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NCT06568627 · ClinicalTrials.gov registry record · Phase 3
A Double Blind Study Performed to Evaluate the Efficacy and the Safety of EscharEx in Debridement of VLU (VALUE)
A Phase 3 study of Venous Leg Ulcer (VLU), sponsored by MediWound.
- Recruiting
- Registry status
- Phase 3
- Development phase
- 216
- Enrollment target
- 5
- Study locations
NCT06568627 is a Phase 3 study of Venous Leg Ulcer (VLU) that is actively recruiting participants, run by MediWound. The registered enrollment target is 216 participants, roughly in line with the 202-participant average among 6 other Venous Leg Ulcer (VLU) trials with a reported enrollment target. The trial reports 5 study locations across 3 states.
The verdict
NCT06568627, a Phase 3 study of Venous Leg Ulcer (VLU), is actively recruiting participants, sponsored by MediWound.
- RECRUITING
- Registry status
- Phase 3
- Development phase
- 216 participants
- Enrollment target
- 5
- Study locations
Study 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).
Conditions Studied
Interventions
- DRUG EscharEx (EX-03)
- DRUG Placebo (Gel vehicle)
Study Locations (5)
California
- Limb Preservation Platform, Inc - Fresno
- Center for Clinical Research INC - San Francisco
Texas
- JPS Health Network/Acclaim Multispecialty Clinic - Fort Worth
- University of Texas Health Science Center at San Antonio - San Antonio
New York
- Northwell Health Comprehensive Wound Healing Center - Lake Success
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 216 participants |
| Start Date | 2025-06-01 |
| Est. Completion | 2027-03 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06568627
The ClinicalTrials.gov registry entry for NCT06568627 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 216 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 202-participant average among 6 other Venous Leg Ulcer (VLU) trials with a reported enrollment target. The listed sponsor is MediWound, which has 7 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Venous Leg Ulcer (VLU) appearing as the primary indexed condition, and to 2 interventions - of which EscharEx (EX-03) is the first listed.
NCT06568627 reports 5 study locations spanning 3 distinct geographic areas - top geographies include California, Texas, New York.
Frequently Asked Questions
What is clinical trial NCT06568627 about?
NCT06568627 is a clinical study titled "A Double Blind Study Performed to Evaluate the Efficacy and the Safety of EscharEx in Debridement of VLU (VALUE)". 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).
What is the current status of trial NCT06568627?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 216 participants. The study started on 2025-06-01. Estimated completion is 2027-03.
What conditions does trial NCT06568627 study?
This clinical trial studies the following conditions: Venous Leg Ulcer (VLU).
What interventions are being tested in trial NCT06568627?
The interventions under investigation include: EscharEx (EX-03) (DRUG), Placebo (Gel vehicle) (DRUG).
Who is sponsoring clinical trial NCT06568627?
This trial is sponsored by MediWound, which has 7 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06568627 being conducted?
This trial has 5 study locations across California, New York, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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