Status:

COMPLETED

Registry For Patients Treated With BeneFix In Usual Care Setting In Germany

Lead Sponsor:

Pfizer

Conditions:

Hemophilia B

Eligibility:

All Genders

Brief Summary

The purpose of this observational study is to describe the incidence of adverse events among patients treated with BeneFix® in usual health care settings in Germany.

Detailed Description

Non-interventional study: subjects to be selected according to the usual clinical practice of their physician

Eligibility Criteria

Inclusion

  • Patients with hemophilia B already receiving or starting treatment with reformulated BeneFIX®.

Exclusion

  • Patients with hemophilia B treated with a product other than BeneFIX®.
  • Inclusion in the ongoing prospective registry of European hemophilia B patients using BeneFIX®.

Key Trial Info

Start Date :

January 1 2008

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

October 1 2016

Estimated Enrollment :

80 Patients enrolled

Trial Details

Trial ID

NCT00714415

Start Date

January 1 2008

End Date

October 1 2016

Last Update

October 25 2018

Active Locations (21)

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Page 1 of 6 (21 locations)

1

Allgemeines Krankenhaus Linz, Kinderklinik

Linz, Austria, 4020

2

Sonnengesundheitszentrum

München, Bavaria, Germany, 80336

3

Werlhof-Institut für Haemostaseologie GmbH

Hanover, Lower Saxony, Germany, 30159

4

Institut für Thrombophilie und Hämostaseologie

Münster, North Rhine-Westphalia, Germany, 48143

Registry For Patients Treated With BeneFix In Usual Care Setting In Germany | DecenTrialz