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A Clinical Study of the Safety and Efficacy of MEBO Wound Ointment in Subjects With Venous Leg Ulcers

2014-07-23 21:08:52 | BioPortfolio

Summary

This is a Phase II, randomized, controlled, two-center pilot study designed to assess the safety and efficacy of MEBO in the treatment of 14 subjects with VLUs. Subjects meeting entry criteria will be randomly assigned in a 1:1 ratio for up to 8 weeks of treatment with either MEBO or SOC (7 subjects per treatment arm).

Study Design

Allocation: Randomized, Control: Active Control, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Conditions

Ulcers

Intervention

MEBO Wound Ointment (MEBO), Standard of Care

Location

University of California San Diego Medical Center
San Diego
California
United States
92106

Status

Not yet recruiting

Source

Skingenix, Inc.

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-07-23T21:08:52-0400

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