The LSM change with elinzanetant 120 mg versus placebo from baseline in VMS frequency indicated a significant decrease at week 4 (–3.93 VMS/day, p < 0.001) and week 12 (–2.95 VMS/day, p = 0.01); reductions in VMS severity followed a similar trend (–0.51 at week 4 and –0.56 at week 12), but did not reach statistical significance (coprimary endpoints).
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