Phase 2Active, not recruiting

A Phase II Clinical Study on the Efficacy and Safety of HRS-1780 in Participants With Primary Aldosteronism

A Multicenter, Randomized, Double-blind, Parallel, Placebo-controlled Phase II Clinical Study to Evaluate the Efficacy and Safety of HRS-1780 in Participants With Primary Aldosteronism

Sponsor
Shandong Suncadia Medicine Co., Ltd. (Industry)
Enrolment
61 enrolled
Conditions
Primary Aldosteronism
Interventions
HRS-1780 Tablets; Placebo
Ages
adults, older adults
Registry
NCT07470983

Full record on ClinicalTrials.gov

From the registry

This study is a multicenter, randomized, double-blind, placebo-parallel-controlled phase II clinical trial to evaluate the efficacy and safety of HRS-1780 compared with placebo in participants with primary aldosteronism. The study plans to enroll 60 participants.

Primary outcomes

  • Change from baseline in office systolic blood pressure (SBP);

History

  1. Primary completion expected

  2. Last registry update

  3. Started

  4. Registered