Claims for Patent: 10,154,963

Summary for Patent: 10,154,963

Title:	Controlled-release formulations comprising Torsemide
Abstract:	Disclosed herein are controlled-release (GR, e.g., extended-release (ER) or prolonged-release (PR)) oral dosage formulation comprising an effective amount of Torsemide or a pharmaceutically acceptable salt thereof and at least one sustained release excipient comprising a polymer, wherein the at least one matrix component is selected from the group consisting of: hydroxy propyl cellulose (HPC), hydroxpropyl methyl cellulose (HPMC), glyceryl behenate, and a polyethylene glycol glyceride. Torsemide may be present in the formulation in a range of about 1 wt % to about 20 wt %, or about 5 wt % to about 10 wt % and the matrix component is present in the formulation in a range of about 5 wt % to about 50 wt %, or about 15 wt % to about 35 wt %. The formulation may further comprise at least one binder, lactose, talc and magnesium stearate. Methods of making and using the controlled-release oral dosage Torsemide formulation are also disclosed. A novel mechanism for Torsemide action in diuresis is further disclosed.
Inventor(s):	Shah; Salim (Vienna, VA)
Assignee:	SARFEZ PHARMACEUTICALS, INC. (Vienna, VA)
Application Number:	15/027,355
Patent Claims:	1. An extended-release oral dosage formulation manufactured by wet granulation comprising: torsemide or a pharmaceutically acceptable salt thereof as an active ingredient; 27 wt % to 34 wt % of hydroxypropyl methyl cellulose; 25 wt % to 53 wt % of high density microcrystalline cellulose of nominal particle size of about 100 micrometer; and 6.5 wt % to 8 wt % of lactose monohydrate. 2. An extended-release oral dosage formulation manufactured by wet granulation comprising: torsemide or a pharmaceutically acceptable salt thereof as an active ingredient; 27 wt % to 34 wt % of hydroxypropyl methyl cellulose; 25 wt % to 53 wt % of high density microcrystalline cellulose of nominal particle size of about 100 micrometer; and 5 wt % to 8 wt % of lactose monohydrate. 3. The extended-release oral dosage formulation of claim 2, wherein said dosage formulation when administered orally to a subject, Cmax decreases by 60.87% wt-75.94% wt of a corresponding (by API weight) immediate release dosage form. 4. The extended-release oral dosage formulation of claim 2, wherein said dosage formulation when administered orally to a subject, Tmax increases by 281%-422% compared to that of a corresponding (by API weight) immediate release dosage form. 5. The extended-release oral dosage formulation of claim 2, wherein said dosage formulation when administered orally to a subject decreases AUC1-3 (1-3 hours after drug administration and measured as hr/ngml-1) between 48%-67% and increases AUC8-10 (8-10 hours after drug administration and measured as hr/ngml-1) between 149%-263% compared to that of a corresponding (by API weight) immediate release dosage form. 6. The extended-release oral dosage formulation of claim 2, wherein said dosage formulation when administered orally to a subject increases T1/2 between 32%-55% compared to that of a corresponding (by API weight) immediate release dosage form. 7. An extended-release oral dosage formulation manufactured by wet granulation comprising torsemide or a pharmaceutically acceptable salt thereof, 27 wt % to 34 wt % of hydroxypropyl methyl cellulose; 25 wt % to 53 wt % of high density microcrystalline cellulose of nominal particle size about 100 micrometer, 5 wt % to 8 wt % of lactose monohydrate, an aldosterone receptor antagonist or a pharmaceutically acceptable salt thereof, wherein said torsemide and said aldosterone receptor antagonist are comprised in an extended release dosage formulation. 8. A method of producing wet granules of an extended-release oral dosage formulation comprising the steps of mixing torsemide with 27 wt % to 34 wt % of hydroxypropyl methyl cellulose; 25 wt % to 53 wt % of high density microcrystalline cellulose; and 5 wt % to 8 wt % of lactose monohydrate by final weight of the granules. 9. A method of producing wet granules of an extended-release oral dosage formulation comprising the steps of mixing torsemide with 32-34 wt % of hydroxypropyl methyl cellulose; 25 wt % to 53 wt % of high density microcrystalline cellulose; and 5 wt % to 8 wt % of lactose monohydrate by final weight of the granules.