JP2007530540A5 - - Google Patents

Download PDF

Info

Publication number
JP2007530540A5
JP2007530540A5 JP2007504971A JP2007504971A JP2007530540A5 JP 2007530540 A5 JP2007530540 A5 JP 2007530540A5 JP 2007504971 A JP2007504971 A JP 2007504971A JP 2007504971 A JP2007504971 A JP 2007504971A JP 2007530540 A5 JP2007530540 A5 JP 2007530540A5
Authority
JP
Japan
Prior art keywords
inhibitor
hiv
pharmaceutically acceptable
acceptable salt
solvate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2007504971A
Other languages
English (en)
Japanese (ja)
Other versions
JP2007530540A (ja
JP4847441B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2005/006277 external-priority patent/WO2005102392A2/en
Publication of JP2007530540A publication Critical patent/JP2007530540A/ja
Publication of JP2007530540A5 publication Critical patent/JP2007530540A5/ja
Application granted granted Critical
Publication of JP4847441B2 publication Critical patent/JP4847441B2/ja
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

JP2007504971A 2004-03-24 2005-03-01 Hiv感染の治療方法 Expired - Lifetime JP4847441B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US55576704P 2004-03-24 2004-03-24
US60/555,767 2004-03-24
PCT/US2005/006277 WO2005102392A2 (en) 2004-03-24 2005-03-01 Combinations for treating hiv infection

Publications (3)

Publication Number Publication Date
JP2007530540A JP2007530540A (ja) 2007-11-01
JP2007530540A5 true JP2007530540A5 (https=) 2008-04-17
JP4847441B2 JP4847441B2 (ja) 2011-12-28

Family

ID=34961940

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007504971A Expired - Lifetime JP4847441B2 (ja) 2004-03-24 2005-03-01 Hiv感染の治療方法

Country Status (30)

Country Link
US (1) US7776863B2 (https=)
EP (1) EP1732604B1 (https=)
JP (1) JP4847441B2 (https=)
KR (1) KR101158140B1 (https=)
CN (1) CN1956720B (https=)
AR (1) AR048333A1 (https=)
AT (1) ATE474602T1 (https=)
AU (1) AU2005235116B2 (https=)
BR (1) BRPI0509140A (https=)
CA (1) CA2561146C (https=)
CY (1) CY1111613T1 (https=)
DE (1) DE602005022420D1 (https=)
DK (1) DK1732604T3 (https=)
ES (1) ES2347801T3 (https=)
GE (1) GEP20104925B (https=)
HR (1) HRP20100434T1 (https=)
IL (1) IL178141A (https=)
IN (1) IN2012DN06436A (https=)
MY (1) MY144318A (https=)
NO (1) NO337116B1 (https=)
NZ (1) NZ549778A (https=)
PE (1) PE20060148A1 (https=)
PL (1) PL1732604T3 (https=)
PT (1) PT1732604E (https=)
RU (1) RU2367439C2 (https=)
SI (1) SI1732604T1 (https=)
TW (1) TWI347184B (https=)
UA (1) UA88463C2 (https=)
WO (1) WO2005102392A2 (https=)
ZA (1) ZA200607959B (https=)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040110785A1 (en) * 2001-02-02 2004-06-10 Tao Wang Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives
US7745625B2 (en) 2004-03-15 2010-06-29 Bristol-Myers Squibb Company Prodrugs of piperazine and substituted piperidine antiviral agents
US20060100432A1 (en) * 2004-11-09 2006-05-11 Matiskella John D Crystalline materials of 1-(4-benzoyl-piperazin-1-yl)-2-[4-methoxy-7-(3-methyl-[1,2,4]triazol-1-yl)-1H-pyrrolo[2,3-c]pyridin-3-yl]-ethane-1,2-dione
US20060100209A1 (en) * 2004-11-09 2006-05-11 Chong-Hui Gu Formulations of 1-(4-benzoyl-piperazin-1-yl)-2-[4-methoxy-7-(3-methyl-[1,2,4]triazol-1-yl)-1H-pyrrolo[2,3-c]pyridin-3-yl]-ethane-1,2-dione
PT1942108E (pt) 2005-10-28 2013-10-24 Ono Pharmaceutical Co Composto com um grupo básico e a sua utilização
WO2007058322A1 (ja) 2005-11-18 2007-05-24 Ono Pharmaceutical Co., Ltd. 塩基性基を含有する化合物およびその用途
US7851476B2 (en) * 2005-12-14 2010-12-14 Bristol-Myers Squibb Company Crystalline forms of 1-benzoyl-4-[2-[4-methoxy-7-(3-methyl-1H-1,2,4-triazol-1-YL)-1-[(phosphonooxy)methyl]-1H-pyrrolo[2,3-C]pyridin-3-YL]-1,2-dioxoethyl]-piperazine
US7501419B2 (en) * 2006-04-25 2009-03-10 Bristol-Myers Squibb Company 4-Squarylpiperazine derivatives as antiviral agents
US7807671B2 (en) 2006-04-25 2010-10-05 Bristol-Myers Squibb Company Diketo-piperazine and piperidine derivatives as antiviral agents
US7572810B2 (en) * 2006-06-08 2009-08-11 Bristol-Myers Squibb Company Alkene piperidine derivatives as antiviral agents
US7504399B2 (en) 2006-06-08 2009-03-17 Bristol-Meyers Squibb Company Piperazine enamines as antiviral agents
JP5433691B2 (ja) * 2008-06-25 2014-03-05 ブリストル−マイヤーズ スクイブ カンパニー Hiv結合阻害剤としてのジケトピペリジン誘導体
JP5433690B2 (ja) 2008-06-25 2014-03-05 ブリストル−マイヤーズ スクイブ カンパニー 抗−hiv薬としてのジケト縮合アゾロピペリジンおよびアゾロピペラジン
US20110293686A1 (en) * 2010-05-28 2011-12-01 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Anti-viral compositions and methods for administration
WO2012019003A1 (en) 2010-08-06 2012-02-09 Bristol-Myers Squibb Company Substituted indole and azaindole oxoacetyl piperazinamide derivatives
WO2012075235A1 (en) 2010-12-02 2012-06-07 Bristol-Myers Squibb Company Alkyl amides as hiv attachment inhibitors
WO2012106189A1 (en) 2011-01-31 2012-08-09 Bristol-Myers Squibb Company Methods of making hiv attachment inhibitor prodrug compound and intermediates
ES2636312T3 (es) 2011-04-12 2017-10-05 VIIV Healthcare UK (No.5) Limited Derivados de tioamida, amidoxima y amidrazona como inhibidores de la fijación del VIH
ES2609579T3 (es) 2011-08-29 2017-04-21 VIIV Healthcare UK (No.5) Limited Derivados espiro de diamina bicíclica como inhibidores de la unión del VIH
EP2751119B1 (en) 2011-08-29 2016-11-23 VIIV Healthcare UK (No.5) Limited Fused bicyclic diamine derivatives as hiv attachment inhibitors
WO2013138436A1 (en) 2012-03-14 2013-09-19 Bristol-Myers Squibb Company Cyclolic hydrazine derivatives as hiv attachment inhibitors
ES2616492T3 (es) 2012-08-09 2017-06-13 VIIV Healthcare UK (No.5) Limited Derivados de piperidina amida como inhibidores de la fijación del VIH
EP2895472B1 (en) 2012-08-09 2016-11-23 VIIV Healthcare UK (No.5) Limited Tricyclic alkene derivatives as HIV attachment inhibitors
US9586957B2 (en) * 2013-03-27 2017-03-07 VIIV Healthcare UK (No.5) Limited 2-keto amide derivatives as HIV attachment inhibitors
US11584797B2 (en) 2015-06-23 2023-02-21 Cytodyn Inc. Inhibition of CCL5 ligand binding to CCR5 receptor and alteration of CCR5/CCL5 axis signaling in inflammation, cancer, autoimmune, and other conditions
WO2023172635A1 (en) * 2022-03-08 2023-09-14 Emory University Predictive model for variants associated with drug resistance and theranostic applications thereof
US12425371B2 (en) * 2022-09-16 2025-09-23 Cisco Technology, Inc. System and method for providing SCHC-based edge firewalling

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU762404B2 (en) * 1998-03-02 2003-06-26 Panacos Pharmaceuticals, Inc. Acylated betulin and dihydrobetulin derivatives, preparation thereof and use thereof
US6476034B2 (en) 2000-02-22 2002-11-05 Bristol-Myers Squibb Company Antiviral azaindole derivatives
US20030207910A1 (en) * 2001-02-02 2003-11-06 Tao Wang Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives
US20040110785A1 (en) * 2001-02-02 2004-06-10 Tao Wang Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives
RU2192870C1 (ru) * 2001-07-02 2002-11-20 Закрытое акционерное общество "Агрофарм ПитерСиб" Антивирусная композиция, способ получения ее активной компоненты и способ лечения вич-инфицированных больных этой композицией
JP2005515206A (ja) * 2001-12-12 2005-05-26 ブリストル−マイヤーズ スクイブ カンパニー Hivインテグラーゼ・インヒビター
CA2467718C (en) * 2001-12-21 2011-04-26 Anormed Inc. Chemokine receptor binding heterocyclic compounds with enhanced efficacy

Similar Documents

Publication Publication Date Title
JP2007530540A5 (https=)
De Clercq Tenofovir alafenamide (TAF) as the successor of tenofovir disoproxil fumarate (TDF)
RU2006137555A (ru) Способы и композиции для лечения вич-инфекции
Piacenti An update and review of antiretroviral therapy
RU2420284C2 (ru) Антагонист ccr5 для усиления иммуновосстановительной терапии и лечения оппортунистической инфекции у пациентов с вич
Ruela Correa et al. Darunavir: a critical review of its properties, use and drug interactions
De Clercq Role of tenofovir alafenamide (TAF) in the treatment and prophylaxis of HIV and HBV infections
US20150133434A1 (en) Compositions and Methods for Reactivating Latent Immunodeficiency Virus
US20150030638A1 (en) Ingenol Derivatives in the Reactivation of Latent HIV
AU2020228361B2 (en) Treatment of herpes simplex with a combination of valacyclovir and famciclovir
CA2920811A1 (en) Medicament comprising a pharmaceutical combination of dolutegravir, emtricitabine and tenofovir
A Waheed et al. Why do we need new drug classes for HIV treatment and prevention?
KR102286386B1 (ko) 아타자나비르 및 코비시스타트의 hiv 치료 제제
WO2011089166A1 (en) Semicarbazone proteasome inhibitors for treating hiv and hepatitis infection
US20200101072A1 (en) Hiv post-exposure prophylaxis
CN111587107A (zh) 药物组合物
Roberts et al. Virologic Failure with a Raltegravir‐Containing Antiretroviral Regimen and Concomitant Calcium Administration
US20160235750A1 (en) Small molecules targeting hiv-1 nef
Rockstroh et al. Pharmacokinetics of faldaprevir and antiretrovirals in patients with HIV/HCV Co-infection
JP2020530024A (ja) 組み合わせ並びにその使用及び治療
JP2020528413A (ja) Hiv感染症及びaidsを治療するためのレジメン
Sension Initial Therapy for Human Immunodeficiency Virus: Broadening the Options
Di Biagio et al. Which patients have greatest need for elvitegravir/cobicistat/emtricitabine/tenofovirDF-based therapy?
HK40065109A (en) Treatment of herpes simplex with a combination of valacyclovir and famciclovir
JP2020529461A (ja) 組み合わせ並びにその使用及び治療