Hatfield, England (ots/PRNewswire) - Child friendly formulation will help treatment of orphan syndrome LGS a severe form of childhood epilepsy Inovelon(R) (rufinamide) oral suspension for adjunctive (add-on) treatment of seizures associated with Lennox-Gastaut syndrome (LGS) in children four years and older is launched today in France. The new formulation of the orphan drug has been developed as a child friendly drinkable liquid to aid the administration of treatment. LGS is one of the most severe forms of childhood epilepsy accounting for four per cent of epilepsy in children.[1] The rare but serious condition affects approximately 11,000 children across Western Europe and the peak age of onset is between ages three and five.[2] The condition is characterised by multiple daily seizures and people with the condition can have up to 70 seizures a day.[3] Two in three individuals with LGS experience at least one prolonged period of seizure causing confusion and a loss of alertness lasting from hours to weeks.[4] Most children with LGS also experience developmental problems leading to impaired intellectual functioning and behavioural issues.[5] LGS is one of the most drug-resistant forms of childhood epilepsy and effective management of the condition is often very difficult, reiterating the importance for … Continue reading
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