Abstract
Objective
This study characterizes the tolerability of ziprasidone in children and adolescents with bipolar mania, schizophrenia, or schizoaffective disorder.
Method
Sixty-three subjects (aged 10–17 years) entered an open-label study consisting of a 3-week fixed-dose period (Period 1) and a subsequent 24-week flexible-dose period (Period 2). In Period 1, subjects received ziprasidone 80 or 160 mg/d in two divided doses, titrated over 10 days. In Period 2, subjects received flexible doses (20–160 mg/d). Tolerability was evaluated using movement rating scales, laboratory tests, and electrocardio- grams. Clinical response was assessed using the Young Mania Rating Scale, the Brief Psychiatric Rating Scale- Anchored Version, and the Clinical Global Impressions–Severity scale.
Results
Adverse events (AEs) occurred mostly during dose titration and in the high-dose (160 mg/d) group. The most common AEs during Period 1 were sedation (32%), somnolence (30%), and nausea (25%) and during Period 2 were sedation (30%), somnolence (30%), and headache (25%). The incidence of movement disorder AEs was 22% and 16% during Periods 1 and 2, respectively. Six percent of study participants discontinued study participation due to AEs during Period 1 and 20% discontinued in Period 2. Thirty-three percent of subjects gained 7% of their baseline weight. No Fridericia-corrected QT (QTcF) intervals of 450 ms were observed during Period 1 and only one occurred during Period 2. No QTcF increase 60 ms from baseline was observed. Symptom reductions were observed in all patient groups.
Conclusions
No unexpected tolerability findings were observed in this prospective trial of ziprasidone in children and adolescents with bipolar mania, schizophrenia, or schizoaffective disorder. On the basis of the results, a starting dose of 20 mg/d titrated to between 80 and 160 mg/d over 1–2 weeks appears optimal for most patients.
