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
- Diseases
- Ankylosing spondylitis
- 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
Sites (35)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU d Angers Coordinator of this site? Confirm its status | Angers | France | Unknown status |
| Chru Besancon Coordinator of this site? Confirm its status | Besançon | France | Unknown status |
| APHP - Hôpital Avicenne Coordinator of this site? Confirm its status | Bobigny | France | Unknown status |
| CHU Bordeaux Coordinator of this site? Confirm its status | Bordeau | France | Unknown status |
| CHRU Brest Coordinator of this site? Confirm its status | Brest | France | Unknown status |
| CHU Clermont-Ferrand Coordinator of this site? Confirm its status | Clermont-Ferrand | France | Unknown status |
| CHU de GRENOBLE ALPES Coordinator of this site? Confirm its status | Grenoble | France | Unknown status |
| CHD Vendée Coordinator of this site? Confirm its status | La Roche-sur-Yon | France | Unknown status |
| CH Le Mans Coordinator of this site? Confirm its status | Le Mans | France | Unknown status |
| CHRU Lille Coordinator of this site? Confirm its status | Lille | France | Unknown status |
| Hopital Saint Philibert Coordinator of this site? Confirm its status | Lomme | France | Unknown status |
| Hopital Edouard Herriot Coordinator of this site? Confirm its status | Lyon | France | Unknown status |
| CH Lyon Sud Coordinator of this site? Confirm its status | Lyon | France | Unknown status |
| CHU Montpellier - 2 - Unité Clinique thérapeutique des Maladies Ostéo-Articulaires Coordinator of this site? Confirm its status | Montpellier | France | Unknown status |
| CHRU Montpellier Coordinator of this site? Confirm its status | Montpellier | France | Unknown status |
| CHU Nancy Coordinator of this site? Confirm its status | Nancy | France | Unknown status |
| CHU de Nantes Coordinator of this site? Confirm its status | Nantes | France | Unknown status |
| CHU de Nice Coordinator of this site? Confirm its status | Nice | France | Unknown status |
| CHR d'Orléans Coordinator of this site? Confirm its status | Orléans | France | Unknown status |
| Aphp - Hopital Bichat Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| APHP - Kremlin-Bicêtre Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| Aphp - Hopital Pitie Salpetriere Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| APHP - Hôpital Saint Antoine Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| APHP - Hôpital Henri Mondor Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| APHP - Hôpital Ambroise Paré Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| Aphp-Hopital Lariboisiere Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| APHP - Hôpital Cochin Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| CHU de Poitiers Coordinator of this site? Confirm its status | Poitiers | France | Unknown status |
| CHU Reims Coordinator of this site? Confirm its status | Reims | France | Unknown status |
| CHU de Rouen Coordinator of this site? Confirm its status | Rouen | France | Unknown status |
| CHU Saint-Etienne Coordinator of this site? Confirm its status | Saint-Etienne | France | Unknown status |
| CHU Strasbourg-Hautepierre Coordinator of this site? Confirm its status | Strasbourg | France | Unknown status |
| CHU Toulouse Coordinator of this site? Confirm its status | Toulouse | France | Unknown status |
| CHRU Tours Coordinator of this site? Confirm its status | Tours | France | Unknown status |
| CH Princesse de Grace Coordinator of this site? Confirm its status | Monaco | Monaco | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.