BENITIONSClinical Trial Intelligence

Study of Aripiprazole in the Treatment of Serious Behavioral Problems in Children and Adolescents With Autistic Disorder (AD)

第3相 完了 NCT00365859

対象疾患Autistic Disorder, Behavioral Symptoms
第3相
スポンサーOtsuka Pharmaceutical Development & Commercialization, Inc.
ステータス完了
参加者数330 名
介入(薬剤)Aripiprazole
開始日2006年9月1日
完了日2009年6月1日
結果公開日2010年1月25日

概要

This study will provide long-term safety data for patients who are taking aripiprazole for up to 1 year. Most patients enrolled in this study will have participated in a short-term study with aripiprazole (CN138-178 \[NCT00332241\] or CN138-179 \[NCT00337571\]).

Number of Participants With Serious Adverse Events (SAEs), Treatment-Emergent Adverse Events (AEs), Deaths, AEs Leading to Discontinuation, Extra Pyramidal Syndrome (EPS)-Related AEs

From Screening (up to 42 days prior to treatment start) through Week 52 (end of study) for SAEs; from Week 0 (Baseline) through Week 52 (End of Study) for AEs · Participants

De Novo0 Participants
Rollover Placebo0 Participants
Rollover Aripiprazole0 Participants
Total0 Participants
De Novo3 Participants
Rollover Placebo1 Participants

Mean Change From Baseline in Total Simpson-Angus Scale (SAS) At Week 8, Week 26, and Week 52

Baseline, Week 8, Week 26, Week 52 · units on a scale

De Novo10.7 ± 1.40 units on a scale
Rollover Placebo10.6 ± 1.17 units on a scale
Rollover Aripiprazole11.0 ± 2.11 units on a scale
Total10.8 ± 1.77 units on a scale
De Novo-0.3 ± 1.13 units on a scale
Rollover Placebo0.1 ± 1.51 units on a scale

Mean Change From Baseline in Abnormal Involuntary Movement Scale (AIMS) At Week 8, Week 26, and Week 52

Baseline, Week 8, Week 26, Week 52 · units on a scale

De Novo0.5 ± 1.90 units on a scale
Rollover Placebo0.5 ± 1.02 units on a scale
Rollover Aripiprazole0.3 ± 1.23 units on a scale
Total0.4 ± 1.40 units on a scale
De Novo-0.3 ± 1.45 units on a scale
Rollover Placebo-0.1 ± 0.87 units on a scale

BENITIONS で見る ClinicalTrials.gov の原文を見る

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