Epidiolex® for Anxiety in Pediatric Epilepsy
Purpose
This is a prospective open label study assessing the efficacy and tolerability of pharmaceutical grade cannabidiol--Epidiolex (R), for the treatment of anxiety in pediatric patients with pediatric epilepsy that has been difficult to treat and requires ongoing use of anticonvulsant medication.
Conditions
- Anxiety
- Epilepsy
Eligibility
- Eligible Ages
- Between 6 Years and 17 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Established diagnosis of epilepsy, characterized by focal or generalized seizures. All participants will have active epilepsy that requires treatment with anticonvulsant medication. 2. No episodes of seizure clusters of status epilepticus within 30 days prior to entry into the study. 3. Established symptoms of anxiety with functional impairment. 4. Baseline behavioral criteria for inclusion will include subscale scores for anxiety above the norm for age and gender inth e 60 days prior to the study on one of the following: 5. Male or female participants equal to or above age 6 and below age 18 at the start of the study. No exclusion will be made on the basis of gender or minority status. 6. Ability to administer medicine orally 7. Previous subjects who failed at any point to meet continuation criteria and withdrew early may be considered for re-enrollment by the PI on a case-by-case basis. 8. Participant or legal caregiver capable of providing informed consent and fully capable of monitoring the subject's disease process and compliance with treatment. 9. Participants who are sexually active, must agree to sexual abstinence, or, to use an approved birth control method for the full duration of study participation. 10. No active use of CBD products within the 14 days prior to screening visit and commitment to only use study product for the duration of the study.
Exclusion Criteria
- Baseline lab tests for liver specific transaminase, ALT, over the upper limit of normal (ULN). 2. Previous allergic or hypersensitivity reactions to Epidiolex® or cannabidiol 3. No access to a phone or internet to complete remote visits (in-person visits acceptable for participants without devices) 4. Active substance abuse or dependence 5. Presence of psychotic illness or imminent risk of harm to self or others. 6. Current standing use of benzodiazepines (except as "rescue" medicine) 7. Serious unstable medical or neurologic conditions such as HIV, liver or kidney disease, cancer or diabetes. 8. Presence of Epilepsy Syndrome such as Sturge-Weber Syndrome that will be more suitable as a candidate in alternate research studies. 9. Participation in a previous experimental drug study within 30 days of baseline visit. 10. Cognitive functional capacity or English literacy that is insufficient to assure validity of clinical rating scales 11. Insufficient capacity of caregiver or legal guardian to understand and appropriately consent for study procedures 12. No exclusions for existing AEDs will be absolute, though consideration of additional monitoring will be in place for patients taking clobazam or valproate. 13. Pregnant, planning to become pregnant, breast feeding, or failing to use an appropriate method of contraception.
Study Design
- Phase
- Phase 4
- Study Type
- Interventional
- Allocation
- N/A
- Intervention Model
- Single Group Assignment
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Other treatment arm |
open label treatment intervention |
|
Recruiting Locations
More Details
- Status
- Recruiting
- Sponsor
- Hugo W. Moser Research Institute at Kennedy Krieger, Inc.
Detailed Description
This study is an open label, adjunctive, proof of concept clinical trial. Prospective participants will be considered for the study if neurologic status suggests the need for continued treatment, and behavioral characteristics are clinically significant. All participants will receive active treatment, involving flexible dose titration of Epidiolex® and will be monitored for a period of four months. The study will be monitored and overseen by the Johns Hopkins Hospital Institutional Review Board.
