For Healthcare Professionals

A Study of Milvexian Versus Apixaban in Participants With Atrial Fibrillation

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About the study

The purpose of this study is to evaluate if milvexian is at least as effective as apixaban for reducing the risk of the composite stroke and non-central nervous system (CNS) systemic embolism.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:

  1. Minimum age of 18 years
  2. Medically stable and appropriate for chronic antithrombotic treatment
  3. Atrial fibrillation eligible to receive anticoagulation
  4. Participant must satisfy one or both of the following categories of risk factors (a or b): a) one or more of the following risk factors: i) age greater than or equal to 75 years, ii) history of any type of stroke including symptomatic stroke of any kind. b) two or more of the following risk factors: i) age between 65 and 74 years, ii) hypertension, iii) diabetes mellitus, iv) atherosclerotic vascular disease, v) heart failure

EXCLUSION CRITERIA

Exclusion Criteria:

  1. Hemodynamically significant valve disease or those with valve disease that will potentially require surgical valve replacement during the study
  2. Any condition other than AF that requires chronic anticoagulation
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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall 844-434-4210Email iconEmail Study Center

Study Details


Contition

Atrial Fibrillation

Age

18+

Phase

PHASE3

Participants Needed

15500

Est. Completion Date

May 5, 2027

Treatment Type

INTERVENTIONAL


Sponsor

Janssen Research & Development, LLC

ClinicalTrials.gov NCT Identifier

NCT05757869

Study Number

70033093AFL3002

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