CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 25 enrolled
Drug / intervention
Placebo +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03714776
NCT03714776Phase 2Completed

A Double-Blind, Placebo-Controlled, Phase 2 Study to Assess the Safety, Tolerability and Efficacy of IONIS-AGT-LRx, an Antisense Inhibitor Administered Subcutaneously to Hypertensive Subjects With Controlled Blood Pressure

Ionis Pharmaceuticals, Inc.·interventional·Posted Oct 22, 2018·Updated Jan 6, 2023

In Brief

A Phase 2 clinical trial evaluating Placebo and ISIS 757456 for Mild Hypertension. Completed, enrolled 25 participants across 6 sites.

Detailed Summary

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

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20192020202120222023202420252026
First PostedOct 22, 2018
Enrollment StartJan 3, 2019
Primary CompletionNov 13, 2019
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 7.7 years ago

Interventions

Placebodrug

Placebo matching solution administered as SC injection.

ISIS 757456drug

Administered as SC injection.