CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 27 enrolled
Drug / intervention
MCI-186 +2 moredrug
Likely dose
MCI-186 60 mgfrom 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/NCT04029090
NCT04029090Phase 1Completed

A Randomized, Single-Blind, Placebo-Controlled, Three-Way Crossover Study to Evaluate the Effect of MCI-186 at Therapeutic and Supra-Therapeutic Doses on the QT/QTc Interval in Healthy Subjects

Tanabe Pharma Corporation·interventional·Posted Jul 23, 2019·Updated May 22, 2026

In Brief

A Phase 1 clinical trial evaluating MCI-186 and Placebo for Healthy Adult Subjects. Completed, enrolled 27 participants across 1 site.

Detailed Summary

To evaluate the effect of MCI-186 on the QT interval corrected for heart rate using Fridericia's formula (QTcF)

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesJapan
Collaborators--

Timeline

Phase 1CompletedFinished
20192020202120222023202420252026
First PostedJul 23, 2019
Enrollment StartSep 18, 2018
Primary CompletionOct 20, 2018
Study CompletionOct 23, 2018
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 6.9 years ago

Interventions

MCI-186drug

A single dose of 60 mg MCI-186 over 60 min will be intravenously administered.

MCI-186drug

A single dose of 300 mg MCI-186 over 60 min will be intravenously administered.

Placebodrug

A single dose of 0.9% w/v saline over 60 min will be intravenously administered.