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Clinical Trial 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.


Clinical Trial Description

Further study details as provided by Nuvelo ;


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00322270
Study type Interventional
Source ARCA Biopharma, Inc.
Contact
Status Completed
Phase Phase 3
Start date January 2006

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