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Myovant, Pfizer Offer Update On Supplemental New Drug Application For MYFEMBREE For Mgmt. Of Moderate To Severe Pain Associated With Endometriosis: FDA Extended Review Period, New PDUFA Date Goal Is Aug. 6, 2022

Myovant Sciences (NYSE:MYOV) and Pfizer Inc. (NYSE:PFE) announced today that the U.S. Food and Drug Administration (FDA) has extended the review period for the supplemental New Drug Application (sNDA) for MYFEMBREE®

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Myovant Investment Sumitomo Pharma’s Urovant Sciences Highlights Publication Of EMPOWUR Trial Subgroup Analysis Showing Similar Efficacy Of GEMTESA In Dry, Wet Overactive Bladder Populations In ‘Int’l. Journal Of Clinical Practice’

Post-hoc analysis indicates significant reductions in urgency episodes and micturitions in patients treated with GEMTESA vs. placebo in both types of overactive bladder (OAB) Article appears in the peer-reviewed

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