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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.
Affiliation
  • Thiele E; Massachusetts General Hospital, Boston, Massachusetts.
  • Marsh E; The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Mazurkiewicz-Beldzinska M; Medical University of Gdansk, Gdansk, Poland.
  • Halford JJ; Medical University of South Carolina, Charleston, South Carolina.
  • Gunning B; Stichting Epilepsie Instellingen Nederland (SEIN), Zwolle, The Netherlands.
  • Devinsky O; NYU Comprehensive Epilepsy Center, New York City, New York.
  • Checketts D; GW Research Ltd, Cambridge, UK.
  • Roberts C; GW Research Ltd, Cambridge, UK.
Epilepsia ; 60(3): 419-428, 2019 03.
Article in En | MEDLINE | ID: mdl-30740695
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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cannabidiol / Lennox Gastaut Syndrome Type of study: Clinical_trials Aspects: Patient_preference Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Language: En Journal: Epilepsia Year: 2019 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cannabidiol / Lennox Gastaut Syndrome Type of study: Clinical_trials Aspects: Patient_preference Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Language: En Journal: Epilepsia Year: 2019 Document type: Article Country of publication: