Methods For Treating Hyperlipidemia with Intermediate Release Nicotinic Acid Compositions Having Unique Biopharmaceutical Characteristics
OwnerEugenio Cefaliinventor
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Abstract
Methods for treating hyperlipidemia with intermediate release nicotinic acid formulations having unique biopharmaceutical characteristics, without causing drug-induced hepatotoxicity to a level which would require discontinuation of the therapy, whereby a majority of the nicotinic acid is release and metabolized in the individual within about 5 to about 9 hours. The present methods of treatment also contemplate administering the intermediate release nicotinic acid formulations composition according to a titrated dosage regimen to reduce flushing.
Claims14
A method for treating hyperlipidemia in a patient, which comprises:
- administering a single daily dose of an intermediate release nicotinic acid composition, wherein the majority of the nicotinic acid is release and metabolized in the individual within about 5 to about 9 hours, and wherein the composition does not cause dose-limiting hepatotoxicity.
A method for treating hyperlipidemia in a patient, which comprises administering to the patient a once daily intermediate release nicotinic acid composition according to a titrated dosage regimen to reduce flushing.
A pharmaceutical composition for once per day administration comprising nicotinic acid or a compound metabolized in an individual's body to nicotinic acid and a pharmaceutically acceptable carrier, wherein the composition comprises about 500 mg of the nicotinic acid or the compound metabolized in an individual's body to nicotinic acid and dissolves in deionized water at a rate of:
- (a) about 10.3-10.8% after 1 hr;
- (b) about 22.5-23.9% after 3 hrs;
- (c) about 37.6-39.0% after 6 hrs;
- (d) about 51.2-51.8% after 9 hrs;
- (e) about 62.8-63.1% after 12 hrs;
- and
- (f) about 87.1-85.2% after 20 hrs.
A pharmaceutical composition for once per day administration comprising nicotinic acid or a compound metabolized in an individual's body to nicotinic acid and a pharmaceutically acceptable carrier, wherein the composition comprises about 500 mg of the nicotinic acid or the compound metabolized in an individual's body to nicotinic acid and dissolves in deionized water at a rate of:
- (a) about 10.6% after 1 hr;
- (h) about 22.9% after 3 hrs;
- (c) about 38.0% after 6 hrs;
- (d) about 51.4% after 9 hrs;
- (e) about 63.4% after 12 hrs;
- and
- (f) about 88.4% after 20 hrs.
A pharmaceutical composition for once per day administration comprising nicotinic acid or a compound metabolized in an individual's body to nicotinic acid and a pharmaceutically acceptable carrier, wherein the composition comprises about 250 mg to about 325 mg of the nicotinic acid or the compound metabolized in an individual's body to nicotinic acid and dissolves in deionized water at a rate of:
- (a) about 11.3% after 1 hr;
- (b) about 24.1% after 3 hrs;
- (c) about 40.2% after 6 hrs;
- (d) about 54.2% after 9 hrs;
- (e) about 67.0 after 12 hrs;
- and
- (f) about 91.7% after 20 hrs.
A pharmaceutical composition for once per day administration comprising nicotinic acid or a compound metabolized in an individual's body to nicotinic acid and a pharmaceutically acceptable carrier, wherein the composition comprises about 750 mg of the nicotinic acid or the compound metabolized in an individual's body to nicotinic acid and dissolves in deionized water at a rate of:
- (a) about 10.3% after 1 hr;
- (b) about 22.0% after 3 hrs;
- (c) about 36.6% after 6 hrs;
- (d) about 49.4% after 9 hrs;
- (e) about 61.6% after 12 hrs;
- and
- (f) about 87.2% after 20 hrs.
A pharmaceutical composition for once per day administration comprising nicotinic acid or a compound metabolized in an individual's body to nicotinic acid and a pharmaceutically acceptable carrier, wherein the composition comprises about 1000 mg of the nicotinic acid or the compound metabolized in an individual's body to nicotinic acid and dissolves in deionized water at a rate of:
- (a) about 11.8% after 1 hr;
- (b) about 25.2% after 3 hrs;
- (c) about 41.3% after 6 hrs;
- (d) about 54.8% after 9 hrs;
- (e) about 66.3% after 12 hrs;
- and
- (f) about 98.4% after 20 hrs.
Dependencies are inferred from the claim text.