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临床试验/NCT01766401
NCT01766401已完成3 期

A Double-Blind, Placebo-Controlled, Flexible-Dose Study of Vilazadone in Patients With Generalized Anxiety Disorder

Forest Laboratories30 个研究点 分布在 1 个国家目标入组 402 人开始时间: 2013年1月31日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
402
试验地点
30
主要终点
Change in Baseline in the Hamilton Rating Scale for Anxiety (HAM-A) Total Score

研究概览

简要总结

The purpose of this study is to evaluate the efficacy, safety, and tolerability of vilazodone relative to placebo in the treatment of generalized anxiety disorder (GAD).

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male and female, 18 - 70 Years of age
  • Currently meet the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) criteria for Generalized Anxiety Disorder (GAD)
  • Minimum score of 20 on the Hamilton Rating Scale for Anxiety (HAM-A)

排除标准

  • Women who are pregnant, women who will be breastfeeding during the study, and women of childbearing potential who are not practicing a reliable method of birth control
  • Patients with a history of meeting DSM-IV-TR criteria for:
  • any manic, hypomanic or mixed episode, including bipolar disorder and substance-induced manic, hypomanic, or mixed episode;
  • any depressive episode with psychotic or catatonic features;
  • panic disorder with or without agoraphobia;
  • obsessive-compulsive disorder;
  • Schizophrenia, schizoaffective, or other psychotic disorder;
  • bulimia or anorexia nervosa;
  • presence of borderline personality disorder or antisocial personality disorder;
  • mental retardation, dementia, amnesia, or other cognitive disorders
  • Patients who are considered a suicide risk

研究组 & 干预措施

Placebo

Placebo Comparator

Matching placebo tablets, oral administration

干预措施: Placebo (Drug)

Vilazadone

Experimental

Vilazadone tablets, oral administration

干预措施: Vilazadone (Drug)

结局指标

主要结局

Change in Baseline in the Hamilton Rating Scale for Anxiety (HAM-A) Total Score

时间窗: Baseline to Week 8

The Hamilton Anxiety Rating Scale (HAM-A) is a clinician-administered scale which consists of 14 items, each rated on a five point scale ranging from 0 (not present) to 4 (very severe). The highest possible score is 56, which represents the most severe form of anxiety; the lowest possible score is 0, which represents an absence of anxiety.

次要结局

  • Change From Baseline in the Sheehan Disability Scale (SDS) Total Score(Baseline to Week 8)

研究者

发起方
Forest Laboratories
申办方类型
Industry
责任方
Sponsor

研究点 (30)

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