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)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Dermatology (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nutrition Science (AREA)
- Physiology (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 (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3351249A1 (fr) | 2010-01-27 | 2018-07-25 | VIIV Healthcare Company | Thérapie antivirale |
| EP2911674A1 (fr) | 2012-10-23 | 2015-09-02 | Cipla Limited | Composition pharmaceutique antirétrovirale |
| EA030003B1 (ru) | 2012-12-21 | 2018-06-29 | Джилид Сайэнс, Инк. | Полициклическое карбамоилпиридоновое соединение и его фармацевтическое применение для лечения вич-инфекции |
| CA2897137A1 (fr) * | 2013-02-18 | 2014-08-21 | Ratiopharm Gmbh | Forme galenique pharmaceutique solide de dolutegravir |
| EP2767272A1 (fr) * | 2013-02-18 | 2014-08-20 | Ratiopharm GmbH | Forme posologique pharmaceutique solide de dolutegravir |
| DK3019503T3 (da) | 2013-07-12 | 2017-11-20 | Gilead Sciences Inc | Polycykliske-carbamoylpyridon-forbindelser og anvendelse deraf til behandling af hiv-infektioner |
| NO2865735T3 (fr) | 2013-07-12 | 2018-07-21 | ||
| CA2924829C (fr) | 2013-09-27 | 2019-10-29 | Merck Sharp & Dohme Corp. | Derives de quinolizine substitues utiles en tant qu'inhibiteurs de l'integrase du vih |
| WO2015140569A1 (fr) | 2014-03-20 | 2015-09-24 | Cipla Limited | Composition pharmaceutique |
| JP6768522B2 (ja) | 2014-06-04 | 2020-10-14 | サンフォード−バーンハム メディカル リサーチ インスティテュート | Hiv治療におけるアポトーシスタンパク質阻害剤(iap)のアンタゴニストの使用 |
| 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 |
| 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 |
| EP3177629B1 (fr) | 2014-07-29 | 2020-01-29 | LEK Pharmaceuticals d.d. | Nouveaux hydrates de sodium de dolutegravir |
| 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 |
| CA2980362C (fr) | 2015-04-02 | 2020-02-25 | Gilead Sciences, Inc. | Composes carbamoylpyridones polycycliques et leur utilisation pharmaceutique |
| 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 |
| WO2019016732A1 (fr) | 2017-07-21 | 2019-01-24 | Viiv Healthcare Company | Régimes pour le traitement des infections du vih et du sida |
| JP2020528413A (ja) * | 2017-07-21 | 2020-09-24 | 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 |
| EP3694522B1 (fr) * | 2017-10-13 | 2025-11-26 | VIIV Healthcare Company | Formulation de comprimé pharmaceutique bicouche |
| KR20240151256A (ko) | 2019-03-22 | 2024-10-17 | 길리애드 사이언시즈, 인코포레이티드 | 가교된 트리시클릭 카르바모일피리돈 화합물 및 그의 제약 용도 |
| AU2020358156B2 (en) | 2019-10-01 | 2024-06-06 | Janssen Sciences Ireland Unlimited Company | Method for treating HIV with cabotegravir and rilpivirine |
| US12678509B2 (en) | 2019-11-08 | 2026-07-14 | Sanford Burnham Prebys Medical Discovery Institute | Inhibitor of apoptosis (IAP) protein antagonists |
| WO2021142150A1 (fr) * | 2020-01-09 | 2021-07-15 | University Of Washington | Combinaisons d'agents thérapeutiques à action prolongée et leurs procédés |
| EP4110783A1 (fr) | 2020-02-24 | 2023-01-04 | Gilead Sciences, Inc. | Composés tétracycliques pour le traitement d'une infection par le vih |
| CN116390924B (zh) | 2020-09-30 | 2025-11-07 | 吉利德科学公司 | 桥连三环氨基甲酰基吡啶酮化合物及其用途 |
| CR20260070A (es) | 2021-01-19 | 2026-04-24 | Gilead Sciences Inc | COMPUESTOS DE PIRIDOTRIAZINA SUSTITUIDOS Y USOS DE ESTOS (Divisional 2023-0315) |
| 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 |
| WO2023164293A1 (fr) * | 2022-02-28 | 2023-08-31 | Jericho Sciences, Llc | Méthodes d'infections virales |
| 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 |
|---|---|---|---|---|
| US7119202B1 (en) | 1989-02-08 | 2006-10-10 | Glaxo Wellcome Inc. | Substituted-1,3-oxathiolanes and substituted-1,3-dioxolanes with antiviral properties |
| US5047407A (en) | 1989-02-08 | 1991-09-10 | Iaf Biochem International, Inc. | 2-substituted-5-substituted-1,3-oxathiolanes 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 |
| IL106507A (en) | 1992-08-07 | 1997-11-20 | Merck & Co Inc | Pharmaceutical compositions containing benzoxazinones and some novel compounds of this type |
| US5663169A (en) | 1992-08-07 | 1997-09-02 | Merck & Co., Inc. | Benzoxazinones as inhibitors of HIV reverse transcriptase |
| 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 |
| KR20000022226A (ko) * | 1996-06-25 | 2000-04-25 | 그레이엄 브레레톤;레슬리 에드워즈 | Hiv 치료에 사용하기 위한 vx478, 지도부딘, ftc 및(또는) 3tc를 포함하는 배합물 |
| 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 |
| WO1999048371A1 (fr) | 1998-03-27 | 1999-09-30 | The Regents Of The University Of California | Nouveaux inhibiteurs de vih integrase et traitement du vih fonde sur des combinaisons de medicaments contenant des inhibiteurs d'integrase |
| 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 |
| KR100880550B1 (ko) | 2000-01-31 | 2009-01-30 | 쿠크 바이오텍, 인코포레이티드 | 판막 기구 및 심장 판막 기구 |
| SI1762567T1 (sl) | 2001-04-10 | 2012-08-31 | Pfizer | Derivati pirazola za zdravljenje HIV-a |
| 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 |
| MY169670A (en) | 2003-09-03 | 2019-05-08 | Tibotec Pharm Ltd | Combinations of a pyrimidine containing nnrti with rt inhibitors |
| 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 |
| BR0311141A (pt) | 2002-06-27 | 2005-06-07 | Medivir Ab | Interação sinergìstica de abacavir e alovudine |
| PT1583542E (pt) * | 2003-01-14 | 2008-09-17 | Gilead Sciences Inc | Composições e métodos para terapia de combinação antiviral |
| TW200510425A (en) | 2003-08-13 | 2005-03-16 | Japan Tobacco Inc | Nitrogen-containing fused ring compound and use thereof as HIV integrase inhibitor |
| CN1976915A (zh) * | 2004-02-11 | 2007-06-06 | 史密丝克莱恩比彻姆公司 | Hiv整合酶抑制剂 |
| 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 |
| SI1742642T1 (sl) * | 2004-04-14 | 2009-04-30 | Gilead Sciences Inc | Fosfonatni analogi inhibitorskih spojin HIV integraze |
| US8633219B2 (en) * | 2004-05-21 | 2014-01-21 | Japan Tobacco Inc. | Combination therapy |
| US7176196B2 (en) | 2004-05-28 | 2007-02-13 | Bristol-Myers Squibb Company | Bicyclic heterocycles as HIV integrase inhibitors |
| ES2358269T3 (es) | 2004-08-23 | 2011-05-09 | Teva Pharmaceutical Industries Ltd | Forma cristalina del ibandronato sódico y procedimientos para su preparación. |
| CA2577288C (fr) | 2004-09-02 | 2010-11-30 | Janssen Pharmaceutica N.V. | Chlorhydrate de 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethyl-phenyl]amino]-2-pyrimidinyl]amino]benzonitrile |
| AU2005305609B2 (en) | 2004-09-17 | 2011-10-06 | Idenix Pharmaceuticals, Inc. | Phosphoindoles as HIV inhibitors |
| 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 |
| WO2006096444A2 (fr) | 2005-03-04 | 2006-09-14 | Smithkline Beecham Corporation | Composes chimiques |
| DK3187225T3 (da) | 2005-04-28 | 2022-02-28 | Viiv Healthcare Co | Polycyklisk carbamoylpyridonderivat med hiv-integrasehæmmende aktivitet |
| CN101212903B (zh) * | 2005-04-28 | 2013-07-24 | 史密丝克莱恩比彻姆公司 | 具有hiv整合酶抑制活性的多环氨基甲酰基吡啶酮衍生物 |
| JP2008542352A (ja) | 2005-06-01 | 2008-11-27 | ビオアリアンス ファルマ | キノリン化合物及び他のhiv感染治療薬を含む相乗作用のコンビネーション |
| UA108605C2 (uk) * | 2005-12-30 | 2015-05-25 | Спосіб покращення фармакокінетики інгібіторів інтегрази віл | |
| US20070219243A1 (en) | 2005-12-30 | 2007-09-20 | Kearney Brian P | Method for improving the pharmacokinetics of HIV integrase inhibitors |
| AR059097A1 (es) * | 2006-01-20 | 2008-03-12 | Tibotec Pharm Ltd | Tratamiento a largo plazo de la infeccion por vih |
| 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 |
| ES2488922T3 (es) | 2006-09-29 | 2014-09-01 | Idenix Pharmaceuticals, Inc. | Fosfoindoles enantiómeramente puros como inhibidores del HIV |
| TW200835693A (en) | 2007-02-23 | 2008-09-01 | Auspex Pharmaceuticals Inc | Preparation and utility of non-nucleoside reverse transcriptase inhibitors |
| PT3150586T (pt) | 2007-02-23 | 2020-03-31 | Gilead Sciences Inc | Moduladores de propriedades farmacocinéticas de agentes terapêuticos |
| CN101784532B (zh) | 2007-06-29 | 2014-10-22 | 韩国化学研究院 | Hiv逆转录酶抑制剂 |
| US8354421B2 (en) | 2007-06-29 | 2013-01-15 | Korea Research Insitute Of Chemical Technology | HIV reverse transcriptase inhibitors |
| KR20100040896A (ko) | 2007-07-06 | 2010-04-21 | 길리애드 사이언시즈, 인코포레이티드 | 치료제의 약동학적 특성의 조절제 |
| 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 |
| JP2011502998A (ja) | 2007-11-01 | 2011-01-27 | ザ ユーエイビー リサーチ ファウンデイション | ウイルス感染の治療および予防 |
| US8108055B2 (en) | 2007-12-28 | 2012-01-31 | Larry Wong | Method, system and apparatus for controlling an electrical device |
| CA2711424A1 (fr) * | 2008-01-03 | 2009-07-09 | Virochem Pharma Inc. | Nouveaux derives de lupane |
| AU2008342536A1 (en) | 2008-01-03 | 2009-07-09 | Virochem Pharma Inc. | Novel C-21-keto lupane derivatives preparation and use thereof |
| PT2231628E (pt) | 2008-01-04 | 2015-12-29 | Gilead Sciences Inc | Inibidores de citocromo 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 |
| WO2010011812A1 (fr) * | 2008-07-25 | 2010-01-28 | Smithkline Beecham Corporation | Composés chimiques |
| EP3617194B1 (fr) | 2008-12-11 | 2023-11-08 | VIIV Healthcare Company | Procédés et intermédiaires pour inhibiteurs de l'intégrase du vih de carbamoylpyridone |
| SG171308A1 (en) | 2008-12-11 | 2011-07-28 | Shionogi & Co | Synthesis of carbamoylpyridone hiv integrase inhibitors and intermediates |
| EP3351249A1 (fr) | 2010-01-27 | 2018-07-25 | VIIV Healthcare Company | Thérapie antivirale |
| GB201006038D0 (en) | 2010-04-12 | 2010-05-26 | Unilever Plc | Improvements relating to antiviral compositions |
| EP2590971A4 (fr) | 2010-06-17 | 2014-12-10 | Fuzians Biomedicals Inc | Composés utiles en tant qu'agents antiviraux, compositions, et procédés d'utilisation |
| RU2623039C2 (ru) | 2011-04-01 | 2017-06-21 | КЬЕЗИ ФАРМАЧЕУТИЧИ С.п.А. | Дигидропиридины (клевидипин) кратковременного действия для применения в восстановлении после инсульта |
-
2011
- 2011-01-24 EP EP18161536.0A patent/EP3351249A1/fr not_active Withdrawn
- 2011-01-24 SM SM20180290T patent/SMT201800290T1/it unknown
- 2011-01-24 HU HUE11737484A patent/HUE026849T2/en unknown
- 2011-01-24 MY MYPI2019000564A patent/MY202778A/en unknown
- 2011-01-24 CA CA3003988A patent/CA3003988C/fr active Active
- 2011-01-24 ES ES19151897T patent/ES2969969T3/es active Active
- 2011-01-24 RS RS20181178A patent/RS57728B1/sr unknown
- 2011-01-24 EP EP15164931.6A patent/EP2932970B1/fr not_active Revoked
- 2011-01-24 US US13/575,380 patent/US20120295898A1/en not_active Abandoned
- 2011-01-24 AU AU2011209788A patent/AU2011209788C1/en active Active
- 2011-01-24 TR TR2018/07704T patent/TR201807704T4/tr unknown
- 2011-01-24 SG SG10201707183TA patent/SG10201707183TA/en unknown
- 2011-01-24 JP JP2012551213A patent/JP2013518107A/ja active Pending
- 2011-01-24 SI SI201131593T patent/SI3127542T1/sl unknown
- 2011-01-24 ES ES15164931.6T patent/ES2670811T3/es active Active
- 2011-01-24 PT PT151649316T patent/PT2932970T/pt unknown
- 2011-01-24 EP EP23214771.0A patent/EP4316599A3/fr active Pending
- 2011-01-24 MA MA35145A patent/MA34002B1/fr unknown
- 2011-01-24 CA CA3060290A patent/CA3060290C/fr active Active
- 2011-01-24 MX MX2012008774A patent/MX2012008774A/es active IP Right Grant
- 2011-01-24 SI SI201132101T patent/SI3494972T1/sl unknown
- 2011-01-24 DK DK19151897.6T patent/DK3494972T3/da active
- 2011-01-24 NZ NZ627827A patent/NZ627827A/en unknown
- 2011-01-24 ES ES11737484.3T patent/ES2543066T3/es active Active
- 2011-01-24 MY MYPI2012003346A patent/MY188334A/en unknown
- 2011-01-24 LT LTEP15164931.6T patent/LT2932970T/lt unknown
- 2011-01-24 SM SM20180594T patent/SMT201800594T1/it unknown
- 2011-01-24 DK DK11737484.3T patent/DK2531027T3/en active
- 2011-01-24 RS RS20240189A patent/RS65183B1/sr unknown
- 2011-01-24 RS RS20150462A patent/RS54123B1/sr unknown
- 2011-01-24 HU HUE16187411A patent/HUE040554T2/hu unknown
- 2011-01-24 NZ NZ627824A patent/NZ627824A/en unknown
- 2011-01-24 RS RS20180667A patent/RS57323B1/sr unknown
- 2011-01-24 PH PH1/2012/501537A patent/PH12012501537A1/en unknown
- 2011-01-24 FI FIEP19151897.6T patent/FI3494972T3/fi active
- 2011-01-24 EA EA201690872A patent/EA032868B1/ru active Protection Beyond IP Right Term
- 2011-01-24 CA CA2967453A patent/CA2967453C/fr active Active
- 2011-01-24 BR BR112012018670-1A patent/BR112012018670A2/pt not_active Application Discontinuation
- 2011-01-24 KR KR1020167025050A patent/KR101883750B1/ko active Active
- 2011-01-24 NO NO15164931A patent/NO2932970T3/no unknown
- 2011-01-24 HU HUE19151897A patent/HUE065569T2/hu unknown
- 2011-01-24 MY MYPI2021001818A patent/MY207233A/en unknown
- 2011-01-24 WO PCT/US2011/022219 patent/WO2011094150A1/fr not_active Ceased
- 2011-01-24 ES ES16187411.0T patent/ES2688925T3/es active Active
- 2011-01-24 PE PE2016000261A patent/PE20160180A1/es unknown
- 2011-01-24 EA EA201290583A patent/EA025176B1/ru active Protection Beyond IP Right Term
- 2011-01-24 EP EP16187411.0A patent/EP3127542B1/fr active Active
- 2011-01-24 PE PE2012001082A patent/PE20121524A1/es active IP Right Grant
- 2011-01-24 DK DK15164931.6T patent/DK2932970T3/en active
- 2011-01-24 SI SI201130539T patent/SI2531027T1/sl unknown
- 2011-01-24 SG SG10201509476RA patent/SG10201509476RA/en unknown
- 2011-01-24 LT LTEP19151897.6T patent/LT3494972T/lt unknown
- 2011-01-24 PT PT191518976T patent/PT3494972T/pt unknown
- 2011-01-24 PT PT16187411T patent/PT3127542T/pt unknown
- 2011-01-24 ME MEP-2015-106A patent/ME02182B/me unknown
- 2011-01-24 SI SI201131492T patent/SI2932970T1/en unknown
- 2011-01-24 NZ NZ627826A patent/NZ627826A/en unknown
- 2011-01-24 LT LTEP16187411.0T patent/LT3127542T/lt unknown
- 2011-01-24 CN CN201510619148.8A patent/CN105311033B/zh active Active
- 2011-01-24 UA UAA201209253A patent/UA105556C2/uk unknown
- 2011-01-24 PL PL19151897.6T patent/PL3494972T3/pl unknown
- 2011-01-24 HU HUE15164931A patent/HUE037812T2/hu unknown
- 2011-01-24 CN CN201180015114.8A patent/CN102791129B/zh active Active
- 2011-01-24 AP AP2012006445A patent/AP3551A/xx active
- 2011-01-24 PL PL16187411T patent/PL3127542T3/pl unknown
- 2011-01-24 MX MX2014014688A patent/MX367937B/es unknown
- 2011-01-24 MX MX2014014689A patent/MX356891B/es unknown
- 2011-01-24 EP EP19151897.6A patent/EP3494972B1/fr active Active
- 2011-01-24 DK DK16187411.0T patent/DK3127542T3/en active
- 2011-01-24 KR KR1020127022254A patent/KR101830715B1/ko active Active
- 2011-01-24 PL PL15164931T patent/PL2932970T3/pl unknown
- 2011-01-24 EP EP11737484.3A patent/EP2531027B1/fr not_active Revoked
- 2011-01-24 PL PL11737484T patent/PL2531027T3/pl unknown
- 2011-01-24 EA EA202190473A patent/EA202190473A3/ru unknown
- 2011-01-24 NZ NZ601319A patent/NZ601319A/en unknown
- 2011-01-24 CA CA2787691A patent/CA2787691C/fr active Active
- 2011-01-24 HR HRP20240168TT patent/HRP20240168T1/hr unknown
- 2011-01-24 PT PT117374843T patent/PT2531027E/pt unknown
- 2011-01-24 HR HRP20150770TT patent/HRP20150770T1/hr unknown
- 2011-01-24 ME MEP-2018-131A patent/ME03058B/fr unknown
- 2011-01-24 EA EA201892277A patent/EA037601B1/ru active Protection Beyond IP Right Term
- 2011-01-24 SG SG2012053492A patent/SG182614A1/en unknown
- 2011-01-24 SM SM20240063T patent/SMT202400063T1/it unknown
- 2011-01-24 KR KR1020177017713A patent/KR20170078868A/ko not_active Ceased
- 2011-01-24 MX MX2014014687A patent/MX367938B/es unknown
- 2011-01-24 KR KR1020187018909A patent/KR101964923B1/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 TN TNP2012000376A patent/TN2012000376A1/en unknown
- 2012-07-24 ZA ZA2012/05586A patent/ZA201205586B/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 US15/366,442 patent/US10426780B2/en active Active
- 2016-12-01 US US15/366,566 patent/US20170119777A1/en not_active Abandoned
-
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/CY2018029I2/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 LU LU00346C patent/LUC00346I2/fr unknown
- 2024-06-04 CY CY2024017C patent/CY2024017I2/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 |
|---|---|---|
| CO6602152A2 (es) | En respuesta al requerimiento de pago de reivindicaciones adicionales a las 10 primeras,presenta nuevo capítulo reivindicatorio y paga. | |
| 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 | |
| DE60318891D1 (de) | Cyclopropylverbindungen als ccr5 antagonisten | |
| NO20064547L (no) | Fremgangsmater for behandling av HIV infeksjon | |
| 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 | |
| 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 | |
| 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 | |
| MA40844A (fr) | Compositions pharmaceutiques à action prolongée pour l'hépatite c | |
| MA39448A1 (fr) | (r)-pirlindole et ses sels pharmaceutiquement acceptables destinés à un usage médical | |
| MA39533A1 (fr) | Composés, composition pharmaceutique et leur utilisation dans le traitement de maladies neurodégénératives | |
| MA39446A1 (fr) | Compositions pharmaceutiques pour traiter des maladies infecteuses | |
| MA46625B1 (fr) | Inhibiteurs de lsd1 et leurs utilisations médicales |