Details for Patent: 6,525,057

Title:	Sustained release ranolazine formulations
Abstract:	A sustained release ranolazine formulation contains an intimate mixture of ranolazine and a partially neutralized pH-dependent binder to form a film that is mostly insoluble in aqueous media below pH 4.5 and soluble in aqueous media above pH 4.5. The formulation is suitable for twice daily administration of ranolazine and is useful for controlling the rate of dissolution of ranolazine, and to maintain human plasma ranolazine levels at between 550 and 7500 ng base/mL.
Inventor(s):	Wolff; Andrew A. (San Francisco, CA), Baker; Fiona (Dunfermline, GB), Langridge; John (Wrexham, GB)
Assignee:	CV Therapeutics, Inc. (Palo Alto, CA)
Filing Date:	Aug 09, 2001
Application Number:	09/925,871
Claims:	1. A method for treating variant or exercise-induced angina in a human, comprising administering to said human a sustained release ranolazine formulation that includes at least 50% by weight ranolazine, and an admixture of at least one pH-dependent binder and at least one pH-independent binder. 2. The method of claim 1, wherein the sustained release ranolazine formulation is administered in no more than two tablets per dose. 3. The method of claim 2, wherein the sustained release ranolazine formulation is administered once, twice or three times over 24 hours. 4. The method of claim 1 wherein the sustained release ranolazine formulation is administered at a frequency such that the peak to trough plasma ranolazine level does not exceed 4:1 over a 24 hour period. 5. The method of claim 1 wherein the sustained release ranolazine formulation is administered at a frequency such that the peak to trough plasma ranolazine level does not exceed 3:1 over a 24 hour period. 6. The method of claim 1 wherein the sustained release ranolazine formulation includes an amount of ranolazine sufficient to maintain ranolazine plasma levels in the human patient of about 550 to about 7500 ng base/mL for at least 24 hours. 7. The method of claim 1 wherein the sustained release ranolazine formulation includes from about 70 to about 80 wt % ranolazine. 8. The method of claim 7 wherein the sustained release ranolazine formulation includes from about 5 to about 12.5 wt % pH-dependent binders. 9. The method of claim 8 wherein the pH-dependent binder is at least one methacrylic acid copolymer. 10. The method of claim 9 wherein the sustained release ranolazine formulation includes from about 1 to about 3 wt % of pH-independent binders. 11. The method of claim 10 wherein the pH-independent binder is hydroxypropylmethyl cellulose. 12. The method of claim 11 wherein each tablet includes from about 350 to about 800 mg ranolazine.