drugset / Trial / NCT06651021

A Phase I PK Study of Balcinrenone/Dapagliflozin in Healthy Chinese Participants

NCT06651021

Phase 1 Completed 10 enrolled AstraZeneca
NaSingle-groupOpen-labelTreatment

Summary

This study is intended to evaluate the PK, safety, and tolerability of balcinrenone/dapagliflozin given as a single dose capsule to healthy Chinese participants.

Timeline

Start
2024-10-21
Primary completion
2024-10-28
Completion
2024-10-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Dapagliflozin Small molecule 10 mg
Subject balcinrenone Small molecule 40 mg

Indications

No indication recorded.