HATFIELD, England, November 6, 2014 /PRNewswire/ --
Eisai announces with utmost disappointment that the German Federal Joint Committee (G-BA) has decided that the additional benefit for new generation anti-epileptic drug (AED) Fycompa (perampanel) has not been proven, when compared to conventional AEDs as defined by the G-BA.[1] The decision, based on methodological rather than clinical considerations, ignores the demands of the German Epilepsy Association (DE) and other epilepsy patient advocacy groups to recognise the additional benefit seen in practical applications as well as in studies.[2] The decision also ignores the recommendations of the German Society of Epileptology (DGfE) to assess the additional benefit of new AEDs.
The efficacy and tolerability of adjunctive perampanel in the treatment of partial onset seizures in real world clinical practice has been demonstrated by a multi-centre, six-month observational study from nine epilepsy centres in Germany and Austria. The results show that half of the 281 people with highly refractory epilepsy treated with perampanel experienced at least a 50% reduction in seizure frequency and up to 15% became seizure free during the observation period.[3] "We are utterly disappointed by the decision of the German Joint Federal Committee (G-BA) not to recognise the additional benefit of perampanel and are totally unable to understand their reasons. It has been demonstrated that there are patients who experience significantly fewer seizures or have even become seizure-free on Fycompa. With this decision, the G-BA is denying people with epilepsy for whom no current treatment has been successful, the benefits of medical progress," said Stefan Conrad, President of the German Epilepsy Association.
Perampanel is the first and only licensed AED to selectively target AMPA receptors, a protein in the brain which plays a critical role in the spread of seizures.[4] This mechanism of action is different to all other, currently available AEDs. In addition, perampanel has the advantage of convenient, once-daily dosing at bedtime[5] and significantly, since its launch, is the only new-generation partial epilepsy treatment approved to treat adolescents (12 years and older) with epilepsy. Perampanel is available in more than 35 countries worldwide.
"To ignore the considerable real world experience data available in Germany for perampanel is a mistake. As a clinician, I understand the impact that epilepsy can have on people and their families and the importance of being able to access new treatment options. I have personally observed the potential of perampanel for my long-time refractory epilepsy patients and hoped that the G-BA would also recognise this potential," commented Professor Bernhard Steinhoff from Epilepsiezentrum Kork, Kehl-Kork, Germany.
Epilepsy is one of the most common neurological conditions in the world[6] and over half a million people in Germany live with the condition.[7] The successful treatment of partial onset seizures remains a challenge; up to a third of people with epilepsy do not achieve seizure freedom despite appropriate therapy with AEDs.[8]
"We are dismayed by the G-BA's decision and what appears to be the lack of consideration displayed for the some 4,000 people in Germany with epilepsy who have already benefited from the treatment with perampanel. All European countries show a flexible, patient-oriented approach to their decision making process, but on this occasion the stringent German system has failed to listen to the patients it should help and the clinical experts treating people with refractory epilepsy. We will strive to continue talks with the G-BA to find a solution for the people who depend on new epilepsy treatments such as perampanel," commented Gary Hendler, President & CEO, Eisai EMEA.
Perampanel was approved by the European Commission in 2012 and is indicated for the adjunctive treatment of partial onset seizures, with or without secondarily generalised seizures, in patients with epilepsy aged 12 years and older.[5] Eisai submitted a Marketing Authorisation Application to the European Commission for perampanel as an adjunctive treatment of primary generalised tonic-clonic seizures (PGTC) in August 2014.
Eisai is committed to the therapeutic area of epilepsy and to addressing the unmet medical needs of people with epilepsy and their families, an integral part of our human health care (hhc) mission. Eisai is proud to currently market more epilepsy products in EMEA than any other company.
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Eisai Speechless With G-BA Decision Which Ignores the Demand of Epilepsy Patients and Denies the Proven Additional ...