drugset / Trial / NCT03714776

A Study to Assess the Safety, Tolerability and Efficacy of IONIS-AGT-LRx, an Antisense Inhibitor Administered Subcutaneously to Hypertensive Participants With Controlled Blood Pressure

NCT03714776 ↗

Phase 2 Completed 25 enrolled Ionis Pharmaceuticals, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This was a Phase 2, double-blind, randomized, placebo-controlled study of IONIS-AGT-LRx conducted in mild hypertensive participants.

Timeline

Start
2019-01-03
Primary completion
2019-11-13
Completion
2019-11-13

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs ISIS 757456 80 mg; p <0.001; ANOVA NCT03714776 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject EVAZARSEN Unknown 80 mg Subcutaneous

Indications