MedPath

Efficacy and Safety Study of Iloperidone Virus Risperidone to Treat Schizophrenia

Phase 2
Completed
Conditions
Iloperidone
Efficacy
Schizophrenia
Interventions
Registration Number
NCT01623713
Lead Sponsor
Jiangsu Hansoh Pharmaceutical Co., Ltd.
Brief Summary

The purpose of this study is to determine whether iloperidone is effective in the treatment of Schizophrenia.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
260
Inclusion Criteria
  • Men or women ages 18-65 years old.
  • DSM-IV diagnosis of schizophrenia.
  • PANSS≥70.
  • Of the 7 PANSS positive symptom subscale, at least two score ≥ 4 points.
  • Written informed consent.
Exclusion Criteria
  • Pregnant or nursing (lactating) women, or women who plan on conceiving during the course of the study.
  • Clinically significant disease of the heart,kidneys,liver,hematonosis or endocrine system.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
RisperidoneRisperidone-
iloperidoneiloperidone-
Primary Outcome Measures
NameTimeMethod
Positive and Negative Symptom Scale(PANSS)-Total Score6 weeks
Secondary Outcome Measures
NameTimeMethod
Effective percentage(PANSS score reduce rate≥50%)6 weeks
Change in scores from baseline to end point assessment on the PANSS Positive subscale (PANSS-P)6 weeks
Change in scores from baseline to end point assessment on the PANSS Negative subscale (PANSS-N)6 weeks
Change in scores from baseline to end point assessment on the PANSS General Psychopathology subscale(PANSS-GP)6 weeks

Trial Locations

Locations (1)

Sixth Hospital of Peking University

🇨🇳

Peking, Beijing, China

© Copyright 2025. All Rights Reserved by MedPath