US2010221354A1PendingUtilityA1

Pharmaceutical composition for once-a-day oral administration of trospium chloride

65
Assignee: SUPERNUS PHARMACEUTICALS INCPriority: Nov 4, 2003Filed: May 12, 2010Published: Sep 2, 2010
Est. expiryNov 4, 2023(expired)· nominal 20-yr term from priority
A61K 9/1652A61P 13/10A61K 9/20A61K 9/5026A61K 9/5047A61K 9/2866A61K 31/46A61P 13/06A61K 9/16A61P 13/02A61K 9/4808A61P 13/00A61K 9/2846A61K 9/5078A61K 9/2086
65
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Claims

Abstract

A pharmaceutical composition of a pharmaceutically acceptable trospium salt, with upon administration to a human patient generates an average steady state blood levels of trospium with a minimum (C min ) and maximum (C max ) blood levels of about 0.5-2.5 ng/ml and about 2.0-6.0 ng/ml, respectively.

Claims

exact text as granted — not AI-modified
1 - 77 . (canceled) 
     
     
         78 . A pharmaceutical composition suitable for a once-a-day oral administration of trospium chloride to a human, the composition comprising:
 a first plurality of particulates comprising trospium chloride, said first plurality of particulates further comprising a first polymer,   a second plurality of particulates comprising trospium chloride, said second plurality of particulates further comprising a second polymer,   said pharmaceutical composition having an in vitro release profile as measured by USP Apparatus II, 50 RPM, at 37° C., in an acidic medium of 750 mL 0.1 N HCl for the first 2 hours and then adjusting the medium to pH 7.5 at 2 hours using phosphate buffer;   whereby said in vitro profile is characterized by a release of up to about 20% of the total trospium chloride during the first two hours in the acidic medium, and a release of between about 60% and about 80% of the total trospium chloride about 2 hours after said pH adjustment.   
     
     
         79 . The pharmaceutical composition of  claim 78 , wherein the second polymer comprises ethylcellulose. 
     
     
         80 . The pharmaceutical composition of  claim 78 , wherein the first polymer comprises a methacrylic acid copolymer. 
     
     
         81 . The pharmaceutical composition of  claim 80 , wherein the second polymer comprises ethylcellulose. 
     
     
         82 . The pharmaceutical composition of  claim 81 , wherein said first plurality of particulates comprises about 30 mg trospium chloride and said second plurality of particulates comprises about 30 mg trospium chloride. 
     
     
         83 . The pharmaceutical composition of  claim 82 , wherein the particulates are substantially spherical. 
     
     
         84 . The pharmaceutical composition of  claim 82 , wherein once daily oral administration to a subject in need thereof provides therapeutically effective amounts of trospium chloride to treat said subject's condition while reducing the occurrence of dry-mouth relative to oral, twice-daily administration of 20 mg immediate release trospium chloride tablets. 
     
     
         85 . The pharmaceutical composition of  claim 78 , wherein the first polymer is selected from the group consisting of a methacrylic acid copolymer, cellulose acetate phthalate, hydroxypropyl methylcellulose phthalate, and polyvinyl acetate phthalate, and wherein the second polymer is selected from the group consisting of a copolymer of acrylic and methacrylic acid esters, a copolymer of polyvinylpyrrolidone and vinyl acetate, and cellulose derivatives. 
     
     
         86 . The pharmaceutical composition of  claim 78 , wherein once-a-day administration of said pharmaceutical composition provides steady state blood levels of trospium chloride less than about 6.0 ng/mL. 
     
     
         87 . The pharmaceutical composition of  claim 78 , wherein once-a-day administration of said pharmaceutical composition provides steady state blood levels of trospium chloride greater than about 0.5 ng/mL. 
     
     
         88 . The pharmaceutical composition of  claim 78 , whereby single-dosage administration of said pharmaceutical composition provides a plasma concentration versus time curve having an area under the curve (AUC 0-72 hrs ) of about 30,000 pg/ml*hr to about 80,000 pg/ml*hr. 
     
     
         89 . The pharmaceutical composition of  claim 78 , whereby single-dosage administration of said pharmaceutical composition provides blood levels of trospium chloride less than about 3.0 ng/mL. 
     
     
         90 . The pharmaceutical composition of  claim 85 , wherein once-a-day administration of said pharmaceutical composition provides steady state blood levels of trospium chloride less than about 6.0 ng/mL. 
     
     
         91 . The pharmaceutical composition of  claim 85 , wherein once-a-day administration of said pharmaceutical composition provides steady state blood levels of trospium chloride greater than about 0.5 ng/mL. 
     
     
         92 . The pharmaceutical composition of  claim 85 , whereby single-dosage administration of said pharmaceutical composition provides a plasma concentration versus time curve having an area under the curve (AUC 0-72 hrs ) of about 30,000 pg/ml*hr to about 80,000 pg/ml*hr. 
     
     
         93 . The pharmaceutical composition of  claim 85 , whereby single-dosage administration of said pharmaceutical composition provides blood levels of trospium chloride less than about 3.0 ng/mL.

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