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WO2006114703A3 - Methode d'administration de (1s,s2)-1-(4-hydroxyphenyl)-2-(4-hydroxy-4-phenylpiperidin-1-yle)-1-propanol - Google Patents

Methode d'administration de (1s,s2)-1-(4-hydroxyphenyl)-2-(4-hydroxy-4-phenylpiperidin-1-yle)-1-propanol Download PDF

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Publication number
WO2006114703A3
WO2006114703A3 PCT/IB2006/001044 IB2006001044W WO2006114703A3 WO 2006114703 A3 WO2006114703 A3 WO 2006114703A3 IB 2006001044 W IB2006001044 W IB 2006001044W WO 2006114703 A3 WO2006114703 A3 WO 2006114703A3
Authority
WO
WIPO (PCT)
Prior art keywords
period
time
phenylpiperidin
hydroxyphenyl
administration
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/IB2006/001044
Other languages
English (en)
Other versions
WO2006114703A2 (fr
Inventor
Jerry John Weaver
Lorraine Yurkewicz
Keith David Wilner
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Products Inc
Original Assignee
Pfizer Products Inc
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 Pfizer Products Inc filed Critical Pfizer Products Inc
Publication of WO2006114703A2 publication Critical patent/WO2006114703A2/fr
Publication of WO2006114703A3 publication Critical patent/WO2006114703A3/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/451—Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

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  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

L'invention concerne, dans un aspect, une méthode pouvant améliorer chez l'être humain la biodisponibilité de (1S,S2)-1-(4-hydroxyphényl)-2-(4-hydroxy-4-phénylpipéridin-1-yle)-1-propanol, ou un sel pharmaceutiquement acceptable dudit composé. La méthode consiste à administrer à un être humain, sur une durée d'au moins 24 heures, (1S,S2)-1-(4-hydroxyphényl)-2-(4-hydroxy-4-phénylpipéridin-1-yle)-1-propanol ou un sel pharmaceutiquement acceptable dudit composé, cette durée représentant la durée totale d'une première durée et d'une seconde durée. Le taux d'administration sur la première durée est supérieur au taux d'administration sur la seconde durée. La biodisponibilité est améliorée par rapport à l'administration d'un taux constant égal au taux d'administration sur la seconde durée.
PCT/IB2006/001044 2005-04-25 2006-04-13 Methode d'administration de (1s,s2)-1-(4-hydroxyphenyl)-2-(4-hydroxy-4-phenylpiperidin-1-yle)-1-propanol Ceased WO2006114703A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US67494705P 2005-04-25 2005-04-25
US60/674,947 2005-04-25

Publications (2)

Publication Number Publication Date
WO2006114703A2 WO2006114703A2 (fr) 2006-11-02
WO2006114703A3 true WO2006114703A3 (fr) 2007-03-22

Family

ID=36688172

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2006/001044 Ceased WO2006114703A2 (fr) 2005-04-25 2006-04-13 Methode d'administration de (1s,s2)-1-(4-hydroxyphenyl)-2-(4-hydroxy-4-phenylpiperidin-1-yle)-1-propanol

Country Status (1)

Country Link
WO (1) WO2006114703A2 (fr)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1186304A2 (fr) * 2000-09-06 2002-03-13 Pfizer Products Inc. Combinations pharmaceutiques pour le traitement d' attaques et de lésions traumatiques du cerveau

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1186304A2 (fr) * 2000-09-06 2002-03-13 Pfizer Products Inc. Combinations pharmaceutiques pour le traitement d' attaques et de lésions traumatiques du cerveau

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
JOHN A MCCAULEY: "NR2B subtype-selective NMDA receptor antagonists: 2001-2004", EXPERT OPINION, vol. 15, no. 4, 1 April 2005 (2005-04-01), pages 389 - 407, XP002392768, Retrieved from the Internet <URL:http://www.expertopin.com/doi/abs/10.1517/13543776.15.4.389> [retrieved on 20060627] *
JOHN. A. KEMP: "NMDA receptor pathways as drug targests", NATURE NEUROSCIENCE SUPPLEMENT, vol. 5, November 2002 (2002-11-01), pages 1039 - 1042, XP002392767, Retrieved from the Internet <URL:http://www.nature.com/neuro/journal/v5/n11s/pdf/nn936.pdf> [retrieved on 20060727] *
JOHNSON KIM ET AL: "Metabolism, pharmacokinetics, and excretion of a highly selective N-methyl-D-aspartate receptor antagonist, traxoprodil, in human cytochrome P450 2D6 extensive and poor metabolizers.", DRUG METABOLISM AND DISPOSITION: THE BIOLOGICAL FATE OF CHEMICALS. JAN 2003, vol. 31, no. 1, January 2003 (2003-01-01), pages 76 - 87, XP009069857, ISSN: 0090-9556, Retrieved from the Internet <URL:http://dmd.aspetjournals.org/cgi/reprint/31/1/76> [retrieved on 20060627] *
LORRAINE YURKEWICZ, JOURNAL OF NEUROTRAUMA, vol. 22, no. 12, December 2005 (2005-12-01), pages 1428 - 1443, XP002392769, Retrieved from the Internet <URL:http://www.liebertonline.com/doi/pdf/10.1089/neu.2005.22.1428> [retrieved on 20060727] *

Also Published As

Publication number Publication date
WO2006114703A2 (fr) 2006-11-02

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