Cited by 906Epilepsy research and treatmentCannabis and Cannabinoid ResearchDiet and metabolism studies

Cannabidiol in patients with seizures associated with Lennox-Gastaut syndrome (GWPCARE4): a randomised, double-blind, placebo-controlled phase 3 trial

Thiele, Elizabeth A, Marsh, Eric D, French, Jacqueline A, Mazurkiewicz-Beldzinska, Maria, Benbadis, Selim R, Joshi, Charuta, Lyons, Paul D, Taylor, Adam +37 more·2018·The Lancet

Abstract

Background Patients with Lennox-Gastaut syndrome, a rare, severe form of epileptic encephalopathy, are frequently treatment resistant to available medications. No controlled studies have investigated the use of cannabidiol for patients with seizures associated with Lennox-Gastaut syndrome. We therefore assessed the efficacy and safety of cannabidiol as an add-on anticonvulsant therapy in this population of patients.Methods In this randomised, double-blind, placebo-controlled trial done at 24 clinical sites in the USA, the Netherlands, and Poland, we investigated the efficacy of cannabidiol as add-on therapy for drop seizures in patients with treatment-resistant Lennox-Gastaut syndrome. Eligible patients (aged 2-55 years) had Lennox-Gastaut syndrome, including a history of slow (<3 Hz) spike-and-wave patterns on electroencephalogram, evidence of more than one type of generalised seizure for at least 6 months, at least two drop seizures per week during the 4-week baseline period, and had not responded to treatment with at least two antiepileptic drugs. Patients were randomly assigned (1:1) using an interactive voice response system, stratified by age group, to receive 20 mg/kg oral cannabidiol daily or matched placebo for 14 weeks. All patients, caregivers, investigators, and individuals assessing data were masked to group assignment. The primary endpoint was percentage change from baseline in monthly frequency of drop seizures during the treatment period, analysed in all patients who received at least one dose of study drug and had post-baseline efficacy data. All randomly assigned patients were included in the safety analyses. This study is registered with ClinicalTrials.gov, number NCT02224690.Findings Between April 28, 2015, and Oct 15, 2015, we randomly assigned 171 patients to receive cannabidiol (n=86) or placebo (n=85). 14 patients in the cannabidiol group and one in the placebo group discontinued study treatment; all randomly assigned patients received at least one dose of study treatment and had post-baseline efficacy data. The median percentage reduction in monthly drop seizure frequency from baseline was 43·9% (IQR -69·6 to -1·9) in the cannibidiol group and 21·8% (IQR -45·7 to 1·7) in the placebo group. The estimated median difference between the treatment groups was -17·21 (95% CI -30·32 to -4·09; p=0·0135) during the 14-week treatment period. Adverse events occurred in 74 (86%) of 86 patients in the cannabidiol group and 59 (69%) of 85 patients in the placebo group; most were mild or moderate. The most common adverse events were diarrhoea, somnolence, pyrexia, decreased appetite, and vomiting. 12 (14%) patients in the cannabidiol group and one (1%) patient in the placebo group withdrew from the study because of adverse events. One patient (1%) died in the cannabidiol group, but this was considered unrelated to treatment.Interpretation Add-on cannabidiol is efficacious for the treatment of patients with drop seizures associated with Lennox-Gastaut syndrome and is generally well tolerated. The long-term efficacy and safety of cannabidiol is currently being assessed in the open-label extension of this trial.Funding GW Pharmaceuticals.

Integrity signals

Registry

Crossref · 10.1016/s0140-6736(18)30136-3

Cites

27 of 27 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • CBD acts as a positive allosteric modulator at GABAA receptors, and controlled trials have shown that CBD in the form of Epidiolex is an effective anticonvulsant in Dravet syndrome and Lennox-Gastaut syndrome.

    “CBD has also been shown to act as a positive allosteric modulator at GABAA receptors, and controlled trials have shown that CBD in the form of Epidiolex is an effective anticonvulsant in Dravet syndrome and Lennox-Gastaut syndrome [120].”
  • Open-blind and double-blind controlled clinical trials confirmed and expanded preliminary findings on the efficacy, security and tolerability of CBD in children and adolescents with treatment-resistant epilepsy, particularly Dravet and Lennox-Gastaut syndromes.

    “More recently, open-blind and double-blind, controlled clinical trials investigated the efficacy, security and tolerability of CBD in children and adolescents with treatment-resistant epilepsy (particularly Dravet and Lennox-Gastaut syndromes) confirmed and expanded these preliminary findings (137–140).”

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Thiele, E. A., Marsh, E. D., French, J. A., Mazurkiewicz-Beldzinska, M., Benbadis, S. R., Joshi, C., Lyons, P. D., Taylor, A., Roberts, C., Sommerville, K., Gunning, B., Gawlowicz, J., Lisewski, P., Mazurkiewicz Beldzinska, M., Mitosek Szewczyk, K., Steinborn, B., Zolnowska, M., Hughes, E., McLellan, A., Benbadis, S., Ciliberto, M., Clark, G., Dlugos, D., Filloux, F., Flamini, R., French, J., Frost, M., Haut, S., Joshi, C., Kapoor, S., Kessler, S., Laux, L., Lyons, P., Marsh, E., Moore, D., Morse, R., Nagaraddi, V., Rosenfeld, W., Seltzer, L., Shellhaas, R., Sullivan, J., Thiele, E., Thio, L. L., Wang, D., & Wilfong, A.
Affiliations
  • GW Pharmaceuticals (United Kingdom) (GB)
  • Duke University (US)
Venue
The Lancet
Publisher
Elsevier BV
Published
2018-03
Volume
391
Issue
10125
Pages
1085-1096
ISSN
  • 0099-5355 (ISSN-L)
  • 0140-6736
OpenAlex
W2785059893
Cited by
905
References
27
Citations by year
2026: 51 · 2025: 114 · 2024: 63 · 2023: 103 · 2022: 110 · 2021: 108 · 2020: 171 · 2019: 116 · 2018: 68
FWCI
91.09
Type
journal article
Language
en
Open access
closed
Locations
  • The Lancet (publishedVersion)
  • PubMed (publishedVersion)
Funders
GW Pharmaceuticals
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Epilepsy research and treatment
  • Health Sciences › Medicine › Pharmacology › Cannabis and Cannabinoid Research
  • Health Sciences › Medicine › Physiology › Diet and metabolism studies
Keywords
cannabidiol, Lennox-Gastaut syndrome, drop seizures, drug-resistant epilepsy, seizure frequency reduction, drug safety, adverse events, pediatric and adult patients, generalized seizures, antiepileptic drugs, treatment efficacy and safety
MeSH terms
Adolescent, Adult, Anticonvulsants, Cannabidiol, Child, Child, Preschool, Double-Blind Method, Drug Therapy, Combination, Female, Humans, Male, Middle Aged, Seizures, Treatment Outcome, Young Adult, Lennox Gastaut Syndrome

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review