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A Study to Evaluate ALN-AGT01 RVR in Adult Patients With Mild to Moderate Hypertension Pretreated With Zilebesiran

StatusRecruiting
PhasePhase 2
Started2026-04-27
View on ClinicalTrials.gov ↗

Amendment history

2026-09-10
minor
Study Status v5
Re-verified, no change to tracked fields
2026-08-12
minor
Study Status, Contacts/Locations v4
Study sitesdetails revised at 2 of 3 sites
2026-07-22
minor
Study Status v3
Re-verified, no change to tracked fields
2026-06-10
minor
Study Status, Contacts/Locations v2
Study sitesdetails revised at 2 of 3 sites
2026-05-13
notable
Study Status, Contacts/Locations v1
Recruitment opened
Study sitesdetails revised at 3 of 3 sites
2026-04-22
minor
Original filing
The purpose of this study is to evaluate the efficacy, pharmacodynamics (PD), and safety of ALN-AGT01 RVR in participants with mild to moderate hypertension pretreated with zilebesiran.
Trial Details
NCT Number NCT07553442
Lead Sponsor Alnylam Pharmaceuticals
Collaborators: Hoffmann-La Roche
Conditions Hypertension
Enrollment 93 participants
Start Date 2026-04-27
Primary Completion 2028-04-01 (estimated)
Study Completion 2028-10-01 (estimated)
Updated on ClinicalTrials.gov 2026-09-14