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Clinical Trial Summary

This non-interventional study concerns a safety data collection based on adverse event data from a third-party registry (European Haemophilia Safety Surveillance System, EUHASS) that includes information about adverse events from patients with haemophilia A treated with turoctocog alfa pegol. There is no extra burden to the patients by participating in this registry-based data collection.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04682145
Study type Observational
Source Novo Nordisk A/S
Contact
Status Enrolling by invitation
Phase
Start date December 9, 2020
Completion date April 1, 2025

See also
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