Participants diagnosed with uncontrolled hypertension were randomly assigned to the low-dose group, middle-dose group, high-dose group or placebo group for a double-blind treatment period. Participants subsequently entered a withdrawal period.
Age
18–75
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
1. Patients 18-75 years old, male or female.
2. Mean seated systolic blood pressure (msSBP) at screening was ≥140 mmHg and \<180 mmHg.
3. Meet either item A or B at screening: A. Uncontrolled hypertension (uHTN); B. Resistant hypertension (rHTN).
4. Mean seated systolic blood pressure (msSBP) prior to randomization was ≥140 mmHg and \<180 mmHg.
5. Voluntarily participate in this study and sign the informed consent form.
6. Agree to comply with contraception and fertility restrictions of this study.
2. Compliance with study drug during the run-in period was less than 80% or greater than 120%.
3. Hypertension complicated with the following conditions: acute coronary syndrome, myocardial infarction, percutaneous coronary intervention, stroke.
4. Positive results for any of human immunodeficiency virus antibody (HIV), hepatitis C virus antibody (HCV), treponema pallidum antibody (TP); or positive hepatitis B surface antigen (HBsAg) with HBVDNA ≥ 1000 IU/mL.
5. Patients with active malignant tumors.
6. Patients receiving hemodialysis or adhering to strict salt restriction therapy.
7. History of adrenal insufficiency.
8. History of solid organ or bone marrow transplantation.
9. Gastrointestinal diseases or post-gastrointestinal surgery.
10. Known or suspected hypersensitivity to aldosterone synthase inhibitors; known or suspected contraindications or hypersensitivity to background medications.
11. History of drug abuse or alcohol abuse.
12. Blood donation or significant blood loss.
Clareo Health | A Phase II Clinical Trial of Efficacy and Safety of SAL0140 at Different Doses in Patients With Uncontrolled Hypertension
