B was first diagnosed with Lennox-Gastaut syndrome (LGS) due to the frequency and severity of his seizures. He was later confirmed to have the genetic mutation that indicates Dravet's.

In addition, among Lennox-Gastaut syndrome patients in the SKYWAY trial, the drug did not significantly reduce the frequency of major motor drop seizures during the treatment period, with a ...

Lennox-Gastaut Syndrome (LGS) is a rare and severe form of childhood-onset epilepsy, characterized by multiple treatment-resistant seizure types and a high burden of comorbidities, including ...

13 May 2020 Schedule affected by COVID-19. Topic update: this appraisal has not been defined as therapeutically critical. The appraisal will therefore be paused. At this stage, we are unable to ...

Amari was born with a rare form of epilepsy known as Lennox-Gastaut syndrome (LGS), and is bound to a wheelchair, requiring around-the-clock support. After the sudden death of Tristan's mother ...

B was first diagnosed with Lennox-Gastaut syndrome (LGS) due to the frequency and severity of his seizures. He was later confirmed to have the genetic mutation that indicates Dravet's. "The only other ...

There is a simple discount patient access scheme for fenfluramine. NHS organisations can get details on the Commercial Access and Pricing (CAP) Portal. Non-NHS organisations can contact ...