Clinical Trials Directory

Trials / Completed

CompletedNCT00719459

Bioequivalency Study Comparing Hospira's Generic Iron Sucrose Injection to Venofer

A Randomized, Open-Label, Single-Dose, Parallel-Design, Bioequivalence Study of Hospira Iron Sucrose Injection Compared to Venofer® Injection USP in Healthy Subjects.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Hospira, now a wholly owned subsidiary of Pfizer · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The primary objective of this study is to assess the bioequivalence of the test product Hospira Iron Sucrose 20 mg/mL (Hospira, Inc.) to the reference product Venofer® 20 mg/mL following intravenous administration to healthy subjects.

Detailed description

Iron is essential to the synthesis of hemoglobin (Hb) to maintain oxygen transport and to the function and formation of other physiologically important heme and nonheme compounds. Iron deficiency may be caused by blood loss during dialysis, increased erythropoiesis following administration of epoetin, and insufficient absorption of iron from the gastro-intestinal tract. Most dialysis patients require intravenous iron supplementation to replenish iron stores. Iron sucrose is used to replenish body iron stores in patients with iron deficiency on chronic hemodialysis and receiving erythropoietin. In these patients iron deficiency is caused by blood loss during dialysis procedure, increased erythropoiesis, and insufficient absorption of iron from the gastrointestinal tract. Most hemodialysis patients require intravenous iron to maintain sufficient iron stores to achieve and maintain a hemoglobin level of 11-12 g/dL. Subjects who fulfill the inclusion/exclusion criteria after screening will be randomized to receive 100 mg of iron sucrose as either Hospira Iron Sucrose or Venofer®.

Conditions

Interventions

TypeNameDescription
DRUGIron SucroseVenofer 20 mg/mL
DRUGIron SucroseIron sucrose 20 mg/mL

Timeline

Start date
2008-06-01
Primary completion
2008-07-01
Completion
2008-07-13
First posted
2008-07-21
Last updated
2017-03-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00719459. Inclusion in this directory is not an endorsement.