CardiologyPhase IIIEnrolling

Lorundrostat Open-Label Extension Study

Uncontrolled Hypertension

Study Overview

An open-label extension evaluating long-term safety and blood pressure-lowering efficacy of lorundrostat, an aldosterone synthase inhibitor, in adults with uncontrolled hypertension who completed prior lorundrostat parent trials.

Inclusion Criteria

  • Adults aged 18 years or older
  • Completed a prior lorundrostat parent study (MLS-101-202, -206, or -301)
  • Fertile subjects must use acceptable contraception
  • Maintained ≥75% compliance with study medication in parent study

Exclusion Criteria

  • Pregnant, planning pregnancy, or breastfeeding
  • Use of prohibited medications (potassium-sparing diuretics, strong CYP3A4 inhibitors)
  • Serum potassium >5.5 mmol/L at baseline
  • Any condition precluding safe participation per Investigator judgment

Study Details

Phase
Phase III
Duration
50 weeks
Location
Main Facility
Compensation
Study drug and care provided at no cost
Check Eligibility

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