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LU92550I2 - Lurasidone, facultativement sous forme de sa base libre ou de ses sels pharmaceutiquement acceptables - Google Patents

Lurasidone, facultativement sous forme de sa base libre ou de ses sels pharmaceutiquement acceptables Download PDF

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Publication number
LU92550I2
LU92550I2 LU92550C LU92550C LU92550I2 LU 92550 I2 LU92550 I2 LU 92550I2 LU 92550 C LU92550 C LU 92550C LU 92550 C LU92550 C LU 92550C LU 92550 I2 LU92550 I2 LU 92550I2
Authority
LU
Luxembourg
Prior art keywords
lurasidone
optionally
pharmaceutically acceptable
acceptable salts
free base
Prior art date
Application number
LU92550C
Other languages
English (en)
Original Assignee
Sumitomo Dainippon Pharma Co Ltd
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=37452103&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=LU92550(I2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sumitomo Dainippon Pharma Co Ltd filed Critical Sumitomo Dainippon Pharma Co Ltd
Publication of LU92550I2 publication Critical patent/LU92550I2/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/10Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
    • 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
    • A61K9/0053Mouth and digestive tract, i.e. intraoral and peroral administration
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2009Inorganic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2013Organic compounds, e.g. phospholipids, fats
    • A61K9/2018Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/2027Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/2031Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyethylene oxide, poloxamers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2059Starch, including chemically or physically modified derivatives; Amylose; Amylopectin; Dextrin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2095Tabletting processes; Dosage units made by direct compression of powders or specially processed granules, by eliminating solvents, by melt-extrusion, by injection molding, by 3D printing
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Nutrition Science (AREA)
  • Physiology (AREA)
  • Psychiatry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
LU92550C 2005-05-26 2014-09-18 Lurasidone, facultativement sous forme de sa base libre ou de ses sels pharmaceutiquement acceptables LU92550I2 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2005153508 2005-05-26

Publications (1)

Publication Number Publication Date
LU92550I2 true LU92550I2 (fr) 2015-11-02

Family

ID=37452103

Family Applications (1)

Application Number Title Priority Date Filing Date
LU92550C LU92550I2 (fr) 2005-05-26 2014-09-18 Lurasidone, facultativement sous forme de sa base libre ou de ses sels pharmaceutiquement acceptables

Country Status (22)

Country Link
US (5) US8729085B2 (fr)
EP (2) EP1884242B1 (fr)
JP (2) JP4733120B2 (fr)
KR (2) KR101552033B1 (fr)
CN (2) CN101184489B (fr)
AU (1) AU2006250340C1 (fr)
BR (2) BR122020005056B1 (fr)
CA (1) CA2606510C (fr)
CY (2) CY1114118T1 (fr)
DK (2) DK1884242T3 (fr)
ES (2) ES2535478T3 (fr)
FR (1) FR14C0069I2 (fr)
HK (1) HK1108379A1 (fr)
HU (1) HUS1400051I1 (fr)
LU (1) LU92550I2 (fr)
MX (1) MX2007014872A (fr)
NL (1) NL300690I2 (fr)
PL (1) PL1884242T3 (fr)
PT (1) PT1884242E (fr)
RU (1) RU2398586C3 (fr)
SI (1) SI1884242T1 (fr)
WO (1) WO2006126681A1 (fr)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1886678B1 (fr) * 2005-05-18 2017-04-19 Sumitomo Dainippon Pharma Co., Ltd. Comprimé stable contenant de la droxidopa
CN101184489B (zh) * 2005-05-26 2011-01-19 大日本住友制药株式会社 药物组合物
KR20100121483A (ko) * 2008-02-11 2010-11-17 다이닛본 스미토모 세이야꾸 가부시끼가이샤 용출성이 개선된 정제
ES2400774T3 (es) 2008-06-13 2013-04-12 Dainippon Sumitomo Pharma Co., Ltd. Tableta que se disgrega rápidamente en la cavidad oral y método para producción de la misma
JP5694773B2 (ja) * 2008-09-30 2015-04-01 テバ製薬株式会社 圧縮成型製剤およびその製造方法
MX342330B (es) 2009-05-19 2016-09-26 Celgene Corp Formulaciones de 4-amino-2-(2, 6-dioxopiperidin-3-il) isoindolin-1, 3-diona.
JP5893616B2 (ja) * 2010-10-18 2016-03-23 大日本住友製薬株式会社 注射用徐放性製剤
WO2012063246A1 (fr) * 2010-11-11 2012-05-18 Mapi Pharma Ltd. Forme amorphe du chlorhydrate de lurasidone
WO2012107890A2 (fr) * 2011-02-10 2012-08-16 Ranbaxy Laboratories Limited Formes cristallines de chlorhydrate de lurasidone
US9433620B2 (en) * 2011-05-13 2016-09-06 Cadila Healthcare Limited Pharmaceutical compositions of lurasidone
US8981095B2 (en) 2011-07-28 2015-03-17 Mapi Pharma Ltd. Intermediate compounds and process for the preparation of lurasidone and salts thereof
CN102911169B (zh) * 2011-08-02 2015-05-06 上海医药工业研究院 一种卢拉西酮的制备方法
WO2013061338A1 (fr) 2011-08-24 2013-05-02 Cadila Healthcare Limited Compositions pharmaceutiques de silodosine
CN103446071B (zh) * 2012-05-29 2017-12-19 江苏豪森药业集团有限公司 一种口服片剂及其制备方法和用途
CN102688209A (zh) * 2012-06-21 2012-09-26 李兴惠 鲁拉西酮片和制备方法
CN102688210A (zh) * 2012-06-21 2012-09-26 李兴惠 鲁拉西酮的药物组合物和制备方法
CN106074414B (zh) * 2012-07-12 2019-01-18 成都康弘药业集团股份有限公司 一种含有鲁拉西酮的口腔崩解片及其制备方法
CN103006661B (zh) * 2012-12-06 2015-02-18 江苏先声药物研究有限公司 一种含有盐酸鲁拉西酮的制剂及其制备方法
US20150157628A1 (en) * 2013-12-11 2015-06-11 Saravanan Kannusamy Pharmaceutical compositions of Lurasidone and Process for preparation thereof
WO2016012898A1 (fr) 2014-07-25 2016-01-28 Lupin Limited Composition pharmaceutique orale de lurasidone
CN104606133A (zh) * 2015-01-07 2015-05-13 万特制药(海南)有限公司 鲁拉西酮口服混悬液及其制备方法
WO2016139683A2 (fr) * 2015-03-05 2016-09-09 Jubilant Generics Limited Compositions pharmaceutiques de lurasidone et son procédé de préparation
DE102016205950A1 (de) * 2016-04-08 2017-10-12 Dietrich Seidel Mittel zur Verwendung bei entzündlichen Zuständen der Schleimhäute
WO2018083117A1 (fr) * 2016-11-02 2018-05-11 Sanovel Ilac Sanayi Ve Ticaret A.S. Compositions pharmaceutiques orales solides de chlorhydrate de lurasidone
CN108567758A (zh) * 2017-03-08 2018-09-25 湖南洞庭药业股份有限公司 盐酸鲁拉西酮片剂及其制备方法
CN107854445A (zh) * 2017-12-17 2018-03-30 佛山市弘泰药物研发有限公司 一种盐酸鲁拉西酮分散片及其制备方法
CN107875122A (zh) * 2017-12-17 2018-04-06 佛山市弘泰药物研发有限公司 一种盐酸鲁拉西酮自微乳制剂及其制备方法
CN107854446A (zh) * 2017-12-19 2018-03-30 佛山市弘泰药物研发有限公司 一种盐酸鲁拉西酮口崩片及其制备方法
WO2019167978A1 (fr) 2018-02-28 2019-09-06 大日本住友製薬株式会社 Préparation pharmaceutique de type suspension aqueuse à dissolution contrôlée
EP3772993A1 (fr) 2018-04-10 2021-02-17 Z-Catering Mitte GmbH Dispositif de réchauffage d'un plat conservé dans des unités d'emballage, destiné à préparer une restauration collective
KR102286499B1 (ko) * 2018-04-13 2021-08-05 주식회사 삼양홀딩스 레날리도마이드를 포함하는 약제학적 조성물
WO2022042646A1 (fr) * 2020-08-26 2022-03-03 浙江华海药业股份有限公司 Composition de chlorhydrate de lurasidone et son procédé de préparation
AT17300U3 (de) * 2020-12-03 2022-02-15 G L Pharma Gmbh Feste orale pharmazeutische Zusammensetzung
US20240100022A1 (en) 2020-12-23 2024-03-28 Sumitomo Pharma Co., Ltd. Oral solid preparation

Family Cites Families (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4600579A (en) * 1983-06-07 1986-07-15 Mallinckrodt, Inc. N-acetyl-p-aminophenol compositions containing partially gelatinized starch and method for preparing same
US4551177A (en) 1984-04-23 1985-11-05 National Starch And Chemical Corporation Compressible starches as binders for tablets or capsules
US4609675A (en) 1984-08-17 1986-09-02 The Upjohn Company Stable, high dose, high bulk density ibuprofen granulations for tablet and capsule manufacturing
US4837031A (en) 1987-09-17 1989-06-06 Mallinckrodt, Inc. Compositions containing ibuprofen
US5047246A (en) 1988-09-09 1991-09-10 Bristol-Myers Company Direct compression cyclophosphamide tablet
US5104648A (en) 1989-02-02 1992-04-14 Mallinckrodt Specialty Chemicals Company High ibuprofen content granulations
US4911921A (en) 1989-02-02 1990-03-27 Mallinckrodt, Inc. High ibuprofen content granulations
JP2800953B2 (ja) 1990-07-06 1998-09-21 住友製薬株式会社 新規なイミド誘導体
US5605889A (en) 1994-04-29 1997-02-25 Pfizer Inc. Method of administering azithromycin
ES2181868T3 (es) 1995-02-28 2003-03-01 Aventis Pharma Inc Composicion farmaceutica para compuestos de piperidinoalcanol.
JP4022269B2 (ja) * 1995-05-26 2007-12-12 協和醗酵工業株式会社 医薬組成物
TR200001056T2 (tr) 1997-10-20 2000-09-21 Dainippon Pharmaceutical Co., Ltd. Hızlı çözülen farmasötik terkipler.
JP4063386B2 (ja) * 1998-01-29 2008-03-19 キッセイ薬品工業株式会社 速放性経口医薬品組成物
US6150366A (en) 1998-06-15 2000-11-21 Pfizer Inc. Ziprasidone formulations
EA005291B1 (ru) * 1999-03-31 2004-12-30 Янссен Фармацевтика Н.В. Применение предварительно желатинированного крахмала в композиции с контролируемым высвобождением
US6586617B1 (en) 1999-04-28 2003-07-01 Sumitomo Chemical Takeda Agro Company, Limited Sulfonamide derivatives
WO2001076557A1 (fr) * 2000-04-10 2001-10-18 Sumitomo Pharmaceuticals Co., Ltd. Preparations a liberation prolongee
JP4868695B2 (ja) * 2000-09-22 2012-02-01 大日本住友製薬株式会社 崩壊性が良好な経口製剤
ATE468325T1 (de) 2001-03-19 2010-06-15 Dainippon Sumitomo Pharma Co Arylsubstituierte alicyclische verbindung und diese enthaltende medizinische zusammensetzung
GB0209265D0 (en) 2002-04-23 2002-06-05 Novartis Ag Organic compounds
EP1944030B1 (fr) * 2002-08-22 2018-08-01 Sumitomo Dainippon Pharma Co., Ltd. Agent de traitement de schizophrénie
MXPA05001707A (es) 2002-08-30 2005-04-19 Pharmacia Corp Formas de dosificacion farmaceutica solidas que presentan un perfil de liberacion de farmaco reproducible,.
JPWO2004078173A1 (ja) * 2003-02-05 2006-06-08 塩野義製薬株式会社 溶出性の改善された錠剤
EP2316442A1 (fr) 2003-09-12 2011-05-04 Amgen Inc. Composition à base de composé actif aux récepteurs au calcium, à vitesse de dissolution rapide
CN1913876B (zh) 2003-12-09 2013-06-26 大日本住友制药株式会社 含药物的颗粒和包含这种颗粒的固体制剂
WO2006096439A2 (fr) 2005-03-04 2006-09-14 Boehringer Ingelheim International Gmbh Compositions pharmaceutiques destinees au traitement et/ou a la prevention de la schizophrenie et de maladies associees
CN101184489B (zh) 2005-05-26 2011-01-19 大日本住友制药株式会社 药物组合物

Also Published As

Publication number Publication date
EP2422783B1 (fr) 2015-04-08
JP4733120B2 (ja) 2011-07-27
DK1884242T3 (da) 2013-05-06
RU2007148997A (ru) 2009-07-10
CY1114118T1 (el) 2016-06-22
BR122020005056B1 (pt) 2023-01-10
ES2408687T3 (es) 2013-06-21
BRPI0611409B8 (pt) 2021-05-25
US8883794B2 (en) 2014-11-11
US20140235651A1 (en) 2014-08-21
ES2535478T3 (es) 2015-05-12
BR122020005056A2 (fr) 2010-11-23
US9907794B2 (en) 2018-03-06
FR14C0069I2 (fr) 2015-11-20
CN101184489A (zh) 2008-05-21
HUS1400051I1 (hu) 2016-10-28
KR20080012306A (ko) 2008-02-11
HK1108379A1 (en) 2008-05-09
JP2011126915A (ja) 2011-06-30
US9555027B2 (en) 2017-01-31
PT1884242E (pt) 2013-05-21
CA2606510C (fr) 2014-07-22
US20090143404A1 (en) 2009-06-04
BRPI0611409B1 (pt) 2020-12-29
DK2422783T3 (en) 2015-05-11
AU2006250340A1 (en) 2006-11-30
MX2007014872A (es) 2008-02-15
US20180161322A1 (en) 2018-06-14
BR122020005056A8 (pt) 2022-11-22
BRPI0611409A8 (pt) 2015-12-15
CY2014039I1 (el) 2016-06-22
CY2014039I2 (el) 2016-06-22
NL300690I2 (nl) 2017-11-02
EP2422783A1 (fr) 2012-02-29
US8729085B2 (en) 2014-05-20
KR101552033B1 (ko) 2015-09-09
CA2606510A1 (fr) 2006-11-30
RU2398586C2 (ru) 2010-09-10
SI1884242T1 (sl) 2013-07-31
KR20130122019A (ko) 2013-11-06
CN101184489B (zh) 2011-01-19
PL1884242T3 (pl) 2013-09-30
AU2006250340B2 (en) 2012-02-09
AU2006250340C1 (en) 2014-06-12
WO2006126681A1 (fr) 2006-11-30
FR14C0069I1 (fr) 2014-10-24
JP5285105B2 (ja) 2013-09-11
EP1884242B1 (fr) 2013-04-17
EP1884242A1 (fr) 2008-02-06
RU2398586C3 (ru) 2017-10-04
CN102048734B (zh) 2013-11-20
US20150265611A1 (en) 2015-09-24
KR101380088B1 (ko) 2014-04-10
CN102048734A (zh) 2011-05-11
BRPI0611409A2 (pt) 2010-11-23
US20150056284A1 (en) 2015-02-26
JPWO2006126681A1 (ja) 2008-12-25
EP1884242A4 (fr) 2009-07-01

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