ORAL PHARMACEUTICAL COMPOSITION OF METHYLERGONOVINE AND METHODS OF USE THEREOF

1 . A solid pharmaceutical oral composition configured for once or twice daily administration, comprising

an immediate release core comprising methylergonovine or a pharmaceutically acceptable salt thereof; and a polymer coating disposed on the immediate release core,

wherein the solid pharmaceutical oral composition comprises from about 0.3 mg to about 0.8 mg in total of methylergonovine or a pharmaceutically acceptable salt thereof.

2 . The solid pharmaceutical oral composition of claim 1 , further comprising an immediate release layer comprising methylergonovine or a pharmaceutically acceptable salt thereof disposed on the polymer coating.

3 . The solid pharmaceutical oral composition of claim 1 , wherein the polymer coating is an extended release coating comprises a first release rate controlling polymer.

4 . The solid pharmaceutical oral composition of claim 3 , wherein the first release rate controlling polymer comprises one or more hydrophilic release rate controlling compound, one or more hydrophobic release rate controlling compound, or combinations thereof.

5 . The solid pharmaceutical oral composition of claim 4 , wherein the first release rate controlling polymer in the extended release coating comprises hydroxypropyl methylcellulose and/or ethyl cellulose.

6 . The solid pharmaceutical oral composition of claim 1 , wherein the polymer coating is a semipermeable osmotic coatingcomprising a second release rate controlling polymer.

7 . The solid pharmaceutical oral composition of claim 6 , wherein the second release rate controlling polymer comprises one or more hydrophilic release rate controlling compound, one or more hydrophobic release rate controlling compound, or combinations thereof.

8 . The solid pharmaceutical oral composition of claim 6 , wherein the second release rate controlling polymer in the semipermeable osmotic coating comprises cellulose acetate phthalate.

9 . The solid pharmaceutical oral composition of claim 1 , wherein the polymer coating defines orifices for allowing release of methylergonovine or a pharmaceutically acceptable salt thereof from the immediate release core.

10 . The solid pharmaceutical oral composition of claim 1 , wherein the solid pharmaceutical oral composition is in a form selected from a tablet; a capsule; granules; pellets; powder; or granules, pellets, powder or a combination thereof filled in a capsule.

11 . The solid pharmaceutical oral composition of claim 1 , wherein the pharmaceutically acceptable salt of methylergonovine is maleate.

12 . The solid pharmaceutical oral composition of claim 1 , wherein the solid pharmaceutical oral composition comprises from about 0.6 mg to about 0.7 mg in total of methylergonovine or a pharmaceutically acceptable salt thereof, and is configured for once daily administration.

13 . The solid pharmaceutical oral composition of claim 12 , wherein the solid pharmaceutical oral composition is configured to provide a dissolution profileof a release of methylergonovine or a pharmaceutically acceptable salt thereof

within 0.5 hours being between about 5% and about 25%,

within 2 hours being between about 15% and about 45%,

within 6 hours being between about 25% and about 65%,

within 10 hours being between about 35% and about 85%, and

within 16 hours being not less than 75%,

as measured by a dissolution method employing a USP Type-II dissolution apparatus equipped with a paddle, a rotation speed of 75 rpm and 900 mL of tartaric acid (1 in 200 w/w) as dissolution medium.

14 . The solid pharmaceutical oral composition of claim 1 , wherein the solid pharmaceutical oral composition comprises from about 0.4 mg to about 0.45 mg in total of methylergonovine or a pharmaceutically acceptable salt thereof, and is configured for twice daily administration.

15 . The solid pharmaceutical oral composition of claim 14 , wherein the solid pharmaceutical oral composition is configured to provide a dissolution profile of a release of methylergonovine or a pharmaceutically acceptable salt thereof

within 0.5 hours being between about 10% and about 35%,

within 3 hours being between about 30% and about 60%,

within 6 hours being between about 40% and about 85%, and

within 10 hours being not less than 70%,

as measured by a dissolution method employing a USP Type-II dissolution apparatus equipped with a paddle, a rotation speed of 75 rpm and 900 mL of tartaric acid (1 in 200 w/w) as dissolution medium.

16 . A method of making the solid pharmaceutical oral composition of claim 1 , comprising preparing the immediate release core comprising methylergonovine or a pharmaceutically acceptable salt thereof.

17 . The method of claim 16 , further comprising coating the immediate release core with the polymer coating.

18 . The method of claim 17 , further comprising forming an immediate release coating comprising methylergonovine or a pharmaceutically acceptable salt thereof on the polymer coating.

19 . A method for treating a subject having a methylergonovine responsive condition comprising a step of administering to the subjectneed thereof a therapeutic effective amount of the solid pharmaceutical oral composition of claim 1 .

20 . The method for treating a subject having a methylergonovine responsive condition of claim 19 , wherein the methylergonovine responsive condition is selected from migraine, refractory migraine, uterine ator uterine haemorrhage, subinvolution of the uterus, or uterine haemorrhage in the second stage of labor.