CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 14 enrolled
Drug / intervention
40mg lurasidone +1 moredrug
Likely dose
40mg lurasidonefrom 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/NCT02174523
NCT02174523Phase 1Completed

Pharmacokinetic Study of Lurasidone After Multiple Oral Administration in Healthy Human Subjects

Sumitomo Pharma (Suzhou) Co., Ltd.·interventional·Posted Jun 25, 2014·Updated Apr 8, 2019

In Brief

A Phase 1 clinical trial evaluating 40mg lurasidone and placebo for Schizophrenia. Completed, enrolled 14 participants across 1 site.

Detailed Summary

To evaluate the pharmacokinetic (PK) characteristics after multiple oral administration of 40 mg lurasidone in healthy Chinese subjects. To evaluate the safety and tolerance after multiple oral administration of 40 mg lurasidone in healthy Chinese subjects.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSchizophrenia
CountriesChina

Timeline

Phase 1CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJun 25, 2014
Enrollment StartApr 1, 2014
Primary CompletionApr 1, 2014
TodayJul 2, 2026
Enrollment to primary: 0 daysPosted 12.0 years ago

Interventions

40mg lurasidonedrug

placebodrug