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Clinical Trial Summary

The primary purpose of this study is to assess the long-term safety and tolerability of Cannabidiol Oral Solution (CBD) in pediatric participants with treatment-resistant childhood absence seizures.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03355300
Study type Interventional
Source Radius Pharmaceuticals, Inc.
Contact
Status Terminated
Phase Phase 2
Start date February 20, 2018
Completion date June 28, 2019

See also
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Terminated NCT06153186 - Flunarizine for Treatment Resistant Absence Epilepsy Phase 2
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Recruiting NCT04666610 - A Study to Evaluate the Efficacy, Safety, and Tolerability of Brivaracetam as Monotherapy in Patients 2 to 25 Years of Age With Childhood Absence Epilepsy or Juvenile Absence Epilepsy Phase 3
Completed NCT00088452 - Childhood Absence Epilepsy Rx PK-PD-Pharmacogenetics Study Phase 3
Terminated NCT03336242 - Cannabidiol Oral Solution in Pediatric Participants With Treatment-Resistant Childhood Absence Seizures Phase 2
Completed NCT00361010 - A Pilot Study of Efficacy and Tolerability of Levetiracetam Monotherapy in Subjects With Childhood Absence Epilepsy N/A
Completed NCT00041951 - Search for Genes Influencing Childhood Absence Epilepsy (CAE) Study N/A
Not yet recruiting NCT06315322 - A Study to Test the Long-term Safety and Tolerability of Brivaracetam in Study Participants With Childhood Absence Epilepsy or Juvenile Absence Epilepsy Phase 3
Recruiting NCT06310772 - Assessing Comorbidities in Epilepsy Using Eye Movement Recordings