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CFDA gives fast track status to Jiangsu Nhwa for epilepsy drug

By Shannon Ellis
Staff Writer

Tuesday, June 10, 2014
SHANGHAI – Jiangsu Nhwa Pharmaceutical Co. Ltd.'s DP-VPA, a modified valproic acid (VPA) treatment for epilepsy, has received fast track status from the CFDA. The drug was first licensed from D-Pharm Ltd., of Rehovot, Israel, in 2011 and holds promise for its targeted technology to be more potent and safer than other forms of VPA.

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