drugset / Trial / NCT06150924

Efficacy and Safety of Lorundrostat in Addition to Sodium-Glucose Cotransporter-2 Inhibitors (SGLT2i) in Subjects With Hypertension and Chronic Kidney Disease (CKD) With Albuminuria

NCT06150924

Phase 2 Completed 60 enrolled Mineralys Therapeutics Inc.
RandomizedCrossoverDouble-blindTreatment

Summary

This is a randomized, double-blind (DB), placebo controlled, crossover study with a two-period, two-sequence (2x2) design evaluating the efficacy and safety of 25 mg QD lorundrostat (an aldosterone synthase inhibitor \[ASI\]) in addition to a SGLT2i for the treatment of hypertension in subjects with CKD and albuminuria while receiving stable treatment with an Angiotensin-converting enzyme inhibitor (ACEi) or an Angiotensin receptor blocker (ARB). Subjects will be at least 18 years old with hypertension, and mild to severe CKD with albuminuria at the Screening Visit.

Timeline

Start
2023-12-14
Primary completion
2025-02-27
Completion
2025-04-23

Drugs

EvaluationDrugModalityDoseRoute
Subject lorundrostat Small molecule 25 mg
Background Dapagliflozin Small molecule 10 mg