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Clinical trialNCT00389792CompletedPhase 2Interventional

Efficacy and Safety Study of an Antiarrhythmic Drug to Treat Atrial Fibrillation in Patients With Pacemakers

SponsorARYx TherapeuticsEnrollment72Atrial Fibrillation
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study is to determine the safety and efficacy of an investigational antiarrhythmic drug (ATI-2042) in the treatment of atrial fibrillation in patients with a dual chamber pacemaker.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

40 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Canada
  • Aryx Investigational Site

    Edmonton, Alberta, Canada

  • Aryx Investigational Site

    Edmonton, Alberta, Canada

  • Aryx Investigational Site

    Campbell River, British Columbia, Canada

  • Aryx Investigational Site

    Vancouver, British Columbia, Canada

  • Aryx Investigational Site

    Victoria, British Columbia, Canada

  • Aryx Investigational Site

    London, Ontario, Canada

  • Aryx Investigational Site

    Niagara Falls, Ontario, Canada

  • Aryx Investigational Site

    Ottawa, Ontario, Canada

  • Aryx Investigational Site

    Montreal, Quebec, Canada

  • Aryx Investigational Site

    Montreal, Quebec, Canada

  • Aryx Investigational Sites

    Montreal, Quebec, Canada

  • Aryx Investigational Site

    Sherbrooke, Quebec, Canada

  • Aryx Investigational Site

    Terrebonne, Quebec, Canada

United States
  • Aryx Investigational Site

    Phoenix, Arizona, United States

  • Aryx Investigational Site

    Scottsdale, Arizona, United States

  • Aryx Investigational Site

    Tucson, Arizona, United States

  • Aryx Investigational Site

    Larkspur, California, United States

  • Aryx Investigational Site

    Aurora, Colorado, United States

  • Aryx Investigational Site

    Hollywood, Florida, United States

  • Aryx Investigational Site

    Jacksonville Beach, Florida, United States

  • Aryx Investigational Site

    Atlanta, Georgia, United States

  • Aryx Investigational Site

    Marietta, Georgia, United States

  • Aryx Investigational Site

    Chicago, Illinois, United States

  • Aryx Investigational Site

    Towson, Maryland, United States

  • Aryx Investigational Site

    Saginaw, Michigan, United States

  • Aryx Investigational Site

    Minneapolis, Minnesota, United States

  • Aryx Investigational Site

    St Louis, Missouri, United States

  • Aryx Investigational Site

    Lincoln, Nebraska, United States

  • Aryx Investigational Site

    Warren Township, New Jersey, United States

  • Aryx Investigational Site

    Albuquerque, New Mexico, United States

  • Aryx Investigational Site

    Buffalo, New York, United States

  • Aryx Investigational Site

    Hershey, Pennsylvania, United States

  • Aryx Investigational Site

    Wynnewood, Pennsylvania, United States

  • Aryx Investigational Site

    Charleston, South Carolina, United States

  • Aryx Investigational Site

    Nashville, Tennessee, United States

  • Aryx Investigational Site

    Austin, Texas, United States

  • Aryx Investigational Site

    Houston, Texas, United States

  • Aryx Investigational Site

    Burlington, Vermont, United States

  • Aryx Investigational Site

    Newport News, Virginia, United States

  • Aryx Investigational Site

    Charleston, West Virginia, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

ATI-2042ATI-2042 200 mg
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Jul 2006
Primary completion
31 Dec 2008
Completion
31 Dec 2008
Last update posted
11 Mar 2009
Registered enrollment
72
Registry id
NCT00389792

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.