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Effects of Intravenous Injection of Erythropoietin on Hepcidin Pharmacokinetics in Healthy Volunteers

Effects of Intravenous Injection of Erythropoietin on Hepcidin Pharmacokinetics in Healthy Volunteers

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00687518
Acronym
HEPEPO
Enrollment
14
Registered
2008-05-30
Start date
2008-02-07
Completion date
2008-09-30
Last updated
2026-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Iron Metabolism Disorders

Brief summary

The aim of this study is to measure the variations of serum and urinary hepcidin levels following a single intravenous injection of erythropoietin in healthy volunteers. Hepcidin is a major regulator of iron homeostasis. It acts by binding on ferroportin, and limits cellular efflux of iron through enterocytes and macrophages. Anemia and hypoxia are known to modulate hepcidin synthesis. In these situations, erythropoietin synthesis is increased, so it can be postulated that erythropoietin could modulate hepcidin synthesis.

Interventions

DRUGErythropoietin

Intravenous injection of 50 U/kg of erythropoietin

DRUGPlacebo

Intravenous injection of equivalent volume of saline serum

Sponsors

Rennes University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy volunteers * male aged 18 - 30 * normal routine laboratory values * normal ECG * normal iron status

Exclusion criteria

* C282Y mutation of the HFE gene * alcohol or tobacco consumption

Design outcomes

Primary

MeasureTime frame
serum hepcidin levelsover 24 hours

Secondary

MeasureTime frame
urinary hepcidin levelsover 24 hours
serum iron and ferritin levelsover 24 hours

Countries

France

Contacts

PRINCIPAL_INVESTIGATORFabrice LAINE, MD

Rennes University Hospital

STUDY_CHAIRBruno LAVIOLLE, MD

RennesUniversity Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 13, 2026