CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 12 enrolled
Drug / intervention
MCI-186drug
Likely dose
MCI-186 30 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/NCT03664544
NCT03664544Phase 1Completed

An Open-Label, Single-Dose Study to Evaluate the Pharmacokinetics of MCI-186 in Subjects With Severe Hepatic Impairment Compared to Subjects With Normal Hepatic Function

Tanabe Pharma Corporation·interventional·Posted Sep 10, 2018·Updated May 8, 2026

In Brief

A Phase 1 clinical trial evaluating MCI-186 for Severe Hepatic Impairment and Healthy. Completed, enrolled 12 participants across 3 sites in 3 countries.

Detailed Summary

This is an open-label, single-dose study in male and female subjects with severe hepatic impairment and in male and female subjects with normal hepatic function.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCzechia, Hungary, Slovakia
Collaborators--

Timeline

Phase 1CompletedFinished
20192020202120222023202420252026
First PostedSep 10, 2018
Enrollment StartNov 6, 2018
Primary CompletionMar 25, 2019
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 7.8 years ago

Interventions

MCI-186drug

30 mg MCI-186 will be administered intravenously over 60 minutes.