Clinical Trials Directory

Trials / Completed

CompletedNCT06046534

Retrospective Medical Chart Review Study to Describe the Experience of SLE Patients Treated With Anifrolumab in the Early Access Programs.

ERYTHRO Retrospective Medical Chart Review Study to Describe the Experience of SLE Patients Treated With Anifrolumab in the Early Access Programs.

Status
Completed
Phase
Study type
Observational
Enrollment
46 (actual)
Sponsor
AstraZeneca · Industry
Sex
All
Age
18 Years – 130 Years
Healthy volunteers
Not accepted

Summary

The ERYTHRO study is a retrospective medical chart review study of patients in the AMANA and ATUc Early Access Programs (EAPs) across a number of countries, to assess anifrolumab usage and patient experience in treating SLE in a real-world setting. Since patient safety data are already collected and reported according to regulatory requirements through EAPs, this study will not collect safety data.

Detailed description

This is a multi-country, multi-site retrospective chart review study that will use data extracted from the medical charts of SLE patients who participated in the anifrolumab EAPs AMANA or ATUc in France, Germany, Greece, Israel, Italy, Portugal, Spain, and the UK. Patient level data will be captured longitudinally for each patient over a 12- to 18-month period. The study period will include retrospective data collection covering a minimum 6- month baseline period prior to the index date and retrospective data collection covering a minimum 6-month FU period from the first Anifrolumab infusion. The index date is defined as the date of first anifrolumab infusion during the indexing period. The indexing period is between the earliest date of patient enrolment into the EAP and the date of last new patient enrolment into EAP. The EAPs have closed by end of February 2023 in all countries included in the ERYTHRO study. One data extraction will be performed per patient.

Conditions

Interventions

TypeNameDescription
OTHERNone (Observational study)Not applicable since this is observational study.

Timeline

Start date
2023-10-27
Primary completion
2024-06-10
Completion
2024-06-10
First posted
2023-09-21
Last updated
2025-05-13

Locations

15 sites across 7 countries: France, Greece, Israel, Italy, Portugal, Spain, United Kingdom

Source: ClinicalTrials.gov record NCT06046534. Inclusion in this directory is not an endorsement.