drugset / Trial / NCT05370235

A Study to Evaluate the Safety and Efficacy of Afamelanotide in Patients With Xeroderma Pigmentosum C and V

NCT05370235 ↗

Phase 2 Unknown 6 enrolled Clinuvel Europe Limited
NaSingle-groupOpen-labelTreatment

Summary

The CUV152 study will evaluate the safety of afamelanotide in XP-C and XP-V patients, as well as the drug's ability to assist reparative processes following ultraviolet (UV) provoked DNA damage of the skin. It will assess whether SCENESSE® increases the amount of UV light needed to cause DNA damage of skin cells, as well as the extent of skin repair before and after treatment.

Timeline

Start
2022-03-28
Primary completion
2024-06
Completion
2024-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Afamelanotide Peptide — Subcutaneous

Indications