EU green light for Zogenix’s Fintepla
Oral solution approved to treat seizures associated with Dravet syndrome
Read Moreby Lucy Parsons | Dec 23, 2020 | News | 0
Oral solution approved to treat seizures associated with Dravet syndrome
Read Moreby Selina McKee | Jun 24, 2020 | News | 0
The cannabinoid has been reclassified as a Schedule 5 medicine meaning that it can be dispensed more easily
Read Moreby Selina McKee | Sep 28, 2018 | News | 0
GW Pharmaceuticals and its subsidiary Greenwich Biosciences are gearing up to launch Epidiolex in the US after drug enforcement officials re-classified the cannabis-based medicine to the lowest restriction.
Read Moreby Selina McKee | Aug 24, 2018 | News | 0
US regulators have approved Biocodex’ Diacomit for the treatment of seizures associated with Dravet syndrome (DS), a rare and difficult to treat form of epilepsy.
Read Moreby Selina McKee | Jul 12, 2018 | News | 0
Zogenix has revealed top-line results from a second late-stage trial of its investigational Dravet syndrome drug ZX008, showing a significant reduction in seizures.
Read Moreby Selina McKee | Jun 26, 2018 | News | 0
GW Pharmaceuticals’ Epidiolex has become the first cannabinoid prescription medicine to be approved in the US, winning clearance to treat two rare forms of epilepsy.
Read Moreby Selina McKee | Apr 20, 2018 | News | 0
As expected, an FDA advisory panel has backed approval of GW Pharmaceuticals/Greenwich Bioscience’s Epidiolex for treating seizures associated with Lennox-Gastaut syndrome and Dravet syndrome.
Read Moreby Selina McKee | Oct 31, 2017 | News | 0
GW Pharmaceuticals and its US subsidiary Greenwich Biosciences have completed the rolling submission of Epidiolex as adjunctive treatment of seizures associated with Lennox-Gastaut syndrome and Dravet syndrome, two difficult-to-treat forms of childhood-onset epilepsy.
Read Moreby Selina McKee | May 25, 2017 | News | 0
GW Pharmaceuticals is on the brink of filing its cannabis-derived therapy Epidiolex in the US as another late-stage study highlights the drug’s efficacy in treating Dravet Syndrome, a rare and severe type of epilepsy.
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