Fezolinetant effect on vasomotor symptoms due to menopause in women unsuitable for hormone therapy.

IF 2.4 4区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Current Medical Research and Opinion Pub Date : 2025-02-01 Epub Date: 2025-03-05 DOI:10.1080/03007995.2025.2470752
Nanette Santoro, Genevieve Neal-Perry, Petra Stute, Martin Blogg, Shayna Mancuso, Antonia Morga, Faith D Ottery, Emad Siddiqui
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引用次数: 0

Abstract

Objective: To assess efficacy and safety of fezolinetant in women unsuitable for hormone therapy (HT), using pooled SKYLIGHT 1 and 2 data.

Methods: SKYLIGHT 1 and 2 were double-blind, placebo-controlled studies of once-daily placebo, fezolinetant 30 mg or 45 mg for 12 weeks in women aged ≥40-≤65 years with moderate to severe vasomotor symptoms (VMS; average ≥7 hot flashes/d), followed by a double-blind, non-controlled extension period for 40 weeks. The HT unsuitable group comprised 4 mutually exclusive subgroups, categorized using the following hierarchy: contraindicated; caution; stopper for medical concerns; averse.

Results: A total of 1,022 participants received ≥1 dose of study medication (fezolinetant 30 mg, n = 339; fezolinetant 45 mg, n = 341). Improvement was seen for the HT unsuitable group in frequency and severity of moderate to severe VMS from baseline to weeks 4 and 12 (mean difference [95% CI] fezolinetant 45 mg vs. placebo: -2.55; 95% CI, -3.29 to -1.80; p < .001 at week 12). Sleep disturbance, measured by Patient-Reported Outcomes Measurement Information System Sleep Disturbance-Short Form 8b (PROMIS-SD SF 8b) total score, improved by weeks 4 and 12 (mean difference [95% CI] fezolinetant 45 mg vs. placebo at week 12: -1.60; 95% CI, -2.71 to -0.49; p = .005). Fezolinetant was well tolerated in the HT unsuitable group, with treatment-emergent adverse events in 39.4% of participants receiving fezolinetant 45 mg vs. 41.3% receiving placebo.

Conclusion: This pooled analysis demonstrated efficacy of fezolinetant vs. placebo in reducing frequency and severity of VMS due to menopause in participants unsuitable for HT.

Clinical trial registration: SKYLIGHT 1 - ClinicalTrials.gov, NCT04003155; https://clinicaltrials.gov/ct2/show/NCT04003155 (conducted between July 2019 and August 2021); SKYLIGHT 2 - ClinicalTrials.gov, NCT04003142; https://clinicaltrials.gov/ct2/show/NCT04003142 (conducted between July 2019 and April 2021).

非唑啉奈坦对不适宜激素治疗的绝经期妇女血管舒缩症状的影响。
目的:利用合并的天窗1和天窗2数据,评价非唑啉坦对不适宜激素治疗(HT)妇女的疗效和安全性。方法:天光1和天光2是双盲、安慰剂对照研究,在年龄≥40-≤65岁有中重度血管舒缩症状(VMS;平均≥7次潮热/d),随后是双盲、非对照延长期40周。HT不适宜组包括4个相互排斥的亚组,按以下等级分类:禁忌症;谨慎;出于医疗考虑的塞子;厌恶。结果:共有1,022名参与者接受了≥1剂量的研究药物(非唑啉奈坦30 mg, n = 339;Fezolinetant 45 mg, n = 341)。从基线到第4周和第12周,HT不适合组在中度至重度VMS的频率和严重程度上有所改善(fezolinetant 45 mg与安慰剂的平均差异[95% CI]: -2.55;95% CI, -3.29 ~ -1.80;第12周P < 0.001)。睡眠障碍,由患者报告结果测量信息系统睡眠障碍-短表8b(承诺- sd SF 8b)总分测量,在第4周和第12周得到改善(fezolinetant 45 mg与安慰剂在第12周的平均差异[95% CI]: -1.60;95% CI, -2.71 ~ -0.49;P = .005)。非唑啉奈坦在HT不适合组中耐受性良好,接受非唑啉奈坦45 mg的参与者中有39.4%出现治疗不良事件,而接受安慰剂的参与者中有41.3%出现治疗不良事件。结论:本汇总分析表明,fezolinetant与安慰剂相比,在不适合HT治疗的患者中,可降低绝经期VMS的发生频率和严重程度。临床试验注册:天窗1 - ClinicalTrials.gov, NCT04003155;https://clinicaltrials.gov/ct2/show/NCT04003155(2019年7月至2021年8月进行);天光2 - ClinicalTrials.gov, NCT04003142;https://clinicaltrials.gov/ct2/show/NCT04003142(2019年7月至2021年4月进行)。
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来源期刊
Current Medical Research and Opinion
Current Medical Research and Opinion 医学-医学:内科
CiteScore
4.40
自引率
4.30%
发文量
247
审稿时长
3-8 weeks
期刊介绍: Current Medical Research and Opinion is a MEDLINE-indexed, peer-reviewed, international journal for the rapid publication of original research on new and existing drugs and therapies, Phase II-IV studies, and post-marketing investigations. Equivalence, safety and efficacy/effectiveness studies are especially encouraged. Preclinical, Phase I, pharmacoeconomic, outcomes and quality of life studies may also be considered if there is clear clinical relevance
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