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临床试验/NCT00694707
NCT00694707已完成2 期

Evaluation of the Safety and Efficacy of RGH-188 in the Acute Exacerbation of Schizophrenia

Forest Laboratories4 个研究点 分布在 2 个国家目标入组 732 人开始时间: 2008年6月30日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
732
试验地点
4
主要终点
Change From Baseline to Week 6 in the PANSS Total Score

研究概览

简要总结

This is a study to evaluate the safety, efficacy, and tolerability of cariprazine (RGH-188) relative to placebo in adult patients (18-60 years of age) with acute exacerbation of schizophrenia.

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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female, 18 to 60 years of age.
  • Meets Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV) criteria for schizophrenia (paranoid type, disorganized type, catatonic type, or undifferentiated type) based on a Structured Clinical Interview for DSM-IV (SCID).
  • Total Positive and Negative Syndrome Scale (PANSS) score ≥ 80 and ≤
  • Diagnosis of schizophrenia for at least 1 year.

排除标准

  • Abnormalities on physical examination or abnormal vital signs, electrocardiogram, or clinical laboratory values.
  • First episode of psychosis.

研究组 & 干预措施

Placebo

Placebo Comparator

Participants received placebo orally once a day for 6 weeks.

干预措施: Placebo (Drug)

Cariprazine 1.5 mg

Experimental

Participants received cariprazine 1.5 mg orally once a day for 6 weeks.

干预措施: Cariprazine (Drug)

Cariprazine 3.0 mg

Experimental

Participants received cariprazine 3.0 mg orally once a day for 6 weeks.

干预措施: Cariprazine (Drug)

Cariprazine 4.5 mg

Experimental

Participants received cariprazine 4.5 mg orally once a day for 6 weeks.

干预措施: Cariprazine (Drug)

Risperidone 4.0 mg

Active Comparator

Participants received risperidone 4.0 mg orally once a day for 6 weeks.

干预措施: Risperidone (Drug)

结局指标

主要结局

Change From Baseline to Week 6 in the PANSS Total Score

时间窗: Baseline to Week 6

The Positive and Negative Syndrome Scale (PANSS) is a 30-item rating scale that assesses the positive and negative symptoms of individuals with schizophrenia. Responses to the 30 items are based on a structured clinical interview with the patient and on supporting clinical information obtained from family, hospital staff, or other reliable informants. Of the 30 psychiatric parameters measured by the scale, 7 assess positive symptoms (eg, delusions, grandiosity); 7 assess negative symptoms (eg, blunted affect, emotional withdrawal); and 16 assess general psychopathology (eg, poor attention, active social avoidance). Each item is scored on a 7-point scale (1 = absent, 2 = minimal, 3 = mild, 4 = moderate, 5 = moderately severe, 6 = severe, and 7 = extreme). The PANSS total score can range from 30 to 210. A higher score indicates worse symptoms. A negative change score indicates improvement.

次要结局

  • Change From Baseline to Week 6 in the CGI-S Score(Baseline to Week 6)

研究者

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

研究点 (4)

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