COVID-19 trials registries data warehouse

https://clinicaltrials.gov/show/NCT04508023

Not reported

Not reported

2020-08-11

Terminated

RCT

Randomized

Parallel

Blind label

multi-center

Treatment

inclusion criteria: - coronavirus disease 2019 (covid-19) positive diagnosis by locally obtained viral diagnostic test (example, polymerase chain reaction [pcr]). this may be nasal swab or saliva test or other available technology to demonstrate current infection - confirm that participant is known to health system, with at least 1 contact in electronic medical records (emr) prior to screening - symptoms attributable to covid-19 (example, fever, cough, loss of taste or smell, muscle aches, shortness of breath, fatigue) - initial treatment plan does not include hospitalization - presence of at least 1 additional risk factor: a) age more than or equal to (>=) 60 years; b) prior history of vte; c) history of thrombophilia; d) history of coronary artery disease (cad); e) history of peripheral artery disease (pad); f) history of cerebrovascular disease or ischemic stroke; g) history of cancer (other than basal cell carcinoma) h) history of diabetes requiring medication; i) history of heart failure; j) body mass index (bmi) greater than or equal to (>=) 35 kilogram per meter square (kg/m^2); k) d-dimer greater than (>) upper limit of normal for local laboratory (within 2 weeks of the date of the covid-19 test and prior to randomization)

- increased risk of bleeding such as a) significant bleeding in the last 3 months; b) active gastroduodenal ulcer in the last 3 months; c) history of bronchiectasis or pulmonary cavitation; d) need for dual antiplatelet therapy or anticoagulation; e) prior intracranial hemorrhage, f) known severe thrombocytopenia g) active cancer and undergoing treatment - any illness or condition that in the opinion of the investigator would significantly increase the risk of bleeding (example recent trauma, recent surgery, severe uncontrolled hypertension, gastrointestinal cancer, renal failure requiring dialysis, severe liver disease, known bleeding diathesis) - known allergies, hypersensitivity, or intolerance to rivaroxaban or its excipients - positive covid-19 antibody or serology test after 2-week period of acute, symptomatic covid-19 infection - known diagnosis of triple positive (positive for lupus anticoagulant, anticardiolipin, and anti-beta 2-glycoprotein i antibodies) antiphospholipid syndrome

2

Janssen Research & Development, LLC

18

100

United States

Mild disease at enrollment

1: Mild disease at enrollment

1284

Number of Participants With Time to First Occurrence of Primary Efficacy Composite Endpoint;Number of Participants With Time to First Occurrence of The Principle Safety Outcome (Fatal Bleeding and Critical Site Bleeding) Based on a Modification of the International Society on Thrombosis and Haemostasis (ISTH) Criteria

None

Phase 3

[{"arm_notes": "", "treatment_id": 1124, "treatment_name": "Rivaroxaban", "treatment_type": "Coagulation modifiers", "pharmacological_treatment": "Pharmacological treatment"}, {"arm_notes": "", "treatment_id": 2187, "treatment_name": "Placebo", "treatment_type": "Placebo", "pharmacological_treatment": "Placebo"}]