Article: Lilly Submits Cymbalta(R) Supplemental New Drug Application for Generalized Anxiety Disorder.

Four Million Americans are Diagnosed Annually with Generalized Anxiety Disorder

INDIANAPOLIS, May 9 /PRNewswire-FirstCall/ -- Eli Lilly and Company today announced the recent submission of a supplemental New Drug Application (sNDA) to the U.S. Food and Drug Administration (FDA) for Cymbalta(R) (duloxetine HCl) for the treatment of generalized anxiety disorder.

Cymbalta is already approved in the United States for the treatment of major depressive disorder and the management of diabetic peripheral neuropathic pain, both in adults. Lilly is also conducting Phase III studies on Cymbalta and its effects on fibromyalgia, a chronic, often debilitating pain ...

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