A secondary data use study of pregnancy and infant outcomes following administration of casirivimab + imdevimab (Ronapreve, REGEN-COV) during pregnancy based on data obtained from the COVID-19 international drug pregnancy registry [COVID-PR]

05/11/2021
28/04/2025
EU PAS number:
EUPAS43694
Study
Discontinued

ENCePP Code of conduct

No
Data sources

Data sources (types)

Disease registry
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
Procedures
No information provided.