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

被引:51
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
[21]   Brexanolone (SAGE-547 injection) in post-partum depression: a randomised controlled trial [J].
Kanes, Stephen ;
Colquhoun, Helen ;
Gunduz-Bruce, Handan ;
Raines, Shane ;
Arnold, Ryan ;
Schacterle, Amy ;
Doherty, James ;
Epperson, C. Neill ;
Deligiannidis, Kristina M. ;
Riesenberg, Robert ;
Hoffmann, Ethan ;
Rubinow, David ;
Jonas, Jeffrey ;
Paul, Steven ;
Meltzer-Brody, Samantha .
LANCET, 2017, 390 (10093) :480-489
[22]   Switching and stopping antidepressants [J].
Keks, Nicholas ;
Hope, Judy ;
Keogh, Simone .
AUSTRALIAN PRESCRIBER, 2016, 39 (03) :76-83
[23]   The descriptive epidemiologv of commonly occurring mental disorders in the United States [J].
Kessler, Ronald C. ;
Wang, Philip S. .
ANNUAL REVIEW OF PUBLIC HEALTH, 2008, 29 :115-129
[24]   Has the rising placebo response impacted antidepressant clinical trial outcome? Data from the US Food and Drug Administration 1987-2013 [J].
Khan, Arif ;
Mar, Kaysee Fahl ;
Faucett, Jim ;
Schilling, Shirin Khan ;
Brown, Walter A. .
WORLD PSYCHIATRY, 2017, 16 (02) :181-192
[25]   Initial severity and antidepressant benefits: A meta-analysis of data submitted to the food and drug administration [J].
Kirsch, Irving ;
Deacon, Brett J. ;
Huedo-Medina, Tania B. ;
Scoboria, Alan ;
Moore, Thomas J. ;
Johnson, Blair T. .
PLOS MEDICINE, 2008, 5 (02) :260-268
[26]   The impact of tonic GABAA receptor-mediated inhibition on neuronal excitability varies across brain region and cell type [J].
Lee, Vallent ;
Maguire, Jamie .
FRONTIERS IN NEURAL CIRCUITS, 2014, 8
[27]   The GABAergic deficit hypothesis of major depressive disorder [J].
Luscher, B. ;
Shen, Q. ;
Sahir, N. .
MOLECULAR PSYCHIATRY, 2011, 16 (04) :383-406
[28]   Recommendations for the primary analysis of continuous endpoints in longitudinal clinical trials [J].
Mallinckrodt, Craig H. ;
Lane, Peter W. ;
Schnell, Dan ;
Peng, Yahong ;
Mancuso, James P. .
DRUG INFORMATION JOURNAL, 2008, 42 (04) :303-319
[29]   ANXIETY IN MAJOR DEPRESSION AND CEREBROSPINAL FLUID FREE GAMMA-AMINOBUTYRIC ACID [J].
Mann, J. John ;
Oquendo, Maria A. ;
Watson, Kalycia Trishana ;
Boldrini, Maura ;
Malone, Kevin M. ;
Ellis, Steven P. ;
Sullivan, Gregory ;
Cooper, Thomas B. ;
Xie, Shan ;
Currier, Dianne .
DEPRESSION AND ANXIETY, 2014, 31 (10) :814-821
[30]   Brexanolone injection in post-partum depression: two multicentre, double-blind, randomised, placebo-controlled, phase 3 trials [J].
Meltzer-Brody, Samantha ;
Colquhoun, Helen ;
Riesenberg, Robert ;
Epperson, C. Neill ;
Deligiannidis, Kristina M. ;
Rubinow, David R. ;
Li, Haihong ;
Sankoh, Abdul J. ;
Clemson, Christine ;
Schacterle, Amy ;
Jonas, Jeffrey ;
Kanes, Stephen .
LANCET, 2018, 392 (10152) :1058-1070