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Cannabidiol in patients with Lennox‐Gastaut syndrome: Interim analysis of an open‐label extension study

OBJECTIVE: Patients with Lennox‐Gastaut syndrome (LGS) who completed 1 of 2 randomized, double‐blind, placebo‐controlled trials of add‐on cannabidiol (CBD) (GWPCARE3, NCT02224560 or GWPCARE4, NCT02224690) were invited to enroll in an open‐label extension (OLE) study evaluating the long‐term safety a...

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Autores principales: Thiele, Elizabeth, Marsh, Eric, Mazurkiewicz‐Beldzinska, Maria, Halford, Jonathan J., Gunning, Boudewijn, Devinsky, Orrin, Checketts, Daniel, Roberts, Claire
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850399/
https://www.ncbi.nlm.nih.gov/pubmed/30740695
http://dx.doi.org/10.1111/epi.14670
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author Thiele, Elizabeth
Marsh, Eric
Mazurkiewicz‐Beldzinska, Maria
Halford, Jonathan J.
Gunning, Boudewijn
Devinsky, Orrin
Checketts, Daniel
Roberts, Claire
author_facet Thiele, Elizabeth
Marsh, Eric
Mazurkiewicz‐Beldzinska, Maria
Halford, Jonathan J.
Gunning, Boudewijn
Devinsky, Orrin
Checketts, Daniel
Roberts, Claire
author_sort Thiele, Elizabeth
collection PubMed
description OBJECTIVE: Patients with Lennox‐Gastaut syndrome (LGS) who completed 1 of 2 randomized, double‐blind, placebo‐controlled trials of add‐on cannabidiol (CBD) (GWPCARE3, NCT02224560 or GWPCARE4, NCT02224690) were invited to enroll in an open‐label extension (OLE) study evaluating the long‐term safety and efficacy of CBD (GWPCARE5, NCT02224573). Herein we present an interim analysis of the safety, efficacy, and patient‐reported outcomes from this trial. METHODS: Patients received a pharmaceutical formulation of highly purified CBD oral solution (Epidiolex; 100 mg/mL), titrated from 2.5 to 20 mg/kg/d over a 2‐week titration period, in addition to their existing medications. Doses could be reduced if not tolerated or increased up to 30 mg/kg/d if thought to be of benefit. RESULTS: This interim analysis was based on a November 2016 data cut. Of 368 patients who completed treatment in GWPCARE3 and GWPCARE4, 366 (99.5%) enrolled in the OLE study (GWPCARE5). Median treatment duration was 38 weeks at a mean modal dose of 23 mg/kg/d. Most patients (92.1%) experienced adverse events (AEs), primarily of mild (32.5%) or moderate (43.4%) severity. The most common AEs were diarrhea (26.8%), somnolence (23.5%), and convulsion (21.3%). Thirty‐five patients (9.6%) discontinued treatment due to AEs. Liver transaminase elevations were reported in 37 patients (10.1%), of whom 29 were receiving concomitant valproic acid; 34 cases resolved spontaneously or with dose modification of CBD or concomitant medication. Median reduction from baseline in drop seizure frequency (quantified monthly over 12‐week periods) ranged from 48% to 60% through week 48. Median reduction in monthly total seizure frequency ranged from 48% to 57% across all 12‐week periods through week 48. Eighty‐eight percent of patients/caregivers reported an improvement in the patient's overall condition per the Subject/Caregiver Global Impression of Change scale. SIGNIFICANCE: In this study, long‐term add‐on CBD treatment had an acceptable safety profile in patients with LGS and led to sustained reductions in seizures.
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spelling pubmed-68503992019-11-18 Cannabidiol in patients with Lennox‐Gastaut syndrome: Interim analysis of an open‐label extension study Thiele, Elizabeth Marsh, Eric Mazurkiewicz‐Beldzinska, Maria Halford, Jonathan J. Gunning, Boudewijn Devinsky, Orrin Checketts, Daniel Roberts, Claire Epilepsia Full‐length Original Research OBJECTIVE: Patients with Lennox‐Gastaut syndrome (LGS) who completed 1 of 2 randomized, double‐blind, placebo‐controlled trials of add‐on cannabidiol (CBD) (GWPCARE3, NCT02224560 or GWPCARE4, NCT02224690) were invited to enroll in an open‐label extension (OLE) study evaluating the long‐term safety and efficacy of CBD (GWPCARE5, NCT02224573). Herein we present an interim analysis of the safety, efficacy, and patient‐reported outcomes from this trial. METHODS: Patients received a pharmaceutical formulation of highly purified CBD oral solution (Epidiolex; 100 mg/mL), titrated from 2.5 to 20 mg/kg/d over a 2‐week titration period, in addition to their existing medications. Doses could be reduced if not tolerated or increased up to 30 mg/kg/d if thought to be of benefit. RESULTS: This interim analysis was based on a November 2016 data cut. Of 368 patients who completed treatment in GWPCARE3 and GWPCARE4, 366 (99.5%) enrolled in the OLE study (GWPCARE5). Median treatment duration was 38 weeks at a mean modal dose of 23 mg/kg/d. Most patients (92.1%) experienced adverse events (AEs), primarily of mild (32.5%) or moderate (43.4%) severity. The most common AEs were diarrhea (26.8%), somnolence (23.5%), and convulsion (21.3%). Thirty‐five patients (9.6%) discontinued treatment due to AEs. Liver transaminase elevations were reported in 37 patients (10.1%), of whom 29 were receiving concomitant valproic acid; 34 cases resolved spontaneously or with dose modification of CBD or concomitant medication. Median reduction from baseline in drop seizure frequency (quantified monthly over 12‐week periods) ranged from 48% to 60% through week 48. Median reduction in monthly total seizure frequency ranged from 48% to 57% across all 12‐week periods through week 48. Eighty‐eight percent of patients/caregivers reported an improvement in the patient's overall condition per the Subject/Caregiver Global Impression of Change scale. SIGNIFICANCE: In this study, long‐term add‐on CBD treatment had an acceptable safety profile in patients with LGS and led to sustained reductions in seizures. John Wiley and Sons Inc. 2019-02-11 2019-03 /pmc/articles/PMC6850399/ /pubmed/30740695 http://dx.doi.org/10.1111/epi.14670 Text en © 2019 The Authors. Epilepsia published by Wiley Periodicals, Inc. on behalf of International League Against Epilepsy This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Full‐length Original Research
Thiele, Elizabeth
Marsh, Eric
Mazurkiewicz‐Beldzinska, Maria
Halford, Jonathan J.
Gunning, Boudewijn
Devinsky, Orrin
Checketts, Daniel
Roberts, Claire
Cannabidiol in patients with Lennox‐Gastaut syndrome: Interim analysis of an open‐label extension study
title Cannabidiol in patients with Lennox‐Gastaut syndrome: Interim analysis of an open‐label extension study
title_full Cannabidiol in patients with Lennox‐Gastaut syndrome: Interim analysis of an open‐label extension study
title_fullStr Cannabidiol in patients with Lennox‐Gastaut syndrome: Interim analysis of an open‐label extension study
title_full_unstemmed Cannabidiol in patients with Lennox‐Gastaut syndrome: Interim analysis of an open‐label extension study
title_short Cannabidiol in patients with Lennox‐Gastaut syndrome: Interim analysis of an open‐label extension study
title_sort cannabidiol in patients with lennox‐gastaut syndrome: interim analysis of an open‐label extension study
topic Full‐length Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850399/
https://www.ncbi.nlm.nih.gov/pubmed/30740695
http://dx.doi.org/10.1111/epi.14670
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