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2024-510746-14-00Active, not recruitingPhase 4

DAPHNE

Detailed assessment of axial and peripheral entheses and joints in axial spondyloarthritis and psoriatic arthritis patients treated with ixekizumab – a 2-year study applying whole-body MRI, MRI-based synthetic CT, and CT

Source: EU CTIS (euclinicaltrials.eu) · Last updated 19 Feb 2026

Next steps

Brief summary (registry, in English)

To assess the effect of ixekizumab (IXE) on the total inflammatory burden in the entire body (peripheral and axial joints and entheses) of patients with axSpA and PsA, as assessed by WB-MRI

Status (registry)
Active, not recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
65 (estimated)
First submitted
19 Jan 2024
Start date
28 Aug 2024
Lead sponsor
Rigshospitalet
EU CT number
2024-510746-14-00

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 65
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Contraindications for ixekizumab. • Contraindication for MRI. • Previous exposure to ixekizumab or other biologic drug directly targeting IL-17 or IL-17 receptor • Has received more than 1 prior anti-TNF inhibitor • Previous exposure to other types of bDMARDs than TNF inhibitor. • Active inflammatory bowel disease • DMARDs are allowed during the study, but the dose cannot be changed from 1 month before the first MRI. • Use of any investigational drug and/or devices within 1 month before randomization or a period of 5 half-lives of the investigational drug, whichever is longer. • Any use of oral, intravenous, intra-articular, or intra-muscular corticosteroids within 1 month before the baseline MRI. • Pregnant or nursing (lactating) women. • Known recent drug or alcohol abuse. • Known severe psychiatric disease. • Incapable of complying with the examination program for physical or mental reasons. • Unable to speak, read, or understand Danish.

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

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (4)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Frederiksberg HospitalFrederiksbergDenmarkActive, not recruiting
RigshospitaletGlostrupDenmarkActive, not recruiting
Gentofte HospitalHellerupDenmarkActive, not recruiting
Slagelse HospitalSlagelseDenmarkActive, not recruiting

Are you the coordinator? Confirm the details

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