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NCT06690177 · ClinicalTrials.gov registry record · Phase 2

Clinical Study to Evaluate the Safety and the Efficacy of EscharEx Drug Product (EX-03 Formulation) and Its Placebo Compared to Collagenase, Non-surgical Standard of Care, in Patients With Venous Leg Ulcers

A Phase 2 study, sponsored by MediWound.

Not yet
Registry status
Phase 2
Development phase
45
Enrollment target

NCT06690177: Clinical Trial Phase 2 study, sponsored by MediWound.

NCT06690177 is a Phase 2 study that has not yet begun recruiting, run by MediWound. The registered enrollment target is 45 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (66% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06690177, a Phase 2 study, has not yet begun recruiting, sponsored by MediWound.

NOT YET RECRUITING
Registry status
Phase 2
Development phase
45 participants
Enrollment target

Study Summary

The main objective of this study is: To assess the safety of EscharEx (EX-03 5% formulation) compared to placebo control and compared to Collagenase (NSSOC) in patients with VLU.

Primary Outcome

The endpoint will assess number of patients, in each arm, with reported local (target wound related) AEs

Interventions

  • DRUG EscharEx (EX-03)
  • DRUG Placebo (Gel vehicle)

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2025-04-30
Est. Completion 2028-09-30
Phase Phase 2
MediWound

7 total trials

What is known before NCT06690177 opens enrollment

NCT06690177 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 45 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (66% lower).

The record links to 0 conditions, and to 2 interventions - of which EscharEx (EX-03) is the first listed.

NCT06690177 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06690177 about?

NCT06690177 is a clinical study titled "Clinical Study to Evaluate the Safety and the Efficacy of EscharEx Drug Product (EX-03 Formulation) and Its Placebo Compared to Collagenase, Non-surgical Standard of Care, in Patients With Venous Leg Ulcers". The main objective of this study is: To assess the safety of EscharEx (EX-03 5% formulation) compared to placebo control and compared to Collagenase (NSSOC) in patients with VLU.

What is the current status of trial NCT06690177?

This trial is currently not yet recruiting. It is a Phase 2 study. The enrollment target is 45 participants. The study started on 2025-04-30. Estimated completion is 2028-09-30.

What interventions are being tested in trial NCT06690177?

The interventions under investigation include: EscharEx (EX-03) (DRUG), Placebo (Gel vehicle) (DRUG).

Who is sponsoring clinical trial NCT06690177?

This trial is sponsored by MediWound, which has 7 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06690177's enrollment target sits among peer trials

45 1296th of 2000 higher than 679 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06690177, the US trial registry maintained by the National Library of Medicine. NCT06690177 (small enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.