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Clinical Trial Summary

This is a three-part, Phase I, first-in-human study designed to evaluate the safety, tolerability, and potential systemic exposure of multiple topical doses of TCP-25. Part I includes healthy volunteers with acute epidermal wounds formed by the suction blister technique. Part II includes patients with non-healing leg ulcers and Part III patients with dystrophic epidermolysis bullosa (DEB).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05378997
Study type Interventional
Source Xinnate AB
Contact
Status Completed
Phase Phase 1
Start date April 7, 2022
Completion date March 16, 2024

See also
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