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Completed Phase 2 Interventional Results available

A Study to Evaluate Efficacy and Safety of ALN-AGT01 in Patients With Mild To-Moderate Hypertension

ClinicalTrials.gov ID: NCT04936035

Public ClinicalTrials.gov record NCT04936035. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 3:15 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Placebo-Controlled, Dose-Ranging Multicenter Study to Evaluate the Efficacy and Safety of ALN-AGT01 in Patients With Mild-to-Moderate Hypertension

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the effect of ALN-AGT01 on systolic and diastolic blood pressure and to characterize the pharmacodynamic (PD) effects and safety of ALN-AGT01.

Study identification

NCT ID
NCT04936035
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Alnylam Pharmaceuticals
Industry
Enrollment
394 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 7, 2021 (Actual)
Primary completion
Apr 4, 2023 (Actual)
Completion
Dec 5, 2024 (Actual)
Last update posted
Dec 23, 2025

2021 – 2024

United States locations

U.S. sites
54
U.S. states
21
U.S. cities
47
Facility City State ZIP Site status
Clinical Trial Site Birmingham Alabama 35209 —
Clinical Trial Site Tempe Arizona 85281 —
Clinical Trial Site Tempe Arizona 85282 —
Clinical Trial Site Beverly Hills California 90211 —
Clinical Trial Site La Mesa California 91942 —
Clinical Trial Site Los Angeles California 90057 —
Clinical Trial Site San Diego California 92103 —
Clinical Trial Site South Gate California 90280 —
Clinical Trial Site Vista California 92083 —
Clinical Trial Site Washington D.C. District of Columbia 20011 —
Clinical Trial Site Clearwater Florida 33756 —
Clinical Trial Site Coral Gables Florida 33134 —
Clinical Trial Site Fleming Island Florida 32003 —
Clinical Trial Site Hollywood Florida 33021 —
Clinical Trial Site Hollywood Florida 33024 —
Clinical Trial Site Inverness Florida 34452 —
Clinical Trial Site Jacksonville Florida 32204 —
Clinical Trial Site Jacksonville Florida 32216 —
Clinical Trial Site Jacksonville Florida 32256 —
Clinical Trial Site Miami Florida 33126 —
Clinical Trial Site Miami Florida 33135 —
Clinical Trial Site Naples Florida 34102 —
Clinical Trial Site Orlando Florida 32801 —
Clinical Trial Site Acworth Georgia 30101 —
Clinical Trial Site Columbus Georgia 31904 —
Clinical Trial Site Fayetteville Georgia 30214 —
Clinical Trial Site Macon Georgia 31210 —
Clinical Trial Site Champaign Illinois 61822 —
Clinical Trial Site Valparaiso Indiana 46383 —
Clinical Trial Site West Des Moines Iowa 50266 —
Clinical Trial Site Lake Charles Louisiana 70601 —
Clinical Trial Site New Orleans Louisiana 70124 —
Clinical Trial Site Prairieville Louisiana 70769 —
Clinical Trial Site Baltimore Maryland 21229 —
Clinical Trial Site Jackson Mississippi 39209 —
Clinical Trial Site Jefferson City Missouri 65109 —
Clinical Trial Site Las Vegas Nevada 89119 —
Clinical Trial Site New York New York 10036 —
Clinical Trial Site The Bronx New York 10456 —
Clinical Trial Site Greensboro North Carolina 27408 —
Clinical Trial Site Greensboro North Carolina 27410 —
Clinical Trial Site Medford Oregon 97504 —
Clinical Trial Site Greenville South Carolina 29607 —
Clinical Trial Site Memphis Tennessee 38119 —
Clinical Trial Site Cedar Park Texas 78613 —
Clinical Trial Site Houston Texas 77074 —
Clinical Trial Site Houston Texas 77081 —
Clinical Trial Site Magnolia Texas 77355 —
Clinical Trial Site Pearland Texas 77584 —
Clinical Trial Site San Antonio Texas 78229 —
Clinical Trial Site Stephenville Texas 76401 —
Clinical Trial Site Tomball Texas 77375 —
Clinical Trial Site Waco Texas 76708 —
Clinical Trial Site Burke Virginia 22015 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 21 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04936035, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 23, 2025 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04936035 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →