drugset / Trial / NCT06153693

Efficacy and Safety of Lorundrostat in Subjects With Uncontrolled and Resistant Hypertension

NCT06153693

Phase 3 Completed 1083 enrolled Mineralys Therapeutics Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a Phase 3 trial to evaluate the BP-lowering effect of lorundrostat (an aldosterone synthase inhibitor) in subjects with uncontrolled and resistant hypertension taking between 2 and 5 anti-hypertensive (AHT) medications.

Timeline

Start
2023-11-22
Primary completion
2024-12-10
Completion
2025-01-24

Drugs

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

Indications