CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 593 enrolled
Drug / intervention
Iloperidone +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00254202
NCT00254202Phase 3Completed

A Randomized, Double-blind, Placebo- and Active-controlled, Multicenter Study to Evaluate the Efficacy, Safety and Tolerability of Iloperidone in Schizophrenic Patients in Acute Exacerbation Followed by a Long-term Treatment Phase.

Vanda Pharmaceuticals·interventional·Posted Nov 15, 2005·Updated Dec 13, 2024

In Brief

A Phase 3 clinical trial evaluating Iloperidone, Ziprasidone, and 1 other intervention for Schizophrenia. Completed, enrolled 593 participants across 42 sites in 2 countries.

Detailed Summary

The purpose of this study is to determine the safety and efficacy of iloperidone compared to placebo and an active comparator in the treatment of patients with schizophrenia in acute exacerbation.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSchizophrenia
CountriesIndia, United States
Collaborators--

Timeline

Phase 3CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedNov 15, 2005
Enrollment StartNov 18, 2005
Primary CompletionSep 26, 2006
Study CompletionMar 21, 2007
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 20.6 years ago

Interventions

Iloperidonedrug

Ziprasidonedrug

Placebodrug