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RECRUITING
NCT05648591
PHASE4

Safety and Tolerability of Open-Labeled Iloperidone in Adolescents

Sponsor: Vanda Pharmaceuticals

View on ClinicalTrials.gov

Summary

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

Official title: Open-label Safety Study of a 1-year 8 to 24 mg/Day Dose Regimen of Iloperidone (FANAPT®) in Adolescent Patients With Schizophrenia or Bipolar I Disorder

Key Details

Gender

All

Age Range

12 Years - 17 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2023-05-24

Completion Date

2026-11-30

Last Updated

2025-03-04

Healthy Volunteers

No

Interventions

DRUG

Iloperidone

oral tablet

Locations (9)

Vanda Investigational Site

Little Rock, Arkansas, United States

Vanda Investigational Site

Denver, Colorado, United States

Vanda Investigational Site

Atlanta, Georgia, United States

Vanda Investigational Site

Atlanta, Georgia, United States

Vanda Investigational Site

Decatur, Georgia, United States

Vanda Investigational Site

Cincinnati, Ohio, United States

Vanda Investigational Site

Garfield Heights, Ohio, United States

Vanda Investigational Site

Westlake, Ohio, United States

Vanda Investigational Site

Everett, Washington, United States