AR015900A1 - Una formulacion farmaceutica que comprende voriconazol o un derivado farmaceuticamente aceptable del mismo y un derivado de ciclodextrina. - Google Patents

Una formulacion farmaceutica que comprende voriconazol o un derivado farmaceuticamente aceptable del mismo y un derivado de ciclodextrina.

Info

Publication number
AR015900A1
AR015900A1 ARP980102924A ARP980102924A AR015900A1 AR 015900 A1 AR015900 A1 AR 015900A1 AR P980102924 A ARP980102924 A AR P980102924A AR P980102924 A ARP980102924 A AR P980102924A AR 015900 A1 AR015900 A1 AR 015900A1
Authority
AR
Argentina
Prior art keywords
derivative
pharmaceutically acceptable
pharmaceutical formulation
voriconazol
same
Prior art date
Application number
ARP980102924A
Other languages
English (en)
Spanish (es)
Original Assignee
Pfizer
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10814734&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR015900(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer filed Critical Pfizer
Publication of AR015900A1 publication Critical patent/AR015900A1/es

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • A61K47/40—Cyclodextrins; Derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/69—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
    • A61K47/6949—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
    • A61K47/6951—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
    • 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
    • A61P31/10—Antimycotics
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nanotechnology (AREA)
  • Epidemiology (AREA)
  • Biotechnology (AREA)
  • Oncology (AREA)
  • Medical Informatics (AREA)
  • Molecular Biology (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Biophysics (AREA)
  • Communicable Diseases (AREA)
  • General Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Inorganic Chemistry (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
ARP980102924A 1997-06-21 1998-06-18 Una formulacion farmaceutica que comprende voriconazol o un derivado farmaceuticamente aceptable del mismo y un derivado de ciclodextrina. AR015900A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB9713149.4A GB9713149D0 (en) 1997-06-21 1997-06-21 Pharmaceutical formulations

Publications (1)

Publication Number Publication Date
AR015900A1 true AR015900A1 (es) 2001-05-30

Family

ID=10814734

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP980102924A AR015900A1 (es) 1997-06-21 1998-06-18 Una formulacion farmaceutica que comprende voriconazol o un derivado farmaceuticamente aceptable del mismo y un derivado de ciclodextrina.

Country Status (47)

Country Link
US (1) US6632803B1 (enExample)
EP (1) EP1001813B8 (enExample)
JP (2) JP2000513029A (enExample)
KR (1) KR100372988B1 (enExample)
CN (1) CN1125653C (enExample)
AP (1) AP912A (enExample)
AR (1) AR015900A1 (enExample)
AT (1) ATE238812T1 (enExample)
AU (1) AU724799B2 (enExample)
BG (1) BG64584B1 (enExample)
BR (1) BRPI9809468B8 (enExample)
CA (1) CA2295035C (enExample)
CO (1) CO4940450A1 (enExample)
CZ (1) CZ289570B6 (enExample)
DE (1) DE69814091T2 (enExample)
DK (1) DK1001813T3 (enExample)
DZ (1) DZ2523A1 (enExample)
EA (1) EA001924B1 (enExample)
EG (1) EG23910A (enExample)
ES (1) ES2195355T3 (enExample)
GB (1) GB9713149D0 (enExample)
HR (1) HRP980341B1 (enExample)
HU (1) HU228338B1 (enExample)
ID (1) ID22939A (enExample)
IL (1) IL132918A (enExample)
IS (1) IS2004B (enExample)
MA (1) MA26508A1 (enExample)
ME (1) ME00907B (enExample)
MY (1) MY118151A (enExample)
NO (1) NO313125B1 (enExample)
NZ (1) NZ501066A (enExample)
OA (1) OA11232A (enExample)
PA (1) PA8453201A1 (enExample)
PE (1) PE84899A1 (enExample)
PL (1) PL191295B1 (enExample)
PT (1) PT1001813E (enExample)
RS (1) RS49633B (enExample)
SA (1) SA98190159B1 (enExample)
SI (1) SI1001813T1 (enExample)
SK (1) SK282946B6 (enExample)
TN (1) TNSN98090A1 (enExample)
TR (1) TR199903191T2 (enExample)
TW (1) TW406023B (enExample)
UA (1) UA57083C2 (enExample)
UY (1) UY25055A1 (enExample)
WO (1) WO1998058677A1 (enExample)
ZA (1) ZA985364B (enExample)

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GB9818258D0 (en) * 1998-08-21 1998-10-14 Pfizer Ltd Antifungal compositions
PE20020300A1 (es) 2000-08-22 2002-05-10 Pharmacia Corp Composicion de solucion de un farmaco antibiotico a base de oxazolidinona con mejoramiento de la carga de farmaco
AR031135A1 (es) 2000-10-10 2003-09-10 Upjohn Co Composiciones de antibiotico topico para el tratamiento de infecciones oculares
NZ537995A (en) * 2002-08-20 2007-11-30 Bristol Myers Squibb Co Inclusion complex of aripiprazole in a substituted b-cyclodextrin
GB0327390D0 (en) * 2003-11-25 2003-12-31 Pfizer Ltd Pharmaceutical formulations
ZA200604579B (en) * 2003-12-08 2007-10-31 Univ Arizona Synergistic anti-cancer compositions
CA2572223C (en) 2004-06-25 2014-08-12 The Johns Hopkins University Angiogenesis inhibitors
US20100204178A1 (en) 2006-10-02 2010-08-12 James Cloyd Novel parenteral carbamazepine formulation
WO2007047253A2 (en) * 2005-10-11 2007-04-26 Eastman Chemical Company Pharmaceutical formulations of cyclodextrins and antifungal azole compounds
AR061889A1 (es) 2006-07-13 2008-10-01 Medichem Sa Proceso mejorado para la preparacion de voriconazol
CN1919846B (zh) * 2006-09-14 2013-01-02 大道隆达(北京)医药科技发展有限公司 伏立康唑及其药用盐、中间体的一种新定向合成制备方法
BG1110U1 (bg) * 2007-06-19 2008-09-30 Рудолф ПОДЛИПСКИ Отоплителен съд за експресно локално загряване навода
EP2018866A1 (en) * 2007-07-27 2009-01-28 Sandoz AG Pharmaceutical compositions containing voriconazole
US8192721B2 (en) * 2007-12-13 2012-06-05 Verrow Pharmaceuticals, Inc. Compositions useful for reducing toxicity associated with gadolinium-based contrast agents
US20110224232A1 (en) * 2008-05-06 2011-09-15 Board Of Regents, The University Of Texas System Treatment of Pulmonary Fungal Infection With Voriconazole via Inhalation
RU2472510C2 (ru) * 2008-06-06 2013-01-20 Гленмарк Фармасьютикалс Лимитед Стабильная лекарственная форма для местного применения, содержащая вориконазол
CN101390825B (zh) * 2008-10-01 2010-12-29 山东省眼科研究所 一种伏立康唑眼内释药系统
JP5675629B2 (ja) 2008-10-21 2015-02-25 オニキス セラピューティクス, インク.Onyx Therapeutics, Inc. ペプチドエポキシケトンを用いた併用療法
CN101444510B (zh) * 2008-12-31 2011-03-09 南京卡文迪许生物工程技术有限公司 含有伏立康唑的药物制剂及其制备方法
EA201270283A1 (ru) 2009-08-19 2012-12-28 Рациофарм Гмбх Способ получения соэвапоратов и комплексы, содержащие вориконазол и циклодекстрин
WO2011064558A2 (en) 2009-11-30 2011-06-03 Cipla Limited Pharmaceutical composition
PL3391890T3 (pl) 2010-06-29 2021-12-20 Merck Sharp & Dohme Corp. Preparaty dożylnego roztworu pozakonazolu stabilizowane podstawioną beta-cyklodekstryną
EP2409699B1 (en) 2010-07-23 2014-04-30 Combino Pharm, S.L. Stable compositions of voriconazole
CN102058519B (zh) * 2010-11-19 2013-01-02 苏州特瑞药业有限公司 一种伏立康唑缓释栓剂及其制备方法
PL2720723T3 (pl) 2011-06-15 2018-10-31 Synthon Bv Stabilizowana kompozycja worykonazolu
EP2561863A1 (en) 2011-08-22 2013-02-27 Farmaprojects, S.A.U. Pharmaceutical compositions comprising voriconazole
US20130202681A1 (en) * 2012-01-05 2013-08-08 Frederick Timothy Guilford Liposomally encapsulated reduced glutathione for management of cancer and disruption of cancer energy cycles
US8853248B2 (en) 2012-04-05 2014-10-07 Hubert Maehr (1,2,3-triazolyl)sulfonyl derivatives
AU2013259573B2 (en) 2012-05-08 2018-02-15 Onyx Therapeutics, Inc. Cyclodextrin complexation Methods for Formulating Peptide Proteasome Inhibitors
BR112014028069A2 (pt) 2012-05-11 2017-08-08 Cipla Ltd composição farmacêutica oftálmica, processo para a preparação de uma composição farmacêutica oftálmica, uso de uma composição farmacêutica oftálmica, e, método para a prevenção ou tratamento de uma infecção fúngica
BR112015016331B1 (pt) 2013-01-11 2020-05-12 Xellia Pharmaceuticals Aps Formulação farmacêutica estabilizada e método de estabilização de uma composição compreendendo voriconazol
US20140275122A1 (en) 2013-03-14 2014-09-18 Fresenius Kabi Usa, Llc Voriconazole Formulations
GB201312737D0 (en) 2013-07-17 2013-08-28 Univ Greenwich Cyclodextrin
CN103690968A (zh) * 2013-11-21 2014-04-02 石药集团中奇制药技术(石家庄)有限公司 一种伏立康唑组合物及其制备方法
PT109117B (pt) * 2016-01-28 2019-02-01 Hovione Farm Sa Complexação de ingredientes ativos farmacêuticos
CN110022857A (zh) 2016-11-18 2019-07-16 艾库里斯抗感染治疗有限公司 基于改性环糊精和酸化剂的脒取代β-内酰胺化合物的新制剂、其制备及作为抗微生物药物组合物的用途
EP3584245A4 (en) * 2017-02-17 2020-08-26 Wuhan LL Science And Technology Development Co., Ltd. TRIAZOLE ANTIBACTERIAL DERIVATIVE, ASSOCIATED PHARMACEUTICAL COMPOSITION AND USE
CN113750034A (zh) * 2020-06-05 2021-12-07 中南大学湘雅三医院 耳用温敏凝胶及其制备方法
WO2021245703A2 (en) 2020-06-06 2021-12-09 Inventia Healthcare Limited Stable liquid compositions of posaconazole
CN116570558B (zh) * 2023-06-21 2023-12-26 广州仁恒医药科技股份有限公司 一种伏立康唑眼用纳米缓释组合物及其制备方法和应用

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DE3346123A1 (de) 1983-12-21 1985-06-27 Janssen Pharmaceutica, N.V., Beerse Pharmazeutische praeparate von in wasser schwerloeslichen oder instabilen arzneistoffen und verfahren zu ihrer herstellung
DE3347421A1 (de) 1983-12-29 1985-07-11 Hoechst Ag, 6230 Frankfurt Verfahren zur herstellung von fluorarmen alkaliphosphatloesungen
GB8819308D0 (en) * 1988-08-13 1988-09-14 Pfizer Ltd Triazole antifungal agents
US5376645A (en) * 1990-01-23 1994-12-27 University Of Kansas Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
KR0166088B1 (ko) * 1990-01-23 1999-01-15 . 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도
US5278175A (en) * 1990-02-02 1994-01-11 Pfizer Inc. Triazole antifungal agents
GB9002375D0 (en) * 1990-02-02 1990-04-04 Pfizer Ltd Triazole antifungal agents
GB9512961D0 (en) * 1995-06-26 1995-08-30 Pfizer Ltd Antifungal agents
GB9602080D0 (en) 1996-02-02 1996-04-03 Pfizer Ltd Pharmaceutical compounds

Also Published As

Publication number Publication date
NO313125B1 (no) 2002-08-19
HUP0003323A2 (hu) 2001-06-28
MY118151A (en) 2004-09-30
SA98190159B1 (ar) 2005-12-21
DZ2523A1 (fr) 2003-02-01
EA199900937A1 (ru) 2000-08-28
WO1998058677A1 (en) 1998-12-30
CA2295035A1 (en) 1998-12-30
DE69814091D1 (de) 2003-06-05
NO995565D0 (no) 1999-11-12
AU8110498A (en) 1999-01-04
HUP0003323A3 (en) 2002-01-28
NO995565L (no) 1999-11-30
JP2002332234A (ja) 2002-11-22
BG103882A (en) 2000-07-31
EP1001813A1 (en) 2000-05-24
JP5089004B2 (ja) 2012-12-05
HRP980341A2 (en) 1999-02-28
TNSN98090A1 (fr) 2005-03-15
BR9809468B1 (pt) 2013-11-12
HRP980341B1 (en) 2001-12-31
KR20010014006A (ko) 2001-02-26
AP912A (en) 2001-12-08
KR100372988B1 (ko) 2003-02-25
SK282946B6 (sk) 2003-01-09
PT1001813E (pt) 2003-07-31
ATE238812T1 (de) 2003-05-15
UA57083C2 (uk) 2003-06-16
TR199903191T2 (xx) 2000-09-21
CN1261287A (zh) 2000-07-26
CZ289570B6 (cs) 2002-02-13
NZ501066A (en) 2001-01-26
IL132918A (en) 2001-09-13
PL191295B1 (pl) 2006-04-28
CN1125653C (zh) 2003-10-29
TW406023B (en) 2000-09-21
IS2004B (is) 2005-04-15
EP1001813B1 (en) 2003-05-02
CA2295035C (en) 2005-04-19
EP1001813B8 (en) 2014-02-12
IS5248A (is) 1999-11-15
HU228338B1 (en) 2013-03-28
EG23910A (en) 2007-12-30
CZ409699A3 (cs) 2000-02-16
ME00907B (me) 2007-08-03
GB9713149D0 (en) 1997-08-27
SK159399A3 (en) 2000-06-12
PL337692A1 (en) 2000-08-28
BR9809468A (pt) 2000-06-20
ID22939A (id) 1999-12-16
CO4940450A1 (es) 2000-07-24
IL132918A0 (en) 2001-03-19
ES2195355T3 (es) 2003-12-01
BG64584B1 (bg) 2005-08-31
PE84899A1 (es) 1999-09-17
JP2000513029A (ja) 2000-10-03
MA26508A1 (fr) 2004-12-20
EA001924B1 (ru) 2001-10-22
RS49633B (sr) 2007-08-03
AU724799B2 (en) 2000-09-28
SI1001813T1 (en) 2004-02-29
AP9801268A0 (en) 1998-06-30
US6632803B1 (en) 2003-10-14
BRPI9809468B8 (pt) 2022-01-18
HK1027966A1 (en) 2001-02-02
DK1001813T3 (da) 2003-07-28
ZA985364B (en) 1999-12-20
UY25055A1 (es) 2000-12-29
DE69814091T2 (de) 2004-01-22
YU68199A (sh) 2002-06-19
PA8453201A1 (es) 2000-05-24
OA11232A (en) 2003-05-26

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