Modified release gamma-hydroxybutyrate formulations having improved pharmacokinetics
Modified release formulations of gamma-hydroxybutyrate having improved dissolution and pharmacokinetic properties are provided, and therapeutic uses thereof.
1. A method of treating a disorder treatable with gamma-hydroxybutyrate in a human subject in need thereof, the method comprising:
initiating a dosage of a pharmaceutical formulation equivalent to 4.5 g of sodium oxybate once per night orally, wherein the pharmaceutical formulation comprises an immediate-release (IR) portion and a modified-release (MR) portion;
up-titrating the once per night dosage in an amount equivalent to 1.5 g of sodium oxybate;
maintaining the up-titrated once per night dosage for at least a week before any further up-titrating; and
ceasing any further up-titrating upon effect.
2. The method of claim 1 , wherein the once per night dosage is increased by an amount equivalent to 1.5 g of sodium oxybate per night to an effective dosage range of an amount equivalent to 6 g to 9 g of sodium oxybate per night.
3. The method of claim 2 , wherein the once per night dosage is increased by an amount equivalent to 1.5 g of sodium oxybate per night to an effective dosage amount equivalent to 6 g of sodium oxybate per night.
4. The method of claim 2 , wherein the once per night dosage is increased by an amount equivalent to 1.5 g of sodium oxybate per night to an effective dosage amount equivalent to 7.5 g of sodium oxybate per night.
5. The method of claim 2 , wherein the once per night dosage of sodium oxybate is increased by an amount equivalent to 1.5 g of sodium oxybate per night to an effective dosage amount equivalent to 9 g of sodium oxybate per night.
6. The method of claim 1 , wherein the up-titrated once per night dosage is maintained for at least two weeks before any further up-titrating occurs.
7. The method of claim 1 , wherein initiating comprises dosing at an amount equivalent to 4.5 g of sodium oxybate for week 1, and then up-titrating to a dosage amount equivalent to 6 g of sodium oxybate once per night dosage for at least weeks 2-3.
8. The method of claim 7 , wherein the method comprises up-titrating to a dosage amount equivalent to 7.5 g of sodium oxybate once per night dosage for at least weeks 4-8.
9. The method of claim 8 , wherein the method comprises up-titrating to a dosage amount equivalent to 9 g of sodium oxybate once per night dosage for at least weeks 9-13.
10. The method of claim 1 , wherein the ceasing comprises maintaining a stable dosage amount equivalent to 6 g, 7.5 g, or 9 g of sodium oxybate once per night orally.
11. The method of claim 1 , wherein the once per night dosage does not change once a dosage amount equivalent to 9 g of sodium oxybate per night is reached.
12. The method of claim 1 , further comprising administering a stimulant to the human patient.
13. The method of claim 1 , wherein doses higher than an amount equivalent to 9 g of sodium oxybate per night are not to be administered to the human patient.
14. A method of treating a disorder treatable with gamma-hydroxybutyrate in a human subject in need thereof, the method comprising:
initiating a dosage of a pharmaceutical formulation equivalent to 4.5 g of sodium oxybate once per night orally, wherein the pharmaceutical formulation comprises an immediate-release (IR) portion and a modified-release (MR) portion; and
up-titrating the once per night dosage to effect in increments equivalent to 1.5 g of sodium oxybate per night;
maintaining each up-titrated once per night dosage for at least one week before any further up-titrating.
15. The method of claim 14 , wherein the effective once per night dosage is equivalent to 6 g of sodium oxybate per night.
16. The method of claim 14 , wherein the effective once per night dosage is equivalent to 7.5 g of sodium oxybate per night.
17. The method of claim 14 , wherein the effective once per night dosage is equivalent to 9 g of sodium oxybate per night.
18. The method of claim 14 , wherein the up-titrating occurs over a period of at least three weeks.
19. The method of claim 14 , wherein the up-titrating occurs over a period of at least five weeks.
20. A method of treating a disorder treatable with gamma-hydroxybutyrate in a human subject in need thereof, the method comprising:
initiating a dosage of a pharmaceutical formulation equivalent to 4.5 g of sodium oxybate once per night orally, wherein the pharmaceutical formulation comprises an immediate-release (IR) portion and a modified-release (MR) portion; and
maintaining the dosage at an amount equivalent to 4.5 g of sodium oxybate once per night for week 1;
up-titrating the dosage to an amount equivalent to 6 g of sodium oxybate once per night; and
maintaining the up-titrated dosage for at least weeks 2-3.
21. The method of claim 20 , further comprising:
further up-titrating the dosage to an amount equivalent to 7.5 g of sodium oxybate once per night; and
maintaining the further up-titrated dosage for at least weeks 4-8.
22. The method of claim 21 , further comprising:
still further up-titrating the dosage to an amount equivalent to 9 g of sodium oxybate once per night; and
maintaining the still further up-titrated dosage for at least weeks 9-13.
23. A method of treating a disorder treatable with gamma-hydroxybutyrate in a human subject in need thereof, the method comprising:
initiating a dosage of a pharmaceutical formulation equivalent to 4.5 g of sodium oxybate once per night orally, wherein the pharmaceutical formulation comprises an immediate-release portion and a modified-release portion; and
up-titrating the once per night dosage to effect in increments equivalent to 1.5 g of sodium oxybate per night at weekly intervals for at least one week.
24. The method of claim 23 , wherein the once per night dosage is increased by an amount equivalent to 1.5 g of sodium oxybate per night at weekly intervals to an effective dosage range of an amount equivalent to 6 g to 9 g of sodium oxybate once per night orally.
25. The method of claim 23 , wherein the titrating occurs over a period of eight weeks.
26. The method of claim 23 , further comprising maintaining a stable dosage amount equivalent to 6 g, 7.5 g, or 9 g of sodium oxybate once per night, wherein the maintaining occurs after the up-titrating.