Stopped: Terminated due to pipeline prioritization
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.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Percentage of Participants With Discontinued, Delayed or Interrupted Therapy
Timeframe: up to week 21
Percentage of Participants Without Graft Failure or Need for Intervention
Timeframe: 24 weeks
Stenosis (%) of the Index Lesion at Venous Anastomosis Using Angiography at Week 12
Timeframe: 12 weeks
Stenosis (%) of the Index Lesion at Venous Anastomosis Using Angiography at Week 24
Timeframe: 24 weeks
Stenosis (%) of the Index Lesion at Venous Anastomosis Using Angiography at Month 9
Timeframe: 9 months
Stenosis (%) of the Index Lesion at Venous Anastomosis Using Angiography at Month 12
Timeframe: 12 months
Stenosis (%) of a Non-index Lesion Using Angiography at Week 12
Timeframe: 12 weeks
Stenosis (%) of a Non-index Lesion Using Angiography at Week 24
Timeframe: 24 weeks
Stenosis (%) of a Non-index Lesion Using Angiography at Month 9
Timeframe: 9 months
Stenosis (%) of a Non-index Lesion Using Angiography at Month 12
Timeframe: 12 months