Clinical Trial

A Dose Finding Study of IBI3016 in Mild to Moderate Hypertensive Patients

Not Yet Recruiting Phase 2
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Summary
The purpose of this study is to evaluate the efficacy, safety and tolerability of IBI3016 or placebo, given subcutaneously, every 3 or 6 months, at different dose levels in patients with mild to moderate hypertension
Trial Details
NCT Number NCT07352969
Lead Sponsor Innovent Biologics (Suzhou) Co. Ltd.
Conditions Hypertension
Enrollment 352 participants
Start Date 2026-02-06
Primary Completion 2029-03-27 (estimated)
Study Completion 2029-03-27 (estimated)
Updated on ClinicalTrials.gov 2026-01-20