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NCT00318812

Heme Iron Polypeptide for the Treatment of Iron Deficiency Anemia in Pre-Dialysis Patients: A Pilot Randomized Controlled Study

Completed Phase 2/Phase 3 Results posted Last updated 5 April 2016
What this trial tests

Phase 2/Phase 3 trial testing Heme Iron Polypeptide (Proferrin) in Anemia in 55 participants. Completed in 1 December 2011.

Timeline
1 May 2007
Primary endpoint
1 December 2011
1 December 2011

Quick facts

Lead sponsorOttawa Hospital Research Institute
PhasePhase 2/Phase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment55
Start date1 May 2007
Primary completion1 December 2011
Estimated completion1 December 2011
Sites1 location across Canada

Drugs / interventions tested

Conditions studied

Sponsor

Ottawa Hospital Research Institute

Who can join

18 and older, any sex, with Anemia or Renal Failure. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The purpose of this study is to determine if oral Heme Iron Polypeptide is as effective as intravenous (IV) iron sucrose in the treatment of iron-deficiency anemia for patients with chronic kidney disease.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Heme iron polypeptide for the treatment of iron deficiency anemia in non-dialysis chronic kidney disease patients: a randomized controlled trial.
    Nagaraju SP, Cohn A, Akbari A, Davis JL, et al · · 2013 · cited 28× · PMID 23514036 · DOI 10.1186/1471-2369-14-64

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Other recruiting trials for Anemia

Currently open trials in the same condition.

Other Ottawa Hospital Research Institute trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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