PE20051049A1 - Composiciones farmaceuticas que comprenden un antagonista de neuroquinina nk1 - Google Patents

Composiciones farmaceuticas que comprenden un antagonista de neuroquinina nk1

Info

Publication number
PE20051049A1
PE20051049A1 PE2005000022A PE2005000022A PE20051049A1 PE 20051049 A1 PE20051049 A1 PE 20051049A1 PE 2005000022 A PE2005000022 A PE 2005000022A PE 2005000022 A PE2005000022 A PE 2005000022A PE 20051049 A1 PE20051049 A1 PE 20051049A1
Authority
PE
Peru
Prior art keywords
compound
antagonist
sodium
neuroquinin
sulfobutilic
Prior art date
Application number
PE2005000022A
Other languages
English (en)
Inventor
Mengwei Hu
Original Assignee
Schering Corp
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 Schering Corp filed Critical Schering Corp
Publication of PE20051049A1 publication Critical patent/PE20051049A1/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0019Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4747Quinolines; Isoquinolines spiro-condensed
    • 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
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • A61K47/40Cyclodextrins; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/19Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Dermatology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Inorganic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

SE REFIERE A UNA COMPOSICION FARMACEUTICA QUE COMPRENDE UN COMPUESTO ANTAGONISTA DEL RECEPTOR DE NEUROPEPTIDO NEUROQUININA NK 1, TALES COMO LOS COMPUESTOS DESCRITOS EN LA SOLICITUD DE PATENTE US 20030158173 A1, SIENDO PREFERIDO EL COMPUESTO DE FORMULA (I), ESTOS COMPUESTOS SE ENCUENTRAN MEZCLADOS CON UN DERIVADO POLIANIONICO DE ß-CICLODEXTRINA CON APROXIMADAMENTE 1 O 7 GRUPOS SULFONATO DE SODIO SEPARADOS DE LA CAVIDAD LIPOFILICA POR AL MENOS UN GRUPO ESPACIADOR DE ETER BUTILICO, ESPECIFICAMENTE LA SAL SODICA DE ESTERES SULFOBUTILICOS DE ß-CICLODEXTRINA (CAPTISOL), EL CUAL MEJORA LA SOLUBILIDAD DEL COMPUESTO QUE SE ENCUENTRA EN FORMA DE SAL CLORHIDRICA O DE UNA BASE LIBRE BUFFERIZADA CON ACIDO CITRICO O ACIDO FOSFORICO. ESTA FORMULACION PRESENTA UN Ph DE 4 A 8 Y ADEMAS PUEDEN ESTAR COMPRENDIDA POR: a) UN INHIBIDOR SELECTIVO DE LA RECAPTACION DE SEROTONINA TALES COMO FLUOXETINA, FLUVOXAMINA, PAROXETINA, ENTRE OTROS; b) UN ANTAGONISTA DEL RECEPTOR DE SEROTONINA 5-HT3 TALES COMO ONDANSETRONA, DOLASETRONA, ENTRE OTROS; O c) UNA BENZAMIDA SUSTITUIDA O UN CORTICOSTEROIDE. SON PREFERIDAS LAS FORMULACIONES DE ADMINISTRACION PARENTERAL, SIENDO MAS ESTABLE LA SOLUCION OBTENIDA A PARTIR DE UNA FORMULACION LIOFILIZADA
PE2005000022A 2003-12-22 2005-01-03 Composiciones farmaceuticas que comprenden un antagonista de neuroquinina nk1 PE20051049A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US53173503P 2003-12-22 2003-12-22

Publications (1)

Publication Number Publication Date
PE20051049A1 true PE20051049A1 (es) 2006-01-03

Family

ID=34738689

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2005000022A PE20051049A1 (es) 2003-12-22 2005-01-03 Composiciones farmaceuticas que comprenden un antagonista de neuroquinina nk1

Country Status (16)

Country Link
US (1) US20050153999A1 (es)
EP (1) EP1706116A1 (es)
JP (1) JP2007515425A (es)
KR (1) KR20060113737A (es)
CN (1) CN1897942A (es)
AR (1) AR046769A1 (es)
AU (1) AU2004308935A1 (es)
BR (1) BRPI0417950A (es)
CA (1) CA2550432A1 (es)
MX (1) MXPA06007210A (es)
NO (1) NO20063393L (es)
PE (1) PE20051049A1 (es)
PL (1) PL380482A1 (es)
TW (1) TW200531686A (es)
WO (1) WO2005063243A1 (es)
ZA (1) ZA200605080B (es)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5155998B2 (ja) * 2006-04-05 2013-03-06 オプコ ヘルス, インコーポレイテッド 薬学的処方物:8−[{1−(3,5−ビス−(トリフルオロメチル)フェニル)−エトキシ}−メチル]−8−フェニル−1,7−ジアザ−スピロ[4.5]デカン−2−オンの塩およびそれを使用した処置方法
PE20080353A1 (es) * 2006-04-05 2008-04-25 Schering Corp Sales de 8-[{1-(3,5-bis-(trifluorometil)fenil)-etoxi}-metil]-8-fenil-1,7-diaza-espiro[4,5]decan-2-ona y proceso de preparacion de las mismas
CA2648604C (en) * 2006-04-05 2016-05-24 Schering Corporation Hydrochloride salts of 8-[{1-(3,5-bis-(trifluoromethyl)phenyl)-ethoxy}-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one and preparation process therefor
AR066191A1 (es) * 2007-03-22 2009-08-05 Schering Corp Proceso e intermediarios para la sintesis de compuestos 8- [ ( 1- (3,5- bis- ( trifluorometil) fenil) - etoxi ) - metil]- 8 fenil - 1,7- diaza - espiro (4, 5) decan -2 ona
AR065802A1 (es) * 2007-03-22 2009-07-01 Schering Corp Formulaciones de comprimidos que contienen sales de 8- [( 1- ( 3,5- bis- (trifluorometil) fenil) -etoxi ) - metil) -8- fenil -1, 7- diaza- spiro [ 4,5] decan -2- ona y comprimidos elaborados a partir de estas
GEP20135806B (en) * 2008-11-23 2013-04-10 Pfizer Lactams as beta secretase inhibitors
AU2014271269B2 (en) * 2009-08-14 2016-11-03 Opko Health, Inc. Intravenous formulations of neurokinin-1 antagonists
WO2011019911A1 (en) * 2009-08-14 2011-02-17 Opko Health, Inc. Intravenous formulations of neurokinin-1 antagonists
BR112014018110B1 (pt) * 2012-01-23 2022-06-07 Sage Therapeutics, Inc Composições farmacêutica aquosas formuladas para administração parenteral e uso de alopregnanolona e sulfobutiléter-b-ciclodextrina
NL2018041B1 (en) * 2016-12-22 2018-06-28 Land Life Company B V Process to prepare a biodegradable pulp product
US10973780B2 (en) * 2019-05-15 2021-04-13 Bexson Biomedical, Inc. Ketamine formulation for subcutaneous injection
MX2021015827A (es) * 2019-06-28 2022-04-11 Shanghai Shengdi Pharmaceutical Co Ltd Antagonista de neurokinin -1.
IL296635A (en) 2020-04-03 2022-11-01 Nerre Therapeutics Ltd An nk-1 receptor antagonist for the treatment of a disease selected from sepsis, septic shock, acute respiratory distress syndrome (ARDS), or multiple organ dysfunction syndrome (MODS)
KR20230018485A (ko) 2020-06-02 2023-02-07 네르 쎄라퓨틱스 리미티드 폐에 대한 기계적 손상에 의해 촉진된 폐 섬유증 상태의 치료에 사용하기 위한 뉴로키닌 (nk)-1 수용체 길항제
EP4268818A4 (en) * 2020-12-25 2024-06-19 Shanghai Shengdi Pharmaceutical Co Ltd USE OF AN NK1 ANTAGONIST PRODRUG COMPOUND IN COMBINATION WITH A 5-HT3 RECEPTOR ANTAGONIST

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2791346B3 (fr) * 1999-03-25 2001-04-27 Sanofi Sa Nouveaux derives de morpholine, procede pour leur preparation et compositions pharmaceutiques les contenant
EP1383445A4 (en) * 2001-03-20 2005-04-13 Cydex Inc PREPARATION CONTAINING PROPOFOL AND SULFOALKYL ETHER CYCLODEXTRIN
PE20030762A1 (es) * 2001-12-18 2003-09-05 Schering Corp Compuestos heterociclicos como antagonistas nk1

Also Published As

Publication number Publication date
ZA200605080B (en) 2008-06-25
TW200531686A (en) 2005-10-01
AR046769A1 (es) 2005-12-21
WO2005063243A1 (en) 2005-07-14
US20050153999A1 (en) 2005-07-14
MXPA06007210A (es) 2006-08-18
EP1706116A1 (en) 2006-10-04
AU2004308935A1 (en) 2005-07-14
PL380482A1 (pl) 2007-02-05
CN1897942A (zh) 2007-01-17
NO20063393L (no) 2006-07-21
JP2007515425A (ja) 2007-06-14
BRPI0417950A (pt) 2007-04-17
KR20060113737A (ko) 2006-11-02
CA2550432A1 (en) 2005-07-14

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