发明名称 Controlled release tolterodine formulation that releases not less than 80% of the active compound in under 18 hours
摘要 Described is a pharmaceutical formulation containing tolterodine or a tolterodine-related compound, or a pharmacologically acceptable salt thereof, as active ingredient, in which the formulation exhibits a controlled in vitro release of the active ingredient in a phosphate buffer at pH 6.8 of not less than about 80% after 18 hours, and after oral administration to a patient is capable of maintaining a substantially constant serum level of the active moiety or moieties for 24 hours. The use of the pharmaceutical formulation for treating overactive bladder, nocturia and gastrointestinal disorders is also described.
申请公布号 NZ518309(A) 申请公布日期 2003.05.30
申请号 NZ20000518309 申请日期 2000.10.24
申请人 PHARMACIA AB 发明人 NILVEBRANT, LISBETH;HALLEN, BENGT;OLSSON, BIRGITTA;STROMBOM, JAN;GREN, TORKEL;RINGBERG, ANDERS;WIKBERG, MARTIN
分类号 A61K45/00;A61K;A61K9/10;A61K9/16;A61K9/22;A61K9/26;A61K9/50;A61K9/52;A61K9/54;A61K31/135;A61K31/137;A61P1/00;A61P13/00;A61P13/10 主分类号 A61K45/00
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