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NCT05323591Completed

Prospective Observational Study of Filgotinib in Participants With Rheumatoid Arthritis in France

A Prospective, Non-interventional Study in Patients With Moderate to Severe Active Rheumatoid Arthritis in France Receiving Filgotinib for 2 Years

Source: ClinicalTrials.gov · Last updated 22 May 2026

Brief summary (registry, in English)

An observational study to describe the effectiveness, safety, and patient-reported outcomes (PROs) in participants with moderate to severe active rheumatoid arthritis (RA) in France receiving filgotinib in real-world setting.

Status (registry)
Completed
Study type
Observational
Enrollment
155 (actual)
First submitted
5 Apr 2022
Start date
May 2022
Primary completion date
Mar 2026
Lead sponsor
Alfasigma S.p.A.
NCT number
NCT05323591

What you commit to

  • Study type: Observational
  • Participants enrolled: 155
  • From May 2022 to the primary completion date, Mar 2026
  • 17 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participation in any interventional or non-interventional study without prior approval from the Medical Lead. This does not preclude inclusion of participants enrolled to national registries.

Other

  • Female participant is pregnant or intending to become pregnant while taking filgotinib.

Who the study is looking for

  • Participants aged ≥18 years with a diagnosis of moderate to severe active RA being prescribed filgotinib in accordance with the local treatment practices and product label for the first time.
  • Female participants of childbearing potential must agree to use contraception while taking filgotinib as per product label.
  • Participants must be willing and able to use an electronic device to complete the study PROs.
  • Participant must sign and date the Informed Consent Form (ICF) before enrollment into the study.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (17)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU de Amiens Picardie
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AmiensFranceUnknown status
CHU Amiens Picardie site Nord
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AmiensFranceUnknown status
Hôpital Avicenne - AP-HP
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BobignyFranceUnknown status
CHU Bordeaux
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BordeauxFranceUnknown status
CH de Cahors
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CahorsFranceUnknown status
Clinique De L'infirmerie Protestante De Lyon
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Caluire-et-CuireFranceUnknown status
Hopital Sud Francilien Corbeil Essonne
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Corbeil-EssonnesFranceUnknown status
Hopital Roger Salengro
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LilleFranceUnknown status
CHU de Nice
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NiceFranceUnknown status
Centre Hospitalier Regional d Orleans
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OrléansFranceUnknown status
Hopital Cochin Service A
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ParisFranceUnknown status
Hôpital Saint-Antoine
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ParisFranceUnknown status
Hopital Robert Debré
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ReimsFranceUnknown status
CHU de Rouen
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RouenFranceUnknown status
Centre Hospitalier Universitaire de Saint Etienne
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Saint-EtienneFranceUnknown status
CHU Toulouse
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ToulouseFranceUnknown status
CHRU de Tours
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ToursFranceUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.