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      Efficacy and safety of elinzanetant, a selective neurokinin-1,3 receptor antagonist for vasomotor symptoms: a dose-finding clinical trial (SWITCH-1)

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          Abstract

          SWITCH-1 was a phase 2b study assessing the efficacy, safety, and dose-response relationship of elinzanetant, a selective neurokinin-1,3 receptor antagonist, for the treatment of vasomotor symptoms. Elinzanetant resulted in significant and clinically meaningful improvements in vasomotor symptoms, sleep and quality of life and was well tolerated across all doses.

          Abstract

          Objective

          Neurokinin (NK)-3 and NK-1 receptors have been implicated in the etiology of vasomotor symptoms (VMS) and sleep disturbances associated with menopause. This phase 2b, adaptive, dose-range finding study aimed to assess the efficacy and safety of multiple doses of elinzanetant (NT-814), a selective NK-1,3 receptor antagonist, in women experiencing VMS associated with menopause, and investigate the impact of elinzanetant on sleep and quality of life.

          Methods

          Postmenopausal women aged 40 to 65 years who experienced seven or more moderate-to-severe VMS per day were randomized to receive elinzanetant 40, 80, 120, or 160 mg or placebo once daily using an adaptive design algorithm. Coprimary endpoints were reduction in mean frequency and severity of moderate-to-severe VMS at weeks 4 and 12. Secondary endpoints included patient-reported assessments of sleep and quality of life.

          Results

          Elinzanetant 120 mg and 160 mg achieved reductions in VMS frequency versus placebo from week 1 throughout 12 weeks of treatment. Least square mean reductions were statistically significant versus placebo at both primary endpoint time points for elinzanetant 120 mg (week 4: −3.93 [SE, 1.02], P < 0.001; week 12: −2.95 [1.15], P = 0.01) and at week 4 for elinzanetant 160 mg (−2.63 [1.03]; P = 0.01). Both doses also led to clinically meaningful improvements in measures of sleep and quality of life. All doses of elinzanetant were well tolerated.

          Conclusions

          Elinzanetant is an effective and well-tolerated nonhormone treatment option for postmenopausal women with VMS and associated sleep disturbance. Elinzanetant also improves quality of life in women with VMS.

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          Most cited references45

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          Psychometric evaluation of the Pittsburgh Sleep Quality Index.

          The Pittsburgh Sleep Quality Index (PSQI) measures sleep quality and disturbance retrospectively over a 1-month period using self-reports. Although the PSQI has been used in a variety of populations, published psychometric data are limited. The goal of this study was to examine psychometric properties of the PSQI among four populations: bone marrow transplant patients (n=155); renal transplant patients (n=56); women with breast cancer (n=102); and women with benign breast problems (n=159). Results supported PSQI internal consistency reliability and construct validity. Cronbach's alphas were 0.80 across groups and correlations between global and component scores were moderate to high. PSQI scores were moderately to highly correlated with measures of sleep quality and sleep problems, and poorly correlated with unrelated constructs. Individuals with sleep problems, poor sleep quality, and sleep restlessness had significantly higher PSQI scores in comparison to individuals without such problems.
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            Minireview: kisspeptin/neurokinin B/dynorphin (KNDy) cells of the arcuate nucleus: a central node in the control of gonadotropin-releasing hormone secretion.

            Recently, a subset of neurons was identified in the arcuate nucleus of the hypothalamus that colocalize three neuropeptides, kisspeptin, neurokinin B, and dynorphin, each of which has been shown to play a critical role in the central control of reproduction. Growing evidence suggests that these neurons, abbreviated as the KNDy subpopulation, are strongly conserved across a range of species from rodents to humans and play a key role in the physiological regulation of GnRH neurons. KNDy cells are a major target for steroid hormones, form a reciprocally interconnected network, and have direct projections to GnRH cell bodies and terminals, features that position them well to convey steroid feedback control to GnRH neurons and potentially serve as a component of the GnRH pulse generator. In addition, recent work suggests that alterations in KNDy cell peptides may underlie neuroendocrine defects seen in clinical reproductive disorders such as polycystic ovarian syndrome. Taken together, this evidence suggests a key role for the KNDy subpopulation as a focal point in the control of reproductive function in health and disease.
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              Duration of menopausal vasomotor symptoms over the menopause transition.

              The expected duration of menopausal vasomotor symptoms (VMS) is important to women making decisions about possible treatments.
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                Author and article information

                Contributors
                Journal
                Menopause
                Menopause
                MENO
                Menopause (New York, N.y.)
                Lippincott Williams & Wilkins
                1072-3714
                1530-0374
                March 2023
                30 January 2023
                : 30
                : 3
                : 239-246
                Affiliations
                From the [1 ]George Washington University, IntimMedicine Specialists, Washington, DC
                [2 ]MRC Centre for Reproductive Health, Queens Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom
                [3 ]NeRRe Therapeutics, Stevenage, United Kingdom
                [4 ]Cytel, Waltham, MA
                [5 ]Bayer CC AG, Basel, Switzerland
                [6 ]Brigham and Women's Hospital, Harvard Medical School, Boston, MA
                [7 ]Queen Charlotte's and Chelsea and Westminster Hospitals, Imperial College, London, United Kingdom
                [8 ]Bayer AG, Berlin, Germany.
                Author notes
                [*]Address correspondence to: James A. Simon, MD, IntimMedicine Specialists, 1850 M St, NW, Suite 450, Washington, DC 20036. E-mail: jsimon@ 123456intimmedicine.com
                Article
                MENO_220155 00003
                10.1097/GME.0000000000002138
                9970022
                36720081
                b710f205-4aa8-47a7-90ff-3724279c81b8
                © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The North American Menopause Society.

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.

                History
                : 29 September 2022
                : 26 October 2022
                : 26 October 2022
                Categories
                Original Studies
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                kndy neuron,menopause,neurokinin b,neurokinin-1,3 receptor antagonist,substance p,vasomotor symptoms

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