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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | EVAZARSEN | Unknown | 80 mg | Subcutaneous |