COMPOSITIONS AND METHODS FOR TREATING METABOLIC DISORDERS
Compositions and methods for improving the pharmacokinetics and reducing the risk of adverse events resulting from biguanide compound administration are provided, comprising administering delayed release formulations of such compounds having a lag phase release.
1 . (canceled)
2 . (canceled)
3 . The method according to claim 25 , wherein said enteric coating is applied to said oral dosage form to about a 2.5% to about a 7% (wt/wt) weight gain.
4 . The method according to claim 3 , wherein said enteric coating is applied to said oral dosage form to at least about a 3.0% to at least about a 6.0% (wt/wt) weight gain
5 . The method according to claim 4 , wherein said enteric coating is applied to said oral dosage form to about a 2.5% to about a 5% (wt/wt) weight gain.
6 . The method according to claim 5 , wherein said enteric coating is applied to said oral dosage form to about a 2.5% to about a 4% (wt/wt) weight gain.
7 . The method according to claim 25 , wherein said oral dosage form releases about 75% to about 100% of the therapeutically effective amount of said metformin or a salt thereof over about 90 minutes after contacting said pH of at least about 6.5.
8 . The method according to claim 25 , wherein said oral dosage form releases about 100% of the therapeutically effective amount of said metformin or a salt thereof over about 90 minutes after contacting said pH of at least about 6.8.
9 . The method according to claim 25 , wherein said enteric coating comprises a first copolymer based on methyl acrylate, methyl methacrylate and methacrylic acid.
10 . (canceled)
11 . The method according to claim 25 , wherein said enteric coating further comprises a second copolymer based on a methacrylic acid copolymer.
12 - 14 . (canceled)
15 . The method according to claim 25 , further comprising a seal coating between the core and the enteric coating, providing a total coating thickness of at least about 4% to 8% (wt./wt.) weight gain.
16 . The method according to claim 15 , further comprising a seal coating between the core and the enteric coating, providing a total coating thickness of at least about 4.5% to 6% (wt./wt.) weight gain.
17 . The method according to claim 25 , wherein the seal coating comprises hypromellose, titanium dioxide, polyethylene glycol 400, polysorbate 80, triacetin, talc, or combinations thereof.
18 . (canceled)
19 . (canceled)
20 . The method according to claim 25 , wherein said metformin or a salt thereof is metformin hydrochloride.
21 . The method according to claim 25 , where said oral dosage form comprises an enterically-coated tablet, capsule or microsphere.
22 - 24 . (canceled)
25 . A method of treating a metabolic disorder associated with or that results from a hyperglycemic condition in a patient, comprising administering to said patient a delayed-release oral dosage form having a core comprising metformin or salt thereof, and an enteric coating surrounding said core, wherein said enteric coating releases less than 5% of said metformin in an aqueous medium of 0.1 N HCl for 2 hours, has an onset of release at a pH of at-least about 6.5 for a lag phase of at least about ten minutes after contacting said pH of at least about 6.5; and wherein said oral dosage form releases about 75% to 100% of said metformin over about 90 to 120 minutes after contacting said pH of at least about 6.5.
26 - 33 . (canceled)
34 . The method according to claim 25 , wherein said lag phase is at least about 15 minutes after contacting said pH of at least about 6.5.
35 . The method according to claim 25 , wherein said lag phase is at least about 20 minutes at said pH of at least about 6.5.
36 . The method according to claim 25 , wherein said oral dosage form releases greater than 90% of the therapeutically effective amount of said metformin or a salt thereof over about 90 to 120 minutes after contacting said pH of at least about 6.5.
37 . The method according to claim 25 , wherein said dosage form releases less than 20% of the therapeutically effective amount of said metformin or a salt thereof after contacting said pH of about 6.5 or about 6.8 for a total of 30 minutes.
38 . The method according to claim 25 , wherein the oral dosage form, after oral administration, delivers metformin, or a salt thereof, downstream of the distal small intestine.
39 . The method form according to claim 25 , wherein said oral dosage form comprises either 400 mg or 600 mg metformin, or a salt thereof.