Clinical Trials in the EU / 2025-523266-24-00
Authorised, not yet recruiting
Phase II
“A phase 2 multi-center study investigating the efficacy, safety and tolerability of pioglitazone in adult participants with non-segmental vitiligo”
2025-523266-24-00 · tracked via the Priya Life Science EU tracker
Condition studied
Vitiligo
Investigational medicinal product(s)
Pioglitazone Mylan 15 mg compresse
Every trial of Pioglitazone across our registers →
Eligibility
Primary endpoint
- Proportion of subjects achieving F-VASI50 (defined as at least 50% improvement in F-VASI from baseline) at Week 16
Official registry record
This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View 2025-523266-24-00 on CTIS ↗ ← All trials in the EU