Authorised Therapeutic confirmatory (Phase III) Symptomatic Venous Thromboembolism (VTE)

REGN7508 versus Acetylsalicylic Acid (ASA) for Venous Thromboprophylaxis after Total Knee Arthroplasty in Adult Participants

EU CTIS ID: 2025-520479-25-00

What this study is testing

To evaluate the efficacy of IV REGN7508 for the prevention of symptomatic VTE after TKA compared to ASA

  • Therapeutic confirmatory (Phase III)

A plain-language read of the study's public EU CTIS listing. The study team confirms the details.

Who can take part

You may be able to join if

  • Is undergoing a primary elective unilateral TKA.
  • Is in good health based on laboratory safety testing as described in the protocol
  • Other protocol-defined Inclusion criteria apply

You likely can't join if

  • Has 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.
  • Has a history of bleeding in the 6 months prior to randomization requiring hospitalization or transfusion; history of intracranial or intraocular bleeding, excessive operative or post-operative bleeding, and traumatic spinal or epidural anesthesia; history of bleeding diathesis (eg, hemophilia A or B, von Willebrand’s Factor deficiency).
  • Has a history of thromboembolic disease or thrombophilia.
  • Has a history of platelet dysfunction.
  • Has received or plans to receive preoperative enoxaparin on the day prior to TKA surgery
  • Other protocol-defined Exclusion criteria apply

The study team makes the final eligibility decision.

Where it's taking place

  • Malaysia
  • Canada
  • Moldova, Republic of
  • United States

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18-64 years, 65+ years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Malaysia; Canada; Moldova, Republic of; United States. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from EU CTIS; the study team decides eligibility.