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Completed Phase 2 Interventional Results available

Study of ARO-ANG3 in Adults With Mixed Dyslipidemia

ClinicalTrials.gov ID: NCT04832971

Public ClinicalTrials.gov record NCT04832971. 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 Sep 12, 2026, 7:17 AM 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 Double-blind, Placebo-controlled Phase 2b Study to Evaluate the Efficacy and Safety of ARO-ANG3 in Adults With Mixed Dyslipidemia

Brief summary

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

The purpose of AROANG3-2001 is to evaluate the efficacy and safety of ARO-ANG3 in participants with mixed dyslipidemia. Participants will initially receive 2 subcutaneous injections of ARO-ANG3 or placebo. Participants who complete the double-blind treatment period may opt to continue in an open-label extension during which they will receive up to 8 doses of ARO-ANG3.

Study identification

NCT ID
NCT04832971
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Arrowhead Pharmaceuticals
Industry
Enrollment
204 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Jun 27, 2021
Primary completion
Aug 29, 2022
Completion
Sep 24, 2024
Last update posted
Dec 2, 2025

2021 – 2024

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Research Site 5 Huntington Park California 90255
Research Site 7 Hialeah Florida 33012
Research Site 17 Miami Florida 33144
Research Site 8 Port Orange Florida 32127
Research Site 24 Minneapolis Minnesota 55455
Research Site 10 Omaha Nebraska 68114
Research Site 23 Las Vegas Nevada 89121
Research Site 22 New York New York 10029
Research Site 15 Greensboro North Carolina 27408
Research Site 2 Morehead City North Carolina 28557
Research Site 1 Marion Ohio 43302
Research Site 4 Camp Hill Pennsylvania 17011
Research Site 11 Houston Texas 77030

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 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04832971, 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 2, 2025 · Synced Sep 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04832971 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →