Sprout Pharmaceuticals, Inc
14
0
0
9
Key Highlights
Risk & Performance
Pipeline Risk Assessment
Pipeline Risk Assessment
Based on historical performance
Moderate Risk
Score: 50/100
35.7%
5 terminated/withdrawn out of 14 trials
64.3%
-22.2% vs industry average
86%
12 trials in Phase 3/4
133%
12 of 9 completed trials have results
Key Signals
Enrollment Performance
Analytics
Activity Timeline
Global Presence
Clinical Trials (14)
Hypoactive Sexual Desire Disorder in Males
Role: collaborator
12 Week Safety Trial of Flibanserin in Depressed Women Taking an SSRI or SNRI With Decreased Sexual Desire and Distress
Role: lead
Uptitration Trial of Flibanserin Versus Placebo in Premenopausal Women With Hypoactive Sexual Desire Disorder
Role: lead
24-week Placebo-controlled Trial of Flibanserin Once Daily in Premenopausal Women With Hypoactive Sexual Desire Disorder
Role: lead
6-mo. Min Eff Dose of Flibanserin: 25 v 50 mg Bid v 50 mg hs v Pbo in Younger Women in NA
Role: lead
Flibanserin Evaluation Over 28 Additional Weeks in Hypoactive Sexual Desire Disorder
Role: lead
Flibanserin for the Treatment of Hypoactive Sexual Desire Disorder in Postmenopausal Women in North America
Role: lead
A One-year Safety Study of Flibanserin to Treat Pre-Menopausal Women With Hypoactive Sexual Desire Disorder (HSDD).
Role: lead
Flibanserin for the Treatment of Hypoactive Sexual Desire Disorder in Postmenopausal Women
Role: lead
Flibanserin Versus Placebo in Premenopausal Women With HSDD
Role: lead
Pharmacokinetics of Flibanserin in Postmenopausal Women With Hypoactive Sexual Desire Disorder (HSDD)
Role: lead
Fixed 100 mg Every Evening of Flibanserin vs Placebo in Premenopausal Women With Hypoactive Sexual Desire Disorder
Role: lead
A 28-week Safety Study of Flibanserin in Pre- and Postmenopausal Women With Hypoactive Sexual Desire Disorder
Role: lead
Flibanserin Randomized Withdrawal Trial in Pre-menopausal Women
Role: lead
All 14 trials loaded