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
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