CA2108575A1 - Method of manufacturing solid dispersion - Google Patents

Method of manufacturing solid dispersion

Info

Publication number
CA2108575A1
CA2108575A1 CA002108575A CA2108575A CA2108575A1 CA 2108575 A1 CA2108575 A1 CA 2108575A1 CA 002108575 A CA002108575 A CA 002108575A CA 2108575 A CA2108575 A CA 2108575A CA 2108575 A1 CA2108575 A1 CA 2108575A1
Authority
CA
Canada
Prior art keywords
solid dispersion
manufacturing solid
solid
twin
dissolving
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.)
Granted
Application number
CA002108575A
Other languages
French (fr)
Other versions
CA2108575C (en
Inventor
Kouichi Nakamichi
Shogo Izumi
Hiroyuki Yasuura
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.)
Nippon Shinyaku Co Ltd
Original Assignee
Individual
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=14589572&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CA2108575(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Individual filed Critical Individual
Publication of CA2108575A1 publication Critical patent/CA2108575A1/en
Application granted granted Critical
Publication of CA2108575C publication Critical patent/CA2108575C/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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
    • A61K9/1682Processes
    • A61K9/1694Processes resulting in granules or microspheres of the matrix type containing more than 5% of excipient
    • 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
    • A61K9/141Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
    • A61K9/146Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds

Abstract

The object of this invention is to provide a process for producing a solid dispersion, which has overcome the disadvantages of the conventional production technology for solid dispersions, The invention comprises employing a twin-screw extruder in the production of a solid dispersion.
In accordance with the invention, a solid dispersion can be expediently produced without heating a drug and a polymer to or beyond their melting points and without using an organic solvent for dissolving both components and the resulting solid dispersion has excellent performance characteristics.
CA002108575A 1991-04-16 1992-04-14 Method of manufacturing solid dispersion Expired - Lifetime CA2108575C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP11255491 1991-04-16
JPHEI-3/112,554 1991-04-16
PCT/JP1992/000470 WO1992018106A1 (en) 1991-04-16 1992-04-14 Method of manufacturing solid dispersion

Publications (2)

Publication Number Publication Date
CA2108575A1 true CA2108575A1 (en) 1992-10-17
CA2108575C CA2108575C (en) 2002-10-22

Family

ID=14589572

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002108575A Expired - Lifetime CA2108575C (en) 1991-04-16 1992-04-14 Method of manufacturing solid dispersion

Country Status (12)

Country Link
US (1) US5456923A (en)
EP (1) EP0580860B2 (en)
JP (1) JP2527107B2 (en)
KR (1) KR0182801B1 (en)
AT (1) ATE159426T1 (en)
AU (1) AU1537292A (en)
CA (1) CA2108575C (en)
DE (1) DE69222847T3 (en)
DK (1) DK0580860T4 (en)
ES (1) ES2111065T5 (en)
GR (1) GR3025864T3 (en)
WO (1) WO1992018106A1 (en)

Families Citing this family (273)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5266331A (en) * 1991-11-27 1993-11-30 Euroceltique, S.A. Controlled release oxycodone compositions
JP3722293B2 (en) 1991-12-18 2005-11-30 ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー Novel pharmaceutical solid dispersion
US5968551A (en) 1991-12-24 1999-10-19 Purdue Pharma L.P. Orally administrable opioid formulations having extended duration of effect
US5958459A (en) * 1991-12-24 1999-09-28 Purdue Pharma L.P. Opioid formulations having extended controlled released
US5478577A (en) * 1993-11-23 1995-12-26 Euroceltique, S.A. Method of treating pain by administering 24 hour oral opioid formulations exhibiting rapid rate of initial rise of plasma drug level
DE69327877T2 (en) * 1992-10-14 2000-10-05 Nippon Shinyaku Co Ltd METHOD FOR SHIFTING A CRYSTAL CONDITION
US5811547A (en) * 1992-10-14 1998-09-22 Nippon Shinyaju Co., Ltd. Method for inducing crystalline state transition in medicinal substance
ATE223704T1 (en) * 1992-10-16 2002-09-15 Nippon Shinyaku Co Ltd METHOD FOR PRODUCING WAX MATRICES
US20080075781A1 (en) * 1992-11-25 2008-03-27 Purdue Pharma Lp Controlled release oxycodone compositions
US20070275062A1 (en) * 1993-06-18 2007-11-29 Benjamin Oshlack Controlled release oxycodone compositions
IL110014A (en) 1993-07-01 1999-11-30 Euro Celtique Sa Solid controlled-release oral dosage forms of opioid analgesics
US7740881B1 (en) 1993-07-01 2010-06-22 Purdue Pharma Lp Method of treating humans with opioid formulations having extended controlled release
US5879705A (en) * 1993-07-27 1999-03-09 Euro-Celtique S.A. Sustained release compositions of morphine and a method of preparing pharmaceutical compositions
WO1995005809A1 (en) * 1993-08-20 1995-03-02 Nippon Shinyaku Co., Ltd. Gastric remaining preparation, swollen molding, and production process
GB2281697A (en) 1993-09-14 1995-03-15 Euro Celtique Sa Laxative compositions in capsules
US5688510A (en) * 1993-11-18 1997-11-18 Nippon Shinyaku Co. Ltd. Process for producing stable medicinal composition, and pharmaceutical preparation
DE19509807A1 (en) * 1995-03-21 1996-09-26 Basf Ag Process for the preparation of active substance preparations in the form of a solid solution of the active substance in a polymer matrix, and active substance preparations produced using this method
GB9422154D0 (en) 1994-11-03 1994-12-21 Euro Celtique Sa Pharmaceutical compositions and method of producing the same
US20020006438A1 (en) * 1998-09-25 2002-01-17 Benjamin Oshlack Sustained release hydromorphone formulations exhibiting bimodal characteristics
US5965161A (en) 1994-11-04 1999-10-12 Euro-Celtique, S.A. Extruded multi-particulates
ES2210321T3 (en) * 1994-12-19 2004-07-01 Daiichi Pharmaceutical Co., Ltd. GRANULAR PREPARATION OF PROLONGED RELEASE AND PRODUCTION PROCEDURE.
FR2736550B1 (en) * 1995-07-14 1998-07-24 Sandoz Sa PHARMACEUTICAL COMPOSITION IN THE FORM OF A SOLID DISPERSION COMPRISING A MACROLIDE AND A VEHICLE
ATE240734T1 (en) * 1995-07-26 2003-06-15 Kyowa Hakko Kogyo Kk PREPARATION OF XANTHINDERIVATES AS A SOLID DISPERSION
TW487582B (en) 1995-08-11 2002-05-21 Nissan Chemical Ind Ltd Method for converting sparingly water-soluble medical substance to amorphous state
BR9706897B1 (en) * 1996-05-20 2010-09-21 pharmaceutical dosage form.
US6139872A (en) * 1996-08-14 2000-10-31 Henkel Corporation Method of producing a vitamin product
JPH10114682A (en) * 1996-10-11 1998-05-06 Shimizu Kagaku Kk Sustained release medicine mixed with clucomannan for internal use
US5955475A (en) * 1997-06-30 1999-09-21 Endo Pharmaceuticals Inc. Process for manufacturing paroxetine solid dispersions
DE69837903T2 (en) 1997-08-11 2008-02-14 Pfizer Products Inc., Groton Solid pharmaceutical dispersions with increased bioavailability
EP1741424B1 (en) 1997-08-11 2018-10-03 Pfizer Products Inc. Solid pharmaceutical dispersions with enhanced bioavailabilty
HN1998000115A (en) * 1997-08-21 1999-06-02 Warner Lambert Co SOLID PHARMACEUTICAL DOSAGE FORMS
US6013280A (en) * 1997-10-07 2000-01-11 Fuisz Technologies Ltd. Immediate release dosage forms containing microspheres
WO1999034780A1 (en) * 1998-01-12 1999-07-15 Bühler AG Method and device for capsulating active ingredients
IE980115A1 (en) * 1998-02-16 2000-02-09 Biovail Internat Ltd Solubilizing delivery systems and method of manufacture
AU759264B2 (en) * 1998-05-27 2003-04-10 Euro-Celtique S.A. Preparations for the application of anti-inflammatory, especially antiseptic agents and/or agents promoting the healing of wounds, to the upper respiratory tract and/or the ear
DE19842914A1 (en) * 1998-09-18 2000-03-23 Basf Ag Test system to characterize the compatibility of biologically active substances and polyvinylpyrrolidone
DE19842753A1 (en) 1998-09-18 2000-03-23 Bayer Ag Multiple-unit retard oral dosage formulation having controlled release independent of agitation and food effect, containing particles of combination of drug and hydroxypropyl cellulose
US6350786B1 (en) 1998-09-22 2002-02-26 Hoffmann-La Roche Inc. Stable complexes of poorly soluble compounds in ionic polymers
US6806294B2 (en) 1998-10-15 2004-10-19 Euro-Celtique S.A. Opioid analgesic
US6455526B1 (en) 1998-12-16 2002-09-24 Aventis Pharmaceuticals, Inc. Biodegradable polymer encapsulated pharmaceutical compositions and method for preparing the same
OA11728A (en) * 1998-12-16 2005-02-01 Aventis Pharma Inc Biodegradable polymer encapsulated serotonin receptor antagonist and method for preparing the same.
DE60039377D1 (en) 1999-02-09 2008-08-21 Pfizer Prod Inc Compositions of basic drugs with improved bioavailability
US6706283B1 (en) * 1999-02-10 2004-03-16 Pfizer Inc Controlled release by extrusion of solid amorphous dispersions of drugs
EP1027886B1 (en) 1999-02-10 2008-07-09 Pfizer Products Inc. Pharmaceutical solid dispersions
JP2000281561A (en) * 1999-03-26 2000-10-10 Ajinomoto Co Inc New solid dispersion preparation by solvent method
DE19918325A1 (en) 1999-04-22 2000-10-26 Euro Celtique Sa Extruded drug dosage form, e.g. granulate for tableting, comprising an active agent in a polysaccharide-containing matrix, giving a release profile which is controllable by extrusion conditions and/or the inclusion of additives
US7300667B1 (en) 1999-05-27 2007-11-27 Euro-Celtique, S.A. Preparations for the application of anti-inflammatory, especially antiseptic agents and/or agents promoting the healing of wounds, to the lower respiratory tract
US7297344B1 (en) 1999-05-27 2007-11-20 Euro-Celtique, S.A. Preparations for the promotion of wound healing in the upper respiratory tract and/or ear
ES2274372T3 (en) 1999-05-27 2007-05-16 Euro-Celtique S.A. USE OF ANTISEPTICS IN THE MANUFACTURE OF A PHARMACEUTICAL PREPARATION FOR THE PREVENTION OR TREATMENT OF INFLAMMATIONS INSIDE THE HUMAN BODY.
DE19945982A1 (en) 1999-09-24 2001-03-29 Knoll Ag Velocity-determined particles
DE19949897A1 (en) * 1999-10-15 2001-04-19 Rainer Rogasch Shaped article, e.g. in stick form, for controlled release of drugs in wounds or body cavities, comprising hydrophilic outer phase, lipophilic inner phase and drug, e.g. antibiotic
EP2295043A1 (en) 1999-10-29 2011-03-16 Euro-Celtique S.A. Controlled release hydrocodone formulations
US10179130B2 (en) 1999-10-29 2019-01-15 Purdue Pharma L.P. Controlled release hydrocodone formulations
WO2001034119A2 (en) 1999-11-12 2001-05-17 Abbott Laboratories Inhibitors of crystallization in a solid dispersion
US7364752B1 (en) 1999-11-12 2008-04-29 Abbott Laboratories Solid dispersion pharamaceutical formulations
TR200201617T2 (en) 1999-12-23 2002-10-21 Pfizer Products Inc. Pharmaceutical compositions that provide enhanced drug concentrations
KR20030019326A (en) * 2000-03-21 2003-03-06 니뽄 신야쿠 가부시키가이샤 Sustained release oral preparations
DE10026698A1 (en) 2000-05-30 2001-12-06 Basf Ag Self-emulsifying active ingredient formulation and use of this formulation
DE10031044A1 (en) 2000-06-26 2002-01-03 Bayer Ag Endoparasiticidal agents for voluntary oral ingestion by animals
JP3563070B2 (en) * 2000-07-17 2004-09-08 山之内製薬株式会社 Oral absorption improving pharmaceutical composition
US7115279B2 (en) 2000-08-03 2006-10-03 Curatolo William J Pharmaceutical compositions of cholesteryl ester transfer protein inhibitors
US20040013736A1 (en) * 2000-09-25 2004-01-22 Tomio Nakano Process for producing medicinal solid dispersion
CN101317825A (en) 2000-10-30 2008-12-10 欧罗赛铁克股份有限公司 Controlled release hydrocodone formulations
ITMI20010141A1 (en) * 2001-01-26 2002-07-26 Giuliani Spa PROCEDURE FOR THE PREPARATION OF PHARMACEUTICAL OR DIETETIC COMPOSITIONS FOR VEHICULATION IN THE INTESTINE OF LABILE SUBSTANCES
GB0104752D0 (en) * 2001-02-27 2001-04-18 Astrazeneca Ab Pharmaceutical compositions
CA2439366A1 (en) * 2001-02-27 2002-09-06 Julie Cahill Pharmaceutical formulation comprising bicalutamide
US6465014B1 (en) * 2001-03-21 2002-10-15 Isp Investments Inc. pH-dependent sustained release, drug-delivery composition
US20110104214A1 (en) 2004-04-15 2011-05-05 Purdue Pharma L.P. Once-a-day oxycodone formulations
UA81224C2 (en) 2001-05-02 2007-12-25 Euro Celtic S A Dosage form of oxycodone and use thereof
KR20040011549A (en) * 2001-06-22 2004-02-05 화이자 프로덕츠 인크. Pharmaceutical Compositions Comprising Low-Solubility and/or Acid-Sensitive Drugs and Neutralized Acidic Polymers
EP1269994A3 (en) 2001-06-22 2003-02-12 Pfizer Products Inc. Pharmaceutical compositions comprising drug and concentration-enhancing polymers
ES2333645T3 (en) * 2001-06-22 2010-02-25 Bend Research, Inc. PHARMACEUTICAL COMPOSITIONS OF DISPERSIONS OF MEDICINES AND NEUTRAL POLYMERS.
JP2004534811A (en) * 2001-06-22 2004-11-18 ファイザー・プロダクツ・インク Pharmaceutical composition comprising a polymer and drug assembly
ES2284871T3 (en) * 2001-06-22 2007-11-16 Pfizer Products Inc. PHARMACEUTICAL COMPOSITIONS CONTAINING A SOLID DISPERSION OF LITTLE SOLUBLE PHARMACO AND A SOLUBILITY POTENTIATING POLYMER.
DE10141650C1 (en) 2001-08-24 2002-11-28 Lohmann Therapie Syst Lts Safe transdermal therapeutic system for administration of fentanyl or analogous analgesics, having matrix layer of carboxy group-free polyacrylate adhesive providing high permeation rate
SE0103424D0 (en) * 2001-10-15 2001-10-15 Astrazeneca Ab Pharmaceutical formulation
US7491407B2 (en) * 2001-10-31 2009-02-17 North Carolina State University Fiber-based nano drug delivery systems (NDDS)
AR038375A1 (en) * 2002-02-01 2005-01-12 Pfizer Prod Inc PHARMACEUTICAL COMPOSITIONS OF INHIBITORS OF THE PROTEIN OF TRANSFER OF ESTERES DE COLESTERILO
EP1920766B1 (en) 2002-02-01 2017-08-23 Bend Research, Inc Pharmaceutical compositions of amorphous dispersions of drugs and lipophilic microphase-forming materials
KR20040083493A (en) * 2002-02-01 2004-10-02 화이자 프로덕츠 인크. Controlled release pharmaceutical dosage forms of a cholesteryl ester transfer protein inhibitor
KR100664822B1 (en) 2002-02-01 2007-01-04 화이자 프로덕츠 인코포레이티드 Method for making homogeneous spray-dried solid amorphous drug dispersions utilizing modified spray-drying apparatus
US20030204180A1 (en) * 2002-04-30 2003-10-30 Kimberly-Clark Worldwide, Inc. Temperature responsive delivery systems
ES2333318T3 (en) 2002-08-12 2010-02-19 Bend Research, Inc. PHARMACEUTICAL COMPOSITIONS OF MEDICINES WITH SEMIORDENATED STRUCTURE AND OF POLYMER.
ATE407670T1 (en) 2002-12-20 2008-09-15 Pfizer Prod Inc DOSAGE FORM CONTAINING A CETP INHIBITOR AND A HMG-COA REDUCTASE INHIBITOR
WO2004069180A2 (en) * 2003-01-31 2004-08-19 Smithkline Beecham Corporation Solid dispersion compositions
EP1594468A2 (en) * 2003-02-03 2005-11-16 Novartis AG Process for preparing a solid dispersion pharmaceutical product
US8377952B2 (en) 2003-08-28 2013-02-19 Abbott Laboratories Solid pharmaceutical dosage formulation
US8025899B2 (en) 2003-08-28 2011-09-27 Abbott Laboratories Solid pharmaceutical dosage form
JP2007511500A (en) * 2003-11-14 2007-05-10 ファイザー・プロダクツ・インク Solid amorphous dispersion of MTP inhibitors for the treatment of obesity
WO2005056542A1 (en) * 2003-12-09 2005-06-23 Pfizer Inc. Compositions comprising an hiv protease inhibitor
JP2007520543A (en) 2004-02-04 2007-07-26 ファイザー・プロダクツ・インク Substituted quinoline compounds
US20050238721A1 (en) * 2004-04-07 2005-10-27 Acquarulo Lawrence A Jr One step compounding extrusion of drug filled polymers
EP1750669A1 (en) * 2004-05-04 2007-02-14 Boehringer Ingelheim International Gmbh Solid pharmaceutical form comprising an ltb4 antagonist
GEP20094723B (en) 2004-05-25 2009-07-10 Pfizer Prod Inc Tetraazabenzo [e] azulene derivatives and analogs thereof
JP2008501009A (en) * 2004-05-28 2008-01-17 ファイザー・プロダクツ・インク Pharmaceutical composition with enhanced performance
MY191349A (en) * 2004-08-27 2022-06-17 Bayer Pharmaceuticals Corp New pharmaceutical compositions for the treatment of hyper-proliferative disorders
US8604055B2 (en) 2004-12-31 2013-12-10 Dr. Reddy's Laboratories Ltd. Substituted benzylamino quinolines as cholesterol ester-transfer protein inhibitors
ES2644450T3 (en) 2004-12-31 2017-11-29 Dr. Reddy's Laboratories Ltd. New benzylamine derivatives as CETP inhibitors
US8617604B2 (en) 2005-02-03 2013-12-31 Bend Research, Inc. Pharmaceutical compositions with enhanced performance
EP1690528A1 (en) * 2005-02-11 2006-08-16 Abbott GmbH & Co. KG Process for the preparation of dosage forms comprising a solid dispersion of a microcrystalline active agent
US20100047338A1 (en) 2008-03-14 2010-02-25 Angela Brodie Novel C-17-Heteroaryl Steroidal CYP17 Inhibitors/Antiandrogens, In Vitro Biological Activities, Pharmacokinetics and Antitumor Activity
US20080213339A1 (en) * 2005-08-02 2008-09-04 Roger Imboden Pharmaceutical Composition Containing Indometacin and/or Acemetacin
EP2664337B1 (en) 2005-09-27 2019-08-14 TissueTech, Inc. Amniotic membrane preparations and purified compositions and methods of use
US8187639B2 (en) 2005-09-27 2012-05-29 Tissue Tech, Inc. Amniotic membrane preparations and purified compositions and anti-angiogenesis treatment
US8022054B2 (en) 2005-11-28 2011-09-20 Marinus Pharmaceuticals Liquid ganaxolone formulations and methods for the making and use thereof
EP1832281A1 (en) 2006-03-10 2007-09-12 Abbott GmbH & Co. KG Process for producing a solid dispersion of an active ingredient
EP2056818B1 (en) 2006-08-11 2011-05-25 The Johns Hopkins University Compositions and methods for neuroprotection
HUE028086T2 (en) 2006-09-22 2016-11-28 Pharmacyclics Llc Inhibitors of bruton's tyrosine kinase
WO2008063888A2 (en) 2006-11-22 2008-05-29 Plexxikon, Inc. Compounds modulating c-fms and/or c-kit activity and uses therefor
US7638541B2 (en) * 2006-12-28 2009-12-29 Metabolex Inc. 5-ethyl-2-{4-[4-(4-tetrazol-1-yl-phenoxymethyl)-thiazol-2-yl]-piperidin-1-yl}-pyrimidine
US7607596B1 (en) 2007-03-07 2009-10-27 Exxpharma, LLC Process for enhancing the solubility of poorly soluble drugs
US8703204B2 (en) 2007-05-03 2014-04-22 Bend Research, Inc. Nanoparticles comprising a cholesteryl ester transfer protein inhibitor and anon-ionizable polymer
US8309129B2 (en) 2007-05-03 2012-11-13 Bend Research, Inc. Nanoparticles comprising a drug, ethylcellulose, and a bile salt
US9545384B2 (en) 2007-06-04 2017-01-17 Bend Research, Inc. Nanoparticles comprising drug, a non-ionizable cellulosic polymer and tocopheryl polyethylene glocol succinate
WO2008149192A2 (en) 2007-06-04 2008-12-11 Pfizer Products Inc. Nanoparticles comprising a non-ionizable cellulosic polymer and an amphiphilic non-ionizable block copolymer
MX2010000617A (en) 2007-07-17 2010-05-17 Plexxikon Inc Compounds and methods for kinase modulation, and indications therefor.
AU2008279447A1 (en) * 2007-07-19 2009-01-29 Metabolex, Inc. N-azacyclic substituted pyrrole, pyrazole, imidazole, triazole and tetrazole derivatives as agonists of the RUP3 or GPR119 receptor for the treatment of diabetes and metabolic disorders
CA2990445C (en) 2007-08-21 2020-05-05 Board Of Regents, The University Of Texas System Thermo-kinetic mixing for pharmaceutical applications
US8263641B2 (en) 2007-09-10 2012-09-11 Calcimedica, Inc. Compounds that modulate intracellular calcium
US20100240711A1 (en) * 2007-09-21 2010-09-23 Shionogi & Co., Ltd. Solid preparation comprising npyy5 receptor antagonist
EP2601935A1 (en) * 2007-09-25 2013-06-12 Solubest Ltd. Compositions comprising lipophilic active compounds and method for their preparation
WO2009053635A1 (en) * 2007-10-11 2009-04-30 L'oreal Structured cosmetic composition
FR2922100B1 (en) * 2007-10-11 2009-12-11 Oreal PROCESS FOR THE PREPARATION OF SEMI-SOLID PARTICLES WITH COSMETIC INTEREST
US9724362B2 (en) 2007-12-06 2017-08-08 Bend Research, Inc. Pharmaceutical compositions comprising nanoparticles and a resuspending material
US9233078B2 (en) 2007-12-06 2016-01-12 Bend Research, Inc. Nanoparticles comprising a non-ionizable polymer and an Amine-functionalized methacrylate copolymer
US20090163561A1 (en) * 2007-12-21 2009-06-25 Url Pharma, Inc. Amorphous metaxalone and amorphous dispersions thereof
JP5711655B2 (en) * 2008-03-31 2015-05-07 シマベイ セラピューティクス, インコーポレーテッド Oxymethylene aryl compounds and uses thereof
WO2010027875A2 (en) 2008-08-27 2010-03-11 Calcimedica Inc. Compounds that modulate intracellular calcium
US20110160222A1 (en) * 2008-11-26 2011-06-30 Metabolex, Inc. Modulators of glucose homeostasis for the treatment of diabetes and metabolic disorders
WO2010067233A1 (en) 2008-12-08 2010-06-17 Pfizer Inc. 1,2,4 triazolo [4, 3 -a] [1,5] benzodiazepin-5 (6h) -ones as agonists of the cholecystokinin-1 receptor (cck-ir)
CA2761389A1 (en) 2009-02-05 2010-08-12 Tokai Pharmaceuticals, Inc. Novel prodrugs of steroidal cyp17 inhibitors/antiandrogens
WO2010114928A2 (en) 2009-04-03 2010-10-07 F.Hoffmann-La Roche Ag Compositions and uses thereof
EP2421901B1 (en) 2009-04-24 2015-10-28 Tissue Tech, Inc. Compositions containing hc ha complex and methods of use thereof
RU2012101214A (en) 2009-06-16 2013-07-27 Пфайзер Инк. DOSAGE FORMS OF APIKSABAN
US8329724B2 (en) 2009-08-03 2012-12-11 Hoffmann-La Roche Inc. Process for the manufacture of pharmaceutically active compounds
CN102666553B (en) 2009-10-01 2015-05-06 赛马拜制药公司 Substituted tetrazol-1-yl-phenoxymethyl-thiazol-2-yl-piperidinyl-pyrimidine salts
US7718662B1 (en) 2009-10-12 2010-05-18 Pharmacyclics, Inc. Pyrazolo-pyrimidine inhibitors of bruton's tyrosine kinase
NZ629615A (en) 2009-11-06 2016-01-29 Plexxikon Inc Compounds and methods for kinase modulation, and indications therefor
CN102821754B (en) * 2010-03-26 2014-06-18 陶氏环球技术有限责任公司 Multilayer melt-extruded film
US20110236666A1 (en) * 2010-03-26 2011-09-29 Hall Mark J Melt-extruded film
KR20130080004A (en) * 2010-03-26 2013-07-11 다우 글로벌 테크놀로지스 엘엘씨 Melt-extruded film
EP2558866B1 (en) 2010-04-15 2016-08-17 Tracon Pharmaceuticals, Inc. Potentiation of anti-cancer activity through combination therapy with ber pathway inhibitors
WO2011139489A2 (en) 2010-04-27 2011-11-10 Calcimedica Inc. Compounds that modulate intracellular calcium
JP2013525448A (en) 2010-04-27 2013-06-20 カルシメディカ,インク. Compounds that regulate intracellular calcium
US20130072519A1 (en) 2010-05-21 2013-03-21 Edward Lee Conn 2-phenyl benzoylamides
CA2800913C (en) 2010-06-03 2019-07-23 Pharmacyclics, Inc. The use of inhibitors of bruton's tyrosine kinase (btk)
EP2585048B1 (en) 2010-06-23 2018-04-11 CymaBay Therapeutics, Inc. Compositions of 5-ethyl-2-{4-[4-(4-tetrazol-1-yl-phenoxymethyl)-thiazol-2-yl]-piperidin-1-yl}-pyrimidine
MX2013000201A (en) 2010-07-02 2013-08-21 Procter & Gamble Methods of delivering a health care active by administering personal health care articles comprising a filament.
AU2011293201B2 (en) 2010-08-27 2015-11-05 Calcimedica Inc. Compounds that modulate intracellular calcium
JP5941069B2 (en) 2011-02-07 2016-06-29 プレキシコン インコーポレーテッドPlexxikon Inc. Compounds and methods for kinase regulation and indications therefor
RU2013139701A (en) 2011-02-17 2015-03-27 Ф. Хоффманн-Ля Рош Аг METHOD FOR CONTROLLED CRYSTALLIZATION OF AN ACTIVE PHARMACEUTICAL INGREDIENT FROM THE STATE OF A COOLED LIQUID BY EXTRUSION OF HOT DECAY
AR085279A1 (en) 2011-02-21 2013-09-18 Plexxikon Inc SOLID FORMS OF {3- [5- (4-CHLORINE-PHENYL) -1H-PIRROLO [2,3-B] PIRIDINA-3-CARBONIL] -2,4-DIFLUOR-PHENIL} -AMIDE OF PROPANE ACID-1- SULFONIC
DE102011015370A1 (en) * 2011-03-29 2012-10-04 Emodys Gmbh Preparing a matrix comprises preparing a mixture containing an active agent and a biopolymer e.g. alginate, gum arabic, locust bean gum, karaya gum, tara gum or tragacanth and extruding the obtained mixture
WO2012149486A1 (en) 2011-04-28 2012-11-01 Tissuetech, Inc. Methods of modulating bone remodeling
ES2822301T3 (en) 2011-06-10 2021-04-30 Tissuetech Inc Fetal Support Tissue Processing Methods
US9199967B2 (en) 2011-08-18 2015-12-01 Dr. Reddy's Laboratories Ltd. Substituted heterocyclic amine compounds as cholestryl ester-transfer protein (CETP) inhibitors
CN103917231B (en) 2011-09-13 2016-09-28 药品循环有限责任公司 Combination formulations of histone deacetylase inhibitor and bendamustine and application thereof
CN103958511A (en) 2011-09-27 2014-07-30 雷迪博士实验室有限公司 5 - benzylaminomethyl - 6 - aminopyrazolo [3, 4 -b] pyridine derivatives as cholesteryl ester -transfer protein (cetp) inhibitors useful for the treatment of atherosclerosis
US8377946B1 (en) 2011-12-30 2013-02-19 Pharmacyclics, Inc. Pyrazolo[3,4-d]pyrimidine and pyrrolo[2,3-d]pyrimidine compounds as kinase inhibitors
MY168791A (en) 2012-01-06 2018-12-04 Abide Therapeutics Inc Carbamate compounds and of making and using same
IN2012DE00674A (en) 2012-03-07 2015-08-21 Nat Inst Of Pharmaceutical Education And Res Niper
SG11201405477XA (en) 2012-04-06 2014-11-27 Pfizer Diacylglycerol acyltransferase 2 inhibitors
US9150570B2 (en) 2012-05-31 2015-10-06 Plexxikon Inc. Synthesis of heterocyclic compounds
CN110354132A (en) 2012-06-04 2019-10-22 药品循环有限责任公司 The crystalline form of bruton's tyrosine kinase inhibitor
JP2015528001A (en) 2012-07-11 2015-09-24 ティッシュテック,インク. Composition comprising HC-HA / PTX3 complex and method of use thereof
DK2900674T3 (en) 2012-09-28 2017-07-03 Univ Washington Through Its Center For Commercialization RELATIONSHIPS AND PROCEDURES FOR PREVENTION, TREATMENT AND / OR PROTECTION AGAINST SENSITIVE CELL DEATH
WO2014059333A1 (en) 2012-10-12 2014-04-17 Calcimedica, Inc. Compounds that modulate intracellular calcium
KR102191562B1 (en) * 2012-11-07 2020-12-15 에스케이바이오팜 주식회사 Solid dispersions of insoluble drug and preparation method therof
US20170071930A1 (en) 2012-11-19 2017-03-16 Dr. Reddy's Laboratories Ltd. Pharmaceutical compositions of cetp inhibitors
JP6150518B2 (en) 2012-12-27 2017-06-21 花王株式会社 Method for producing polyphenol composition
WO2014128564A2 (en) 2013-02-21 2014-08-28 Dr. Reddy's Laboratories Ltd. Pharmaceutical compositions of cetp inhibitors
AU2014236135A1 (en) 2013-03-14 2015-09-10 Thomas Jefferson University Androgen receptor down-regulating agents and uses thereof
EP2837391B1 (en) 2013-08-12 2017-05-10 Shin-Etsu Chemical Co., Ltd. Hypromellose acetate succinate for use as hot-melt extrusion carrier, hot-melt extrusion composition, and method for producing hot-melt extrudate
US9808472B2 (en) 2013-08-12 2017-11-07 Tokai Pharmaceuticals, Inc. Biomarkers for treatment of neoplastic disorders using androgen-targeted therapies
US9296882B2 (en) 2013-09-04 2016-03-29 Zzyzx Polymers LLC Methods for increasing throughput rates of solid-state extrusion devices
WO2015054283A1 (en) 2013-10-08 2015-04-16 Calcimedica, Inc. Compounds that modulate intracellular calcium
US20150104508A1 (en) * 2013-10-12 2015-04-16 Zzyzx Polymers LLC Devices, compositions, and methods for fabricating drug delivery systems
AU2014360446A1 (en) 2013-12-05 2016-06-09 Pharmacyclics, Llc Inhibitors of Bruton's tyrosine kinase
EP3104853B1 (en) 2014-02-10 2019-10-02 Respivant Sciences GmbH Mast cell stabilizers treatment for systemic disorders
SI3104854T1 (en) 2014-02-10 2020-09-30 Respivant Sciences Gmbh Mast cell stabilizers for lung disease treatment
MX2016012008A (en) 2014-03-17 2016-12-07 Pfizer Diacylglycerol acyltransferase 2 inhibitors for use in the treatment of metabolic and related disorders.
JP6537147B2 (en) * 2014-03-18 2019-07-03 武田薬品工業株式会社 Solid dispersion
EP3134418A4 (en) 2014-04-23 2018-01-03 The Research Foundation for The State University of New York A rapid and efficient bioorthogonal ligation reaction and boron-containing heterocycles useful in conjuction therewith
TW201603818A (en) 2014-06-03 2016-02-01 組織科技股份有限公司 Compositions and methods
WO2016031651A1 (en) 2014-08-29 2016-03-03 花王株式会社 Method for producing solid dispersion containing hardly soluble polyphenol
US9839644B2 (en) 2014-09-09 2017-12-12 ARKAY Therapeutics, LLC Formulations and methods for treatment of metabolic syndrome
US20160113906A1 (en) * 2014-09-19 2016-04-28 Board Of Regents, The University Of Texas System Methods of preparing extrudates
US9359316B1 (en) 2014-11-25 2016-06-07 Concentric Analgesics, Inc. Prodrugs of phenolic TRPV1 agonists
EP3253766B1 (en) 2015-02-06 2019-09-04 University of Washington Compounds and methods for preventing or treating sensory hair cell death
US10227333B2 (en) 2015-02-11 2019-03-12 Curtana Pharmaceuticals, Inc. Inhibition of OLIG2 activity
US20160243288A1 (en) 2015-02-23 2016-08-25 Tissuetech, Inc. Apparatuses and methods for treating ophthalmic diseases and disorders
CA2977521C (en) 2015-02-27 2024-03-19 Curtana Pharmaceuticals, Inc. 1-(aryl)-3-(heteroaryl) urea compounds and their use as olig2 inhibitors
AU2016226279B2 (en) 2015-03-03 2021-11-11 Pharmacyclics Llc Pharmaceutical formulations of Bruton's tyrosine kinase inhibtor
MA41827A (en) 2015-03-27 2018-01-30 Pharmacyclics Llc SOLVATED FORMS OF A BRUTON TYROSINE KINASE INHIBITOR
MA41828A (en) 2015-03-27 2018-01-30 Pharmacyclics Llc CO-CRYSTALS OF A TYROSINE KINASE INHIBITOR FROM BRUTON
MX2017014344A (en) 2015-05-11 2018-04-11 Abide Therapeutics Inc Methods of treating inflammation or neuropathic pain.
CN107847526A (en) 2015-05-20 2018-03-27 组织技术公司 For preventing the propagation of epithelial cell and the composition and method of the conversion of epithelium mesenchyma
MX2017015238A (en) 2015-05-28 2018-02-19 Dr Reddy´S Laboratories Ltd Oral composition of celecoxib for treatment of pain.
US10265296B2 (en) 2015-08-07 2019-04-23 Respivant Sciences Gmbh Methods for the treatment of systemic disorders treatable with mast cell stabilizers, including mast cell related disorders
EP3331522A1 (en) 2015-08-07 2018-06-13 Patara Pharma LLC Methods for the treatment of mast cell related disorders with mast cell stabilizers
AR106018A1 (en) 2015-08-26 2017-12-06 Achillion Pharmaceuticals Inc ARYL, HETEROARYL AND HETEROCYCLIC COMPOUNDS FOR THE TREATMENT OF MEDICAL DISORDERS
EP3340982B1 (en) 2015-08-26 2021-12-15 Achillion Pharmaceuticals, Inc. Compounds for treatment of immune and inflammatory disorders
US20170209462A1 (en) 2015-08-31 2017-07-27 Pharmacyclics Llc Btk inhibitor combinations for treating multiple myeloma
JP2019505498A (en) 2015-12-16 2019-02-28 ザ・ウォルター・アンド・エリザ・ホール・インスティテュート・オブ・メディカル・リサーチ Inhibition of cytokine-induced SH2 protein in NK cells
MA43649A (en) 2016-01-19 2018-11-28 Janssen Pharmaceutica Nv FORMULATIONS / COMPOSITIONS INCLUDING A BTK INHIBITOR
WO2017125424A1 (en) 2016-01-19 2017-07-27 Janssen Pharmaceutica Nv Formulations/compositions comprising a btk inhibitor
TW201733600A (en) 2016-01-29 2017-10-01 帝聖工業公司 Fetal support tissue products and methods of use
US10851123B2 (en) 2016-02-23 2020-12-01 Concentric Analgesics, Inc. Prodrugs of phenolic TRPV1 agonists
CN116509869A (en) 2016-04-04 2023-08-01 希诺皮亚生物科学公司 Treatment of extrapyramidal syndrome with trapidil
CA3024556A1 (en) 2016-05-12 2017-11-16 The Regents Of The University Of Michigan Ash1l inhibitors and methods of treatment therewith
BR112018071722B1 (en) 2016-05-13 2024-02-27 Merck Patent Gmbh USE OF AMINO SUGAR AS PLASTIFICANT, POWDER COMPOSITION AND ITS PRODUCTION PROCESS
WO2017194578A1 (en) 2016-05-13 2017-11-16 Merck Patent Gmbh Particle size and distribution of polymer for melt extrusion application
JP2019516773A (en) 2016-05-25 2019-06-20 コンセントリック アナルジジックス,インク. Prodrugs of phenol TRPV1 agonists in combination with local anesthetics and vasoconstrictors for improved local anesthesia
WO2017205762A1 (en) 2016-05-27 2017-11-30 Pharmacyclics Llc Inhibitors of interleukin-1 receptor-associated kinase
WO2017205769A1 (en) 2016-05-27 2017-11-30 Pharmacyclics Llc Inhibitors of interleukin-1 receptor-associated kinase
WO2017205766A1 (en) 2016-05-27 2017-11-30 Pharmacyclics Llc Inhibitors of interleukin-1 receptor-associated kinase
CA3029262A1 (en) 2016-06-27 2018-01-04 Achillion Pharmaceuticals, Inc. Quinazoline and indole compounds to treat medical disorders
EP3957629B1 (en) 2016-07-18 2023-09-06 Arthrosi Therapeutics, Inc. Process for making deuterated hydroxy-benzbromarone and intermediates thereof
EP3493807A1 (en) 2016-08-03 2019-06-12 CymaBay Therapeutics, Inc. Oxymethylene aryl compounds for treating inflammatory gastrointestinal diseases or gastrointestinal conditions
AR109179A1 (en) 2016-08-19 2018-11-07 Pfizer DIACILGLICEROL ACILTRANSFERASA 2 INHIBITORS
JP7028860B2 (en) 2016-08-26 2022-03-02 カーテナ ファーマシューティカルズ,インク. Inhibition of OLIG2 activity
EP3506893A4 (en) 2016-08-31 2020-01-22 Respivant Sciences GmbH Cromolyn compositions for treatment of chronic cough due to idiopathic pulmonary fibrosis
WO2018067341A1 (en) 2016-10-07 2018-04-12 Patara Pharma, LLC Cromolyn compositions for treatment of pulmonary fibrosis
EP3534883A1 (en) 2016-11-07 2019-09-11 Merck Patent GmbH Instant release capsule based on hot melt extruded polyvinyl alcohol
EP3534882A1 (en) 2016-11-07 2019-09-11 Merck Patent GmbH Anti-alcohol-induced dose dumping tablet based on polyvinyl alcohol
KR20190082848A (en) 2016-11-07 2019-07-10 메르크 파텐트 게엠베하 Controlled release tablet based on polyvinyl alcohol and its preparation
WO2018093950A1 (en) 2016-11-16 2018-05-24 Abide Therapeutics, Inc. Pharmaceutical formulations
PE20191239A1 (en) 2016-11-16 2019-09-16 Abide Therapeutics Inc CRYSTAL FORMS OF A MAGL INHIBITOR
CA3056030A1 (en) 2017-03-10 2018-09-13 Pfizer Inc. Novel imidazo[4,5-c]quinoline derivatives as lrrk2 inhibitors
CN109320428A (en) * 2017-08-01 2019-02-12 浙江普利药业有限公司 A kind of Trimebutine Maleate crystal form and preparation method thereof
EP3675865A4 (en) 2017-09-01 2021-06-02 University of Washington Crystalline forms of compounds for preventing or treating sensory hair cell death
EP3706867A4 (en) 2017-11-07 2021-08-11 The Regents Of The University Of Michigan Therapeutic combination for treatment of cerebellar ataxia
US10632209B2 (en) 2017-11-10 2020-04-28 The Regents Of The University Of Michigan ASH1L inhibitors and methods of treatment therewith
WO2019113469A1 (en) 2017-12-07 2019-06-13 The Regents Of The University Of Michigan Nsd family inhibitors and methods of treatment therewith
US11685722B2 (en) 2018-02-28 2023-06-27 Curtana Pharmaceuticals, Inc. Inhibition of Olig2 activity
EP4155293A1 (en) 2018-06-07 2023-03-29 The Regents of The University of Michigan Prc1 inhibitors and methods of treatment therewith
EP3830078A4 (en) 2018-07-27 2022-03-30 Concentric Analgesics, Inc. Pegylated prodrugs of phenolic trpv1 agonists
US20230022157A1 (en) 2018-08-20 2023-01-26 Achillion Pharmaceuticals, Inc. Pharmaceutical compounds for the treatment of complement factor d medical disorders
US20200069742A1 (en) 2018-08-29 2020-03-05 Myos Rens Technology Inc. Methods for alleviating, inhibiting or reversing muscle disuse atrophy in mammals
KR102614808B1 (en) 2018-08-31 2023-12-19 화이자 인코포레이티드 Combination for the treatment of NASH/NAFLD and related diseases
US20200108102A1 (en) 2018-10-03 2020-04-09 Myos Rens Technology Inc. Spray dried follistatin product
EP3866773A4 (en) 2018-10-16 2022-10-26 Georgia State University Research Foundation, Inc. Carbon monoxide prodrugs for the treatment of medical disorders
WO2020096660A1 (en) 2018-11-06 2020-05-14 Myos Rens Technology, Inc. Methods and compositions for improving skeletal muscle protein fractional synthetic rate
SG11202106304RA (en) 2018-12-31 2021-07-29 Biomea Fusion Llc Irreversible inhibitors of menin-mll interaction
US11833186B2 (en) 2019-02-01 2023-12-05 Myos Corp. Methods and compositions for improving quality of life and increasing activity in aging and chronically ill mammals
US20220265630A1 (en) 2019-03-15 2022-08-25 Unicycive Therapeutics Inc. Nicorandil derivatives
EP3883548A4 (en) * 2019-04-08 2022-11-09 Cosci Med-tech Co. Ltd. Methods of improving pharmaceutical substance solubilization and products thereof
JP2022529930A (en) 2019-04-19 2022-06-27 ファイザー・インク Antiproliferative drug for treating PAH
US20220387402A1 (en) 2019-05-20 2022-12-08 Pfizer Inc. Combinations comprising benzodioxol as glp-1r agonists for use in the treatment of nash/nafld and related diseases
CA3144848C (en) 2019-06-28 2023-11-21 Pfizer Inc. 5-(thiophen-2-yl)-1h-tetrazole derivatives as bckdk inhibitors useful for treating various diseases
TW202115086A (en) 2019-06-28 2021-04-16 美商輝瑞大藥廠 Bckdk inhibitors
TWI771766B (en) 2019-10-04 2022-07-21 美商輝瑞股份有限公司 Diacylglycerol acyltransferase 2 inhibitor
JP2022058085A (en) 2020-02-24 2022-04-11 ファイザー・インク Combination of inhibitors of diacylglycerol acyltransferase 2 and inhibitors of acetyl-coa carboxylase
JP2021134211A (en) 2020-02-24 2021-09-13 ファイザー・インク Combinations for treating nafld/nash and related diseases
CN115427403A (en) 2020-04-21 2022-12-02 H.隆德贝克有限公司 Synthesis of monoacylglycerol lipase inhibitors
BR112022024527A2 (en) 2020-06-09 2022-12-27 Pfizer SPYRO COMPOUNDS AS MELANOCORTIN 4 RECEPTOR ANTAGONISTS AND USES THEREOF
JP2023533982A (en) 2020-07-10 2023-08-07 ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン GAS41 inhibitor and method of use thereof
WO2022133064A1 (en) 2020-12-16 2022-06-23 Biomea Fusion, Inc. Fused pyrimidine compounds as inhibitors of menin-mll interaction
WO2022150525A1 (en) 2021-01-06 2022-07-14 Awakn Life Sciences Mdma in the treatment of alcohol use disorder
EP4337316A1 (en) 2021-05-11 2024-03-20 Awakn Ls Europe Holdings Limited Therapeutic aminoindane compounds and compositions
EP4346788A2 (en) 2021-06-03 2024-04-10 Arcadia Medicine, Inc. Enantiomeric entactogen compositions and methods of their use
CA3228627A1 (en) 2021-08-11 2023-02-16 Thomas Butler Covalent inhibitors of menin-mll interaction for diabetes mellitus
WO2023022912A1 (en) 2021-08-20 2023-02-23 Biomea Fusion, Inc. Crystalline form of n-[4-[4-(4-morpholinyl)-7h-pyrrolo[2,3-d]pyrimidin-6-yl]phenyl]-4-[[3(r)-[(1-oxo -2-propen-1-yl)amino]-1-piperidinyl]methyl]-2-pyridinecarboxamide, an irreversible menin-mll inhibitor for the treatment of cancer
WO2023027966A1 (en) 2021-08-24 2023-03-02 Biomea Fusion, Inc. Pyrazine compounds as irreversible inhibitors of flt3
WO2023039240A1 (en) 2021-09-13 2023-03-16 Biomea Fusion, Inc. IRREVERSIBLE INHIBITORS OF KRas
WO2023086341A1 (en) 2021-11-09 2023-05-19 Biomea Fusion, Inc. Inhibitors of kras
TW202337429A (en) 2021-12-01 2023-10-01 美商輝瑞股份有限公司 Bckdk inhibitors and/or degraders
WO2023105387A1 (en) 2021-12-06 2023-06-15 Pfizer Inc. Melanocortin 4 receptor antagonists and uses thereof
TW202340177A (en) 2021-12-30 2023-10-16 美商拜歐米富士恩股份有限公司 Pyrazine compounds as inhibitors of flt3
WO2023139163A1 (en) 2022-01-19 2023-07-27 Awakn Ls Europe Holdings Limited 1,3-benzodioxole esters and their therapeutic use
WO2023156565A1 (en) 2022-02-16 2023-08-24 Awakn Ls Europe Holdings Limited Bridged ring compounds and their therapeutic use as cns agents
WO2023235618A1 (en) 2022-06-03 2023-12-07 Biomea Fusion, Inc. Fused pyrimidine compounds as inhibitors of menin
US20240010649A1 (en) 2022-07-06 2024-01-11 Oppilan Pharma Limited Crystalline forms of an s1p receptor modulator

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5257315A (en) * 1975-11-04 1977-05-11 Sandoz Ag Tablet for medical preparation
DE2549740A1 (en) * 1975-11-17 1977-05-18 Sandoz Ag NEW GALENIC FORMS AND METHODS FOR THEIR PRODUCTION
US4230687A (en) * 1978-05-30 1980-10-28 Griffith Laboratories U.S.A., Inc. Encapsulation of active agents as microdispersions in homogeneous natural polymeric matrices
JPS5785316A (en) * 1980-11-14 1982-05-28 Kanebo Ltd Preparation of easily absorbable nifedipine preparation
JPS58109411A (en) * 1981-12-23 1983-06-29 Shionogi & Co Ltd Nifedipine composition for solid preparation
JPS6240277A (en) * 1985-08-15 1987-02-21 Ajinomoto Co Inc Production of granular food
US4778676A (en) * 1985-12-20 1988-10-18 Warner-Lambert Company Confectionery delivery system for actives
DE3612212A1 (en) * 1986-04-11 1987-10-15 Basf Ag METHOD FOR PRODUCING SOLID PHARMACEUTICAL FORMS
DE3612211A1 (en) * 1986-04-11 1987-10-15 Basf Ag CONTINUOUS TABLET METHOD
US4760094A (en) * 1986-10-21 1988-07-26 American Home Products Corporation (Del.) Spray dried acetaminophen
US4842761A (en) * 1988-03-23 1989-06-27 International Flavors & Fragrances, Inc. Compositions and methods for controlled release of fragrance-bearing substances
DE3812567A1 (en) * 1988-04-15 1989-10-26 Basf Ag METHOD FOR PRODUCING PHARMACEUTICAL MIXTURES
DE3827061C1 (en) * 1988-08-10 1990-02-15 Deutsche Gelatine-Fabriken Stoess & Co Gmbh, 6930 Eberbach, De
DE3830353A1 (en) * 1988-09-07 1990-03-15 Basf Ag METHOD FOR THE CONTINUOUS PRODUCTION OF SOLID PHARMACEUTICAL FORMS
AU645003B2 (en) * 1988-11-08 1994-01-06 Takeda Chemical Industries Ltd. Sustained release preparations
JP2893191B2 (en) * 1988-11-08 1999-05-17 武田薬品工業株式会社 Controlled release matrix agent
IL92343A0 (en) * 1988-12-20 1990-07-26 Gist Brocades Nv Granulate for multiparticulate controlled release oral compositions,their preparation and oral pharmaceutical compositions containing them
US5102668A (en) * 1990-10-05 1992-04-07 Kingaform Technology, Inc. Sustained release pharmaceutical preparation using diffusion barriers whose permeabilities change in response to changing pH
FR2670398B1 (en) * 1990-12-14 1995-02-17 Roquette Freres DIRECTLY COMPRESSIBLE POWDER COMPOSITION AND PROCESS FOR OBTAINING SAME.
JP3722293B2 (en) * 1991-12-18 2005-11-30 ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー Novel pharmaceutical solid dispersion
ATE223704T1 (en) * 1992-10-16 2002-09-15 Nippon Shinyaku Co Ltd METHOD FOR PRODUCING WAX MATRICES
DE19509807A1 (en) * 1995-03-21 1996-09-26 Basf Ag Process for the preparation of active substance preparations in the form of a solid solution of the active substance in a polymer matrix, and active substance preparations produced using this method
WO1996009115A1 (en) * 1994-09-21 1996-03-28 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Adsorbent for interleukins, method of removal thereof by adsorption, and device for adsorption
HN1998000115A (en) * 1997-08-21 1999-06-02 Warner Lambert Co SOLID PHARMACEUTICAL DOSAGE FORMS
US5954175A (en) * 1997-09-02 1999-09-21 Northrop Grumman Corporation Modularized parallel drivetrain
EP0966269A1 (en) * 1997-10-07 1999-12-29 Fuiz Technologies Ltd. Immediate release drug delivery forms
US6029764A (en) * 1997-11-12 2000-02-29 Case Corporation Coordinated control of an active suspension system for a work vehicle
DE60039377D1 (en) * 1999-02-09 2008-08-21 Pfizer Prod Inc Compositions of basic drugs with improved bioavailability
ATE433318T1 (en) * 1999-02-10 2009-06-15 Pfizer Prod Inc OSMOTIC SYSTEM FOR ADMINISTRATION OF ACTIVE INGREDIENTS CONTAINING SOLID AMORPHOUS DISPERSIONS
EP1027886B1 (en) * 1999-02-10 2008-07-09 Pfizer Products Inc. Pharmaceutical solid dispersions

Also Published As

Publication number Publication date
DE69222847T3 (en) 2005-09-15
ES2111065T3 (en) 1998-03-01
DK0580860T3 (en) 1998-05-25
US5456923A (en) 1995-10-10
DE69222847D1 (en) 1997-11-27
JP2527107B2 (en) 1996-08-21
CA2108575C (en) 2002-10-22
EP0580860B1 (en) 1997-10-22
EP0580860A4 (en) 1994-06-15
WO1992018106A1 (en) 1992-10-29
KR0182801B1 (en) 1999-05-01
GR3025864T3 (en) 1998-04-30
EP0580860B2 (en) 2004-12-15
DK0580860T4 (en) 2005-03-21
AU1537292A (en) 1992-11-17
EP0580860A1 (en) 1994-02-02
ATE159426T1 (en) 1997-11-15
DE69222847T2 (en) 1998-05-20
ES2111065T5 (en) 2005-06-16

Similar Documents

Publication Publication Date Title
CA2108575A1 (en) Method of manufacturing solid dispersion
WO2002014430A3 (en) Biodegradable polymeric blend
AU4565900A (en) Reinforced polymers
WO1999014336A3 (en) Thermostable luciferases and methods of production
EP1630231A3 (en) Thermostable luciferases from photuris pennsylvanica and pyrophorus plagiophthalamus and methods of production
EP0724947A4 (en) Biaxially oriented polyester film and process for production thereof
AU2001254914A1 (en) Extruded joinery work element reinforced with continuous fibres, method and device
WO2001064774A3 (en) Extrusion process for dispersion production
EP0747113A3 (en) Polyvinyl alcohol-based hollow fiber membrane and process for producing the same
EP0288315A3 (en) Process for producing polyester resin composition
EP0934968A3 (en) Polycarbonate articles with photochromic properties
CA2302487A1 (en) Method for producing dyed moulding materials
CA2033095A1 (en) Process for continuous production of elastic polyesters
EP0281295A3 (en) Process and composition for producing bonded magnet
CA2237032A1 (en) Process for producing the drawn molded article of a fluoroplastic
CA2330928A1 (en) Extruder die head
WO1994018243A3 (en) Polyvinyl alcohol esterified with lactic acid and process therefor
ITMI922476A1 (en) MULTIFILAMENT YARN OF THERMOPLASTIC POLYMERS BASED ON TETRAFLUOROETHYLENE AND RELATED PREPARATION PROCESS
KR960701735A (en) Improved process for resin transfer molding
CA2106086A1 (en) Thermoplastic saturated norbornene resin sheet and process for production thereof
CA2071758A1 (en) Polyvinyl alcohol-based synthetic fiber and process for producing the same
AU1725992A (en) Process for producing foamable particles of styrenic polymers, endowed with improved processability and mechanical properties
FI940625A (en) An electrically conductive polymer and a method of making the same
EP0299468A3 (en) Polycarbonate resin composition with dienic impact modifiers
EP0401942A3 (en) Whitened wire of ultra-high-molecular-weight polyethylene and production thereof

Legal Events

Date Code Title Description
EEER Examination request
MKEX Expiry
MKEX Expiry

Effective date: 20120414