drugset / Trial / NCT00322270

Safety and Efficacy Study of Alfimeprase in Subjects With Occluded Catheters

NCT00322270 ↗

Phase 3 Completed ARCA Biopharma, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To evaluate the safety profile of alfimeprase as assessed by monitoring of adverse events, serious adverse events and major bleeding events for up to 120 minutes following the instillation of study drug to an occluded central venous access device.

Timeline

Start
2006-01
Primary completion
—
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject Alfimeprase Protein / enzyme biologic 10 mg Other