218
Participants
Start Date
January 31, 2004
Primary Completion Date
October 31, 2011
Study Completion Date
October 31, 2011
activated recombinant human factor VII
A prospective, observational multi-national registry collecting data and evaluating the efficacy and safety of rFVIIa in patients with GT with past or present refractoriness to platelet transfusions. The registry will also collect data from a broader range of GT patients treated with systemic haemostatic treatment (with or without antifibrinolytic drugs or other agents) used in the clinics. Data collection will continue for a maximum of six years. Baseline data as well as data obtained during either bleeding episodes or invasive procedures/surgeries will be recorded in the registry.
Budapest
Brussels
Sofia
Algiers
Madrid
Mainz
Paris La Défense Cedex
Novo Nordisk Clinical Trial Call Center, Princeton
Vienna
Rome
Alphen aan den Rijn
Karachi
Malmo
Zurich
Crawley
Lead Sponsor
Novo Nordisk A/S
INDUSTRY