Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6a569b1f7828cb235d1ee2af578b7bf7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_aa483f86cc4003166ba4a17f7117bc12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cf32b60391b469c41e86c353437f5751 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d85899b09a301b541d4b49d4809d3162 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2d3911a97372cb96f24081487cf4eb5d http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0a70b05f3bdf7f6e9aaf7a41ac3aacdc |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-1617 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2081 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2095 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-1617 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-20 |
filingDate |
2005-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7f39a26844a424b81cc53c276b03fd60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3592d9210058b25f2f06bf625f0f3ba6 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_21c5b40e36bd3d0e0d7a43fdba64b936 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3847dc69d3eb24c77122f3a1e006a656 |
publicationDate |
2006-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
WO-2006021455-A1 |
titleOfInvention |
Fast release composition including melt granules of a moisture sensitive drug and process for manufacturing thereof |
abstract |
Solid oral dosage forms that include melt granules of a moisture-sensitive therapeutic compound and a hydrophobic melt component. The melt granules better protect the therapeutic compound from hydrolytic degradation. Such solid oral dosage forms also possess immediate-release characteristics rather than that associated with extended-release or controlled-release drug products. |
isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TR-201002256-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7915427-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2007128801-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2018050892-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2377518-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7754757-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8053465-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10369108-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2009129943-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3087975-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8143427-B2 |
priorityDate |
2004-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |