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Completed Phase 2 Interventional Results available

Genetically Targeted Therapy for the Prevention of Symptomatic Atrial Fibrillation in Patients With Heart Failure

ClinicalTrials.gov ID: NCT01970501

Public ClinicalTrials.gov record NCT01970501. 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 21, 2026, 1:22 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

GENETIC-AF - A Genotype-Directed Comparative Effectiveness Trial of Bucindolol and Toprol-XL for Prevention of Symptomatic Atrial Fibrillation/Atrial Flutter in Patients With Heart Failure

Brief summary

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

This study is being done to compare the effects of bucindolol hydrochloride (bucindolol) to metoprolol succinate (Toprol-XL) on the recurrence of symptomatic atrial fibrillation/atrial flutter in patients with heart failure who have a specific genotype for the beta-1 adrenergic receptor.

Study identification

NCT ID
NCT01970501
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
ARCA Biopharma, Inc.
Industry
Enrollment
267 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Apr 2014 (Type not available)
Primary completion
Dec 28, 2017 (Actual)
Completion
Dec 28, 2017 (Actual)
Last update posted
Sep 26, 2022

2014 – 2017

United States locations

U.S. sites
48
U.S. states
27
U.S. cities
46
Facility City State ZIP Site status
ARCA Clinical Research Site #157 Anchorage Alaska 99508 —
ARCA Clinical Research Site #383 Phoenix Arizona 85004 —
ARCA Clinical Research Site #385 Phoenix Arizona 85018 —
ARCA Clinical Research Site #381 East Palo Alto California 94303 —
ARCA Clinical Research Site #186 Loma Linda California 92357 —
ARCA Clinical Research Site #320 Pasadena California 91105 —
ARCA Clinical Research Site #390 Stanford California 94305 —
ARCA Clinical Research Site #153 Aurora Colorado 80045 —
ARCA Clinical Research Site #380 Denver Colorado 80120 —
ARCA Clinical Research Site #195 Miami Florida 33136 —
ARCA Clinical Research Site #184 Tampa Florida 33606 —
ARCA Clinical Research Site #351 Athens Georgia 30606 —
ARCA Clinical Research Site #389 Atlanta Georgia 30322 —
ARCA Clinical Research Site #342 Oakbrook Terrace Illinois 60181 —
ARCA Clinical Research Site #303 Hammond Indiana 46320 —
ARCA Clinical Research Site #388 Iowa City Iowa 52242 —
ARCA Clinical Site #396 New Orleans Louisiana 70121 —
ARCA Clinical Research Site #398 Baltimore Maryland 21287 —
ARCA Clinical Research Site #127 Ypsilanti Michigan 48197 —
ARCA Clinical Research Site #156 Minneapolis Minnesota 55417 —
ARCA Clinical Research Site #174 Saint Paul Minnesota 55102 —
ARCA Clinical Research Site #108 St Louis Missouri 63110 —
ARCA Clinical Research Site #201 St Louis Missouri 63128 —
ARCA Clinical Research Site #152 Lincoln Nebraska 68506 —
ARCA Clinical Research Site #161 Elmer New Jersey 08318 —
ARCA Clinical Research Site #202 Hillsborough New Jersey 08844 —
ARCA Clinical Research Site # 179 Albany New York 12205 —
ARCA Clinical Research Site #397 New York New York 10029 —
ARCA Clinical Research Site #181 Durham North Carolina 27705 —
ARCA Clinical Research Site #349 Greensboro North Carolina 27401 —
ARCA Clinical Research Site #173 Akron Ohio 44304 —
ARCA Clinical Research Site #392 Cincinnati Ohio 45219 —
ARCA Clinical Research Site #322 Cleveland Ohio 44106 —
ARCA Clinical Research Site #151 Columbus Ohio 43210 —
ARCA Clinical Research Site #399 Oklahoma City Oklahoma 73135 —
ARCA Clinical Research Site #115 Portland Oregon 97201 —
ARCA Clinical Research Site # 189 Hershey Pennsylvania 17033 —
ARCA Clinical Research Site #109 Lancaster Pennsylvania 17603 —
ARCA Clinical Research Site #133 Philadelphia Pennsylvania 19104 —
ARCA Clinical Site #393 Germantown Tennessee 38138 —
ARCA Clinical Research Site #198 Jackson Tennessee 38305 —
ARCA Clinical Research Site #387 Dallas Texas 75230 —
ARCA Clinical Research Site #379 Salt Lake City Utah 84132 —
ARCA Clinical Site #391 Charlottesville Virginia 22908 —
ARCA Clinical Research Site #386 Falls Church Virginia 22042 —
ARCA Clinical Research Site #200 Manassas Virginia 20109 —
ARCA Research Site #131 Norfolk Virginia 23507 —
ARCA Clinical Research Site #196 Puyallup Washington 98372 —

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 49 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01970501, 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 Sep 26, 2022 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01970501 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →