Phase 2 Uveitis Trial, Recruiting NCT06285539 Sponsor: UMC Utrecht Condition: Uveitis
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Phase 2 Uveitis Trial, Recruiting

NCT06285539
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are 18 years of age or older (but under 65)
  • You have been diagnosed with one of the following rare inflammatory conditions, with active disease:
  • Behçet's disease that does not currently involve life-, organ-, or sight-threatening symptoms, but is considered active based on a standard scoring system or your doctor's assessment (e.g., you need new or additional medication)
  • Dermatomyositis or anti-synthetase syndrome (types of inflammatory muscle disease), confirmed by recognised diagnostic guidelines, with signs of active disease shown by specific blood test results, a muscle scan done within the last 3 months, or your doctor's clinical judgement
  • IgG4-related disease, diagnosed using 2019 international guidelines, with active disease shown by a standard scoring tool or your doctor's assessment
  • Your condition has not responded well to at least 12 weeks of steroid treatment, plus at least one other immune-suppressing medication (such as methotrexate, azathioprine, mycophenolate mofetil, or rituximab), or you are unable to tolerate standard treatments
  • You have no signs of active or latent tuberculosis (TB), confirmed by two negative TB tests done within the past 3 months, a clear chest X-ray, and no history of untreated TB

Who may not be able to join:

  • You are under 18 or 65 years of age or older
  • Your life expectancy is less than 6 months
  • You have a specific type of myositis such as juvenile dermatomyositis, myositis linked to another autoimmune disease, immune-mediated necrotising myopathy, inclusion-body myositis, or cancer-related myositis
  • Your muscle weakness is thought to be due to permanent muscle damage rather than active inflammation
  • You have a significantly increased risk of major heart or blood vessel problems
  • You are a current smoker or have a long history of smoking
  • You are pregnant or breastfeeding
  • You have previously used a type of medication called a JAK inhibitor
  • You have taken an experimental drug within the past month (or longer, depending on the drug)
  • You have HIV infection
  • You have an active infection, or hepatitis B or C
  • You have a history of shingles or repeated herpes simplex infections
  • You have been diagnosed with cancer in the last 5 years (with some exceptions for certain minor skin cancers)
  • You are considered at increased risk of developing cancer
  • Your kidneys are functioning at a very low level (confirm with trial site)
  • You have severe liver failure (confirm with trial site)
  • Your blood counts (white cells, neutrophils, or haemoglobin) are below certain levels (confirm with trial site)
  • You are unable or unlikely to follow the study procedures and attend follow-up appointments
  • You have a known recent history of alcohol or drug misuse
  • You have difficulty with blood draws or poor vein access for the blood tests required during the study
  • You have previously not taken immunosuppressant medications as prescribed
  • You are allergic to the study drug or any of its ingredients
  • You have a rare inherited condition affecting how your body processes certain sugars, such as galactose intolerance, lactase deficiency, or glucose-galactose malabsorption

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Jaap M van Laar, Prof. dr., UMC Utrecht

Phone: +887550459

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
UMC Utrecht
Registry
ClinicalTrials.gov
Start date
12 March 2024
Est. completion
1 December 2026

Where this trial is recruiting

🇳🇱 Netherlands

Primary endpoints

EQ-5D-5L; Disease activity in Behcet's patients; Disease activity in myositis patients; Disease activity in IgG4-RD patients

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov