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Phase 2 clinical trial to evaluate the efficacy and safety of zasocitinib in participants with non-segmental vitiligo

Status
In recruitment
headquarters
Madrid
Early phase

Technical Summary

  • A PHASE 2, MULTICENTER, RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND, DOSE-RANGING TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF ZASOCITINIB IN PARTICIPANTS WITH NON-SEGMENTAL VITILIGO
  • Code EudraCT: 2025-522309-40
  • Protocol number: TAK-279-VT-2001
  • Promoter: Takeda Pharmaceuticals International Co.
  • Molecule/Drug: zasocitinib

* The trials only admit a limited number of patients and are subject to inclusion and exclusion criteria. The specialist who assesses your case will inform you of the conditions required to participate in the clinical trial.

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