drugset / Trial / NCT06087835

Study to Investigate Efficacy, Safety, and Tolerability of Zibotentan/Dapagliflozin Compared to Dapagliflozin in Participants With Chronic Kidney Disease and High Proteinuria (ZENITH High Proteinuria)

NCT06087835

Phase 3 Active not recruiting 1835 enrolled AstraZeneca
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Phase III, randomised, multicentre, double-blinded study to evaluate efficacy, safety and tolerability of treatment with zibotentan/dapagliflozin and dapagliflozin alone in participants with chronic kidney disease (CKD) and high proteinuria

Timeline

Start
2023-11-07
Primary completion
2027-02-18
Completion
2027-02-18

Drugs

EvaluationDrugModalityDoseRoute
Comparator Dapagliflozin Small molecule Oral
Subject Zibotentan Small molecule Oral