MA34002B1 - Thérapie antivirale - Google Patents
Thérapie antiviraleInfo
- Publication number
- MA34002B1 MA34002B1 MA35145A MA35145A MA34002B1 MA 34002 B1 MA34002 B1 MA 34002B1 MA 35145 A MA35145 A MA 35145A MA 35145 A MA35145 A MA 35145A MA 34002 B1 MA34002 B1 MA 34002B1
- Authority
- MA
- Morocco
- Prior art keywords
- antiviral therapy
- treatment
- hiv
- aids
- combinations
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/536—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines ortho- or peri-condensed with carbocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2121/00—Preparations for use in therapy
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Dermatology (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physiology (AREA)
- Nutrition Science (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
La présente invention concerne des combinaisons de composés comprenant des inhibiteurs de l'intégrase du vih et d'autres agents thérapeutiques. Lesdites combinaisons peuvent être utilisées dans le cadre de l'inhibition de la réplication du vih, de la prévention et/ou du traitement de l'infection par le vih et du traitement du sida et/ou du syndrome pré-sida.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US29858910P | 2010-01-27 | 2010-01-27 | |
| PCT/US2011/022219 WO2011094150A1 (fr) | 2010-01-27 | 2011-01-24 | Thérapie antivirale |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA34002B1 true MA34002B1 (fr) | 2013-02-01 |
Family
ID=44319704
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA35145A MA34002B1 (fr) | 2010-01-27 | 2011-01-24 | Thérapie antivirale |
Country Status (45)
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SMT201800290T1 (it) | 2010-01-27 | 2018-07-17 | Viiv Healthcare Co | Terapia antivirale |
| NZ706223A (en) | 2012-10-23 | 2018-11-30 | Cipla Ltd | Pharmaceutical antiretroviral composition |
| PE20151499A1 (es) | 2012-12-21 | 2015-10-29 | Gilead Sciences Inc | Compuestos de carbamoilpiridona policiclicos y su uso farmaceutico |
| EP2767272A1 (fr) * | 2013-02-18 | 2014-08-20 | Ratiopharm GmbH | Forme posologique pharmaceutique solide de dolutegravir |
| CA2897137A1 (fr) * | 2013-02-18 | 2014-08-21 | Ratiopharm Gmbh | Forme galenique pharmaceutique solide de dolutegravir |
| EP3252058B1 (fr) | 2013-07-12 | 2021-01-20 | Gilead Sciences, Inc. | Composés polycycliques-carbamoylpyridone et leur utilisation pour le traitement des infections par vih |
| NO2865735T3 (fr) | 2013-07-12 | 2018-07-21 | ||
| AU2014324829B2 (en) | 2013-09-27 | 2017-09-07 | Merck Sharp & Dohme Corp. | Substituted Quinolizine Derivatives useful as HIV integrase inhibitors |
| IN2014MU00916A (fr) | 2014-03-20 | 2015-09-25 | Cipla Ltd | |
| EP3151920B1 (fr) | 2014-06-04 | 2025-08-06 | Sanford-Burnham Medical Research Institute | Utilisation d'un inhibiteur des antagonistes de la protéine d'apoptose (iap) dans une thérapie contre le vih |
| TWI744723B (zh) | 2014-06-20 | 2021-11-01 | 美商基利科學股份有限公司 | 多環型胺甲醯基吡啶酮化合物之合成 |
| NO2717902T3 (fr) | 2014-06-20 | 2018-06-23 | ||
| TW201613936A (en) | 2014-06-20 | 2016-04-16 | Gilead Sciences Inc | Crystalline forms of(2R,5S,13aR)-8-hydroxy-7,9-dioxo-n-(2,4,6-trifluorobenzyl)-2,3,4,5,7,9,13,13a-octahydro-2,5-methanopyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxamide |
| JP6603306B2 (ja) | 2014-07-29 | 2019-11-06 | レツク・フアーマシユーテイカルズ・デー・デー | ドルテグラビルナトリウムの新規な水和物 |
| TWI695003B (zh) | 2014-12-23 | 2020-06-01 | 美商基利科學股份有限公司 | 多環胺甲醯基吡啶酮化合物及其醫藥用途 |
| KR20190057158A (ko) | 2015-04-02 | 2019-05-27 | 길리애드 사이언시즈, 인코포레이티드 | 폴리시클릭-카르바모일피리돈 화합물 및 그의 제약 용도 |
| EP3334419A1 (fr) * | 2015-08-14 | 2018-06-20 | Sandoz AG | Composition pharmaceutique solide d'abacavir, de lamivudine et d'éfavirenz |
| WO2017205585A1 (fr) * | 2016-05-27 | 2017-11-30 | Viiv Healthcare Company | Combinaisons, utilisations et traitements correspondants |
| WO2018028841A1 (fr) * | 2016-08-12 | 2018-02-15 | Sandoz Ag | Composé pharmaceutique solide d'abacavir, de lamivudine et d'éfavirenz. |
| WO2018042332A1 (fr) * | 2016-08-31 | 2018-03-08 | Glaxosmithkline Intellectual Property (No.2) Limited | Combinaisons, utilisations et traitements correspondants |
| US20200138845A1 (en) * | 2017-07-18 | 2020-05-07 | Viiv Healthcare Company | Combination Drug Therapy |
| JP7384783B2 (ja) | 2017-07-21 | 2023-11-21 | ヴィーブ ヘルスケア カンパニー | Hiv感染症及びaidsを治療するためのレジメン |
| US20200147092A1 (en) * | 2017-07-21 | 2020-05-14 | Viiv Healthcare Company | Regimens for treating hiv infections and aids |
| MX2020003377A (es) * | 2017-10-13 | 2020-09-28 | Viiv Healthcare Co | Formulacion de tableta farmaceutica de dos capas. |
| TW202544011A (zh) | 2019-03-22 | 2025-11-16 | 美商基利科學股份有限公司 | 橋鍵聯三環胺甲醯吡啶酮化合物及其醫藥用途 |
| CN114901363A (zh) * | 2020-01-09 | 2022-08-12 | 华盛顿大学 | 长效治疗剂组合物及其方法 |
| JP7453399B2 (ja) | 2020-02-24 | 2024-03-19 | ギリアード サイエンシーズ, インコーポレイテッド | Hiv感染症を治療するための四環式化合物及びその使用 |
| KR20230079137A (ko) | 2020-09-30 | 2023-06-05 | 길리애드 사이언시즈, 인코포레이티드 | 가교된 트리사이클릭 카르바모일피리돈 화합물 및 이의 용도 |
| PL4196479T3 (pl) | 2021-01-19 | 2024-03-18 | Gilead Sciences, Inc. | Podstawione związki pirydotriazynowe i ich zastosowania |
| CN114230579A (zh) * | 2021-11-12 | 2022-03-25 | 南京艾迪医药科技有限公司 | 多环氨基甲酰基吡啶酮衍生物及其制备方法和药物组合物 |
| AU2023225805A1 (en) * | 2022-02-28 | 2024-10-17 | Jericho Sciences, Llc | Methods for viral infections |
| TWI856796B (zh) | 2022-04-06 | 2024-09-21 | 美商基利科學股份有限公司 | 橋聯三環胺甲醯基吡啶酮化合物及其用途 |
Family Cites Families (78)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5047407A (en) | 1989-02-08 | 1991-09-10 | Iaf Biochem International, Inc. | 2-substituted-5-substituted-1,3-oxathiolanes with antiviral properties |
| US7119202B1 (en) | 1989-02-08 | 2006-10-10 | Glaxo Wellcome Inc. | Substituted-1,3-oxathiolanes and substituted-1,3-dioxolanes with antiviral properties |
| GB8815265D0 (en) | 1988-06-27 | 1988-08-03 | Wellcome Found | Therapeutic nucleosides |
| GB9009861D0 (en) | 1990-05-02 | 1990-06-27 | Glaxo Group Ltd | Chemical compounds |
| ZA923641B (en) | 1991-05-21 | 1993-02-24 | Iaf Biochem Int | Processes for the diastereoselective synthesis of nucleosides |
| GB9111902D0 (en) | 1991-06-03 | 1991-07-24 | Glaxo Group Ltd | Chemical compounds |
| GB9204015D0 (en) | 1992-02-25 | 1992-04-08 | Wellcome Found | Therapeutic nucleosides |
| US5663169A (en) | 1992-08-07 | 1997-09-02 | Merck & Co., Inc. | Benzoxazinones as inhibitors of HIV reverse transcriptase |
| IL106507A (en) | 1992-08-07 | 1997-11-20 | Merck & Co Inc | Pharmaceutical compositions containing benzoxazinones and some novel compounds of this type |
| GB9402161D0 (en) | 1994-02-04 | 1994-03-30 | Wellcome Found | Chloropyrimidine intermediates |
| IL113432A (en) | 1994-04-23 | 2000-11-21 | Glaxo Group Ltd | Process for the diastereoselective synthesis of nucleoside analogues |
| UA49803C2 (uk) | 1994-06-03 | 2002-10-15 | Дж.Д. Сьорль Енд Ко | Спосіб лікування ретровірусних інфекцій |
| MY115461A (en) | 1995-03-30 | 2003-06-30 | Wellcome Found | Synergistic combinations of zidovudine, 1592u89 and 3tc |
| US5914332A (en) | 1995-12-13 | 1999-06-22 | Abbott Laboratories | Retroviral protease inhibiting compounds |
| US5849911A (en) | 1996-04-22 | 1998-12-15 | Novartis Finance Corporation | Antivirally active heterocyclic azahexane derivatives |
| AU727983B2 (en) * | 1996-06-25 | 2001-01-04 | Glaxo Group Limited | Combinations comprising VX478, zidovudine, FTC and/or 3TC for use in the treatment of HIV |
| US5922695A (en) | 1996-07-26 | 1999-07-13 | Gilead Sciences, Inc. | Antiviral phosphonomethyoxy nucleotide analogs having increased oral bioavarilability |
| US5965729A (en) | 1997-02-05 | 1999-10-12 | Merck & Co., Inc. | Process for the crystallization of a reverse transcriptase inhibitor using an anti-solvent |
| GB9709945D0 (en) | 1997-05-17 | 1997-07-09 | Glaxo Group Ltd | A novel salt |
| US5935946A (en) | 1997-07-25 | 1999-08-10 | Gilead Sciences, Inc. | Nucleotide analog composition and synthesis method |
| GB9717928D0 (en) | 1997-08-22 | 1997-10-29 | Glaxo Group Ltd | Process for the enatioselective hydrolysis of n-derivatised lactams |
| GB9721780D0 (en) | 1997-10-14 | 1997-12-10 | Glaxo Group Ltd | Process for the synthesis of chloropurine intermediates |
| US6436989B1 (en) | 1997-12-24 | 2002-08-20 | Vertex Pharmaceuticals, Incorporated | Prodrugs of aspartyl protease inhibitors |
| US6087383A (en) | 1998-01-20 | 2000-07-11 | Bristol-Myers Squibb Company | Bisulfate salt of HIV protease inhibitor |
| GB9805898D0 (en) | 1998-03-20 | 1998-05-13 | Glaxo Group Ltd | Process for the sythesis of hiv protease inhibitors |
| AU3366899A (en) | 1998-03-27 | 1999-10-18 | Regents Of The University Of California, The | Novel hiv integrase inhibitors and hiv therapy based on drug combinations including integrase inhibitors |
| UA72207C2 (uk) | 1998-04-07 | 2005-02-15 | Брістол- Майєрс Сквібб Фарма Компані | Фармацевтична композиція ефавіренцу з добавкою дезінтегруючих агентів у вигляді швидкорозчинних капсул або таблеток та спосіб її виготовлення |
| GB9809213D0 (en) * | 1998-04-29 | 1998-07-01 | Glaxo Group Ltd | Pharmaceutical compositions |
| GB9815567D0 (en) | 1998-07-18 | 1998-09-16 | Glaxo Group Ltd | Antiviral compound |
| AU784782B2 (en) | 2000-01-31 | 2006-06-15 | Cook Biotech, Incorporated | Stent valves and uses of same |
| BRPI0208811B8 (pt) | 2001-04-10 | 2021-05-25 | Pfizer | derivados de pirazol, seu uso e processo de preparação, bem como composição farmacêutica compreendendo os mesmos |
| MY169670A (en) | 2003-09-03 | 2019-05-08 | Tibotec Pharm Ltd | Combinations of a pyrimidine containing nnrti with rt inhibitors |
| US7638522B2 (en) * | 2001-08-13 | 2009-12-29 | Janssen Pharmaceutica N.V. | Salt of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]amino] benzonitrile |
| JO3429B1 (ar) | 2001-08-13 | 2019-10-20 | Janssen Pharmaceutica Nv | مشتقات برميدينات مثبطة فيروس الايدز |
| TW200403061A (en) | 2002-06-04 | 2004-03-01 | Glaxo Group Ltd | Pharmaceutical compositions |
| CN1302779C (zh) * | 2002-06-27 | 2007-03-07 | 美迪维尔公司 | 含有阿巴卡韦和阿洛夫定的药物制剂及其用途 |
| EA201100293A1 (ru) * | 2003-01-14 | 2011-08-30 | Джилид Сайэнс, Инк. | Способ (варианты) и фармацевтическая композиция (варианты) для лечения или профилактики симптомов вич-инфекции |
| TW200510425A (en) | 2003-08-13 | 2005-03-16 | Japan Tobacco Inc | Nitrogen-containing fused ring compound and use thereof as HIV integrase inhibitor |
| EP1720856B1 (fr) * | 2004-02-11 | 2013-08-14 | GlaxoSmithKline LLC | Inhibiteurs de l'integrase du vih |
| JP4285353B2 (ja) | 2004-03-05 | 2009-06-24 | 清水建設株式会社 | 化学物質放散度評価方法 |
| EP1742642B1 (fr) * | 2004-04-14 | 2008-10-15 | Gilead Sciences, Inc. | Analogues de phosphonate de composes inhibiteurs de l'integrase du vih |
| EP3287130A1 (fr) | 2004-05-21 | 2018-02-28 | Japan Tobacco Inc. | Combinaisons comportant un dérivé d'isoquinolone 4 et inhibiteurs de la protease |
| US7176196B2 (en) | 2004-05-28 | 2007-02-13 | Bristol-Myers Squibb Company | Bicyclic heterocycles as HIV integrase inhibitors |
| EP1930011B1 (fr) | 2004-08-23 | 2011-08-17 | Teva Pharmaceutical Industries Ltd | Forme cristalline de ibandronate de sodium |
| WO2006024668A1 (fr) | 2004-09-02 | 2006-03-09 | Janssen Pharmaceutica N.V. | Chlorhydrate de 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethyl-phenyl]amino]-2-pyrimidinyl]amino]benzonitrile |
| ATE479693T1 (de) | 2004-09-17 | 2010-09-15 | Idenix Pharmaceuticals Inc | Phosphoindole als hiv-inhibitoren |
| US7250421B2 (en) | 2005-01-31 | 2007-07-31 | University Of Georgia Research Foundation, Inc. | Diketo acids with nucleobase scaffolds: anti-HIV replication inhibitors targeted at HIV integrase |
| US20090093454A1 (en) | 2005-03-04 | 2009-04-09 | Kristjan Gudmundsson | Chemical Compounds |
| UA96568C2 (en) * | 2005-04-28 | 2011-11-25 | Глаксосмиткляйн Ллк | Polycyclic carbamoyl pyridone derivative as hiv-integrase inhibitor |
| BRPI0610030B8 (pt) * | 2005-04-28 | 2022-01-11 | Glaxosmithkline Llc | Composto, composição farmacêutica, e, uso de um composto |
| CA2610029A1 (fr) | 2005-06-01 | 2006-12-07 | Bioalliance Pharma | Combinaisons synergiques comprenant un compose de styrylquinoleine et d'autres agents therapeutiques contre une infection au vih |
| UA108605C2 (uk) * | 2005-12-30 | 2015-05-25 | Спосіб покращення фармакокінетики інгібіторів інтегрази віл | |
| SG170795A1 (en) | 2005-12-30 | 2011-05-30 | Gilead Sciences Inc | Methods for improving the pharmacokinetics of hiv integrase inhibitors |
| JP5754005B2 (ja) * | 2006-01-20 | 2015-07-22 | ヤンセン・アールアンドデイ・アイルランド | Tcm278を用いるhiv−感染症の長期間処置 |
| US20080039428A1 (en) | 2006-06-29 | 2008-02-14 | Panacos Pharmaceuticals, Inc. | Antiretroviral combination therapy |
| PT2069303E (pt) | 2006-07-21 | 2016-06-08 | Gilead Sciences Inc | Inibidores de protease antiviral |
| NZ575831A (en) | 2006-09-29 | 2011-12-22 | Idenix Pharmaceuticals Inc | Enantiomerically pure phosphoindoles as hiv inhibitors |
| PL2487161T5 (pl) | 2007-02-23 | 2024-09-09 | Gilead Sciences, Inc. | <div>Modulatory właściwości farmakokinetycznych środków terapeutycznych</div><div> </div> |
| TW200835693A (en) | 2007-02-23 | 2008-09-01 | Auspex Pharmaceuticals Inc | Preparation and utility of non-nucleoside reverse transcriptase inhibitors |
| US8354421B2 (en) | 2007-06-29 | 2013-01-15 | Korea Research Insitute Of Chemical Technology | HIV reverse transcriptase inhibitors |
| EA200971115A1 (ru) | 2007-06-29 | 2010-04-30 | Корея Рисерч Инститьют Оф Кемикал Текнолоджи | Новые ингибиторы обратной транскриптазы вич |
| CA2692331A1 (fr) | 2007-07-06 | 2009-01-15 | Gilead Sciences, Inc. | Modulateurs des proprietes pharmacocinetiques de substances therapeutiques |
| HRP20131128T1 (hr) * | 2007-07-12 | 2013-12-20 | Janssen R&D Ireland | Kristalni oblik (e) 4-[[4-[[4-(2-cijanoetenil)-2,6-dimetilfenil]amino]-2-pirimidinil]amino]benzonitrila |
| WO2009058923A1 (fr) | 2007-10-31 | 2009-05-07 | Smithkline Beecham Corporation | Antagonistes de ccr5 en tant qu'agents thérapeutiques |
| EP2217573A4 (fr) | 2007-11-01 | 2011-08-31 | Uab Research Foundation | Traitement et prévention d'infections virales |
| US8108055B2 (en) | 2007-12-28 | 2012-01-31 | Larry Wong | Method, system and apparatus for controlling an electrical device |
| JP2011508748A (ja) * | 2008-01-03 | 2011-03-17 | バイロケム ファーマ インコーポレイテッド | 新規のルパン誘導体 |
| MX2010007374A (es) | 2008-01-03 | 2010-10-05 | Virochem Pharma Inc | Nuevos derivados de c-21-ceto lupano, preparacion y uso de los mismos. |
| AU2008346823B2 (en) | 2008-01-04 | 2015-03-12 | Gilead Sciences, Inc. | Inhibitors of cytochrome P450 |
| JP2011511812A (ja) | 2008-02-14 | 2011-04-14 | バイロケム ファーマ インコーポレイテッド | 新規17βルパン誘導体 |
| WO2009148600A2 (fr) * | 2008-06-06 | 2009-12-10 | Concert Pharmaceuticals, Inc. | Composés à base de lysine deutérée |
| DK2320908T3 (en) * | 2008-07-25 | 2014-03-10 | Viiv Healthcare Co | DOLUTEGRAVIR prodrugs |
| JP5572168B2 (ja) | 2008-12-11 | 2014-08-13 | ビーブ・ヘルスケア・カンパニー | カルバモイルピリドンhivインテグラーゼ阻害剤の製造方法および中間体 |
| JP5086478B2 (ja) | 2008-12-11 | 2012-11-28 | 塩野義製薬株式会社 | カルバモイルピリドンhivインテグラーゼ阻害剤及びそれらの中間体の合成 |
| SMT201800290T1 (it) | 2010-01-27 | 2018-07-17 | Viiv Healthcare Co | Terapia antivirale |
| GB201006038D0 (en) | 2010-04-12 | 2010-05-26 | Unilever Plc | Improvements relating to antiviral compositions |
| CN103402516B (zh) | 2010-06-17 | 2018-01-30 | 富津世生物技术有限公司 | 用作抗病毒药物的化合物、组合物及使用方法 |
| AU2012236332A1 (en) | 2011-04-01 | 2013-10-31 | Chiesi Farmaceutici S.P.A. | Short -acting dihydropyridines (clevidipine) for use in reducing stroke damage |
-
2011
- 2011-01-24 SM SM20180290T patent/SMT201800290T1/it unknown
- 2011-01-24 MX MX2014014688A patent/MX367937B/es unknown
- 2011-01-24 MX MX2014014689A patent/MX356891B/es unknown
- 2011-01-24 RS RS20240189A patent/RS65183B1/sr unknown
- 2011-01-24 MY MYPI2012003346A patent/MY188334A/en unknown
- 2011-01-24 SG SG10201707183TA patent/SG10201707183TA/en unknown
- 2011-01-24 SG SG2012053492A patent/SG182614A1/en unknown
- 2011-01-24 PH PH1/2012/501537A patent/PH12012501537A1/en unknown
- 2011-01-24 ES ES19151897T patent/ES2969969T3/es active Active
- 2011-01-24 SI SI201131593T patent/SI3127542T1/sl unknown
- 2011-01-24 MX MX2012008774A patent/MX2012008774A/es active IP Right Grant
- 2011-01-24 RS RS20180667A patent/RS57323B1/sr unknown
- 2011-01-24 MY MYPI2021001818A patent/MY207233A/en unknown
- 2011-01-24 EA EA201892277A patent/EA037601B1/ru active Protection Beyond IP Right Term
- 2011-01-24 PL PL16187411T patent/PL3127542T3/pl unknown
- 2011-01-24 AP AP2012006445A patent/AP3551A/xx active
- 2011-01-24 LT LTEP16187411.0T patent/LT3127542T/lt unknown
- 2011-01-24 CA CA2967453A patent/CA2967453C/fr active Active
- 2011-01-24 RS RS20181178A patent/RS57728B1/sr unknown
- 2011-01-24 DK DK15164931.6T patent/DK2932970T3/en active
- 2011-01-24 AU AU2011209788A patent/AU2011209788C1/en active Active
- 2011-01-24 DK DK11737484.3T patent/DK2531027T3/en active
- 2011-01-24 NZ NZ601319A patent/NZ601319A/en unknown
- 2011-01-24 SG SG10201509476RA patent/SG10201509476RA/en unknown
- 2011-01-24 PT PT151649316T patent/PT2932970T/pt unknown
- 2011-01-24 PT PT191518976T patent/PT3494972T/pt unknown
- 2011-01-24 PL PL11737484T patent/PL2531027T3/pl unknown
- 2011-01-24 DK DK16187411.0T patent/DK3127542T3/en active
- 2011-01-24 PL PL15164931T patent/PL2932970T3/pl unknown
- 2011-01-24 FI FIEP19151897.6T patent/FI3494972T3/fi active
- 2011-01-24 BR BR112012018670-1A patent/BR112012018670A2/pt not_active Application Discontinuation
- 2011-01-24 HR HRP20150770TT patent/HRP20150770T1/hr unknown
- 2011-01-24 WO PCT/US2011/022219 patent/WO2011094150A1/fr not_active Ceased
- 2011-01-24 ES ES11737484.3T patent/ES2543066T3/es active Active
- 2011-01-24 EA EA202190473A patent/EA202190473A3/ru unknown
- 2011-01-24 SM SM20240063T patent/SMT202400063T1/it unknown
- 2011-01-24 PE PE2016000261A patent/PE20160180A1/es unknown
- 2011-01-24 NZ NZ627826A patent/NZ627826A/en unknown
- 2011-01-24 EP EP16187411.0A patent/EP3127542B1/fr active Active
- 2011-01-24 ES ES15164931.6T patent/ES2670811T3/es active Active
- 2011-01-24 UA UAA201209253A patent/UA105556C2/uk unknown
- 2011-01-24 EP EP15164931.6A patent/EP2932970B1/fr not_active Revoked
- 2011-01-24 CN CN201510619148.8A patent/CN105311033B/zh active Active
- 2011-01-24 CA CA3060290A patent/CA3060290C/fr active Active
- 2011-01-24 KR KR1020187018909A patent/KR101964923B1/ko active Active
- 2011-01-24 PT PT117374843T patent/PT2531027E/pt unknown
- 2011-01-24 JP JP2012551213A patent/JP2013518107A/ja active Pending
- 2011-01-24 EP EP19151897.6A patent/EP3494972B1/fr active Active
- 2011-01-24 EP EP23214771.0A patent/EP4316599A3/fr active Pending
- 2011-01-24 PT PT16187411T patent/PT3127542T/pt unknown
- 2011-01-24 SI SI201131492T patent/SI2932970T1/en unknown
- 2011-01-24 HR HRP20240168TT patent/HRP20240168T1/hr unknown
- 2011-01-24 EA EA201690872A patent/EA032868B1/ru active Protection Beyond IP Right Term
- 2011-01-24 MA MA35145A patent/MA34002B1/fr unknown
- 2011-01-24 NZ NZ627824A patent/NZ627824A/en unknown
- 2011-01-24 KR KR1020177017713A patent/KR20170078868A/ko not_active Ceased
- 2011-01-24 EA EA201290583A patent/EA025176B1/ru active Protection Beyond IP Right Term
- 2011-01-24 CN CN201180015114.8A patent/CN102791129B/zh active Active
- 2011-01-24 PE PE2012001082A patent/PE20121524A1/es active IP Right Grant
- 2011-01-24 MY MYPI2019000564A patent/MY202778A/en unknown
- 2011-01-24 HU HUE19151897A patent/HUE065569T2/hu unknown
- 2011-01-24 ES ES16187411.0T patent/ES2688925T3/es active Active
- 2011-01-24 US US13/575,380 patent/US20120295898A1/en not_active Abandoned
- 2011-01-24 ME MEP-2015-106A patent/ME02182B/me unknown
- 2011-01-24 ME MEP-2018-131A patent/ME03058B/fr unknown
- 2011-01-24 LT LTEP19151897.6T patent/LT3494972T/lt unknown
- 2011-01-24 SI SI201130539T patent/SI2531027T1/sl unknown
- 2011-01-24 EP EP18161536.0A patent/EP3351249A1/fr not_active Withdrawn
- 2011-01-24 PL PL19151897.6T patent/PL3494972T3/pl unknown
- 2011-01-24 KR KR1020167025050A patent/KR101883750B1/ko active Active
- 2011-01-24 EP EP11737484.3A patent/EP2531027B1/fr not_active Revoked
- 2011-01-24 HU HUE16187411A patent/HUE040554T2/hu unknown
- 2011-01-24 CA CA2787691A patent/CA2787691C/fr active Active
- 2011-01-24 MX MX2014014687A patent/MX367938B/es unknown
- 2011-01-24 SM SM20180594T patent/SMT201800594T1/it unknown
- 2011-01-24 LT LTEP15164931.6T patent/LT2932970T/lt unknown
- 2011-01-24 NZ NZ627827A patent/NZ627827A/en unknown
- 2011-01-24 RS RS20150462A patent/RS54123B1/sr unknown
- 2011-01-24 HU HUE15164931A patent/HUE037812T2/hu unknown
- 2011-01-24 CA CA3003988A patent/CA3003988C/fr active Active
- 2011-01-24 DK DK19151897.6T patent/DK3494972T3/da active
- 2011-01-24 SI SI201132101T patent/SI3494972T1/sl unknown
- 2011-01-24 NO NO15164931A patent/NO2932970T3/no unknown
- 2011-01-24 HU HUE11737484A patent/HUE026849T2/en unknown
- 2011-01-24 TR TR2018/07704T patent/TR201807704T4/tr unknown
- 2011-01-24 KR KR1020127022254A patent/KR101830715B1/ko active Active
-
2012
- 2012-07-18 IL IL221007A patent/IL221007A/en active IP Right Grant
- 2012-07-18 DO DO2012000205A patent/DOP2012000205A/es unknown
- 2012-07-24 ZA ZA2012/05586A patent/ZA201205586B/en unknown
- 2012-07-24 TN TNP2012000376A patent/TN2012000376A1/en unknown
- 2012-07-26 CO CO12125933A patent/CO6602152A2/es active IP Right Grant
- 2012-07-26 CL CL2012002080A patent/CL2012002080A1/es unknown
- 2012-08-13 CR CR20120423A patent/CR20120423A/es unknown
- 2012-08-14 EC ECSP12012106 patent/ECSP12012106A/es unknown
-
2013
- 2013-06-06 HK HK18109751.0A patent/HK1250335A1/en unknown
-
2015
- 2015-05-13 US US14/710,952 patent/US20150238496A1/en not_active Abandoned
- 2015-07-17 CY CY20151100633T patent/CY1116509T1/el unknown
- 2015-07-24 SM SM201500177T patent/SMT201500177B/xx unknown
-
2016
- 2016-01-28 PH PH12016500195A patent/PH12016500195B1/en unknown
- 2016-01-29 JP JP2016015242A patent/JP2016145204A/ja active Pending
- 2016-03-18 US US15/073,728 patent/US20160199379A1/en not_active Abandoned
- 2016-04-18 IL IL245182A patent/IL245182B/en active IP Right Grant
- 2016-08-01 US US15/224,865 patent/US20160339033A1/en not_active Abandoned
- 2016-08-22 JP JP2016161610A patent/JP6268386B2/ja active Active
- 2016-12-01 US US15/366,566 patent/US20170119777A1/en not_active Abandoned
- 2016-12-01 US US15/366,442 patent/US10426780B2/en active Active
-
2017
- 2017-04-19 US US15/490,944 patent/US20170216284A1/en not_active Abandoned
- 2017-06-13 US US15/620,859 patent/US20170281636A1/en not_active Abandoned
- 2017-12-12 US US15/838,738 patent/US20180098992A1/en not_active Abandoned
-
2018
- 2018-01-31 IL IL257267A patent/IL257267B/en active IP Right Grant
- 2018-03-15 US US15/922,240 patent/US20180200254A1/en not_active Abandoned
- 2018-04-05 JP JP2018072861A patent/JP2018127473A/ja active Pending
- 2018-05-23 CY CY20181100548T patent/CY1120457T1/el unknown
- 2018-05-30 HR HRP20180855TT patent/HRP20180855T1/hr unknown
- 2018-09-26 HR HRP20181531TT patent/HRP20181531T1/hr unknown
- 2018-10-15 FR FR18C1043C patent/FR18C1043I2/fr active Active
- 2018-10-15 NO NO2018036C patent/NO2018036I1/no unknown
- 2018-10-16 CY CY2018029C patent/CY2018029I1/el unknown
- 2018-10-22 LT LTPA2018013C patent/LTC2932970I2/lt unknown
- 2018-10-23 CY CY181101087T patent/CY1121040T1/el unknown
- 2018-10-26 HU HUS1800042C patent/HUS1800042I1/hu unknown
- 2018-10-31 LU LU00090C patent/LUC00090I2/en unknown
- 2018-11-26 PH PH12018502489A patent/PH12018502489A1/en unknown
-
2019
- 2019-06-07 JP JP2019106635A patent/JP2019167371A/ja active Pending
- 2019-06-26 IL IL267658A patent/IL267658B/en active IP Right Grant
-
2020
- 2020-03-31 US US16/835,733 patent/US11234985B2/en active Active
-
2021
- 2021-02-26 JP JP2021030306A patent/JP7724619B2/ja active Active
- 2021-04-01 IL IL281959A patent/IL281959B/en unknown
- 2021-07-14 DO DO2021000147A patent/DOP2021000147A/es unknown
- 2021-09-08 US US17/468,794 patent/US20210401850A1/en not_active Abandoned
-
2022
- 2022-03-03 JP JP2022032464A patent/JP2022071126A/ja active Pending
-
2023
- 2023-04-04 JP JP2023060638A patent/JP2023085431A/ja active Pending
-
2024
- 2024-02-16 CY CY20241100135T patent/CY1126771T1/el unknown
- 2024-05-31 LT LTPA2024516C patent/LTC3494972I2/lt unknown
- 2024-05-31 FI FIC20240016C patent/FIC20240016I1/fi unknown
- 2024-06-03 HU HUS2400017C patent/HUS2400017I1/hu unknown
- 2024-06-04 CY CY2024017C patent/CY2024017I1/el unknown
- 2024-06-06 FR FR24C1024C patent/FR24C1024I2/fr active Active
- 2024-10-01 US US18/903,013 patent/US20250017939A1/en active Pending
-
2025
- 2025-06-02 JP JP2025091741A patent/JP2025131664A/ja active Pending
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA34002B1 (fr) | Thérapie antivirale | |
| MA44674A (fr) | Inhibiteurs de bromodomaine | |
| MA34170B1 (fr) | Inhibiteurs de transcriptase inverse non nucléosidiques | |
| MA42410B1 (fr) | Oxystérols et leurs méthodes d'utilisation | |
| MA39721A (fr) | Nouvelles héteroaryldihydropyrimidines condensées en position 6 pour le traitement et la prophylaxie d'une infection à virus de l'hépatite b | |
| MA31036B1 (fr) | Inhibiteurs non nucleosidiques de la transcriptase inverse | |
| MA38182A1 (fr) | Compositions pharmaceutiques a action prolongée pur une utilisation dans le traitement ou la prévention d'infections par le virus de l’immunodéficience humaine (vih) | |
| MY186986A (en) | Compositions and methods of use of phorbol esters | |
| BRPI0509140A (pt) | processos para o tratamento de infecção por hiv | |
| MA38349A1 (fr) | Œstra-1,3,5(10),16-tétraéno-3-carboxamide pour inhiber la 17-bêta-hydroxystéroïde déshydrogénase (akr1c3) | |
| EP2555798A4 (fr) | Procédés et compositions pour l'inhibition de la transmission du vih | |
| WO2018033941A3 (fr) | Compositions pharmaceutiques à base d'ibrutinib | |
| WO2015126930A3 (fr) | Pharmacothérapie à effet "booster" pour lutter contre les infections à mycobacterium | |
| MA39447B1 (fr) | Pirlindole ou ses sels pharmaceutiquement acceptables pour une utilisation en médecine | |
| MA31902B1 (fr) | Oxazolidinones pour le traitement et/ou la prophylaxie de l'insuffisance cardiaque | |
| TW200738700A (en) | HIV integrase inhibitors | |
| MA39448A1 (fr) | (r)-pirlindole et ses sels pharmaceutiquement acceptables destinés à un usage médical | |
| MA40844A (fr) | Compositions pharmaceutiques à action prolongée pour l'hépatite c | |
| MA39533B1 (fr) | Composés, composition pharmaceutique et leur utilisation dans le traitement de maladies neurodégénératives | |
| MA46625B1 (fr) | Inhibiteurs de lsd1 et leurs utilisations médicales |