Abstract | OBJECTIVE: METHODS: Thirteen subjects with refractory epilepsy concomitantly taking CLB and CBD under IND 119876 were included in this study. Demographic information was collected for each subject including age, sex, and etiology of seizures, as well as concomitant antiepileptic drugs (AEDs). CLB, N-desmethylclobazam ( norclobazam; nCLB), and CBD levels were measured over the course of CBD treatment. CLB doses were recorded at baseline and at weeks 4 and 8 of CBD treatment. Side effects were monitored. RESULTS: We report elevated CLB and nCLB levels in these subjects. The mean (± standard deviation [SD]) increase in CLB levels was 60 ± 80% (95% confidence interval (CI) [-2-91%] at 4 weeks); the mean increase in nCLB levels was 500 ± 300% (95% CI [+90-610%] at 4 weeks). Nine of 13 subjects had a >50% decrease in seizures, corresponding to a responder rate of 70%. The increased CLB and nCLB levels and decreases in seizure frequency occurred even though, over the course of CBD treatment, CLB doses were reduced for 10 (77%) of the 13 subjects. Side effects were reported in 10 (77%) of the 13 subjects, but were alleviated with CLB dose reduction. SIGNIFICANCE: Monitoring of CLB and nCLB levels is necessary for clinical care of patients concomitantly on CLB and CBD. Nonetheless, CBD is a safe and effective treatment of refractory epilepsy in patients receiving CLB treatment.
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Authors | Alexandra L Geffrey, Sarah F Pollack, Patricia L Bruno, Elizabeth A Thiele |
Journal | Epilepsia
(Epilepsia)
Vol. 56
Issue 8
Pg. 1246-51
(Aug 2015)
ISSN: 1528-1167 [Electronic] United States |
PMID | 26114620
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Wiley Periodicals, Inc. © 2015 International League Against Epilepsy. |
Chemical References |
- Benzodiazepines
- Cannabidiol
- Clobazam
- Cytochrome P-450 Enzyme System
- N-desmethylclobazam
|
Topics |
- Adolescent
- Benzodiazepines
(metabolism, therapeutic use)
- Cannabidiol
(metabolism, therapeutic use)
- Child
- Child, Preschool
- Clobazam
- Cytochrome P-450 Enzyme System
(metabolism)
- Drug Interactions
- Epilepsy
(drug therapy)
- Female
- Humans
- Male
- Young Adult
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