CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 207 enrolled
Drug / intervention
SelK2 +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03812328
NCT03812328Phase 2Completed

A Phase 2, Randomized, Active Comparator-Controlled, Open-Label, Adaptive Design Study to Assess the Safety and Efficacy of Intravenously-Administered SelK2 in Patients Undergoing Total Knee Arthroplasty

Tetherex Pharmaceuticals Corporation·interventional·Posted Jan 23, 2019·Updated Jan 6, 2021

In Brief

A Phase 2 clinical trial evaluating SelK2 and Enoxaparin for Venous Thromboembolism. Completed, enrolled 207 participants across 21 sites in 5 countries.

Detailed Summary

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 Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBulgaria, Latvia, Lithuania, Poland, Ukraine
Collaborators--

Timeline

Phase 2CompletedFinished
20192020202120222023202420252026
First PostedJan 23, 2019
Enrollment StartFeb 20, 2019
Primary CompletionOct 1, 2019
Study CompletionNov 14, 2019
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 7.4 years ago

Interventions

SelK2drug

I.V., single-dose

Enoxaparinbiological

SC, QD for up to 10 ± 2 days