A Study of Milvexian Versus Apixaban in Participants With Atrial Fibrillation (LIBREXIA-AF)

J
John Strobel, MD

Primary Investigator

Enrolling By Invitation
18 years and older
All
Phase 3
15500 participants needed
1 Location

Brief description of study

The purpose of this study is to evaluate if milvexian is at least as effective as apixabanducing the risk of the composite stroke and non- central nervous system (CNS) systemicbolism.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Atrial Fibrillation
  • Age: 18 Years
  • Gender: All

Inclusion Criteria:
  • Minimum age of 18 years
  • Medically stable and appropriate for chronic antithrombotic treatment
  • Atrial fibrillation eligible to receive anticoagulation
  • Participant must satisfy one or both of the following categories of risk factors (a orb): a) one or more of the following risk factors: i) age greater than or equal to 75years, ii) history of a clinical symptomatic stroke. b) two or more of the followingk factors: i) age between 65 and 74 years, ii) hypertension, iii) diabetesus, iv) atherosclerotic vascular disease, v) heart failure
Exclusion Criteria:
  • Hemodynamically significant valve disease or those with valve disease that willy require surgical valve replacement during the study
  • Any condition other than AF that requires chronic anticoagulation

Updated on 01 Aug 2024. Study ID: CR109220
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