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NCT03445845CompletedPhase 4

Rotation or Change of Biotherapy After TNF Blocker Treatment Failure for Axial Spondyloarthritis

Source: ClinicalTrials.gov · Last updated 18 Nov 2024

Brief summary (registry, in English)

Axial spondyloarthritis (axSpA) is a chronic inflammatory disease characterized by inflammatory arthritis and enthesitis involving the spine. AxSpA prevalence is around 0.17% of the French population. Tumor necrosis factor (TNF) was the first target defined in axSpA. Since one third of axSpA patients failed to the first TNF blocker, many axSpA patients received a second biological Disease-Modifying AntiRheumatic Drugs (bDMARDs). Until few months, the only choice was to use a second TNF blocker.Since 2003, pharmaceutical companies investigated efficacy of TNF blockers already used in rheumatoid arthritis. Etanercept is a fusion protein with TNF receptor type II p75 and IgG1 Fc fragment, whereas adalimumab, infliximab, and golimumab are monoclonal antibodies. Certolizumab is a fusion between a fab fragment targeting TNF and a Peg fraction. All demonstrated efficacy versus placebo in a randomized double blinded study In case of failure to the first TNF blockers, rheumatologists will follow the "Treat-to-Target" principle. This approach already demonstrated its benefit in rheumatoid arthritis or in psoriatic arthritis. This concept was also suggested for axSpA with low levels of evidence and recommendation. So rheumatologist will provide the best treatment in case of failure to the first TNF blockers, which is a daily clinical situation. Since few months, rheumatologists have the choice between targeting IL-23/17 axis compared to a second TNF blocker.

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
300 (actual)
First submitted
20 Feb 2018
Start date
14 Dec 2018
Primary completion date
21 Sept 2024
Lead sponsor
Centre Hospitalier Universitaire de Saint Etienne
NCT number
NCT03445845
EudraCT number
2017-004700-22

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 300
  • From 14 Dec 2018 to the primary completion date, 21 Sept 2024
  • 35 sites in 2 countries
  • 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.

Other illness

  • Inflammatory bowel diseases
  • Existing pregnancy, lactation, or intended pregnancy within the next 15 months Active tuberculosis or other severe infections such as sepsis or opportunistic infections
  • Active infections, including chronic or localised infections.
  • Moderate to severe heart failure (NYHA classes III/IV)

Other

  • Any contra-indication to TNF blocker and/or secukinumab
  • Impossibility to give informed consent
  • Impossibility to be followed for 12 months

Who the study is looking for

  • Active axSPA with BASDAI\>4 or ASDAS\>3.5, who need change in TNF blocker treatment
  • Aged over 18 years
  • Inadequate response after at least 3 months to the 1st TNF blocker
  • If non biologic DMARD treatment : stable dose for at least on month before inclusion
  • If oral corticosteroids treatment : stable dose for at least on month before inclusion
  • If NSAIDs treatment : stable dose for at least on month before inclusion
  • Ability to complete questionnaires
  • Social security affiliation
  • Informed written consent given

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

Full criteria on ClinicalTrials.gov

Sites (35)

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

SiteCityCountrySite status
CHU d Angers
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AngersFranceUnknown status
Chru Besancon
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BesançonFranceUnknown status
APHP - Hôpital Avicenne
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BobignyFranceUnknown status
CHU Bordeaux
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BordeauFranceUnknown status
CHRU Brest
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BrestFranceUnknown status
CHU Clermont-Ferrand
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Clermont-FerrandFranceUnknown status
CHU de GRENOBLE ALPES
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GrenobleFranceUnknown status
CHD Vendée
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La Roche-sur-YonFranceUnknown status
CH Le Mans
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Le MansFranceUnknown status
CHRU Lille
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LilleFranceUnknown status
Hopital Saint Philibert
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LommeFranceUnknown status
Hopital Edouard Herriot
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LyonFranceUnknown status
CH Lyon Sud
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LyonFranceUnknown status
CHU Montpellier - 2 - Unité Clinique thérapeutique des Maladies Ostéo-Articulaires
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MontpellierFranceUnknown status
CHRU Montpellier
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MontpellierFranceUnknown status
CHU Nancy
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NancyFranceUnknown status
CHU de Nantes
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NantesFranceUnknown status
CHU de Nice
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NiceFranceUnknown status
CHR d'Orléans
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OrléansFranceUnknown status
Aphp - Hopital Bichat
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ParisFranceUnknown status
APHP - Kremlin-Bicêtre
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ParisFranceUnknown status
Aphp - Hopital Pitie Salpetriere
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ParisFranceUnknown status
APHP - Hôpital Saint Antoine
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ParisFranceUnknown status
APHP - Hôpital Henri Mondor
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ParisFranceUnknown status
APHP - Hôpital Ambroise Paré
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ParisFranceUnknown status
Aphp-Hopital Lariboisiere
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ParisFranceUnknown status
APHP - Hôpital Cochin
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ParisFranceUnknown status
CHU de Poitiers
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PoitiersFranceUnknown status
CHU Reims
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ReimsFranceUnknown status
CHU de Rouen
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RouenFranceUnknown status
CHU Saint-Etienne
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Saint-EtienneFranceUnknown status
CHU Strasbourg-Hautepierre
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StrasbourgFranceUnknown status
CHU Toulouse
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ToulouseFranceUnknown status
CHRU Tours
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ToursFranceUnknown status
CH Princesse de Grace
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MonacoMonacoUnknown status

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