drugset / Trial / NCT04857047

A Multi Doses Study to Compare the Pharmacokinetics of BR9003A and BR9003 in Healthy Adult Subjects

NCT04857047 ↗

Phase 1 Completed 27 enrolled Boryung Pharmaceutical Co., Ltd
RandomizedCrossoverOpen-labelTreatment

Summary

This is a randomized, multiple doses, crossover clinical study to compare the pharmacokinetic characteristics and the safety between administration of BR9003 and BR9003A in healthy adult subjects. Within each period, randomized subjects will be taken 2 dosing regimens of administrating BR9003 once a day for six days or BR9003A twice a day for six days.

Timeline

Start
2021-03-31
Primary completion
2021-06-15
Completion
2021-06-28

Drugs

EvaluationDrugModalityDoseRoute
Subject BR9003 Unknown 2 mg Oral
Subject BR9003A Unknown 1 mg Oral

Indications

No indication recorded.