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 cataplexy or excessive daytime sleepiness in a human subject with narcolepsy, the method comprising:
administering to the subject a single daily dose of a gamma-hydroxybutyrate formulation comprising an immediate-release portion and a modified-release portion,
wherein the single daily dose comprises an amount of gamma-hydroxybutyrate equivalent to 3.0 g, 4.5 g, 6 g, 7.5 g, or 9 g of sodium oxybate,
wherein the administering occurs at bedtime, and
wherein 2% or fewer subjects administered the formulation experience a confusional state.
2. The method of claim 1 , wherein the subject has a decreased risk of falls or headaches.
3. The method of claim 1 , wherein the subject has a decreased risk of car and work accidents.
4. The method of claim 1 , wherein the subject has a decreased risk of work-related errors or lack of energy.
5. The method of claim 1 , wherein the subject has a decreased risk of irritability or mood problems.
6. The method of claim 1 , wherein the subject has a decreased risk of gastrointestinal, cardiovascular, or metabolic disorders.
7. The method of claim 1 , wherein the subject has a decreased risk of drug or alcohol abuse.
8. The method of claim 1 , wherein the subject has a decreased risk of one or more of the sleep deprivation side effects selected from the group consisting of lack of alertness, irritation, memory lapses, lack of focus, difficulty retaining new concepts, difficulty making decisions, slower reaction times, and combinations thereof.
9. The method of claim 1 , where the subject has a decreased risk of developing diabetes, obesity, and heart disease associated with long-term sleep deprivation.
10. A method of treating cataplexy or excessive daytime sleepiness in a human subject with narcolepsy, the method comprising:
administering to the subject a single daily dose of a gamma-hydroxybutyrate formulation comprising an immediate-release portion and a modified-release portion,
wherein the single daily dose comprises an amount of gamma-hydroxybutyrate equivalent to 3.7 g, 5.0 g, 6.2 g, or 7.4 g of oxybate,
wherein the administering occurs at bedtime, and
wherein 3% or fewer subjects administered the formulation experience sleepwalking.
11. The method of claim 10 , wherein the sleepwalking is a parasomnia that occurs during non-REM sleep.