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REGN7508 Versus Apixaban and Enoxaparin for Thromboprophylaxis After Total Knee Arthroplasty in Adults

RecruitingPhase 3

A Phase 3, Multicenter, Randomized, Open-Label, Study to Evaluate REGN7508, A Factor XI Monoclonal Antibody, Versus Apixaban and Enoxaparin for Prophylaxis of Venous Thromboembolism After Elective Total Knee Arthroplasty (ROXI-APEX)

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Key Inclusion Criteria:

1. Is undergoing a primary elective unilateral TKA
2. Is in good health based on laboratory safety testing as described in the protocol
3. Body weight ≤130 kg at screening visit as described in the protocol

Key Exclusion Criteria:

1. Any condition that, as assessed by the investigator, may confound the results of the study or pose an additional risk to the participant by study participation
2. History of bleeding in the 6 months prior to randomization requiring hospitalization or transfusion as described in the protocol
3. History of thromboembolic disease or thrombophilia
4. History of major surgery, including brain, spinal, or ocular, or major trauma within approximately the past 6 months prior to randomization
5. Has an estimated Glomerular Filtration Rate (GFR) of \<30 mL/min/1.73 m2 at the screening visit as described in the protocol

Note: Other protocol-defined Inclusion/ Exclusion Criteria apply

About the study

This study is researching an experimental drug called REGN7508 (called "study drug"). The study is focused on adults undergoing elective, unilateral (one side) total knee replacement surgery.

The aim of the study is to see how effective the study drug is at preventing Venous Thromboembolism (VTE) and other related diseases after total knee replacement surgery.

The study is looking at several other research questions, including:

* What side effects may happen from taking the study drug * How much study drug is in the blood at different times * Whether the body makes antibodies against the study drug (which could make the study drug less effective or could lead to side effects)

What is being tested

Sponsor: Regeneron Pharmaceuticals · Participants: 2,000 · Started: Jun 25, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07015905

Locations in the U.S.

AlabamaShoals Medical Trials, Inc., Sheffield
CaliforniaCARI Clinical Trials, Riverside
ColoradoDenver Metro Orthopedics, P.C. Englewood Location, Englewood
FloridaDelray Physician Care Center, Delray Beach
Bioresearch Partner, Miami
Sacred Heart Health System Inc, Pensacola
Gulfcoast Research Institute, Sarasota
Phoenix Clinical Research, Tamarac
MarylandSinai Hospital of Baltimore, Inc., Baltimore
MassachusettsBrigham and Women's Hospital, Boston
New JerseyCuralta Clinical Trials, Westwood
North CarolinaDuke University Health System (Duke Health), Duke University Hospital, Durham
TexasHD Research - First Surgical Hospital, Bellaire
University of Texas (UT); Southwestern Medical Center, Dallas
NextStage Clinical Research, All American Orthopedics and Sports Medicine, Houston
Futuro Clinical Trials, McAllen
DRx Clinical Research, LLC; South Texas Bone and Joint Institute, San Antonio
Flourish Research - San Antonio (Formerly Clinical Trials of Texas), San Antonio
UtahDRx Clinical Research, LLC, St. George

Conditions

From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.