Dermacyte® Liquid for Treatment of Cutaneous Ulcers and Wounds
Available (expanded access)
Conditions studied: Cutaneous Ulcer, Diabetic Ulcer, Surgical Wound Dehiscence, Burns - Multiple, Pressure Ulcers, Mixed Ulcer, Ischemic Ulcer
In brief
The objective of this study is to make Dermacyte Liquid available on an expanded access basis to treat cutaneous ulcers and wounds refractory to initial treatment or that do not have adequate alternative treatments. Minimal data will be collected to evaluate the efficacy and safety of Dermacyte Liquid.
Key facts
- Study ID
- NCT06730022
- Run by
- Merakris Therapeutics
- Last updated by the study team
- 2025-02-25
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Must be 18 years of age or older
- Must have a cutaneous ulcer or wound refractory to initial treatment or does not have an adequate treatment alternative, as determined by the Investigator
You may not qualify if…
- Must not be pregnant or lactating
- Must not have known malignancies
- Must not be less than 18 years of age
Where it is running
- The WISH Clinic — Arvada, Colorado, United States
Full record on ClinicalTrials.gov
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