EA199801045A1 - Комбинации, содержащие vx478, зидовудин, ftc и/или 3тс, для применения при лечении вич - Google Patents

Комбинации, содержащие vx478, зидовудин, ftc и/или 3тс, для применения при лечении вич

Info

Publication number
EA199801045A1
EA199801045A1 EA199801045A EA199801045A EA199801045A1 EA 199801045 A1 EA199801045 A1 EA 199801045A1 EA 199801045 A EA199801045 A EA 199801045A EA 199801045 A EA199801045 A EA 199801045A EA 199801045 A1 EA199801045 A1 EA 199801045A1
Authority
EA
Eurasian Patent Office
Prior art keywords
amino
ftc
hiv
treating hiv
zidovudin
Prior art date
Application number
EA199801045A
Other languages
English (en)
Other versions
EA001517B1 (ru
Inventor
Марта Хайдер Сейнт-Клэр
Дейвид Уолтер Бэрри
Original Assignee
Глаксо Груп Лимитед
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from GBGB9614022.3A external-priority patent/GB9614022D0/en
Application filed by Глаксо Груп Лимитед filed Critical Глаксо Груп Лимитед
Publication of EA199801045A1 publication Critical patent/EA199801045A1/ru
Publication of EA001517B1 publication Critical patent/EA001517B1/ru

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
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • 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
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • 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
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • 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
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
    • A61K31/7072—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
    • 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
    • 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

Abstract

Настоящее изобретение относится к терапевтическим комбинациям тетрагидро-3-фуранилового эфира 3S-[3R*(1R*, 2S*)-[3-[[(4-аминофенил)сульфонил](2-метилпропил)-амино]-2-гидрокси-1-фенил-метил)пропил] карбаминовой кислоты (141W94), 3'-азидо-3'-дезокситимидина (зидовудина) и (2R, цис)-4-амино-1-(2-гидроксиметил-1,3-оксатиолан-5-ил)-(1Н)-пиримидин-2-она (3ТС) (или, альтернативно 3ТС, (2R, цис)-4-амино-5-фтор-1-(2-гидроксиметил)-1,3-оксатиолан-5-ил)-(1Н)-пиримидин-2-она (FTC)), которые обладают анти-ВИЧ активностью. Настоящее изобретение также относится к фармацевтическим композициям, содержащим указанные комбинации, и к их применению при лечении ВИЧ инфекций, включая инфекции ВИЧ мутантов, несущих резистентность к нуклеозидным и/или ненуклеозидным ингибиторам.Международная заявка была опубликована вместе с отчетом о международном поиске.
EA199801045A 1996-06-25 1997-06-23 Комбинации, содержащие vx478, зидовудин и 3tc, для применения при лечении вич EA001517B1 (ru)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US2054396P 1996-06-25 1996-06-25
US2102796P 1996-07-02 1996-07-02
GBGB9614022.3A GB9614022D0 (en) 1996-07-04 1996-07-04 Antiviral therapeutic combinations
PCT/EP1997/003247 WO1997049411A1 (en) 1996-06-25 1997-06-23 Combinations comprising vx478, zidovudine, ftc and/or 3tc for use in the treatment of hiv

Publications (2)

Publication Number Publication Date
EA199801045A1 true EA199801045A1 (ru) 1999-08-26
EA001517B1 EA001517B1 (ru) 2001-04-23

Family

ID=27268358

Family Applications (1)

Application Number Title Priority Date Filing Date
EA199801045A EA001517B1 (ru) 1996-06-25 1997-06-23 Комбинации, содержащие vx478, зидовудин и 3tc, для применения при лечении вич

Country Status (26)

Country Link
US (1) US6544961B1 (ru)
EP (1) EP0938321B1 (ru)
JP (1) JP2000515852A (ru)
KR (1) KR20000022226A (ru)
CN (1) CN1228026A (ru)
AP (1) AP9801419A0 (ru)
AT (1) ATE257708T1 (ru)
AU (1) AU727983B2 (ru)
BR (1) BR9709939A (ru)
CA (1) CA2258956A1 (ru)
CO (1) CO4900074A1 (ru)
CZ (1) CZ429498A3 (ru)
DE (1) DE69727240T2 (ru)
EA (1) EA001517B1 (ru)
ES (1) ES2213217T3 (ru)
HU (1) HUP9903249A3 (ru)
ID (1) ID19490A (ru)
IL (1) IL127351A0 (ru)
IS (1) IS4915A (ru)
NO (1) NO986034L (ru)
NZ (1) NZ333099A (ru)
PL (1) PL330747A1 (ru)
TR (1) TR199802704T2 (ru)
TW (1) TW469132B (ru)
WO (1) WO1997049411A1 (ru)
YU (1) YU58398A (ru)

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MY115461A (en) 1995-03-30 2003-06-30 Wellcome Found Synergistic combinations of zidovudine, 1592u89 and 3tc
US6875773B1 (en) 1998-05-29 2005-04-05 Ben M. Dunn Combination therapy for treatment of FIV infection
AU4219799A (en) * 1998-05-29 1999-12-13 University Of Florida Combination therapy for treatment of fiv infection
GB0011903D0 (en) * 2000-05-18 2000-07-05 Astrazeneca Ab Combination chemotherapy
NZ554779A (en) * 2005-02-01 2011-02-25 Troikaa Pharmaceuticals Ltd Injectable preparations of diclofenac ((2,6-dichloranilino)phenylacetic acid) and its pharmaceutically acceptable salts
ES2279707B1 (es) * 2005-11-10 2008-06-01 Combino Pharm, S.L. Formulaciones orales que comprenden 3'-azidonucleosidos.
US8168662B1 (en) 2006-11-06 2012-05-01 Poniard Pharmaceuticals, Inc. Use of picoplatin to treat colorectal cancer
US8168661B2 (en) * 2006-11-06 2012-05-01 Poniard Pharmaceuticals, Inc. Use of picoplatin to treat colorectal cancer
US8178564B2 (en) * 2006-11-06 2012-05-15 Poniard Pharmaceuticals, Inc. Use of picoplatin to treat colorectal cancer
US8173686B2 (en) 2006-11-06 2012-05-08 Poniard Pharmaceuticals, Inc. Use of picoplatin to treat colorectal cancer
US20110033528A1 (en) * 2009-08-05 2011-02-10 Poniard Pharmaceuticals, Inc. Stabilized picoplatin oral dosage form
US20100260832A1 (en) * 2007-06-27 2010-10-14 Poniard Pharmaceuticals, Inc. Combination therapy for ovarian cancer
TW200916094A (en) * 2007-06-27 2009-04-16 Poniard Pharmaceuticals Inc Stabilized picoplatin dosage form
WO2009011861A1 (en) * 2007-07-16 2009-01-22 Poniard Pharmaceuticals, Inc. Oral formulations for picoplatin
US20110052580A1 (en) * 2008-02-08 2011-03-03 Poniard Pharmaceuticals, Inc. Use of picoplatin and bevacizumab to treat colorectal cancer
MX367937B (es) * 2010-01-27 2019-09-12 Viiv Healthcare Co Combinaciones de compuestos que comprenden inhibidores de la integrasa de vih y otros agentes terapéuticos.

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US4724232A (en) * 1985-03-16 1988-02-09 Burroughs Wellcome Co. Treatment of human viral infections
US5047407A (en) 1989-02-08 1991-09-10 Iaf Biochem International, Inc. 2-substituted-5-substituted-1,3-oxathiolanes with antiviral properties
MY104575A (en) * 1989-12-22 1994-04-30 The Wellcome Foundation Ltd Therapeutic nucleosides.
US5204466A (en) 1990-02-01 1993-04-20 Emory University Method and compositions for the synthesis of bch-189 and related compounds
GB9009861D0 (en) 1990-05-02 1990-06-27 Glaxo Group Ltd Chemical compounds
IL100502A (en) 1991-01-03 1995-12-08 Iaf Biochem Int PHARMACEUTICAL PREPARATIONS CONTAINING CIS-4-AMINO-1-) 2-HYDROXIMETHIL-1,3-OXETYOLEN-5-IL (-
IL100965A (en) * 1991-02-22 1999-12-31 Univ Emory 2 - Hydroxymethyl - 5 -) 5 - Fluorocytocin - 1 - Eyal (- 1, 3 - Oxathiolane, its resolution and pharmaceuticals containing it
GB9104740D0 (en) * 1991-03-06 1991-04-17 Wellcome Found Antiviral nucleoside combination
SK279262B6 (sk) 1991-05-16 1998-08-05 Glaxo Group Limited Protivírusová zmes, farmaceutický prostriedok s je
GB9111902D0 (en) 1991-06-03 1991-07-24 Glaxo Group Ltd Chemical compounds
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DK0656887T3 (da) 1992-08-25 1999-07-05 Searle & Co Hydroxyethylaminosulfonamider til anvendelse som inhibitorer af retrovirale proteaser
IS2334B (is) * 1992-09-08 2008-02-15 Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) Aspartyl próteasi hemjari af nýjum flokki súlfonamíða
US5723490A (en) * 1992-09-08 1998-03-03 Vertex Pharmaceuticals Incorporated THF-containing sulfonamide inhibitors of aspartyl protease
UA49803C2 (ru) * 1994-06-03 2002-10-15 Дж.Д. Сьорль Енд Ко Способ лечения ретровирусных инфекций
GB9503850D0 (en) 1995-02-25 1995-04-19 Glaxo Group Ltd Medicaments
US5869461A (en) 1995-03-16 1999-02-09 Yale University Reducing toxicity of L-nucleosides with D-nucleosides
MY115461A (en) * 1995-03-30 2003-06-30 Wellcome Found Synergistic combinations of zidovudine, 1592u89 and 3tc
US5646180A (en) * 1995-12-05 1997-07-08 Vertex Pharmaceuticals Incorporated Treatment of the CNS effects of HIV
TW536403B (en) 1997-03-24 2003-06-11 Glaxo Group Ltd An ethanol and ethylenediaminetetraacetic acid free pharmaceutical composition comprising lamivudine and exhibiting antimicrobial preservative efficacy

Also Published As

Publication number Publication date
HUP9903249A3 (en) 2001-04-28
ES2213217T3 (es) 2004-08-16
CA2258956A1 (en) 1997-12-31
US6544961B1 (en) 2003-04-08
ID19490A (id) 1998-07-16
DE69727240T2 (de) 2004-11-25
AU727983B2 (en) 2001-01-04
KR20000022226A (ko) 2000-04-25
CO4900074A1 (es) 2000-03-27
ATE257708T1 (de) 2004-01-15
EA001517B1 (ru) 2001-04-23
BR9709939A (pt) 1999-08-10
NO986034D0 (no) 1998-12-22
YU58398A (en) 1999-11-22
WO1997049411A1 (en) 1997-12-31
NZ333099A (en) 2000-06-23
AP9801419A0 (en) 1998-12-31
CZ429498A3 (cs) 1999-06-16
EP0938321A1 (en) 1999-09-01
NO986034L (no) 1999-02-23
IS4915A (is) 1998-11-30
AU3262797A (en) 1998-01-14
JP2000515852A (ja) 2000-11-28
TW469132B (en) 2001-12-21
EP0938321B1 (en) 2004-01-14
HUP9903249A2 (hu) 2000-10-28
IL127351A0 (en) 1999-10-28
TR199802704T2 (xx) 1999-03-22
PL330747A1 (en) 1999-05-24
CN1228026A (zh) 1999-09-08
DE69727240D1 (de) 2004-02-19

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Legal Events

Date Code Title Description
MM4A Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s)

Designated state(s): AM AZ BY KZ KG MD TJ TM RU