A cohort event monitoring study to characterise use of eplontersen in patients with prior liver transplant and pre-existing severe hepatic impairment and to assess long-term safety among all new users of eplontersen (sTTRing)

05/01/2026
05/01/2026
EU PAS number:
EUPAS1000000890
Study
Planned

ENCePP Code of conduct

Yes
Data sources

Data source(s), other

1. DD8450R00003
2. US claims data
3. AZ PV database (Argus)

Data sources (types)

Administrative healthcare records (e.g., claims)
Non-interventional study
Other

Data sources (types), other

Individual case safety reports (ICSRs)
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