drugset / Trial / NCT05001945

Trial on the Safety and Efficacy of MLS-101 in Patients With Uncontrolled Hypertension

NCT05001945

Phase 2 Completed 200 enrolled Mineralys Therapeutics Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A randomized, double-blind, placebo-controlled, dose-ranging, Phase II study to evaluate the safety, efficacy, and tolerability of MLS-101 in Subjects With Uncontrolled Hypertension

Timeline

Start
2021-07-01
Primary completion
2022-09-07
Completion
2022-10-07

Drugs

EvaluationDrugModalityDoseRoute
Subject lorundrostat Small molecule 12.5 mg Oral
Subject lorundrostat Small molecule 25 mg Oral
Subject lorundrostat Small molecule 50 mg Oral
Subject lorundrostat Small molecule 100 mg Oral

Indications