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An Observational, Prospective, Safety Study of Mircera (Monopegylated Epoetin Beta) in Clinical Practice

Kidney Disease, Chronic Clinical Trial

Official title:
Post Marketing Surveillance of Mircera®

Clinical Trial Summary

This national study was a post-marketing surveillance study conducted in Korea from 29 August 2008 to 28 August 2012 to meet local regulatory requirements for Mircera (monopegylated-epoetin beta). Prospective patient-based data collection was evaluated for safety/risk assessments and effectiveness. No specific study-related procedures are required. Patients were to be followed up as long as possible at the physician's discretion.

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02263833
Study type Observational
Source Hoffmann-La Roche
Contact
Status Completed
Phase N/A
Start date September 2009
Completion date August 2012
View Details
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