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 patient in need thereof, the method comprising:
orally administering a dosage of a composition comprising gamma-hydroxybutyrate only once per night,
wherein the composition comprises an immediate-release portion and a modified-release portion, and
wherein the patient experiences fewer adverse reactions as compared to administration of a comparable amount of a twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses, wherein a first dose of the liquid solution is administered 2.5-4 hours prior to administration of a second dose of the liquid solution each night.
2. The method of claim 1 , wherein the patient experiences no adverse reactions.
3. The method of claim 1 , wherein the patient experiences less or no obtundation as compared to the twice-nightly, immediate release liquid solution administration.
4. The method of claim 1 , wherein the patient experiences less or no clinically significant respiratory depression as compared to the twice-nightly, immediate release liquid solution gamma-hydroxybutyrate administration.
5. The method of claim 1 , wherein the patient does not have profound CNS depression or severe difficulty breathing at doses equivalent to 4.5 g to 9 g of sodium oxybate per night.
6. The method of claim 1 , wherein the patient does not have a clinically significant worsening of respiratory function as measured by apnea/hypopnea index and pulse oximetry at doses equivalent to 4.5 g to 9 g of sodium oxybate per night.
7. The method of claim 1 , wherein the patient has statistically significant improvement on the Maintenance of Wakefulness Test at dosages equivalent to 6 g, 7.5 g, and 9 g of sodium oxybate as compared to placebo and/or wherein the patient has a latency to sleep onset about 5 minutes or more than placebo.
8. The method of claim 1 , wherein the patient has a decrease in daytime sleepiness when measured by the Maintenance of Wakefulness Test based on EEG measures of wakefulness, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
9. The method of claim 1 , wherein the patient has a decrease in excessive daytime sleepiness (EDS) as measured by patient report via the Epworth Sleepiness Scale (ESS), compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
10. The method of claim 1 , wherein the patient has an increase in mean sleep latency compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
11. The method of claim 1 , wherein the patient has statistically significant improvement on the Clinical Global Impression-Improvement (CGI) rating at dosages equivalent to 6 g, 7.5 g, and 9 g of sodium oxybate as compared to placebo and/or wherein the patient is 5 times or more likely to respond as much or very much improved as compared to placebo.
12. The method of claim 1 , wherein administration of the composition improves the CGI rating of sleepiness, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
13. The method of claim 1 , wherein the patient has statistically significant improvement in mean weekly cataplexy attacks at dosages equivalent to 6 g, 7.5 g, and 9 g of sodium oxybate as compared to placebo and/or wherein the patient has about 4 or fewer mean cataplexy attacks per week as compared to placebo.
14. The method of claim 1 , wherein the patient has a decrease in the number of cataplexy attacks (NCA), compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
15. The method of claim 1 , wherein the patient has less confusion, less depressive syndrome, less incontinence, less nausea, or less sleepwalking, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
16. The method of claim 1 , wherein the patient has a decrease in PSG transitions from N/2 to N/3 and REM sleep to wake and N1 sleep, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
17. The method of claim 1 , wherein the patient has a decrease in a number of arousals or wakenings obtained from a polysomnogram, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
18. The method of claim 1 , wherein the patient has a decrease in disturbed nocturnal sleep (DNS), disturbed nocturnal events, or adverse respiratory events as determined by polysomnographic measures of sleep fragmentation, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
19. The method of claim 1 , wherein the patient has a decrease in hypnagogic hallucinations or sleep paralysis symptoms in Type 1 narcolepsy patients, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
20. The method of claim 1 , wherein the dosage of the composition initially administered comprises an amount of gamma-hydroxybutyrate equivalent to 4.5 g of sodium oxybate.
21. The method of claim 20 , further comprising increasing the dosage by 1.5 g per night at weekly intervals to an effective dosage range equivalent to 6 g to 9 g of sodium oxybate per night.
22. The method of claim 1 , wherein the composition is a powder for oral suspension.
23. The method of claim 22 , wherein the composition further comprises microcrystalline cellulose spheres, povidone K30, hydrogenated vegetable oil, methacrylic acid copolymer, malic acid, xanthan gum, hydroxyethyl cellulose, carrageenan, and/or magnesium stearate.
24. The method of claim 22 , further comprising providing the composition in a nightly dose packet in an amount of gamma-hydroxybutyrate equivalent to 4.5 g, 6 g, 7.5, g, or 9 g of sodium oxybate.
25. The method of claim 24 , further comprising preparing the dosage by suspending the composition from the dose packet in in approximately 50 mL of water.
26. The method of claim 1 , wherein the dosage is administered without regard for meals.
27. The method of claim 1 , wherein the patient is in bed prior to orally administering the dosage and/or wherein the patient lays down immediately after administering the dosage.
28. The method of claim 1 , wherein the patient falls asleep within 5 minutes to 15 minutes after administering the dosage.
29. The method of claim 1 , wherein the patient is an adult.
30. A method of treating a disorder treatable with gamma-hydroxybutyrate in a human patient in need thereof, the method comprising:
orally administering a dosage of a composition comprising gamma-hydroxybutyrate only once per night,
wherein the composition comprises an immediate-release portion and a modified-release portion, and
wherein the patient experiences less obtundation as compared to administration of a comparable amount of a twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses, wherein a first dose of the liquid solution is administered 2.5-4 hours prior to administration of a second dose of the liquid solution each night.
31. The method of claim 30 , wherein the patient experiences no obtundation.
32. The method of claim 30 , wherein the patient experiences less or no clinically significant respiratory depression as compared to the twice-nightly, immediate release liquid solution administration.
33. The method of claim 30 , wherein the patient does not have profound CNS depression or severe difficulty breathing at doses equivalent to 4.5 g to 9 g of sodium oxybate per night.
34. The method of claim 30 , wherein the patient does not have a clinically significant worsening of respiratory function as measured by apnea/hypopnea index and pulse oximetry at doses equivalent to 4.5 g to 9 g of sodium oxybate per night.
35. The method of claim 30 , wherein the patient has statistically significant improvement on the Maintenance of Wakefulness Test at dosages equivalent to 6 g, 7.5 g, and 9 g of sodium oxybate as compared to placebo and/or wherein the patient has a latency to sleep onset about 5 minutes or more than placebo.
36. The method of claim 30 , wherein the patient has a decrease in daytime sleepiness when measured by the Maintenance of Wakefulness Test based on EEG measures of wakefulness, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
37. The method of claim 30 , wherein the patient has a decrease in excessive daytime sleepiness (EDS) as measured by patient report via the Epworth Sleepiness Scale (ESS), compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
38. The method of claim 30 , wherein the patient has an increase in mean sleep latency compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
39. The method of claim 30 , wherein the patient has statistically significant improvement on the Clinical Global Impression-Improvement (CGI) rating at dosages equivalent to 6 g, 7.5 g, and 9 g of sodium oxybate as compared to placebo and/or wherein the patient is 5 times or more likely to respond as much or very much improved as compared to placebo.
40. The method of claim 30 , wherein the patient improves the CGI rating of sleepiness, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
41. The method of claim 30 , wherein the patient has statistically significant improvement in mean weekly cataplexy attacks at dosages equivalent to 6 g, 7.5 g, and 9 g of sodium oxybate as compared to placebo and/or wherein the patient has about 4 or fewer mean cataplexy attacks per week as compared to placebo.
42. The method of claim 30 , wherein the patient has a decrease in the number of cataplexy attacks (NCA), compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
43. The method of claim 30 , wherein the patient has less confusion, less depressive syndrome, less incontinence, less nausea, or less sleepwalking, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
44. The method of claim 30 , wherein the patient has a decrease in PSG transitions from N/2 to N/3 and REM sleep to wake and N1 sleep, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
45. The method of claim 30 , wherein the patient has a decrease in the number of arousals or wakenings obtained from a polysomnogram, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
46. The method of claim 30 , wherein the patient has a decrease in hypnagogic hallucinations or sleep paralysis symptoms in Type 1 narcolepsy patients, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
47. A method of treating a disorder treatable with gamma-hydroxybutyrate in a human patient in need thereof, the method comprising:
orally administering a dosage of a composition comprising gamma-hydroxybutyrate only once per night,
wherein the composition comprises an immediate-release portion and a modified-release portion, and
wherein the patient experiences less respiratory depression as compared to administration of a comparable amount of a twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses, wherein a first dose of the liquid solution is administered 2.5-4 hours prior to administration of a second dose of the liquid solution each night.
48. The method of claim 47 , wherein the patient experiences no clinically significant respiratory depression.
49. The method of claim 47 , wherein the patient experiences less or no obtundation as compared to the twice-nightly, immediate release liquid solution administration.
50. The method of claim 47 , wherein the patient does not have profound CNS depression or severe difficulty breathing at doses equivalent to 4.5 g to 9 g of sodium oxybate per night.
51. The method of claim 47 , wherein the patient does not have a clinically significant worsening of respiratory function as measured by apnea/hypopnea index and pulse oximetry at doses equivalent to 4.5 g to 9 g of sodium oxybate per night.
52. The method of claim 47 , wherein the patient has statistically significant improvement on the Maintenance of Wakefulness Test at dosages equivalent to 6 g, 7.5 g, and 9 g of sodium oxybate as compared to placebo and/or wherein the patient has a latency to sleep onset about 5 minutes or more than placebo.
53. The method of claim 47 , wherein the patient has a decrease in daytime sleepiness when measured by the Maintenance of Wakefulness Test based on EEG measures of wakefulness, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
54. The method of claim 47 , wherein the patient has a decrease in excessive daytime sleepiness (EDS) as measured by patient report via the Epworth Sleepiness Scale (ESS), compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
55. The method of claim 47 , wherein the patient has an increase in mean sleep latency compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
56. The method of claim 47 , wherein the patient has statistically significant improvement on the Clinical Global Impression-Improvement (CGI) rating at dosages equivalent to 6 g, 7.5 g, and 9 g of sodium oxybate as compared to placebo and/or wherein the patient is 5 times or more likely to respond as much or very much improved as compared to placebo.
57. The method of claim 47 , wherein the patient improves on the CGI rating of sleepiness, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
58. The method of claim 47 , wherein the patient has statistically significant improvement in mean weekly cataplexy attacks at dosages equivalent to 6 g, 7.5 g, and 9 g of sodium oxybate as compared to placebo and/or wherein the patient has about 4 or fewer mean cataplexy attacks per week as compared to placebo.
59. The method of claim 47 , wherein the patient has a decrease in the number of cataplexy attacks (NCA), compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
60. The method of claim 47 , wherein the patient has less confusion, less depressive syndrome, less incontinence, less nausea, or less sleepwalking, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
61. The method of claim 47 , wherein the patient has a decrease in PSG transitions from N/2 to N/3 and REM sleep to wake and N1 sleep, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
62. The method of claim 47 , wherein the patient has a decrease in a number of arousals or wakenings obtained from a polysomnogram, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.
63. The method of claim 47 , wherein the patient has a decrease in hypnagogic hallucinations or sleep paralysis symptoms in Type 1 narcolepsy patients, compared to administration of the comparable amount of the twice-nightly, immediate release liquid solution of sodium oxybate divided into two separate doses.