Phase 4 Eczema Trial, Recruiting NCT06004986 Sponsor: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) Condition: Eczema
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Phase 4 Eczema Trial, Recruiting

NCT06004986
Recruiting Phase 4

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:

  • People who are adults (18 years of age or older)
  • People who have been diagnosed with atopic eczema (a chronic skin condition that causes itching and inflammation)
  • People who are currently receiving a medication called dupilumab at a dose of 300 mg every two weeks to treat their atopic eczema
  • People whose eczema is considered well-controlled based on a specific set of medical measurements called the Treat-to-Target criteria
  • People who are comfortable with the possibility that their dupilumab dose may be reduced as part of the trial
  • People who have voluntarily signed and dated a consent form before any trial-related procedures take place

Who may not be able to join:

  • People who are currently using, or plan to start using, another medication that affects the immune system (taken as a tablet, injection, or infusion rather than a cream) — whether for atopic eczema or for any other condition

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 19 July 2026
Phase 4 trials study a drug that has already been approved, monitoring long-term safety and effectiveness in real-world use.

Contact this trial

Principal Investigator: Louise AA Gerbens, MD PhD, Amsterdam UMC, location VUmc

Phone: +3120 566 9111

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 4
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Registry
ClinicalTrials.gov
Start date
14 August 2023
Est. completion
1 October 2025

Where this trial is recruiting

🇳🇱 Netherlands

Primary endpoints

Mean EASI

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: 19 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