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US 2010/0160431 A1Published application
Methods and Compositions for the Treatment of Viral Infections
OwnerGregory Went, David Chernoff +3inventors
InventorsGregory Went, David Chernoff, Paul Spence, Terry Burkoth, Timothy Fultz
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Abstract
Compositions for treating flu comprise an M2 inhibitor, and optionally a neuraminidase inhibitor, wherein at least one of said M2 inhibitor or said neuraminidase inhibitor is provided in an extended release dosage form.
Claims20
A pharmaceutical composition comprising:
- (a) an M2 inhibitor;
- (b) a neuraminidase inhibitor,
- wherein at least one of said M2 inhibitor or said neuraminidase inhibitor is provided in an extended release dosage form and wherein at least one of said active pharmaceutical ingredients in said extended release dosage form has an in vitro dissolution profile less than 70% in one hour, less than 90% in two hours, greater than 40% in six hours, and greater than 85% in 12 hours as measured using a USP type 2 (paddle) dissolution system at 50 rpm, at a temperature of 37±0.5° with water as a dissolution medium.
A method of preventing or treating flu or a flu-related condition comprising administering to a subject in need thereof a therapeutically effective amount of:
- (a) an M2 inhibitor;
- and
- (b) a neuraminidase inhibitor,
- wherein at least one of said M2 inhibitor or said neuraminidase inhibitor is provided in an extended release dosage form and wherein at least one of said active pharmaceutical ingredients in said extended release dosage form has an in vitro dissolution profile less than 70% in one hour, less than 90% in two hours, greater than 40% in six hours, and greater than 85% in 12 hours as measured using a USP type 2 (paddle) dissolution system at 50 rpm, at a temperature of 37±0.5° with water as a dissolution medium.
1 more element
A pharmaceutical composition comprising:
- (a) amantadine in a dose ranging between 200 and 500 mg;
- and
- (b) oseltamivir in a dose ranging between 75 and 150 mg;
- wherein amantadine and oseltamivir are both provided in an extended release dosage form, said extended release dosage form having an in vitro dissolution profile less than 70% in one hour, less than 90% in two hours, greater than 40% in six hours, and greater than 85% in 12 hours as measured using a USP type 2 (paddle) dissolution system at 50 rpm, at a temperature of 37±0.5° with water as a dissolution medium;
1 more element
Dependencies are inferred from the claim text.