A Study to Evaluate ALN-AGT01 RVR in Adult Patients With Mild to Moderate Hypertension Pretreated With Zilebesiran
Recruiting now · Phase 2 · Has a placebo group
Conditions studied: Hypertension
In brief
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.
Key facts
- Study ID
- NCT07553442
- Run by
- Alnylam Pharmaceuticals
- People needed
- 93
- Starts
- 2026-04-27
- Expected to finish
- 2028-10-01
- Last updated by the study team
- 2026-07-23
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Clinical Trial Site — Lake Forest, California, United States (enrolling)
- Clinical Trial Site — Tampa, Florida, United States (enrolling)
- Clinical Trial Site — Savannah, Georgia, United States (enrolling)
Full record on ClinicalTrials.gov
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