Bioavailability, Safety and Tolerability of Diazepam Nasal Spray Versus Diazepam Rectal Gel (Diastat®)
Status: | Terminated |
---|---|
Conditions: | Neurology |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 12 - 65 |
Updated: | 10/18/2018 |
Start Date: | June 2015 |
End Date: | July 2016 |
An Open-Label, Randomized, Crossover Pharmacokinetic Study to Determine the Bioavailability, Safety and Tolerability of Single Doses of Diazepam Nasal Spray Versus Diazepam Rectal Gel (Diastat®) in Patients With Refractory Epilepsy
This is a multi-center, open-label, crossover, pharmacokinetic, bio-availability study
involving adolescents and adults with refractory (drug-resistant) epilepsy. Cohort 1
comprises the subjects used to determine the relative bioavailability of DZNS versus DRG
(Diastat)
involving adolescents and adults with refractory (drug-resistant) epilepsy. Cohort 1
comprises the subjects used to determine the relative bioavailability of DZNS versus DRG
(Diastat)
To determine the bioavailability of diazepam nasal spray versus diazepam rectal gel
(Diastat®) under conditions of use in adolescent and adult persons with epilepsy (PWE)
meeting the definition of refractory epilepsy.
(Diastat®) under conditions of use in adolescent and adult persons with epilepsy (PWE)
meeting the definition of refractory epilepsy.
Inclusion Criteria:
- Diagnosis of refractory epilepsy
- Body weight 26 to 111 kilogram (kg) inclusive
- Other inclusion criteria apply
Exclusion Criteria:
- Male or female subject who is not surgically sterile or female subject who is less
than 2 years postmenopausal, and does not agree to use a highly effective birth
control method during the study and up to 3 months after the last dose of
investigational product
- Female subject who is pregnant, breastfeeding, or planning to become pregnant
- Presence or history of any abnormality or illness that may affect the absorption,
distribution, metabolism or elimination of diazepam
- Other exclusion criteria apply
We found this trial at
22
sites
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