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Long-term safety and treatment effects of cannabidiol in children and adults with treatment-resistant epilepsies: Expanded access program results

  • CBD EAP study group
    ,
  • Jerzy P. Szaflarski(corresponding author)
    ,
  • Elizabeth Martina Bebin
    ,
  • Anne M. Comi
    ,
  • Anup D. Patel
    ,
  • Charuta Joshi
*Corresponding author for this work
  • University of Alabama at Birmingham
    ,
  • Kennedy Krieger Institute
    ,
  • Nationwide Children’s Hospital
    ,
  • University of Iowa
    ,
  • GW Pharmaceuticals
    ,
  • Yeshiva University
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Objective: Since 2014, cannabidiol (CBD) has been administered to patients with treatment-resistant epilepsies (TREs) in an ongoing expanded-access program (EAP). We report interim results on the safety and efficacy of CBD in EAP patients treated through December 2016. Methods: Twenty-five US-based EAP sites enrolling patients with TRE taking stable doses of antiepileptic drugs (AEDs) at baseline were included. During the 4-week baseline period, parents/caregivers kept diaries of all countable seizure types. Patients received oral CBD starting at 2-10 mg/kg/d, titrated to a maximum dose of 25-50 mg/kg/d. Patient visits were every 2-4 weeks through 16 weeks and every 2-12 weeks thereafter. Efficacy endpoints included the percentage change from baseline in median monthly convulsive and total seizure frequency, and percentage of patients with ≥50%, ≥75%, and 100% reductions in seizures vs baseline. Data were analyzed descriptively for the efficacy analysis set and using the last-observation-carried-forward method to account for missing data. Adverse events (AEs) were documented at each visit. Results: Of 607 patients in the safety dataset, 146 (24%) withdrew; the most common reasons were lack of efficacy (89 [15%]) and AEs (32 [5%]). Mean age was 13 years (range, 0.4-62). Median number of concomitant AEDs was 3 (range, 0-10). Median CBD dose was 25 mg/kg/d; median treatment duration was 48 weeks. Add-on CBD reduced median monthly convulsive seizures by 51% and total seizures by 48% at 12 weeks; reductions were similar through 96 weeks. Proportion of patients with ≥50%, ≥75%, and 100% reductions in convulsive seizures were 52%, 31%, and 11%, respectively, at 12 weeks, with similar rates through 96 weeks. CBD was generally well tolerated; most common AEs were diarrhea (29%) and somnolence (22%). Significance: Results from this ongoing EAP support previous observational and clinical trial data showing that add-on CBD may be an efficacious long-term treatment option for TRE.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1540-1548 (9 pages)

Journal (Volume, Issue Number)

Epilepsia (Volume 59, Issue 8)

Publication milestones

  • Published - 08/2018

Publication status

Published - 08/2018

ISSN

0013-9580

Publication IDs

  • Scopus: 85050490233
  • PubMed: 29998598

Publication metrics

Metrics

Fractional count
1
Fractional count
0.04
Fractional count
23
Fractional count
0.96
Fractional count
1
Fractional count
1
SciVal
citations
89
SciVal
FWCI
9.69
SciVal
Author count
24
SciVal
Paper percentile
99
SciVal
Top percentile
1
Scopus
citations

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Funding Details

The expanded‐access program was supported by grants from GW Research Ltd and the Epilepsy Therapy Project of the Epilepsy Foundation. State of Alabama General Funds supported the Alabama EAP (Carly's Law). Funding for the EAP in New York was provided by the New York State Department of Health. GW Research Ltd provided CBD free of charge, administrative support across all sites, and provided some sites with funds to support the study. At some sites, funds were provided for salary support for staff time spent on activities required for the EAP. GW Research Ltd collected the data from the sites and conducted the statistical analyses. The authors would like to thank the patients, their families, and the sites that provided data for this analysis. The expanded-access program was supported by grants from GW Research Ltd and the Epilepsy Therapy Project of the Epilepsy Foundation. State of Alabama General Funds supported the Alabama EAP (Carly's Law). Funding for the EAP in New York was provided by the New York State Department of Health. GW Research Ltd provided CBD free of charge, administrative support across all sites, and provided some sites with funds to support the study. At some sites, funds were provided for salary support for staff time spent on activities required for the EAP. GW Research Ltd collected the data from the sites and conducted the statistical analyses. The authors would like to thank the patients, their families, and the sites that provided data for this analysis.
FundersFunding number
Alabama EAP
-
GW Research Ltd
-
NCATS
UL1TR001420
GW Research Ltd
-