MediWound's EscharEx® Outshines Collagenase in Healing Trials
Breakthrough Findings in Chronic Wound Treatment
Recently, MediWound Ltd. (Nasdaq: MDWD), a leader in enzymatic therapies, has achieved a significant milestone with the publication of critical trial data on EscharEx®, a topical treatment specifically designed for challenging venous leg ulcers (VLUs). This research highlights EscharEx®'s considerable efficacy compared to collagenase ointment, commonly known as SANTYL.
Key Insights from the Latest Study
The peer-reviewed analysis, published in the journal Wounds, stems from the Phase II ChronEx clinical trial focusing on VLUs, which affect a substantial number of individuals worldwide. It provides compelling evidence on how EscharEx® performs in wound debridement, a crucial step in healing such ulcers. The analysis examined two groups of patients: those treated with SANTYL and others with EscharEx®, with the findings highlighting several promising results.
Comparative Efficacy
Among the key findings, debridement efficacy stood out vividly. The data revealed that:
- Complete Debridement: A remarkable 63% of patients receiving EscharEx® achieved complete debridement within two weeks, whereas none in the SANTYL group reached this goal.
- Median Time to Debridement: Patients treated with EscharEx® experienced faster debridement, taking only 9 days, compared to SANTYL, which was not able to achieve debridement within the study duration.
Wound Bed Preparation Results
Wound bed preparation (WBP), involving both complete debridement and granulation, was assessed, revealing:
- Within the two-week timeframe, 50% of EscharEx® cases reached WBP, while the SANTYL group saw 0%.
- Extending over the entire 12-week study, the proportion of EscharEx® patients achieving WBP increased to 78%, contrasting with 38% for those using SANTYL.
Closure Rates and Timeframes
When examining closure rates, findings suggested:
- Closure was attained in 33% of EscharEx® patients, compared to 25% for those on SANTYL.
- Among those who achieved closure, the average time needed was significantly shorter for EscharEx® at 48 days, in comparison to 76 days for the counterpart treatment.
Safety and Tolerability
As safety remains a priority in treatment selections, the trial demonstrated:
- Adverse events occurred at similar rates for both EscharEx® and SANTYL, bagging positive notes on tolerability.
- Deep wound infections were notably lower in the EscharEx® group, recorded at 11%, while 38% in the SANTYL group experienced complications.
About EscharEx®
EscharEx® is an innovative bromelain-based therapy currently undergoing advanced clinical development, demonstrating a strong safety profile and effective outcomes in multiple trials. Designed for easy topical application, it effectively addresses the removal of non-viable tissue, supporting the promotion of granulation tissue and reducing bioburden, setting the stage for comprehensive wound management.
MediWound Ltd.'s Vision
As a prominent biotechnology enterprise, MediWound Ltd. continues to focus on pioneering enzymatic interventions for non-surgical tissue repair. Apart from EscharEx®, the company is also known for NexoBrid®, an FDA-approved biologic aimed at treatment in severe burn cases. With ongoing trials of EscharEx® and a progressive approach to chronic wound treatment, MediWound looks forward to making substantial advancements in the field.
Frequently Asked Questions
What is EscharEx®?
EscharEx® is a bromelain-based enzymatic therapy intended for the debridement of chronic and hard-to-heal wounds, notably venous leg ulcers.
How does EscharEx® compare to SANTYL?
The recent data revealed that EscharEx® demonstrates superior efficacy in debridement speed, wound bed preparation, and safety profiles compared to SANTYL.
Who conducted the trial for EscharEx®?
The peer-reviewed study was part of the Phase II ChronEx trial conducted by MediWound, assessing its effectiveness against collagenase treatments.
What are the safety findings for EscharEx®?
EscharEx® exhibited a favorable safety profile, with a lower incidence of deep wound infections compared to the SANTYL group.
Is there a market for EscharEx®?
Yes, EscharEx® targets a significant global market for chronic wound treatments, exhibiting promising clinical advantages that set it apart in the field.
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