Estetrol Is Safe and Well Tolerated during Treatment of Hospitalized Men and Women with Moderate COVID-19 in a Randomized, Double-Blind Study

被引:2
作者
Foidart, Jean Michel [1 ,2 ]
Simon, Krzysztof [3 ]
Utian, Wulf H. [4 ]
Mauvais-Jarvis, Franck [5 ]
Douxfils, Jonathan [6 ,7 ]
Dixon, Graham [1 ]
Barrington, Philip [8 ]
机构
[1] Mithra Pharmaceut, B-4000 Liege, Belgium
[2] Univ Liege, Dept Obstet & Gynecol, B-4000 Liege, Belgium
[3] Wroclaw Med Univ, Dept Infect Dis & Hepatol, 51149 Wroclaw, Wroclaw, Poland
[4] Case Western Reserve Med Sch, Dept Reprod Biol, Cleveland, OH 44106 USA
[5] Tulane Univ, Sch Med, Dept Endocrinol & Metab, New Orleans, LA 70112 USA
[6] Univ Namur, Fac Med, Namur Thrombosis & Hemostasis Ctr, Dept Pharm, B-5000 Namur, Belgium
[7] QUALIblood Sa, B-5000 Namur, Belgium
[8] TranScrip Ltd, Wokingham RG41 5TP, Berks, England
关键词
estetrol; E4; COVID-19; estrogen; human fetal estrogen; postmenopausal; hospitalization; coagulation; thromboembolic events; THERAPY;
D O I
10.3390/jcm12123928
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Epidemiological data suggest that the severe acute respiratory syndrome coronavirus 2 infection rate is higher in women than in men, but the death rate is lower, while women (>50 years) on menopausal hormone therapy (MHT) have a higher survival rate than those not on MHT. Classical oral estrogen enhances the synthesis of coagulation markers and may increase the risk of thromboembolic events that are common in coronavirus disease 2019 (COVID-19). The favorable hemostatic profile of estetrol (E4) might be suitable for use in women who are receiving estrogen treatment and contract COVID-19. A multicenter, randomized, double-blind, placebo-controlled, phase 2 study (NCT04801836) investigated the efficacy, safety, and tolerability of E4 versus placebo in hospitalized patients with moderate COVID-19. Eligible postmenopausal women and men (aged & GE; 18 years old) were randomized to E4 15 mg or placebo, once daily for 21 days, in addition to the standard of care (SoC). The primary efficacy endpoint of improvement in COVID-19 (percentage of patients recovered at day 28) between the placebo and E4 arms was not met. E4 was well tolerated, with no safety signals or thromboembolic events, suggesting that postmenopausal women can safely continue E4-based therapy in cases of moderate COVID-19 managed with SoC.
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页数:14
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