drugset / Trial / NCT00249002

Use of ABI-007 for the Prevention of Vascular Access Graft Failure in Patients Undergoing Hemodialysis

NCT00249002 ↗

Phase 2 Terminated 9 enrolled Celgene Corporation
NaSingle-groupOpen-labelPrevention

Summary

This study is designed to confirm the safety of the proposed dose and schedule of ABI-007 for hemodialysis patients with vascular access device failure, and to obtain preliminary data on the effectiveness of such treatment.

Timeline

Start
2005-11-01
Primary completion
2007-11-01
Completion
2007-11-01

Outcome

Outcome not reported

Stopped: “Terminated due to pipeline prioritization”

Drugs

EvaluationDrugModalityDoseRoute
Subject ABI-007 Unknown 35 mg/m2 Intravenous

Indications

No indication recorded.