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Letters to the Editor

Fezolinetant for VMS: a balanced view on efficacy and safety needed

Jonathan Douxfilsa Department of Pharmacy, Research Unit in Clinical Pharmacology and Toxicology, Namur Research Institute for Life Sciences (NARILIS), Faculty of Medicine, University of Namur, Namur, Belgium;b QUALIblood s.a., Namur, Belgium;c Department of Biological Hematology, CHU Clermont-Ferrand, Hôpital Estaing, Clermont-Ferrand, FranceCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0002-7644-5298
ORCID Icon,
Charlotte Beaudartd Department of Biomedical Sciences, Research Unit in Clinical Pharmacology and Toxicology, Namur Research Institute for Life Sciences (NARILIS), Faculty of Medicine, University of Namur, Namur, Belgium;e WHO Collaborating Center for Epidemiology of Musculoskeletal Health and Aging Division of Public Health, Epidemiology and Health Economics, University of Liège, Liège, Belgium
&
Jean-Michel Dognéa Department of Pharmacy, Research Unit in Clinical Pharmacology and Toxicology, Namur Research Institute for Life Sciences (NARILIS), Faculty of Medicine, University of Namur, Namur, Belgium
Received 16 May 2024, Accepted 18 Jun 2024, Published online: 09 Jul 2024
 
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"Fezolinetant for VMS: a balanced view on efficacy and safety needed." Climacteric, ahead-of-print(ahead-of-print), pp. 1–2

Disclosure statement

J. Douxfils reports personal fees from Daiichi-Sankyo, Diagnostica Stago, Gedeon Richter, GyneBio Pharma, Mithra Pharmaceuticals, Norgine, Roche, Roche Diagnostics, Technoclone, Werfen and YHLO, outside the submitted work. All other authors declare no competing interests.

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