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NCT04340076CompletedPhase 4

Dose Reduction of IL17 and IL23 Inhibitors in Psoriasis

Dose Reduction of the New Generation Biologicals (IL17 and IL23 Inhibitors) in Psoriasis: A Pragmatic, Multicentre, Randomized, Controlled, Non-inferiority Study - BeNeBio Study

Source: ClinicalTrials.gov · Last updated 17 Mar 2026

Brief summary (registry, in English)

The main objective of this study is to investigate whether controlled dose reduction of IL17 or IL23 inhibiting biologics is not inferior compared to usual care in psoriasis patients. Therefore, a pragmatic, multicentre, randomized, controlled, non-inferiority study will be carried out.

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
244 (actual)
First submitted
20 Mar 2020
Start date
20 Aug 2020
Primary completion date
30 Jan 2025
Lead sponsor
Radboud University Medical Center
Diseases
Psoriasis
NCT number
NCT04340076
EudraCT number
2019-004230-42

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 244
  • From 20 Aug 2020 to the primary completion date, 30 Jan 2025
  • 19 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.

Prior treatment

  • Concomitant use of systemic immunosuppressants other than methotrexate or acitretin (e.g. prednisone, cyclosporine etc).

Other

  • Another indication than plaque psoriasis as the main indication for biologic use (e.g. patient receives biologic for rheumatoid arthritis as the main indication).
  • Severe comorbidities with short life-expectancy (e.g. metastasized tumor).
  • Presumed inability to follow the study protocol.

Who the study is looking for

  • Plaque psoriasis (primarily)
  • Treatment for at least 6 months with IL23 or IL17 inhibitor in a normal dose (dose advised by the label)
  • PASI≤ 5 at inclusion and in previous 6 months (if no PASI scores are available, it should be clear from the patient record that psoriasis was clear/almost clear in previous 6 months).
  • DLQI ≤ 5 at inclusion

Age in the registry: 18 years to - · 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
ULB Erasme
Coordinator of this site? Confirm its status
BrusselsBelgiumUnknown status
AZ Maria Middelares
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GhentBelgiumUnknown status
AZ St. Lucas
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GhentBelgiumUnknown status
Ghent university hospital
Coordinator of this site? Confirm its status
GhentBelgiumUnknown status
UCL Saint Luc
Coordinator of this site? Confirm its status
LeuvenBelgiumUnknown status
UZ Leuven
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LeuvenBelgiumUnknown status
CHU Liège
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LiègeBelgiumUnknown status
Dermatologie Maldegem
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MaldegemBelgiumUnknown status
Ziekenhuisgroep Twente
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AlmeloNetherlandsUnknown status
Bravis hospital
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Bergen op ZoomNetherlandsUnknown status
Amphia Hospital
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BredaNetherlandsUnknown status
Slingeland Hospital
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DoetinchemNetherlandsUnknown status
Catharina hospital
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EindhovenNetherlandsUnknown status
UMC Groningen
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GroningenNetherlandsUnknown status
Maastricht UMC
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MaastrichtNetherlandsUnknown status
Radboudumc
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NijmegenNetherlandsUnknown status
Erasmus MC
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RotterdamNetherlandsUnknown status
UMC Utrecht
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UtrechtNetherlandsUnknown status
Maxima Medisch Centrum
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VeldhovenNetherlandsUnknown status

Related publications

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