MA35717B1 - Preparation a liberation prolongee - Google Patents

Preparation a liberation prolongee

Info

Publication number
MA35717B1
MA35717B1 MA37034A MA37034A MA35717B1 MA 35717 B1 MA35717 B1 MA 35717B1 MA 37034 A MA37034 A MA 37034A MA 37034 A MA37034 A MA 37034A MA 35717 B1 MA35717 B1 MA 35717B1
Authority
MA
Morocco
Prior art keywords
pioglitazone
preparation
sustained
salt
hours
Prior art date
Application number
MA37034A
Other languages
English (en)
Inventor
Yusuke Murakawa
Yutaka Tanoue
Yumiko Ishii
Kaoru Takenaka
Original Assignee
Takeda Pharmaceutical
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=47178262&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA35717(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Takeda Pharmaceutical filed Critical Takeda Pharmaceutical
Publication of MA35717B1 publication Critical patent/MA35717B1/fr

Links

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
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • 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
    • A61K9/2013—Organic compounds, e.g. phospholipids, fats
    • A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
    • 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
    • A61K9/2031—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyethylene oxide, poloxamers
    • 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
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics

Landscapes

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

Abstract

L'invention concerne une préparation à libération prolongée contenant de la pioglitazone ou un sel de celle-ci en tant que principe actif et présentant une durabilité accrue. L'invention concerne une préparation à libération prolongée contenant de la pioglitazone ou un sel de celle-ci, qui présente un rapport de dissolution de pioglitazone en moyenne de 25-58% à un moment de 2 heures, et en moyenne de 60-100% à un moment de 4 heures, dans un essai de dissolution selon la méthode de la pharmacopée américaine (usp) faisant intervenir des palettes tournant à 50 tr/min et avec une substance tampon kcl/hcl de ph 2,0 à 37 °c en tant que solution d'essai.
MA37034A 2011-10-21 2014-05-15 Preparation a liberation prolongee MA35717B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2011232302 2011-10-21
PCT/JP2012/077662 WO2013058409A1 (fr) 2011-10-21 2012-10-19 Préparation à libération prolongée

Publications (1)

Publication Number Publication Date
MA35717B1 true MA35717B1 (fr) 2014-12-01

Family

ID=47178262

Family Applications (1)

Application Number Title Priority Date Filing Date
MA37034A MA35717B1 (fr) 2011-10-21 2014-05-15 Preparation a liberation prolongee

Country Status (29)

Country Link
US (1) US9907789B2 (fr)
EP (1) EP2768487B1 (fr)
JP (1) JP6093762B2 (fr)
KR (1) KR20140081826A (fr)
CN (1) CN104039313A (fr)
AP (1) AP2014007645A0 (fr)
AR (1) AR088398A1 (fr)
AU (1) AU2012326976B2 (fr)
BR (1) BR112014008744A2 (fr)
CA (1) CA2852417A1 (fr)
CL (1) CL2014000992A1 (fr)
CO (1) CO6960544A2 (fr)
CR (1) CR20140213A (fr)
DO (1) DOP2014000077A (fr)
EA (1) EA201490840A1 (fr)
EC (1) ECSP14013328A (fr)
IL (1) IL232114A0 (fr)
IN (1) IN2014DN03169A (fr)
MA (1) MA35717B1 (fr)
MX (1) MX2014004679A (fr)
NZ (1) NZ624275A (fr)
PE (1) PE20141189A1 (fr)
SG (2) SG2014012025A (fr)
TN (1) TN2014000152A1 (fr)
TW (1) TW201323018A (fr)
UA (1) UA113858C2 (fr)
UY (1) UY34403A (fr)
WO (1) WO2013058409A1 (fr)
ZA (1) ZA201403103B (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104039313A (zh) 2011-10-21 2014-09-10 武田药品工业株式会社 缓释制剂
MD20140063A2 (ro) 2012-04-20 2014-12-31 Gilead Sciences, Inc. Derivaţi de acid benzotiazol-6-il acetic şi utilizarea acestora pentru tratarea unei infecţii HIV
US20150141517A1 (en) * 2013-11-15 2015-05-21 Shin-Etsu Chemical Co., Ltd. Granulated composite, rapid release tablet and method for producing same
KR102485766B1 (ko) 2019-12-11 2023-01-09 한국유나이티드제약 주식회사 생체이용률이 향상된 피오글리타존 함유 약학조성물

Family Cites Families (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4810502A (en) 1987-02-27 1989-03-07 Alza Corporation Pseudoephedrine brompheniramine therapy
US4820522A (en) 1987-07-27 1989-04-11 Mcneilab, Inc. Oral sustained release acetaminophen formulation and process
JPH0624991A (ja) 1991-06-20 1994-02-01 Tokyo Tanabe Co Ltd ウルソデスオキシコール酸持続性製剤
JPH0624959A (ja) 1991-10-04 1994-02-01 Bayer Yakuhin Kk 胃内浮遊型薬物徐放性固形製剤
SK281042B6 (sk) 1992-09-18 2000-11-07 Yamanouchi Pharmaceutical Co., Ltd Prípravok hydrogélového typu s ustáleným uvoľňovaním
JPH06316517A (ja) 1993-02-22 1994-11-15 Grelan Pharmaceut Co Ltd 放出制御製剤
WO1998056359A2 (fr) 1997-06-13 1998-12-17 Roland Bodmeier Compositions retardant la liberation de principes actifs
US6191154B1 (en) * 1998-11-27 2001-02-20 Case Western Reserve University Compositions and methods for the treatment of Alzheimer's disease, central nervous system injury, and inflammatory diseases
WO2003013609A1 (fr) 2001-08-03 2003-02-20 Takeda Chemical Industries, Ltd. Medicaments a liberation continue
WO2004026241A2 (fr) 2002-09-20 2004-04-01 Andrx Labs Llc Nouvelle preparation pharmaceutique contenant un biguanide et un derive de la thiazolidinedione
US9060941B2 (en) 2002-09-20 2015-06-23 Actavis, Inc. Pharmaceutical formulation containing a biguanide and a thiazolidinedione derivative
JP4493970B2 (ja) 2002-10-16 2010-06-30 武田薬品工業株式会社 持続性製剤
MY148805A (en) 2002-10-16 2013-05-31 Takeda Pharmaceutical Controlled release preparation
IN192749B (fr) 2002-11-15 2004-05-15 Ranbaxy Lab Ltd
US7442387B2 (en) 2003-03-06 2008-10-28 Astellas Pharma Inc. Pharmaceutical composition for controlled release of active substances and manufacturing method thereof
JP4933033B2 (ja) 2003-03-17 2012-05-16 武田薬品工業株式会社 放出制御組成物
CA2519208A1 (fr) 2003-03-17 2004-09-30 Takeda Pharmaceutical Company Limited Composition a liberation controlee
JP2005015477A (ja) 2003-06-06 2005-01-20 Takeda Chem Ind Ltd 固形製剤
BRPI0410555A (pt) 2003-06-06 2006-06-20 Takeda Pharmaceutical preparação sólida
US20060003002A1 (en) 2003-11-03 2006-01-05 Lipocine, Inc. Pharmaceutical compositions with synchronized solubilizer release
WO2005099760A1 (fr) 2004-04-14 2005-10-27 Takeda Pharmaceutical Company Limited Préparation pharmaceutique solide
EP1789022A2 (fr) 2004-08-31 2007-05-30 Pfizer Products Incorporated Formes posologiques a liberation controlee combinant une liberation immediate et une liberation prolongee d'un medicament a faible solubilite
WO2007038115A2 (fr) 2005-09-22 2007-04-05 Sb Pharmco Puerto Rico Inc. Procede d'amelioration de la fonction cognitive
WO2007054976A2 (fr) 2005-11-08 2007-05-18 Panacea Biotec Ltd. Nouvelles compositions pharmaceutiques a liberation controlee a base de lipides
BRPI0620020A2 (pt) 2005-12-22 2011-10-25 Takeda Pharmaceutical preparação sólida, e, partìcula revestida
CN101410103B (zh) 2006-03-30 2013-04-10 日本脏器制药株式会社 固体药物制剂
TW200800299A (en) 2006-04-27 2008-01-01 Takeda Pharmaceutical Pharmaceutical composition
US9095519B2 (en) 2007-02-09 2015-08-04 Alphapharm Pty Ltd Dosage form containing two or more active pharmaceutical ingredients in different physical forms
TW200914006A (en) * 2007-07-12 2009-04-01 Takeda Pharmaceutical Coated preparation
CN101269040A (zh) 2008-05-16 2008-09-24 北京正大绿洲医药科技有限公司 盐酸吡格列酮缓释滴丸及其制备方法
AU2009298684B2 (en) 2008-09-30 2015-11-19 Konstantinos Ritis Method of inhibiting biomaterial-induced procoagulant activity using complement inhibitors
TWI478712B (zh) * 2008-09-30 2015-04-01 Astellas Pharma Inc 釋控性醫藥組成物
JP5827952B2 (ja) 2009-10-09 2015-12-02 ユンジン・ファーム・カンパニー・リミテッドＹｕｎｇｊｉｎ Ｐｈａｒｍ． Ｃｏ． Ｌｔｄ． 速効性と持続性を同時に有する薬剤学的組成物
JP2011232302A (ja) 2010-04-30 2011-11-17 Ricoh Elemex Corp 画像検査方法及び画像検査装置
CN101884627B (zh) 2010-07-07 2012-01-25 青岛黄海制药有限责任公司 盐酸吡格列酮胃内滞留缓释片及其制备方法
KR20180050420A (ko) * 2011-01-10 2018-05-14 진판델 파마슈티컬스 인코포레이티드 알츠하이머 병 치료를 위한 방법 및 약품
CN104039313A (zh) 2011-10-21 2014-09-10 武田药品工业株式会社 缓释制剂
KR20160056691A (ko) 2014-11-12 2016-05-20 삼성에스디아이 주식회사 이차전지

Also Published As

Publication number Publication date
EP2768487A1 (fr) 2014-08-27
BR112014008744A2 (pt) 2017-04-18
AU2012326976A1 (en) 2014-05-29
US20140248362A1 (en) 2014-09-04
WO2013058409A1 (fr) 2013-04-25
TW201323018A (zh) 2013-06-16
SG2014012025A (en) 2014-06-27
AU2012326976A2 (en) 2014-06-12
PE20141189A1 (es) 2014-09-24
CR20140213A (es) 2014-06-18
AR088398A1 (es) 2014-05-28
TN2014000152A1 (en) 2015-09-30
IN2014DN03169A (fr) 2015-05-22
CL2014000992A1 (es) 2014-09-05
US9907789B2 (en) 2018-03-06
EA201490840A1 (ru) 2014-08-29
ZA201403103B (en) 2015-08-26
UA113858C2 (uk) 2017-03-27
AU2012326976B2 (en) 2017-08-17
AP2014007645A0 (en) 2014-05-31
IL232114A0 (en) 2014-06-30
JP2014530802A (ja) 2014-11-20
JP6093762B2 (ja) 2017-03-08
UY34403A (es) 2013-05-31
NZ624275A (en) 2016-09-30
EP2768487B1 (fr) 2020-06-03
KR20140081826A (ko) 2014-07-01
CO6960544A2 (es) 2014-05-30
MX2014004679A (es) 2014-08-01
SG10201700121YA (en) 2017-03-30
ECSP14013328A (es) 2014-05-31
CA2852417A1 (fr) 2013-04-25
DOP2014000077A (es) 2014-07-15
CN104039313A (zh) 2014-09-10

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