Key result
Zilebesiran demonstrated a dose-dependent reduction in blood pressure and serum angiotensinogen levels with sustained effects up to 6 months in Phase I clinical trials.
Why the study?
Despite widespread use of antihypertensive drugs, only a fifth of diagnosed patients achieve adequate blood pressure control, driving the pursuit for novel antihypertensive therapies.
Does zilebesiran reduce blood pressure and serum angiotensinogen levels in patients with systemic hypertension?
Does zilebesiran reduce blood pressure and serum angiotensinogen levels in patients with systemic hypertension?
Zilebesiran is a promising novel siRNA therapy that post-transcriptionally silences the AGT gene, showing dose-dependent reductions in blood pressure and angiotensinogen levels in early trials.
Zilebesiran merits Phase II/III evaluation in hypertension; leaves open its clinical role pending larger efficacy and safety data.
Systemic hypertension is one of the most common noncommunicable diseases globally, with over one billion people affected. Despite the widespread use of numerous antihypertensive drugs, it is estimated that only a fifth of diagnosed patients achieve adequate blood pressure control. For this reason, the pursuit for novel antihypertensive therapies is ongoing. Zilebesiran, an siRNA designed to target the liver, is the newest potential addition to the renin-angiotensin-aldosterone system-inhibiting drugs. This subcutaneous injection post-transcriptionally silences the AGT gene responsible for the synthesis of angiotensinogen. By preventing the progenitor protein of the renin-angiotensin-aldosterone system, zilebesiran blocks the downstream production of angiotensin II, which plays multiple roles in blood pressure elevation. Phase I clinical trials have demonstrated a dose-dependent negative relationship between zilebesiran and blood pressure/serum angiotensinogen levels-with sustained effects up to 6 months. Researchers also demonstrated a promising safety profile, as most of the adverse events were mild to moderate in nature. Phase II trials assessing efficacy and optimal dosing are currently underway, with a predicted completion by 2025.
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Khan et al. (2024) conducted a review in Systemic hypertension. Zilebesiran was evaluated on Blood pressure and serum angiotensinogen levels. Zilebesiran demonstrated a dose-dependent reduction in blood pressure and serum angiotensinogen levels with sustained effects up to 6 months in Phase I clinical trials.
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