A Study of Risk Factors for Anti-erythropoietin Antibody Positive Pure Red Cell Aplasia Among Patients With Chronic Kidney Disease Receiving Epoetin Alfa

CompletedOBSERVATIONAL
Enrollment

124

Participants

Timeline

Start Date

March 31, 2004

Study Completion Date

March 31, 2006

Conditions
Pure Red-cell Aplasia
Interventions
DRUG

No intervention

This study is an observational study. No medication will be provided or administered to the participants. Participants will receive standard-of-care treatment from their individual physicians.

Trial Locations (22)

Unknown

São Paulo

Sorocaba

Bois-Guillaume

Grenoble

Nantes

Orléans

Paris

Tvnsberg

Bloemfontein

Karlshamn

Stockholm

Trollhättan

Vlissingen

Birmingham

Brighton

Bristol

Chelmsford

Edinburgh

London

Manchester

Omagh

Westcliff-on-Sea

All Listed Sponsors
lead

Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

INDUSTRY

NCT00211068 - A Study of Risk Factors for Anti-erythropoietin Antibody Positive Pure Red Cell Aplasia Among Patients With Chronic Kidney Disease Receiving Epoetin Alfa | Biotech Hunter | Biotech Hunter