drugset / Trial / NCT05750355

Evaluate the Effect of TPN171H on the QT/QTc Interval in Healthy Volunteers

NCT05750355

Phase 1 Completed 32 enrolled Vigonvita Life Sciences
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a single-dose orally administered, dose-escalation, single-center, randomized, double-blind, placebo-parallel controlled clinical study evaluating the effect of TPN171H tablets on QT/QTc interval in healthy subjects.The main objective was to evaluate the effect of TPN171H tablets on QT/QTc interval in healthy Chinese subjects after a single oral administration.

Timeline

Start
2022-10-10
Primary completion
2022-12-07
Completion
2022-12-07

Drugs

EvaluationDrugModalityDoseRoute
Subject TPN171H Unknown 10 mg Oral
Subject TPN171H Unknown 30 mg Oral
Subject TPN171H Unknown 40 mg Oral
Subject TPN171H Unknown 50 mg Oral

Indications

No indication recorded.