Clinical Trial

QT Interval Effects Study of Oral FXS5626 Tablets

Not Yet Recruiting Phase 1
View on ClinicalTrials.gov →
Summary
The purpose of this study is to evaluate the Exposure-Response Relationship Between the Plasma Drug Concentrations and the Change From Baseline in QTc interval of a single oral dose of FXS5626 in healthy subjects.
Trial Details
NCT Number NCT07695779
Lead Sponsor Shanghai Fosun Pharmaceutical Industrial Development Co. Ltd.
Conditions Evaluation of QTc Interval
Enrollment 28 participants
Start Date 2026-08-05
Primary Completion 2026-09-25 (estimated)
Study Completion 2026-09-25 (estimated)
Updated on ClinicalTrials.gov 2026-07-10