ASTER: Anifrolumab Study for Treatment Effectiveness in the Real World Multi-National, Observational, Post-Launch Effectiveness Study Among SLE Patients Receiving Anifrolumab in Routine Clinical Practice

Status: Active_not_recruiting
Location: See all (78) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY

Anifrolumab Study of Treatment Effectiveness in the Real World (ASTER) study will collect real world data to obtain a good understanding of the (sustained) clinical effect and patient quality of life outcomes among diagnosed SLE patients who initiate anifrolumab treatment. ASTER will generate critical real-world evidence on the benefits of adding anifrolumab to standard of care treatment for SLE in routine clinical practice, to inform physicians, payers and patients.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 130
Healthy Volunteers: f
View:

• Fulfilled the 2019 EULAR (European League Against Rheumatism)/ACR (American College of Rheumatology) criteria for SLE at the time of study entry.

• Prescribed anifrolumab for their SLE treatment for the first time, according to approved country-specific label.

• The Physician's decision to prescribe anifrolumab must occur prior to any study-related discussion.

• In countries where prescription reimbursements are authorised on a case-by-case basis, authorisation (ie, patient access to treatment) will be required for study entry.

Locations
Other Locations
Austria
Research Site
Innsbruck
Research Site
Linz
Research Site
Vienna
Belgium
Research Site
Aalst
Research Site
Bruges
Research Site
Leuven
Research Site
Liège
Canada
Research Site
Calgary
Research Site
Hamilton
Research Site
Orillia
Research Site
Rimouski
Research Site
Sherbrooke
Research Site
Ste-foy
Research Site
Toronto
Research Site
Winnipeg
France
Research Site
Bordeaux
Research Site
Bouches-du-rh Ne
Research Site
Clermont-ferrand
Research Site
Dijon
Research Site
Finist Re
Research Site
Fort De France Cedex
Research Site
Grenoble
Research Site
Lille
Research Site
Nantes
Research Site
Nice
Research Site
Paris
Research Site
Paris
Research Site
Paris
Research Site
Paris
Research Site
Paris
Research Site
Saint-denis
Research Site
Seine-maritime
Research Site
Strasbourg
Germany
Research Site
Bad Bramstedt
Research Site
Berlin
Research Site
Cologne
Research Site
D Sseldorf
Research Site
Erlangen
Research Site
Greifswald
Research Site
Greifwald
Research Site
Heidelberg
Research Site
Herne
Research Site
Magdeburg
Research Site
Mainz A. Rhein
Research Site
Munich
Research Site
Schleswig-holstein
Israel
Research Site
Afula
Research Site
Haifa
Research Site
Haifa
Research Site
Jerusalem
Research Site
Kfar Saba
Research Site
Ramat Gan
Research Site
Tel Aviv
Research Site
Tel Hashomer
Research Site
Tiberias
Italy
Research Site
Ancona
Research Site
Bari
Research Site
Brescia
Research Site
Cagliari
Research Site
Cona
Research Site
Florence
Research Site
Milan
Research Site
Milan
Research Site
Milan
Research Site
Napoli
Research Site
Pisa
Research Site
Roma
Research Site
Roma
Research Site
Rome
Research Site
Turin
Research Site
Udine
Sweden
Research Site
Danderyd
Research Site
Örebro
Research Site
Stockholm
United Arab Emirates
Research Site
Abu Dhabi
Research Site
Dubai
Research Site
Dubai
Research Site
Sharjah City
Time Frame
Start Date: 2023-02-27
Completion Date: 2030-12-30
Participants
Target number of participants: 551
Treatments
Prospective Cohort
All patients aged ≥18 years diagnosed with SLE who initiate anifrolumab as prescribed by their healthcare provider (HCP) per the approved country-specific label and are treated at the study sites will be eligible for inclusion.
Related Therapeutic Areas
Sponsors
Leads: AstraZeneca
Collaborators: Parexel

This content was sourced from clinicaltrials.gov