BENITIONSClinical Trial Intelligence

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

3상 완료 NCT00365859

대상 질환Autistic Disorder, Behavioral Symptoms
임상 단계3상
스폰서Otsuka Pharmaceutical Development & Commercialization, Inc.
상태완료
참여자 수330 명
중재(약물)Aripiprazole
시작일2006년 9월 1일
완료일2009년 6월 1일
결과 공개일2010년 1월 25일

요약

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

BENITIONS에서 보기 ClinicalTrials.gov 원문 보기

전체 임상

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