JP2010500411A5 - - Google Patents
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- Publication number
- JP2010500411A5 JP2010500411A5 JP2009524659A JP2009524659A JP2010500411A5 JP 2010500411 A5 JP2010500411 A5 JP 2010500411A5 JP 2009524659 A JP2009524659 A JP 2009524659A JP 2009524659 A JP2009524659 A JP 2009524659A JP 2010500411 A5 JP2010500411 A5 JP 2010500411A5
- Authority
- JP
- Japan
- Prior art keywords
- mixture
- extrudate
- solubilizer
- therapeutic compound
- heating
- 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
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- 150000001875 compounds Chemical class 0.000 claims description 51
- 230000001225 therapeutic effect Effects 0.000 claims description 41
- 238000000034 method Methods 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 25
- 239000002904 solvent Substances 0.000 claims description 12
- 238000002844 melting Methods 0.000 claims description 10
- 230000008018 melting Effects 0.000 claims description 10
- 239000007962 solid dispersion Substances 0.000 claims description 9
- 239000007787 solid Substances 0.000 claims description 7
- 239000004014 plasticizer Substances 0.000 claims description 6
- BMGQWWVMWDBQGC-IIFHNQTCSA-N midostaurin Chemical compound CN([C@H]1[C@H]([C@]2(C)O[C@@H](N3C4=CC=CC=C4C4=C5C(=O)NCC5=C5C6=CC=CC=C6N2C5=C43)C1)OC)C(=O)C1=CC=CC=C1 BMGQWWVMWDBQGC-IIFHNQTCSA-N 0.000 claims description 5
- 229950010895 midostaurin Drugs 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 3
- CTKXFMQHOOWWEB-UHFFFAOYSA-N Ethylene oxide/propylene oxide copolymer Chemical group CCCOC(C)COCCO CTKXFMQHOOWWEB-UHFFFAOYSA-N 0.000 claims description 3
- 229920001993 poloxamer 188 Polymers 0.000 claims description 3
- 229940044519 poloxamer 188 Drugs 0.000 claims description 3
- 239000000600 sorbitol Substances 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims 7
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical group C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 claims 4
- 229920001983 poloxamer Polymers 0.000 claims 4
- 229960000502 poloxamer Drugs 0.000 claims 4
- 239000008194 pharmaceutical composition Substances 0.000 description 11
- 239000000546 pharmaceutical excipient Substances 0.000 description 6
- 239000003826 tablet Substances 0.000 description 5
- 239000003814 drug Substances 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 239000006069 physical mixture Substances 0.000 description 4
- 241000124008 Mammalia Species 0.000 description 3
- 239000001961 anticonvulsive agent Substances 0.000 description 3
- -1 cerebral dilators Substances 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000000634 powder X-ray diffraction Methods 0.000 description 3
- 229940035676 analgesics Drugs 0.000 description 2
- 239000000730 antalgic agent Substances 0.000 description 2
- 230000003474 anti-emetic effect Effects 0.000 description 2
- 239000003146 anticoagulant agent Substances 0.000 description 2
- 229940125681 anticonvulsant agent Drugs 0.000 description 2
- 239000002111 antiemetic agent Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003172 expectorant agent Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000006187 pill Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 101710175516 14 kDa zinc-binding protein Proteins 0.000 description 1
- 241000251730 Chondrichthyes Species 0.000 description 1
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- 208000031226 Hyperlipidaemia Diseases 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 208000019695 Migraine disease Diseases 0.000 description 1
- 229940123924 Protein kinase C inhibitor Drugs 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 230000003044 adaptive effect Effects 0.000 description 1
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- 230000001195 anabolic effect Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 230000000954 anitussive effect Effects 0.000 description 1
- 229940069428 antacid Drugs 0.000 description 1
- 239000003159 antacid agent Substances 0.000 description 1
- 230000003257 anti-anginal effect Effects 0.000 description 1
- 230000001142 anti-diarrhea Effects 0.000 description 1
- 230000003556 anti-epileptic effect Effects 0.000 description 1
- 230000003276 anti-hypertensive effect Effects 0.000 description 1
- 230000002924 anti-infective effect Effects 0.000 description 1
- 239000002260 anti-inflammatory agent Substances 0.000 description 1
- 230000003579 anti-obesity Effects 0.000 description 1
- 230000002785 anti-thrombosis Effects 0.000 description 1
- 239000000924 antiasthmatic agent Substances 0.000 description 1
- 229940127219 anticoagulant drug Drugs 0.000 description 1
- 239000003472 antidiabetic agent Substances 0.000 description 1
- 229940125683 antiemetic agent Drugs 0.000 description 1
- 229960003965 antiepileptics Drugs 0.000 description 1
- 229940125715 antihistaminic agent Drugs 0.000 description 1
- 239000000739 antihistaminic agent Substances 0.000 description 1
- 229960005475 antiinfective agent Drugs 0.000 description 1
- 239000002246 antineoplastic agent Substances 0.000 description 1
- 239000002221 antipyretic Substances 0.000 description 1
- 229940125716 antipyretic agent Drugs 0.000 description 1
- 229940043671 antithyroid preparations Drugs 0.000 description 1
- 239000003434 antitussive agent Substances 0.000 description 1
- 229940124584 antitussives Drugs 0.000 description 1
- 239000002249 anxiolytic agent Substances 0.000 description 1
- 230000006793 arrhythmia Effects 0.000 description 1
- 206010003119 arrhythmia Diseases 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 239000007894 caplet Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 230000002490 cerebral effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000003218 coronary vasodilator agent Substances 0.000 description 1
- 239000000850 decongestant Substances 0.000 description 1
- 229940124581 decongestants Drugs 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000002934 diuretic Substances 0.000 description 1
- 229940030606 diuretics Drugs 0.000 description 1
- 210000003743 erythrocyte Anatomy 0.000 description 1
- 230000003419 expectorant effect Effects 0.000 description 1
- 229940066493 expectorants Drugs 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000000864 hyperglycemic agent Substances 0.000 description 1
- 229940126904 hypoglycaemic agent Drugs 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000008141 laxative Substances 0.000 description 1
- 229940125722 laxative agent Drugs 0.000 description 1
- 206010027599 migraine Diseases 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 210000000214 mouth Anatomy 0.000 description 1
- 229940066491 mucolytics Drugs 0.000 description 1
- 230000002232 neuromuscular Effects 0.000 description 1
- 235000020939 nutritional additive Nutrition 0.000 description 1
- 239000000810 peripheral vasodilating agent Substances 0.000 description 1
- 229960002116 peripheral vasodilator Drugs 0.000 description 1
- 229940124531 pharmaceutical excipient Drugs 0.000 description 1
- 238000001907 polarising light microscopy Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 238000001144 powder X-ray diffraction data Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 239000003881 protein kinase C inhibitor Substances 0.000 description 1
- 239000004089 psychotropic agent Substances 0.000 description 1
- 229940125723 sedative agent Drugs 0.000 description 1
- 239000000932 sedative agent Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 210000001685 thyroid gland Anatomy 0.000 description 1
- 229940043672 thyroid preparations Drugs 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 239000005526 vasoconstrictor agent Substances 0.000 description 1
- 229940124549 vasodilator Drugs 0.000 description 1
- 239000003071 vasodilator agent Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US82255606P | 2006-08-16 | 2006-08-16 | |
| US60/822,556 | 2006-08-16 | ||
| PCT/US2007/017960 WO2008021347A2 (en) | 2006-08-16 | 2007-08-14 | Method for making solid dispersions of highly crystalline therapeutic compounds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010500411A JP2010500411A (ja) | 2010-01-07 |
| JP2010500411A5 true JP2010500411A5 (https=) | 2010-09-24 |
| JP5546860B2 JP5546860B2 (ja) | 2014-07-09 |
Family
ID=38657762
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009524659A Expired - Fee Related JP5546860B2 (ja) | 2006-08-16 | 2007-08-14 | 高結晶性治療化合物の固体分散体を製造するための方法 |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US20100038816A1 (https=) |
| EP (1) | EP2054040B1 (https=) |
| JP (1) | JP5546860B2 (https=) |
| KR (1) | KR101462693B1 (https=) |
| CN (1) | CN101516339B (https=) |
| AT (1) | ATE503484T1 (https=) |
| AU (1) | AU2007284615B2 (https=) |
| BR (1) | BRPI0714963A2 (https=) |
| CA (1) | CA2660086C (https=) |
| DE (1) | DE602007013567D1 (https=) |
| ES (1) | ES2363725T3 (https=) |
| MX (1) | MX2009001636A (https=) |
| PL (1) | PL2054040T3 (https=) |
| PT (1) | PT2054040E (https=) |
| RU (1) | RU2454220C2 (https=) |
| WO (1) | WO2008021347A2 (https=) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1923053A1 (en) | 2006-09-27 | 2008-05-21 | Novartis AG | Pharmaceutical compositions comprising nilotinib or its salt |
| WO2009100176A2 (en) * | 2008-02-07 | 2009-08-13 | Abbott Laboratories | Pharmaceutical dosage form for oral administration of tyrosine kinase inhibitor |
| MX2010011962A (es) * | 2008-04-30 | 2010-11-30 | Novartis Ag | Proceso continuo para hacer composiciones farmaceuticas. |
| EP2327706A1 (en) | 2009-11-30 | 2011-06-01 | Novartis AG | Polymorphous forms III and IV of N-benzoyl-staurosporine |
| UA113500C2 (xx) | 2010-10-29 | 2017-02-10 | Одержані екструзією розплаву тверді дисперсії, що містять індукуючий апоптоз засіб | |
| CN102525879B (zh) * | 2010-12-31 | 2015-01-21 | 正大天晴药业集团股份有限公司 | 制备阿瑞匹坦固体分散组合物的方法 |
| BR112016021739B1 (pt) * | 2014-03-25 | 2021-11-03 | Genentech, Inc | Método para preparar um poloxâmero para uso em um meio de cultura de célula |
| CN107001322B (zh) | 2014-12-18 | 2020-07-28 | 默沙东公司 | 用于药物制剂的组合物 |
| GB201502073D0 (en) * | 2015-02-09 | 2015-03-25 | Cubic Pharmaceuticals Ltd And Delta Pharmaceuticals Ltd | HDEG technology |
| CN108024939B (zh) | 2015-08-20 | 2024-06-07 | 联合利华知识产权控股有限公司 | 包封的内酰胺 |
| ES2758300T3 (es) | 2015-08-20 | 2020-05-05 | Unilever Nv | Solubilidad de lactama mejorada |
| EP3337451B1 (en) | 2015-08-20 | 2018-12-26 | Unilever PLC | Improved lactam solubility |
| CN107848968B (zh) | 2015-08-20 | 2021-06-18 | 荷兰联合利华有限公司 | 从乙醛酸制备内酰胺的方法 |
| WO2017029093A1 (en) | 2015-08-20 | 2017-02-23 | Unilever Plc | Improved lactam solubility |
| CN107920976A (zh) | 2015-08-20 | 2018-04-17 | 荷兰联合利华有限公司 | 改善的内酰胺溶解度 |
| BR112018003082B1 (pt) * | 2015-08-20 | 2021-12-14 | Unilever Ip Holdings B.V. | Lactama em uma dispersão sólida, método de produção de uma composição compreendendo uma lactama e método de formação de lactama em uma dispersão sólida |
| JP7021182B2 (ja) * | 2016-03-24 | 2022-02-16 | ロケート・バイオ・リミテッド | 足場材料、方法および使用 |
| MX383740B (es) * | 2016-05-13 | 2025-03-14 | Merck Patent Gmbh | Composición de extrusión fundida en caliente que usa un excipiente compresible directo como plastificante. |
| CN111615389A (zh) | 2018-02-01 | 2020-09-01 | 科尔沃斯制药股份有限公司 | 药物调配物 |
| EP3520782A3 (en) * | 2018-02-01 | 2019-11-13 | Corvus Pharmaceuticals, Inc. | Pharmaceutical formulations containing adenosine a2a receptor antagonists |
| CN113573712A (zh) | 2019-02-18 | 2021-10-29 | 斯莱班克制药有限责任公司 | 尼洛替尼的药物组合物 |
| CN116887866A (zh) | 2020-12-03 | 2023-10-13 | 巴特尔纪念研究院 | 聚合物纳米颗粒和dna纳米结构组合物及用于非病毒递送的方法 |
| WO2022216977A1 (en) | 2021-04-07 | 2022-10-13 | Batelle Memorial Institute | Rapid design, build, test, and learn technologies for identifying and using non-viral carriers |
| CN114796149A (zh) * | 2022-04-27 | 2022-07-29 | 苏州中化药品工业有限公司 | 一种高生物利用度的双醋瑞因胶囊剂及其制备方法 |
| WO2025072751A1 (en) | 2023-09-29 | 2025-04-03 | Battelle Memorial Institute | Polymer nanoparticle compositions for in vivo expression of polypeptides |
| US12441996B2 (en) | 2023-12-08 | 2025-10-14 | Battelle Memorial Institute | Use of DNA origami nanostructures for molecular information based data storage systems |
Family Cites Families (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3346123A1 (de) | 1983-12-21 | 1985-06-27 | Janssen Pharmaceutica, N.V., Beerse | Pharmazeutische praeparate von in wasser schwerloeslichen oder instabilen arzneistoffen und verfahren zu ihrer herstellung |
| IE80467B1 (en) | 1995-07-03 | 1998-07-29 | Elan Corp Plc | Controlled release formulations for poorly soluble drugs |
| US5837714A (en) * | 1997-03-03 | 1998-11-17 | Sanofi | Solid pharmaceutical dispersions |
| ATE232087T1 (de) * | 1997-10-27 | 2003-02-15 | Merck Patent Gmbh | Feste lösungen und dispersionen von eines schlecht wasserlöslichen wirkstoffes |
| US6706283B1 (en) * | 1999-02-10 | 2004-03-16 | Pfizer Inc | Controlled release by extrusion of solid amorphous dispersions of drugs |
| GB9903547D0 (en) * | 1999-02-16 | 1999-04-07 | Novartis Ag | Organic compounds |
| US20060034937A1 (en) * | 1999-11-23 | 2006-02-16 | Mahesh Patel | Solid carriers for improved delivery of active ingredients in pharmaceutical compositions |
| US6593308B2 (en) * | 1999-12-03 | 2003-07-15 | The Regents Of The University Of California | Targeted drug delivery with a hyaluronan ligand |
| US20020015730A1 (en) * | 2000-03-09 | 2002-02-07 | Torsten Hoffmann | Pharmaceutical formulations and method for making |
| DE10013289A1 (de) * | 2000-03-17 | 2001-09-20 | Knoll Ag | Torasemid enthaltende pharmazeutische Zubereitungen |
| EP1372611B1 (en) | 2001-03-26 | 2006-05-17 | Novartis AG | Pharmaceutical composition comprising a poorly water-soluble staurosporine, a surfactant and a water-soluble polymer |
| HU229938B1 (en) * | 2001-05-03 | 2015-01-28 | Hoffmann La Roche | Pharmaceutical dosage form of amorphous nelfinavir mesylate |
| US20030212102A1 (en) * | 2001-06-12 | 2003-11-13 | Koretke Todd W | Novel solid dispersion compositions |
| JP4644397B2 (ja) * | 2001-09-05 | 2011-03-02 | 信越化学工業株式会社 | 難溶性薬物を含む医薬用固形製剤の製造方法 |
| US6756381B2 (en) * | 2002-02-21 | 2004-06-29 | Supergen, Inc. | Compositions and formulations of 9-nitrocamptothecin polymorphs and methods of use thereof |
| GB0205253D0 (en) * | 2002-03-06 | 2002-04-17 | Univ Gent | Immediate release pharmaceutical granule compositions and a continuous process for making them |
| US8268352B2 (en) * | 2002-08-05 | 2012-09-18 | Torrent Pharmaceuticals Limited | Modified release composition for highly soluble drugs |
| US7230012B2 (en) * | 2002-11-14 | 2007-06-12 | Celgene Corporation | Pharmaceutical compositions and dosage forms of thalidomide |
| GB0315012D0 (en) * | 2003-06-27 | 2003-07-30 | Leuven K U Res & Dev | Zeotiles |
| AR047938A1 (es) * | 2003-08-25 | 2006-03-15 | Combinatorx Inc | Formulaciones, conjugados y combinaciones de farmacos para el tratamiento de neoplasmas |
| US20050208095A1 (en) * | 2003-11-20 | 2005-09-22 | Angiotech International Ag | Polymer compositions and methods for their use |
| KR20060101762A (ko) * | 2003-11-21 | 2006-09-26 | 쉐링 코포레이션 | 포스포디에스테라제 v 억제제 제형 |
| US7498309B2 (en) * | 2003-11-29 | 2009-03-03 | Sangstat Medical Corporation | Pharmaceutical compositions for bioactive peptide agents |
| CN102127057A (zh) * | 2004-03-15 | 2011-07-20 | 武田药品工业株式会社 | 二肽基肽酶抑制剂 |
| US20050288481A1 (en) * | 2004-04-30 | 2005-12-29 | Desnoyer Jessica R | Design of poly(ester amides) for the control of agent-release from polymeric compositions |
| US20060246109A1 (en) * | 2005-04-29 | 2006-11-02 | Hossainy Syed F | Concentration gradient profiles for control of agent release rates from polymer matrices |
| MX2007002415A (es) * | 2004-08-31 | 2007-04-23 | Novartis Ag | Uso de midostaurina para el tratamiento de tumores estromales gastrointestinales. |
| US20080038316A1 (en) * | 2004-10-01 | 2008-02-14 | Wong Vernon G | Conveniently implantable sustained release drug compositions |
| JO2897B1 (en) * | 2004-11-05 | 2015-09-15 | نوفارتيس ايه جي | Organic compounds |
| US20090088465A1 (en) * | 2004-12-02 | 2009-04-02 | Stephen Craig Dyar | Pharmaceutical Compositions of Amorphous Atorvastatin and Process for Preparing Same |
| WO2007068615A2 (en) * | 2005-12-14 | 2007-06-21 | F. Hoffmann-La Roche Ag | Hcv prodrug formulation |
| BRPI0622054B8 (pt) * | 2006-09-22 | 2021-05-25 | Oxford Amherst Llc | composto e composição farmacêutica |
| US8258137B2 (en) * | 2008-01-29 | 2012-09-04 | Katholieke Universiteit Leuven | Process for release of biologically active species from mesoporous oxide systems |
| MX2011009312A (es) * | 2009-03-06 | 2012-02-29 | Medimmune Llc | Formulaciones de anticuerpos humanizados anti-cd19. |
| TW201120037A (en) * | 2009-10-26 | 2011-06-16 | Sunesis Pharmaceuticals Inc | Compounds and methods for treatment of cancer |
| EP2327706A1 (en) * | 2009-11-30 | 2011-06-01 | Novartis AG | Polymorphous forms III and IV of N-benzoyl-staurosporine |
| CN107898791A (zh) * | 2010-06-03 | 2018-04-13 | 药品循环有限责任公司 | 布鲁顿酪氨酸激酶(btk)抑制剂的应用 |
| EP2618846A1 (en) * | 2010-09-24 | 2013-07-31 | Mallinckrodt LLC | Aptamer conjugates for targeting of therapeutic and/or diagnostic nanocarriers |
| US9295673B2 (en) * | 2011-02-23 | 2016-03-29 | Intellikine Llc | Combination of mTOR inhibitors and P13-kinase inhibitors, and uses thereof |
-
2007
- 2007-08-14 RU RU2009109357/15A patent/RU2454220C2/ru not_active IP Right Cessation
- 2007-08-14 CN CN2007800302086A patent/CN101516339B/zh not_active Expired - Fee Related
- 2007-08-14 EP EP07811314A patent/EP2054040B1/en not_active Not-in-force
- 2007-08-14 PL PL07811314T patent/PL2054040T3/pl unknown
- 2007-08-14 DE DE602007013567T patent/DE602007013567D1/de active Active
- 2007-08-14 KR KR1020097005216A patent/KR101462693B1/ko not_active Expired - Fee Related
- 2007-08-14 AU AU2007284615A patent/AU2007284615B2/en not_active Ceased
- 2007-08-14 ES ES07811314T patent/ES2363725T3/es active Active
- 2007-08-14 CA CA2660086A patent/CA2660086C/en active Active
- 2007-08-14 US US12/376,692 patent/US20100038816A1/en not_active Abandoned
- 2007-08-14 MX MX2009001636A patent/MX2009001636A/es active IP Right Grant
- 2007-08-14 AT AT07811314T patent/ATE503484T1/de active
- 2007-08-14 BR BRPI0714963-8A patent/BRPI0714963A2/pt not_active IP Right Cessation
- 2007-08-14 PT PT07811314T patent/PT2054040E/pt unknown
- 2007-08-14 JP JP2009524659A patent/JP5546860B2/ja not_active Expired - Fee Related
- 2007-08-14 WO PCT/US2007/017960 patent/WO2008021347A2/en not_active Ceased
-
2012
- 2012-03-19 US US13/423,329 patent/US8641948B2/en not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
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| JP2010500411A5 (https=) | ||
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