Gamma-hydroxybutyrate compositions having improved pharmacokinetics in the fed state
Oral pharmaceutical compositions of sodium oxybate having improved pharmacokinetic properties when administered less than two hours after eating are provided, and therapeutic uses thereof.
1. A method of decreasing excessive daytime sleepiness in a human subject in need thereof, the method comprising:
orally administering a pharmaceutical composition comprising first and second salts of gamma-hydroxybutyrate to said human subject, wherein
said first salt is selected from the group consisting of sodium oxybate, calcium oxybate, magnesium oxybate, and potassium oxybate,
said second salt differs from said first salt and is selected from the group consisting of sodium oxybate, calcium oxybate, magnesium oxybate, and potassium oxybate, and
wherein the orally administering occurs only once daily, and most adverse events (AEs) occur 1.5-2 hours after dosing.
2. The method of claim 1 , wherein the pharmaceutical composition comprises calcium oxybate, magnesium oxybate, potassium oxybate, and sodium oxybate.
3. The method of claim 1 , wherein the pharmaceutical composition comprises calcium oxybate, magnesium oxybate, and potassium oxybate.
4. The method of claim 1 , wherein the human subject achieves a decrease in excessive daytime sleepiness when measured by the Epworth Sleepiness Scale (ESS).
5. The method of claim 1 , wherein the human subject achieves a decrease in excessive daytime sleepiness when measured by the Maintenance of Wakefulness Test.
6. The method of claim 1 , wherein the human subject achieves an improved Clinical Global Impression (CGI) rating of sleepiness.
7. The method of claim 1 , wherein the human subject achieves a decrease in weekly cataplexy attacks.
8. The method of claim 1 , wherein the human subject has hepatic impairment.
9. The method of claim 1 , comprising mixing the pharmaceutical composition with water prior to orally administering.
10. The method of claim 1 , wherein the pharmaceutical composition is in the form of a powder.
11. The method of claim 1 , wherein the pharmaceutical composition comprises from 1 to 15% of viscosifying or suspending agents.
12. The method of claim 11 , wherein the viscosifying or suspending agents comprise xanthan gum, medium viscosity sodium carboxymethyl cellulose, mixtures of microcrystalline cellulose and sodium carboxymethyl cellulose, mixtures of microcrystalline cellulose and guar gum, medium viscosity hydroxyethyl cellulose, agar, sodium alginate, mixtures of sodium alginate and calcium alginate, gellan gum, carrageenan gum grade iota, kappa or lambda, or medium viscosity hydroxypropylmethyl cellulose.
13. The method of claim 1 , wherein the pharmaceutical composition comprises an immediate release portion and modified release portion.
14. A method of decreasing excessive daytime sleepiness in a human subject, the method comprising:
orally administering a pharmaceutical composition comprising first and second salts of gamma-hydroxybutyrate to said human subject, wherein
said first salt is selected from the group consisting of sodium oxybate, calcium oxybate, magnesium oxybate, and potassium oxybate,
said second salt differs from said first salt and is selected from the group consisting of sodium oxybate, calcium oxybate, magnesium oxybate, and potassium oxybate, and
wherein the orally administering occurs only once daily, and most adverse events (AEs) occur close to Tmax during the Cmax period.
15. The method of claim 14 , wherein the pharmaceutical composition comprises calcium oxybate, magnesium oxybate, potassium oxybate, and sodium oxybate.
16. The method of claim 14 , wherein the pharmaceutical composition comprises calcium oxybate, magnesium oxybate, and potassium oxybate.
17. The method of claim 14 , wherein the human subject achieves a decrease in excessive daytime sleepiness when measured by the Epworth Sleepiness Scale (ESS).
18. The method of claim 14 , wherein the human subject achieves a decrease in excessive daytime sleepiness when measured by the Maintenance of Wakefulness Test.
19. The method of claim 14 , wherein the human subject achieves an improved Clinical Global Impression (CGI) rating of sleepiness.
20. The method of claim 14 , wherein the human subject achieves a decrease in weekly cataplexy attacks.
21. The method of claim 14 , wherein the human subject has hepatic impairment.
22. The method of claim 14 , comprising mixing the pharmaceutical composition with water prior to orally administering.
23. The method of claim 14 , wherein the pharmaceutical composition is in the form of a powder.
24. The method of claim 14 , wherein the pharmaceutical composition comprises from 1 to 15% of viscosifying or suspending agents.
25. The method of claim 24 , wherein the viscosifying or suspending agents comprise xanthan gum, medium viscosity sodium carboxymethyl cellulose, mixtures of microcrystalline cellulose and sodium carboxymethyl cellulose, mixtures of microcrystalline cellulose and guar gum, medium viscosity hydroxyethyl cellulose, agar, sodium alginate, mixtures of sodium alginate and calcium alginate, gellan gum, carrageenan gum grade iota, kappa or lambda, or medium viscosity hydroxypropylmethyl cellulose.
26. The method of claim 14 , wherein the pharmaceutical composition comprises an immediate release portion and modified release portion.