Zuranolone for the Treatment of Adults With Major Depressive Disorder: A Randomized, Placebo-Controlled Phase 3 Trial

被引:52
作者
Clayton, Anita H. [1 ]
Lasser, Robert [2 ]
Parikh, Sagar, V [3 ]
Iosifescu, Dan, V [4 ]
Jung, Jungah [2 ]
Kotecha, Mona [5 ]
Forrestal, Fiona [5 ]
Jonas, Jeffrey [2 ]
Kanes, Stephen J. [2 ]
Doherty, James [2 ]
机构
[1] Univ Virginia, Sch Med, Dept Psychiat & Neurobehav Sci, Charlottesville, VA 22903 USA
[2] Sage Therapeut, Cambridge, MA USA
[3] Univ Michigan, Dept Psychiat, Ann Arbor, MI USA
[4] NYU, Dept Psychiat, Sch Med, New York, NY USA
[5] Biogen, Cambridge, MA USA
关键词
STAR-ASTERISK-D; UNITED-STATES; ANTIDEPRESSANT; GABA; BENZODIAZEPINE; INHIBITION; EFFICACY; OUTCOMES;
D O I
10.1176/appi.ajp.20220459
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: This study assessed the efficacy and safety of a 14-day treatment course of once-daily zuranolone 50 mg, an investigational oral positive allosteric modulator of the g-aminobutyric acid type A (GABAA) receptor, for the treat-ment of major depressive disorder. Methods: Patients 18-64 years of age with severe major depressive disorder were enrolled in this randomized, double-blind, placebo-controlled trial. Patients self-administered zur-anolone 50 mg or placebo once daily for 14 days. The primary endpoint was change from baseline in total score on the 17-item Hamilton Depression Rating Scale (HAM-D) at day 15. Safety and tolerability were assessed by incidence of adverse events. Results: Of 543 randomized patients, 534 (266 in the zur-anolone group, 268 in the placebo group) constituted the full analysis set. Compared with patients in the placebo group, patients in the zuranolone group demonstrated a statistically significant improvement in depressive symptoms at day 15 (least squares mean change from baseline HAM-D score,-14.1 vs.-12.3). Numerically greater improvements in depressive symptoms for zuranolone versus placebo were observed by day 3 (least squares mean change from baseline HAM-D score,-9.8 vs.-6.8), which were sus-tained at all visits throughout the treatment and follow-up periods of the study (through day 42, with the difference remaining nominally significant through day 12). Two pa-tients in each group experienced a serious adverse event; nine patients in the zuranolone group and four in the placebo group discontinued treatment due to adverse events. Conclusions: Zuranolone at 50 mg/day elicited a significantly greater improvement in depressive symptoms at day 15, with a rapid time to effect (day 3). Zuranolone was generally well tolerated, with no new safety findings compared with pre-viously studied lower dosages. These findings support the potential of zuranolone in treating adults with major de-pressive disorder. Am J Psychiatry 2023; 180:676-684; doi: 10.1176/appi.ajp.20220459
引用
收藏
页码:676 / 684
页数:9
相关论文
共 44 条
[1]   Neurosteroids promote phosphorylation and membrane insertion of extrasynaptic GABAA receptors [J].
Abramian, Armen M. ;
Comenencia-Ortiz, Eydith ;
Modgil, Amit ;
Vien, Thuy N. ;
Nakamura, Yasuko ;
Moore, Yvonne E. ;
Maguire, Jamie L. ;
Terunuma, Miho ;
Davies, Paul A. ;
Moss, Stephen J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (19) :7132-7137
[2]   Preclinical characterization of zuranolone (SAGE-217), a selective neuroactive steroid GABAA receptor positive allosteric modulator [J].
Althaus, Alison L. ;
Ackley, Michael A. ;
Belfort, Gabriel M. ;
Gee, Steven M. ;
Dai, Jing ;
Nguyen, David P. ;
Kazdoba, Tatiana M. ;
Modgil, Amit ;
Davies, Paul A. ;
Moss, Stephen J. ;
Salituro, Francesco G. ;
Hoffmann, Ethan ;
Hammond, Rebecca S. ;
Robichaud, Albert J. ;
Quirk, Michael C. ;
Doherty, James J. .
NEUROPHARMACOLOGY, 2020, 181
[3]  
[Anonymous], 2019, Zulresso (brexanolone)
[4]   Allopregnanolone Mediates Affective Switching Through Modulation of Oscillatory States in the Basolateral Amygdala [J].
Antonoudiou, Pantelis ;
Colmers, Phillip L. W. ;
Walton, Najah L. ;
Weiss, Grant L. ;
Smith, Anne C. ;
Nguyen, David P. ;
Lewis, Mike ;
Quirk, Michael C. ;
Barros, Lea ;
Melon, Laverne C. ;
Maguire, Jamie L. .
BIOLOGICAL PSYCHIATRY, 2022, 91 (03) :283-293
[5]   Neuroactive Steroids. 2.3α-Hydroxy-3β-methyl-21-(4-cyano-1H-pyrazol-1′-yl)-19-nor-5β-pregnan-20-one (SAGE-217): A Clinical Next Generation Neuroactive Steroid Positive Allosteric Modulator of the (γ-Aminobutyric Acid)A Receptor [J].
Botella, Gabriel Martinez ;
Salituro, Francesco G. ;
Harrison, Boyd L. ;
Beresis, Richard T. ;
Bai, Zhu ;
Blanco, Maria-Jesus ;
Belfort, Gabriel M. ;
Dai, Jing ;
Loya, Carlos M. ;
Ackley, Michael A. ;
Althaus, Alison L. ;
Grossman, Scott J. ;
Hoffmann, Ethan ;
Doherty, James J. ;
Robichaud, Albert J. .
JOURNAL OF MEDICINAL CHEMISTRY, 2017, 60 (18) :7810-7819
[6]   Simultaneous Antidepressant and Benzodiazepine New Use and Subsequent Long-term Benzodiazepine Use in Adults With Depression, United States, 2001-2014 [J].
Bushnell, Greta A. ;
Sturmer, Til ;
Gaynes, Bradley N. ;
Pate, Virginia ;
Miller, Matthew .
JAMA PSYCHIATRY, 2017, 74 (07) :747-755
[7]   Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications [J].
Cosci, Fiammetta ;
Chouinard, Guy .
PSYCHOTHERAPY AND PSYCHOSOMATICS, 2020, 89 (05) :283-306
[8]   Effect of Zuranolone vs Placebo in Postpartum Depression A Randomized Clinical Trial [J].
Deligiannidis, Kristina M. ;
Meltzer-Brody, Samantha ;
Gunduz-Bruce, Handan ;
Doherty, James ;
Jonas, Jeffrey ;
Li, Sigui ;
Sankoh, Abdul J. ;
Silber, Christopher ;
Campbell, Andrew D. ;
Werneburg, Brian ;
Kanes, Stephen J. ;
Lasser, Robert .
JAMA PSYCHIATRY, 2021, 78 (09) :951-959
[9]   Altered Connectivity in Depression: GABA and Glutamate Neurotransmitter Deficits and Reversal by Novel Treatments [J].
Duman, Ronald S. ;
Sanacora, Gerard ;
Krystal, John H. .
NEURON, 2019, 102 (01) :75-90
[10]   Prevalence of Depression Symptoms in US Adults Before and During the COVID-19 Pandemic [J].
Ettman, Catherine K. ;
Abdalla, Salma M. ;
Cohen, Gregory H. ;
Sampson, Laura ;
Vivier, Patrick M. ;
Galea, Sandro .
JAMA NETWORK OPEN, 2020, 3 (09)