drugset / Trial / NCT01151592

Safety Assessment of Iron Sucrose (Venofer) in Patients With Chronic Kidney Disease Who Cannot Tolerate Ferumoxytol (Feraheme) or Iron Dextran (INFed or Dexferrum)

NCT01151592 ↗

Phase 4 Withdrawn American Regent, Inc.
NaSingle-groupOpen-labelTreatment

Summary

The objective of this study is to assess the safety and tolerability of Venofer in patients with chronic kidney disease who cannot tolerate Ferumoxytol (Feraheme) or intravenous iron containing a dextran (INFed or Dexferrum).

Timeline

Start
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Primary completion
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Completion
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Outcome

Outcome not reported

Stopped (Business): “Sponsor Decision”

Drugs

EvaluationDrugModalityDoseRoute
Subject Iron sucrose Unknown 1000 mg Intravenous