{"id":2729,"date":"2020-07-06T00:00:00","date_gmt":"2021-03-18T02:28:51","guid":{"rendered":"https:\/\/www.eisai.com.cn\/?p=2729"},"modified":"2021-03-18T10:28:51","modified_gmt":"2021-03-18T02:28:51","slug":"new-fine-granule-formulation-of-anti-epileptic-drug-fycompa-launched-in-japan","status":"publish","type":"post","link":"https:\/\/www.eisai.com.cn\/en\/2020\/07\/06\/new-fine-granule-formulation-of-anti-epileptic-drug-fycompa-launched-in-japan\/","title":{"rendered":"NEW FINE GRANULE FORMULATION OF ANTI-EPILEPTIC DRUG FYCOMPA\u00ae LAUNCHED IN JAPAN"},"content":{"rendered":"
Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, \u201cEisai\u201d) announced today that it has launched a new fine granule formulation of its in-house-discovered antiepileptic drug (AED) Fycompa\u00ae<\/sup>\u00a0(perampanel hydrate) in Japan on July 6, 2020. Eisai received marketing and manufacturing approval for this formulation on January 23, 2020, and the fine granule formulation was added to Japan\u2019s National Health Insurance drug price list on April 23 of the same year.<\/p>\n In Japan, it is estimated that there are approximately 1 million patients with epilepsy. While epilepsy is a disease that may occur regardless of age, it is said that incidence is particularly high in children and the elderly. This newly launched fine granule formula was developed so that even patients who have difficulty taking tablets such as children or those who have difficulties in taking tablets due to reduced swallowing ability may take this drug. Additionally, greater ability to adjust dosage to match patients\u2019 symptoms becomes possible.<\/p>\n Fycompa is a first-in-class AED discovered at Eisai\u2019s Tsukuba Research Laboratories and was developed in-house. It is a highly selective, noncompetitive AMPA receptor antagonist that reduces neuronal hyperexcitation associated with seizures by targeting glutamate activity at postsynaptic AMPA receptors. In Japan, Fycompa is currently approved for monotherapy and adjunctive use in the treatment of partial-onset seizures (with or without secondarily generalized seizures) in patients with epilepsy 4 years of age and older, as well as adjunctive treatment for primary generalized tonic-clonic seizures in patients with epilepsy 12 years of age and older.<\/p>\n With the launch of this fine granule formulation in Japan, Eisai will continue to prioritize the provision of safety information. Furthermore, Eisai will pursue its mission of delivering \u201cseizure freedom\u201d to as many patients as possible, and seek to address the diverse needs of, as well as increasing the benefits provided to, patients with epilepsy and their families.<\/p>\n <\/p>\n Media Inquiries:<\/span><\/strong> [Notes to editors]<\/b> <\/span>4)<\/span>\u00a0Price\u00a0<\/span><\/strong> 5)\u00a0<\/span>Packaging<\/span><\/strong> 6)<\/span>\u00a0Product image<\/span><\/strong><\/p>\n
\nPublic Relations Department,
\nEisai Co., Ltd.
\n+81-(0)3-3817-5120<\/p>\n
\n1. Product Information
\n1)<\/span>\u00a0Product name<\/span><\/strong>
\nFycompa\u00ae<\/sup>\u00a0Fine Granules 1%
\n
\n2)<\/span>\u00a0Generic name<\/span><\/span><\/strong>
\nperampanel hydrate<\/span>
\n
\n<\/span><\/strong>3)<\/span>\u00a0Indications\u00a0<\/strong>
\n\u00a0\u00a0\u00a0 Partial-onset seizures (including secondarily generalized seizures)<\/span>
\nAdjunctive therapy with antiepileptic drugs for tonic-clonic seizures below in patients with epilepsy showing\u00a0inadequate response to other antiepileptic drugs<\/p>\n
\n<\/span>Fycompa Fine Granules 1%: 1,068.90 yen per 1g containing 1% (package price: 106,890 yen)<\/span><\/p>\n
\nBottles of 100 g<\/span><\/p>\n