Clinical Trial

Effect of YAP1-inhibition in Surgical Wounds.

Not Yet Recruiting Phase 1/2
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Record status
This record was last updated April 25, 2025 (before its estimated April 30, 2026 completion). Its status may not reflect the trial's current state.
Summary
When we get injured, our body naturally tries to heal. In adults, this healing often leads to scars - thick, stiff tissue known as fibrotic tissue. Unlike normal tissue, fibrotic tissue doesn't function properly and can cause serious health problems, depending on the affected organ. Once it forms, fibrosis is usually permanent. A good example of the fibrosis process is the healing of our skin: after a cut or surgery, the resulting scar is a type of fibrosis. Special cells called fibroblasts are key players in this process. Our study looks at a drug called verteporfin, which is already approved both in Europe and the U.S. Previous research on mice and human cells suggests it can reduce or even prevent fibrosis. We are now testing, clinically, histologically and by scRNA-seq, whether injecting verteporfin into the skin during wound healing, specifically after surgical procedures, can prevent thick, rigid scars from forming. Since the skin is easy to observe and sample, it offers a great model for studying this. Will verteporfin have an impact on how surgical wounds heal? That's what we aim to find out.
Trial Details
NCT Number NCT06944249
Lead Sponsor Jöri Pünchera
Collaborators: University of Geneva, Switzerland, University Hospital, Geneva
Conditions Scar Formation
Enrollment 24 participants
Start Date 2025-05-08
Primary Completion 2026-04-30 (estimated)
Study Completion 2026-07-31 (estimated)
Updated on ClinicalTrials.gov 2025-04-25