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Sunovion’s once-daily epilepsy drug Aptiom debuts in US

Sunovion’s once-daily epilepsy drug Aptiom debuts in US

FDA-approves-Aptiom-to-treat-seizures-in-adultsUSA-based Sunovion Pharmaceuticals, a subsidiary of Japanese drug major Dainippon Sumitomo (TYO: 4506), has launched its Aptiom (eslicarbazepine acetate), a once-daily antiepileptic drug (AED) indicated for use as adjunctive treatment of partial-onset seizures, is now available by prescription in pharmacies across the USA.

Aptiom, a voltage-gated sodium channel blocker, is a new chemical entity approved by the US Food and Drug Administration late last year (The Pharma Letter November 9, 2013), and is available in four tablet strengths (200mg, 400mg, 600mg and 800mg), which can be taken whole or crushed, with or without food. Aptiom is not classified as a controlled substance by the FDA.

“The availability of APTIOM is a significant milestone for Sunovion. Aptiom not only marks our entry into the epilepsy therapeutic area, but also reinforces our commitment to improving the lives of people living with CNS disorders,” said Rick Russell, executive vice president and chief commercial officer at Sunovion

“Epilepsy is a serious condition that not only affects the people who suffer from seizures, but also their family, caregivers and friends,” commented Michael Sperling, Professor of Neurology at Thomas Jefferson University and director of the Jefferson Comprehensive Epilepsy Center in Philadelphia, Pennsylvania, adding: “Approximately one-third of those with epilepsy still have inadequate seizure control despite treatment, so we need new therapies. Aptiom is a welcome addition to our therapeutic toolkit that may help some patients.”

Sunovion Support, a prescription assistance program, may help people who are eligible to receive their medication at no cost, said Sunovion

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