Thursday, August 6, 2009

Abstral file submitted to the FDA for approval in the USA

August 6, 2009 - Orexo AB today announces that its partner, UK-based international specialty pharmaceutical company ProStrakan Group plc, has submitted the New Drug Application (NDA) for Abstral™ (rapinyl)(for the treatment of breakthrough cancer pain in opioid-tolerant patients) to the US FDA.

the details can be read here.

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