EscharEx

Enzymatic Therapeutic for
Non-Surgical Tissue Repair

EscharEx®

Plastic ampule NO Shadow(2)
Next-Generation Enzymatic Therapy Candidate for Wound Care
Indication: Debridement of chronic/hard-to-heal wounds
Classification: Biological drug
Target Audience: Patients in all wound care settings
Status: Phase 3 in VLU ongoing; DFU trial planned for H2 2026

How to Use

EscharEx® is a bromelain-based, bioactive enzymatic therapy in advanced clinical development for the debridement of chronic and hard-to-heal wounds. Designed for topical, once-daily application, EscharEx has demonstrated a favorable safety profile and effective wound bed preparation in multiple Phase II trials. The therapy has shown the ability to remove non-viable tissue, promote granulation tissue, and reduce bioburden and biofilm. A global Phase III study in venous leg ulcers (VLUs) is currently underway, and a clinical study in diabetic foot ulcers (DFUs) is in preparation. EscharEx has shown clinical advantages over the leading enzymatic debridement product and targets a substantial global market opportunity.

EscharEx®

Let's Talk Numbers
Clinical Trials
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Strategic Partners
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Potential U.S. Patients
0 Million
Publications
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U.S. TAM
$ 0 Billion+

Phase 2 ChronEx Trial Data

Clinical Sites
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Patients
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EscharEx® development is being supported in part by the European Innovation Council (EIC) through its accelerator program for the indication of diabetic foot ulcers.