Phase 3Not yet recruiting
A Study Evaluating Aprocitentan Tablets(SYH9108) for the Treatment of Resistant Hypertension
A Multicenter, Randomized, Double-blind, Placebo-controlled Phase 3 Study of Aprocitentan Tablets in the Treatment of Resistant Hypertension
- Sponsor
- CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd. (Industry)
- Enrollment
- 382 planned
- Conditions
- Resistant Hypertension
- Interventions
- Aprocitentan tablets(SYH9108); Placebo
- Ages
- adults, older adults
- Registry
- NCT07635914
Full record on ClinicalTrials.gov
From the registry
Aprocitentan tablets are currently the only endothelin dual receptor antagonist approved internationally for the treatment of resistant hypertension.This is a multicenter, randomized, double-blind, placebo-controlled Phase 3 study to evaluate the efficacy and safety of aprocitentan tablets(SYH9108) in patients with treatment-resistant hypertension (rHTN)
Primary outcomes
- Change from baseline in Sitting Systolic Blood Pressure (SiSBP) after 8 weeks of treatment.
History
Study completion expected
Primary completion expected
Registered
Started