Once daily dosage forms of trospium
View Patent ↗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.
1. A once-a-day dosage formulation of a pharmaceutical composition suitable for treating a bladder dysfunction comprising:
(a) a first plurality of sugar spheres coated with a layer comprising hydroxypropylmethylcellulose (HPMC) and a pharmaceutically acceptable salt of trospium (Tr + ), said layer being coated in turn with a layer comprising a methacrylic acid copolymer, thereby providing a delayed release (DR) component; and
(b) a second plurality of sugar spheres coated with a layer comprising hydroxypropylmethylcellulose (HPMC) and a pharmaceutically acceptable salt of trospium (Tr + ), said layer being coated in turn with a layer comprising ethyl cellulose, thereby providing an extended release (XR) component;
wherein at least a portion of said formulation releases trospium in the lower gastrointestinal (GI) tract;
wherein said formulation, when administered orally to a patient suffering from a bladder dysfunction provides average steady state blood levels of Tr + ranging between 500 pg/ml and 2400 pg/ml, and
wherein the bladder dysfunction is selected from the group consisting of urinary frequency, urgency, nocturia, urge-incontinence associated with detrusor instability, urge syndrome and detrusor hyperreflexia.
2. The formulation of claim 1 in which the pharmaceutically acceptable salt of trospium is selected from the group consisting of a fluoride, chloride, bromide and iodide salt of trospium.
3. The formulation of claim 1 in which the pharmaceutically acceptable salt of trospium is trospium chloride.
4. The formulation of claim 1 in which the DR component includes 30 mg of trospium chloride.
5. The formulation of claim 1 in which the XR component includes 30 mg of trospium chloride.
6. The formulation of claim 3 in which the DR component includes 30 mg of trospium chloride and the XR component includes 30 mg of trospium chloride.