NO20013585L - Kompleks av ras-farnesyltransferaseinhibitor og sulfobutyleter-7-<beta>-cyklodekstrin eller 2-hydroksypropyl-<beta>-cyklodekstrin og fremgangsmate - Google Patents

Kompleks av ras-farnesyltransferaseinhibitor og sulfobutyleter-7-<beta>-cyklodekstrin eller 2-hydroksypropyl-<beta>-cyklodekstrin og fremgangsmate

Info

Publication number
NO20013585L
NO20013585L NO20013585A NO20013585A NO20013585L NO 20013585 L NO20013585 L NO 20013585L NO 20013585 A NO20013585 A NO 20013585A NO 20013585 A NO20013585 A NO 20013585A NO 20013585 L NO20013585 L NO 20013585L
Authority
NO
Norway
Prior art keywords
ras
complex
sulfobutyl ether
farnesyltransferase inhibitor
farnesyltransferase
Prior art date
Application number
NO20013585A
Other languages
English (en)
Norwegian (no)
Other versions
NO20013585D0 (no
Inventor
Krishnaswamy S Raghavan
Timothy M Malloy
Sailesh A Varia
Original Assignee
Bristol Myers Squibb Co
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
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of NO20013585D0 publication Critical patent/NO20013585D0/no
Publication of NO20013585L publication Critical patent/NO20013585L/no

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/55131,4-Benzodiazepines, e.g. diazepam or clozapine
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal 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
    • A61K47/69Medicinal 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
    • A61K47/6949Medicinal 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
    • A61K47/6951Medicinal 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nanotechnology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Medical Informatics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Biophysics (AREA)
  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Plural Heterocyclic Compounds (AREA)
NO20013585A 1999-01-21 2001-07-20 Kompleks av ras-farnesyltransferaseinhibitor og sulfobutyleter-7-<beta>-cyklodekstrin eller 2-hydroksypropyl-<beta>-cyklodekstrin og fremgangsmate NO20013585L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US11664799P 1999-01-21 1999-01-21
PCT/US1999/030424 WO2000042849A1 (en) 1999-01-21 1999-12-21 COMPLEX OF RAS-FARNESYLTRANSFERASE INHIBITOR AND SULFOBUTYLETHER-7-β-CYCLODEXTRIN OR 2-HYDROXYPROPYL-β-CYCLODEXTRIN AND METHOD

Publications (2)

Publication Number Publication Date
NO20013585D0 NO20013585D0 (no) 2001-07-20
NO20013585L true NO20013585L (no) 2001-09-04

Family

ID=22368422

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20013585A NO20013585L (no) 1999-01-21 2001-07-20 Kompleks av ras-farnesyltransferaseinhibitor og sulfobutyleter-7-<beta>-cyklodekstrin eller 2-hydroksypropyl-<beta>-cyklodekstrin og fremgangsmate

Country Status (33)

Country Link
US (1) US6218375B1 (pl)
EP (1) EP1143796A4 (pl)
JP (1) JP2002535253A (pl)
KR (1) KR100708360B1 (pl)
CN (1) CN1219517C (pl)
AR (1) AR022323A1 (pl)
AU (1) AU772204B2 (pl)
BG (1) BG105666A (pl)
BR (1) BR9916566A (pl)
CA (1) CA2359646C (pl)
CO (1) CO5160253A1 (pl)
CZ (1) CZ20012601A3 (pl)
EE (1) EE200100382A (pl)
GE (1) GEP20043214B (pl)
HK (1) HK1038865A1 (pl)
HU (1) HUP0105160A3 (pl)
ID (1) ID30139A (pl)
IL (1) IL144025A (pl)
LT (1) LT4893B (pl)
LV (1) LV12712B (pl)
MY (1) MY119700A (pl)
NO (1) NO20013585L (pl)
NZ (1) NZ511995A (pl)
PE (1) PE20001419A1 (pl)
PL (1) PL195280B1 (pl)
RU (1) RU2230062C2 (pl)
SK (1) SK9602001A3 (pl)
TR (1) TR200102109T2 (pl)
TW (1) TWI232752B (pl)
UA (1) UA67825C2 (pl)
UY (2) UY25987A1 (pl)
WO (1) WO2000042849A1 (pl)
ZA (1) ZA200104416B (pl)

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US6566347B1 (en) * 2001-08-22 2003-05-20 Duquesne University Of The Holy Ghost Controlled release pharmaceutical
WO2003041658A2 (en) * 2001-11-13 2003-05-22 Bristol-Myers Squibb Company Process for the preparation of 3,7-disubstituted-2,3,4,5- tetrahydro-1h-1,4-benzodiazepine compounds
KR100451485B1 (ko) 2002-03-28 2004-10-06 주식회사종근당 푸마질롤 유도체 또는 그 염의 포접 화합물, 및 이를포함하는 약제학적 조성물
US6869939B2 (en) * 2002-05-04 2005-03-22 Cydex, Inc. Formulations containing amiodarone and sulfoalkyl ether cyclodextrin
US6818662B2 (en) * 2002-05-28 2004-11-16 Taisho Pharmaceutical Co., Ltd. Pharmaceutical composition
WO2003106628A2 (en) * 2002-06-17 2003-12-24 Bristol-Myers Squibb Company Benzodiazepine inhibitors of mitochondial f1f0 atp hydrolase and methods of inhibiting f1f0 atp hydrolase
US7157446B2 (en) * 2003-05-02 2007-01-02 Bristol Myers Squibb Company Complex of ras-farnesyltransferase inhibitor, a cyclodextrin, and ethanol
US20070020299A1 (en) 2003-12-31 2007-01-25 Pipkin James D Inhalant formulation containing sulfoalkyl ether cyclodextrin and corticosteroid
PT1928464E (pt) * 2005-09-30 2014-07-10 Lundbeck Inc Nova formulação parentérica de carbamazepina
US20100204178A1 (en) 2006-10-02 2010-08-12 James Cloyd Novel parenteral carbamazepine formulation
CN100503647C (zh) * 2005-11-02 2009-06-24 南京师范大学 羟丙基-磺丁基-β-环糊精及其制备方法、分析方法以及在药学上的应用
TW200806284A (en) * 2006-03-31 2008-02-01 Alcon Mfg Ltd Prenyltransferase inhibitors for ocular hypertension control and the treatment of glaucoma
CA2669705A1 (en) * 2006-11-21 2008-05-29 Novartis Ag Stable parenteral formulation containing a rsv inhibitor of a benzodiazepine structure
US12370352B2 (en) 2007-06-28 2025-07-29 Cydex Pharmaceuticals, Inc. Nasal and ophthalmic delivery of aqueous corticosteroid solutions
AR074052A1 (es) 2008-10-22 2010-12-22 Array Biopharma Inc Compuestos pirazolo{1,5-a}pirimidina sustituida como inhibidores de trk cinasa
NZ604498A (en) * 2010-05-26 2014-10-31 Neurophyxia B V 2-iminobiotin formulations and uses thereof
WO2012034038A2 (en) * 2010-09-09 2012-03-15 H. Lee Moffitt Cancer Center And Research Institute, Inc. Dual inhibitors of farnesyltransferase and geranylgeranyltransferase i
CA2849421C (en) * 2011-10-07 2020-04-28 Pisces Therapeutics Llc Malignant and non-malignant disease treatment with ras antagonists
CN105194685A (zh) * 2015-10-15 2015-12-30 重庆大学 磺胺脒的磺丁基醚-β-环糊精包合物及其粉针制剂
JP6975165B2 (ja) 2015-12-16 2021-12-01 ニューロフィシア・ベー・フェー 脳細胞傷害の処置における使用のための2−イミノビオチン
US10045991B2 (en) 2016-04-04 2018-08-14 Loxo Oncology, Inc. Methods of treating pediatric cancers
ES2987474T3 (es) 2016-04-04 2024-11-15 Loxo Oncology Inc Formulaciones líquidas de (S)-N-(5-((R)-2-(2,5-difluorofenil)-pirrolidin-1-IL)-pirazolo[1,5-A]pirimidin-3-IL)-3-hidroxipirrolidina-1-carboxamida
ES2836222T3 (es) 2016-05-18 2021-06-24 Loxo Oncology Inc Preparación de (S)-N-(5-((R)-2-(2,5-difluorofenil)pirrolidin-1-il)pirazolo[1,5-a]pirimidin-3-il)-3-hidroxipirrolidina-1-carboxamida
JOP20190092A1 (ar) 2016-10-26 2019-04-25 Array Biopharma Inc عملية لتحضير مركبات بيرازولو[1، 5-a]بيريميدين وأملاح منها
US20210145816A1 (en) * 2019-11-15 2021-05-20 Cyclolab Cyclodextrin Research And Development Laboratory Ltd. Pharmaceutical formulation of lonafarnib with a sulfobutylether beta-cyclodextrin
CN114929704B (zh) 2019-12-27 2024-07-23 微境生物医药科技(上海)有限公司 含螺环的喹唑啉化合物
MX2024007452A (es) * 2021-12-15 2024-07-09 Sillajen Inc Composiciones farmaceuticas que comprenden beta-ciclodextrinas modificadas.
AU2024265078A1 (en) 2023-05-04 2025-12-11 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
IL326136A (en) 2023-08-07 2026-03-01 Revolution Medicines Inc RMC-6291 for use in the treatment of a disease or disorder associated with the RAS protein
US20250154171A1 (en) 2023-10-12 2025-05-15 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
WO2025240847A1 (en) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Ras inhibitors
US20250375445A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025265060A1 (en) 2024-06-21 2025-12-26 Revolution Medicines, Inc. Therapeutic compositions and methods for managing treatment-related effects
WO2026006747A1 (en) 2024-06-28 2026-01-02 Revolution Medicines, Inc. Ras inhibitors
WO2026015825A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Use of ras inhibitor for treating pancreatic cancer
WO2026015796A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015790A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015801A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026050446A1 (en) 2024-08-29 2026-03-05 Revolution Medicines, Inc. Ras inhibitors
WO2026072904A2 (en) 2024-09-26 2026-04-02 Revolution Medicines, Inc. Compositions and methods for treating lung cancer

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JPS5630927A (en) * 1979-08-24 1981-03-28 Zeria Shinyaku Kogyo Kk Stabilization of guaiazulene and its derivative
US4371673A (en) * 1980-07-21 1983-02-01 The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Water soluble forms of retinoids
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US4596795A (en) * 1984-04-25 1986-06-24 The United States Of America As Represented By The Secretary, Dept. Of Health & Human Services Administration of sex hormones in the form of hydrophilic cyclodextrin derivatives
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US5376645A (en) 1990-01-23 1994-12-27 University Of Kansas Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
JPH07165616A (ja) * 1993-12-09 1995-06-27 Hisamitsu Pharmaceut Co Inc シクロデキストリンの複合組成物及び複合化法
US6011029A (en) * 1996-02-26 2000-01-04 Bristol-Myers Squibb Company Inhibitors of farnesyl protein transferase
JPH1067639A (ja) * 1996-08-26 1998-03-10 Shiseido Co Ltd ビタミンe−ビタミンcリン酸ジエステル/シクロデキストリン包接物及び該包接物を配合した皮膚外用剤

Also Published As

Publication number Publication date
TR200102109T2 (tr) 2001-12-21
GEP20043214B (en) 2004-04-26
AU2374000A (en) 2000-08-07
NO20013585D0 (no) 2001-07-20
UY25986A1 (es) 2000-09-29
HK1038865A1 (zh) 2002-04-04
UY25987A1 (es) 2000-09-29
SK9602001A3 (en) 2002-06-04
LT2001064A (en) 2001-10-25
WO2000042849A1 (en) 2000-07-27
PE20001419A1 (es) 2001-02-21
AU772204B2 (en) 2004-04-22
KR20010101611A (ko) 2001-11-14
US6218375B1 (en) 2001-04-17
CN1219517C (zh) 2005-09-21
PL366338A1 (pl) 2005-01-24
PL195280B1 (pl) 2007-08-31
LV12712B (en) 2002-01-20
ID30139A (id) 2001-11-08
NZ511995A (en) 2003-11-28
EP1143796A4 (en) 2002-03-20
HUP0105160A2 (hu) 2002-05-29
IL144025A0 (en) 2002-04-21
BG105666A (en) 2002-04-30
MY119700A (en) 2005-06-30
CA2359646A1 (en) 2000-07-27
CO5160253A1 (es) 2002-05-30
CN1333651A (zh) 2002-01-30
RU2230062C2 (ru) 2004-06-10
ZA200104416B (en) 2002-05-29
HUP0105160A3 (en) 2003-01-28
JP2002535253A (ja) 2002-10-22
AR022323A1 (es) 2002-09-04
CA2359646C (en) 2008-12-02
UA67825C2 (uk) 2004-07-15
CZ20012601A3 (cs) 2002-05-15
LT4893B (lt) 2002-02-25
TWI232752B (en) 2005-05-21
BR9916566A (pt) 2001-11-13
LV12712A (lv) 2001-09-20
KR100708360B1 (ko) 2007-04-17
IL144025A (en) 2004-05-12
EE200100382A (et) 2002-12-16
EP1143796A1 (en) 2001-10-17

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