A hormonal therapy for menopausal women with MS: A phase Ib/IIa randomized controlled trial

Introduction: Most women develop MS before menopause. Menopausal hot flashes can worsen MS symptoms, and could be relieved with hormone therapy. Our objective was to evaluate feasibility, tolerability and symptom response of Duavee® (bazedoxifene + conjugated estrogen) in a Phase Ib/IIa double-blind...

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Main Authors: Anderson, A. (Author), Bove, R. (Author), Carleton, M. (Author), Chan, J.R (Author), Cooper, J. (Author), Cree, B.A.C (Author), Gelfand, J.M (Author), Graves, J.S (Author), Green, A.J (Author), Henry, R.G (Author), Hills, N.K (Author), Joffe, H. (Author), Krysko, K.M (Author), Rankin, K.A (Author), Rowles, W. (Author), Rush, G. (Author), Zamvil, S.S (Author)
Format: Article
Language:English
Published: Elsevier B.V. 2022
Subjects:
Online Access:View Fulltext in Publisher
LEADER 02863nam a2200385Ia 4500
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008 220420s2022 CNT 000 0 und d
020 |a 22110348 (ISSN) 
245 1 0 |a A hormonal therapy for menopausal women with MS: A phase Ib/IIa randomized controlled trial 
260 0 |b Elsevier B.V.  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1016/j.msard.2022.103747 
520 3 |a Introduction: Most women develop MS before menopause. Menopausal hot flashes can worsen MS symptoms, and could be relieved with hormone therapy. Our objective was to evaluate feasibility, tolerability and symptom response of Duavee® (bazedoxifene + conjugated estrogen) in a Phase Ib/IIa double-blind randomized controlled clinical trial. Methods: We randomized 24 peri/postmenopausal women with MS and symptomatic hot flashes 1:1 to Duavee® versus placebo. Evaluations occurred at baseline and 2 months. Results: Groups were balanced for age (mean 51.2 ± 3.6 years), EDSS [median 3 (IQR:2.5, 4.5)], and MS duration. 21/24 participants completed the study. Feasibility: Enrollment was protracted (34 months), partially due to concerns about hormone therapy safety. Tolerability: treatment group participants reported greater satisfaction and fewer missed doses; one participant (placebo) developed new MRI lesions; liver function testing remained normal for all patients. Symptoms: Hot Flash Related Daily Interference scale at 2 months was lower in treatment vs. placebo group [median (IQR) of 4 (0.5, 14) vs. 9 (0, 33)]. Between-group differences were not statistically significant. Conclusion: Despite perceived benefits in MS, estrogens have perceived risks that represent a hurdle to enrollment. With appropriate education and screening of participants, the favorable study retention (87%) and treatment satisfaction observed in the current study support the feasibility of a longer, powered trial to evaluate whether a proven treatment for menopausal symptoms, Duavee®, could also improve MS-related function in menopausal women with MS. © 2022 The Author(s) 
650 0 4 |a Estrogen 
650 0 4 |a Gender 
650 0 4 |a Hormone therapy 
650 0 4 |a Menopause 
650 0 4 |a SERM 
700 1 0 |a Anderson, A.  |e author 
700 1 0 |a Bove, R.  |e author 
700 1 0 |a Carleton, M.  |e author 
700 1 0 |a Chan, J.R.  |e author 
700 1 0 |a Cooper, J.  |e author 
700 1 0 |a Cree, B.A.C.  |e author 
700 1 0 |a Gelfand, J.M.  |e author 
700 1 0 |a Graves, J.S.  |e author 
700 1 0 |a Green, A.J.  |e author 
700 1 0 |a Henry, R.G.  |e author 
700 1 0 |a Hills, N.K.  |e author 
700 1 0 |a Joffe, H.  |e author 
700 1 0 |a Krysko, K.M.  |e author 
700 1 0 |a Rankin, K.A.  |e author 
700 1 0 |a Rowles, W.  |e author 
700 1 0 |a Rush, G.  |e author 
700 1 0 |a Zamvil, S.S.  |e author 
773 |t Multiple Sclerosis and Related Disorders