | Merck Sharp & Dohme Corp. | Markers associated with ribavirin-induced anemia |
| WO2011063076A1 (en) | 2009-11-19 | 2011-05-26 | Itherx Pharmaceuticals, Inc. | Methods of treating hepatitis c virus with oxoacetamide compounds |
| US8623416B2 (en) | 2009-11-25 | 2014-01-07 | Michael Zasloff | Formulations comprising aminosterols |
| WO2011081918A1 (en) * | 2009-12-14 | 2011-07-07 | Enanta Pharmaceuticals, Inc | Hepatitis c virus inhibitors |
| PH12012501216A1 (en) | 2009-12-18 | 2012-11-05 | Boehringer Ingelheim Int | Hcv combination therapy |
| WO2011079016A1 (en) | 2009-12-22 | 2011-06-30 | Gilead Sciences, Inc. | Methods of treating hbv and hcv infection |
| KR101762466B1 (ko) | 2009-12-23 | 2017-07-27 | 노파르티스 아게 | 지질, 지질 조성물 및 이의 사용 방법 |
| RU2424794C1 (ru) | 2009-12-30 | 2011-07-27 | Государственное образовательное учреждение высшего профессионального образования "Уральская государственная медицинская академия Федерального агентства по здравоохранению и социальному развитию" (ГОУ ВПО УГМА Росздрава) | Способ лечения врожденного гепатита с у детей первого года жизни |
| EP2528436A4 (en) * | 2010-01-25 | 2013-07-10 | Enanta Pharm Inc | INHIBITORS OF HEPATITIS C VIRUS |
| CN102844030A (zh) * | 2010-01-29 | 2012-12-26 | 沃泰克斯药物股份有限公司 | 用于治疗丙型肝炎病毒感染的疗法 |
| WO2011112558A2 (en) * | 2010-03-10 | 2011-09-15 | Abbott Laboratories | Solid compositions |
| US8530497B2 (en) | 2010-03-11 | 2013-09-10 | Boehringer Ingelheim International Gmbh | Crystalline salts of a potent HCV inhibitor |
| WO2011123668A2 (en) * | 2010-03-31 | 2011-10-06 | Pharmasset, Inc. | Stereoselective synthesis of phosphorus containing actives |
| NZ605440A (en) | 2010-06-10 | 2014-05-30 | Abbvie Bahamas Ltd | Solid compositions comprising an hcv inhibitor |
| TW201211047A (en) | 2010-06-10 | 2012-03-16 | Gilead Sciences Inc | Methods for treating HCV |
| US8592372B2 (en) | 2010-06-29 | 2013-11-26 | King Saud University Liver Disease | Pharmaceutical composition and method of use to improve organ function |
| RU2429877C1 (ru) | 2010-06-30 | 2011-09-27 | Общество с ограниченной ответственностью "ИНГИЛС" | Способ лечения хронического вирусного гепатита с |
| EP2593105A1 (en) | 2010-07-14 | 2013-05-22 | Vertex Pharmaceuticals Incorporated | Palatable pharmaceutical composition comprising vx-950 |
| US20140162942A1 (en) | 2010-07-30 | 2014-06-12 | Anima Ghosal | Inhibition of cyp3a drug metabolism |
| US20120196272A1 (en) | 2010-08-05 | 2012-08-02 | Roche Molecular Systems, Inc. | Prediction of HCV Viral Kinetics in Interferon-Free Treatment |
| US20120196794A1 (en) | 2010-08-06 | 2012-08-02 | Bristol-Myers Squibb Company | Combinations of Hepatitis C Virus Inhibitors |
| NZ607996A (en) | 2010-09-22 | 2014-07-25 | Alios Biopharma Inc | Substituted nucleotide analogs |
| US20130280214A1 (en) | 2010-09-29 | 2013-10-24 | Merck Sharp & Dohme Corp. | Polycyclic heterocycle derivatives and methods of use thereof for the treatment of viral diseases |
| US20120135949A1 (en) | 2010-09-30 | 2012-05-31 | Boehringer Ingelheim International Gmbh | Combination therapy for treating hcv infection |
| BR112013009789A2 (pt) * | 2010-10-26 | 2016-07-19 | Presidio Pharmaceuticals Inc | inibidores do vírus da hepatite c |
| US20120107278A1 (en) | 2010-10-29 | 2012-05-03 | Pharmasset, Inc. | Abbreviated hcv therapy for hcv infected patients with il28b c/c genotype |
| CA2822037A1 (en) | 2010-12-20 | 2012-06-28 | Gilead Sciences, Inc. | Methods for treating hcv |
| WO2012139028A2 (en) | 2011-04-06 | 2012-10-11 | The Trustees Of Princeton University | Anti-viral combination therapy |
| US20140127159A1 (en) | 2011-06-23 | 2014-05-08 | Stella Aps | HCV Combination Therapy |
| WO2013000856A1 (en) | 2011-06-30 | 2013-01-03 | Santaris Pharma A/S | Hcv combination therapy |
| KR20140064765A (ko) | 2011-06-30 | 2014-05-28 | 스텔라 에이피에스 | Hcv 조합 치료 |
| WO2013024155A1 (en) | 2011-08-17 | 2013-02-21 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Combinations of anti-hcv-entry factor antibodies and direct acting antivirals for the treatment and the prevention of hcv infection |
| WO2013025975A1 (en) | 2011-08-17 | 2013-02-21 | Glaxosmithkline Llc | Combination treatments for hepatitis c |
| WO2013024158A1 (en) | 2011-08-17 | 2013-02-21 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Combinations of protein kinase inhibitors and interferons or of protein kinase inhibitors and direct acting antivirals for the treatment and the prevention of hcv infection |
| AU2012298750A1 (en) | 2011-08-24 | 2014-03-13 | Glaxosmithkline Llc | Combination treatments for Hepatitis C |
| SG10201602044WA (en) * | 2011-09-16 | 2016-04-28 | Gilead Pharmassett Llc | Methods For Treating HCV |
| DE112012003457T5 (de) | 2011-10-21 | 2015-03-12 | Abbvie Inc. | Kombinationsbehandlung (z.B. mit ABT-072 oder ABT-333 von DAAs zur Verwendung in der Behandlung von HCV) |
| TWI532487B (zh) | 2011-10-21 | 2016-05-11 | 艾伯維有限公司 | 治療c型肝炎病毒(hcv)之方法 |
| US8466159B2 (en) * | 2011-10-21 | 2013-06-18 | Abbvie Inc. | Methods for treating HCV |
| US8492386B2 (en) * | 2011-10-21 | 2013-07-23 | Abbvie Inc. | Methods for treating HCV |
| KR20140098759A (ko) | 2011-10-31 | 2014-08-08 | 머크 샤프 앤드 돔 코포레이션 | 바이러스성 질환의 치료에 유용한 조성물 |
| US20130137084A1 (en) | 2011-11-28 | 2013-05-30 | Roche Molecular Systems, Inc. | Single Nucleotide Polymorphism on Chromosome 15 That Predicts HCV Treatment Responses |
| AU2012358804B2 (en) | 2011-12-22 | 2018-04-19 | Alios Biopharma, Inc. | Substituted phosphorothioate nucleotide analogs |
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