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Trials / Completed

CompletedNCT04873323

A QT/QTc Evaluation Study of TS-142 in Healthy Adult Subjects

A Study to Evaluate the Effects on QT/QTc Interval of TS-142 in Healthy Adult Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
59 (actual)
Sponsor
Taisho Pharmaceutical Co., Ltd. · Industry
Sex
All
Age
20 Years – 39 Years
Healthy volunteers
Accepted

Summary

A clinical study to evaluate the effects on QT/QTc Interval of TS-142 in Healthy Adult Subjects

Conditions

Interventions

TypeNameDescription
DRUGTS-142Single dose of TS-142 10 mg or TS-142 30 mg in the morning under fasting in each period
DRUGMoxifloxacinSingle dose of moxifloxacin 400 mg in the morning under fasting in each period
DRUGPlaceboSingle dose of TS-142 placebo in the morning under fasting in each period

Timeline

Start date
2021-06-07
Primary completion
2021-09-28
Completion
2021-09-28
First posted
2021-05-05
Last updated
2025-02-28

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT04873323. Inclusion in this directory is not an endorsement.