New Drug Decreased the Frequency, Severity of Hot Flashes

Fezolinetant reduced the frequency and severity of moderate-to-severe vasomotor symptoms (VMS), or hot flashes, associated with menopause significantly.

Fezolinetant reduced the frequency and severity of vasomotor symptoms (VMS), or hot flashes significantly in women going through menopause.

The SKYLIGHT 2 trial was a 52-week study to investigate the safety and efficacy of Fezolinetant on the frequency and severity of moderate-to-severe VMS and sleep disturbance.

‘Researchers evaluated the efficacy, safety and tolerability of Fezolinetant among women suffering from hot flashes and reported satisfactory results.’
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The mean change in patient-reported sleep disturbance, from baseline to week 12, was a key secondary endpoint in the study.

“VMS associated with menopause, which are characterized by hot flashes and/or night sweats, affect millions of women worldwide and can impact daily activities and quality of life,” said Genevieve Neal-Perry, MD, PhD, distinguished professor and chair of Obstetrics and Gynecology at the University of North Carolina School of Medicine in Chapel Hill, NC, USA.

The double-blind phase 3 study randomized 501 post-menopausal women ages 40 to 65 with an average of seven or more moderate-to-severe hot flashes/day to placebo or one of two once-daily doses of Fezolinetant — 30 mg or 45 mg — for 12 weeks.

Those on placebo were re-randomized to Fezolinetant 30 or 45 mg, and those originally on Fezolinetant remained on their dose for the remaining 40 weeks. The extension period analysis comprised 484 women.

Effectiveness of Fezolinetant:

30 and 45 mg doses of Fezolinetant were associated with a statistically significant reduction in the frequency and severity of hot flashes, which was maintained through the 52-week study period. Data support the overall safety and tolerability previously observed for Fezolinetant at the 30 and 45 mg doses.

About Hot Flash
The frequency of the hot flash can be from 1 to 2 two hot flashes a week to 10 or greater in a day. The silver lining is that it usually decreases over time.

Those who were re-randomized from placebo to Fezolinetant experienced a reduction in frequency and severity of VMS consistent with the women initially randomized to Fezolinetant. The treatment also reduced sleep disturbances as assessed by Patient-Reported Outcomes Measurement Information System Sleep Disturbance.

“These results, along with other Fezolinetant studies, will be important in understanding the use of this oral nonhormonal selective NK3 receptor antagonist to treat moderate-to-severe VMS associated with menopause,” Neal-Perry said.

Source-Medindia