EU panel recommends approval of Alexza's Adasuve

Alexza says European Union panel recommends approval for its agitation drug Adasuve

Associated Press

MOUNTAIN VIEW, Calif. (AP) -- Alexza Pharmaceuticals Inc. said Friday that a panel of European Union regulators recommended marketing approval for its drug Adasuve, an inhaled treatment for agitation in patients with schizophrenia or bipolar disorder.

Shares of Alexza rose about 10 percent in morning trading.

The company and its partner Grupo Ferrer Internacional said the advisory panel recommended that Adasuve be approved for the control of mild to moderate agitation in adult patients. The panel recommended that patients receive regular treatment as soon as their agitation symptoms are under control, and that Adasuve be administered only at a hospital under supervision of a health care professional.

Alexza does not have any products on the market, and Adasuve is its most advanced drug candidate. If the drug is approved in Europe, the companies will be able to market it in all 27 EU countries and Iceland, Liechtenstein, and Norway. A decision on the drug is expected in the first quarter of 2013.

Privately held Grupo Ferrer is based in Barcelona, Spain.

Shares of Alexza Pharmaceuticals added 51 cents, or 9.7 percent, to $5.75 in morning trading. The stock has traded in a 52-week range of $2.55 to $10.

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