HUP0101012A2 - Orálisan adagolható gyógyszerkompozíció - Google Patents

Orálisan adagolható gyógyszerkompozíció

Info

Publication number
HUP0101012A2
HUP0101012A2 HU0101012A HUP0101012A HUP0101012A2 HU P0101012 A2 HUP0101012 A2 HU P0101012A2 HU 0101012 A HU0101012 A HU 0101012A HU P0101012 A HUP0101012 A HU P0101012A HU P0101012 A2 HUP0101012 A2 HU P0101012A2
Authority
HU
Hungary
Prior art keywords
pharmaceutical composition
oral administration
effect
tetrahydropyridine
trifluoromethylfend
Prior art date
Application number
HU0101012A
Other languages
English (en)
Inventor
Claude Aleman
Philippe Bastard
Marielle Bonnel
Thierry Breul
Original Assignee
Sanofi-Synthelabo
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 Sanofi-Synthelabo filed Critical Sanofi-Synthelabo
Publication of HUP0101012A2 publication Critical patent/HUP0101012A2/hu
Publication of HUP0101012A3 publication Critical patent/HUP0101012A3/hu

Links

Classifications

    • 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
    • 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
    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/10Laxatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Nanotechnology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Molecular Biology (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Biophysics (AREA)
  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • Medical Informatics (AREA)
  • Child & Adolescent Psychology (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Physical Or Chemical Processes And Apparatus (AREA)

Abstract

Találmányunk tárgya iható vizes oldat, amely 1-[2-(2-naftil)-etil]-4-(3-trifluormetil-fend)-1,2,3,6-tetrahidropiridin-hidrokloridot <-ciklodextrint (<-CD), és valamely gyógyászatilag elfogadott savat vagypuffert tartalmaz, amely 3 vagy ennél alacsonyabb pH-t biztosít. Afenti tetrahidropiridinszármazéknak ismert az antidepresszív hatása,az idegszövetet tápláló hatása, székrekedés ellenes hatása. Ó
HU0101012A 1997-12-24 1998-12-14 Pharmaceutical composition for oral administration HUP0101012A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9716529A FR2772614B1 (fr) 1997-12-24 1997-12-24 Solution aqueuse a base de chlorhydrate de 1- [ 2-(2-naphtyl)ethyl]-4- (3-trifluoromethylphenyl) -1,2,3,6-tetrahydropyridine et composition pharmaceutique buvable en contenant
PCT/FR1998/002712 WO1999033466A1 (fr) 1997-12-24 1998-12-14 Composition pharmaceutique buvable

Publications (2)

Publication Number Publication Date
HUP0101012A2 true HUP0101012A2 (hu) 2001-08-28
HUP0101012A3 HUP0101012A3 (en) 2002-12-28

Family

ID=9515152

Family Applications (1)

Application Number Title Priority Date Filing Date
HU0101012A HUP0101012A3 (en) 1997-12-24 1998-12-14 Pharmaceutical composition for oral administration

Country Status (25)

Country Link
US (1) US6191137B1 (hu)
EP (1) EP1041984B1 (hu)
JP (1) JP2002510599A (hu)
AR (1) AR017722A1 (hu)
AT (1) ATE252384T1 (hu)
AU (1) AU1880599A (hu)
BR (1) BR9814414A (hu)
CA (1) CA2315696C (hu)
CO (1) CO4970813A1 (hu)
DE (1) DE69819203T2 (hu)
DK (1) DK1041984T3 (hu)
DZ (1) DZ2676A1 (hu)
ES (1) ES2209238T3 (hu)
FR (1) FR2772614B1 (hu)
GT (1) GT199800204A (hu)
HU (1) HUP0101012A3 (hu)
MY (1) MY117156A (hu)
NO (1) NO20003284L (hu)
PT (1) PT1041984E (hu)
SA (2) SA99191002B1 (hu)
SI (1) SI1041984T1 (hu)
TW (1) TW536409B (hu)
UY (1) UY25320A1 (hu)
WO (1) WO1999033466A1 (hu)
ZA (1) ZA9811824B (hu)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004087870A2 (en) * 2003-03-25 2004-10-14 The Johns Hopkins University Neuronal cell lineages and methods of production thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2702656B1 (fr) * 1993-03-18 1995-06-16 Sanofi Elf Utilisation de derives de la tetrahydropyridine pour la preparation de medicaments cardioprotecteurs.

Also Published As

Publication number Publication date
CA2315696C (en) 2008-01-29
FR2772614A1 (fr) 1999-06-25
GT199800204A (es) 2000-06-14
AU1880599A (en) 1999-07-19
HUP0101012A3 (en) 2002-12-28
FR2772614B1 (fr) 2000-03-10
US6191137B1 (en) 2001-02-20
PT1041984E (pt) 2004-02-27
DE69819203T2 (de) 2004-07-15
EP1041984B1 (fr) 2003-10-22
CA2315696A1 (en) 1999-07-08
WO1999033466A1 (fr) 1999-07-08
NO20003284D0 (no) 2000-06-22
SA99191002B1 (ar) 2006-03-07
JP2002510599A (ja) 2002-04-09
ZA9811824B (en) 1999-06-29
TW536409B (en) 2003-06-11
MY117156A (en) 2004-05-31
DZ2676A1 (fr) 2004-09-19
SI1041984T1 (en) 2004-04-30
EP1041984A1 (fr) 2000-10-11
SA99191003B1 (ar) 2006-10-02
BR9814414A (pt) 2000-10-10
NO20003284L (no) 2000-08-24
DE69819203D1 (de) 2003-11-27
AR017722A1 (es) 2001-09-12
ES2209238T3 (es) 2004-06-16
DK1041984T3 (da) 2004-02-16
UY25320A1 (es) 2000-10-31
ATE252384T1 (de) 2003-11-15
CO4970813A1 (es) 2000-11-07

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Legal Events

Date Code Title Description
FA9A Lapse of provisional patent protection due to relinquishment or protection considered relinquished