Timely addition to Bayer’s case for elinzanetant in hot flashes
Germany’s Bayer (BAYN: DE) has presented results from the Phase III OASIS 3 study further supporting efficacy data and sustained safety data of elinzanetant over 52 weeks in vasomotor symptoms (VMS).
Only last month, Bayer submitted a filing to the US Food and Drug Administration (FDA) for approval to market elinzanetant for VMS, commonly known as hot flashes and associated with menopause.
Hot flashes are a leading cause for women to seek medical attention during menopause, and are expected to impact 1.2 billion women worldwide by 2030.
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