CA2199954A1 - Microparticules sechees par pulverisation utilisees comme excipient therapeutique - Google Patents
Microparticules sechees par pulverisation utilisees comme excipient therapeutiqueInfo
- Publication number
- CA2199954A1 CA2199954A1 CA002199954A CA2199954A CA2199954A1 CA 2199954 A1 CA2199954 A1 CA 2199954A1 CA 002199954 A CA002199954 A CA 002199954A CA 2199954 A CA2199954 A CA 2199954A CA 2199954 A1 CA2199954 A1 CA 2199954A1
- Authority
- CA
- Canada
- Prior art keywords
- microparticles
- microparticles according
- water
- soluble material
- microcapsules
- 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.)
- Abandoned
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- 238000003384 imaging method Methods 0.000 description 1
- 230000002163 immunogen Effects 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229940125396 insulin Drugs 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 230000001057 ionotropic effect Effects 0.000 description 1
- 239000002502 liposome Substances 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 238000009549 lung scintigraphy Methods 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 238000011587 new zealand white rabbit Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000000199 parathyroid hormone Substances 0.000 description 1
- 229960001319 parathyroid hormone Drugs 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000000137 peptide hydrolase inhibitor Substances 0.000 description 1
- 230000002572 peristaltic effect Effects 0.000 description 1
- 102000013415 peroxidase activity proteins Human genes 0.000 description 1
- 108040007629 peroxidase activity proteins Proteins 0.000 description 1
- 229920000747 poly(lactic acid) Polymers 0.000 description 1
- 239000001259 polydextrose Substances 0.000 description 1
- 235000013856 polydextrose Nutrition 0.000 description 1
- 229940035035 polydextrose Drugs 0.000 description 1
- 229920000656 polylysine Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 238000002731 protein assay Methods 0.000 description 1
- 238000000163 radioactive labelling Methods 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000004366 reverse phase liquid chromatography Methods 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 238000000527 sonication Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000001839 systemic circulation Effects 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 239000002753 trypsin inhibitor Substances 0.000 description 1
- 238000013385 tryptic peptide mapping Methods 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 210000005166 vasculature Anatomy 0.000 description 1
Classifications
-
- 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
-
- 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
- A61K9/007—Pulmonary tract; Aromatherapy
- A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
- A61K9/0075—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy for inhalation via a dry powder inhaler [DPI], e.g. comprising micronized drug mixed with lactose carrier particles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/22—Echographic preparations; Ultrasound imaging preparations ; Optoacoustic imaging preparations
- A61K49/222—Echographic preparations; Ultrasound imaging preparations ; Optoacoustic imaging preparations characterised by a special physical form, e.g. emulsions, liposomes
- A61K49/223—Microbubbles, hollow microspheres, free gas bubbles, gas microspheres
-
- 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
-
- 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1682—Processes
- A61K9/1688—Processes resulting in pure drug agglomerate optionally containing up to 5% of excipient
-
- 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1682—Processes
- A61K9/1694—Processes resulting in granules or microspheres of the matrix type containing more than 5% of excipient
-
- 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
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
-
- 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
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5089—Processes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
Abstract
L'invention concerne des microparticules d'un produit hydrosoluble, lisses et de forme sphérique, dont au moins 90 % ont une granulométrie moyenne en masse de 1 à 10 µm et qui soit comportent un agent thérapeutique ou diagnostique, soit utilisent cet agent comme produit hydrosoluble. Ces microparticules peuvent être employées avec succès dans des inhalateurs à poudre sèche pour délivrer ledit agent.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP94307126.6 | 1994-09-20 | ||
EP94307126 | 1994-09-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2199954A1 true CA2199954A1 (fr) | 1996-04-04 |
Family
ID=8217866
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002199954A Abandoned CA2199954A1 (fr) | 1994-09-29 | 1995-09-26 | Microparticules sechees par pulverisation utilisees comme excipient therapeutique |
Country Status (16)
Country | Link |
---|---|
EP (1) | EP0783298A1 (fr) |
JP (1) | JPH10506406A (fr) |
KR (1) | KR970705979A (fr) |
AU (1) | AU701440B2 (fr) |
BR (1) | BR9509171A (fr) |
CA (1) | CA2199954A1 (fr) |
CZ (1) | CZ92497A3 (fr) |
FI (1) | FI971332A0 (fr) |
HU (1) | HUT77373A (fr) |
MX (1) | MX9702357A (fr) |
NO (1) | NO971438L (fr) |
NZ (1) | NZ292980A (fr) |
PL (1) | PL319600A1 (fr) |
RU (1) | RU2147226C1 (fr) |
WO (1) | WO1996009814A1 (fr) |
ZA (1) | ZA958239B (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9827205B2 (en) | 2008-12-12 | 2017-11-28 | Mallinckrodt Pharma Ip Trading D.A.C. | Dry powder fibrin sealant |
Families Citing this family (86)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6051256A (en) * | 1994-03-07 | 2000-04-18 | Inhale Therapeutic Systems | Dispersible macromolecule compositions and methods for their preparation and use |
US5955108A (en) * | 1994-12-16 | 1999-09-21 | Quadrant Healthcare (Uk) Limited | Cross-linked microparticles and their use as therapeutic vehicles |
GB9606188D0 (en) * | 1996-03-23 | 1996-05-29 | Danbiosyst Uk | Pollysaccharide microspheres for the pulmonary delivery of drugs |
GB9606677D0 (en) * | 1996-03-29 | 1996-06-05 | Glaxo Wellcome Inc | Process and device |
GB9607035D0 (en) * | 1996-04-03 | 1996-06-05 | Andaris Ltd | Spray-dried microparticles as therapeutic vehicles |
EP0914096B1 (fr) * | 1996-05-17 | 2003-08-13 | Elan Drug Delivery Limited | Microparticules et utilisation de ces dernieres pour soigner des plaies |
GB9610341D0 (en) * | 1996-05-17 | 1996-07-24 | Andaris Ltd | Formulation for inhalation |
US5855913A (en) * | 1997-01-16 | 1999-01-05 | Massachusetts Instite Of Technology | Particles incorporating surfactants for pulmonary drug delivery |
US5985309A (en) * | 1996-05-24 | 1999-11-16 | Massachusetts Institute Of Technology | Preparation of particles for inhalation |
US6254854B1 (en) | 1996-05-24 | 2001-07-03 | The Penn Research Foundation | Porous particles for deep lung delivery |
US5874064A (en) * | 1996-05-24 | 1999-02-23 | Massachusetts Institute Of Technology | Aerodynamically light particles for pulmonary drug delivery |
USRE37053E1 (en) | 1996-05-24 | 2001-02-13 | Massachusetts Institute Of Technology | Particles incorporating surfactants for pulmonary drug delivery |
GB9615435D0 (en) | 1996-07-23 | 1996-09-04 | Andaris Ltd | Spray-dried product and its therapeutic use |
GB9621825D0 (en) * | 1996-10-19 | 1996-12-11 | Andaris Ltd | Microparticles and their use as therapeutic vehicles |
EP0949932A1 (fr) * | 1996-10-19 | 1999-10-20 | Quadrant Healthcare (UK) Limited | Utilisation de microcapsules creuses a des fins diagnostiques et therapeutiques |
AU6014098A (en) * | 1996-12-31 | 1998-07-31 | Inhale Therapeutic Systems | Aerosolized hydrophobic drug |
EP1498115A1 (fr) * | 1997-01-16 | 2005-01-19 | Massachusetts Institute Of Technology | Préparation de particules pour inhalation |
JP3884484B2 (ja) * | 1997-01-16 | 2007-02-21 | マサチューセッツ インスティチュート オブ テクノロジー | 吸入用粒子の調製 |
SE9700133D0 (sv) * | 1997-01-20 | 1997-01-20 | Astra Ab | New formulation |
US6309623B1 (en) * | 1997-09-29 | 2001-10-30 | Inhale Therapeutic Systems, Inc. | Stabilized preparations for use in metered dose inhalers |
US20060165606A1 (en) | 1997-09-29 | 2006-07-27 | Nektar Therapeutics | Pulmonary delivery particles comprising water insoluble or crystalline active agents |
ATE248583T1 (de) * | 1997-09-29 | 2003-09-15 | Nektar Therapeutics | In dosierinhalatoren verwendbare, stabilisierte zubereitungen |
US6565885B1 (en) * | 1997-09-29 | 2003-05-20 | Inhale Therapeutic Systems, Inc. | Methods of spray drying pharmaceutical compositions |
SE9704186D0 (sv) | 1997-11-14 | 1997-11-14 | Astra Ab | New composition of matter |
GB9727102D0 (en) * | 1997-12-22 | 1998-02-25 | Andaris Ltd | Microparticles and their therapeutic use |
CA2320219A1 (fr) * | 1998-02-20 | 1999-08-26 | Quadrant Healthcare (Uk) Limited | Produits contenant du fibrinogene pour une utilisation therapeutique |
DE69907456T2 (de) * | 1998-06-24 | 2004-03-25 | Advanced Inhalation Research, Inc., Cambridge | Grosse poröse partikel ausgestossen von einem inhalator |
EP1273290A1 (fr) * | 1998-06-24 | 2003-01-08 | Advanced Inhalation Research, Inc. | Particules poreuses de grande taille émises par inhalateur |
EP1169065B1 (fr) * | 1999-04-21 | 2005-03-02 | 1355540 Ontario Inc. | Formulations a base de methacoline ou d'histamine pour detecter l'asthme |
US6858199B1 (en) | 2000-06-09 | 2005-02-22 | Advanced Inhalation Research, Inc. | High efficient delivery of a large therapeutic mass aerosol |
US8771740B2 (en) | 1999-12-20 | 2014-07-08 | Nicholas J. Kerkhof | Process for producing nanoparticles by spray drying |
CA2395129C (fr) | 1999-12-20 | 2008-12-16 | Nicholas J. Kerkhof | Procede de production de particules d'echelle nanometrique par sechage par atomisation en lit fluidise |
US7871598B1 (en) | 2000-05-10 | 2011-01-18 | Novartis Ag | Stable metal ion-lipid powdered pharmaceutical compositions for drug delivery and methods of use |
AU2001264789A1 (en) * | 2000-06-08 | 2001-12-17 | Eli Lilly And Company | Protein powder for pulmonary delivery |
DE60127175T2 (de) * | 2000-12-21 | 2007-11-08 | Nektar Therapeutics, San Carlos | Lagerstabile pulverzusammensetzungen mit interleukin-4 rezeptor |
GB0111420D0 (en) * | 2001-05-10 | 2001-07-04 | Biovector Solutions Ltd | Soluble polymer systems for drug delivery |
AU2002342241B2 (en) | 2001-11-01 | 2007-07-19 | Novartis Ag | Spray drying methods and compositions thereof |
SI1458360T1 (sl) | 2001-12-19 | 2011-08-31 | Novartis Ag | Pulmonalno dajanje aminoglikozidov |
US9339459B2 (en) | 2003-04-24 | 2016-05-17 | Nektar Therapeutics | Particulate materials |
AU2003299795A1 (en) | 2002-12-20 | 2004-07-22 | Xeris Pharmaceuticals, Inc. | Intracutaneous injection |
EP1635786A2 (fr) * | 2003-05-28 | 2006-03-22 | Nektar Therapeutics | Sechage par pulverisation d'une solution aqueuse alcoolique pour la fabrication d'une microparticule contenant un principe actif insoluble dans l'eau et ayant un enrobage partiel ou complet comprenant un acide amine ou un phospholipide |
US8075919B2 (en) | 2003-07-18 | 2011-12-13 | Baxter International Inc. | Methods for fabrication, uses and compositions of small spherical particles prepared by controlled phase separation |
DE10339197A1 (de) * | 2003-08-22 | 2005-03-24 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Sprühgetrocknete amorphe Pulver mit geringer Restfeuchte und guter Lagerstabilität |
US7727962B2 (en) | 2004-05-10 | 2010-06-01 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Powder comprising new compositions of oligosaccharides and methods for their preparation |
US7611709B2 (en) | 2004-05-10 | 2009-11-03 | Boehringer Ingelheim Pharma Gmbh And Co. Kg | 1,4 O-linked saccharose derivatives for stabilization of antibodies or antibody derivatives |
US7723306B2 (en) | 2004-05-10 | 2010-05-25 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Spray-dried powder comprising at least one 1,4 O-linked saccharose-derivative and methods for their preparation |
US8333995B2 (en) | 2004-05-12 | 2012-12-18 | Baxter International, Inc. | Protein microspheres having injectable properties at high concentrations |
CA2702340C (fr) | 2006-10-12 | 2014-12-16 | The University Of Queensland | Compositions et procedes destines a moduler des reponses immunes |
EP2050437A1 (fr) * | 2007-10-15 | 2009-04-22 | Laboratoires SMB | Compositions de poudre sèche pharmaceutiquement améliorées pour l'inhalation |
UA90013C2 (ru) * | 2008-03-19 | 2010-03-25 | Давид Анатолійович Нога | Фармацевтическая композиция, содержащая инсулин, и способ его получения |
US10463608B2 (en) | 2008-09-29 | 2019-11-05 | The Corporation Of Mercer University | Microneedle-based transdermal delivery system and method of making same |
US10004790B2 (en) | 2008-09-29 | 2018-06-26 | The Corporation Of Mercer University | Nanospheres encapsulating bioactive material and method for formulation of nanospheres |
WO2010037142A1 (fr) * | 2008-09-29 | 2010-04-01 | The Corporation Of Mercer University | Materiau bioactif d'encapsulation de nanospheres et procede de preparation de nanospheres |
US11524058B2 (en) | 2008-09-29 | 2022-12-13 | The Corporation Of Mercer University | Oral dissolving films containing microencapsulated vaccines and methods of making same |
EP2216054A1 (fr) | 2009-02-06 | 2010-08-11 | ProFibrix BV | Support extravasculaire biodégradable |
GB0909131D0 (en) | 2009-05-28 | 2009-07-01 | Quadrant Drug Delivery Ltd | Dry powder fibrin sealant |
GB0909136D0 (en) | 2009-05-28 | 2009-07-01 | Profibrix Bv | Dry powder composition |
CN102448443A (zh) * | 2009-05-28 | 2012-05-09 | 普罗菲布瑞克斯公司 | 干粉纤维蛋白密封剂 |
WO2011005756A1 (fr) | 2009-07-06 | 2011-01-13 | Puretech Ventures, Llc | Administration d'agents ciblés contre des niches de microbiote |
KR20120125465A (ko) | 2010-01-08 | 2012-11-15 | 프로피브릭스 비.브이. | 건조 분말 피브린 실란트 |
US20120046225A1 (en) | 2010-07-19 | 2012-02-23 | The Regents Of The University Of Colorado, A Body Corporate | Stable glucagon formulations for the treatment of hypoglycemia |
WO2012058715A1 (fr) | 2010-11-01 | 2012-05-10 | University Of Technology, Sydney | Agents immuno-modulateurs et leurs utilisations |
EP3225235B1 (fr) | 2011-03-10 | 2020-12-16 | Xeris Pharmaceuticals, Inc. | Formulations stables pour injection parentérale de médicaments peptidiques |
WO2012122535A2 (fr) | 2011-03-10 | 2012-09-13 | Xeris Pharmaceuticals, Inc. | Formulations stables pour injection parentérale de médicaments peptidiques |
RU2013155713A (ru) | 2011-07-06 | 2015-08-20 | Профибрикс Бв | Составы для лечения ран |
US9138479B2 (en) | 2011-10-31 | 2015-09-22 | Xeris Pharmaceuticals, Inc. | Formulations for the treatment of diabetes |
WO2013153146A1 (fr) | 2012-04-13 | 2013-10-17 | Glaxosmithkline Intellectual Property Development Limited | Particules agrégées |
IN2014DN10714A (fr) * | 2012-06-26 | 2015-09-04 | Ge Healthcare As | |
US9125805B2 (en) | 2012-06-27 | 2015-09-08 | Xeris Pharmaceuticals, Inc. | Stable formulations for parenteral injection of small molecule drugs |
ES2752021T3 (es) | 2013-02-01 | 2020-04-02 | Glialogix Inc | Composiciones y métodos para el tratamiento de enfermedades neurodegenerativas y otras enfermedades |
WO2014124096A1 (fr) | 2013-02-06 | 2014-08-14 | Perosphere Inc. | Formulations de glucagon stables |
US9018162B2 (en) | 2013-02-06 | 2015-04-28 | Xeris Pharmaceuticals, Inc. | Methods for rapidly treating severe hypoglycemia |
CN113768881A (zh) | 2013-10-08 | 2021-12-10 | 人工智能治疗公司 | 用于治疗淋巴管平滑肌瘤病的雷帕霉素 |
PL3125875T3 (pl) | 2014-04-04 | 2023-11-20 | AI Therapeutics, Inc. | Nadający się do inhalacji preparat rapamycyny do leczenia stanów związanych z wiekiem |
EP3149049B1 (fr) | 2014-05-27 | 2022-10-26 | The University Of Queensland | Il-22 pour utilisation dans le traitement des maladies métaboliques |
CN106573106B (zh) | 2014-08-06 | 2021-06-22 | Xeris药物公司 | 用于皮内和/或皮下注射糊剂的注射器、试剂盒和方法 |
KR20170095807A (ko) | 2014-10-07 | 2017-08-23 | 램 테라퓨틱스, 인코포레이티드 | 폐 고혈압의 치료를 위한 흡입가능 라파마이신 제제 |
WO2016196976A1 (fr) | 2015-06-04 | 2016-12-08 | Xeris Pharmaceuticals, Inc. | Appareils d'administration de glucagon et procédés associés |
US9649364B2 (en) | 2015-09-25 | 2017-05-16 | Xeris Pharmaceuticals, Inc. | Methods for producing stable therapeutic formulations in aprotic polar solvents |
WO2016201248A1 (fr) | 2015-06-10 | 2016-12-15 | Xeris Pharmaceuticals, Inc. | Utilisation de glucagon à faible dose |
US11590205B2 (en) | 2015-09-25 | 2023-02-28 | Xeris Pharmaceuticals, Inc. | Methods for producing stable therapeutic glucagon formulations in aprotic polar solvents |
US11628208B2 (en) | 2015-10-05 | 2023-04-18 | The Corporation Of Mercer University | System and method for microneedle delivery of microencapsulated vaccine and bioactive proteins |
WO2017062463A1 (fr) | 2015-10-05 | 2017-04-13 | The Corporation Of Mercer University | Matériau bioactif d'encapsulation de nanosphères et procédé de préparation de nanosphères |
US20180110760A1 (en) | 2016-10-21 | 2018-04-26 | Glialogix, Inc. | Compositions and methods for the treatmentof neurodegenerative and other diseases |
US11020403B2 (en) | 2017-06-02 | 2021-06-01 | Xeris Pharmaceuticals, Inc. | Precipitation resistant small molecule drug formulations |
WO2021090214A2 (fr) * | 2019-11-04 | 2021-05-14 | Alesco S.R.L. | Berbérine bertrypanosomial®, ses compositions et leur utilisation |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69332240T2 (de) * | 1992-06-12 | 2003-04-10 | Teijin Ltd | Ultrafeines pulver zur inhalation und dessen herstellung |
ES2159524T3 (es) * | 1992-06-12 | 2001-10-16 | Teijin Ltd | Preparacion farmaceutica para administrarse en el interior de las vias respiratorias. |
-
1995
- 1995-09-26 MX MX9702357A patent/MX9702357A/es unknown
- 1995-09-26 CA CA002199954A patent/CA2199954A1/fr not_active Abandoned
- 1995-09-26 HU HU9702161A patent/HUT77373A/hu unknown
- 1995-09-26 PL PL95319600A patent/PL319600A1/xx unknown
- 1995-09-26 BR BR9509171A patent/BR9509171A/pt not_active Application Discontinuation
- 1995-09-26 RU RU97106769A patent/RU2147226C1/ru not_active IP Right Cessation
- 1995-09-26 JP JP8511495A patent/JPH10506406A/ja not_active Ceased
- 1995-09-26 NZ NZ292980A patent/NZ292980A/xx not_active IP Right Cessation
- 1995-09-26 EP EP95932122A patent/EP0783298A1/fr not_active Ceased
- 1995-09-26 KR KR1019970702043A patent/KR970705979A/ko not_active Application Discontinuation
- 1995-09-26 WO PCT/GB1995/002279 patent/WO1996009814A1/fr not_active Application Discontinuation
- 1995-09-26 CZ CZ97924A patent/CZ92497A3/cs unknown
- 1995-09-26 AU AU35302/95A patent/AU701440B2/en not_active Ceased
- 1995-09-29 ZA ZA958239A patent/ZA958239B/xx unknown
-
1997
- 1997-03-26 NO NO971438A patent/NO971438L/no not_active Application Discontinuation
- 1997-04-01 FI FI971332A patent/FI971332A0/fi not_active IP Right Cessation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9827205B2 (en) | 2008-12-12 | 2017-11-28 | Mallinckrodt Pharma Ip Trading D.A.C. | Dry powder fibrin sealant |
Also Published As
Publication number | Publication date |
---|---|
FI971332A (fi) | 1997-04-01 |
BR9509171A (pt) | 1997-09-16 |
AU3530295A (en) | 1996-04-19 |
JPH10506406A (ja) | 1998-06-23 |
WO1996009814A1 (fr) | 1996-04-04 |
RU2147226C1 (ru) | 2000-04-10 |
CZ92497A3 (en) | 1997-08-13 |
KR970705979A (ko) | 1997-11-03 |
NZ292980A (en) | 1999-02-25 |
NO971438D0 (no) | 1997-03-26 |
HUT77373A (hu) | 1998-03-30 |
EP0783298A1 (fr) | 1997-07-16 |
NO971438L (no) | 1997-03-26 |
MX9702357A (es) | 1997-06-28 |
ZA958239B (en) | 1996-09-30 |
PL319600A1 (en) | 1997-08-18 |
AU701440B2 (en) | 1999-01-28 |
FI971332A0 (fi) | 1997-04-01 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
FZDE | Discontinued |