핵심 개념
Zilebesiran shows promising results in reducing systolic blood pressure in patients with hypertension.
초록
The phase 2 KARDIA-1 study evaluated the efficacy and safety of zilebesiran in treating hypertension. Key highlights include:
- Zilebesiran met primary and secondary endpoints with an "encouraging" safety profile.
- Patients showed a dose-dependent reduction in systolic blood pressure with zilebesiran.
- The study supports quarterly or biannual dosing of zilebesiran.
- Adverse events were reported but not considered related to the study drug.
- Results are promising for addressing unmet needs in patients with uncontrolled hypertension.
통계
Topline data show a placebo-subtracted reduction greater than 15 mm Hg in systolic blood pressure with 300 mg and 600 mg doses.
Serious adverse events were reported in 3.6% of zilebesiran-treated patients and 6.7% of placebo-treated patients.
인용구
"As a physician, I believe these KARDIA-1 results, which demonstrate clinically significant reductions in systolic blood pressure of greater than 15 mm Hg, along with the ability to achieve durable tonic blood pressure control, provide hope that we may one day have access to a novel therapy with the potential to address the significant unmet needs of patients with uncontrolled hypertension who are at high risk of future cardiovascular events." - George L. Bakris, MD