drugset / Trial / NCT04083222

A Study to Assess the Safety, Tolerability and Efficacy of IONIS-AGT-LRx

NCT04083222 ↗

Phase 2 Completed 26 enrolled Ionis Pharmaceuticals, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This study evaluated the effect of ISIS 757456 (IONIS-AGT-LRx) on plasma angiotensinogen (AGT) and systolic blood pressure (SBP) in uncontrolled hypertensive participants who were on two to three antihypertensive medications.

Timeline

Start
2019-11-13
Primary completion
2020-07-20
Completion
2020-07-20

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs ISIS 757456; p < 0.001; ANOVA; NCT04083222 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject EVAZARSEN Unknown 80 mg Subcutaneous

Indications