TAK-577-4005: Estimating Risk of Selected Adverse Events in Patients with Von Willebrand Disease Treated With VEYVONDI® (Vonicog Alfa; Recombinant Von Willebrand Factor)

03/03/2022
02/07/2024
EU PAS number:
EUPAS45617
Study
Finalised

ENCePP Code of conduct

No
Data sources

Data sources (types)

Electronic healthcare records (EHR)
Other

Data sources (types), other

The primary source for this retrospective study is the electronic or paper medical records of enrolled participants. Participant’s data will be collected from the records and will be entered in a web-based electronic case report form (eCRF).
Use of a Common Data Model (CDM)

CDM mapping

No
Data quality specifications

Check conformance

Unknown

Check completeness

Unknown

Check stability

Unknown

Check logical consistency

Unknown
Data characterisation

Data characterisation conducted

No