drugset / Trial / NCT06568627

A Double Blind Study Performed to Evaluate the Efficacy and the Safety of EscharEx in Debridement of VLU (VALUE)

NCT06568627 ↗

Phase 3 Recruiting 216 enrolled MediWound Ltd
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The main objective of this study is: To assess the efficacy and safety of EscharEx (EX-03 5% formulation) compared to placebo control,in debridement and wound bed preparation of Venous Leg Ulcers (VLU).

Timeline

Start
2025-06-01
Primary completion
2026-12
Completion
2027-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator anacaulase-bcdb Protein / enzyme biologic 5 % Topical

Indications