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filingDate 2003-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2011-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-101068253-B1
titleOfInvention Pharmaceutical composition for oral administration containing cyclosporin
abstract The present invention is suitable for oral administration in the form of a homogeneous solution which forms an emulsion with a particle size of less than 5 microns when exposed to water or gastrointestinal fluid, the solution comprising: a) a pharmaceutically effective amount of cyclosporin , In particular cyclosporine A, b) a carrier medium comprising triglycerol monoesters of fatty acids having 6 to 30 carbon atoms or mixtures thereof, c) polyethylene glycols, d) hydrophilic-lipophilic equilibrium greater than 10 ( Nonionic surfactant with HLB), and e) optionally, a viscosity reducing agent, wherein the composition is substantially free of ethanol. Preferred carrier medium is triglycerol monooleate. Examples of viscosity relaxants are glycerol monocaprylate and glycerol monooleate.n n n Cyclosporin, carrier medium, nonionic surfactant
priorityDate 2002-08-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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