CARVEDILOL FORMS, COMPOSITIONS, AND METHODS OF PREPARATION THEREOF
Disclosed are amorphous carvedilol salt forms, controlled-release carvedilol compositions, and methods of preparing the forms and compositions.
1 . A controlled-release composition, comprising:
a capsule comprising
a first plurality of controlled-release subunits, wherein each controlled-release subunit comprises an immediate-release subunit comprising a carvedilol phosphate salt or a hydrate, solvate, or polymorph form thereof, and a coating surrounding the immediate-release subunit, the coating comprising a methacrylic acid-methyl methacrylate copolymer as a release-retarding coating material; and
a second plurality of controlled-release subunits, wherein each controlled-release subunit comprises an immediate-release subunit comprising a carvedilol phosphate salt or a hydrate, solvate, or polymorph form thereof, and a coating surrounding the immediate-release subunit comprising a methacrylic acid-ethyl acrylate copolymer as a release-retarding coating material; and
wherein the controlled-release composition exhibits a single T max within the first 10 hours after oral administration to a patient, wherein the T max is between 4 and 10 hours.
2 . The controlled-release composition of claim 1 , wherein the ratio by weight of the second plurality of controlled-release subunits to first plurality of controlled-release subunits is about 3.6:1.
3 . The controlled-release composition of claim 1 , wherein the methacrylic acid-methyl methacrylate copolymer is present in an amount of about 5 to about 16 weight percent based on the total weight of the controlled-release subunit.
4 . The controlled-release composition of claim 1 , wherein the methacrylic acid-methyl methacrylate copolymer is present in an amount of about 10 to about 12 weight percent based on the total weight of the controlled-release subunit.
5 . The controlled-release composition of claim 1 , wherein the methacrylic acid-ethyl acrylate copolymer is present in an amount of about 2 to about 10 weight percent based on the total weight of the controlled-release subunit.
6 . The controlled-release composition of claim 1 , wherein the methacrylic acid-ethyl acrylate copolymer is present in an amount of about 3 to about 5 weight percent based on the total weight of the controlled-release subunit.
7 . The controlled-release composition of claim 1 , wherein the carvedilol phosphate salt is carvedilol dihydrogen phosphate hemihydrate.
8 . The controlled-release composition of claim 1 , wherein the capsule comprises 10, 20, 40, or 80 mg carvedilol phosphate.
9 . The controlled-release composition of claim 1 , wherein the capsule comprises about 80 mg carvedilol phosphate.
10 . The controlled-release composition of claim 1 , wherein the first and second controlled-release subunits each have a mean diameter of greater than about 2100 micrometers.
11 . The controlled-release composition of claim 1 , wherein the first and second controlled-release subunits each have a mean diameter of about 1000 to about 3000 micrometers.
12 . The controlled-release composition of claim 1 , wherein the first and second controlled-release subunits each have a mean diameter of about 2100 to about 2500 micrometers.
13 . The controlled-release composition of claim 1 , wherein the immediate-release subunits are compressed tablets.
14 . The controlled-release composition of claim 1 , wherein the controlled-release composition exhibits a second T max2 of greater than 10 hours after oral administration to a patient.
15 . The controlled-release composition of claim 1 , wherein the composition is bioequivalent to a reference drug according to New Drug Application No. 022012.
16 . A controlled-release composition, comprising:
a capsule consisting of
a first plurality of controlled-release subunits, wherein each controlled-release subunit comprises an immediate-release subunit comprising a carvedilol phosphate salt or a hydrate, solvate, or polymorph form thereof, and a coating surrounding the immediate-release subunit, the coating comprising a methacrylic acid-methyl methacrylate copolymer as a release-retarding coating material; and
a second plurality of controlled-release subunits, wherein each controlled-release subunit comprises an immediate-release subunit comprising a carvedilol phosphate salt or a hydrate, solvate, or polymorph form thereof, and a coating surrounding the immediate-release subunit comprising a methacrylic acid-ethyl acrylate copolymer as a release-retarding coating material; and
wherein the controlled-release composition exhibits a single T max within the first 10 hours after oral administration to a patient, wherein the T max is between 4 and 10 hours, and further wherein the controlled-release composition exhibits a second T max2 of greater than 10 hours.
17 . A controlled-release composition, comprising:
a capsule comprising
a first plurality of controlled-release subunits, wherein each controlled-release subunit comprises an immediate-release subunit comprising a carvedilol phosphate salt or a hydrate, solvate, or polymorph form thereof, and a coating surrounding the immediate-release subunit, the coating comprising a polymer consisting of a methacrylic acid-methyl methacrylate copolymer as a release-retarding coating material, wherein the methacrylic acid-methyl methacrylate copolymer is present in an amount of about 5 to about 16 weight percent based on the total weight of the controlled-release subunit; and
a second plurality of controlled-release subunits, wherein each controlled-release subunit comprises an immediate-release subunit comprising a carvedilol phosphate salt or a hydrate, solvate, or polymorph form thereof, and a coating surrounding the immediate-release subunit, the coating comprising a polymer consisting of a methacrylic acid-ethyl acrylate copolymer as a release-retarding coating material, wherein the methacrylic acid-ethyl acrylate copolymer is present in an amount of about 2 to about 10 weight percent based on the total weight of the controlled-release subunit; and
wherein the ratio by weight of the second plurality of controlled-release subunits to first plurality of controlled-release subunits is about 3.6:1.
18 . The controlled-release composition of claim 17 ,
wherein the methacrylic acid-methyl methacrylate copolymer is present in an amount of about 10 to about 12 weight percent based on the total weight of the controlled-release subunit; and
wherein the methacrylic acid-ethyl acrylate copolymer is present in an amount of about 3 to about 5 weight percent based on the total weight of the controlled-release subunit.