Overview

A Phase I Study of the Co-administration of VLX-1005 and Argatroban in Healthy Human Subjects

Status:
Recruiting
Trial end date:
2022-10-15
Target enrollment:
Participant gender:
Summary
The study is designed to characterize the safety and tolerability of VLX-1005 and argatroban administered intravenously, either alone or in combination; and the pharmacokinetics and pharmacodynamics and potential interaction of both agents in a population of healthy subjects.
Phase:
Phase 1
Details
Lead Sponsor:
Veralox Therapeutics
Collaborator:
Celerion
Treatments:
Argatroban