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Resurrected Flibanserin Filing Tests FDA Position On Female Sexual Desire Disorders

This article was originally published in Pharmaceutical Approvals Monthly

Executive Summary

With a decision by FDA on a new filing for flibanserin possible by the fall, Sprout hopes to gain the first U.S. approval for treating women with low sexual desire. Meanwhile, Palatin forges on to Phase III with its female sexual desire disorder drug bremelanotide after discussing endpoints with FDA.

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