Safety and Tolerability of Open-Labeled Iloperidone in Adolescents

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age12-17
SponsorVanda Pharmaceuticals

About this trial

To evaluate the safety and tolerability of iloperidone in adolescent patients with schizophrenia or bipolar I disorder for up to 52 weeks of treatment.

Eligibility criteria

Qualifiers

Patient is willing and able to provide assent and willing to complete all aspects of the study

Patient's parent or legal guardian willing and able to provide consent

Male or female patients 12 through 17 years of age (inclusive)

Clinical diagnosis of either schizophrenia or bipolar I disorder

Disqualifiers

Use of other investigational drugs at the time of enrollment, or within 30 days or 5 half-lives of enrollment, whichever is longer

A positive test for drugs of abuse

Trial design

Treatments tested in this trial

  • Iloperidone

Treatment groups

100 Participants
are divided into 1 treatment group

Sponsors and collaborators