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NCT01885598

Eliquis Regulatory Post Marketing Surveillance

Completed Last updated 31 October 2017
What this trial tests

trial testing Apixaban in NonValvular Atrial Fibrillation in 3,335 participants. Completed in 29 September 2017.

Timeline
10 July 2013
Primary endpoint
29 September 2017
29 September 2017

Quick facts

Lead sponsorBristol-Myers Squibb
StatusCompleted
Study typeOBSERVATIONAL
Enrollment3,335
Start date10 July 2013
Primary completion29 September 2017
Estimated completion29 September 2017
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Bristol-Myers Squibb — full company profile →

Who can join

19 and older, any sex, with NonValvular Atrial Fibrillation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary objective of this study is to examine the safety profile of Eliquis in Korean nonvalvular atrial fibrillation patients.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Apixaban for Secondary Stroke Prevention: Coexistant Cerebral Atherosclerosis May Increase Recurrent Strokes.
    Kim JS, Koo J, Shin DI, Kim BS, et al · · 2022 · cited 6× · PMID 35135065 · DOI 10.5853/jos.2021.02355

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Other trials of Apixaban

Trials testing the same drug.

Other Bristol-Myers Squibb trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01885598.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing