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Phase 3 N=228 Randomized Double-blind Treatment

An Efficacy and Safety Study of Extended-Release (ER) Paliperidone in Adolescent Participants With Schizophrenia

Schizophrenia

Enrolled (actual)
228
Serious AEs
6.2%
Results posted
Jun 2013
Primary outcome: Primary: Change From Baseline in the Positive and Negative Syndrome Scale (PANSS) Total Score at Day 56 — 89.6; 92.0; -19.3; -19.8 Units on a scale — p=0.935

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Paliperidone extended release (ER) (Drug); Aripiprazole (Drug)
Age
Pediatric · 12+ yrs
Sex
All
Sponsor
Janssen Research & Development, LLC
Primary completion
Jun 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline in the Positive and Negative Syndrome Scale (PANSS) Total Score at Day 56
89.6; 92.0; -19.3; -19.8 0.935
SECONDARY
Change From Baseline in PANSS Total Score at Day 182
89.6; 92.0; -25.6; -26.8 0.877
SECONDARY
Change From Baseline in Marder Factor Negative Symptoms Score at Day 56 and 182
23.2; 23.3; -4.3; -4.7; -6.0; -6.2 0.341
SECONDARY
Change From Baseline in Other Marder Factors Scores at Day 56 and 182
24.6; 24.9; -6.1; -5.6; -7.8; -7.8 0.351
SECONDARY
Change From Baseline in Other PANSS Factors and Subscales at Day 56 and 182
21.5; 22.5; -6.4; -6.2; -8.0; -8.3
SECONDARY
Number of Participants With Clinical Stability
58; 68 0.296
SECONDARY
Change From Baseline in Clinical Global Impression - Severity (CGI-S) Score at Days 56 and 182
4.0; 4.0; -1.0; -1; -1.0; -1.0 0.843
SECONDARY
Change From Baseline in Personal and Social Performance (PSP) Scores at Day 56 and 182
49.8; 49.2; 12.2; 12.2; 17.1; 17.1 0.895
SECONDARY
Number of Participants With PANSS Response
76; 87; 86; 93 0.119

Summary

The purpose of this study is to evaluate the efficacy and safety of extended-release (ER) paliperidone compared to aripiprazole (atypical antipsychotic) in symptomatic (having symptoms) adolescent participants with schizophrenia (psychiatric disorder with symptoms of emotional instability, detachment from reality, often with delusions and hallucinations [imagining things], and withdrawal into the self) .

Eligibility Criteria

Inclusion Criteria

  • Participants must currently meet the Diagnostic and Statistical Manual of Mental Disorders Fourth Edition (DSM-IV) criteria for schizophrenia and have experienced symptoms of the illness for at least 1 year, and they should have had at least treatment with 1 antipsychotic before participation in this study
  • Participants having a Positive and Negative Syndromes Scale (PANSS) score between 60 and 120 inclusive at Screening
  • Female participants must be incapable of pregnancy, or if heterosexually active and capable of pregnancy, have been using an acceptable method of contraception for at least 1 month before study entry and agree to continue use contraception methods for the duration of the study, or if sexually abstinent (not having sexual intercourse) and capable of pregnancy, must agree to continue abstinence or to use an acceptable method of birth control
  • Participants must not be a danger to themselves or others, and must have family support available to be maintained as out-patients
  • Participants with a weight of equal to or greater than 29 kilogram

Exclusion Criteria

  • Participants with mild (not serious), moderate (medium level of seriousness), or severe (very serious, life threatening) mental retardation
  • Participants with a known or suspected history of substance dependence (including alcohol, but excluding nicotine or caffeine) as per the DSM-IV criteria in the 3 months before Screening
  • Participants with a history of certain neurological (pertaining to the nervous system) disorders or insulin-dependent diabetes mellitus (disorder in which there is decreased insulin in the body or the body's insulin is not effective, resulting in high blood sugar, increased thirst and urine, and many other side effects)
  • Participants who have received a depot injectable antipsychotic within 2 treatment cycles before the Screening visit
  • Participants who have received clozapine in 2 months before the Baseline visit (Day 1 of Week 1)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01009047). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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