drugset / Trial / NCT05385770

Study to Evaluate and Compare the Efficacy and Safety of AZM and AML Combined and Alone in Mild-to-moderate Essential Hypertensive Subjects

NCT05385770 ↗

Phase 3 Completed 890 enrolled Celltrion
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is an 8-week, randomized, double-blind Phase 3, multicentre study to determine the optimal dose of AZM and AML in combination therapy and to compare efficacy and tolerability of the combined therapy to each of the monotherapy in essential hypertensive subjects who are not adequately controlled on AZM and AML monotherapy.

Timeline

Start
2022-07-08
Primary completion
2024-07-11
Completion
2024-07-19

Drugs

EvaluationDrugModalityDoseRoute
Comparator AML Unknown — Oral
Comparator AZM Unknown — Oral