drugset / Trial / NCT05769608

A Pivotal Study to Evaluate the Efficacy of Lorundrostat in Subjects With Uncontrolled Hypertension on a Standardized Antihypertensive Medication Regimen

NCT05769608

Phase 2 Completed 285 enrolled Mineralys Therapeutics Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

A Phase 2 trial to evaluate the blood pressure-lowering effect of lorundrostat an aldosterone synthase inhibitor (ASI), administered as an add-on to a standardized anti-hypertensive (AHT) medication regimen, in subjects with hypertension.

Timeline

Start
2023-03-13
Primary completion
2025-01-15
Completion
2025-01-15

Drugs

EvaluationDrugModalityDoseRoute
Subject lorundrostat Small molecule 50 mg
Subject lorundrostat Small molecule 100 mg

Indications