CA2796063A1 - Polysaccharide compositions and methods of use for the treatment and prevention of disorders associated with progenitor cell mobilization - Google Patents
Polysaccharide compositions and methods of use for the treatment and prevention of disorders associated with progenitor cell mobilization Download PDFInfo
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- CA2796063A1 CA2796063A1 CA2796063A CA2796063A CA2796063A1 CA 2796063 A1 CA2796063 A1 CA 2796063A1 CA 2796063 A CA2796063 A CA 2796063A CA 2796063 A CA2796063 A CA 2796063A CA 2796063 A1 CA2796063 A1 CA 2796063A1
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- polysaccharide
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| US12/762,268 | 2010-04-16 | ||
| US12/762,268 US8592393B2 (en) | 2007-11-02 | 2010-04-16 | Polysaccharide compositions and methods of use for the treatment and prevention of disorders associated with progenitor cell mobilization |
| PCT/US2011/032581 WO2011130572A1 (en) | 2010-04-16 | 2011-04-14 | Polysaccharide compositions and methods of use for the treatment and prevention of disorders associated with progenitor cell mobilization |
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| CA2796063A1 true CA2796063A1 (en) | 2011-10-20 |
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| JP (1) | JP2013525306A (https=) |
| CN (1) | CN103096924A (https=) |
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| US8569262B2 (en) | 2007-11-02 | 2013-10-29 | Momenta Pharmaceuticals, Inc. | Polysaccharide compositions and methods of use for the treatment and prevention of disorders associated with progenitor cell mobilization |
| ES2567079T3 (es) | 2007-11-02 | 2016-04-19 | Momenta Pharmaceuticals, Inc. | Composiciones de polisacáridos que no son anticoagulantes |
| US8592393B2 (en) | 2007-11-02 | 2013-11-26 | Momenta Pharmaceuticals, Inc. | Polysaccharide compositions and methods of use for the treatment and prevention of disorders associated with progenitor cell mobilization |
| BR112012026542A2 (pt) | 2010-04-16 | 2016-07-12 | Momenta Pharmaceuticals Inc | abordagem seletiva de tecido |
| CA2795868A1 (en) | 2010-06-17 | 2011-12-22 | Momenta Pharmaceuticals, Inc. | Methods and compositions for modulating hair growth |
| WO2012003457A1 (en) * | 2010-07-01 | 2012-01-05 | Mtm Research Llc | Anti-fibroblastic fluorochemical emulsion therapies |
| US20140351961A1 (en) * | 2011-08-31 | 2014-11-27 | Alexzander A. Asea | Compositions and methods for treatment of metastatic cancer |
| CN104144950B (zh) * | 2011-12-19 | 2017-09-05 | 迪乐方有限责任公司 | 含有重复的二糖单元的非抗凝的葡糖胺聚糖及其医药用途 |
| WO2013095215A1 (en) * | 2011-12-19 | 2013-06-27 | Dilaforette Ab | Low anticoagulant heparins |
| JP2016520613A (ja) | 2013-05-28 | 2016-07-14 | モメンタ ファーマシューティカルズ インコーポレイテッド | 薬学的組成物 |
| GB2515315A (en) | 2013-06-19 | 2014-12-24 | Dilafor Ab | New Processes |
| WO2016164264A1 (en) * | 2015-04-07 | 2016-10-13 | Immunomedics, Inc. | Y-90-labeled anti-cd22 antibody (epratuzumab tetraxetan) in refractory/relapsed adult cd22+ b-cell acute lymphoblastic leukemia |
| US20190201556A1 (en) | 2016-05-16 | 2019-07-04 | Mtm Research, Llc | Fluorochemical targeted therapies |
| WO2018208933A1 (en) * | 2017-05-09 | 2018-11-15 | Crosby Innovations, LLC | Handheld sanitizing device |
| US12239707B2 (en) | 2018-05-07 | 2025-03-04 | Mt Research, Llc | Photodynamic compositions and methods of use |
| CN109248171A (zh) * | 2018-09-13 | 2019-01-22 | 黄泳华 | 含有伊马替尼与植物多糖的组合物 |
| CN109010354A (zh) * | 2018-09-15 | 2018-12-18 | 黄泳华 | 含有伊马替尼与植物多糖的组合物 |
| CN112949370A (zh) | 2019-12-10 | 2021-06-11 | 托比股份公司 | 眼睛事件检测 |
Family Cites Families (74)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE620906A (https=) | ||||
| US3118816A (en) * | 1962-04-03 | 1964-01-21 | Abbott Lab | N-succinyl heparin and process |
| US4235871A (en) | 1978-02-24 | 1980-11-25 | Papahadjopoulos Demetrios P | Method of encapsulating biologically active materials in lipid vesicles |
| CA1136620A (en) * | 1979-01-08 | 1982-11-30 | Ulf P.F. Lindahl | Heparin fragments having selective anticoagulation activity |
| FR2538404B1 (https=) * | 1982-12-28 | 1985-08-23 | Anic Spa | |
| IT1195497B (it) * | 1983-03-08 | 1988-10-19 | Opocrin Spa | Procedimento per la preparazione di frazioni oligosaccaridiche dotate di proprieta' farmacologiche per degradazione chimica di eparina |
| FR2553287B1 (fr) | 1983-10-18 | 1986-09-12 | Choay Sa | Compositions a base de mucopolysaccharides ou d'oligosaccharides, notamment a base de fractions ou fragments d'heparine, appropriees au traitement de desordres de la proliferation cellulaire |
| IT1169888B (it) * | 1983-10-25 | 1987-06-03 | Italfarmaco Spa | Glicosaminoglicani modificati dotati di attivita' antitrombotica |
| US4847338A (en) * | 1985-03-28 | 1989-07-11 | University Of Iowa Research Foundation | Low molecular weight heparin fragments as inhibitors of complement activation |
| US4916219A (en) * | 1985-03-28 | 1990-04-10 | University Of Iowa Research Foundation | Oligosaccharide heparin fragments as inhibitors of complement cascade |
| US4868103A (en) | 1986-02-19 | 1989-09-19 | Enzo Biochem, Inc. | Analyte detection by means of energy transfer |
| US5262403A (en) | 1986-03-10 | 1993-11-16 | Board Of Regents, The University Of Texas System | Glycosaminoglycan derivatives and their use as inhibitors of tumor invasiveness of metastatic profusion-II |
| US5541166A (en) * | 1987-01-23 | 1996-07-30 | The Australian National University | Sulphated polysaccharides having anti-metastatic and/or anti-inflammatory activity |
| US5668116A (en) * | 1987-03-19 | 1997-09-16 | Anthropharm Pty. Limited | Anti-inflammatory compounds and compositions |
| FR2614026B1 (fr) * | 1987-04-16 | 1992-04-17 | Sanofi Sa | Heparines de bas poids moleculaire, a structure reguliere, leur preparation et leurs applications biologiques |
| US5264425A (en) * | 1988-06-03 | 1993-11-23 | Italfarmaco S.P.A. | Glycosaminoglycan salts and pharmaceutical compositions containing them |
| IL86753A0 (en) | 1988-06-15 | 1988-11-30 | Hadassah Med Org | Pharmaceutical compositions for treatment of lupus |
| DK191889D0 (da) | 1989-04-20 | 1989-04-20 | Bukh Meditec | Kosmetisk middel |
| SE9002550D0 (sv) | 1990-08-01 | 1990-08-01 | Kabivitrum Ab | Heparinfragment |
| IT1243987B (it) * | 1990-10-29 | 1994-06-28 | Derivati Organici Lab | Procedimento per la preparazione di epossi-eparidi prodotti ottenuti ecomposizioni farmaceutiche che li contengono |
| US5280016A (en) | 1991-03-29 | 1994-01-18 | Glycomed Incorporated | Non-anticoagulant heparin derivatives |
| US5250519A (en) | 1991-03-29 | 1993-10-05 | Glycomed Incorporated | Non-anticoagulant heparin derivatives |
| SE9101155D0 (sv) | 1991-04-18 | 1991-04-18 | Kabi Pharmacia Ab | Novel heparin derivatives |
| IT1254216B (it) | 1992-02-25 | 1995-09-14 | Opocrin Spa | Derivati polisaccaridici di eparina, eparan solfato, loro frazioni e frammenti, procedimento per la loro preparazione e composizioni farmaceutiche che li contengono |
| US5668118A (en) * | 1992-07-24 | 1997-09-16 | Cavalier Pharmaceuticals | Method of synthesis of 2-O-desulfated Heparin and use thereof for inhibition of elastase and Cathepspin G |
| US5696100A (en) * | 1992-12-22 | 1997-12-09 | Glycomed Incorporated | Method for controlling O-desulfation of heparin and compositions produced thereby |
| US5296471A (en) * | 1992-12-22 | 1994-03-22 | Glycomed Incorporated | Method for controlling o-desulfation of heparin and compositions produced thereby |
| EP0690720B1 (en) | 1993-03-12 | 2001-06-27 | XOMA Technology Ltd. | Therapeutic uses of bactericidal/permeability increasing protein products |
| IT1264709B1 (it) * | 1993-07-12 | 1996-10-04 | Italfarmaco Spa | Derivati eparinici ad attivita' antimetastatica |
| US5583121A (en) * | 1994-01-12 | 1996-12-10 | Michigan State University | Non-anticoagulant chemically modified heparinoids for treating hypovolemic shock and related shock syndromes |
| US6127347A (en) * | 1994-01-12 | 2000-10-03 | Univ Michigan | Non-anticoagulant chemically modified heparinoids for treating hypovolemic shock and related shock syndromes |
| AU2435795A (en) * | 1994-05-06 | 1995-11-29 | Glycomed Incorporated | O-desulfated heparin derivatives, methods of making and uses thereof |
| US6140481A (en) * | 1994-07-01 | 2000-10-31 | Seikagaku Corporation | Process for producing desulfated polysaccharide, and desulfated heparin |
| US5733893A (en) | 1995-03-15 | 1998-03-31 | Washington University | Method of identifying molecules that regulate FGF activity |
| EP0735050B1 (en) * | 1995-03-31 | 2002-09-25 | Hamilton Civic Hospitals Research Development, Inc. | Compositions for inhibiting thrombogenesis |
| US5744457A (en) | 1995-03-31 | 1998-04-28 | Hamilton Civic Hospitals Research Development Inc. | Compositions and methods for inhibiting thrombogenesis |
| US6001820A (en) * | 1995-03-31 | 1999-12-14 | Hamilton Civic Hospitals Research Development Inc. | Compositions and methods for inhibiting thrombogenesis |
| US5690910A (en) * | 1995-08-18 | 1997-11-25 | Baker Norton Pharmaceuticals, Inc. | Method for treating asthma |
| ES2231880T3 (es) * | 1996-07-29 | 2005-05-16 | Paringenix, Inc. | Procedimiento para tratar el asma con heparina o-desulfatada. |
| US5767269A (en) * | 1996-10-01 | 1998-06-16 | Hamilton Civic Hospitals Research Development Inc. | Processes for the preparation of low-affinity, low molecular weight heparins useful as antithrombotics |
| AUPO573697A0 (en) | 1997-03-20 | 1997-04-10 | Prince Henry's Institute Of Medical Research | Diagnosis of endometrial cancer |
| US6596705B1 (en) * | 1998-02-09 | 2003-07-22 | The Regents Of The University Of California | Inhibition of L-selectin and P-selection mediated binding using heparin |
| US7781416B2 (en) * | 2000-01-25 | 2010-08-24 | Sigma-Tau Research Switzerland S.A. | Derivatives of partially desulphated glycosaminoglycans as heparanase inhibitors, endowed with antiangiogenic activity and devoid of anticoagulating effect |
| IT1316986B1 (it) * | 2000-01-25 | 2003-05-26 | Sigma Tau Ind Farmaceuti | Derivati glicosamminoglicani parzialmente desolfatati nonanticoagulanti ad attivita' antiangiogenica. |
| CN1197587C (zh) * | 2000-06-09 | 2005-04-20 | 中国科学院上海细胞生物学研究所 | N－位脱硫酸肝素在预防和治疗炎症中的应用 |
| US6514866B2 (en) | 2001-01-12 | 2003-02-04 | North Carolina State University | Chemically enhanced focused ion beam micro-machining of copper |
| BRPI0101486B1 (pt) | 2001-04-17 | 2017-09-19 | Cristália Produtos Químicos Farmacêuticos Ltda. | Pharmaceutical composition for topic use containing heparin for the treatment of skin or mucosal injuries caused by burns |
| SK288335B6 (sk) | 2001-09-12 | 2016-02-02 | Sigma-Tau Research Switzerland S.A. | Čiastočne alebo úplne N-desulfatovaný, N-reacetylovaný heparín, spôsob jeho prípravy, jeho použitie na prípravu liečiva s inhibičným účinkom na heparanázu, s antiangiogénnym a protizápalovým účinkom a farmaceutický prostriedok s jeho obsahom |
| US7575886B2 (en) | 2002-03-11 | 2009-08-18 | Momenta Pharmaceuticals, Inc. | Analysis of sulfated polysaccharides |
| EP1551852A4 (en) | 2002-04-25 | 2007-03-21 | Momenta Pharmaceuticals Inc | METHOD AND PRODUCTS FOR MUCOSAL DELIVERY |
| US8071569B2 (en) * | 2002-09-20 | 2011-12-06 | Mousa Shaker A | Oxidized heparin fractions and their use in inhibiting angiogenesis |
| US7964439B2 (en) | 2002-12-20 | 2011-06-21 | The Trustees Of Princeton University | Methods of fabricating devices by transfer of organic material |
| WO2004113278A2 (en) | 2003-05-20 | 2004-12-29 | Genentech, Inc. | Acylsulfamide inhibitors of factor viia |
| US7560444B2 (en) | 2003-10-01 | 2009-07-14 | Momenta Pharmaceuticals, Inc. | Polysaccharides for pulmonary delivery of active agents |
| FR2866650B1 (fr) * | 2004-02-24 | 2006-04-28 | Aventis Pharma Sa | Oligosaccharides, procede de preparation, utilisation et compositions pharmaceutiques les renfermant |
| US20050282775A1 (en) * | 2004-06-16 | 2005-12-22 | Paringenix, Inc. | Method and medicament for sulfated polysaccharide treatment of inflammation without inducing platelet activation and heparin-induced thrombocytopenia syndrome |
| US20060040896A1 (en) * | 2004-08-18 | 2006-02-23 | Paringenix, Inc. | Method and medicament for anticoagulation using a sulfated polysaccharide with enhanced anti-inflammatory activity |
| US7767420B2 (en) | 2005-11-03 | 2010-08-03 | Momenta Pharmaceuticals, Inc. | Heparan sulfate glycosaminoglycan lyase and uses thereof |
| AU2006315348A1 (en) | 2005-11-16 | 2007-05-24 | Beth Israel Deaconess Medical Center | Method to assess breast cancer risk |
| CN101495517B (zh) | 2006-05-25 | 2012-10-10 | 莫曼塔医药品有限公司 | 低分子量肝素及其用途 |
| EP1867995A1 (en) | 2006-06-15 | 2007-12-19 | Cézanne S.A.S. | In vitro method for diagnosing and monitoring metastasized bladder cancer using the determination of MMP-7 in the circulation of patients |
| US10166271B2 (en) | 2006-06-21 | 2019-01-01 | The Regents Of The University Of California | Methods for promoting hair growth |
| JP4964577B2 (ja) | 2006-12-15 | 2012-07-04 | 有限会社応用糖質化学研究所 | 親脂質性ヘパリン修飾体、その製造方法及び毛髪成長促進剤 |
| FR2912409B1 (fr) | 2007-02-14 | 2012-08-24 | Sanofi Aventis | Heparines de bas poids moleculaire comprenant au moins une liaison covalente avec la biotine ou un derive de la biotine leur procede de preparation,leur utilisation |
| US8088753B2 (en) | 2007-06-29 | 2012-01-03 | Mediplex Corporation, Korea | Heparin conjugates and methods |
| US20090012165A1 (en) | 2007-07-03 | 2009-01-08 | Sucampo Ag | Pharmaceutical combination of nsaid and prostaglandin compound |
| WO2009007224A1 (en) | 2007-07-10 | 2009-01-15 | Sigma-Tau Industrie Farmaceutiche Riunite S.P.A. | Low molecular weight heparin derivatives having neuroprotective activity |
| US8592393B2 (en) | 2007-11-02 | 2013-11-26 | Momenta Pharmaceuticals, Inc. | Polysaccharide compositions and methods of use for the treatment and prevention of disorders associated with progenitor cell mobilization |
| EP2207811B1 (en) | 2007-11-02 | 2017-01-04 | Momenta Pharmaceuticals, Inc. | Non-anticoagulant polysaccharide compositions |
| US8569262B2 (en) | 2007-11-02 | 2013-10-29 | Momenta Pharmaceuticals, Inc. | Polysaccharide compositions and methods of use for the treatment and prevention of disorders associated with progenitor cell mobilization |
| WO2009105522A1 (en) | 2008-02-20 | 2009-08-27 | Momenta Pharmaceuticals, Inc. | Methods of making low molecular weight heparin compositions |
| JP5421366B2 (ja) | 2008-07-21 | 2014-02-19 | オトノミ―，インク． | 制御放出性の耳の構造体調節および生来の免疫システム調節化合物および耳の障害の処置のための方法 |
| US20100331746A1 (en) | 2009-02-20 | 2010-12-30 | Aventis Pharma S.A. | Method of using enoxaparin for reducing the risk of death in acutely ill medical patients |
| US8435795B2 (en) | 2010-01-19 | 2013-05-07 | Momenta Pharmaceuticals, Inc. | Evaluating heparin preparations |
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Also Published As
| Publication number | Publication date |
|---|---|
| JP2013525306A (ja) | 2013-06-20 |
| US8592393B2 (en) | 2013-11-26 |
| CN103096924A (zh) | 2013-05-08 |
| US20160060366A1 (en) | 2016-03-03 |
| US20140031315A1 (en) | 2014-01-30 |
| EP2558124A4 (en) | 2013-07-24 |
| EP2558124A1 (en) | 2013-02-20 |
| US9212233B2 (en) | 2015-12-15 |
| US20100324276A1 (en) | 2010-12-23 |
| WO2011130572A1 (en) | 2011-10-20 |
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