http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2007042160-A1

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inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f77f9d97bac447669ae654676ea12a4b
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publicationDate 2007-04-19^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2007042160-A1
titleOfInvention Retard formulation for pralnacasan
abstract The inventive retard tablets comprising at least two layers, wherein at least one layer rapidly releases a drug 1S 9S (RS, 3S) N-(2-Ethoxy-5-oxo- tetrafuran-3-yl)-6, 10-dioxo-9-(isochinolin-1-oyl-amino)-1, 2, 3, 4, 7, 8, 9, 10-octahydro- 6-H-pyridazino [1 , 2-a] [1, 2] diazepin-1-carboxamide and/or the salts or derivatives thereof and/or acids released therefrom and at least one layer releases a drug 1S, 9S (RS, 3S) N-(2-Ethoxy-5-oxo-tetrafuran-3-yl)-6,10- dioxo-9-(isochinolin-1-oyl-amino)-1, 2, 3, 4, 7, 8, 9, 10-octahydro-6-H-pyridazino [1, 2-a] [1, 2] diazepin-1-carboxamide and/or the salts or derivatives thereof and/or acids released therefrom in a delayed manner for treating autoimmune diseases, type I and type II diabetes, rheumatoid arthritis, osteoarthritis and/or psoriasis
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