ConditionPrimary Aldosteronism
Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorShenzhen Salubris Pharmaceuticals Co., Ltd.
About this trial
This is a multicenter, randomized, double-blind, placebo-controlled phase II study designed to explore the efficacy and safety of different doses of SAL0140 in primary aldosteronism.
Eligibility criteria
Qualifiers
Aged ≥18 years , regardless of gender.
Diagnosed with primary aldosteronism (PA).
Mean seated office systolic blood pressure (msSBP) ≥145 mmHg.
Receiving stable background antihypertensive therapy.
Disqualifiers
Mean seated office systolic blood pressure (msSBP) ≥180 mmHg and/or mean seated office diastolic blood pressure (msDBP) ≥110 mmHg.
History or diagnosis of malignant hypertension, hypertensive emergency, hypertensive crisis or hypertensive encephalopathy.
History or diagnostic evidence of other secondary hypertension.
Prior surgical resection for adrenal adenoma.
Trial design
Treatments tested in this trial
- SAL0140 Tablets
- SAL0140 Tablets
- SAL0140 placebo
Treatment groups
50 Participants
are divided into 3 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov