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临床试验/NCT03595579
NCT03595579已完成2 期

A Randomized, Double-Blind, Active-Controlled Trial of AXS-05 Administered Orally to Subjects With Major Depressive Disorder

Axsome Therapeutics, Inc.1 个研究点 分布在 1 个国家目标入组 97 人开始时间: 2018年5月30日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
97
试验地点
1
主要终点
MADRS Score - Overall Change From Baseline

研究概览

简要总结

Randomized, Double-Blind, Active-Controlled Study of AXS-05 for MDD.

详细描述

This study will evaluate the safety and efficacy of AXS-05 in a randomized, double-blind, active-controlled study in patients diagnosed with major depressive disorder (MDD) experiencing an acute episode.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Currently meets DSM-5 criteria for MDD
  • Body mass index (BMI) between 18 and 40 kg/m^2, inclusive
  • Agree to use adequate method of contraception for the duration of the study
  • Additional criteria may apply

排除标准

  • Suicide risk
  • History of treatment resistance in current depressive episode
  • History of electroconvulsive therapy, vagus nerve stimulation, transcranial magnetic stimulation or any experimental central nervous system treatment during the current episode or in the past 6 months
  • Pregnant, breastfeeding, or planning to become pregnant or breastfeed during the study
  • Additional criteria may apply

研究组 & 干预措施

AXS-05

Experimental

干预措施: AXS-05 (Drug)

Bupropion

Active Comparator

干预措施: Bupropion (Drug)

结局指标

主要结局

MADRS Score - Overall Change From Baseline

时间窗: Assessed at week 1, 2, 3, 4, 5 and 6 (averaged over the entire 6-week treatment period)

The primary objective of the study was to assess the effect of AXS-05 versus bupropion as measured by the Montgomery-Åsberg Depression Rating Scale (MADRS) for change in severity of depressive symptoms. The MADRS is a 10-item scale and items are scored between 0-6 points. For each item, a score of 0 indicates the absence of symptoms, and a score of 6 indicates symptoms of maximum severity. A maximum total score is 60 points.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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