BENITIONSClinical Trial Intelligence

Intramuscular Depot Formulation of Aripiprazole as Maintenance Treatment in Patients With Schizophrenia

3상 완료 NCT00706654

대상 질환Schizophrenia
임상 단계3상
스폰서Otsuka Pharmaceutical Development & Commercialization, Inc.
상태완료
참여자 수937 명
중재(약물)Aripiprazole depot 300 or 400 mg, Aripiprazole 10-30 mg orally, Aripiprazole depot 25 or 50 mg, Placebo depot, Placebo tablets
시작일2008년 9월 1일
완료일2012년 8월 1일
결과 공개일2013년 8월 14일

요약

The purpose of the this trial is to evaluate the efficacy, safety, and tolerability of an intramuscular (IM) depot formulation of aripiprazole as maintenance treatment in patients with schizophrenia The trial is designed into three treatment phases. Phase 1 is designed to allow for a subject to be converted from the current anti-psychotic treatment to oral non-generic aripiprazole monotherapy (oral conversion phase from 4 to 6 weeks). During Phase 2 the subject will be stabilized on oral non-generic aripiprazole monotherapy. Once the subject is stabilized in Phase 2 (oral stabilization phase from minimum 8 weeks to maximum 28 weeks), they are eligible to be randomized into the double-blind IM depot maintenance phase, Phase 3. During Phase 3, the subject will be assessed for exacerbation of psychotic symptoms and impending relapse for up to 38 weeks.

Percentage of Patients Meeting Exacerbation of Psychotic Symptoms/Impending Relapse Criteria by the End of Week 26

Baseline to Week 26 · Percentage of patients

Aripiprazole Depot 300 or 400 mg - Depot Maintenance Phase7.12 Percentage of patients
Aripiprazole 10-30 mg Orally - Depot Maintenance Phase7.76 Percentage of patients
Aripiprazole Depot 25 or 50 mg - Depot Maintenance Phase21.80 Percentage of patients
p-value0.7871
Mean Difference (Final Values)-0.64 (95% CI -5.26–3.99)

BENITIONS에서 보기 ClinicalTrials.gov 원문 보기

전체 임상

이 페이지는 ClinicalTrials.gov의 공개 데이터를 정리한 것입니다. 의학적 조언이 아니며 투자 권유나 자문도 아닙니다. 반드시 전문의와 상담하세요.