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Compound · clinical trials

Apixaban

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 7 trials in our USA, China, UK and India registers that name Apixaban as an intervention. Synced 24 Sep 2026
7Trials tracked
6Recruiting now
3Lead sponsors
4Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards

Apixaban is named as a drug or biological intervention in 7 clinical trials in our USA, China, UK and India trial registers, 6 of which are recruiting. Lead sponsors include Regeneron Pharmaceuticals (4), Northern Jiangsu People's Hospital (2) and Janssen Research & Development, LLC (1). Registered phases: Phase 3, Not applicable and Phase 2. Conditions studied include Atrial Fibrillation (AF); Venous Thromboembolism (VTE); Cirrhosis.

Apixaban also has an approved-drug profile on this site (FDA label data): Eliquis (Apixaban) →
01

Clinical trials of Apixaban

7 trials
NCT IDStudyPhaseStatusLead sponsorRegister
NCT07015905 REGN7508 Versus Apixaban and Enoxaparin for Thromboprophylaxis After Total Knee Arthroplasty in Adults (ClinicalTrials.gov ↗)
Venous Thromboembolism (VTE)
Phase 3 Recruiting Regeneron Pharmaceuticals USA
NCT07493304 Treatment and Secondary Prevention of Venous Thromboembolism (VTE) in Adult Participants With Solid and Hematologic Cancers (ClinicalTrials.gov ↗)
Venous Thromboembolism (VTE)
Phase 3 Recruiting Regeneron Pharmaceuticals USA
NCT07626411 Stroke and Systemic Embolism Prevention in Adult Participants With Atrial Fibrillation (ClinicalTrials.gov ↗)
Atrial Fibrillation (AF)
Phase 3 Recruiting Regeneron Pharmaceuticals USA
NCT07175428 Safety in Adult Participants With Atrial Fibrillation Who Are Treated With Anticoagulation (ClinicalTrials.gov ↗)
Atrial Fibrillation (AF)
Phase 2 Recruiting Regeneron Pharmaceuticals USA
NCT07461532 Efficacy of Apixaban in Treating Portal Vein Thrombosis Occurring More Than One Year After LSD (ClinicalTrials.gov ↗)
Cirrhosis, Splenectomy, Portal Vein Thrombosis
Not applicable Recruiting Northern Jiangsu People's Hospital China
NCT07461545 Efficacy of Apixaban in the Treatment of Portal Vein Thrombosis Occurring More Than One Year After LS (ClinicalTrials.gov ↗)
Cirrhosis, Splenectomy, Portal Vein Thrombosis
Not applicable Recruiting Northern Jiangsu People's Hospital China
NCT05757869 A Study of Milvexian Versus Apixaban in Participants With Atrial Fibrillation (ClinicalTrials.gov ↗)
Atrial Fibrillation
Phase 3 Active, closed Janssen Research & Development, LLC UK, USA, India, China

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied

7 conditions
Condition (as registered)Trials
Atrial Fibrillation (AF)2
Venous Thromboembolism (VTE)2
Cirrhosis2
Splenectomy2
Portal Vein Thrombosis2
Hypertension, Portal2
Atrial Fibrillation1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Regeneron Pharmaceuticals4
Northern Jiangsu People's Hospital2
Janssen Research & Development, LLC1
04

Trials by country register

A trial with sites in more than one country appears in each of those registers.

How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records โ€” it is not written from memory, and nothing here describes how Apixaban works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Apixaban (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 24 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician โ€” our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us โ€” we correct promptly and log it.