PE20000544A1 - Forma de dosificacion de nefazodona - Google Patents

Forma de dosificacion de nefazodona

Info

Publication number
PE20000544A1
PE20000544A1 PE1999000481A PE00048199A PE20000544A1 PE 20000544 A1 PE20000544 A1 PE 20000544A1 PE 1999000481 A PE1999000481 A PE 1999000481A PE 00048199 A PE00048199 A PE 00048199A PE 20000544 A1 PE20000544 A1 PE 20000544A1
Authority
PE
Peru
Prior art keywords
nefazodone
micropells
cps
polymer
hours
Prior art date
Application number
PE1999000481A
Other languages
English (en)
Inventor
Peter Timmins
Andrew B Dennis
Alison C Hodsdon
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 PE20000544A1 publication Critical patent/PE20000544A1/es

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2022—Organic macromolecular compounds
    • A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • 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
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2022—Organic macromolecular compounds
    • A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants

Landscapes

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

Abstract

SE REFIERE A UNA FORMULACION FARMACEUTICA DE LIBERACION CONTROLADA/PROLONGADA DE NEFAZODONA Y QUE SE CARACTERIZA PORQUE LA LIBERACION DEL FARMACO SE DA DE LAS 4 A 16 HORAS, CON NIVELES TERAPEUTICOS PROLONGADOS HASTA POR 24 HORAS, CANTIDADES REDUCIDAS DE METABOLITOS DE NEFAZODONA TAL COMO m-CLOROFENILPIPERAZINA, NO ES INCOMPATIBLE CON EL ALIMENTO; TRATANDOSE DE UNA FORMA DE DOSIFICACION MODULADA POR EL pH, CON UNA VISCOSIDAD DE 3 cps A 100 cps; COMPRENDE DE 33% A 45.5% DE CLORHIDRATO DE NEFAZODONA, DE 16% A 33% DE UN POLIMERO DE GELIFICACION NO IONICO (HIDROXIPROPILMETILCELULOSA), DE 10% A 21% DE UN POLIMERO DE GELIFICACION IONICO (ALGINATO DE SODIO), DE 16% A 22% DE UN AGENTE HIDROFILICO INSOLUBLE (CELULOSA MICROCRISTALINA). LOS EXCIPIENTES DE LA FORMULACION PUEDEN SER COLORANTES, SILICE COLOIDAL, ESTEARATO DE MAGNESIO. LA NEFAZODONA ESTA INCRUSTADA EN UNA MATRIZ, FORMADA EN MICROPELLAS o FORMADA EN MICROPELLAS RECUBIERTAS. UNA COMPOSICION PREFERIDA CONTIENE DE 40%-45% DE CLORHIDRATO DE NEFAZODONA, DE 16% A 20% DE HIDROXIPROPILMETILCELULOSA, DE 19%-22% DE ALGINATO DE SODIO, DE 19%-22% DE CELULOSA MICROCRISTALINA, DE 1%-15% DE ESTEARATO DE MAGNESIO. LA NEFAZODONA ES UTIL COMO BLOQUEADOR DEL RECEPTOR 5HT DE SEROTONINA ACTUANDO COMO ANTIDEPRESOR
PE1999000481A 1998-06-05 1999-06-04 Forma de dosificacion de nefazodona PE20000544A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US8821198P 1998-06-05 1998-06-05

Publications (1)

Publication Number Publication Date
PE20000544A1 true PE20000544A1 (es) 2000-06-29

Family

ID=22210038

Family Applications (1)

Application Number Title Priority Date Filing Date
PE1999000481A PE20000544A1 (es) 1998-06-05 1999-06-04 Forma de dosificacion de nefazodona

Country Status (20)

Country Link
US (1) US6143325A (es)
EP (1) EP0966966A3 (es)
JP (1) JP2000007567A (es)
KR (1) KR20000005930A (es)
CN (1) CN1238181A (es)
AR (1) AR018862A1 (es)
AU (1) AU3319999A (es)
BR (1) BR9901782A (es)
CA (1) CA2273546A1 (es)
CO (1) CO5060477A1 (es)
HU (1) HUP9901830A2 (es)
ID (1) ID23458A (es)
IL (1) IL130022A0 (es)
NO (1) NO992692L (es)
NZ (1) NZ336001A (es)
PE (1) PE20000544A1 (es)
PL (1) PL333524A1 (es)
SG (1) SG77244A1 (es)
UY (1) UY25544A1 (es)
ZA (1) ZA993345B (es)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6143325A (en) * 1998-06-05 2000-11-07 Bristol-Myers Squibb Company Nefazodone dosage form
EP1428535A1 (en) * 1998-11-02 2004-06-16 ALZA Corporation Controlled delivery of antidepressants
DE69930952T2 (de) * 1998-11-02 2006-08-31 Alza Corp., Mountain View Verfahren und Vorrichtung zur kontrollierten Abgabe pharmazeutischer Mittel sowie Dosierungsform hierfür
US6706282B1 (en) 1998-11-02 2004-03-16 Evangeline Cruz Controlled delivery of phenoxyethyl-substituted 1,2,4-triazolones
US20030083338A1 (en) * 2001-03-02 2003-05-01 Currie Mark G. Compositions and methods for management of serotonin-mediated disorders
US8329216B2 (en) 2001-07-06 2012-12-11 Endo Pharmaceuticals Inc. Oxymorphone controlled release formulations
US9820982B2 (en) 2001-07-06 2017-11-21 Endo Pharmaceuticals Inc. Oxymorphone controlled release formulations
BR0210855A (pt) 2001-07-06 2006-10-24 Penwest Pharmaceuticals Compan Método de fabricação de formulações de liberação prolongada
US20040220240A1 (en) * 2001-11-28 2004-11-04 Pellegrini Cara A. Method of increasing the extent of absorption of tizanidine
US6455557B1 (en) 2001-11-28 2002-09-24 Elan Pharmaceuticals, Inc. Method of reducing somnolence in patients treated with tizanidine
US6407128B1 (en) 2001-12-03 2002-06-18 Elan Pharmaceuticals, Inc. Method for increasing the bioavailability of metaxalone
US7714006B1 (en) 2001-12-03 2010-05-11 King Pharmaceuticals Research & Development, Inc. Methods of modifying the bioavailability of metaxalone
DE50312523D1 (de) * 2002-05-24 2010-04-29 Carl-Fr Coester Pharmazeutische wirkstoffkombination sowie deren verwendung
TWI319713B (en) 2002-10-25 2010-01-21 Sustained-release tramadol formulations with 24-hour efficacy
US8487002B2 (en) 2002-10-25 2013-07-16 Paladin Labs Inc. Controlled-release compositions
GB0306604D0 (en) * 2003-03-21 2003-04-30 Curidium Ltd Second medical use
KR101087464B1 (ko) * 2003-08-08 2011-11-25 밸리언트 인터내셔널(바베이도스) 에스알엘 부프로피온 히드로클로라이드의 개질 방출형 정제
US7893261B2 (en) 2004-03-26 2011-02-22 Baylor University Serotonin reuptake inhibitors
RU2008113439A (ru) 2005-09-09 2009-10-20 Лабофарм Инк. (CA) Композиции с замедленным высвобождением лекарственного средства
EA014739B1 (ru) * 2005-09-09 2011-02-28 Лабофарм Инк. Композиция тразодона для введения один раз в день
US20080287508A1 (en) * 2007-05-18 2008-11-20 Intermune, Inc. Altering pharmacokinetics of pirfenidone therapy
US20100160363A1 (en) * 2008-12-19 2010-06-24 Aaipharma Services Corp. Extended-release pharmaceutical formulations
US20100159001A1 (en) * 2008-12-19 2010-06-24 Cardinal John R Extended-Release Pharmaceutical Formulations
WO2012072665A1 (en) 2010-11-30 2012-06-07 Pharmaneuroboost N.V. Compositions comprising pipamperone and serotonin antagonist reuptake inhibitors
JP2011140510A (ja) * 2011-03-17 2011-07-21 Biovail Lab Inc 塩酸ブプロピオンの放出調節錠剤
CN105050708A (zh) 2012-11-14 2015-11-11 格雷斯公司 含有生物活性材料与无序无机氧化物的组合物
JP6184903B2 (ja) * 2014-06-04 2017-08-23 ヴァレアント インターナショナル バミューダValeant International Bermuda 塩酸ブプロピオン放出調節錠剤
JP6078514B2 (ja) * 2014-10-30 2017-02-08 コリア ユナイテッド ファーム,インク 溶出率向上と副作用発現が最小化されたシルロスタゾール徐放錠

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4792452A (en) * 1987-07-28 1988-12-20 E. R. Squibb & Sons, Inc. Controlled release formulation
US4983398A (en) * 1987-12-21 1991-01-08 Forest Laboratories, Inc. Sustained release drug dosage forms containing hydroxypropylmethylcellulose and alkali metal carboxylates
US5431922A (en) * 1991-03-05 1995-07-11 Bristol-Myers Squibb Company Method for administration of buspirone
US5169638A (en) * 1991-10-23 1992-12-08 E. R. Squibb & Sons, Inc. Buoyant controlled release powder formulation
US5536507A (en) * 1994-06-24 1996-07-16 Bristol-Myers Squibb Company Colonic drug delivery system
EP0859597B1 (en) * 1995-09-29 2003-04-09 LAM Pharmaceutical Corporation Sustained release delivery system and long acting narcotic analgesics and antagonists
WO1997047285A1 (en) * 1996-06-10 1997-12-18 Depomed, Inc. Gastric-retentive oral controlled drug delivery system with enhanced retention properties
US6143325A (en) * 1998-06-05 2000-11-07 Bristol-Myers Squibb Company Nefazodone dosage form

Also Published As

Publication number Publication date
AR018862A1 (es) 2001-12-12
KR20000005930A (ko) 2000-01-25
IL130022A0 (en) 2000-02-29
JP2000007567A (ja) 2000-01-11
CO5060477A1 (es) 2001-07-30
SG77244A1 (en) 2000-12-19
NO992692D0 (no) 1999-06-03
EP0966966A2 (en) 1999-12-29
HUP9901830A2 (hu) 2001-06-28
UY25544A1 (es) 2001-08-27
AU3319999A (en) 1999-12-16
ID23458A (id) 2000-04-27
EP0966966A3 (en) 2000-02-09
CA2273546A1 (en) 1999-10-10
PL333524A1 (en) 1999-12-06
CN1238181A (zh) 1999-12-15
NO992692L (no) 1999-12-06
ZA993345B (en) 2000-08-22
NZ336001A (en) 2000-09-29
BR9901782A (pt) 2000-05-09
US6143325A (en) 2000-11-07
HU9901830D0 (en) 1999-07-28

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