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Completed Phase 2Phase 3 Interventional Results available

Study to Evaluate the Efficacy and Safety of AZD4831 in Participants With Heart Failure With Left Ventricular Ejection Fraction > 40%

ClinicalTrials.gov ID: NCT04986202

Public ClinicalTrials.gov record NCT04986202. 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 Jul 22, 2026, 10:07 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 Randomised, Double-blind, Placebo-controlled, Multi-center Sequential Phase 2b and Phase 3 Study to Evaluate the Efficacy and Safety of AZD4831 Administered for Up to 48 Weeks in Participants With Heart Failure With Left Ventricular Ejection Fraction > 40%

Study identification

NCT ID
NCT04986202
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
711 participants

Conditions and interventions

Interventions

  • AZD4831 Drug
  • Placebo Other

Drug · Other

Eligibility (public fields only)

Age range
40 Years to 85 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
Jun 29, 2021
Primary completion
Mar 26, 2024
Completion
Mar 26, 2024
Last update posted
Aug 26, 2025

2021 – 2024

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
Research Site Alexander City Alabama 35010
Research Site Little Rock Arkansas 72205
Research Site Sacramento California 95821
Research Site Miami Florida 33144
Research Site Miami Beach Florida 33140
Research Site Ocala Florida 34471
Research Site Evanston Illinois 60208
Research Site Hazel Crest Illinois 60429
Research Site Shreveport Louisiana 71105
Research Site Baltimore Maryland 21229
Research Site St Louis Missouri 63136
Research Site Buffalo New York 14215
Research Site New York New York 10019
Research Site Rosedale New York 11422
Research Site Chapel Hill North Carolina 27599
Research Site Pinehurst North Carolina 28374
Research Site Cleveland Ohio 44195
Research Site Philadelphia Pennsylvania 19107
Research Site Knoxville Tennessee 37916
Research Site Tullahoma Tennessee 37388
Research Site Norfolk Virginia 23510

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 150 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04986202, 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 Aug 26, 2025 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04986202 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →