NO329930B1 - Farmasoytisk parenteral blanding inneholdende bifosfonat, et chelaterende middel og farmasoytisk akseptabelt tilsetningsmiddel, fremgangsmate for fremstilling av slike samt anordning for frigjoring inneholdende slike - Google Patents
Farmasoytisk parenteral blanding inneholdende bifosfonat, et chelaterende middel og farmasoytisk akseptabelt tilsetningsmiddel, fremgangsmate for fremstilling av slike samt anordning for frigjoring inneholdende slike Download PDFInfo
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- NO329930B1 NO329930B1 NO20023469A NO20023469A NO329930B1 NO 329930 B1 NO329930 B1 NO 329930B1 NO 20023469 A NO20023469 A NO 20023469A NO 20023469 A NO20023469 A NO 20023469A NO 329930 B1 NO329930 B1 NO 329930B1
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- Norway
- Prior art keywords
- preparation according
- pharmaceutically acceptable
- bisphosphonic acid
- approx
- acid
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
- A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/66—Phosphorus compounds
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/66—Phosphorus compounds
- A61K31/662—Phosphorus acids or esters thereof having P—C bonds, e.g. foscarnet, trichlorfon
- A61K31/663—Compounds having two or more phosphorus acid groups or esters thereof, e.g. clodronic acid, pamidronic acid
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
- A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
- A61K47/183—Amino acids, e.g. glycine, EDTA or aspartame
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A—HUMAN NECESSITIES
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- A61P23/00—Anaesthetics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
- A61P3/14—Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Physical Education & Sports Medicine (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Anesthesiology (AREA)
- Dermatology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Endocrinology (AREA)
- Toxicology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP00101044 | 2000-01-20 | ||
| PCT/EP2001/000417 WO2001052859A1 (en) | 2000-01-20 | 2001-01-16 | Pharmaceutical parenteral composition containing a biphosphonate |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20023469L NO20023469L (no) | 2002-07-19 |
| NO20023469D0 NO20023469D0 (no) | 2002-07-19 |
| NO329930B1 true NO329930B1 (no) | 2011-01-24 |
Family
ID=8167661
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20023469A NO329930B1 (no) | 2000-01-20 | 2002-07-19 | Farmasoytisk parenteral blanding inneholdende bifosfonat, et chelaterende middel og farmasoytisk akseptabelt tilsetningsmiddel, fremgangsmate for fremstilling av slike samt anordning for frigjoring inneholdende slike |
Country Status (29)
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| EP (1) | EP1251857B1 (sr) |
| JP (1) | JP3933933B2 (sr) |
| KR (1) | KR100518391B1 (sr) |
| CN (1) | CN1311835C (sr) |
| AR (1) | AR027245A1 (sr) |
| AT (1) | ATE318137T1 (sr) |
| AU (1) | AU779677B2 (sr) |
| BR (1) | BR0107755A (sr) |
| CA (1) | CA2406798C (sr) |
| CY (1) | CY1106482T1 (sr) |
| CZ (1) | CZ301961B6 (sr) |
| DE (1) | DE60117362T2 (sr) |
| DK (1) | DK1251857T3 (sr) |
| ES (1) | ES2258070T3 (sr) |
| HR (1) | HRP20020594B1 (sr) |
| HU (1) | HU229054B1 (sr) |
| IL (2) | IL150549A0 (sr) |
| MA (1) | MA26865A1 (sr) |
| MX (1) | MXPA02007057A (sr) |
| NO (1) | NO329930B1 (sr) |
| NZ (1) | NZ519881A (sr) |
| PL (1) | PL199784B1 (sr) |
| PT (1) | PT1251857E (sr) |
| RS (1) | RS50166B (sr) |
| RU (1) | RU2238736C2 (sr) |
| SI (1) | SI1251857T1 (sr) |
| WO (1) | WO2001052859A1 (sr) |
| ZA (1) | ZA200205241B (sr) |
Families Citing this family (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR0010808A (pt) * | 1999-05-21 | 2002-08-27 | Novartis Ag | Composições farmacêuticas e usos |
| CA2372450A1 (en) * | 2001-05-10 | 2001-09-19 | Pharmaceutical Partners Of Canada Inc. | Liquid injectable formulation of disodium pamidronate |
| ITTO20020406A1 (it) * | 2002-05-13 | 2003-11-13 | Chiesi Farma Spa | Formulazioni di bisfosfonati ad uso iniettabile. |
| DE602004015407D1 (de) * | 2003-01-17 | 2008-09-11 | Teva Pharma | Verfahren zur reduzierung des eisengehalts bei risedronat natrium |
| US20050181043A1 (en) * | 2004-02-12 | 2005-08-18 | Indranil Nandi | Alendronate salt tablet compositions |
| WO2005107714A2 (en) * | 2004-05-05 | 2005-11-17 | Alkermes Controlled Therapeutics, Inc. | Method of forming microparticles that include a bisphosphonate and a polymer |
| US7645459B2 (en) * | 2004-05-24 | 2010-01-12 | The Procter & Gamble Company | Dosage forms of bisphosphonates |
| US20080287400A1 (en) * | 2004-05-24 | 2008-11-20 | Richard John Dansereau | Low Dosage Forms Of Risedronate Or Its Salts |
| US20080286359A1 (en) * | 2004-05-24 | 2008-11-20 | Richard John Dansereau | Low Dosage Forms Of Risedronate Or Its Salts |
| US7645460B2 (en) * | 2004-05-24 | 2010-01-12 | The Procter & Gamble Company | Dosage forms of risedronate |
| US20060069068A1 (en) * | 2004-07-15 | 2006-03-30 | Nanobac Pharmaceuticals, Inc. | Methods and compositions for the treatment of diseases characterized by pathological calcification |
| EP1796683A1 (en) * | 2004-07-15 | 2007-06-20 | Nanobac Life Sciences | Methods and compositions for the administration of calcium chelators, bisphosphonates and/or citrate compounds and their pharmaceutical uses |
| US7728038B2 (en) * | 2004-08-04 | 2010-06-01 | University Of Utah Research Foundation | Methods for chelation therapy |
| EP1713489B1 (en) * | 2004-08-23 | 2011-01-19 | Teva Pharmaceutical Industries Ltd | Crystalline form of ibandronate sodium and processes for preparation thereof |
| KR20070067189A (ko) * | 2004-12-02 | 2007-06-27 | 비너스 레머디스 리미티드 | 주사제에 유용한 베타-락타마제 억제제를 이용한베타-락타마제-매개 항생제 내성에 대처하기 위한 조성물 |
| US20060134190A1 (en) * | 2004-12-16 | 2006-06-22 | Banner Pharmacaps Inc. | Formulations of bisphosphonate drugs with improved bioavailability |
| US7582789B2 (en) * | 2005-02-01 | 2009-09-01 | Hoffmann-La Roche Inc. | Ibandronate polymorph |
| ES2712644T3 (es) | 2005-02-01 | 2019-05-14 | Atnahs Pharma Uk Ltd | Uso médico del polimorfo A de Ibandronato |
| US8071574B2 (en) * | 2005-02-22 | 2011-12-06 | John Dennis Bobyn | Implant improving local bone formation |
| BRPI0606280A2 (pt) * | 2005-03-17 | 2009-06-09 | Elan Pharma Int Ltd | composições de bisfosfonato nanoparticulado |
| US20070088161A1 (en) * | 2005-10-19 | 2007-04-19 | Stockel Richard F | Novel chelated bisphosphonates for use as pharmaceutical agents |
| WO2007074475A2 (en) * | 2005-12-27 | 2007-07-05 | Natco Pharma Limited | Novel polymorphic forms of ibandronate |
| US20070264130A1 (en) * | 2006-01-27 | 2007-11-15 | Phluid, Inc. | Infusion Pumps and Methods for Use |
| US20070191315A1 (en) * | 2006-02-16 | 2007-08-16 | Bengt Bergstrom | Method for administering ibandronate |
| US8974801B2 (en) * | 2006-12-21 | 2015-03-10 | Amphastar Pharmaceuticals Inc. | Long term sustained release pharmaceutical composition containing aqueous suspension of bisphosphonate |
| US20090023683A1 (en) * | 2007-07-16 | 2009-01-22 | Chandrasekhar Kocherlakota | Complexes comprising zoledronic acid and cyclodextrins |
| WO2009055014A2 (en) | 2007-10-23 | 2009-04-30 | Nektar Therapeutics Al, Corporation | Hydroxyapatite-targeting multiarm polymers and conjugates made therefrom |
| US8986253B2 (en) * | 2008-01-25 | 2015-03-24 | Tandem Diabetes Care, Inc. | Two chamber pumps and related methods |
| CN101530415A (zh) * | 2008-03-10 | 2009-09-16 | 北京德众万全医药科技有限公司 | 一种含有双膦酸盐的药物组合物及其制备方法 |
| US20090287180A1 (en) * | 2008-05-19 | 2009-11-19 | Diperna Paul M | Disposable pump reservoir and related methods |
| CA2665501A1 (en) * | 2008-09-02 | 2010-03-02 | Ohio University | Methods and compositions for the treatment and prevention of bone loss |
| US8408421B2 (en) * | 2008-09-16 | 2013-04-02 | Tandem Diabetes Care, Inc. | Flow regulating stopcocks and related methods |
| AU2009293019A1 (en) * | 2008-09-19 | 2010-03-25 | Tandem Diabetes Care Inc. | Solute concentration measurement device and related methods |
| EP2180003A1 (en) * | 2008-10-21 | 2010-04-28 | Zentiva, k.s. | Preparation of ibandronate trisodium |
| WO2011014704A2 (en) * | 2009-07-30 | 2011-02-03 | Tandem Diabetes Care, Inc. | Infusion pump system with disposable cartridge having pressure venting and pressure feedback |
| US9169279B2 (en) | 2009-07-31 | 2015-10-27 | Thar Pharmaceuticals, Inc. | Crystallization method and bioavailability |
| WO2011097269A1 (en) * | 2010-02-06 | 2011-08-11 | Thar Pharmaceuticals, Inc. | Crystallization method and bioavailability |
| US20160016982A1 (en) | 2009-07-31 | 2016-01-21 | Thar Pharmaceuticals, Inc. | Crystallization method and bioavailability |
| ES2650665T3 (es) * | 2009-07-31 | 2018-01-19 | Grünenthal GmbH | Método de cristalización y biodisponibilidad |
| WO2012054807A2 (en) | 2010-10-22 | 2012-04-26 | President And Fellows Of Harvard College | Vaccines comprising bisphosphonate and methods of use thereof |
| WO2012071517A2 (en) | 2010-11-24 | 2012-05-31 | Thar Pharmaceuticals, Inc. | Novel crystalline forms |
| GB201200868D0 (en) * | 2012-01-19 | 2012-02-29 | Depuy Int Ltd | Bone filler composition |
| US9180242B2 (en) | 2012-05-17 | 2015-11-10 | Tandem Diabetes Care, Inc. | Methods and devices for multiple fluid transfer |
| CN103070824B (zh) * | 2013-01-24 | 2014-07-16 | 天津红日药业股份有限公司 | 一种含有伊班膦酸钠的注射液 |
| US9173998B2 (en) | 2013-03-14 | 2015-11-03 | Tandem Diabetes Care, Inc. | System and method for detecting occlusions in an infusion pump |
| CN103385882B (zh) * | 2013-07-03 | 2016-02-24 | 江苏奥赛康药业股份有限公司 | 一种伊班膦酸钠注射用组合物 |
| CN108261393B (zh) * | 2015-09-27 | 2020-10-27 | 山东则正医药技术有限公司 | 一种含有唑来膦酸的注射用药物组合物 |
| CN105267145B (zh) * | 2015-11-01 | 2019-06-21 | 袁旭东 | 双膦酸盐的自乳化配方和相关剂型 |
| RU2657833C2 (ru) | 2015-12-01 | 2018-06-15 | Общество С Ограниченной Ответственностью "Остерос Биомедика" | Стабилизированная лекарственная форма конъюгата этидроната с цитарабином и её применение |
| EA033181B1 (ru) * | 2015-12-09 | 2019-09-30 | Общество С Ограниченной Ответственностью "Остерос Биомедика" | Стабилизированная лекарственная форма конъюгата этидроната с цитарабином и ее применение |
| WO2017208070A1 (en) | 2016-05-31 | 2017-12-07 | Grünenthal GmbH | Bisphosphonic acid and coformers with lysin, glycin, nicotinamide for treating psoriatic arthritis |
| EA030671B1 (ru) | 2016-07-20 | 2018-09-28 | Общество С Ограниченной Ответственностью "Остерос Биомедика" | Препарат для лечения костных поражений, вызванных злокачественными новообразованиями |
| JP7492463B2 (ja) * | 2018-07-03 | 2024-05-29 | ブリストル－マイヤーズ スクイブ カンパニー | Ｆｇｆ－２１製剤 |
Family Cites Families (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2405254C2 (de) | 1974-02-04 | 1982-05-27 | Henkel KGaA, 4000 Düsseldorf | Verwendung von 3-Amino-1-Hydroxypropan-1, 1-diphosphonsäure oder ihrer wasserlöslichen Salze bei der Beeinflußung von Calciumstoffwechselstörungen im menschlichen oder tierischen Körper |
| DE2534391C2 (de) | 1975-08-01 | 1983-01-13 | Henkel KGaA, 4000 Düsseldorf | 1-Hydroxy-3-aminoalkan-1,1-diphosphonsäuren |
| DE2745083C2 (de) | 1977-10-07 | 1985-05-02 | Henkel KGaA, 4000 Düsseldorf | Hydroxydiphosphonsäuren und Verfahren zu deren Herstellung |
| US4252742A (en) | 1979-07-13 | 1981-02-24 | Ciba-Geigy Corporation | Chemical process for the preparation of 2,6-dialkylcyclohexylamines from 2,6-dialkylphenols |
| DE2943498C2 (de) | 1979-10-27 | 1983-01-27 | Henkel KGaA, 4000 Düsseldorf | Verfahren zur Herstellung von 3-Amino-1-hydroxypropan-1,1-diphosphonsäure |
| DE3016289A1 (de) | 1980-04-28 | 1981-10-29 | Henkel KGaA, 4000 Düsseldorf | Verfahren zur herstellung von omega -amino-1-hydroxyalkyliden-1,1-bis-phosphonsaeuren |
| IT1201087B (it) | 1982-04-15 | 1989-01-27 | Gentili Ist Spa | Bifosfonati farmacologicamente attivi,procedimento per la loro preparazione e relative composizioni farmaceutiche |
| FR2531088B1 (fr) | 1982-07-29 | 1987-08-28 | Sanofi Sa | Produits anti-inflammatoires derives de l'acide methylenediphosphonique et leur procede de preparation |
| DE3428524A1 (de) | 1984-08-02 | 1986-02-13 | Boehringer Mannheim Gmbh, 6800 Mannheim | Neue diphosphonsaeurederivate, verfahren zu deren herstellung und diese verbindungen enthaltende arzneimittel |
| DE3434667A1 (de) | 1984-09-21 | 1986-04-03 | Henkel KGaA, 4000 Düsseldorf | 4-dimethylamino-1-hydroxybutan-1,1-diphosphonsaeure, deren wasserloesliche salze, verfahren zu ihrer herstellung sowie ihre verwendung |
| DE3512536A1 (de) | 1985-04-06 | 1986-10-16 | Boehringer Mannheim Gmbh, 6800 Mannheim | Neue diphosphonsaeure-derivate, verfahren zu deren herstellung und diese verbindungen enthaltende arzneimittel |
| IT1187828B (it) | 1985-05-24 | 1987-12-23 | Gentili Ist Spa | Composizione farmaceutica a base di difosfonati per il trattamento dell aretrosi |
| US4761406A (en) | 1985-06-06 | 1988-08-02 | The Procter & Gamble Company | Regimen for treating osteoporosis |
| DE3540150A1 (de) | 1985-11-13 | 1987-05-14 | Boehringer Mannheim Gmbh | Neue diphosphonsaeurederivate, verfahren zu deren herstellung und diese verbindungen enthaltende arzneimittel |
| DE3623397A1 (de) | 1986-07-11 | 1988-01-14 | Boehringer Mannheim Gmbh | Neue diphosphonsaeurederivate, verfahren zu deren herstellung und diese verbindungen enthaltende arzneimittel |
| DE3626058A1 (de) | 1986-08-01 | 1988-02-11 | Boehringer Mannheim Gmbh | Neue diphosphonsaeurederivate, verfahren zu deren herstellung und diese verbindungen enthaltende arzneimittel |
| DE3640938A1 (de) | 1986-11-29 | 1988-06-01 | Boehringer Mannheim Gmbh | Neue diphosphonsaeurederivate, verfahren zu deren herstellung und diese verbindung enthaltende arzneimittel |
| CA1283827C (en) | 1986-12-18 | 1991-05-07 | Giorgio Cirelli | Appliance for injection of liquid formulations |
| CA1339805C (en) | 1988-01-20 | 1998-04-07 | Yasuo Isomura | (cycloalkylamino)methylenebis(phosphonic acid) and medicines containing the same as an active |
| DE3822650A1 (de) | 1988-07-05 | 1990-02-01 | Boehringer Mannheim Gmbh | Neue diphosphonsaeurederivate, verfahren zu deren herstellung und diese verbindungen enthaltende arzneimittel |
| US4958839A (en) | 1988-07-12 | 1990-09-25 | Guzik Technical Enterprises, Inc. | Disc clamp employing resilient cone for spreading balls |
| US4922077A (en) | 1989-01-31 | 1990-05-01 | Raytheon Company | Method of laser marking metal packages |
| CA2035179C (en) | 1990-01-31 | 2001-08-14 | Gerald S. Brenner | Pharmaceutical compositions containing insoluble salts of bisphosphonic acids |
| US5019651A (en) | 1990-06-20 | 1991-05-28 | Merck & Co., Inc. | Process for preparing 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid (ABP) or salts thereof |
| DE4244423A1 (de) | 1992-12-29 | 1994-06-30 | Boehringer Mannheim Gmbh | Wasserlösliche Calciumsalze der 1-Hydroxy-3-(methylpentylamino)propan-1,1-bisphosphonsäure, ihre Herstellung und Verwendung als Arzneimittel |
| DE4244422A1 (de) | 1992-12-29 | 1994-06-30 | Boehringer Mannheim Gmbh | Schwerlösliche Zink- und Magnesiumsalze von 1,1-Bisphosphonsäuren, ihre Herstellung und Verwendung als Arzneimittel |
| US5462932A (en) | 1994-05-17 | 1995-10-31 | Merck & Co., Inc. | Oral liquid alendronate formulations |
| US5780455A (en) * | 1994-08-24 | 1998-07-14 | Merck & Co., Inc. | Intravenous alendronate formulations |
| JP3672342B2 (ja) * | 1994-09-26 | 2005-07-20 | アステラス製薬株式会社 | ビスホスホン酸又はその誘導体を含有する注射液とその安定化方法、及び注射液アンプル |
| US5616571A (en) * | 1995-06-06 | 1997-04-01 | Merck & Co., Inc. | Bisphosphonates prevent bone loss associated with immunosuppressive therapy |
| US5730715A (en) * | 1996-06-14 | 1998-03-24 | Becton Dickinson And Company | Method for the iontophoretic administration of bisphosphonates |
| US6720001B2 (en) | 1999-10-18 | 2004-04-13 | Lipocine, Inc. | Emulsion compositions for polyfunctional active ingredients |
-
2001
- 2001-01-11 US US09/758,605 patent/US6677320B2/en not_active Expired - Lifetime
- 2001-01-16 CA CA002406798A patent/CA2406798C/en not_active Expired - Fee Related
- 2001-01-16 IL IL15054901A patent/IL150549A0/xx active IP Right Grant
- 2001-01-16 NZ NZ519881A patent/NZ519881A/en not_active IP Right Cessation
- 2001-01-16 PT PT01900452T patent/PT1251857E/pt unknown
- 2001-01-16 KR KR10-2002-7009365A patent/KR100518391B1/ko not_active IP Right Cessation
- 2001-01-16 AT AT01900452T patent/ATE318137T1/de active
- 2001-01-16 RU RU2002121643A patent/RU2238736C2/ru not_active IP Right Cessation
- 2001-01-16 EP EP01900452A patent/EP1251857B1/en not_active Expired - Lifetime
- 2001-01-16 JP JP2001552906A patent/JP3933933B2/ja not_active Expired - Lifetime
- 2001-01-16 BR BR0107755-4A patent/BR0107755A/pt not_active Application Discontinuation
- 2001-01-16 DK DK01900452T patent/DK1251857T3/da active
- 2001-01-16 AU AU25165/01A patent/AU779677B2/en not_active Ceased
- 2001-01-16 SI SI200130514T patent/SI1251857T1/sl unknown
- 2001-01-16 MX MXPA02007057A patent/MXPA02007057A/es active IP Right Grant
- 2001-01-16 CN CNB018039510A patent/CN1311835C/zh not_active Expired - Fee Related
- 2001-01-16 WO PCT/EP2001/000417 patent/WO2001052859A1/en active IP Right Grant
- 2001-01-16 PL PL357675A patent/PL199784B1/pl unknown
- 2001-01-16 HU HU0204114A patent/HU229054B1/hu not_active IP Right Cessation
- 2001-01-16 DE DE60117362T patent/DE60117362T2/de not_active Expired - Lifetime
- 2001-01-16 ES ES01900452T patent/ES2258070T3/es not_active Expired - Lifetime
- 2001-01-16 CZ CZ20022821A patent/CZ301961B6/cs not_active IP Right Cessation
- 2001-01-18 AR ARP010100224A patent/AR027245A1/es not_active Application Discontinuation
- 2001-11-16 RS YUP-548/02A patent/RS50166B/sr unknown
-
2002
- 2002-06-28 ZA ZA200205241A patent/ZA200205241B/en unknown
- 2002-07-02 IL IL150549A patent/IL150549A/en not_active IP Right Cessation
- 2002-07-16 HR HR20020594A patent/HRP20020594B1/xx not_active IP Right Cessation
- 2002-07-17 MA MA26732A patent/MA26865A1/fr unknown
- 2002-07-19 NO NO20023469A patent/NO329930B1/no not_active IP Right Cessation
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2006
- 2006-05-19 CY CY20061100651T patent/CY1106482T1/el unknown
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