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Timing Better For Sprout’s Latest Shot At First Female Sex Desire Drug

 
• By Emily Hayes

Sprout’s flibanserin resubmission should have an easier time at FDA, as experts backed key aspects of trial design used in flibanserin studies and patients sought treatment options at last year’s workshop on female sexual dysfunction.

Sprout Pharmaceuticals Inc. has submitted a new regulatory package to FDA for its centrally-acting flibanserin in what the company hopes is now a better regulatory climate for drugs aimed at hypoactive sexual desire disorder.

Privately held Sprout announced Feb. 17 that it had resubmitted the NDA for flibanserin in premenopausal HSDD

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