drugset / Trial / NCT05785819

A Phase 2 Study of VLX-1005 Versus Placebo in Suspected Heparin Induced Thrombocytopenia

NCT05785819

Phase 2 Terminated 24 enrolled Veralox Therapeutics
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of VLX-1005, a 12-lipoxygenase (12-LOX) enzyme inhibitor in treating heparin induced thrombocytopenia (HIT). Participants with suspected HIT will receive the usual standard of care, and will be assigned randomly to either VLX-1005 or placebo treatment. The study will measure important outcomes including platelet count, stroke, pulmonary embolus (clot to the lungs) and bleeding.

Timeline

Start
2023-09-26
Primary completion
2025-11-17
Completion
2025-11-17

Drugs

EvaluationDrugModalityDoseRoute
Subject VLX-1005 Small molecule 200 mg Intravenous