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NCT03679546CompletedPhase 4

EFFICACI : EFFicacy of Intravenous Infliximab Versus Vedolizumab After Failure of subCutaneous Anti-TNF in Patients With UlCerative Colitis

EFFICACI : EFFicacy of Intravenous Infliximab Versus Vedolizumab After Failure of subCutaneous Anti-TNF in Patients With UlCerative Colitis : A Double Blinded Randomized Clinical Trial

Source: ClinicalTrials.gov · Last updated 24 Jun 2025

Brief summary (registry, in English)

Ulcerative colitis (UC) is a chronic inflammatory bowel disease (IBD) that results from immune dysregulation. Arguably, the development of Tumor Necrosis Factor (TNF) antagonists (including infliximab, adalimumab and golimumab) revolutionized the management of immune-mediated chronic diseases in the past two decades. However, about one third of patients will not respond to a first anti-TNF treatment and 10% to 30% will loose response to anti-TNF during the follow-up. Historically, a switch between anti-TNF was performed to recapture remission and response to anti-TNF. Recently, a new biologic therapy blocking another target has been approved and is now reimbursed during ulcerative colitis, namely vedolizumab. Vedolizumab is an anti-integrin agent avoiding the recruitment of lymphocytes specifically in inflamed gut tissue. Emerging data suggest that a switch of therapeutic class (meaning a change of biologic target with Non-TNF-targeted biologic) in case of clinical failure or insufficient response to anti-TNF may be the best choice. This idea of a switch out of the anti-TNF class is also supported by data on drug monitoring that may help physician decision making in case of loss of response. However, no trial is currently available and ongoing to assess the best therapeutic strategy. The aim of the proposed study is to assess the best biological based strategy in patient losing response to a first subcutaneous anti-TNF (golimumab and/or adalimumab).

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
151 (actual)
First submitted
18 Sept 2018
Start date
4 Jan 2019
Primary completion date
16 Dec 2024
Lead sponsor
Rennes University Hospital
NCT number
NCT03679546
EudraCT number
2018-002673-21

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 151
  • From 4 Jan 2019 to the primary completion date, 16 Dec 2024
  • 19 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.

Who the study is looking for

  • Male or non-pregnant female, non-lactating female;
  • 18 years of age or older and less than 75 years ;
  • Documented diagnosis of UC for at least 6 months ;
  • Left side colitis or pancolitis ;
  • Moderate to severe disease according to a Mayo score equal or above 6 with a Mayo endoscopic sub-score of 2 or 3 ;
  • Active disease despite ongoing treatment with adalimumab or golimumab for at least 12 weeks (inadequate response, failure, loss of response or intolerance) ;
  • Ability of the subject to participate fully in all aspects of this clinical trial ;
  • Written informed consent must be obtained and documented ;
  • Naïve to Janus kinase inhibitor (JAK inhibitor) ;
  • Affiliation to the national health insurance.
    • Non inclusion Criteria:
  • Contraindication to continue TNF antagonist (ongoing abscess(es), clinical suspicion of tuberculosis, past allergic reaction) ;
  • Contraindication to vedolizumab treatment ;
  • Steroid treatment \> 20 mg/day for at least two weeks before baseline ;
  • Proctitis ;
  • Stoma ;
  • Proctocolectomy or subtotal colectomy ;
  • Planned surgery within the year of the trial ;
  • Previous exposure to vedolizumab or infliximab ;
  • History of cancer during the past 5 years ;
  • Pregnancy or breastfeeding
  • Adults legally protected (under judicial protection, guardianship, or supervision), persons deprived of their liberty.
  • Ongoing participation to another interventional study

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (19)

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

SiteCityCountrySite status
Centre Hospitalier Universitaire d'Amiens-Picardie
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AmiensFranceUnknown status
Centre Hospitalier Universitaire de Besançon
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BesançonFranceUnknown status
Centre hospitalier Universitaire de Bordeaux
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BordeauxFranceUnknown status
Centre Hospitalier Universitaire de Caen
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CaenFranceUnknown status
Centre Hospitalier Universitaire de Clermont-Ferrand
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Clermont-FerrandFranceUnknown status
Assistance Publique des Hôpitaux de Paris - Hôpital Beaujon
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ClichyFranceUnknown status
Assistance Publique des Hôpitaux de Paris - Hôpital Henri Mondor
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CréteilFranceUnknown status
Centre Hospitalier Universitaire de Lille
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LilleFranceUnknown status
Hospices Civils de Lyon
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LyonFranceUnknown status
Assistance Publique Des Hopitaux de Marseille
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MarseilleFranceUnknown status
Centre Hospitalier Universitaire de Montpellier
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MontpellierFranceUnknown status
Centre Hospitalier Universitaire De Nancy
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NancyFranceUnknown status
Centre Hospitalier Universitaire de Nantes
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NantesFranceUnknown status
Centre Hospitalier Universitaire de Nice
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NiceFranceUnknown status
Centre Hospitalier Universitaire de Nîmes
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NîmesFranceUnknown status
Assistance Publique des Hôpitaux de Paris - Hôpital Saint-Louis
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ParisFranceUnknown status
Centre Hospitalier De Saint-Brieuc
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Saint-BrieucFranceUnknown status
Centre Hospitalier Universitaire de Saint Etienne
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Saint-EtienneFranceUnknown status
Centre Hospitalier Universitaire de Toulouse
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ToulouseFranceUnknown status

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