A committee will judge the safety and effectiveness of edoxaban and the regular treatment (standard of care). All children in the study will receive free treatment. They will have a 2 in 3 chance to receive edoxaban, and a 1 in 3 chance to receive the standard of care for preventing blood clots. The study will find out if edoxaban is safer and more effective than the standard of care.



Eligible Ages
Under 17 Years
Eligible Genders
Accepts Healthy Volunteers

Inclusion Criteria

  • Is a child with cardiac disease who is at risk for thromboembolic complications and requires at least 3 months antithrombotic anticoagulant prophylaxis Either one of the following: 1. a child with cardiac disease who has a history of cardiac shunt occlusion/thrombosis, with shunt still in place (secondary prevention). OR 2. a child with cardiac disease who requires (including those already taking, and those not yet taking) anticoagulation for primary prevention of TE. Cardiac conditions known to significantly increase the risk of thrombosis (hence, indications for primary TE prevention) are defined in Antithrombotic Therapy and Prevention of Thrombosis. Some examples of cardiac conditions at risk of thrombosis are Fontan surgery, heart failure, Kawasaki disease, and Blalock-Taussig and Glenn surgery. - Is a male or female child between 1 and <18 years of age (children between 38 weeks gestational age and 1 year of age will be included in the study, however, only after the safety and efficacy data of 50 subjects between 1 and <18 years of age in the edoxaban arm have been evaluated at the end of the 3-month treatment period) - Has parent(s)/legal guardian(s) or legally acceptable representative who is informed and provides signed consent for the child, to participate in the study with edoxaban treatment. Pediatric participants with appropriate intellectual maturity will be required to sign an assent form in addition to the signed informed consent from the parent(s)/legal guardian(s) or any legally acceptable representative. - If a female subject of childbearing potential, tests negative for pregnancy at Screening and consents to avoid becoming pregnant by using a locally approved contraception method throughout the study

Exclusion Criteria

  • Has evidence of symptomatic venous or arterial thrombosis and/or asymptomatic intracardiac thrombosis confirmed by a transthoracic echocardiogram during study screening period - Has mechanical heart valve(s) - Has active bleeding or high risk of bleeding contraindicating treatment with anticoagulant - Takes antithrombotic therapy (other than low-dose aspirin) that is not protocol-related - Administration of rifampin is prohibited during the study and subjects on concomitant use of rifampin are excluded - Has any hepatic disease associated with coagulopathy leading to a clinically relevant bleeding risk - Has estimated glomerular filtration rate (eGFR) <30% of normal for age and size - Has stage 2 hypertension defined as blood pressure systolic and/or diastolic confirmed >99th percentile plus 5 mmHg - Has thrombocytopenia or life expectancy less than three months - Has had Fontan procedure with a history of or signs/symptoms suggestive of protein-losing enteropathy - Is pregnant or breastfeeding - Has a contraindication to the use of heparin and/or vitamin K antagonist (VKA) - Has any condition that, as judged by the Investigator, would place the participant at increased risk of harm if he/she participated in the study, including contraindicated medications identified in the protocol

Study Design

Phase 3
Study Type
Intervention Model
Parallel Assignment
Primary Purpose
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Two out of three participants will be randomized for treatment with edoxaban solution or tablets
  • Drug: Edoxaban
    Edoxaban 15 mg or 30 mg tablets for participants 12 to <18 years of age, or 60 mg edoxaban suspension (dosed as mg/kg) for participants under 12 years of age (and optionally, 12 or older), for oral administration
    Other names:
    • Lixiana
    • Savaysa
Active Comparator
Standard of Care (SOC)
One out of three participants will be randomized for treatment with the institution's SOC regimen
  • Drug: Standard of Care (SOC)
    Standard of care could include low molecular weight heparin (LMWH) and/or VKA according to the clinical site's SOC treatment regimen
    Other names:
    • Warfarin/heparin
    • Enoxaparin

Recruiting Locations

University of Alabama at Birmingham
Birmingham, Alabama 35233
Study Coordinator

More Details

Daiichi Sankyo, Inc.

Study Contact

Daiichi Sankyo Contact for Clinical Trial Information

Detailed Description

The primary objective is to compare the safety of edoxaban with the standard of care (SOC) in pediatric subjects with cardiac diseases at risk of thromboembolic complications who need primary or secondary anticoagulant prophylaxis with regard to the combination of major and clinically relevant non-major (CRNM) bleeding per International Society on Thrombosis and Haemostasis [ISTH] definition. The key secondary objective is to compare the efficacy of edoxaban against SOC with regard to the development of symptomatic thromboembolic events (TE) in the systemic arterial or venous pathways including deep vein thrombosis (DVT), pulmonary embolism (PE), stroke, intracardiac thrombus and myocardial infarction (MI), and asymptomatic intracardiac thrombus identified by cardiac imaging.


Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.