Study to Assess the Safety and Efficacy of SelK2 to Prevent Blood Clots in Patients Undergoing Total Knee Replacement

Tetherex Pharmaceuticals Corporation207 enrolled

Overview

The main purpose of this study is to determine if an investigational medication called SelK2 works in preventing a condition called "venous thromboembolism" (VTE) in patients having a total knee replacement. SelK2 has been designed to attach to a protein found on blood cells and blood vessels. By attaching to this protein, SelK2 is designed to decrease the inflammatory process in the blood vessel wall that leads to the formation of blood clots in the vessel (called thrombosis). By decreasing the inflammatory process, SelK2 may reduce the risk of VTE following joint replacement surgery. In addition, because SelK2 is not a blood thinner, it is expected that the risk for bleeding will also be reduced.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

SINGLE

Enrollment

207

Conditions

Venous Thromboembolism

Interventions

Eligibility

Sex: ALLMin age: 18 YearsMax age: 80 Years

Medical Language ↔ Plain English

Key Inclusion Criteria: * Males or females, 18-80 years of age (inclusive) * Planned to undergo elective, primary total unilateral Total Knee Arthroplasty under general anesthesia Key Exclusion Criteria: * Previous deep vein thrombosis (DVT) of the leg or pulmonary embolism (PE) within the past year * Any underlying condition (e.g., atrial fibrillation, mechanical heart valve, or recent pulmonary embolism) that may lead to the required concomitant use of anticoagulants/antiplatelet agents (e.g., warfarin, dabigatran, rivaroxaban, apixaban, clopidogrel) that may affect study outcome or any other drug influencing coagulation (except low dose aspirin (100 mg or less)) * Anticipated use of intermittent pneumatic compression devices and/or electrical/mechanical muscle stimulators post Total Knee Arthroplasty procedure

Locations (21)

UMHAT Kanev AD

Rousse, Bulgaria

Acibadem City Clinic Tokuda Hospital EAD

Sofia, Bulgaria

UMHAT Tsaritsa Yoanna - ISUL

Sofia, Bulgaria

Regional Hospital of Liepaja

Liepāja, Latvia

Hospital of Traumatology and Orthopaedics

Riga, Latvia

ORTO Clinic

Riga, Latvia

Riga's 2nd Hospital

Riga, Latvia

Vidzemes Hospital

Valmiera, Latvia

Kaunas Clinical Hospital

Kaunas, Lithuania

Klaipeda University Hospital

Klaipėda, Lithuania

...and 11 more locations

Outcomes

Primary Outcomes

Percentage of Participants With Total Venous Thromboembolism

The primary efficacy endpoint was incidence of total VTE (reported as a percentage of patients) during the Treatment Phase up to venography day (10 ± 2 days after total knee replacement). All efficacy endpoint data was adjudicated by the blinded Central Independent Adjudication Committee (CIAC).

Time frame: 10 ± 2 Days After Total Knee Replacement

Percentage of Participants With Major or Clinically Relevant Non-major Bleeding Events

All suspected bleeding events were reviewed by the Central Independent Adjudication Committee (CIAC) in a blinded fashion and were adjudicated for categorization as Major Bleeding (MB), Clinically Relevant Non-Major Bleeding (CRNMB), Minor Bleeding, or combination of MB and CRNMB. The outcome measure assessed the incidence of MB or CRNMB.

Time frame: 10 ± 2 Days After Total Knee Replacement