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2025-522216-17-00CompletedPhase 1

A multi-part, adaptive, Phase 1, first time in human study in healthy participants and participants with atopic dermatitis (AD) to assess the safety, tolerability, pharmacokinetics (PK) of single ascending (SAD), multiple ascending doses (MAD) and selected dose of SYX-5219 (AD Participants)

Source: EU CTIS (euclinicaltrials.eu) · Last updated 12 Jun 2026

Next steps

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
28 (actual)
First submitted
7 Jul 2025
Start date
26 Jan 2026
Lead sponsor
Sitryx Therapeutics Limited
EU CT number
2025-522216-17-00

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 28
  • 7 sites in 4 countries
  • 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.

Sites (7)

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

SiteCityCountrySite status
Medical Center Comac Medical Ltd.SofiaBulgariaCompleted
Charite Universitaetsmedizin Berlin KöRBerlinGermanyCompleted
Goethe University FrankfurtFrankfurt Am MainGermanyCompleted
Medical Center- University of FreiburgFreiburg im BreisgauGermanyCompleted
University Medical Center Hamburg-EppendorfHamburgGermanyCompleted
Sanos A/SHerlevDenmarkCompleted
St James's HospitalDublin 8IrelandCompleted

Are you the coordinator? Confirm the details

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