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ENROLLING BY INVITATION
NCT03690336

Adverse Event Data Collection From External Registries on Nonacog Beta Pegol

Sponsor: Novo Nordisk A/S

View on ClinicalTrials.gov

Summary

The purpose of this study is to collect data on adverse events from third party registries that include information about adverse events from patients with haemophilia B treated with nonacog beta pegol. The third party registries include PedNet Haemophilia Registry (PedNet) and the European Haemophilia Safety Surveillance System (EUHASS). Data from national and international registries in countries where nonacog beta pegol has been approved and marketed could be included in the data collection.

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

10

Start Date

2018-10-01

Completion Date

2027-10-01

Last Updated

2025-06-02

Healthy Volunteers

No

Conditions

Interventions

DRUG

Nonacog beta pegol

Treatment with commercially available nonacog beta pegol according to routine clinical practice at the discretion of the treating physician.

Locations (2)

PedNet Haemophilia Registry

Baarn, Netherlands

European Haemophilia Safety Surveillance Registry

Sheffield, United Kingdom