Cannabidiol with clobazam for treating seizures associated with Lennox–Gastaut syndrome
Closed for comments This consultation ended on at Request commenting lead permission
2 Information about cannabidiol
Anticipated marketing authorisation indication | On 26 July 2019 the Committee for Medicinal Products for Human Use adopted a positive opinion and recommended the granting of a marketing authorisation for cannabidiol (Epidyolex, GW Pharma), for use as 'adjunctive therapy for seizures associated with Lennox-Gastaut syndrome (LGS) or Dravet syndrome (DS) in conjunction with clobazam, for patients 2 years of age or older'. |
Dosage in the marketing authorisation | It is administered orally as 100 mg/ml cannabidiol solution. The recommended starting dose is 2.5 mg/kg taken twice daily for 1 week. After 1 week, the dose should be increased to a maintenance dose of 5 mg/kg twice daily (10 mg/kg/day). Based on individual clinical response and tolerability, each dose can be further increased in weekly increments of 2.5 mg/kg taken twice daily up to a maximum recommended dose of 10 mg/kg twice daily (20 mg/kg/day). Any dose increases above 10 mg/kg/day should take into account individual benefit and risk. |
Price | The company has not confirmed the list price with the Department of Health and Social Care. The proposed list price is considered confidential by the company. |
How are you taking part in this consultation?
You will not be able to change how you comment later.
You must be signed in to answer questions
Question on Consultation
Question on Consultation
Question on Consultation
Question on Consultation