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BI Drops Flibanserin; BioSante Gets Excited

This article was originally published in The Pink Sheet Daily

Executive Summary

Boehringer Ingelheim shuts down development of its female desire drug due to complications in the regulatory process.

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Resurrected Flibanserin Filing Tests FDA Position On Female Sexual Desire Disorders

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.

Resurrected Flibanserin Filing Tests FDA Position On Female Sexual Desire Disorders

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.

BioSante LibiGel Study Design Changes Could Yield Better Results For Sexual Dysfunction

Two more Phase III studies for the hypoactive sexual desire disorder therapy is the firm’s best financial investment, CEO Simes says, because the revised design is expected to eliminate the greater-than-expected placebo response that derailed the previous studies.

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