StockMarketWire.com - Drug maker Hutchmed said the European Medicines Agency had validated and accepted its marketing authorization application for a drug used to treat advanced neuroendocrine tumors.

The submission followed scientific advice from the EMA's Committee for Medicinal Products for Human Use, from which it was concluded that the two positive phase III studies of surufatinib in patients with pancreatic and extra-pancreatic neuroendocrine in China, both previously reported in The Lancet Oncology, along with existing data from surufatinib in U.S. extra-pancreatic and pancreatic NET patients, could form the basis to support a MAA.

'With its launch earlier this year in China, surufatinib has given NET patients an important new therapeutic option and we now hope to soon be able to bring this important treatment to patients across the U.S. and Europe,' the company said.


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